Previous Article in Journal
Hypermucoviscous Multidrug-Resistant Klebsiella variicola Strain LL2208 Isolated from Chinese Longsnout Catfish (Leiocassis longirostris): Highly Similar to Human K. variicola Strains
Previous Article in Special Issue
Lecanicillium psalliotae (Hypocreales: Cordycipitaceae) Exerts Ovicidal and Larvicidal Effects against the Sheep Blood-Feeding Nematode Haemonchus contortus through Its Liquid Culture Filtrates
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

Survey of Gastrointestinal Parasites and Lungworms in Cats and Dogs from Terceira and São Miguel Islands, Azores

by
Romana Teixeira
1,2,*,
Isilda Flor
3,
Telmo Nunes
1,2,
Carlos Pinto
4,
Maria Constança Pomba
1,2 and
Luís Madeira de Carvalho
1,2,*
1
Centre for Interdisciplinary Research in Animal Health, Faculty of Veterinary Medicine, Lisbon University, (CIISA-FMV-ULisboa), Avenida da Universidade Técnica, 1300-477 Lisboa, Portugal
2
Associate Laboratory for Animal and Veterinary Sciences (AL4AnimalS), 1300-477 Lisbon, Portugal
3
Laboratory of Parasitology, Regional Veterinary Laboratory, Vinha Brava, 9700-236 Angra do Heroísmo, Portugal
4
Faculty of Agricultural and Environmental Sciences, University of the Azores, 9700-042 Angra do Heroísmo, Portugal
*
Authors to whom correspondence should be addressed.
Pathogens 2024, 13(8), 648; https://doi.org/10.3390/pathogens13080648
Submission received: 24 June 2024 / Revised: 28 July 2024 / Accepted: 30 July 2024 / Published: 31 July 2024

Abstract

:
Parasitic diseases can affect animal health and welfare, and they may also constitute a danger to public health, particularly in island ecosystems. Fecal samples were collected from 205 dogs and 115 cats on the islands of São Miguel and Terceira, Azores archipelago (Portugal), using the Willis flotation technique and modified Baermann method, for further analysis. The overall prevalence of gastrointestinal parasitism in dogs was 53%, with the following results: Ancylostomatidae (hookworms) (42.44%), Trichuris vulpis (17.56%), Toxocara canis (12.68%) and Cystoisospora spp. (4.39%). In cats, the overall prevalence was also 53%, with the following results: Toxocara cati (31.3%), Ancylostomatidae (30.43%), Cystoisospora spp. (14.78%) and Trichuris sp. (0.87%). The prevalence of lungworms was 0.49% in canines and 20.87% in felines, with Angiostrongylus vasorum and Aelurostrongylus abstrusus species being detected in dogs and cats, respectively. The present survey detected a high prevalence of gastrointestinal infection, in both dogs and cats, probably because the samples came mainly from kennels and catteries and due to the peculiar climatic conditions in this insular territory, with mild temperature and high relative humidity. A considerable prevalence of aelurostrongylosis was also detected (20.87%), so it should be included in the list of differential diagnoses of diseases concerning the respiratory tract in cats of the archipelago.

1. Introduction

Parasites are still one of the main problems that strongly affect our pets. Despite being undervalued, parasitic diseases can seriously affect animal health and well-being, and some of them are zoonotic, which in itself constitutes a danger to public health [1,2].
However, the fact that animals often do not show signs of infection leads to the incorrect prophylaxis and treatment of these infections [3].
Also, at veterinary clinics, the administration of antiparasitic drugs is mainly intended for prophylactic purposes or as a first line in preparing a differential diagnosis, so identification and registration are often undervalued or ruled out. This is due to the small number of parasitological records existing at European, national and island autonomous regions. The only study carried out on the island of São Miguel by Afonso-Roque (1995) of terrestrial vertebrates referred only to the existence of certain helminths in the domestic dog (Ancylostoma caninum, Toxocara canis, Trichuris vulpis and Uncinaria stenocephala), with no record of their prevalence on the island or region [4]. For this reason, the present study focused on the Azores archipelago, more specifically the two most representative islands of this insular region—Terceira and São Miguel. Dogs and cats were introduced to these islands when the archipelago was first populated by the Portuguese people, in the years 1439 to 1444 [5,6]. Since then, these species have developed a closer relationship with humans, moving from working animals to companion animals. However, these animals also contribute to the loss of biodiversity in ecosystems due to their predatory habits, habitat invasion and spread of infectious agents [7,8].
The dog population on the Azores islands is mainly composed of privately owned animals with free-roaming lifestyles. This scenario is visible not only in rural areas but also in cities. Furthermore, most of the islands have kennels for stray and abandoned animals, where prophylaxis and treatment protocols are not regularly applied. A similar case is observed in the cat population of the Azores, where its impact on biodiversity is due to the numerous cats kept by humans in a state of semi-dependence, especially in rural areas, where the cats have greater contact with the native fauna that constitutes their prey [7,8,9].
Another factor to consider is that the number of dogs and cats traveling to and from this insular territory is increasing in proportion to tourism, which has increased in recent years and represents a risk since these pets can acquire or introduce pathogens globally [10,11].
For this purpose, and to obtain as much information as possible, coprological examinations were carried out on both cats and dogs for a further investigation of gastrointestinal and pulmonary parasites. Moreover, a questionnaire was applied to caregivers to determine risk factors associated with the presence of parasites.

2. Materials and Methods

2.1. Study Area

The study took place on two islands of the Azores archipelago, located in the Atlantic Ocean, between September 2019 and January 2020, where a total of 320 samples were collected: 153 on Island A—São Miguel (37.7804° N, 25.4970° W); 167 on Island B—Terceira (38.4315° N, 27.1313° W) (Figure 1). The majority of samples were collected on Terceira Island, given its proximity to the laboratory where the analysis took place. Geographic location is a strong determinant of the climate present on the islands of the archipelago. Therefore, the different islands have different climatic features. Also, within each island, there are climatic asymmetries related to the morphology, geological structure, vegetation and, in some cases, the influence of neighboring islands. Some locations on the islands are recognized for having a well-defined microclimate. Nonetheless, the sample collection took place almost entirely in Cfb locations (Figure 2) distinctive of the general climate classification of the Azores archipelago [12]. Likewise, the level of precipitation differs across the various islands, being higher on islands in the western group and lower on those in the eastern group. Even so, in general, the climate of the Azores is characterized by high levels of air humidity, mild temperatures, low insolation rates, regular and abundant rainfall, and severe winds. The climate is temperate, with average temperatures of 13 °C in winter and 24 °C in summer [13].

2.2. Sample Collection

For each fecal sample, a questionnaire was filled out not only to determine predisposing factors but also to record the data of each animal. The evaluated factors were age, sex, breed, lifestyle, exterior access, cohabitation, deworming frequency, diagnosed diseases, origin of samples and length of time spent in shelters. Both species were distributed in two age categories: young (age ≤ 1 year) and adults (age > 1 year).
This questionnaire was preceded by a small pilot survey for which five animal tutors were invited to answer the questions so that the type of questions, extent and time to be answered was reviewed and corrected. The fecal collection was carried out directly from the substrate or sandbox after the animals defecated and then placed in individual plastic bags, identified and stored in a refrigerated isothermal box. The study involved animals from kennels, catteries and tutors, mostly from kennels and catteries, given the high population density present, the greater proximity between the animals and the low deworming frequency. The collected samples were transported to the Regional Veterinary Laboratory (LRV) on Terceira Island for macroscopic and microscopic examinations.
The minimum sample size was calculated to perform this pilot study. However, it is important to highlight that there are no records of the number of animals in the dog and cat populations of the Azores archipelago. Therefore, we accessed the epidemiological platform WinEpi 2.0, which allowed us to determine the sample size without knowing the population estimated numbers. For dogs, an expected proportion of 20% was used, which was obtained from another study carried out on Madeira Island, Portugal [14], and a confidence level of 95%. For cats, only the expected proportion differed, using a value of 23%, which was obtained from a study carried out on Gran Canaria Island, Spain [15] (http://www.winepi.net/f101.php, accessed on 4 September 2019 [16]) (Table 1).

