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Article

Survey on the Traditional Use of Medicinal Herbs in Haiti: A Study on Knowledge, Practices, and Efficacy Prevention

by
Valendy Thesnor
1,2,3,
Yvens Cheremond
2,
Muriel Sylvestre
1,
Patrick Meffre
3,
Gerardo Cebrián-Torrejón
1,*,† and
Zohra Benfodda
3,*,†
1
COVACHIM-M2E Laboratory EA 3592, Department of Chemistry, Université des Antilles, UFR SEN, Fouillole Campus, Cedex, 97157 Pointe-a-Pitre, France
2
URE, Université d’État d’Haïti, Port-au-Prince HT6110, Haiti
3
UPR CHROME, University Nimes, cedex 1, 30021 Nimes, France
*
Authors to whom correspondence should be addressed.
These authors contributed equally to this work.
Plants 2024, 13(17), 2383; https://doi.org/10.3390/plants13172383
Submission received: 11 July 2024 / Revised: 1 August 2024 / Accepted: 6 August 2024 / Published: 26 August 2024

Abstract

:
The use of medicinal herbs is highly developed in Haiti. However, there is a significant lack of knowledge in the literature on medicinal plants and their uses. The objective of this study was to determine the knowledge and practices of Haitian families for the prevention/treatment of COVID-19, influenza, and respiratory diseases, as well as the mode of preparation and administration of the plants. Individuals were interviewed using the TRAMIL questionnaire as the information holder. The data obtained were analyzed by calculating 5 indices (relative frequency of citation, use value, the family use value, informant consensus factor, and fidelity level). The study surveyed 120 Haitians and collected 75 plants from 43 botanical families. The botanical family most used for all these preventions and remedies is the Lamiaceae. The highest ranked species with a relative frequency of citation value > 0.3. Infusion, decoction, and in the form of punch are the methods used for the remedies. The study found that the use of herbal remedies is still prevalent in the study area, and many of the commonly used plants have been scientifically validated. However, some plants, such as Samyda rosea Sims, lack sufficient research and are recommended for further investigation.

1. Introduction

The use of traditional plant-based medicine in Haiti and the Caribbean comes from a combination of African, European, and Indigenous cultural influences, first during the colonial period, which was influenced by the medical conceptions prevailing in Europe from the 16th to the 19th century through the practice of medicine leaves, and second, during the slave period, through African heritage: under the weight of a hard life, the Black slaves tried to cure their ills by resorting to their own knowledge of African medicinal plants for which they found substitutes of American origin or species adapted from their native lands [1]. This knowledge is based on empirical observations but has repeatedly proven its accuracy [2].
In Haiti, the use of medicinal plants is highly developed as the majority of the population uses them, mainly in rural areas but also in the cities [1]. Traditional medicine is often used in Haiti due to its accessibility and affordability compared to conventional drugs, as well as its potential for fewer side effects and a wider range of plant species to choose from for medicinal purposes [1,3]. The use of plants with healing properties is as old as human civilization. According to WHO, in 2008, nearly 80% of the world’s population currently relied on herbal medicines for their primary healthcare needs [4]. Natural products play a dominant role in the discovery of leads for the development of drugs for the treatment of human diseases [5]. Moreover, the effectiveness of medicinal plants used as traditional treatment has been proven by scientific studies [6,7]. Literature data show that several plant extracts, commonly used for the treatment of infectious diseases such as influenza and cold illnesses, demonstrate antiviral, anti-influenza, antibacterial, and anti-inflammatory activities [8,9,10,11,12]. Those infectious diseases are caused by pathogens (bacteria, viruses, parasites, and fungi) and are spread, directly or indirectly, from one person to another [13]. An example of a recent disease is coronavirus 2019 (COVID-19), also known as Coronavirus Disease 2019, a new pandemic resulting from severe acute respiratory syndrome Coronavirus 2 (SARS-CoV-2), which was first reported in late 2019 in Wuhan, China [14,15,16]. Human-to-human contamination is the main mode of transmission of COVID-19 through droplets generated by breathing, sneezing, and coughing [17,18], just like the influenza/cold virus. Other forms of contamination are also possible, such as airborne from infectious aerosols [19,20], contact with an infected surface, and environments in which we live and work [21]. The most common signs and symptoms are fever, cough, myalgia or fatigue and shortness of breath [22], dysfunction of smell and taste [23]. Other symptoms are reported as diarrhea, vomiting, or abdominal pain [24] and also psychological problems such as anxiety and depressive symptoms [25]. COVID-19 has disrupted the lives of many people around the world and has had a huge effect on the health, economy, environment, and social sectors [26]. At this time, there is no specific treatment for the SARS-CoV-2 virus that causes COVID-19.
In Haiti, where conventional health systems are not very accessible, treating oneself with plants is the patient’s first resort [3]. Due to the traditional plant knowledge of Haitians, the following study was conducted in the western department of Haiti between July and September 2021 to obtain data on the types of plants used for the treatment and/or prevention of these diseases: influenza, colds, COVID-19, and respiratory diseases (Figure 1). Ethnopharmacological information has an undeniable value of its own as it not only preserves age-old tradition but also effectively guides modern research on bioactive ingredients [27].
In this study, we delved into the realm of Haitian folklore medicine. Using a TRAMIL (Program of Applied Research to Popular Medicine in the Caribbean) inspired methodology, we conducted an ethnobotanical survey through face-to-face interviews and telephone conversations. Our research meticulously documented the local use of medicinal plants in Haiti, underscoring their crucial role in community healthcare. We carried out a comprehensive analysis comparing the use of these plants in treating various infectious diseases. Moreover, we evaluated several ethnobotanical indices to gain a deeper understanding of the cultural and medicinal significance of these plants. This investigation aims to pave the way for the scientific community to explore new antiviral strategies and for the local community to enhance their traditional medicine practices.

2. Results

2.1. Profile of Medicinal Plant Users

A total of 120 families were interviewed in this study, with one member in each family. Each person in the survey represents a household in general, meaning that several members of the same household are not represented in the survey as multiple different participants, but rather, they are considered to be one respondent for each household. In other words, the survey is designed to capture the opinions and behaviors of households as a unit rather than individual family members separately. Therefore, if multiple members of a household participated in the survey, their responses would be aggregated and considered to be one for that particular household. The representatives of the 120 families were 81.67% (98/120) female and 18.33% (22/120) male. A total of 81% of the respondents were women in our survey because, in Haiti, women appear to be better informed than men [3]. They were all adults between the ages of 18 and 70 years, with an average age of 39 years (Table 1). They were all Haitians living in Haiti. Families living in Delmas represent 35.83% (43/120), those living in Port-au-Prince represent 16.67% (20/120), those living in Pétion-Ville represent 16.67% (20/120), those living in Tabarre represent 8.33% (10/120), those living in Croix-des-Bouquets represent 8.33% (10/120), those living in Léogâne represent 5% (6/120), those living in Gressier represent 5% (6/120) and those living in Carrefour represent 4.17% (5/120).

2.2. Plant Families and Remedies

The plants collected represent 75 plants divided into 43 botanical families. The 120 Haitians participants who were interviewed mentioned a total of 149 remedies for flu/cold, respiratory diseases, and COVID-19. Each family participating in the survey could use more than one remedy for a given condition.
The botanical families most used for all these preventions and remedies are the Lamiaceae (Table 2), with 8 plant species (9.39% were mentioned to fight respiratory diseases, 57.14% flu and cold, and 33.47% to fight COVID-19), the Rutaceae with 5 plant species (8.13% used against respiratory diseases, 51.20% against flu and cold and 40.67% against COVID-19), the Amaryllidaceae with 2 plant species (0.88% used against respiratory diseases, 25.66% against flu and cold and 73.45% against COVID-19), Asteraceae with 3 plant species (5.5% used against respiratory diseases, 49.54% against flu and cold and 44.95% against COVID-19), Zingiberaceae with 2 plant species (10.68% used against respiratory diseases, 11.65% against flu and cold and 77.67% against COVID-19), Myrtaceae with 2 plant species (25% used against respiratory diseases, 21% against flu and cold and 54% against COVID-19) and Curcubitaceae with 1 plant species (7.61% against flu and cold and 92.39% against COVID-19). The highest ranked species with an RFC value > 0.3 (Table 3) is the Zingiber officinale Roscoe (0.79), Mormordica charantia L. (0.76), Aloe vera L. (0.53), Allium cepa L. (0.51), Syzygium aromaticum L. (0.51), Samyda rosea Sims (0.51), Citrus aurantiifolia (Christm.) Swingle (0.49), Allium sativum L. (0.43), Eupatorium odoratum L. (0.42), Cinnamomum verum J. S. Presl (0.41), Citrus aurantium L. (0.39), Artemisia vulgaris L. (0.39), Phyllanthus niruri L. (0.33), Cymbopogon citratus (DC.) Stapf. (0.32), Malpighia emarginata Dc (0.32), Mentha nemorosa wild. (0.32) Citrus sinensis L. (0.31) and Citrus maxima Merr. (0.31). The results showed the ICF values of the 3 conditions mentioned by the families in the study. Flu/cold (0.97) and COVID-19 (0.96) had the highest ICF values, followed by respiratory diseases (0.91). These high ICF values for the different ailments could indicate that they were common, that there is agreement on the need to treat these diseases, and that there is common knowledge among local people using herbal medicines. The highest UV values for each chosen category have functions of a UV value ≥ 0.1. For the plants used against COVID-19 the most important (Figure 2) were Mormordica charantia L. (0.71), Zingiber officinale Roscoe (0.6), Aloe vera L. (0.53), Syzygium aromaticum L. (0.42), Allium sativum L. (0.41), Artemisia (0.39) and Phyllanthus niruri L. (0.33). For influenza and cold the most important (Figure 3) were Samyda rosea Sims or Samyda dodecandra Jacq (0.49), Eupatorium odoratum L. (0.35), Malpighia emarginata DC. (0.29), Mentha nemorosa wild (0.28), Citrus aurantium L. (0.28), Hibiscus rosa-sinensis L. (0.28), and Citrus aurantiifolia (Christm.) Swingle (0.26) and for respiratory diseases the most important were Eucalyptus globulus Labill. (0.13) and Ricinus communis L. (1.13).

2.3. Plants, Remedies, and Methods of Administration

A total of 149 remedies were reported for 75 plants, with 16 used for respiratory diseases, 53 for COVID-19, and 55 for flu and/or colds. Traditional preparations included decoctions and infusions (63.33%), punch (16%), inhalation (9.67%), fruit/leaf juice (8.67%), and baths and massage (2.33%).
Infusion is the most preferable method of preparation for the softer parts, such as flowers and leaves, because the plant part does not boil with water [28]. Examples of flu remedies are the flowers and leaves of Moringa oleifera L. and the flowers of Hibiscus rosa-sinensis L., the latter given mainly to children by most of the families interviewed. The harder parts, such as roots, rhizomes, underground parts, seeds, and fruits, are proposed to be prepared in decoction because boiling with water extracts the maximum of bioactive compounds. We have as an example the Cymbopogon citratus (DC) Stapf. that is used in decoction form (root and leaf). When it is with the leaves only, the decoction time is minimum specified by the informants and can also be used in infusion.
Punch is a commonly used preparation method for COVID-19 remedies (Table 4) [33], which consists of a mixture of up to 6 plants believed to help fight against symptoms and complications. Certain punch remedies may incorporate protein-rich ingredients like milk and eggs, which can fortify the immune system and provide essential strength, while others may feature the addition of rum [33]. Proteins, being essential macronutrients, play a crucial role in antibody production and can aid in the fight against COVID-19 [34]. Inhalation of hot steam with plants like Eucalyptus globulus Labill, Syzygium aromaticum L., Zingiber officinale Roscoe, or the effects of oils like Ricinus communis, is another method that has been used for specific plants. This method is believed to help thin mucus and fight against microbes in the throat or nose [28,29,33]. For fruit/leaf and/or edible juices, families consume more fruit and vegetables to strengthen their immune systems. Also, there are plants like Eupatorium odoratum L. and Allium cepa L., or they can rub/blend to take a spoonful of juice against flu [28,33]. For baths and/or massages [28,29,33], we have, for example, the oil of Ricinus communis L., which is used to massage the body that has aches or to massage the stomach in the case of strong flu or the leaves for baths with other plants like Mormordica charantia L. and Ocimum basilicum L.
Therefore, for all the remedies quoted in the survey, 88% are administered orally and recommended 1 to 2 times a day for prevention against COVID-19 and up to 3 times a day for people with COVID-19. For punches (Table 4) that have both medicinal and aromatic plants with protein additives or rum it is recommended once a day. In Haiti before COVID-19, people with flu/cold and respiratory diseases used to take the remedies up to 2 times a day [28,29]. For some remedies COVID-19, unlike other teas that families took in the form of a mixture before COVID-19 for flu/cold, there are more herbs added in the decoctions COVID-19, which are aimed at combating flu/cold, fever, and pain associated with the disease [33]. For contraindications most of the complex punch remedies are not recommended for children and pregnant or nursing women. In the worst case, they are advised only once a day for those who are severely affected at a lower dose. For decoctions and/or infusions, there was only mugwort (Artemisia vulgaris L.) that some families have drawn attention to the toxicity, and as a solution, there are some families that use it more or put a small amount (a small branch) in 1 to 2 L of water.

2.4. Plants and Fidelity Levels

The level of fidelity (FL) of a given plant for a given use was calculated to rank the recorded plant species according to their claimed relative efficacy. Species with RFCs less than 0.1 (Table 2) were not included in the FL calculations (Table 5). Table 5 shows the FL% value for the efficacy of a certain plant to treat a certain disease (Table 6) or to be designated for primary use.
For the treatment of influenza, the species recorded at 100% FL were Abrus precatorius L., Argemone mexicana L., Cissus sicyoides L., Corchorus siliquosus L., Guazuma ulmifolia Lam., Lantana camara L., Musa x paradisiaca L., Passiflora foetida L., Prosopis juliflora Sw DC, Rhoeo spathacea (Sw.) Steam., Saccharum officinarum L., Senecioides cinerea L. O. Ktze, Verbascum thapsus L., Waltheria indica L. followed by Samyda rosea Sims (96.72%), Malpighia emarginata DC (92.11%), Mentha nemorosa wild. (89.47%), Ocimum micranthum wild. (82.76%), Lipia alba L. (74.36%), Phaseolus vulgaris L. (70.59%), Melicoccus bijugatus Jacq (75%), Cymbopogon citratus (DC) Stapf (71.05%), Plectranthus amboinicus (Lour.) Spreng (69.23%), Ocimum basilicum L. (64.1%), Myristica fragrans L. (61.54%), Mammea americana L. (61.11%), Annona muricata L. (57.14%), Cinnamomum verum J. S. Presl (61.22%), Citrus aurantiifolia (Christm.) Swingle (52.54%), Citrus aurantium L. (70.21%) and Eucalyptus globulus Labill. (51.28%). For COVID-19 treatments, the species obtained at 100% fidelity level were Aloe vera L., Phyllanthus niruri L., Portulaca oleracea L., Artemisia vulgaris L et Stachytarpheta jamaicensis (L.) Vahl., followed by Allium sativum L. (94.23%), Mormordica charantia L. (92.39%), Syzygium aromaticum L. (81.97%), Zingiber officinale Roscoe (75.79%), Thymus vulgaris L. (68%), Citrus reticulata Blanco (64.29%), Moringa oleifera L. (60%), Allium cepa L. (55.74%), Citrus maxima Merr. (59.46%) and Hyptis suaveolens L. Poit. (53.13%).

3. Discussion

This study documents the traditional medicinal plants used for the prevention and/or treatment of influenza, respiratory diseases, and COVID-19 in eight communes of the West Department in Haiti. Using the TRAMIL method, herbal remedies identified in the survey were included in the data when the calculated frequency (Freq = Ni/Np × 100) was 20% or higher [94]. Also, a minimum value of five was set for the values Ni and Np. The TRAMIL group chose this minimum frequency to exclude anecdotal uses. Plants commonly used to treat various conditions, such as Mormordica charantia L., Zingiber officinale Roscoe, Aloe vera L., and Eupatorium odoratum L., have been found to possess antimicrobial properties that can help the body fight against bacterial and viral infections [10,57,95,96]. The extract of Mormordica charantia L. in Trinidad and Tobago has demonstrated strong potential in inhibiting multi-resistant clinical bacterial isolates [95]. The presence of kaempferol and quercetin derivatives, including rutin, in the extract, suggests that these compounds may be responsible for the observed activity [95]. Aloe vera L. in Iran has been clinically proven to reduce the frequency of infections and fever and increase the count of white and red blood cells in 60 children who have acute lymphocytic leukemia. In the survey, the 120 informants used different parts of the plants [97]. Different parts of plants produce chemicals that are known as bioactive secondary metabolites [57]. These metabolites include alkaloids, quinines, flavones, lectins, polypeptides, flavonols, flavonoids, coumarin, tannins, terpenoids, essential oils, etc. These compounds are available and can be derived from leaves, bark, roots, flowers, fruits, and seeds [38,57,98]. Regarding the pathologies, the remedies for the prevention and treatment of COVID-19 are the most cited. For not only did Haitians use remedies with one herb but also with several herbs as a mixture as they targeted almost all symptoms related to COVID-19, such as: cough, respiratory problems, fever, gastrointestinal problems, pain, etc. As recently reported by the authors [99], herbal mixtures reduce hospitalization rates and time to recovery from symptoms. Most recipes involved decoctions. Administration was either oral or applied topically for soreness. Several plants that were frequently mentioned in the survey, such as Zingiber officinale Roscoe, Mormordica charantia L., Aloe vera L., Allium cepa L., Allium sativum L., Syzygium aromaticum L, Citrus aurantiifolia (Christm.) Swingle, Eupatorium odoratum L., Cinnamomum verum J. S. Presl, Citrus aurantium L., Artemisia vulgaris L., and Phyllanthus niruri L., have been validated through pharmacological studies for their antiviral, antibacterial, or pain management properties. These plants were found to be potential remedies for COVID-19 in the study, as they were mentioned frequently with an RFC value higher than 0.3. However, there is limited information available regarding the pharmacological properties of Samyda rosea Sims (also known as Samyda dodecandra Jack.), which was also frequently cited. This plant is naturalized in Haiti and can be found in other Caribbean regions like Cuba, Bonaire, and Curacao [100]. Haitians have been using it mainly against flu for many years (FL = 96.72%), but there is no literature available regarding its use elsewhere. For the other most cited plants in the survey, despite their frequent use in natural medicine, the Caribbean wild variety is poorly studied for pharmacological activities related to COVID-19 and its corresponding symptoms.
Zingiber officinale Roscoe (Ginger) aromatic herb with leafy stem and horizontal rhizomes, native to and naturalized in India, was the most frequently cited herb in the remedies; it was described as being used mainly against COVID-19 (FL = 75.789%) in a study the authors showed that ginger compounds, specifically 6-gingerol, 8-gingerol, and 6-shogaol, can induce rapid relaxation in human airway smooth muscle and attenuate airway resistance in mice [101]. Recently, another study showed that 6-gingerol, a compound found in Z. officinale (ginger), has significant anti-influenza activity against the PR8 strain of the H1N1 influenza virus, with an IC50 value of 2.25 ± 0.18 μM [102]. In Morocco, it is traditionally used for gastrointestinal disorders (FL = 86%) [103] and The administration of an acetone extract (at 1000 mg/kg), zingiberene (at 100 mg/kg, the main terpenoid of the extract), and 6-gingerol (at 100 mg/kg) resulted in significant inhibition of HCl/ethanol-induced gastric lesions, with reductions of 98%, 54%, and 54%, respectively [10,104]. The hydroethanol extract of ginger shows antibiotic activity against Gram-positive and Gram-negative bacteria [10,105]. 10-Gingerol and 6-gingerdiol had potent antifungal activity against 13 human pathogens at concentrations below 1 mg/mL [106]. Treatment of ginger root with boiling water abolished the antibacterial effect against E. coli, Salmonella typhimurium, Vibrio parahaemolyticus, Pseudomonas aeruginosa, Proteus vulgaris, Staphylococcus aureus, Mycobacterium phlei, Streptococcus faecalis and Bacillus cereus except that against the growth of Micrococcus luteus. This indicates that the antibacterial principle is heat labile [10,107]. It has been shown that fresh ginger could prevent human respiratory syncytial virus (HRSV) infection largely by inhibiting viral attachment [9]. This may partly explain the common use of Zingiber officinale Roscoe against COVID-19 with associated symptoms.
Mormordica charantia L is a plant that originated from Asia and has been naturalized in the Caribbean [28,29]. Although it is a climbing plant that can reach 3 to 4 m in height [28], in Haiti, it is traditionally used mainly to combat fever (FL = 92.391%) as a possible treatment against COVID-19. The fleshy part and seeds of the plant are also a good source of phenolic compounds, such as catechin, epicatechin, and gallic acid [108]. The plant is used in traditional medicine as an antidiabetic, anthelmintic, laxative, or aphrodisiac [12,108]. The different parts of the plant are also used to treat ailments related to colic, diarrhea, eczema, fever, hemorrhoids, inflammation, malaria, dysentery, sores, anemia, cough, scabies, asthma, wounds, and infections [12]. The protein purified from Bitter Gourd seed possessed effective antiviral activity against a wide range of influenza A subtypes, including H1N1, H3N2, and H5N1 [11]. Another study conducted in Trinidad and Tobago found that the plant extract contains phenolic acid derivatives and flavonoid glycosides that have strong antimicrobial potential against multi-resistant clinical bacterial isolates, likely due to the presence of flavonoids such as quercetin, kaempferol, quercitrin, and rutin [95]. These reports therefore correlate with the traditional uses of Mormordica charantia L.
Aloe vera L. (Aloe) is an ornamental and medicinal plant native to North Africa. Aloe is used in traditional medicine and the treatment of burns and wounds. It has various therapeutic properties such as antiviral, antidiabetic, laxative, protective against radiation, antiallergic, anti-inflammatory, anticancer and immunostimulant, antibacterial, anti-oxidant, and photoprotective activities [39,96]. In Haiti, it was described as being used mainly against COVID-19 (FL = 100%). Recently, researchers have assessed the antibacterial, anti-oxidant, photoprotective, and cytotoxic activities of extracts from Aloe vera L. The results indicated that the n-butanol fraction, as well as the acetone and methanol extracts, demonstrated antibacterial effects against a variety of bacterial strains, including S. aureus, B. cereus, E. coli, P. aeruginosa, and A. baumanii, with MIC values ranging from 1.25 to 10 mg/mL [96]. Another study aimed to evaluate the antibacterial potential of methanol and acetone extracts of aloe vera against various bacterial strains [109]. The findings revealed that the methanol extract exhibited the highest antibacterial activity against B. cereus, with a zone of inhibition of 22.33 mm, while the acetone extract exhibited lower values of zones of inhibition, ranging from 6.00 mm for E. coli to 7.33 mm for S. pyogenes [109]. The extracts showed greater antibacterial activity against Gram-positive bacteria compared to Gram-negative bacteria. Moreover, the study authors identified Pyrocatechol, Cinnamic acid, p-coumaric acid, and Ascorbic acid as the active compounds responsible for the maximum antibacterial activity [109].
Allium cepa L. (onion) is a perennial herbaceous plant characterized by its bulb. It is native to Asia and cultivated in various countries. In this survey, almost all families using onion in remedies specified red onions, which they use for COVID-19 with symptoms such as cough and respiratory problems (FL = 55.737%). However, according to the literature, red onions have more pronounced anti-oxidant activities than white onions [109]. Moreover, it has been demonstrated that red onions can increase the rate of respiration [110], which could be beneficial against respiratory viruses such as COVID-19. In fact, it has been suggested that breathing in the odor emanating from a raw cut onion for a few minutes could be helpful against such viruses [110]. In another study, four polysaccharide fractions were extracted from onion and tested for their antibacterial activity against Gram-positive bacteria (S. aureus, B. subtilis) and Gram-negative bacteria (E. coli, S. typhimurium). The results showed that all four polysaccharide extracts inhibited the growth of both types of bacteria [111].
Allium sativum L. (Garlic) is an annual bulbous herb that originates from Central and South Asia and is widely cultivated in warm and dry climates worldwide [112]. In this survey, Haitians reported using garlic with an FL of 94.23% and a UV of 0.41 to prevent COVID-19 and its various symptoms. In contrast, a study from Morocco reported a lower FL of 64% and a UV of 0.10 for the use of garlic in microbial infections [103]. Garlic is commonly used in food and traditional medicine to treat various ailments, including colds, fever, coughs, asthma, and wounds, and as an antimicrobial agent [38,112]. A study has identified organosulfur compounds, such as allicin and its derivatives (ajoene, allitridin, and garlicin), as the most promising compounds responsible for garlic’s therapeutic activities, especially in the prevention of viral infections [112]. Garlic has been used in African traditional medicine, such as in Ethiopia and Nigeria, to treat various infections, including sexually transmitted diseases, tuberculosis, respiratory tract infections, and wounds [112]. Allicin has been identified as one of the main organosulfur compounds responsible for antiviral activity [113]. In vitro and in vivo studies have demonstrated the antiviral potential of garlic and its organosulfur compounds against a wide range of viruses [112].
Syzygium aromaticum, also known as clove, is native to Indonesia but is now cultivated in many parts of the world [90]. In our study, clove was reported as a COVID-19 remedy with a frequency of 81.967%. According to a study, the aqueous extract of clove seeds showed antimicrobial activity against Escherichia coli, Pseudomonas aeruginosa, and Staphylococcus aureus with minimum inhibitory concentration (MIC) and minimum bactericidal concentration (MBC) values of 0.06 and 0.10 mg/mL, respectively [90]. Another study found that the MeOH crude extract of Syzygium aromaticum inhibited the growth of Gram-negative anaerobic periodontal pathogens, including Porphyromonas gingivalis and Prevotella intermedia [114]. Eight active compounds were identified, including 5,7-dihydroxy-2-methylchromone 8-C-β-d-glucopyranoside, biflorin, kaempferol, rhamnocitrin, myricetin, gallic acid, ellagic acid and oleanolic acid [114]. These findings suggest that clove has potential antimicrobial properties that could be useful in the treatment of COVID-19 and other infections.
Citrus aurantiifolia (Christm.) Swingle (Lemon) is a shrubby tree widely cultivated in warm subtropical and tropical regions of the world. The Haitians use the native lemon mainly for flu (FL = 52.542). In the literature, lemon oil has antimicrobial, fungicidal, insecticidal, and anticancer properties [31]. In a study, the results showed promising in vitro anti-oxidant and cytotoxic activities, especially for the essential oil of the leaves [31]. The essential oil of Citrus aurantifolia (Christm.) Swingle was extracted using hydrodistillation, and its antimicrobial activity was assessed against a representative range of Gram-positive bacteria, Gram-negative bacteria, and yeasts, including both ATCC and clinical strains. The disc diffusion and broth microdilution methods were used for evaluation. The major components of the lime essential oil were found to be β-pinene (12.6%), limonene (53.8%), γ-terpinene (16.5%), terpinolene (0.6%), α-terpineol (0.4%), and citral (2.5%). These compounds are likely responsible for the oil’s good antimicrobial activity, particularly against Gram-positive bacteria such as Staphylococcus aureus, Bacillus subtilis, and Staphylococcus epidermidis [115].
Eupatorium odoratum L. (Siam weed). A study performed a phytochemical analysis on siam weed to study the anti-oxidant and antimicrobial activities of ethanolic and aqueous extracts of its leaves [57]. The authors show that the ethanolic extract of leaves showed anti-oxidant activity and antibacterial properties superior to those of the aqueous extract [57]. This may explain the use of this plant by the Haitians for flu (FL = 84%). The study examined the antibacterial activity of Eupatorium odoratum L leaf extracts against several bacterial strains, including Klebsiella oxytoca, Salmonella enterica, Shigella sonnei, and Vibrio cholerae. The results showed that the extracts displayed antibacterial activity within the range of 0.156 to 1.25 mg/mL. Among the strains tested, V. cholerae exhibited the highest susceptibility to the extracts, with a minimum inhibitory concentration (MIC) of 0.156 mg/mL for the dichloromethane extract and 0.312 mg/mL for the butanol extract. The study also identified sinensetin and scutellareintetramethyl ether as the active components responsible for the antibacterial properties of Eupatorium odoratum L. [116].
Cinnamomum verum J. S. Presl. (Cinnamon) native to Sri Lanka and southern India but also distributed in Southeast Asia, China, Burma, Indonesia, Madagascar, the Caribbean, Australia, and Africa. In a study, authors show the antibacterial effect of methanol, ethanol, petroleum ether, and ethyl acetate extracts of C. verum against Staphylococcus aureus, Bacillus subtilis, Escherichia coli, and Pseudomonas aeruginosa. Ethyl acetate extract was reported to possess the strongest antibacterial activity against Staphylococcus aureus, Escherichia coli, and Pseudomonas aeruginosa, while Bacillus subtilis had shown the maximum sensitivity towards petroleum ether extract [30]. In another study, the chemical composition of cinnamon bark extract was analyzed, revealing cinnamal and coumarin as the main compounds [117]. The extract showed antimicrobial activity against various pathogenic and spoilage microorganisms, including Staphylococcus aureus, Staphylococcus epidermidis, Salmonella abony, Escherichia coli, and Candida albicans, except for some strains of Pseudomonas species [117]. It also reduces the metabolism of bacterial cells, coagulates cellular materials, and limits the rate of replication [30,118]. These studies can explain the use of this plant by the Haitians for flu FL = 61.22%.
Citrus aurantium L. is used in traditional medicine in India for treating stomach aches, vomiting, high blood pressure, dysentery, diarrhea, cardiovascular analeptic, as a sedative, for boils, and for urinary tract infections. Its essential oil from fruit peels has anti-oxidant, antimicrobial, antifungal, antiparasitic, and anti-inflammatory activities [32]. In our study, Haitians use Citrus aurantium L. mainly for flu (FL = 70.21%). In a study the auteurs show essential oil extracted from leaves exhibited strong antifungal activity against two strains of Candida albicans, with fungicidal effect. The MIC of essential oil against Candida albicans strains was 0.15–0.31% (v/v) [32]. Another study investigated the antibacterial properties of citrus oil and identified d-limonene as its primary chemical constituent [119]. The results showed that the essential oil exerted dose-dependent antibacterial activity, with a greater impact on S. aureus (5.8–7.9 mm) compared to E. coli (1.7–3.1 mm), as demonstrated by the diameter of the zone of inhibition [119].
Artemisia vulgaris L. (mugwort) is one of the important medicinal plant species of the genus Artemisia and probably the most common in Haiti today. This medicinal plant has a wide spectrum of therapeutic properties, among which are antimalarial, anti-inflammatory, antihypertensive, anti-oxidant, antitumor, immunomodulatory, hepatoprotective, antispasmodic and antiseptic [44]. The antimicrobial activity of mugwort oil was studied against Staphylococcus aureus, Staphylococcus epidermidis, Enterococcus faecalis, Enterobacter cloacae, Escherichia coli, Salmonella typhimurium, and Candida albicans using the disc diffusion method in comparison with the positive control (ceftazidime and ketoconazole) [44,120]. In a study, the antibacterial activity of the methanol extract and essential oil of A. vulgaris was investigated, with both showing significant activity against the test organism [121]. The methanol extract exhibited higher activity against Bacillus subtilis and Enterococcus spp., with zones of inhibition of 12.48 mm and 12.06 mm, respectively [121]. The essential oil of A. vulgaris was found to contain mono- and sesquiterpenes, including sabinene, β-thujone, chrysanthenone, camphor, borneol, and germacrene [121]. In our study, Haitian use mugwort only for COVID-19, and they mentioned in the survey that they need a very small quantity for the infusions, and this corresponds with these studies [122,123]. It is reported to become toxic at high or repeated doses, as is the case with some other Artemisia species.
Phyllanthus niruri L. this plant is also commonly used to treat hypertension, diabetes, and intestinal infections. It also has a lipid-lowering effect and hepatoprotective activity [98]. In a study, the methanolic extract of Phyllanthus niruri L. demonstrated antibacterial activities against all the Gram-positive and Gram-negative was investigated against pathogenic bacteria responsible for common infections of the skin and urinary and gastrointestinal tracts [124]. In this survey, Haitian use it for COVID-19.
The plants described above, including Zingiber officinale Roscoe, Mormordica charantia L., Aloe vera L., Allium cepa L., Allium sativum L., Syzygium aromaticum L., Citrus aurantiifolia (Christm.) Swingle, Eupatorium odoratum L., Cinnamomum verum J. S. Presl, Citrus aurantium L., Artemisia vulgaris L., and Phyllanthus niruri L. contain active ingredients that can be found in the recipes for herbal remedies for COVID-19 and symptoms [37,56,57,125]. These substances can act against flu, fever, and pain. Other secondary substances, such as flavonoids, anthranoids, cyanogenic glycosides, and alkaloids, can act on many symptoms of covid. To take only the example of flavonoids here, let’s say that quercetin, rutin, naringin, and apigenin, found in several species used in recipes, are recognized and sought after for their antiviral, antibacterial, and anti-inflammatory properties. A study using computational analysis has suggested that various flavonoids, such as kaempferol, quercetin, luteolin-7-glucoside, apigenin-7-glucoside, naringenin, catechin, and epigallocatechin, may hold significance as potential inhibitors of the SARS-CoV-2 Mpro [126]. Another study found that quercetin may be effective in treating early-stage COVID-19. The quercetin group recovered faster and had more negative SARS-CoV-2 tests than the control group [127].
Studies suggest that environmental factors like temperature, humidity, and air pollution may affect COVID-19 transmission [17,18,19,20,21,128,129]. No specific drug has been validated for COVID-19 treatment in large-scale studies, but remdesivir shows promise as an antiviral. Other treatments, such as umifenovir combined with lopinavir/ritonavir and hydroxychloroquine with azithromycin, have shown some efficacy. Research on teicoplanin and monoclonal and polyclonal antibodies is ongoing. The pandemic has significantly increased deaths, particularly among those with comorbidities like hypertension, obesity, cardiovascular issues, diabetes, and respiratory disorders, overwhelming healthcare systems [128]. Rapid identification and risk stratification of high-risk patients, along with appropriate resource allocation, are crucial for healthcare systems globally.
In response to the pandemic, Haitians have extensively used herbal remedies for COVID-19 prevention and treatment, involving mixtures of herbs targeting symptoms like cough, respiratory issues, fever, gastrointestinal problems, and pain. Typically, these remedies are decoctions, infusions, or punches, often including 6 to 7 plant extracts with ingredients like milk, eggs, and honey. Similarly, traditional Chinese medicines have been used as preventative measures based on past use against H1N1 and SARS, but clinical data on their effectiveness for COVID-19 is lacking [128,130]. Six traditional Chinese medicines were notably prevalent, requiring rigorous clinical studies for validation. Additionally, enhancing immunity with vitamins (A, D, and E) and minerals has been suggested as a preventative measure [129]. Therefore, even if the treatment is successful, it is difficult to indicate an active and beneficial component. Further studies are needed to protect high-risk groups and to investigate the efficacy of herbal mixtures. In the research for new antibacterial, antiviral, and even anti-analgesic molecules with new modes of action, it will be interesting to identify the compounds responsible for the activities and thus to discover new mechanisms to relieve these ailments.