2.3. Coprological Methods

The samples were examined using qualitative coprological methods: the Willis flotation technique with a 33% zinc sulfate (ZnSO4) solution for detection of lethargic larvae and a Sheather’s sugar solution [17,18,19] for the identification of gastrointestinal parasites and a modified Baermann method for the detection of the L1 larvae of pulmonary nematodes [20]. In addition, a macroscopic examination of all samples was previously performed to assess factors such as consistency, color, existence of blood, mucus and the presence of parasitic forms. The parasites’ identification was based on morphological and morphometric features such as length, width, the posterior and anterior ends of larvae, size, shape, color, shell thickness, surface morphology and content [17,18,19,20,21,22,23,24].

Statistical Analysis

The information collected from the questionnaires and the results of the coprological methods carried out were inserted into a file in the Microsoft Excel 2010® program and later imported into the R program, version 3.3.0, with the R Commander extension. Using the R program, the data were analyzed using contingency tables (two-way table) and Pearson’s chi-square test to evaluate the association of the predisposing factors with infections detected in the examined animals. The results were considered statistically significant when the p-value was less than 0.05.
Binary multiple univariate generalized linear models (GLMs) were used to test the two islands and species mentioned with the presence of gastrointestinal parasites, lungworms and positivity for zoonotic pathogens (hookworms and Toxocara spp.) [25]. The same analysis was performed to test whether the occurrence of infection with certain parasite species was related to the island of origin.

3. Results

3.1. Sampled Population

On Island A, the study sample comprised 101 canines (67.97% of the total sample on this island) and 49 felines (32.03%). On Island B, the study included 104 canines (60.48%) and 66 felines (39.52%). On Island A, 77% of dogs (80/104) and 71% of cats (35/49) were adults. On Island B, the proportion of adults recorded was 77% in dogs (63/104) and 76% in cats (27/49). In the sample under study, most of the dogs analyzed on Island A were males (60.58%), while for cats, most were females (55.1%). On Island B, 63.37% of the dogs (64/101) were males, and 56.06% of the cats (37/66) were females. In this survey, on Island A, the majority of animals were mixed-breed, with a prevalence of 72.12% in dogs (75/104) and 91.84% in cats (45/49). The same scenario occurred on Island B, where 67.33% of the dogs (68/101) and 86.36% of the cats (57/66) (p < 0.05) were mixed-breed (Table 2 and Table 3).
Lifestyle, related to the area of housing/accommodation where the animal lives, was distributed in two classifications: exterior and interior. In addition, another factor considered was the possibility of access to the outside/street for the animals, especially dogs, which can live inside or in yards/gardens but have regular access to the street. On Island A, most dogs lived outside in yards (90%) but did not have access to the streets (93%). In cats, 80% had outdoor housing, in yards or private gardens, with access to the street only allowed for one cat (2%). This was due to the confinement of the majority of cats sheltered in catteries, where this access is denied. On Island B, 83% of dogs (84/101) lived outside, in yards, where outside access was allowed for to 31% (p < 0.05). Of the felines, 80% had indoor housing, with outdoor access allowed to 32% (p < 0.05) (Table 2 and Table 3).
Regarding cohabitation with other animals in the same space, 94.23% of the dogs (98/104) from Island A cohabited with other animals, while among the cats, the prevalence of cohabitation was 95.92% (47/49) (p < 0.05). On Island B, 91.09% of the dogs (92/101) cohabited with other animals, while for the cats, the prevalence of cohabiting animals was 93.94% (62/66) (p < 0.05) (Table 2 and Table 3).
Another evaluated criterion was the deworming frequency, with animals distributed across four classifications: dewormed for less than 2 weeks; dewormed for 3–4 weeks (monthly); dewormed for 2–3 months; and dewormed for more than 3 months. This range was based on the totality of responses obtained in the questionnaire, with many of the participants being unaware of the adequate deworming frequency. On Island A, the dogs were frequently dewormed every 2–3 months (50.96%) or every 3–4 weeks (41.35%). For the cats, 57.14% (28/49) were dewormed every 3–4 weeks and 42.86% (21/49) every 2–3 months (p < 0.05). On Island B, 59.41% (60/101) of dogs were dewormed in periods of more than 3 months and 22.77% (23/101) every 2–3 months. In cats, 51.52% (34/66) were dewormed in periods of more than 3 months and 36.35% (24/66) every 2–3 months (p < 0.05) (Table 2 and Table 3). In sum, the administration of antiparasitic prophylactics, on Island A, was applied mainly monthly or every 2 to 3 months, with protocols established in kennels and catteries and a growing awareness, although still reduced, on the part of tutors. On Island B, deworming was predominantly applied every 2 to 3 months or longer. It is noteworthy that, on this island, tutors with a higher level of education and training were more sensitive to the issue and applied antiparasitic drugs with some regularity, while the rest, who represent the majority, only administrated them annually or had indoor animals for which the probability of occurrence of parasitosis is lower.
Regarding the presence of previously diagnosed diseases, on Island A, 4.81% (5/104) of the canines had concomitant diseases, while in the felines, the prevalence of cats that had concomitant diseases was 2.04% (1/49). On Island B, 7.92% (8/101) of the canines had been previously diagnosed with concomitant diseases, while for the felines, this value was 15.15% (10/66) (Table 2 and Table 3). This diagnosis of concomitant diseases was previously carried out by veterinary clinicians working at clinics, animal shelters or kennels. In general, the sampled animals were considered healthy and without clinical signs that could show disease. Of the few cases in which a concomitant disease was registered, pathologies such as arthrosis were present in older animals (especially dogs), feline asthma and dermatological problems such as folliculitis, yeast infections and allergic dermatitis, which were adequately followed up with and previously treated. For these animals, the obtained results were negative.
On São Miguel Island, 92.31% (96/104) of the dog samples came from kennels and associations, while the remaining 7.69% (8/104) were provided by tutors (p < 0.05). In cats, 79.59% (39/49) came from catteries and associations, while the remaining 20.41% (10/49) were provided by tutors (p < 0.05). On Terceira Island, 61.38% (62/101) of sampled dogs were accommodated in kennels and associations, while the remaining 38.61% (39/101) had tutors (p < 0.05). In cats, 56.06% (37/66) of the samples came from catteries and associations, while the remaining 43.94% (29/66) were provided by tutors (p < 0.05) (Table 2 and Table 3).
The presence of parasitic infection was significantly related to the length of time the animals had spent in the kennels/catteries (p < 0.05) (Table 4). Both dogs and cats housed in these shelters for more than a year were more likely to develop infection.

3.2. Macroscopic Examination

Significantly more infections occurred in animals when parasitic macroscopic forms were observed in the feces (p < 0.05). The remaining factors (consistency, color, blood and mucus) had no association with the occurrence of parasite infection (p > 0.05) Also, the infected animals usually presented normal feces (Table 5 and Table 6).

3.3. Distribution and Prevalence of Gastrointestinal Parasites and Lungworms

Overall, 205 dog samples and 115 cat feces were subjected to microscopic examinations on Islands A and B (Table 3 and Table 4). The overall prevalence of gastrointestinal parasitism in dogs was 53% (108/205), where the results obtained for each parasite were the following: Ancylostomatidae (hookworms) (42.44%), Trichuris vulpis (17.56%), Toxocara canis (12.68%) and Cystoisospora spp. (4.39%) (Figure 2). Of these 108 positive samples, 46 (42.6%) animals were identified with mixed infections, while the remaining 62 (57.4%) were only infected with one parasitic pathogen. The most prevalent parasites were nematodes, followed by protozoa. Island A (São Miguel) showed the highest prevalence of infection with gastrointestinal parasites (65%), and also the highest prevalence of each zoonotic parasite in dogs was attributed to hookworms (51%) and Toxocara canis (15.4%) (p < 0.05) on Island B (Table 7, Table 8 and Table 9).
The overall prevalence of gastrointestinal parasitism in cats was also 53% (61/115), and each parasite was registered at the following prevalence: Toxocara cati (32.17%), Ancylostomatidae (hookworms) (29.57%), Cystoisospora spp. (14.78%) and Trichuris sp. (0.87%) (Figure 3 and Figure 4).
Of these 61 positive samples, 26 (42.62%) animals were identified with mixed infections, while the remaining 35 (57.38%) were only infected with one parasitic pathogen. The most prevalent parasites were also nematodes. Island B (Terceira) showed the highest prevalence of infection with gastrointestinal parasites in cats (56%) and zoonotic parasites: Toxocara cati (39.4%) and hookworms (38%) (p < 0.05) (Table 8, Table 9 and Table 10).
The prevalence of pulmonary parasitism was 0.49% (1/205) in canines and 20.87% (24/115) in felines, with Angiostrongylus vasorum and Aelurostrongylus abstrusus being the only species detected in dogs and cats, respectively (Figure 5).
In dogs, only one specimen was identified on Island B (p < 0.05). Island B (Terceira) also showed the highest prevalence of infection with lungworms in cats (24.24%) (p < 0.05) (Table 7, Table 8, Table 9 and Table 10).

4. Discussion

Using the information collected through the questionnaires, it was found that, on both islands, the samples were predominantly made up of adult dogs and cats. This may have been due to the origin of the samples; animals with a more advanced age predominated. Since these animals are more prone to the development of chronic diseases, the low prevalence obtained could lead to the hypothesis that certain diseases are underdiagnosed. Regarding the breed factor, in both species, the samples were mainly from animals of mixed breeds, a finding that is related to the fact that they were mostly rescued from the street. This is a result of the current concern that has developed with regard to relocating and collecting stray or abandoned animals to ensure not only animal welfare but also public health [14]. In the region, dogs and cats frequently cohabit with other animals, usually of the same species, constituting a risk factor for parasitic transmission [2,26,27,28,29,30,31]. The length of time spent in shelters was also related to the presence of parasitic infection since both species housed in these shelters for more than a year are more likely to develop infections. All the animals who entered the shelter were confined in isolation units for 15 days and properly dewormed, suggesting that infection occurs within the facilities through direct contact and the fecal–oral route. This can be explained by the lack of proper prophylactic protocols and the less hygienic conditions that these animals normally live in, combined with the high population density that usually exists in shelters [27,32]. In the future, it would be advisable to carry out parasitological studies of quarantined animals upon their entry into shelters to eliminate the significance of the time spent in the facilities as a risk factor.
Regarding the administration of antiparasitic prophylactics, positive samples were associated with the poor deworming frequency of the affected animals, which constitutes an important risk and prevention factor. Moreover, most of the samples were collected in kennels, catteries and associations, which resulted in a greater number of positive results [25,32,33,34,35]. It is important to highlight the intermittent excretion of parasites, so it would be advisable, in future studies, to analyze three samples from different days in order to obtain a higher prevalence [18,24]. More infections occurred in animals when parasitic forms were observed in feces, which was predictable since the animals were already infected. Moreover, the infected animals usually presented normal feces, which indicates that the presence of infection may not be directly related to macroscopic changes in their feces. It is important to highlight this point since normal feces may hide parasite shedding, and regular fecal monitoring still makes sense as a major tool for the good control of a pet’s gastrointestinal parasites [36].
The present survey detected a high prevalence of gastrointestinal infection in both dogs and cats, probably due to the origin of samples and the ideal climatic conditions for the development of parasites. Similar results were found in other insular territories [2,30,31]. On Greek islands, a study of cats showed endoparasitism’s prevalence at around 58% (Mykonos) and 64% (Skopeles) [25]. On Sardinia Island (Italy), the prevalence of recorded endoparasites was 34.9% (dogs) and 43.4% (cats) [36]. On Mallorca Island (Spain), a study performed on a sample of feral cats recorded a prevalence of 100%, with all animals being parasitized by helminths [37]. On the Philippine islands, the recorded prevalence of intestinal helminths in dogs was 97.45% [38], while the Galápagos islands (which have a similar climate to the Azores) recorded 53.6% of simple infections and 11.4% co-infections [39]. However, it is thought that the lack of awareness among a part of the population regarding the occurrence and risk that these parasites entail for their animals and for public health is the main factor in the manifestation of the results obtained, as verified in other studies carried out in Portugal [2,29,30,31,32]. Furthermore, the environment and population density, together with the sample being mainly composed of stray animals, favor the occurrence of parasites, which justifies the obtained results [14,28,29,30,31].
The higher occurrence of gastrointestinal and zoonotic parasites in dogs from São Miguel (Island A) is most likely due to the large number of stray dogs sampled. However, the opposite scenario occurred on Island B, where a higher prevalence of gastrointestinal and zoonotic parasitism was observed in cats. Although these findings may be attributed to chance, they can also be explained by the hygienic and sanitary conditions in which cattery cats were found. Island B has only one cattery, where the animals are sheltered in indoor facilities with a high and alarming population density, which makes their hygiene difficult and, therefore, promotes the spread of infections. On the other hand, cats from Island A are housed in outdoor catteries with fewer individuals per cage and better hygiene conditions. Furthermore, the island has three centers available to provide shelter to these animals. It could also be possible that differences in veterinary care in terms of prevention, diagnosis and treatment played a certain role, although further investigations are needed to clarify these issues [2,25,32].
Another aspect to consider is the period in which the collection took place. This study was carried out from September to January, and although the Azores archipelago presents high rainfall and relative humidity throughout the year, in September and October, these values usually reach their maximums. It was, in fact, in these months that the number of positive animals detected was higher, with the seasonality factor standing out.
In this survey performed in an insular territory, the high prevalence of hookworm eggs was highlighted due to its potential health risk as a zoonotic disease. In humans, hookworm larvae can penetrate the skin and cause follicular, papular and ephemeral lesions, muscular damage, and eosinophilic enteritis [40]. This can be due to the facilities and origin of the animals, as well as the presence of ideal temperatures and relative humidity, which provide the optimum conditions for their proliferation [41]. The Toxocara cati infection in this insular environment is also of importance, given its zoonotic nature, which may lead either to subclinical infections or to different larva migrans syndromes (visceral, ocular and neural), which may have serious clinical manifestations in humans [17,34]. It is also interesting to note that a specimen of Trichuris sp. was detected in the cat sample, and this is a rare parasite according to some of the existing literature [16,36]. Another factor that stood out was the important prevalence of Cystoisospora spp. in cats of the archipelago, which, in the present survey, was 14.78%. According to ESCCAP (2018), cats that come from catteries or that are in situations with a high population density are at greater risk of contracting protozoan infections [42]. This factor, together with the region’s favorable climatic conditions, may have been the origin of the obtained results.
The prevalence of aelurostrongylosis in the region is also considerable (20.87%), so it should not be neglected and should be included in the list of differential diagnoses of pathologies concerning the respiratory tract in the felids of the Azores archipelago. A. abstrusus is a parasite that affects feline lung tissues; severe infections can lead to verminous pneumonia, which can be fatal [43,44,45,46]. This cosmopolitan nematode is the most frequent lungworm diagnosed in felids, being reported in Europe, South America, Australia, the Middle East, Russia, the Far East, the USA, China and Africa [47,48,49,50,51,52,53,54,55,56,57,58,59]. As was said before, studies related to cats in this insular region are practically nonexistent. Therefore, this study contributes to the knowledge of pulmonary nematodes affecting cats in the Azores islands, providing new data on the prevalence and distribution of these parasites. Only one specimen of A. vasorum was detected, and studies of this parasite in Portugal are scarce [14,60,61,62,63,64]. Other studies carried out on European islands obtained the following prevalence of A. vasorum: 4.6% in Tenerife Island (Spain); 15% in El Hierro Island (Spain) [65]; 18.1% in Aegean islands (Greece); 5.5% in Ionian islands (Greece) [66]; 9.8% in Giglio Island (Italy) [67]; and 3.4% in Sardinia Island (Italy) [68].
This could be due to numerous factors, such as the diagnostic method used. The method of choice used corresponds to the Baermann technique. Despite being a quick and easy-to-perform method, these parasites have peculiarities that often make their detection impossible. Within these particularities, the long pre-patent periods (28 to 108 days) and the intermittent excretion that this parasite can present stand out [18,24]. Therefore, in a future study, it is advisable to collect feces for three successive days, and if possible, repeat the collection after a pre-established period [18,24]. Given these results, it is thought that the use of different diagnostic methods can be a determinant and complementary factor in the detection of these metastrongylids such that, given the high abundance of terrestrial gastropods and paratenic hosts in the region, it is estimated that the prevalence of A. vasorum is higher than that determined in this screening [69].