4. Materials and Methods

4.1. Study Areas

This ethnopharmacological survey was conducted in 8 communes in Haiti between July and September 2021, such as: Port-au-Prince, (18°32′24″ N, 72°20′24″ W), Carrefour (18°32′ N, 72°24′ W), Gressier (18°27′ N, 72°17′ W), Léogâne (18°30′39″ N, 72°38′02″ W), Pétion-Ville (18°31′ N, 72°17′ W), Delmas (18°33′ N, 72°18′ W), Tabarre (18°35′ N, 72°16′ W), and Croix-des-Bouquets (18°35′ N, 72°14′ W) (Figure 1).

4.2. Data Collection

The interviews were conducted in Haitian Creole (native language) in the field and also by telephone for certain areas: Carrefour, Gressier, Léogâne and Croix-des-Bouquets. They were a total of 120 people with one person per family. Three of these people were “machann fèy” or, in English, medicinal plant traders, and the others were people who had acquired knowledge of the use of medicinal plants from their parents or relatives.
The interview methodology (Figure 4) adopted for this survey was inspired by that used by TRAMIL (TRAditional Medicine in the Islands) which is an applied research program on the popular use of medicinal plants in the Caribbean. TRAMIL’s mission is to scientifically validate the traditional uses of medicinal plants for primary health care [28]. The interviews were conducted in the form of discussions in order to collect information about medicinal plants used for respiratory diseases, influenza, colds, and COVID-19. All participants provided oral prior informed consent before the interviews. The participants were asked to share their experiences (or those of relatives) of the plants they used for the mentioned ailments. During these interviews, the local names of the plants used in the treatment of the conditions, the parts of the plants, the route of administration, and the methods of preparation were recorded on a Microsoft Excel page. During the survey, photos of some plants were requested and provided by the interviewees over the phone. In the process, the plant specimens concerned were collected and then stored in the herbarium of the biomolecule department of COVACHIM-M2E, Faculty of Science, University of West Indies. The identity of each plant species mentioned by the families was verified and their scientific names confirmed by the books: plantes médicinale en Haïti [29], pharmacopée caribéenne [28] and flore illustrée des phanérogames de Guadeloupe et de Martinique 1 and 2 [100], the site Tramil [94] and the botanist at the University of West Indies.
The sampling technique used in this study is stratified sampling. In stratified sampling, the entire population U of N units is divided into a number (K) of mutually exclusive and exhaustive groups, which are called strata [131], each of which corresponds to a commune. The sample size (N = 120) has been selected as being representative of the population. From each of the strata, samples of suitable sizes are selected independently by some suitable sampling design. Eligible participants were people ages ≥ 18 years, Haitian living in the country for 18 years before. People were excluded if they had a disability that prevented them from hearing, understanding, or answering questions, and people who were members of the same family.

4.3. Data Analysis

Relative frequency of citation (RFC) was used to demonstrate the importance of each species. RFC was calculated with this formula: RFC = FC/N; where FC is the number of families mentioning the use of the species, and N is the total number of families participating in the survey [132].
The use value (UV) demonstrates the relative importance of the suggested plant species. UV was calculated using the following formula: UV = (∑Ui)/N where Ui is the number of use statements cited for a given plant species and N is the total number of families surveyed [132]. The UV was useful in determining the most commonly used plant species; these were those that were most frequently indicated in the treatment of a condition [132].
The family use value (FUV) was calculated to identify the importance of medicinal plant families. It was calculated as FUV = ∑UVs/ns × 100 where UVs: use values of the species, and ns: total number of species within each family [133].
The Informant Consensus Factor (ICF) was calculated to test for homogeneity of information using the following formula [134]: ICF = (Nur − Nt)/(Nur − 1) With Nur is the number of utilization reports for each disease category and Nt is the number of plant species used. The diseases were classified as respiratory, influenza, cold, and COVID-19 in order to calculate the ICF. The ICF is the value suggestive of how uniformly participants agree on the use of a particular plant species to treat a particular disease category. The ICF value ranges from 0 to 1. A value near 1 indicates that few plant species were used by a large group of participants. Alternatively, a low value indicates disagreement among participants regarding the use of a plant species for the treatment of a specific disease within a disease category. Medicinal plants presumed to be effective in the treatment of a certain disease have higher ICF values.
The level of fidelity (FL) of each plant was first determined, i.e., the ratio of the number of families that independently suggested the use of a species for the same diseases (Ip) to the total number of families that mentioned the plant for a major disease (Iu). FL was calculated by the following formula [135]: FL = (Ip × 100)/Iu. A high FL value means that the plant species was frequently used to treat a specific disease category by the participants.

5. Conclusions

According to the TRAMIL methodology, medicinal plant uses that are mentioned with a frequency of 20% or more are considered significant. Our study, conducted in Haiti, revealed that several plants are commonly used to treat influenza, colds, and respiratory diseases and are also used for COVID-19. Most of the frequently cited plants were tested for their antibacterial and/or antiviral activities, but the molecules responsible for these activities have not been identified or isolated for most of these plants. Additionally, Samyda dodecandra rosea Sims, which is the most commonly cited plant for influenza treatment in Haiti, has not been tested for biological activity in the literature. Therefore, it is recommended that further pharmacological studies be conducted on these plants.
We want to highlight that in this study, the intellectual property of indigenous knowledge owners and participants is explicitly recognized in accordance with the Nagoya Protocol on Access and Benefit Sharing of the Convention on Biological Diversity.

Author Contributions

The interview was carried out by V.T., with the direct supervision of Y.C. Literature search and data analysis were done by V.T., who also prepared the first draft of the manuscript, which was further improved by Z.B., G.C.-T., P.M., M.S. and V.T.: investigator, data retention, and manuscript writer; Y.C.: article reviewer; Z.B.: investigation author, article critic, and phytochemical, and writing—original project preparation advisor; G.C.-T.: conceptualization, methodology, and writing—original project preparation; V.T.: conceptualization, methodology, and writing—original project preparation; G.C.-T. and P.M.: investigation author, reviewer, and phytochemical advisor; M.S.: investigation author, article critic, and phytochemical advisor; V.T.: writing—revision and editing. All authors have read and agreed to the published version of the manuscript.

Funding

This research was funded by the Anténor Firmin grant, which supported V.T.’s project.

Informed Consent Statement

We did not seek approval from the ethics committee because there is no collection of personal data. Moreover, the consent was obtained orally.

Data Availability Statement

The original contributions presented in the study are included in the article, further inquiries can be directed to the corresponding authors.

Acknowledgments

We gratefully thank the Embassy of France in Haiti, the Agence Universitaire de la Francophonie, the Banque de la République d’Haïti, and the Université de Nîmes for the financial support. With the oral consent of the Haitian participants, the authors thank them. The authors also thank the Haitian community and local herbal healers for their help in data sampling and allowed us to carry out this study. We also thank Alain Rousteau, botanist at the Université des Antilles for his help in identifying some plants.

Conflicts of Interest

The authors declare no conflicts of interest.