5. Conclusions

The present survey was a pioneering one regarding the study of gastrointestinal and pulmonary parasites in populations of domestic carnivores in the Autonomous Region of the Azores. It allowed us to successfully confirm the presence of these helminths and determine associated risk factors, thus remedying the scarcity of studies in this archipelago. Such information is critical, given the potential impact it has on local biodiversity, domestic carnivores and public health due to the identification of zoonotic species while also contributing to new aspects to be explored in works of this nature or others that are intended to pore over the parasitology of companion animals in this insular region.
As future perspectives for research on parasites in domestic carnivores of the Azores, we include (a) sampling the other seven islands to complete the data on the prevalence of gastrointestinal and pulmonary parasites across the Azores archipelago, (b) the evaluation of this prevalence in a sample with more animals from caregivers, (c) the use of or complementing with different diagnosis methods, (d) determining environmental contamination with these zoonotic agents and (e) evaluating the incidence of Aelurostrongylus abstrusus, as it is a very reliable indicator of cats’ hunting behavior and the reduction in biodiversity.

Author Contributions

R.T. and L.M.d.C. designed the study; R.T. and I.F. collected samples; R.T. processed the samples; R.T., T.N. and L.M.d.C. analyzed the data; software, T.N.; writing—original draft preparation, R.T. and L.M.d.C.; writing—review and editing, R.T. and L.M.d.C.; supervision, L.M.d.C., M.C.P. and C.P. All authors have read and agreed to the published version of the manuscript.

Funding

This research was funded by CIISA/FMV Project UIDB/00276/2020 and LA/P/0059/2020—AL4AnimalS (both funded by FCT). Furthermore, Romana Teixeira was awarded a PhD research fellowship, M3.1.a/F/005/2022 (funded by FRCT).

Institutional Review Board Statement

Not applicable since the fecal samples were collected from the ground, so there was no interference with animals.

Informed Consent Statement

Informed consent was obtained from all subjects involved in the study.

Data Availability Statement

Raw data supporting the conclusions of this study are available from the authors upon request.

Acknowledgments

The authors would like to thank the Inter-disciplinary Centre of Research in Animal Health (CIISA), as well as the Regional Veterinary Laboratory (LRV)—Angra do Heroísmo, and all the owners and organizations who kindly cooperated with this study.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Alho, A.M.; Seixas, R.; Rafael, T.; Madeira de Carvalho, L. Formas Larvares dos Helmintas: O elo mais forte na Desparasitação do cão e do gato. Vet. Med. 2010, 33–46. Available online: https://www.researchgate.net/publication/231072442 (accessed on 2 February 2020).
  2. Matos, M.; Alho, A.M.; Owen, S.P.; Nunes, T.; Madeira de Carvalho, L. Parasite control practices and public perception of parasitic diseases: A survey of dog and cat owners. Prev. Vet. Med. 2015, 122, 174–180. [Google Scholar] [CrossRef] [PubMed]
  3. Pirzada, N.; Sahito, H.A.; Gopang, M.A.; Memon, M.; Pirzada, M.; Sanjrani, M.I.; Memon, M.A.; Khuhro, A.P. Prevalence of Intestinal Parasites and Risk Perception of Zoonotic Infection for Humans. J. Dyn. Microbiol. Infect. Dis. 2014, 1, 1–7. Available online: https://www.researchgate.net/publication/264790353 (accessed on 10 March 2020).
  4. Afonso-Roque, M.M. The helminth fauna of the terrestrial vertebrates from S. Miguel Island (Azores): An annotated check list of the known species. Arquipélago. Life Mar. Sci. 1995, 99–104, N° 13A. Available online: http://hdl.handle.net/10400.3/2117 (accessed on 4 April 2020).
  5. Ribeiro, L. Formação histórica do povo dos Açores, in Açoriana, Angra; Angra do Heroísmo, Portugal, 1941; pp. 237–242. [Google Scholar]
  6. Arruda, M. Colecção de Documentos Relativos ao Descobrimento e Povoamento dos Açores, Ponta Delgada; Oficina de Artes Gráficas: Ponta Delgada, Portugal, 1932; pp. 251–259. [Google Scholar]
  7. Medina, F.; Bonnaud, E.; Vidal, E.; Tershy, B.; Zavaleta, E.; Donlan, C.J.; Keitt, B.S.; Le Corre, M.; Horwath, S.; Nogales, M. A global review of the impacts of invasive cats on island endangered vertebrates. Glob. Chang. Biol. 2011, 17, 3503–3510. [Google Scholar] [CrossRef]
  8. Portal da Agricultura dos Açores. Cão de Fila de São Miguel. Raças Autóctones. Melhoramento Animal. Direção Geral da Agricultura, Veterinária e Alimentação. Governo dos Açores. Available online: https://agricultura.azores.gov.pt/apresentacao-e-organica/direcao-regional-da-agricultura/melhoramento-animal-e-recursos-geneticos/planos/cao-de-fila-de-sao-miguel/ (accessed on 20 June 2024).
  9. Silva, L.; Ojeda Land, E.; Rodríguez Luengo, J.L. Flora e Fauna Terrestre Invasora na Macaronésia. TOP 100 nos Açores, Madeira e Canárias; ARENA: Ponta Delgada, Portugal, 2008; 546p, Available online: https://islandlab.uac.pt/fotos/publicacoes/publicacoes_Part1_Inicio.pdf (accessed on 24 June 2024).
  10. IT-Açores. Indicador de Turismo; Serviço Regional de Estatística dos Açores: Azores, Portugal, 2024. [Google Scholar]
  11. Elavai, A. Estudo sobre os turistas que visitam os Açores; Serviço Regional de Estatística dos Açores: Azores, Portugal, 2001. [Google Scholar]
  12. Chazarra, A.; Mestre, A.; Pires, V.; Cunha, S.; Silva, A.; Marques, J.; Carvalho, F.; Mendes, M.; Neto, J.; Mendes, L.; et al. Climate Atlas of the archipelagos of the Canary Islands, Madeira and the Azores; Agência Estatal de Meteorologia—Ministério de Agricultura, Alimentação e Meio Ambiente; Instituto de Meteorologia de Portugal: Lisboa, Portugal, 2011. [Google Scholar]
  13. Azevedo, E.B. O Clima dos Açores (Monografia). Centro do Clima, Meteorologia e Mudanças Globais da Universidade dos Açores. 2015. Available online: https://www.researchgate.net/publication/280921853 (accessed on 4 April 2020).
  14. Gomes, B. Contribuição Para o Estudo dos Parasitas Gastrointestinais, Pulmonares e Hemáticos em cães na Cidade do Funchal, ilha da Madeira. Master’s Thesis, Ulisboa—Faculty of Veterinary Medicine, Técnica, Lisboa, 2019. [Google Scholar]
  15. Rodríguez-Ponce, E.; González, J.F.; Conde de Felipe, M.; Hernández, J.N.; Raduan Jaber, J. Epidemiological survey of zoonotic helminths in feral cats in Gran Canaria island (Macaronesian archipelago-Spain). Acta. Parasitol. 2016, 61, 443–450. [Google Scholar] [CrossRef] [PubMed]
  16. Working in Epidemiology. 2006. Available online: http://www.winepi.net/f101.php (accessed on 4 September 2019).
  17. Urquhart, G.M.; Armour, J.; Duncan, J.L.; Dunn, A.M.; Jennings, F.W. Veterinary Parasitology, 2nd ed.; Blackwell Science: Oxford, UK, 1996; pp. 95–99. [Google Scholar]
  18. Zajac, A.M.; Conboy, G.A. Veterinary Clinical Parasitology, 8th ed.; John Wiley & Sons: Hoboken, NJ, USA, 2012; pp. 9, 10, 40–87. [Google Scholar]
  19. CAPC Guideline. Ascarid. [WWW Document]. Companion Anim. Parasite Counc. Website. 2020. Available online: https://capcvet.org/guidelines/ascarid/ (accessed on 20 March 2021).
  20. Zajac, A.; Johnson, J.; King, S. Evaluation of the importance of centrifugation as a component of zinc sulfate fecal flotation examinations. J. Am. Anim. Hosp. Assoc. 2002, 38, 221–224. [Google Scholar] [CrossRef] [PubMed]
  21. CAPC Guideline. Hookworms. [WWW Document]. Companion Anim. Parasite Counc. Website. 2020. Available online: https://capcvet.org/guidelines/hookworms/ (accessed on 20 March 2021).
  22. Companion Animal Parasite Council |CAPC|. Parasites of Other Systems—Lungworms. 2007. Available online: http://www.capcvet.org/capcrecommendations/lungworms (accessed on 20 March 2021).
  23. Dubey, J.P.; Lindsay, D.S.; Lappin, M.R. Toxoplasmosis and other intestinal coccidial infections in cats and dogs. Vet. Clin. Small Anim. 2009, 39, 1009–1034. [Google Scholar] [CrossRef] [PubMed]
  24. Bowman, D.D. Georgis’ Parasitology for Veterinarians, 10th ed.; Elsevier Saunder: St. Louis, MO, USA, 2014; pp. 349–354. [Google Scholar]
  25. Diakou, A.; Di Cesare, A.; Morelli, S.; Colombo, M.; Halos, L.; Simonato, G.; Tamvakis, A.; Beugnet, F.; Paoletti, B.; Traversa, D. Endoparasites and vector-borne pathogens in dogs from Greek islands: Pathogen distribution and zoonotic implications. Negl. Trop. Dis. 2019, 13, e0007003. [Google Scholar] [CrossRef] [PubMed]
  26. Santos, B.R. Rastreio de Metastrongilídeos Pulmonares em Gatos Domésticos (Felis silvestris catus) na área Metropolitana de Lisboa, Portugal. Master’s Thesis, Ulisboa—Faculty of Veterinary Medicine, Lisboa, Portugal, 2016. [Google Scholar]
  27. Lebre, F. Rastreio de Parasitas Gastrintestinais e seu Impacto Zoonótico em Cães de Canil da Cidade de Lisboa. Master’s Thesis, Ulisboa—Faculty of Veterinary Medicine, Lisboa, Portugal, 2011. [Google Scholar]
  28. Melo, A. Parasitoses Gastrointestinais e Pulmonares em Canídeos e Felídeos da Região oeste de Portugal Continental. Master’s Thesis, Ulisboa—Faculty of Veterinary Medicine, Lisboa, Portugal, 2017. [Google Scholar]
  29. Diniz, T. Prevalência de Parasitas Gastrointestinais e Frequência de Desparasitação em Cães e Gatos no Concelho de Sintra, Portugal. Master’s Thesis, Ulisboa—Faculty of Veterinary Medicine, Lisboa, Portugal, 2018. [Google Scholar]
  30. Morgado, G. Parasitoses Internas e Frequência de Desparasitação em cães do Concelho de Vila Franca de Xira, Portugal. Master’s Thesis, Ulisboa—Faculty of Veterinary Medicine, Lisboa, Portugal, 2016. [Google Scholar]