References

  1. Weniger, B.; Haag-Berrurier, M.; Anton, R. Plants of Haiti used as antifertility agents. J. Ethnopharmacol. 1982, 6, 67–84. [Google Scholar] [CrossRef]
  2. Danton, O.; Somboro, A.; Fofana, B.; Diallo, D.; Sidibé, L.; Rubat-Coudert, C.; Marchand, F.; Eschalier, A.; Ducki, S.; Chalard, P. Ethnopharmacological survey of plants used in the traditional treatment of pain conditions in Mali. J. Herb. Med. 2019, 17–18, 100271. [Google Scholar] [CrossRef]
  3. Salla, B. Prise en charge des symptômes douloureux par la médecine traditionnelle haïtienne: Résultats d’une enquête réalisée dans le quartier de Martissant à Port-au-Prince. Douleurs Éval. Diagn. Trait. 2017, 18, 223–233. [Google Scholar] [CrossRef]
  4. Vital, P.G.; Rivera, W.L. Antimicrobial activity and cytotoxicity of Chromolaena odorata (L. f.) King and Robinson and Uncaria perrottetii (A. Rich) Merr. Extracts. J. Med. Plants Res. 2009, 3, 511–518. [Google Scholar] [CrossRef]
  5. Newman, D.J.; Cragg, G.M. Natural Products as Sources of New Drugs over the Last 25 Years. J. Nat. Prod. 2007, 70, 461–477. [Google Scholar] [CrossRef] [PubMed]
  6. Al-Sayed, E.; El-Naga, R.N. Protective role of ellagitannins from Eucalyptus citriodora against ethanol-induced gastric ulcer in rats: Impact on oxidative stress, inflammation and calcitonin-gene related peptide. Phytomedicine 2015, 22, 5–15. [Google Scholar] [CrossRef]
  7. Gismondi, A.; Canuti, L.; Impei, S.; Di Marco, G.; Kenzo, M.; Colizzi, V.; Canini, A. Antioxidant extracts of African medicinal plants induce cell cycle arrest and differentiation in B16F10 melanoma cells. Int. J. Oncol. 2013, 43, 956–964. [Google Scholar] [CrossRef] [PubMed]
  8. Liu, Y.; Zhao, L.; Xie, Y.; Chen, Z.; Yang, S.; Yin, B.; Li, G.; Guo, H.; Lin, S.; Wu, J. Antiviral activity of Portulaca oleracea L. extracts against porcine epidemic diarrhea virus by partial suppression on myd88/NF-κb activation in vitro. Microb. Pathog. 2021, 154, 104832. [Google Scholar] [CrossRef]
  9. Chang, J.S.; Wang, K.C.; Yeh, C.F.; Shieh, D.E.; Chiang, L.C. Fresh ginger (Zingiber officinale) has anti-viral activity against human respiratory syncytial virus in human respiratory tract cell lines. J. Ethnopharmacol. 2013, 145, 146–151. [Google Scholar] [CrossRef]
  10. Chrubasik, S.; Pittler, M.H.; Roufogalis, B.D. Zingiberis rhizoma: A comprehensive review on the ginger effect and efficacy profiles. Phytomedicine 2005, 12, 684–701. [Google Scholar] [CrossRef]
  11. Pongthanapisith, V.; Ikuta, K.; Puthavathana, P.; Leelamanit, W. Antiviral Protein of Momordica charantia L. Inhibits Different Subtypes of Influenza, A. Evid.-Based Complement. Altern. Med. 2013, 2013, e729081. [Google Scholar] [CrossRef] [PubMed]
  12. Subratty, A.H.; Gurib-Fakim, A.; Mahomoodally, F. Bitter melon: An exotic vegetable with medicinal values. Nutr. Food Sci. 2005, 35, 143–147. [Google Scholar] [CrossRef]
  13. WHO. WHO EMRO|Maladies Infectieuses|Thèmes de Santé. World Health Organization—Regional Office for the Eastern Mediterranean. 12 May 2019. Available online: http://www.emro.who.int/fr/health-topics/infectious-diseases/index.html (accessed on 28 December 2021).
  14. Lasky, J.A.; Fuloria, J.; Morrison, M.E.; Lanier, R.; Naderer, O.; Brundage, T.; Melemed, A. Design and Rationale of a Randomized, Double-Blind, Placebo-Controlled, Phase 2/3 Study Evaluating Dociparstat in Acute Lung Injury Associated with Severe COVID-19. Adv. Ther. 2021, 38, 782–791. [Google Scholar] [CrossRef] [PubMed]
  15. Wu, X.; Chen, Q.; Li, J.; Liu, Z. Diagnostic techniques for COVID-19: A mini-review. J. Virol. Methods 2021, 301, 114437. [Google Scholar] [CrossRef] [PubMed]
  16. WHO. WHO Director-General’s Opening Remarks at the Media Briefing on COVID-19. 11 March 2020. Available online: https://www.who.int/director-general/speeches/detail/who-director-general-s-opening-remarks-at-the-media-briefing-on-covid-19---11-march-2020 (accessed on 6 March 2022).
  17. La Rosa, G.; Bonadonna, L.; Lucentini, L.; Kenmoe, S.; Suffredini, E. Coronavirus in water environments: Occurrence, persistence and concentration methods—A scoping review. Water Res. 2020, 179, 115899. [Google Scholar] [CrossRef] [PubMed]
  18. Setti, L.; Passarini, F.; De Gennaro, G.; Barbieri, P.; Perrone, M.G.; Borelli, M.; Palmisani, J.; Di Gilio, A.; Piscitelli, P.; Miani, A. Airborne Transmission Route of COVID-19: Why 2 Meters/6 Feet of Inter-Personal Distance Could Not Be Enough. Int. J. Environ. Res. Public Health 2020, 17, 2932. [Google Scholar] [CrossRef]
  19. Ong, S.W.X.; Tan, Y.K.; Chia, P.Y.; Lee, T.H.; Ng, O.T.; Wong, M.S.Y.; Marimuthu, K. Air, Surface Environmental, and Personal Protective Equipment Contamination by Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) from a Symptomatic Patient. JAMA 2020, 323, 1610–1612. [Google Scholar] [CrossRef]
  20. Meselson, M. Droplets and Aerosols in the Transmission of SARS-CoV-2. N. Engl. J. Med. 2020, 382, 2063. [Google Scholar] [CrossRef]
  21. Qian, H.; Miao, T.; Liu, L.; Zheng, X.; Luo, D.; Li, Y. Indoor transmission of SARS-CoV-2. Indoor Air 2021, 31, 639–645. [Google Scholar] [CrossRef]
  22. Jotz, G.P.; Voegels, R.L.; Bento, R.F. Otorhinolaryngologists and Coronavirus Disease 2019 (COVID-19). Int. Arch. Otorhinolaryngol. 2020, 24, 125–128. [Google Scholar] [CrossRef]
  23. Kosugi, E.M.; Lavinsky, J.; Romano, F.R.; Fornazieri, M.A.; Luz-Matsumoto, G.R.; Lessa, M.M.; Piltcher, O.B.; Sant’Anna, G.D. Incomplete and late recovery of sudden olfactory dysfunction in COVID-19. Braz. J. Otorhinolaryngol. 2020, 86, 490–496. [Google Scholar] [CrossRef]
  24. Pan, L.; Mu, M.; Yang, P.; Sun, Y.; Wang, R.; Yan, J.; Li, P.; Hu, B.; Wang, J.; Hu, C.; et al. Clinical Characteristics of COVID-19 Patients With Digestive Symptoms in Hubei, China: A Descriptive, Cross-Sectional, Multicenter Study. Am. J. Gastroenterol. 2020, 115, 766–773. [Google Scholar] [CrossRef]
  25. Sultana, M.S.; Khan, A.H.; Hossain, S.; Hasan, M.T. Mental health difficulties in students with suspected COVID-19 symptoms and students without suspected COVID-19 symptoms: A cross-sectional comparative study during the COVID-19 pandemic. Child. Youth Serv. Rev. 2021, 128, 106137. [Google Scholar] [CrossRef] [PubMed]
  26. Nasir, A.; Shah, M.A.; Ashraf, U.; Khan, A.; Jeon, G. An intelligent framework to predict socioeconomic impacts of COVID-19 and public sentiments. Comput. Electr. Eng. 2021, 96, 107526. [Google Scholar] [CrossRef] [PubMed]
  27. Petrakou, K.; Iatrou, G.; Lamari, F.N. Ethnopharmacological survey of medicinal plants traded in herbal markets in the Peloponnisos, Greece. J. Herb. Med. 2020, 19, 100305. [Google Scholar] [CrossRef]
  28. TRAMIL. Pharmacopée Végétale Caribéenne: Troisième Édition Actualisée Et Enrichie. TRAMIL. CANOPE de Guadeloupe, 2014. 2014. Available online: https://www.tramil.net/fr/content/publications-tramil (accessed on 7 March 2022).
  29. Neptune-Rouzier, M. Plantes Médicinales d’Haïti: Description, Usages et Propriétés; Éditions de l’Université d’État d’Haïti: Port-au Prince, Haiti, 2014. [Google Scholar]
  30. Singh, N.; Rao, A.S.; Nandal, A.; Kumar, S.; Yadav, S.S.; Ganaie, S.A.; Narasimhan, B. Phytochemical and pharmacological review of Cinnamomum verum J. Presl-a versatile spice used in food and nutrition. Food Chem. 2021, 338, 127773. [Google Scholar] [CrossRef] [PubMed]
  31. Weimer, P.; Moura, J.G.L.; Mossmann, V.; Immig, M.L.; de Castilhos, J.; Rossi, R.C. Citrus aurantiifolia (Christm) Swingle: Biological potential and safety profile of essential oils from leaves and fruit peels. Food Biosci. 2021, 40, 100905. [Google Scholar] [CrossRef]
  32. Nidhi, P.; Rolta, R.; Kumar, V.; Dev, K.; Sourirajan, A. Synergistic potential of Citrus aurantium L. essential oil with antibiotics against Candida albicans. J. Ethnopharmacol. 2020, 262, 113135. [Google Scholar] [CrossRef]
  33. Bien-Aimé, A.; Casimir, J.; Civil, M.-F.; Noël, E.; Rouzier, M. Les Recettes Haïtiennes Face à la Pandémie Provoquée par le SARS-CoV-2 Par la Commission D’inventaire et D’évaluation des Remèdes Traditionnels Contre le SARS-CoV-2-UEH, Juillet 2020. Available online: https://ueh.edu.ht/wp-content/uploads/2020/08/Rapport-du-Jury-mis-sur-pied-par-lUEH-sur-les-recettes-traditionnelles-haitiennes-face-%C3%A0-la-Covid-19-1.pdf (accessed on 1 July 2020).
  34. Calcuttawala, F. Nutrition as a key to boost immunity against COVID-19. Clin. Nutr. ESPEN 2022, 49, 17–23. [Google Scholar] [CrossRef]
  35. Adão, C.R.; da Silva, B.P.; Parente, J.P. A new steroidal saponin from Allium ampeloprasum var. porrum with antiinflammatory and gastroprotective effects. Phytochem. Lett. 2011, 4, 306–310. [Google Scholar] [CrossRef]
  36. Okoro, E.E.; Maharjan, R.; Jabeen, A.; Ahmad, M.S.; Azhar, M.; Shehla, N.; Zaman, W.; Shams, S.; Osoniyi, O.R.; Onajobi, F.D.; et al. Isoflavanquinones from Abrus precatorius roots with their antiproliferative and anti-inflammatory effects. Phytochemistry 2021, 187, 112743. [Google Scholar] [CrossRef] [PubMed]
  37. Kumar, M.; Barbhai, M.D.; Hasan, M.; Punia, S.; Dhumal, S.; Radha; Rais, N.; Chandran, D.; Pandiselvam, R.; Kothakota, A.; et al. Onion (Allium cepa L.) peels: A review on bioactive compounds and biomedical activities. Biomed. Pharmacother. 2022, 146, 112498. [Google Scholar] [CrossRef]
  38. Torpol, K.; Wiriyacharee, P.; Sriwattana, S.; Sangsuwan, J.; Prinyawiwatkul, W. Antimicrobia activity of garlic (Allium sativum L.) and holy basil (Ocimum sanctum L.) essential oils applied by liquid vs. vapour phases. Int. J. Food Sci. Technol. 2018, 53, 2119–2128. [Google Scholar] [CrossRef]
  39. Farid, A.; Tawfik, A.; Elsioufy, B.; Safwat, G. In vitro and in vivo anti-Cryptosporidium and anti-inflammatory effects of Aloe vera gel in dexamethasone immunosuppressed mice. Int. J. Parasitol. Drugs Drug Resist. 2021, 17, 156–167. [Google Scholar] [CrossRef] [PubMed]
  40. Ajayi, A.M.; Coker, A.I.; Oyebanjo, O.T.; Adebanjo, I.M.; Ademowo, O.G. Ananas comosus (L) Merrill (pineapple) fruit peel extract demonstrates antimalarial, anti-nociceptive and anti-inflammatory activities in experimental models. J. Ethnopharmacol. 2022, 282, 114576. [Google Scholar] [CrossRef] [PubMed]
  41. Balderrama-Carmona, A.P.; Silva-Beltrán, N.P.; Gálvez-Ruiz, J.-C.; Ruíz-Cruz, S.; Chaidez-Quiroz, C.; Morán-Palacio, E.F. Antiviral, Antioxidant, and Antihemolytic Effect of Annona muricata L. Leaves Extracts. Plants 2020, 9, 1650. [Google Scholar] [CrossRef]
  42. Khairullah, A.R. Review on the Pharmacological and Health Aspects of Apium Graveolens or Celery: An Update. Syst. Rev. Pharm. 2021, 12, 595–601. [Google Scholar]
  43. Andleeb, S.; Alsalme, A.; Al-Zaqri, N.; Warad, I.; Alkahtani, J.; Bukhari, S.M. In-vitro antibacterial and antifungal properties of the organic solvent extract of Argemone mexicana L. J. King Saud Univ. Sci. 2020, 32, 2053–2058. [Google Scholar] [CrossRef]
  44. Abiri, R.; Silva, A.L.M.; de Mesquita, L.S.S.; de Mesquita, J.W.C.; Atabaki, N.; de Almeida, E.B., Jr.; Shaharuddin, N.A.; Malik, S. Towards a better understanding of Artemisia vulgaris: Botany, phytochemistry, pharmacological and biotechnological potential. Food Res. Int. 2018, 109, 403–415. [Google Scholar] [CrossRef]
  45. Camacho-Hernández, I.L.; Chávez-Velázquez, J.A.; Uribe-Beltrán, M.J.; Rı, A.; Delgado-Vargas, F. Antifungal activity of fruit pulp extract from Bromelia pinguin. Fitoterapia 2002, 73, 411–413. [Google Scholar] [CrossRef]
  46. Salazar, M.A.R.; Costa, J.V.; Urbina, G.R.O.; Cunha, V.M.B.; Silva, M.P.; do Nascimento Bezerra, P.; Pinheiro, W.B.S.; Gomes-Leal, W.; Lopes, A.S.; Carvalho Junior, R.N. Chemical composition, antioxidant activity, neuroprotective and anti-inflammatory effects of cipó-pucá (Cissus sicyoides L.) extracts obtained from supercritical extraction. J. Supercrit. Fluids 2018, 138, 36–45. [Google Scholar] [CrossRef]
  47. Chen, Y.; Li, T.; Bai, J.; Nong, L.; Ning, Z.; Hu, Z.; Xu, A.; Xu, C.-P. Chemical Composition and Antibacterial Activity of the Essential Oil of Citrus maxima (Burm.) Merr. cv. Shatian Yu. J. Biol. Act. Prod. Nat. 2018, 8, 228–233. [Google Scholar] [CrossRef]
  48. Ferreira, S.S.; Silva, A.M.; Nunes, F.M. Citrus reticulata Blanco peels as a source of antioxidant and anti-proliferative phenolic compounds. Ind. Crops Prod. 2018, 111, 141–148. [Google Scholar] [CrossRef]
  49. Atolani, O.; Adamu, N.; Oguntoye, O.S.; Zubair, M.F.; Fabiyi, O.A.; Oyegoke, R.A.; Adeyemi, O.S.; Areh, E.T.; Tarigha, D.E.; Kambizi, L.; et al. Chemical characterization, antioxidant, cytotoxicity, Anti-Toxoplasma gondii and antimicrobial potentials of the Citrus sinensis seed oil for sustainable cosmeceutical production. Heliyon 2020, 6, e03399. [Google Scholar] [CrossRef] [PubMed]
  50. Shen, X.; Chen, W.; Zheng, Y.; Lei, X.; Tang, M.; Wang, H.; Song, F. Chemical composition, antibacterial and antioxidant activities of hydrosols from different parts of Areca catechu L. and Cocos nucifera L. Ind. Crops Prod. 2017, 96, 110–119. [Google Scholar] [CrossRef]