  31. Matos, B.M. Parasitoses Pulmonares e Gastrointestinais em Felinos Domésticos no Minho, Portugal. Master’s Thesis, Ulisboa—Faculty of Veterinary Medicine, Lisboa, Portugal, 2016. [Google Scholar]
  32. Ortuño, A.; Castellà, J. Intestinal Parasites in Shelter Dogs and Risk Factors Associated with the Facility and its Management. Isr. J. Vet. Med. 2011, 66, 103–107. [Google Scholar]
  33. Borecka, A. Prevalence of intestinal nematodes of dogs in the Warsaw area, Poland. Helminthologia 2005, 42, 35–39. [Google Scholar] [PubMed]
  34. Martínez-Moreno, F.J.; Hernández, S.; López-Cobos, E.; Becer ra, C.; Acosta, I.; Martínez-Moreno, A. Estimation of canine intestinal parasites in Córdoba (Spain) and their risk to public health. Vet. Parasitol. 2007, 143, 7–13. [Google Scholar] [CrossRef] [PubMed]
  35. Tamponi, C.; Varcasia, A.; Pinna, S.; Melis, E.; Melosu, V.; Zidda, A.; Sanna, G.; Pipia, A.P.; Zedda, M.T.; Pau, S.; et al. Endoparasites detected in faecal samples from dogs and cats referred for routine clinical visit in Sardinia, Italy. Vet. Parasitol. Reg. Stud. Rep. 2017, 10, 13–17. [Google Scholar] [CrossRef] [PubMed]
  36. Murnik, L.C.; Daugschies, A.; Delling, C. Gastrointestinal parasites in young dogs and risk factors associated with infection. Parasitol. Res. 2023, 122, 585–596. [Google Scholar] [CrossRef] [PubMed]
  37. Millán, J.; Casanova, J.C. High prevalence of helminth parasites in feral cats in Majorca Island (Spain). Parasitol. Res. 2009, 106, 183–188. [Google Scholar] [CrossRef] [PubMed]
  38. Urgel, M.F.M.; Ybañez, R.H.D.; Ybañez, A.P. The detection of gastrointestinal parasites in owned and shelter dogs in Cebu, Philippines. Vet. World 2019, 12, 372–376. [Google Scholar] [CrossRef] [PubMed]
  39. Gingrich, E.N.; Scorza, A.V.; Clifford, E.L.; Olea-Popelka, F.J.; Lappin, M.R. Intestinal parasites of dogs on the Galapagos Islands. Vet. Parasitol. 2010, 169, 404–407. [Google Scholar] [CrossRef] [PubMed]
  40. Despommier, D. Toxocariasis: Clinical aspects, epidemiology, medical ecology, and molecular aspects. Clin. Microbiol. Rev. 2003, 16, 265–272. [Google Scholar] [CrossRef] [PubMed]
  41. Lee, A.C.; Schantz, P.M.; Kazacos, K.R.; Montgomery, P.; Bowman, D.D. Epidemiologic and zoonotic aspects of ascarid infections in dogs and cats. Trends Parasitol. 2010, 26, 155–161. [Google Scholar] [CrossRef]
  42. ESCCAP. European Scientific Counsel Companion Animal Parasites. Guideline 6, 2nd ed.; Control of Intestinal Protozoa in Dogs and Cats; ESCCAP: Malvern, UK, 2018; pp. 18–19. [Google Scholar]
  43. Vezzosi, T.; Perrucci, S.; Parisi, F.; Morelli, S.; Maestrini, M.; Mennuni, G.; Traversa, D.; Poli, A. Fatal Pulmonary Hypertension and Right-Sided Congestive Heart Failure in a Kitten Infected with Aelurostrongylus Abstrusus. Animals 2020, 10, 2263. [Google Scholar] [CrossRef]
  44. Scott, D.W. Current knowledge of aelurostrongylosis in the cat: Literature review and case reports. Cornell. Vet. 1973, 63, 483–500. [Google Scholar]
  45. Yildiz, K.; Duru, S.Y.; Gokpinar, S. Alteration in blood gases in cats naturally infected with Aelurostrongylus abstrusus. J. Small Anim. Pract. 2011, 52, 376–379. [Google Scholar] [CrossRef] [PubMed]
  46. Mooney, E.T.; Rozanski, E.A.; King, R.G.P.; Sharp, C.R. Spontaneous pneumothorax in 35 cats (2001–2010). J. Feline Med. Surg. 2012, 14, 384–391. [Google Scholar] [CrossRef] [PubMed]
  47. Giannelli, A.; Capelli, G.; Joachim, A.; Hinney, B.; Losson, B.; Kirkova, Z.; René-Martellet, M.; Papadopoulos, E.; Farkas, R.; Napoli, E.; et al. Lungworms and gastrointestinal parasites of domestic cats: A European perspective. Int. J. Parasitol. 2017, 47, 517–528. [Google Scholar] [CrossRef] [PubMed]
  48. Elsheikha, H.M.; Schnyder, M.; Traversa, D.; Di Cesare, A.; Wright, I.; Lacher, D.W. Updates on feline aelurostrongylosis and research priorities for de next decade. Parasites Vectors 2016, 9, 389. [Google Scholar] [CrossRef] [PubMed]
  49. Elsheikha, H.M.; Wright, I.; Wang, B.; Schaper, R. Prevalence of feline lungworm Aelurostrongylus abstrusus in England. Vet. Parasitol. Reg. Stud. Rep. 2019, 16, 100271. [Google Scholar] [CrossRef] [PubMed]
  50. Foster, S.F.; Martin, P.; Allan, G.S.; Barrs, V.R.; Malik, R. Lower respiratory tract infections in cats: 21 cases (1995–2000). J. Feline Med. Surg. 2004, 6, 167–180. [Google Scholar] [CrossRef]
  51. Fiorello, C.V.; Robbins, R.G.; Maffei, L.; Wade, S.E. Parasites of free-ranging small canids and felids in the Bolivian Chaco. J. Zoo Wildl. Med. 2006, 37, 130–134. [Google Scholar] [CrossRef] [PubMed]
  52. Abu-Madi, M.A.; Al-Ahbabi, D.A.; Al-Mashhadani, M.M.; Al-Ibrahim, R.; Pal, P.; Lewis, J.W. Patterns of parasitic infections in faecal samples from stray cat populations in Qatar. J. Helminthol. 2007, 81, 281–286. [Google Scholar] [CrossRef] [PubMed]
  53. González, P.; Carbonell, E.; Urios, V.; Rozhnov, V.V. Coprology of Panthera tigris altaica and Felis bengalensis euptilurus from the Russian far east. J. Parasitol. 2007, 93, 948–950. [Google Scholar] [CrossRef]
  54. Gerdin, J.A.; Slater, M.R.; Makolinski, K.V.; Looney, A.L.; Appel, L.D.; Martin, N.M.; McDonough, S.P. Post-mortem findings in 54 cases of anesthetic associated death in cats from two spay–neuter programs in New York State. J. Feline Med. Surg. 2011, 13, 959–966. [Google Scholar] [CrossRef]
  55. Yang, Y.; Liang, H. Prevalence and risk factors of intestinal parasites in cats from China. BioMed Res. Int. 2015, 2015, 967238. [Google Scholar] [CrossRef]
  56. Di Cesare, A.; Laiacona, F.; Iorio, R.; Marangi, M.; Menegotto, A. Aelurostrongylus abstrusus in wild felids of South Africa. Parasitol. Res. 2016, 115, 3731–3735. [Google Scholar] [CrossRef]
  57. Penagos-Tabares, F.; Lange, M.K.; Chaparro-Gutiérrez, J.J.; Taubert, A.; Hermosilla, C. Angiostrongylus vasorum and Aelurostrongylus abstrusus: Neglected and underestimated parasites in South America. Parasites Vectors 2018, 11, 208. [Google Scholar] [CrossRef]
  58. Hoggard, K.R.; Jarriel, D.M.; Bevelock, T.J.; Verocai, G.G. Prevalence survey of gastrointestinal and respiratory parasites of shelter cats in northeastern Georgia, USA. Vet. Parasitol. Reg. Stud. Rep. 2019, 16, 100270. [Google Scholar] [CrossRef]
  59. Zottler, E.M.; Bieri, M.; Basso, W.; Schnyder, M. Intestinal parasites and lungworms in stray, shelter and privately owned cats of Switzerland. Parasitol. Int. 2019, 69, 75–81. [Google Scholar] [CrossRef]
  60. Ferreira, F.S.; Pereira-Baltasar, P.; Parreira, R.; Padre, L.; Vilhena, M.; Tavira, L.T.; Atouguia, J.; Centeno-Lima, S. Intestinal parasites in dogs and cats from district of Évora, Portugal. Vet. Parasitol. 2011, 179, 242–245. [Google Scholar] [CrossRef]
  61. Payo-Puente, P.; Botelho-Dinis, M.; Urueña, A.M.C.; Payo-Puente, M.; Gonzalo-Orden, J.M.; Rojo-Vazquez, F.A. Prevalence study of the lungworm Aelurostrongylus abstrusus in stray cats of Portugal. J. Feline Med. Surg. 2008, 10, 242–246. [Google Scholar] [CrossRef]
  62. Alho, A.M.; Schnyder, M.; Schaper, R.; Meireles, J.; Belo, S.; Deplazes, P.; Madeira de Carvalho, L. Seroprevalence of circulating Angiostrongylus vasorum antigen and parasite-specific antibodies in dogs from Portugal. Parasitol. Res. 2016, 115, 2567–2572. [Google Scholar] [CrossRef]
  63. Nabais, J.N.P. Infecção por Aelurostrongylus abstrusus e Angiostrongylus vasorum (Nematoda: Angiostrongylidae), em gatos e cães no distrito de Lisboa, Portugal. Master’s Thesis, Ulisboa—Faculty of Veterinary Medicine, Lisboa, Portugal, 2012. [Google Scholar]
  64. Ferdushy, T.; Hasan, M.T. Angiostrongylus vasorum: The “French Heartworm”. Parasitol. Res. 2010, 107, 765–771. Available online: http://www.ncbi.nlm.nih.gov/pubmed/20714748 (accessed on 11 May 2020). [CrossRef]
  65. Segeritz, L.; Cardona, A.; Taubert, A.; Hermosilla, C.; Ruiz, A. Autochthonous Angiostrongylus cantonensis, Angiostrongylus vasorum and Aelurostrongylus abstrusus infections in native terrestrial gastropods from the Macaronesian Archipelago of Spain. Parasitol. Res. 2021, 120, 2671–2680. [Google Scholar] [CrossRef]
  66. Angelou, A.; Gelasakis, A.I.; Schnyder, M.; Schaper, R.; Papadopoulos, E. The ‘French heartworm’ in Greece: A countrywide serological survey of Angiostrongylus vasorum infection by combined detection of circulating antigens and specific antibodies. Vet. Parasitol. Reg. Stud. Rep. 2020, 19, 100376. [Google Scholar] [CrossRef] [PubMed]
  67. Morelli, S.; Gori, F.; Colombo, M.; Traversa, D.; Sarrocco, G.; Simonato, G.; Nespeca, C.; Di Cesare, A.; Frangipane di Regalbono, A.; Veronesi, F.; et al. Simultaneous Exposure to Angiostrongylus vasorum and Vector-Borne Pathogens in Dogs from Italy. Pathogens 2021, 10, 1200. [Google Scholar] [CrossRef] [PubMed]
  68. Pipia, A.P.; Varcasia, A.; Tosciri, G.; Seu, S.; Manunta, M.L.; Mura, M.C.; Sanna, G.; Tamponi, C.; Brianti, E.; Scala, A. New insights onto cardiopulmonary nematodes of dogs in Sardinia, Italy. Parasitol. Res. 2014, 113, 1505–1509. [Google Scholar] [CrossRef] [PubMed]
  69. Borges, P.A.V.; Cunha, R.; Gabriel, R.; Martins, A.F.; Silva, L.; Vieira, V.; Dinis, F.; Lourenço, P.; Pinto, N. Description of the terrestrial Azorean biodiversity. In A List of the Terrestrial Fauna (Mollusca and Arthropoda) and Flora (Bryophyta, Pteridophyta and Spermatophyta) from the Azores; Borges, P.A.V., Cunha, R., Gabriel, R., Martins, A.M.F., Silva, L., Vieira, V., Eds.; Direção Regional de Ambiente and Universidade dos Açores: Horta, Portugal, 2005; pp. 21–68. Available online: http://hdl.handle.net/10400.3/1903 (accessed on 10 July 2024).
Figure 1. Islands of the Azores Archipelago covered by the study of gastrointestinal parasites and lungworms in cats and dogs living in São Miguel (Island A) and Terceira (Island B). Available at Google Maps: https://earth.google.com/web/search/S%c3%a3o+Miguel+Island/@37.82350696,-26.49535856,566.44337324a,2282754.15127426d,35y,0h,0t,0r/data=CigJgokCSfh6U9lJTNAESXh6U9lJTPAGWq1TRxVrj5AIRWOmV0hVlHAOgMKATA (accessed on 10 June 2024).
Figure 1. Islands of the Azores Archipelago covered by the study of gastrointestinal parasites and lungworms in cats and dogs living in São Miguel (Island A) and Terceira (Island B). Available at Google Maps: https://earth.google.com/web/search/S%c3%a3o+Miguel+Island/@37.82350696,-26.49535856,566.44337324a,2282754.15127426d,35y,0h,0t,0r/data=CigJgokCSfh6U9lJTNAESXh6U9lJTPAGWq1TRxVrj5AIRWOmV0hVlHAOgMKATA (accessed on 10 June 2024).
Pathogens 13 00648 g001
Figure 2. Köppen–Geiger climate classification in the archipelagos of the Azores and Madeira Islands: BWh—hot desert; BWk—cold desert; BSh—hot steppe; BSk—Cold steppe; Csa—temperate with hot and dry summers; Csb—temperate with dry and warm summers; Csc—temperate with dry and cold summers; Cfa—temperate with no dry season and hot summers; Cfb—temperate with no dry season and mild summers; Cfc—temperate with no dry season and cold summers; Dsc—dry summers, subarctic climate; ET—polar tundra [12].
Figure 2. Köppen–Geiger climate classification in the archipelagos of the Azores and Madeira Islands: BWh—hot desert; BWk—cold desert; BSh—hot steppe; BSk—Cold steppe; Csa—temperate with hot and dry summers; Csb—temperate with dry and warm summers; Csc—temperate with dry and cold summers; Cfa—temperate with no dry season and hot summers; Cfb—temperate with no dry season and mild summers; Cfc—temperate with no dry season and cold summers; Dsc—dry summers, subarctic climate; ET—polar tundra [12].
Pathogens 13 00648 g002
Figure 3. (A) Hookworm egg (cat). (B) Toxocara canis egg (dog). (C) Mixed infection with eggs of hookworms (left) and Trichuris vulpis (right) (dog). (D) Oocyst of Cystoisospora sp. (cat).
Figure 3. (A) Hookworm egg (cat). (B) Toxocara canis egg (dog). (C) Mixed infection with eggs of hookworms (left) and Trichuris vulpis (right) (dog). (D) Oocyst of Cystoisospora sp. (cat).
Pathogens 13 00648 g003
Figure 4. Trichuris sp. (cat)—Barrel-shaped and yellow–brown egg (77 × 36 μm) with prominent bipolar end plugs and a smooth shell.
Figure 4. Trichuris sp. (cat)—Barrel-shaped and yellow–brown egg (77 × 36 μm) with prominent bipolar end plugs and a smooth shell.
Pathogens 13 00648 g004
Figure 5. (A) First-stage larvae (L1) of Aelurostrongylus abstrusus (cat). (B) First-stage larvae (L1) of Angiostrongylus vasorum (dog).
Figure 5. (A) First-stage larvae (L1) of Aelurostrongylus abstrusus (cat). (B) First-stage larvae (L1) of Angiostrongylus vasorum (dog).
Pathogens 13 00648 g005
Table 1. Minimum sample size selection.
Table 1. Minimum sample size selection.
AreaEstimated Dog
Numbers
Estimated Cat
Numbers
Min. Sample Size
Dogs/Cats
No. of Collected Samples from DogsNo. of Collected Samples from Cats
São Miguel- *- *14/1210449
Terceira- *- *14/1210166
205115
* No official records at the moment.
Table 2. Physical and parasitological features of the sampled population on Island A. Significant factors are highlighted with p-values in bold.
Table 2. Physical and parasitological features of the sampled population on Island A. Significant factors are highlighted with p-values in bold.
Dogsp-ValueCatsp-Value
n (%)n (%)
Age
      Young24
23
p = 0.0814
29
p = 0.062
      Adult80
77
35
71
Sex
      Female41
39.42
p = 0.1727
55.1
p = 0.21
      Male63
60.58
22
44.9
Breed
      Undeterminate75
72.12
p = 0.0657
91.84
p = 0.4
      Purebreed29
27.88
9
8.16
Lifestyle
      Exterior94
90
p = 0.1139
80
p = 0.34
      Interior10
10
10
20
Exterior Access
      Yes7
7
p = 1.88 × 10−61
2
p = 0.028
      No97
93
48
98
Cohabitation
      Yes98
94.23
p = 0.03847
95.92
p = 0.02
      No6
5.77
2
4.08
Deworming Frequency
      <2 weeks5
4.82
p = 0.0330
0
p = 0.015
      3–4 weeks43
41.35
28
57.14
      2–3 months53
50.96
21
42.86
      >3months3
2.88
0
0
Diagnosed Diseases
      Yes5
4.81
p = 0.231
2.04
p = 0.09
      No99
95.19
48
97.96
Origin of Samples
      Kennels/Catteries/Associations96
92.31
p = 0.0339
79.59
p = 1.93 × 10−6
      Tutors8
7.69
10
20.41
Total104
100
49
100
Table 3. Physical and parasitological features of the sampled population on Island B. Significant factors are highlighted with p-values in bold.
Table 3. Physical and parasitological features of the sampled population on Island B. Significant factors are highlighted with p-values in bold.
Dogsp-ValueCatsp-Value
n (%)n (%)
Age
      Young23
23
p = 0.116
24
p = 0.068
      Adult78
77
50
76
Sex
      Female37
36.63
p = 0.0737
56.06
p = 0.2
      Male64
60.58
29
43.94
Breed
      Undeterminate68
67.33
p = 1.04 × 10−457
86.36
p = 0.04
      Purebreed33
32.67
9
13.64
Lifestyle
      Exterior84
83
p = 0.613
20
p = 0.52
      Interior17
17
53
80
Exterior Access
      Yes31
31
p = 0.0121
32
p = 0.038