  51. Sylvestre, M.; Pichette, A.; Longtin, A.; Nagau, F.; Legault, J. Essential oil analysis and anticancer activity of leaf essential oil of Croton flavens L. from Guadeloupe. J. Ethnopharmacol. 2006, 103, 99–102. [Google Scholar] [CrossRef]
  52. Kim, H.J.; Yoo, H.S.; Kim, J.C.; Park, C.S.; Choi, M.S.; Kim, M.; Choi, H.; Min, J.S.; Kim, Y.S.; Yoon, S.W.; et al. Antiviral effect of Curcuma longa Linn extract against hepatitis B virus replication. J. Ethnopharmacol. 2009, 124, 189–196. [Google Scholar] [CrossRef] [PubMed]
  53. Subramaniam, G.; Yew, X.Y.; Sivasamugham, L.A. Antibacterial activity of Cymbopogon citratus against clinically important bacteria. S. Afr. J. Chem. Eng. 2020, 34, 26–30. [Google Scholar] [CrossRef]
  54. Snene, A.; Mokni, R.E.; Mahdhi, A.; Joshi, R.K.; Hammami, S. Comparative study of essential oils composition and in vitro antibacterial effects of two subspecies of Daucus carota growing in Tunisia. S. Afr. J. Bot. 2020, 130, 366–370. [Google Scholar] [CrossRef]
  55. Bachir, R.G.; Benali, M. Antibacterial activity of the essential oils from the leaves of Eucalyptus globulus against Escherichia coli and Staphylococcus aureus. Asian Pac. J. Trop. Biomed. 2012, 2, 739–742. [Google Scholar] [CrossRef]
  56. Cui, S.; Tan, S.; Ouyang, G.; Jiang, S.; Pawliszyn, J. Headspace solid-phase microextraction gas chromatography–mass spectrometry analysis of Eupatorium odoratum extract as an oviposition repellent. J. Chromatogr. B 2009, 877, 1901–1906. [Google Scholar] [CrossRef]
  57. Vijayaraghavan, K.; Rajkumar, J.; Seyed, M.A. Phytochemical screening, free radical scavenging and antimicrobial potential of Chromolaena odorata leaf extracts against pathogenic bacterium in wound infections—A multispectrum perspective. Biocatal. Agric. Biotechnol. 2018, 15, 103–112. [Google Scholar] [CrossRef]
  58. de Lima, L.F.; de Oliveira, J.O.; Carneiro, J.N.P.; Lima, C.N.F.; Coutinho, H.D.M.; Morais-Braga, M.F.B. Ethnobotanical and antimicrobial activities of the Gossypium (Cotton) genus: A review. J. Ethnopharmacol. 2021, 279, 114363. [Google Scholar] [CrossRef]
  59. Pereira, G.A.; Araujo, N.M.P.; Arruda, H.S.; de P. Farias, D.; Molina, G.; Pastore, G.M. Phytochemicals and biological activities of mutamba (Guazuma ulmifolia Lam.): A review. Food Res. Int. 2019, 126, 108713. [Google Scholar] [CrossRef]
  60. Paz, J.E.W.; Contreras, C.R.; Munguía, A.R.; Aguilar, C.N.; Inungaray, M.L.C. Phenolic content and antibacterial activity of extracts of Hamelia patens obtained by different extraction methods. Braz. J. Microbiol. 2018, 49, 656–661. [Google Scholar] [CrossRef] [PubMed]
  61. Mak, Y.W.; Chuah, L.O.; Ahmad, R.; Bhat, R. Antioxidant and antibacterial activities of hibiscus (Hibiscus rosa-sinensis L.) and Cassia (Senna bicapsularis L.) flower extracts. J. King Saud Univ. Sci. 2013, 25, 275–282. [Google Scholar] [CrossRef]
  62. Asekun, O.T.; Ekundayo, O.; Adeniyi, B.A. Antimicrobial activity of the essential oil of Hyptis suaveolens leaves. Fitoterapia 1999, 70, 440–442. [Google Scholar] [CrossRef]
  63. Kumar, V.P.; Chauhan, N.S.; Padh, H.; Rajani, M. Search for antibacterial and antifungal agents from selected Indian medicinal plants. J. Ethnopharmacol. 2006, 107, 182–188. [Google Scholar] [CrossRef]
  64. Rahu, M.I.; Naqvi, S.H.A.; Memon, N.H.; Idrees, M.; Kandhro, F.; Pathan, N.L.; Sarker, M.N.I.; Bhutto, M.A. Determination of antimicrobial and phytochemical compounds of Jatropha curcas plant. Saudi J. Biol. Sci. 2021, 28, 2867–2876. [Google Scholar] [CrossRef]
  65. Agarwal, H.; Shanmugam, V.K. Anti-inflammatory activity screening of Kalanchoe pinnata methanol extract and its validation using a computational simulation approach. Inform. Med. Unlocked 2019, 14, 6–14. [Google Scholar] [CrossRef]
  66. Dubey, D.; Padhy, R.N. Antibacterial activity of Lantana camara L. against multidrug resistant pathogens from ICU patients of a teaching hospital. J. Herb. Med. 2013, 3, 65–75. [Google Scholar] [CrossRef]
  67. da Silva Júnior, A.Q.; da Silva, D.S.; Figueiredo, P.L.B.; Sarrazin, S.L.F.; Bouillet, L.E.M.; de Oliveira, R.B.; Maia, J.G.S.; Mourão, R.H.V. Seasonal and circadian evaluation of a citral-chemotype from Lippia alba essential oil displaying antibacterial activity. Biochem. Syst. Ecol. 2019, 85, 35–42. [Google Scholar] [CrossRef]
  68. Spinu, K. Antiviral Activity of Tomatoside from Lycopersicon esculentum Mill. In Saponins Used in Traditional and Modern Medicine; Waller, G.R., Yamasaki, K., Eds.; Advances in Experimental Medicine and Biology; Springer: Boston, MA, USA, 1996; pp. 505–509. [Google Scholar] [CrossRef]
  69. Delva, L.; Goodrich-Schneider, R. Antioxidant activity and antimicrobial properties of phenolic extracts from acerola (Malpighia emarginata DC) fruit. Int. J. Food Sci. Technol. 2013, 48, 1048–1056. [Google Scholar] [CrossRef]
  70. Lemus, C.; Smith-Ravin, J.; Marcelin, O. Mammea americana: A review of traditional uses, phytochemistry and biological activities. J. Herb. Med. 2021, 29, 100466. [Google Scholar] [CrossRef]
  71. Khan, M.M.; Harunsani, M.H.; Tan, A.L.; Hojamberdiev, M.; Poi, Y.A.; Ahmad, N. Antibacterial Studies of ZnO and Cu-Doped ZnO Nanoparticles Synthesized Using Aqueous Leaf Extract of Stachytarpheta jamaicensis. BioNanoScience 2020, 10, 1037–1048. [Google Scholar] [CrossRef]
  72. Bystrom, L.M.; Lewis, B.A.; Brown, D.L.; Rodriguez, E.; Obendorf, R.L. Phenolics, Sugars, Antimicrobial and Free-Radical-Scavenging Activities of Melicoccus bijugatus Jacq. Fruits from the Dominican Republic and Florida. Plant Foods Hum. Nutr. 2009, 64, 160–166. [Google Scholar] [CrossRef]
  73. Johnson, M.; Wesely, E.; Kavitha, M.; Uma, V. Antibacterial activity of leaves and inter-nodal callus extracts of Mentha arvensis L. Asian Pac. J. Trop. Med. 2011, 4, 196–200. [Google Scholar] [CrossRef]
  74. Mahato, D.K.; Kargwal, R.; Kamle, M.; Sharma, B.; Pandhi, S.; Mishra, S.; Gupta, A.; Mahmud, M.M.C.; Gupta, M.K.; Singha, L.B.; et al. Ethnopharmacological properties and Nutraceutical potential of Moringa oleifera. Phytomed. Plus 2022, 2, 100168. [Google Scholar] [CrossRef]
  75. Behiry, S.I.; Okla, M.K.; Alamri, S.A.; EL-Hefny, M.; Salem, M.Z.M.; Alaraidh, I.A.; Ali, H.M.; Al-Ghtani, S.M.; Monroy, J.C.; Salem, A.Z.M. Antifungal and Antibacterial Activities of Musa paradisiaca L. Peel Extract: HPLC Analysis of Phenolic and Flavonoid Contents. Processes 2019, 7, 215. [Google Scholar] [CrossRef]
  76. Shafiei, Z.; Shuhairi, N.N.; Yap, N.M.F.S.; Sibungkil, C.-A.H.; Latip, J. Antibacterial Activity of Myristica fragrans against Oral Pathogens. Evid.-Based Complement. Altern. Med. 2012, 2012, e825362. [Google Scholar] [CrossRef]
  77. Al Abbasy, D.W.; Pathare, N.; Al-Sabahi, J.N.; Khan, S.A. Chemical composition and antibacterial activity of essential oil isolated from Omani basil (Ocimum basilicum Linn.). Asian Pac. J. Trop. Dis. 2015, 5, 645–649. [Google Scholar] [CrossRef]
  78. Chimnoi, N.; Reuk-ngam, N.; Chuysinuan, P.; Khlaychan, P.; Khunnawutmanotham, N.; Chokchaichamnankit, D.; Thamniyom, W.; Klayraung, S.; Mahidol, C.; Techasakul, S. Characterization of essential oil from Ocimum gratissimum leaves: Antibacterial and mode of action against selected gastroenteritis pathogens. Microb. Pathog. 2018, 118, 290–300. [Google Scholar] [CrossRef] [PubMed]
  79. Sacchetti, G.; Medici, A.; Maietti, S.; Radice, M.; Muzzoli, M.; Manfredini, S.; Braccioli, E.; Bruni, R. Composition and Functional Properties of the Essential Oil of Amazonian Basil, Ocimum micranthum Willd., Labiatae in Comparison with Commercial Essential Oils. J. Agric. Food Chem. 2004, 52, 3486–3491. [Google Scholar] [CrossRef]
  80. Aruwa, C.E.; Amoo, S.O.; Kudanga, T. Extractable and macromolecular antioxidants of Opuntia ficus-indica cladodes: Phytochemical profiling, antioxidant and antibacterial activities. S. Afr. J. Bot. 2019, 125, 402–410. [Google Scholar] [CrossRef]
  81. Taïwe, G.S.; Kuete, V. Chapter 24—Passiflora edulis. In Medicinal Spices and Vegetables from Africa; Kuete, V., Ed.; Academic Press: Cambridge, MA, USA, 2017; pp. 513–526. [Google Scholar] [CrossRef]
  82. Mohanasundari, C.; Natarajan, D.; Srinivasan, K.; Umamaheswari, S.; Ramachandran, A. Antibacterial properties of Passiflora foetida L.—A common exotic medicinal plant. Afr. J. Biotechnol. 2007, 6, 2650–2653. [Google Scholar] [CrossRef]
  83. Slighoua, M.; Mahdi, I.; Amrati, F.E.-Z.; Di Cristo, F.; Amaghnouje, A.; Grafov, A.; Boucetta, N.; Bari, A.; Bousta, D. Assessment of in vivo estrogenic and anti-inflammatory activities of the hydro-ethanolic extract and polyphenolic fraction of parsley (Petroselinum sativum Hoffm.). J. Ethnopharmacol. 2021, 265, 113290. [Google Scholar] [CrossRef] [PubMed]
  84. Amarowicz, R.; Dykes, G.A.; Pegg, R.B. Antibacterial activity of tannin constituents from Phaseolus vulgaris, Fagoypyrum esculentum, Corylus avellana and Juglans nigra. Fitoterapia 2008, 79, 217–219. [Google Scholar] [CrossRef] [PubMed]
  85. Adedotun, I.O.; Abdul-Hammed, M.; Hamzat, B.A.; Adepoju, A.J.; Akinboade, M.W.; Afolabi, T.I.; Ismail, U.T. Molecular docking, ADMET analysis, and bioactivity studies of phytochemicals from Phyllanthus niruri as potential inhibitors of hepatitis C virus NSB5 polymerase. J. Ind. Chem. Soc. 2022, 99, 100321. [Google Scholar] [CrossRef]
  86. Gurgel, A.P.A.D.; da Silva, J.G.; Grangeiro, A.R.S.; Oliveira, D.C.; Lima, C.M.P.; da Silva, A.C.P.; Oliveira, R.A.G.; Souza, I.A. In vivo study of the anti-inflammatory and antitumor activities of leaves from Plectranthus amboinicus (Lour.) Spreng (Lamiaceae). J. Ethnopharmacol. 2009, 125, 361–363. [Google Scholar] [CrossRef]
  87. Malini, S.; Kumar, S.V.; Hariharan, R.; Bharathi, A.P.; Devi, P.R.; Hemananthan, E. Antibacterial, photocatalytic and biosorption activity of chitosan nanocapsules embedded with Prosopis juliflora leaf extract synthesized silver nanoparticles. Mater. Today Proc. 2020, 21, 828–832. [Google Scholar] [CrossRef]
  88. Ribeiro, P.R.; de Castro, R.D.; Fernandez, L.G. Chemical constituents of the oilseed crop Ricinus communis and their pharmacological activities: A review. Ind. Crops Prod. 2016, 91, 358–376. [Google Scholar] [CrossRef]
  89. Amalia, A.V.; Pukan, K.K.; Setyawati, N.; Widiatningrum, T.; Khasanah, U. Antibacterial activity of Saccharum officinarum leaves extract against food-borne disease. J. Phys. Conf. Ser. 2019, 1321, 032043. [Google Scholar] [CrossRef]
  90. Ajiboye, T.O.; Mohammed, A.O.; Bello, S.A.; Yusuf, I.I.; Ibitoye, O.B.; Muritala, H.F.; Onajobi, I.B. Antibacterial activity of Syzygium aromaticum seed: Studies on oxidative stress biomarkers and membrane permeability. Microb. Pathog. 2016, 95, 208–215. [Google Scholar] [CrossRef]
  91. Iseppi, R.; Sabia, C.; de Niederhäusern, S.; Pellati, F.; Benvenuti, S.; Tardugno, R.; Bondi, M.; Messi, P. Antibacterial activity of Rosmarinus officinalis L. and Thymus vulgaris L. essential oils and their combination against food-borne pathogens and spoilage bacteria in ready-to-eat vegetables. Nat. Prod. Res. 2019, 33, 3568–3572. [Google Scholar] [CrossRef] [PubMed]
  92. Weldegebrieal, G.K. Photocatalytic and antibacterial activityof CuO nanoparticles biosynthesized using Verbascum thapsus leaves extract. Optik 2020, 204, 164230. [Google Scholar] [CrossRef]
  93. Zongo, F.; Ribuot, C.; Boumendjel, A.; Guissou, I. Botany, traditional uses, phytochemistry and pharmacology of Waltheria indica L. (syn. Waltheria americana): A review. J. Ethnopharmacol. 2013, 148, 14–26. [Google Scholar] [CrossRef] [PubMed]
  94. TRAMIL. 2017. Available online: https://tramil.net/en (accessed on 7 December 2022).
  95. Svobodova, B.; Barros, L.; Calhelha, R.C.; Heleno, S.; Alves, M.J.; Walcott, S.; Bittova, M.; Kuban, V.; Ferreira, I.C.F.R. Bioactive properties and phenolic profile of Momordica charantia L. medicinal plant growing wild in Trinidad and Tobago. Ind. Crops Prod. 2017, 95, 365–373. [Google Scholar] [CrossRef]
  96. Bendjedid, S.; Lekmine, S.; Tadjine, A.; Djelloul, R.; Bensouici, C. Analysis of phytochemical constituents, antibacterial, antioxidant, photoprotective activities and cytotoxic effect of leaves extracts and fractions of Aloe vera. Biocatal. Agric. Biotechnol. 2021, 33, 101991. [Google Scholar] [CrossRef]
  97. Hashemi, A.S.; Kokab, M.; Kamalian, M.; Zarezadeh, M.; Sheikhpour, E.; Azod, L.; Fallah, T. The effect of Aloe vera syrup on prevention of fever and neutropenia in children with acute lymphoid leukemia. Iran.J. Pediatr. Hematol. Oncol. 2020, 10, 144. [Google Scholar]
  98. Paula, V.G.; Cruz, L.L.; Sene, L.B.; Gratão, T.B.; Soares, T.S.; Moraes-Souza, R.Q.; Damasceno, D.C.; Volpato, G.T. Maternal-fetal repercussions of Phyllanthus niruri L. treatment during rat pregnancy. J. Ethnopharmacol. 2020, 254, 112728. [Google Scholar] [CrossRef]
  99. Gajewski, A.; Kośmider, A.; Nowacka, A.; Puk, O.; Wiciński, M. Potential of herbal products in prevention and treatment of COVID-19. Literature review. Biomed. Pharmacother. 2021, 143, 112150. [Google Scholar] [CrossRef] [PubMed]
  100. Fournet, J. Flore Illustrée des Phanérogames de Guadeloupe et de Martinique. CIRAD, 2002. Consulté le: 7. Available online: https://agritrop.cirad.fr/490202/ (accessed on 7 March 2022).
  101. Townsend, E.A.; Siviski, M.E.; Zhang, Y.; Xu, C.; Hoonjan, B.; Emala, C.W. Effects of Ginger and Its Constituents on Airway Smooth Muscle Relaxation and Calcium Regulation. Am. J. Respir. Cell Mol. Biol. 2013, 48, 157–163. [Google Scholar] [CrossRef]
  102. Dutta, A.; Hsiao, S.-H.; Hung, C.-Y.; Chang, C.-S.; Lin, Y.-C.; Lin, C.-Y.; Chen, T.-C.; Huang, C.-T. Effect of [6]-gingerol on viral neuraminidase and hemagglutinin-specific T cell immunity in severe influenza. Phytomed. Plus 2023, 3, 100387. [Google Scholar] [CrossRef]
  103. Eddouks, M.; Ajebli, M.; Hebi, M. Ethnopharmacological survey of medicinal plants used in Daraa-Tafilalet region (Province of Errachidia), Morocco. J. Ethnopharmacol. 2017, 198, 516–530. [Google Scholar] [CrossRef]
  104. Johji, Y.; Michihiko, M.; Rong, H.Q.; Hisashi, M.; Hajime, F. The anti-ulcer effect in rats of ginger constituents. J. Ethnopharmacol. 1988, 23, 299–304. [Google Scholar] [CrossRef] [PubMed]
  105. Mascolo, N.; Jain, R.; Jain, S.C.; Capasso, F. Ethnopharmacologic investigation of ginger (Zingiber officinale). J. Ethnopharmacol. 1989, 27, 129–140. [Google Scholar] [CrossRef]
  106. Ficker, C.; Smith, M.L.; Akpagana, K.; Gbeassor, M.; Zhang, J.; Durst, T.; Assabgui, R.; Arnason, J.T. Bioassay-guided isolation and identification of antifungal compounds from ginger. Phytother. Res. 2003, 17, 897–902. [Google Scholar] [CrossRef] [PubMed]
  107. Chen, H.C.; Chang, M.D.; Chang, T.J. [Antibacterial properties of some spice plants before and after heat treatment]. Zhonghua Min Guo Wei Sheng Wu Ji Mian Yi Xue Za Zhi 1985, 18, 190–195. [Google Scholar]
  108. Horax, R.; Hettiarachchy, N.; Kannan, A.; Chen, P. Proximate composition and amino acid and mineral contents of Mormordica charantia L. pericarp and seeds at different maturity stages. Food Chem. 2010, 122, 1111–1115. [Google Scholar] [CrossRef]
  109. Lawrence, R.; Tripathi, P.; Jeyakumar, E. Isolation, Purification and Evaluation of Antibacterial Agents from Aloe vera. Braz. J. Microbiol. 2009, 40, 906–915. [Google Scholar] [CrossRef]
  110. Fonseca, S.C.; Gil, L.; Manso, M.C.; Cunha, L.M. Modelling the influence of storage temperature and time after cutting on respiration rate of diced red onions (Allium cepa L. cv. Vermelha da Póvoa). Postharvest Biol. Technol. 2018, 140, 27–33. [Google Scholar] [CrossRef]
  111. Ma, Y.-L.; Zhu, D.-Y.; Thakur, K.; Wang, C.-H.; Wang, H.; Ren, Y.-F.; Zhang, J.-G.; Wei, Z.-J. Antioxidant and antibacterial evaluation of polysaccharides sequentially extracted from onion (Allium cepa L.). Int. J. Biol. Macromol. 2018, 111, 92–101. [Google Scholar] [CrossRef]
  112. Rouf, R.; Uddin, S.J.; Sarker, D.K.; Islam, M.T.; Ali, E.S.; Shilpi, J.A.; Nahar, L.; Tiralongo, E.; Sarker, S.D. Antiviral potential of garlic (Allium sativum) and its organosulfur compounds: A systematic update of pre-clinical and clinical data. Trends Food Sci. Technol. 2020, 104, 219–234. [Google Scholar] [CrossRef] [PubMed]
  113. Yamaguchi, Y.; Kumagai, H. Characteristics, biosynthesis, decomposition, metabolism and functions of the garlic odour precursor, S-allyl-l-cysteine sulfoxide (Review). Exp. Ther. Med. 2020, 19, 1528–1535. [Google Scholar] [CrossRef]
  114. Cai, L. Compounds from Syzygium aromaticum Possessing Growth Inhibitory Activity Against Oral Pathogens. J. Nat. Prod. 1996, 59, 987–990. [Google Scholar] [CrossRef]
  115. Costa, R.; Bisignano, C.; Filocamo, A.; Grasso, E.; Occhiuto, F.; Spadaro, F. Antimicrobial activity and chemical composition of Citrus aurantifolia (Christm.) Swingle essential oil from Italian organic crops. J. Essent. Oil Res. 2014, 26, 400–408. [Google Scholar] [CrossRef]
  116. Atindehou, M.; Lagnika, L.; Guérold, B.; Strub, J.M.; Zhao, M.; Van Dorsselaer, A.; Marchioni, E.; Prévost, G.; Haikel, Y.; Taddéi, C.; et al. Isolation and Identification of Two Antibacterial Agents from Chromolaena odorata L. Active against Four Diarrheal Strains. Adv. Microbiol. 2013, 3, 29382. [Google Scholar] [CrossRef]
  117. Nenov, N.; Gochev, V.; Girova, T.; Stoilova, I.; Atanasova, T.; Stanchev, V.; Stoyanova, A. Low Temperature Extraction of Essential Oil Bearing Plants by Liquefied Gases. 6. Barks from Cinnamon (Cinnamomum zeylanicum Nees). J. Essent. Oil Bear. Plants 2011, 14, 67–75. [Google Scholar] [CrossRef]
  118. Kothiwale, S.V.; Patwardhan, V.; Gandhi, M.; Sohoni, R.; Kumar, A. A comparative study of antiplaque and antigingivitis effects of herbal mouthrinse containing tea tree oil, clove, and basil with commercially available essential oil mouthrinse. J. Indian Soc. Periodontol. 2014, 18, 316–320. [Google Scholar] [CrossRef]
  119. Al-Aamri, M.S.; Al-Abousi, N.M.; Al-Jabri, S.S.; Alam, T.; Khan, S.A. Chemical composition and in-vitro antioxidant and antimicrobial activity of the essential oil of Citrus aurantifolia L. leaves grown in Eastern Oman. J. Taibah Univ. Med. Sci. 2018, 13, 108–112. [Google Scholar] [CrossRef]
  120. Erel, Ş.; Reznicek, G.; Şenol, S.; Yavaşoğlu, N.; Konyalioğlu, S.; Zeybek, A. Antimicrobial and antioxidant properties of Artemisia L. species from western Anatolia. Turk. J. Biol. 2012, 36, 75–84. [Google Scholar] [CrossRef]
  121. Pandey, B.P.; Thapa, R.; Upreti, A. Chemical composition, antioxidant and antibacterial activities of essential oil and methanol extract of Artemisia vulgaris and Gaultheria fragrantissima collected from Nepal. Asian Pac. J. Trop. Med. 2017, 10, 952–959. [Google Scholar] [CrossRef]
  122. Ene, A.C.; Atawodi, S.E.; Fatihu, M.Y. Acute Toxicity of Chloroform Extract of Artemisia macivera Linn in Swiss Albino Mice. J. Pharm. Res. Int. 2014, 4, 1900. [Google Scholar] [CrossRef]
  123. Radulović, N.S.; Genčić, M.S.; Stojanović, N.M.; Randjelović, P.J.; Stojanović-Radić, Z.Z.; Stojiljković, N.I. Toxic essential oils. Part V: Behaviour modulating and toxic properties of thujones and thujone-containing essential oils of Salvia officinalis L., Artemisia absinthium L., Thuja occidentalis L. and Tanacetum vulgare L. Food Chem. Toxicol. 2017, 105, 355–369. [Google Scholar] [CrossRef] [PubMed]
  124. Ibrahim, D.; Hong, L.S.; Kuppan, N. Antimicrobial Activity of Crude Methanolic Extract from Phyllanthus niruri. Nat. Prod. Commun. 2013, 8, 1934578X1300800422. [Google Scholar] [CrossRef]
  125. El-Saber Batiha, G.; Beshbishy, A.M.; Wasef, L.G.; Elewa, Y.H.A.; Al-Sagan, A.A.; El-Hack, M.E.A.; Taha, A.E.; Abd-Elhakim, Y.M.; Devkota, H.P. Chemical Constituents and Pharmacological Activities of Garlic (Allium sativum L.): A Review. Nutrients 2020, 12, 872. [Google Scholar] [CrossRef]
  126. Khaerunnisa, S.; Kurniawan, H.; Awaluddin, R.; Suhartati, S.; Soetjipto, S. Potential Inhibitor of COVID-19 Main Protease (Mpro) From Several Medicinal Plant Compounds by Molecular Docking Study. Preprints 2020, 2020, 2020030226. [Google Scholar] [CrossRef]
  127. Di Pierro, F.; Khan, A.; Iqtadar, S.; Mumtaz, S.U.; Chaudhry, M.N.A.; Bertuccioli, A.; Derosa, G.; Maffioli, P.; Togni, S.; Riva, A.; et al. Quercetin as a possible complementary agent for early-stage COVID-19: Concluding results of a randomized clinical trial. Front. Pharmacol. 2023, 13, 1096853. [Google Scholar] [CrossRef]
  128. Cunningham, A.C.; Goh, H.P.; Koh, D. Treatment of COVID-19: Old tricks for new challenges. Crit. Care Lond. Engl. 2020, 24, 91. [Google Scholar] [CrossRef]
  129. Fitero, A.; Bungau, S.G.; Tit, D.M.; Endres, L.; Khan, S.A.; Bungau, A.F.; Romanul, I.; Vesa, C.M.; Radu, A.-F.; Tarce, A.G.; et al. Comorbidities, Associated Diseases, and Risk Assessment in COVID-19—A Systematic Review. Int. J. Clin. Pract. 2022, 2022, 1571826. [Google Scholar] [CrossRef]
  130. Kabir, M.T.; Uddin, M.S.; Hossain, M.F.; Abdulhakim, J.A.; Alam, M.A.; Ashraf, G.M.; Bungau, S.G.; Bin-Jumah, M.N.; Abdel-Daim, M.M.; Aleya, L. nCOVID-19 Pandemic: From Molecular Pathogenesis to Potential Investigational Therapeutics. Front. Cell Dev. Biol. 2020, 8, 616. [Google Scholar] [CrossRef] [PubMed]
  131. Arnab, R. Chapter 7—Stratified Sampling. In Survey Sampling Theory and Applications; Arnab, R., Ed.; Academic Press: Cambridge, MA, USA, 2017; pp. 213–256. [Google Scholar] [CrossRef]
  132. Sreekeesoon, D.P.; Mahomoodally, M.F. Ethnopharmacological analysis of medicinal plants and animals used in the treatment and management of pain in Mauritius. J. Ethnopharmacol. 2014, 157, 181–200. [Google Scholar] [CrossRef] [PubMed]
  133. Cadena-González, A.L.; Sørensen, M.; Theilade, I. Use and valuation of native and introduced medicinal plant species in Campo Hermoso and Zetaquira, Boyacá, Colombia. J. Ethnobiol. Ethnomed. 2013, 9, 23. [Google Scholar] [CrossRef] [PubMed]
  134. Siddique, H.; Pendry, B.; Rashid, M.A.; Rahman, M.M. Medicinal plants used to treat infectious diseases in the central part and a northern district of Bangladesh—An ethnopharmacological perception. J. Herb. Med. 2021, 29, 100484. [Google Scholar] [CrossRef]
  135. Friedman, J.; Yaniv, Z.; Dafni, A.; Palewitch, D. A preliminary classification of the healing potential of medicinal plants, based on a rational analysis of an ethnopharmacological field survey among Bedouins in the Negev Desert, Israel. J. Ethnopharmacol. 1986, 16, 275–287. [Google Scholar] [CrossRef]
Figure 1. Haiti maps with study areas (Dots correspond to survey locations).
Figure 1. Haiti maps with study areas (Dots correspond to survey locations).
Plants 13 02383 g001
Figure 2. UV value for COVID-19 plants.
Figure 2. UV value for COVID-19 plants.
Plants 13 02383 g002
Figure 3. UV value for plants used for flu and colds.
Figure 3. UV value for plants used for flu and colds.
Plants 13 02383 g003
Figure 4. Survey questions inspired by TRAMIL.
Figure 4. Survey questions inspired by TRAMIL.
Plants 13 02383 g004
Table 1. Sociodemographic factors related to the respondents.
Table 1. Sociodemographic factors related to the respondents.
Male% of MaleFemale% of Female
Gender 2218.339881.67%
Age (mean ± sd) years 39.29 ± 14.07
CommunesZoneNumber of family representatives% of family reprensentativesAge
CarrefourUrban54.1724–67
Croix-des-BouquetRural108.3318–56
DelmasUrban4335.8328–51
GressierRural6545–60
LéogâneRural6521–70
Pétion-VilleUrban2016.6723–70
Port-au-PrinceUrban2016.6719–69
TabarreRural108.3325–56
Table 2. Percentage (%) of botanical families most used for all these preventions and remedies.
Table 2. Percentage (%) of botanical families most used for all these preventions and remedies.
Botanical Families% Respiratory Diseases% Flu and Cold% COVID-19
Amaryllidaceae0.8825.6673.45
Asteraceae5.549.5444.95
Curcubitaceae-7.6192.39
Lamiaceae9.3957.1433.47
Myrtaceae252154
Rutaceae8.1351.2040.67
Zingiberaceae10.6811.6577.67
Table 3. The list of plants mentioned, Creole vernacular names, families, their RFC value, and their traditional uses. RFC = relative frequency of citation. N/A = not available. Traditional plant for flu, COVID-19, and respiratory disease. The voucher specimens are stored at the COVACHIM laboratory in Guadeloupe and, for some, at the URE laboratory at the Faculty of Sciences (UEH) in Haiti.
Table 3. The list of plants mentioned, Creole vernacular names, families, their RFC value, and their traditional uses. RFC = relative frequency of citation. N/A = not available. Traditional plant for flu, COVID-19, and respiratory disease. The voucher specimens are stored at the COVACHIM laboratory in Guadeloupe and, for some, at the URE laboratory at the Faculty of Sciences (UEH) in Haiti.
Scientific NamesCreole Vernacular NamesEnglish Common NamesFamiliesVouchers Specimen CodesNumber of Families Citing It in the SurveyRFCParts Used and Mode of Preparation Flu, Cold, Respiratory Diseases and for a Few COVID-19 SymptomsReferences
Allium ampeloprasum var. porrum.PwawoLeekLiliaceaeURE9120.016Is used in infusions and/or decoction mixtures for COVID-19N/A
Abrus precatorius L.Lyann reglisRosary peaFabaceaeURE73270.225Decoction of leavesN/A
Allium cepa L.ZonyonOnionAmaryllidaceaeURE111610.508Mix the onion and take the juice with honey/or brown sugar for flu, cold[28]
Allium sativum L.LayGarlicAmaryllidaceaeURE68520.433The garlic syrup to use against the or the juice with honey for flu, or bulb in decoction for flu or the stomach pains[3,28]
Aloe vera L.LalwaAloeAloeaceaeURE63630.525Swallow a small butcher of aloe gel with water all morning for COVID-19 or gel in decoction for cold[28,29]
Ananas comosus L.AnanaPineappleBromeliaceaeURE0510.008Fruit juiceN/A
Annona muricata L.KowosolSoursopAnnonaceaeURE61280.233Leaf infusion/fruit juiceN/A
Apium graveolens L.SeleriCeleryApiaceaeURE9580.067For flu syndrome, used fresh leafy stems in infusions and/or decoction[28]
Argemone mexicana L.ChadwonPrickly PoppyPapaveraceaeURE24250.208The root is used for stomach pains and 3 or 4 leaves and put them in a decoction for flu[28,29]
Artemisia vulgaris L.AmwazMugwortAsteraceaeURE04470.392Leaves infusion for COVID-19N/A
Bromelia pinguin L.Grenn pengwenPinuelaBromeliaceaeURE3910.008Leaf decoction or grilled fruitN/A
Carnavalia rosea L.Lyann kayimanCoastal Jack BeanFabaceaeURE7180.067Leaves and stems infusion/decoction for COVID-19N/A
Catalpa longissima L.Bwad chènSpanish OakBignoniaceaeURE2210.008Bark in decoction for stomach pain and fever[28]
Cinnamomum verum J. S. PreslKanèlCinnamonLauraceaeURE51490.408Bark decoction for vomiting and diarrhea[28,30]
Cissus sicyoides L.Lyann mòlPrincess vineVitaceaeURE72230.192Leaves in decoction[28]
Citrus aurantiifolia (Christm.) SwingleSitwonLimeRutaceaeURE98590.492Bark or leaf in decoction or infusion for fever. Leaf in decoction for headaches. Juice for flu, cough, and diarrhea[31]
Citrus aurantium L.Zoranj siBitter OrangeRutaceaeURE84470.392Bark or leaf in decoction or infusion for fever. Leaf in decoction for flu. Juice for flu, cough, and diarrhea[3,28,32]
Citrus maxima Merr.ChadèkPomeloRutaceaeURE23370.308Leaves in decoction for fever[3,28]
Citrus reticulata BlancoMandarinMandarinRutaceaeURE75280.233Fruit juiceN/A
Citrus sinensis L.Zoranj dousSweet OrangeRutaceaeURE112380.317Fruit juice and/or leaf in decoction for flu or cough. The bark in decoction for fever[28,29]
Cocos nucifera L.KokoyeCoconutArecaceaeURE5820.017For flu, the oil of the fruit is used in friction on the chest. Also used against asthma by mouth[28]
Corchorus siliquosus L.Ti laloSlippery DickMalvaceaeURE102120.1Leaves and stems infusion/decoction[29]
Croton flavens L.Ti bonmWelensaliEuphorbiaceaeURE10110.008Leaves in infusionN/A
Curcuma longa L.SafranTurmericZingiberaceaeURE9480.067Is used in infusions and/or decoction mixtures for COVID-19 and is also used in punchN/A
Cymbopogon citratus (DC) StapfSitwonèlLemongrassPoaceaeCOVA21380.317Leaves and/or root in decoction for flu, cold, and fever[28]
Daucus carota subsp. SativusKawótCarrotApioideaeURE5480.067The juiceN/A
Eucalyptus globulus Labill.EkaliptisBluegum eucalyptusMyrtaceaeURE29390.325Infusion and/or decoction of the leaves for flu, cold/leaves for internal infusion and inhalation[28]
Eupatorium odoratum L.LangichatSiam weedAsteraceaeURE65500.417Juice of the leaves to drink in a spoon/infusion of the leaves[3,29]
Grossypium barbadense L.KotonCreole cottonMalvaceaeURE5910.008Aerial parts or leaves in decoction for abdominal pains[28]
Guazuma ulmifolia Lam.Bwa dòmBastard CedarMalvaceaeURE20120.1Leaves in decoction for flu and cold[28]
Hamelia patens Jacq.Fèy korayScarlet bushRubiaceaeURE3540.033Natural leaf applied on the head or in bath[28]
Hibiscus rosa-sinensis L.ChoublakChina-roseMalvaceaeURE25330.275For flu and cold: infusion and/or decoction of young leaves/infusion of flowers for children. Crumpled leaf applied locally for headaches[28,29]
Hyptis suaveolens L. Poit.Gwo tenWild spikenardLamiaceaeURE41320.267Leaves in infusion or decoction[29]
Jatropha gossypifolia L.Ti medsiyenBellyache bushEuphorbiaceaeURE103250.208Leaves in infusion or decoction for diarrhea and pain[28]
Jatropha curcas L.Gwo medsiyenPhysic NutEuphorbiaceaeURE7910.008Fresh leaf for bath[28]
Kalanchoe pinnata (Lam,) Pers.Fèy chòcheCathedral bellsCrassulaceaeURE3020.017Leaves in decoction or juice for flu or cold. For headaches, the leaves are crushed and applied to the forehead[28]
Lantana camara L.BonbonyenLantanaVerbenaceaeCOVA14130.108Infusion and/or decoction of the leaves, flowers, or the aerial part for flu and cold[28]
Lipia alba L.MelisBushy matgrassVerbenaceaeCOVA08390.325Fresh leaves or aerial parts in decoction for flu, cold, and tiredness[28]
Lycopersicon Esculentum Mill.TomatGarden tomatoSolanaceaeURE105240.2Buds in infusion[29]
Malpighia emarginata DCSerizAcerola cherryMalpighiaceaeURE96380.317Leaves in decoction/fruit juice[29]
Mammea americana L.AbrikoMammee appleClusiaceaeURE02180.15Fruit juiceN/A
Melia azedarach L.Fèy lilaChinaberry treeMeliaceaeURE3280.067Infusion of young leaves[29]
Melicoccus bijugatus Jacq.KenèpMamoncilloSapindaceaeURE55160.133Gargle leaf juice/fruit food[29]
Mentha arvensis L.Fèy mantCorn MintLamiaceaeURE33260.217Infusion and/or decoction of the leaves for flu, cold, and stomach pains[28]
Mentha nemorosa Wild.MantMentha nemorosaLamiaceaeURE76380.317Leafy stem in hot infusion[29]
Moringa oleifera L.DolivHorseradish treeMoringaceaeURE17250.208Flower in hot infusionN/A
Mormordica charantia L.Asowosi/asosiBitter GourdCurcubitaceaeCOVA12920.767The aerial parts crushed and/or aqueous maceration, in baths, frictions, and local application. Or the aerial parts are used in decoction for fever and pain[3,28]
Musa x paradisiaca L.BannannPlantainMusaceaeURE12240.2Leaf in decoction/fruit food[29]
Myristica fragrans L.MiskadNutmegMyristicaceaeCOVA04130.108Is used in infusions and/or decoction mixtures for COVID-19 and is also used in punchN/A
Ocimum basilicum L.BazilikBasilLamiaceaeURE15390.325Leaves in decoction for stomach pains and vomiting[28]
Ocimum gratissimum L.FonbazenClove basilLamiaceaeURE0970.058Leaf in decoction for pain[3,28]
Ocimum micranthum Wild.AtiyayoN/ALamiaceaeURE110290.242Leaf juiceN/A
Opuntia antillana Britton & RoseRakètPrickly pearCactaceaeURE9310.0083 small pieces to put in 1 L of water and drink it all dayN/A
Passiflora edulis SimsGenadyaPassion fruitPassiforaceaeURE37300.25Fruit juiceN/A
Passiflora foetida L.MarigouyaWild maracujaPassiforaceaeURE77120.1Leaves in decoction[29]
Petroselinum sativum Hoffm.PèsiParsleyApiaceaeURE8850.042Is used in infusions and/or decoction mixtures for COVID-19N/A
Phaseolus vulgaris L.PwaFrench beanFabaceaeURE90340.283Leaves in decoction[29]
Phyllanthus niruri L.DèyèdoGale Of WindPhyllanthaceaeURE28400.333Infusions and/or decoction for the fever[29]
Physalis angulata L.KòkmòlBalloon cherrySolanaceaeURE5760.05Infusion of young leaves[29]
Pinus occidentalis Sw.Bwa pen/bwa chandèlN/APinaceaeURE21120.1Resin in infusion or essence in friction[29]
Plectranthus amboinicus (Lour.) Spreng.Gwo tenIndian borageLamiaceaeCOVA07390.325Infused leaves for cold[28]
Portulaca oleracea L.KoupyePurslanePortulacaceaeURE60200.167The leaves are edibleN/A
Prosopis juliflora Sw DCBayawondMesquiteMimosaceaeURE14240.2Juice of leaves[29]
Rhoeo spathacea (Sw.) Stearn.Boul di marsBoat lilyCommelinaceaeURE19240.2Leaves in infusion[29]
Ricinus communis L.Fèy maskretiCastor beanEuphorbiaceaeCOVA18390.325Oil for fiction[3,28,29]
Saccharum officinarum L.KannSugar canePoaceaeURE50120.1Syrup/stem juiceN/A
Samyda rosea SimsKasesèk/magripGuayabillaSalicaceaeURE52610.508Infusion and/or decoction of the leaves[29]
Senecioides cinerea L. O. KtzeTòchon salN/AAsteraceaeURE104120.1Aerial part in decoction[29]
Stachytarpheta jamaicensis (L.) Vahl.VèvennBlue porter weedVerbenaceaeURE108170.142Is used in infusions and/or decoction for headaches[3]
Stemodia durantifolia L.Twa zòm fòWhitewoolly twintipPlantaginaceaeURE10670.058Aerial parts in decoction[29]
Syzygium aromaticum L.JiwòfCloveMyrtaceaeURE44610.508Nail decoction for inhalation and/or orallyN/A
Thymus vulgaris L.TenThymeLamiaceaeURE99250.208Plant in decoction and/or infusion[29]
Verbascum thapsus L.MolennBig taperScrophulariaceaeURE81120.1Leaves and flowers in infusion[29]
Waltheria indica L.Bale blanSleepy morningMalvaceaeURE10120.1Leaves in infusion or decoction[29]
Zingiber officinale RoscoeJenjanmGingerZingiberaceaeURE43950.792Decoction, boil the root of the grated ginger for flu, cold, and fever[28,29]
Table 4. Some oral herbal preparations for the prevention and treatment of COVID-19. Some remedies used to prevent/treat COVID-19 by Haitians using up to 6 plants in mixtures or punch with other ingredients.
Table 4. Some oral herbal preparations for the prevention and treatment of COVID-19. Some remedies used to prevent/treat COVID-19 by Haitians using up to 6 plants in mixtures or punch with other ingredients.
Scientific NamesAmount of Plants UsedMode of PreparationReferences
Allium ampeloprasum var. porrum. & Apium graveolens L. & Daucus carota subsp. Sativus 3One leek, one handful of celery, 2 carrots. Mix all together and drink the juiceN/A
Allium sativum L. & Mormordica charantia L. & Phyllanthus niruri L. 3Decoction of a few cloves of garlic with the skin, then add the leaves of the Bitter Gourd and Gale Of Wind[33]
Allium cepa L. & Allium sativum L. & Aloe vera L. Burn & Myristica fragrans & Petroselinum sativum Hoffm. & Zingiber officinale Roscoe 6Mix a spoonful of aloe gel with a few cloves of garlic, nutmeg, parsley and ginger[33]
Allium cepa L. & Allium sativum L & Aloe vera L. Burn & Syzygium aromaticum & Zingiber officinale Roscoe 5Mix half a purple onion, 3 cloves of garlic, a spoonful of aloe gel, a pinch of powdered clove, and a piece of ginger to drink a spoonful twice a day[33]
Allium cepa L. & Aloe vera L. Burn & Myristica fragrans3punch with milk and an egg, a large spoonful of aloe gel[33]
Allium sativum L & Aloe vera L. Burn & Cinnamomum verum L. & Zingiber officinale Roscoe4Punch with milk, egg, and rum[33]
Allium sativum L & Cinnamomum verum L. & Citrus aurantiifolia Swingle & Mormordica charantia L. & Syzygium aromaticum & Zingiber officinale Roscoe6Boil Bitter Gourd and chop a compartment of garlic, then add a few grains of clove and cinnamon, then prick a lime, and finally add a little ginger and put the whole in decoction. After boiling, before drinking it, squeeze the lemon juice[33]
Allium sativum L & Cinnamomum verum L. & Curcuma longa L. & Mormordica charantia L. & Syzygium aromaticum 5Decoction of 5 garlic cloves with a piece of turmeric and some peels of cinnamon, and then add the leaves of Bitter Gourd after a few minutes of boiling[33]
Allium sativum L. & Cinnamomum verum L. & Mormordica charantia L. & Eupatorium odoratum L. & Syzygium aromaticum & Zingiber officinale Roscoe 6Decoction of garlic pods with cinnamon bark and clove grains with ginger root, and after a few minutes of boiling, it is necessary to add the leaves of Bitter Gourd and siam weed[33]
Allium sativum L. & Citrus aurantiifolia Swingle & Zingiber officinale Roscoe 3Boil 2 to 3 cloves of garlic, the lime with its skin, and the grated ginger[33]
Allium sativum L. & Aloe vera L. Burn 21 big spoon of aloe gel, then add half a glass of white rum and let macerate for 5 mn. Then, in a mixer, we put 5 lay pods and a spoon of honey syrup. Then, when the 5 mn approximately has elapsed we put the aloe to macerate with the rum in the mixer. Also, immediately after, we add half a glass of water proportioned to the rum and let mix the whole for 6 to 7 mn[33]
Aloe vera L. Burn 1Swallow a small butcher of aloe gel with water all morning[33]
Aloe vera L. Burn & Zingiber officinale Roscoe22 or 3 pieces of ginger plus 6 cloves of garlic plus a purple onion, we mix them, and we take only the juice after sieving, and we take one or two spoonsN/A
Ananas comosus L.1fruit juice/decoction fruit skinN/A
Artemisia vulgaris L.1Boil 1 to 2 L of water and pour the hot water on a small amount of the plant leaf because it is very strong[33]
Carnavalia rosea L.1Infusion of the stem with young leavesN/A
Catalpa longissima L.1Infusion and/or decoction of the leafN/A
Cinnamomum verum L. & Citrus aurantiifolia Swingle & Mormordica charantia L. & Phyllanthus niruri L. & Zingiber officinale Roscoe 5Boil some cinnamon peels, grated ginger and lime with skin for about 8 min, then add the leafy stems Bitter Gourd and the leafy stems Gale of wind [33]
Cinnamomum verum L. & Citrus aurantium L. & Syzygium aromaticum L.5Boil some cinnamon bark, bitter orange without the skin and cloves[33]
Cinnamomum verum L. & Citrus aurantium L. & Mormordica charantia L. & Petroselinum sativum Hoffm. & Syzygium aromaticum L. & Zingiber officinale Roscoe 6Boil some cinnamon, grated ginger, bitter orange without the skin, and some cloves. Then add the parsley leaves and bitter gourd[33]
Cinnamomum verum L. & Plectranthus amboinicus (Lour.) Spreng. & Syzygium aromaticum L. & Zingiber offinale Roscoe 4Boil some cinnamon bark, grated ginger, and cloves. Then add the leaves of the Indian borage[33]
Cinnamomum verum L. & Syzygium aromaticum L.2Decoction of clove seeds and cinnamon bark to drink every morning and evening[33]
Cinnamomum verum L. & Zingiber officinale Roscoe2Mixed tea in decoction: Boil some cinnamon bark, grated ginger[33]
Cinnamomum verum L.& Croton flavens L.2decoction of the cinnamon, then the leaf for about 2 min to drink twice a week for 1 month, then once a weekN/A
Cinnamomum verum L.& Cymbopogon citratus (DC) Stapf & Zingiber officinale Roscoe 3Tea mixed in decoction. Boil for about 10 min the grated ginger, the cinnamon bark, and the leaf and/or the root of the lemongrass[33]
Citrus aurantiifolia Swingle & Mormordica charantia L & Phyllanthus niruri L. & Stachytarpheta jamaicensis (L.) Vahl.4Tea mixed in decoction. Boil the lime, then add the leaves of Bitter Gourd, blue porter weed, and Gale Of Wind and let them boil for about 5 min [33]
Citrus aurantiifolia Swingle & Mormordica charantia L. 2Tea mixed in decoction. Boil the lime and then add the Bitter Gourd leaves[33]
Citrus aurantiifolia Swingle & Mormordica charantia L. & Syzygium aromaticum L.3Tea mixed in decoction. Boil the lime and cloves, then add the Bitter Gourd leaves[33]
Citrus aurantiifolia Swingle & Mormordica charantia L. & Thymus vulgaris L.3Tea mixed in decoction. Boil the lime and then add the thyme leaves and Bitter Gourd[33]
Citrus aurantiifolia Swingle & Phyllanthus niruri L. 2decoction of the whole plant with the fruit of the lemon with the skin[33]
Citrus aurantium L. & Cymbopogon citratus (D.C) Stapf & Syzygium aromaticum L.3decoction of the bitter orange without the skin with lemongrass leaves and some cloves [33]
Cymbopogon citratus (DC) Stapf1Decoction of the whole plant or leafN/A
Eupatorium odoratum L.1Infusion of the stem with leaf or a spoon of the juice of the leafN/A
Melia azedarach/Azadirachta indica A. Juss1Infusion of young leavesN/A
Mormordica charantia L.1Infusion and/or decoction of the whole plant or maceration in rum[33]
Petroselinum sativum Hoffm. & Syzygium aromaticum L. & Zingiber officinale Roscoe 3Tea mixed in decoction. Boil the ginger and cloves, then add the parsley leavesN/A
Portulaca oleracea L.1Eat as a vegetable by heating it just a little in waterN/A
Samyda rosea Sims1infusion/decoction of the leafN/A
Stemodia durantifolia1Infusion with a small quantity of the leaves because the plant is very strongN/A
Thymus vulgaris L.1Infusion and/or decoction of the whole plant. Or put 2 tablespoons of powdered thyme, add hot water, let it wait for 4–5 min, then cut a lemon, squeeze it, and add 2 spoonfuls of honey[33]
Zingiber officinale Roscoe1Decoction: Cut the ginger into small pieces or use a grater. Boil it for 10 to 15 min. When it is good, add honey or brown sugar[33]
Table 5. List of herbal preparations and related information used for the treatment of COVID-19.
Table 5. List of herbal preparations and related information used for the treatment of COVID-19.
Plant SpeciesNumber of Families Reporting the Use of SpeciesNumber of Ailments Treated by the SpeciesMain UseNumber of Families for the Main UseFL %
Abrus precatorius L.271Flu27100
Allium cepa L.612COVID-193455.737
Allium sativum L.523COVID-194994.231
Aloe vera L.631COVID-1963100
Annona muricata L.283Flu1657.143
Argemone mexicana L.251Flu25100
Artemisia vulgaris L.471COVID-1947100
Cinnamomum verum J. S. Presl492Flu3061.224
Cissus sicyoides L.231Flu23100
Citrus aurantifolia Swingle593Flu3152.542
Citrus aurantium L.473Flu3370.213
Citrus maxima Merr.372COVID-192259.459
Citrus reticulata Blanco282COVID-191864.286
Citrus sinensis L.383Flu1847.364
Corchorus siliquosus L.121Flu12100
Cymbopogon citratus (DC) Stapf.382Flu2771.053
Eucalyptus globulus Labill.393Flu2051.282
Eupatorium odoratum L.503Flu4284
Guazuma ulmifolia Lam.121Flu12100
Hibiscus rosa-sinensis L.331Flu33100
Hyptis suaveolens L. Poit.322COVID-191753.125
Jatropha gossypiifolia L.252Flu2496
Lantana camara L.131Flu13100
Lipia alba L.3910Flu2974.359
Lycopersicon Esculentum Mill.242Flu/COVID-191250
Malpighia emarginata DC382Flu3592.105
Mammea americana L.182Flu1161.11
Melicoccus bijugatus Jacq162Flu1275
Mentha arvensis L.263COVID-191142.307
Mentha nemorosa Wild.382Flu3489.473
Moringa oleifera L.252COVID-191560
Mormordica charantia L.922COVID-198592.391
Musa x paradisiaca L.241Flu24100
Myristica fragrans L.132Flu861.538
Ocimum basilicum L.393Flu2564.102
Ocimum micranthum Wild.292Flu2482.758
Passiflora edulis Sims302Flu2170
Passiflora foetida L.121Flu12100
Phaseolus vulgaris L.342Flu2470.588
Phyllanthus niruri L.401COVID-1940100
Pinus occidentalis Sw.121Flu12100
Plectranthus amboinicus (Lour.) Spreng392Flu2769.231
Portulaca oleracea L.201COVID-1920100
Prosopis juliflora Sw. DC241Flu24100
Rhoeo spathacea (Sw.) Steam241Flu24100
Ricinus communis L.393Respiratory diseases1538.461
Saccharum officinarum L.121Flu12100
Samyda dodecandra Jacq.613Flu5996.721
Senecioides cinerea L. O. Ktze121Flu12100
Stachytarpheta jamaicensis (L.) Vahl.171COVID-1917100
Syzygium aromaticum L.613COVID-195081.967
Thymus vulgaris L.252COVID-191768
Verbascum thapsus L.121Flu12100
Waltheria indica L.121Flu12100
Zingiber officinale Roscoe953COVID-197275.789
Table 6. The list of plants mentioned and parts used. N/A = not available.
Table 6. The list of plants mentioned and parts used. N/A = not available.
Scientific NamesFamiliesParts Used in the LiteratureUses in the LiteratureReferences
Allium ampeloprasum var. porrum.LiliaceaeBulbsInflammatory, gastroprotective activities[35]
Abrus precatorius L.FabaceaeSeeds, fresh rootsAntifungal, apoptotic, antihistaminic, antiproliferative, anti-oxidant, potential anticancer agents [36]
Allium cepa L.AmaryllidaceaeBulbsAnti-oxidant, immuno-modulator, antimicrobial, neuroprotective properties[37]
Allium sativum L.AmaryllidaceaeBulbsFor colds, fever, cough, asthma, antimicrobial[38]
Aloe vera L.AloeaceaeLeaves, gelAntiviral, antidiabetic, laxative, protective against radiation, antiallergic, anti-inflammatory, antibacterial[39]
Ananas comosus L.BromeliaceaePeel, fruit, leafAntimalarial, anti-nociceptive and anti-inflammatory[40]
Annona muricata L.AnnonaceaePlants, leaves, Anti-angiogenic, antibacterial, antiviral, anti-inflammatory, anti-oxidant [41]
Apium graveolens L.ApiaceaePlant, root, leafAntimicrobial, antiparasitic, cardioprotective, gastroprotective, neuroprotective, hypolipidemic, cytotoxic, anti-oxidant, anti-inflammatory, and anti-infertility[42]
Argemone mexicana L.PapaveraceaeFlowers, berries, and leavesAntibacterial and antifungal[43]
Artemisia vulgaris L.AsteraceaePlantAntimalarial, anti-inflammatory, antihypertensive, anti-oxidant, anti-tumoral, immunomodulatory, hepatoprotective, antispasmodic and antiseptic[44]
Bromelia pinguin L.BromeliaceaeFruit pulpAntifungal[45]
Carnavalia rosea L.FabaceaeLeavesIn Haiti, use against fluN/A
Catalpa longissimi L.BignoniaceaeLeaf, plant, barkIn Haiti, use against pneumopathy, antidiarrheal, sore throats, stomach aches[29]
Cinnamomum verum J. S. PreslLauraceaeBarkAnti-oxidant, antimicrobial, anti-inflammatory[30]
Cissus sicyoides L.VitaceaeLeaves and stemsAnti-oxidant activity, neuroprotective and anti-inflammatory[46]
Citrus aurantiifolia (Christm.) SwingleRutaceaeLeaves and fruit peelsAntimicrobial, fungicidal, insecticidal, anticancer, anti-oxidant properties[31]
Citrus aurantium L.RutaceaeLeaves, fruit, fruit peel, fruit peel essential oilAnti-oxidant properties, antimicrobial, antifungal, antiparasitic, and anti-inflammatory activities[32]
Citrus maxima Merr.RutaceaePeel essential oil Antibacterial[47]
Citrus reticulata BlancoRutaceaePeelsAnti-oxidant and antiproliferative[48]
Citrus sinensis L.RutaceaeSeed oil, fruitAnti-oxidant, antimicrobial [49]
Cocos nucifera L.ArecaceaeFloral axis, root, coconut water Antibacterial, anti-oxidant[50]
Corchorus siliquosus L.MalvaceaeLeaves and stemsIn Haiti, use against flu [29]
Croton flavens L.EuphorbiaceaeLeaf essential oilAnticancer activity[51]
Curcuma longa L.ZingiberaceaeCurcumin of rootAntiviral, antitumor, anti-atherogenic, anti-inflammatory[52]
Cymbopogon citratus (DC) StapfPoaceaeLeaves and rootsAntibacterial[53]
Daucus carota subsp. SativusApioideaeAerial parts, oilAntibacterial[54]
Eucalyptus globulus Labill.MyrtaceaeEssential oils, leavesAntibacterial[55]
Eupatorium odoratum L.AsteraceaePlantantimicrobial, anti-inflammatory, analgesic, anti-oxidant, and cytoprotective properties[56,57]
Grossypium barbadense L.MalvaceaeLeaves and rootsAnti-oxidant, antidiarrheal, healing, diuretic, respiratory conditions, pneumonia[58]
Guazuma ulmifolia Lam.MalvaceaeStem bark, fruit, and leavesAntimicrobial, anti-oxidant, antiprotozoal, antidiarrheal activities, and cardioprotective effect[59]
Hamelia patens Jacq.RubiaceaeLeavesAntibacterial [60]
Hibiscus rosa-sinensis L.MalvaceaeParts used and mode of preparation for flu, cold, and respiratory diseasesAntibacterial, anti-oxidant[61]
Hyptis suaveolens L. Poit.LamiaceaeEssential oil of leaves, leavesAntimicrobial, antiviral[62]
Jatropha gossypifolia L.EuphorbiaceaeDifferent parts Antimicrobial[63]
Jatropha curcas L.EuphorbiaceaeRoot, seed, stem, leaf, and flowerAntimicrobial[64]
Kalanchoe pinnata (Lam,) Pers.CrassulaceaeLeavesAnti-inflammatory, antibacterial, anti-tumorous[65]
Lantana camara L.VerbenaceaeLeavesAntibacterial[66]
Lipia alba L.VerbenaceaeEssential oils of leaf, aerial partsAntibacterial[67]
Lycopersicon Esculentum Mill.SolanaceaeTomatosideAntiviral [68]
Malpighia emarginata DCMalpighiaceaeFruitAnti-oxidant activity and antimicrobial[69]
Mammea americana L.ClusiaceaeFruit, leaves, fruit peel, seedAntibacterial[70]
Melia azedarach L.MeliaceaeLeaves, root, and stem barkAntibacterial[71]
Melicoccus bijugatus Jacq.SapindaceaeFruitsAntimicrobial[72]
Mentha arvensis L.LamiaceaeLeavesAntibacterial[73]
Mentha nemorosa Wild.LamiaceaeLeafy stemIn Haiti, use against flu, anti-inflammatory[29]
Moringa oleifera L.MoringaceaeLeaves, roots, pods, seeds, and flowersAntidiabetic, antibacterial, antifungal, and anti-carcinogenic[74]
Mormordica charantia L.CurcubitaceaeLeaves, seeds, whole plant Antibacterial, anti-flu, anti-fever antidiabetic, anthelmintic, antiviral, anti-diarrhea [11,12]
Musa x paradisiaca L.MusaceaePeelAntibacterial[75]
Myristica fragrans L.MyristicaceaeFruitsAntibacterial[76]
Ocimum basilicum L.LamiaceaeLeaves essential oilAntibacterial[77]
Ocimum gratissimum L.LamiaceaeLeaves essential oil, clove Antibacterial, anti-inflammatory, anticancer, hepatoprotective, antidiabetic, antihypertensive, antidiarrhoeal[78]
Ocimum micranthum wild.LamiaceaeEssential oilsAntibacterial[79]
Opuntia antillana Britton & RoseCactaceaeLeafAntibacterial, anti-oxidant[80]
Passiflora edulis SimsPassiforaceaeFruitsAnxiolytic, anti-inflammatory, antibacterial [81]
Passiflora foetida L.PassiforaceaeFlower, leaf, fruitAntibacterial, analgesic, and antidiarrhoeal [82]
Petroselinum sativum Hoffm.ApiaceaeAerial part, plantAnti-inflammatory, anti-oxidant, analgesic and spasmolytic, antidiabetic, immunomodulating, and gastrointestinal effects[83]
Phaseolus vulgaris L.FabaceaeSeeds, homodimeric lectin from seedAntibacterial, antifungal, and antiviral [84]
Phyllanthus niruri L.PhyllanthaceaeLeaves and fruitsAnti-fever, anti-diarrhea, anti-inflammatory[85]
Physalis angulata L.SolanaceaeFruit juice, leafAntidiabetic, anti-inflammatory, antibacterial, anti-oxidant [26]
Pinus occidentalis Sw.PinaceaeResinIn Haiti, use against flu, antirheumatic[29]
Plectranthus amboinicus (Lour.) Spreng.LamiaceaeLeavesAnti-inflammatory, antitumor, antibacterial[86]
Portulaca oleracea L.PortulacaceaeAerial partsAntiviral, antibacterial, anti-inflammatory, antitumor[8]
Prosopis juliflora Sw DCMimosaceaeLeaves, julifloravizoleAntifungal and antibacterial[87]
Rhoeo spathacea (Sw.) Stearn.CommelinaceaePlant, leavesAntifertility, anti-inflammatory, anti-oxidant, and antibacterial[1]
Ricinus communis L.EuphorbiaceaeLeaves, stems, roots, seeds and capsulesAntimicrobial, anti-oxidant, insecticidal, antiasthmatic, anti-inflammatory[88]
Saccharum officinarum L.PoaceaeLeavesAntibacterial[89]
Samyda rosea SimsSalicaceaeLeavesIn Haiti used as an anti-flu/anti-cough [29]
Senecioides cinerea L. O. KtzeAsteraceaePlantIn Haiti, use against flu/cold[29]
Stachytarpheta jamaicensis (L.) Vahl.VerbenaceaeLeavesAntibacterial, antidiarrheal[71]
Stemodia durantifolia L.PlantaginaceaeLeavesAntifertility[1]
Syzygium aromaticum L.MyrtaceaeCloveAnti-oxidant and antimicrobial[90]
Thymus vulgaris L.LamiaceaeEssential oilsAntibacterial[91]
Verbascum thapsus L.ScrophulariaceaeLeavesAntibacterial, inflammatory diseases, diarrhea, asthma[92]
Waltheria indica L.Malvaceae Anti-inflammatory, antiviral, anti-flu[93]
Zingiber officinale RoscoeZingiberaceaeRootAntimicrobial, anti-inflammatory, antiviral [9,10]
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MDPI and ACS Style

Thesnor, V.; Cheremond, Y.; Sylvestre, M.; Meffre, P.; Cebrián-Torrejón, G.; Benfodda, Z. Survey on the Traditional Use of Medicinal Herbs in Haiti: A Study on Knowledge, Practices, and Efficacy Prevention. Plants 2024, 13, 2383. https://doi.org/10.3390/plants13172383

AMA Style

Thesnor V, Cheremond Y, Sylvestre M, Meffre P, Cebrián-Torrejón G, Benfodda Z. Survey on the Traditional Use of Medicinal Herbs in Haiti: A Study on Knowledge, Practices, and Efficacy Prevention. Plants. 2024; 13(17):2383. https://doi.org/10.3390/plants13172383

Chicago/Turabian Style

Thesnor, Valendy, Yvens Cheremond, Muriel Sylvestre, Patrick Meffre, Gerardo Cebrián-Torrejón, and Zohra Benfodda. 2024. "Survey on the Traditional Use of Medicinal Herbs in Haiti: A Study on Knowledge, Practices, and Efficacy Prevention" Plants 13, no. 17: 2383. https://doi.org/10.3390/plants13172383

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