      No70
69
45
68
Cohabitation
      Yes92
91.09
p = 0.01862
93.94
p = 0.03
      No9
8.91
4
6.06
Deworming Frequency
      <2 weeks3
2.97
p = 1 × 10−63
4.55
p = 2.3 × 10−10
      3–4 weeks15
14.85
5
7.58
      2–3 months23
22.77
24
36.35
      >3 months60
59.41
34
51.52
Diagnosed Diseases
      Yes8
7.92
p = 0.3110
15.15
p = 0.19
      No93
92.08
56
84.85
Origin of Samples
      Kennels/Catteries/Associations62
61.38
p = 4.04 × 10−1537
56.06
p = 1.21 × 10−5
      Tutors39
38.61
29
43.94
Total101
100
66
100
Table 4. Length of time spent by animals in kennels and catteries. Significant factors are highlighted with p-values in bold.
Table 4. Length of time spent by animals in kennels and catteries. Significant factors are highlighted with p-values in bold.
Dogsp-ValueCatsp-Value
n
(%)
n
(%)
Length of time spent in kennels/catteries
Island A
<1 month9
9.4
p = 0.00711
28.2
p = 0.012
2–12 months5
5.2
3
7.7
1–5 years75
78.1
22
56.4
>5 years7
7.3
3
7.7
Total96
100
39
100
Island B
<1 month5
8.1
p = 0.0008
21.6
p = 0.020
2–12 months9
14.5
5
13.5
1–5 years39
62.9
22
59.5
>5 years9
14.5
2
5.4
Total62
100
37
100
Table 5. Macroscopic features of sampled feces from Island A. Significant factors are highlighted with p-values in bold.
Table 5. Macroscopic features of sampled feces from Island A. Significant factors are highlighted with p-values in bold.
Dogsp-ValueCatsp-Value
n
(%)
n
(%)
Island A
Consistency
Liquid2
1.9
p = 0.942
4.1
p = 0.92
Very Soft3
2.9
4
8.2
Soft17
16.4
8
16.3
Formed82
78.8
35
71.4
Color
Normal102
98.1
p = 0.7248
98
p = 0.55
Abnormal2
1.9
1
2
Blood
Presence4
4
p = 0.293
6.1
p = 0.2
Absence100
96
46
93.9
Mucus
Presence3
2.9
p = 0.542
4
p = 0.32
Absence101
97.1
47
96
Parasitic Forms
Presence7
6.7
p = 0.0034
8.2
p = 0.04
Absence97
93.3
45
91.8
Total104
100
49
100
Infected animals
Dogs Cats
n
(%)
n
(%)
Feces
Normal51
75
19
79
Abnormal17
25
5
21
Total68
100
24
100
Table 6. Macroscopic features of sampled feces from Island B. Significant factors are highlighted with p-values in bold.
Table 6. Macroscopic features of sampled feces from Island B. Significant factors are highlighted with p-values in bold.
Dogsp-ValueCatsp-Value
n
(%)
n
(%)
Island B
Consistency
Liquid4
4
p = 0.834
6
p = 0.79
Very Soft4
4
5
7.6
Soft14
13.9
11
16.7
Formed79
78.1
46
69.7
Color
Normal98
97
p = 0.4964
97
p = 0.73
Abnormal3
3
2
3
Blood
Presence5
5
p = 0.554
6
p = 0.38
Absence96
95
62
94
Mucus
Presence2
2
p = 0.752
3
p = 0.51
Absence99
98
64
97
Parasitic Forms
Presence4
4
p = 0.046
9
p = 0.03
Absence97
96
60
91
Total101
100
66
100
Infected animals
Dogs Cats
n
(%)
n
(%)
Feces
Normal33
83
29
78
Abnormal7
17
8
22
Total40
100
37
100
Table 7. Microscopic fecal examination: number (n) and percentage (%) of positive dogs for different parasites on Islands A (São Miguel) and B (Terceira).
Table 7. Microscopic fecal examination: number (n) and percentage (%) of positive dogs for different parasites on Islands A (São Miguel) and B (Terceira).
ParasiteIsland A
(n = 104)
n/%
Island B
(n = 101)
n/%
Total
(n = 205)
n/%
Ancylostomatidae (hookworms)53 (51)34 (33.7)87 (42.4)
Trichuris vulpis20 (19.2)16 (15.8)36 (17.6)
Toxocara canis16 (15.4)10 (9.9)26 (12.7)
Cystoisospora spp.7 (6.7)2 (1.98)9 (4.4)
Angiostrongylus vasorum0 (0)1 (1)1(0.5)
Mono-infections44 (64.7)18 (45)62 (57.4)
Mixed infections24 (35.3)22 (55)46 (42.6)
Total number of positive dogs68 (65)40 (40)108 (53)
Table 8. A statistical analysis evaluating two factors (the island where the animals lived and the species) in relation to the different infections detected in the study. Significant factors are highlighted with p-values in bold.
Table 8. A statistical analysis evaluating two factors (the island where the animals lived and the species) in relation to the different infections detected in the study. Significant factors are highlighted with p-values in bold.
Positive for Gastrointestinal ParasitesPositive for LungwormsZoonotic Infections
Variablen (Total)n (Total)n (Total)
%%%
GLM p-valueGLM p-valueGLM p-value
Species
Dogs vs. Cats16925152
53847.5
0.0250.0000.310
IslandDogs
São Miguel vs. Terceira1081100
530.4949
0.0090.0280.001
IslandCats
São Miguel vs. Terceira612452
532145
0.0120.2130.083
Table 9. A statistical analysis evaluating the island of origin concerning the occurrence of infection with certain parasite species. Significant factors are highlighted with p-values in bold.
Table 9. A statistical analysis evaluating the island of origin concerning the occurrence of infection with certain parasite species. Significant factors are highlighted with p-values in bold.
Positive
Variablen (Total)
%
GLM p-value
Hookworms—Island (Dogs)
São Miguel vs. Terceira87
42
0.031
Hookworms—Island (Cats)
São Miguel vs. Terceira34
30
0.007
Toxocara canis—Island (Dogs)
São Miguel vs. Terceira26
13
0.166
Toxocara cati—Island (Cats)
São Miguel vs. Terceira37
32
0.058
Trichuris vulpis—Island (Dogs)
São Miguel vs. Terceira36
18
0.325
Trichuris sp.—Island (Cats)
São Miguel vs. Terceira1
0.9
0.574
Cystoisospora spp.—Island (Dogs)
São Miguel vs. Terceira9
4.4
0.064
Cystoisospora spp.—Island (Cats)
São Miguel vs. Terceira17
15
0.178
Aelurostrongylus abtrusus—Island (Cats)
São Miguel vs. Terceira24
21
0.213
Angiostrongylus vasorum—Island (Dogs)
São Miguel vs. Terceira1
0.5
0.028
Table 10. Microscopic fecal examination: number (n) and percentage (%) of positive cats for different parasites on Islands A (São Miguel) and B (Terceira).
Table 10. Microscopic fecal examination: number (n) and percentage (%) of positive cats for different parasites on Islands A (São Miguel) and B (Terceira).
ParasiteIsland A
(n = 49)
n/%
Island B
(n = 66)
n/%
Total
(n = 115)
n/%
Toxocara cati11 (22.5)26 (39.4)37 (32.2)
Ancylostomatidae9 (18.4)25 (37.9)34 (29.6)
Cystoisospora spp.5 (10.2)12 (18.2)17 (14.8)
Trichuris sp.0 (0)1 (1.5)1 (0.9)
Aelurostrongylus abtrusus8 (16.3)16 (24.2)24 (20.9)
Mono infections18 (75)17 (46)35 (57.4)
Mixed infections6 (25)20 (54)26 (42.6)
Total number of positive cats24 (49)37 (56)61 (53)
Disclaimer/Publisher’s Note: The statements, opinions and data contained in all publications are solely those of the individual author(s) and contributor(s) and not of MDPI and/or the editor(s). MDPI and/or the editor(s) disclaim responsibility for any injury to people or property resulting from any ideas, methods, instructions or products referred to in the content.

Share and Cite

MDPI and ACS Style

Teixeira, R.; Flor, I.; Nunes, T.; Pinto, C.; Pomba, M.C.; de Carvalho, L.M. Survey of Gastrointestinal Parasites and Lungworms in Cats and Dogs from Terceira and São Miguel Islands, Azores. Pathogens 2024, 13, 648. https://doi.org/10.3390/pathogens13080648

AMA Style

Teixeira R, Flor I, Nunes T, Pinto C, Pomba MC, de Carvalho LM. Survey of Gastrointestinal Parasites and Lungworms in Cats and Dogs from Terceira and São Miguel Islands, Azores. Pathogens. 2024; 13(8):648. https://doi.org/10.3390/pathogens13080648

Chicago/Turabian Style

Teixeira, Romana, Isilda Flor, Telmo Nunes, Carlos Pinto, Maria Constança Pomba, and Luís Madeira de Carvalho. 2024. "Survey of Gastrointestinal Parasites and Lungworms in Cats and Dogs from Terceira and São Miguel Islands, Azores" Pathogens 13, no. 8: 648. https://doi.org/10.3390/pathogens13080648

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop