Next Article in Journal
Efficacy of Binary Ethylenimine in the Inactivation of Foot-and-Mouth Disease Virus for Vaccine Production in South Korea
Next Article in Special Issue
A Comparative Study of Genetic Diversity and Multiplicity of Infection in Uncomplicated Plasmodium falciparum Infections in Selected Regions of Pre-Elimination and High Transmission Settings Using MSP1 and MSP2 Genes
Previous Article in Journal
Fluconazole Resistance and Virulence in In Vitro Induced-Fluconazole Resistant Strains and in Clinical Fluconazole Resistant Strain of Cryptococcus deuterogattii
Previous Article in Special Issue
Insights into the Genetic Diversity of Leishmania (Viannia) panamensis in Panama, Inferred via Multilocus Sequence Typing (MLST)
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Review

Lungworms of Non-Ruminant Terrestrial Mammals and Humans in Iran

by
Sina Mohtasebi
1,†,
Alireza Sazmand
2,*,†,
Salman Zafari
3,
Guilherme G. Verocai
4,* and
Domenico Otranto
2,5
1
Faculty of Veterinary Medicine, University of Calgary, Calgary, AB T2N 4Z6, Canada
2
Department of Pathobiology, Faculty of Veterinary Science, Bu-Ali Sina University, Hamedan 6517658978, Iran
3
Department of Medical Parasitology and Mycology, School of Medicine, Hamadan University of Medical Sciences, Hamadan 6517838736, Iran
4
Department of Veterinary Pathobiology, School of Veterinary Medicine and Biomedical Sciences, Texas A&M University, College Station, TX 77843, USA
5
Department of Veterinary Medicine, University of Bari, 70010 Bari, Italy
*
Authors to whom correspondence should be addressed.
These authors contributed equally to this work.
Pathogens 2023, 12(6), 759; https://doi.org/10.3390/pathogens12060759
Submission received: 27 March 2023 / Revised: 10 May 2023 / Accepted: 18 May 2023 / Published: 25 May 2023

Abstract

:
With over 300 terrestrial and aquatic mammalian species, Iran is considered a country with an ample mastofauna. Although many studies have assessed the distribution of gastrointestinal helminth parasites in animals and humans in Iran, lungworms have not received adequate attention. Following a previous article in which we reviewed the diversity and prevalence of lungworm infections in pastoral and wild ruminants of Iran, this report compiles the available scientific information about the occurrence of lungworms in non-ruminant mammals and humans from 1980 to 2022 to provide insights into the epidemiology of these infections. International and national scientific databases were searched, and twenty-six articles in peer-reviewed journals, one conference paper, and one D.V.M. thesis were included in the study. In total, 10 species belonging to seven genera, including Dictyocaulus, Deraiophoronema, Protostrongylus, Crenosoma, Eucoleus, Aelurostrongylus, and Metastrongylus, were reported in the respiratory tract or feces of humans, domestic animals (i.e., camels, equids, dogs, and cats), and wildlife species (i.e., hedgehogs, wild boars, and hares). Most of the studies (22/28) were performed using post-mortem examinations. The overall prevalence of respiratory nematode infection varied according to animal species in camels (14.83%), equids (13.31%), dogs (5%), wild boars (45.66%), hedgehogs (42.57%), and hares (1.6%). In addition, pulmonary capillariasis caused by Eucoleus aerophilus was reported in a 9 year old child. The prevalence of lungworm species in domestic camels, equids, and dogs, combined with a lack of labeled anthelmintic products, supports the need to improve our understanding of these important nematode parasites and inform the development of sustainable control strategies. From a zoo and wildlife medicine point of view, there is a shortage of information about the presence and prevalence of lungworm infections in the majority of mammalian species, pending epidemiological studies that integrate classical parasitology and molecular methods.

1. Introduction

Parasitic infections occur in almost every animal community and play significant roles in the mortality and morbidity of the hosts they inhabit [1]. Many helminths parasitize the lungs and respiratory tracts of many domestic and wild species globally [2,3]. The detrimental economic impacts of these pathogens on farm animals have urged scientists to do research on them, whereas the ecology and fauna of lungworms in many wild species are still unknown [4].
The vast geographical expanses of Iran have provided suitable habitats for a variety of both domesticated and wild animals [5]. Indeed, Iran is a country with an ample mammal fauna, with approximately 192 terrestrial and 16 aquatic species of mammals, including iconic species such as the Asiatic cheetah Acinonyx jubatus (Schreber, 1775), the Persian leopard Panthera pardus saxicolor (Pocock, 1927), the Mesopotamian fallow deer Dama dama subsp. mesopotamica (Brooke, 1875), and the Asiatic wild ass Equus hemionus (Pallas, 1775) [6,7]. As previously reviewed, seven species of lungworms belonging to four genera, i.e., Dictyocaulus filaria (Rudolphi, 1809), Dictyocaulus viviparus (Bloch, 1782), Dictyocaulus eckerti (Skrjabin, 1931), Protostrongylus rufescens (Leuckart, 1865), Protostrongylus raillietti (Schulz, Orlow and Kutass, 1933), Muellerius capillaris (Müller, 1889), and Cystocaulus ocreatus (Railliet and Henry, 1907) have been reported in Iran, in domestic sheep, goats, cattle, water buffaloes and wild ruminants, such as urials, Ovis orientalis (Gmelin, 1774); wild goats, Capra hircus subsp. Aegagrus (Erxleben, 1777); goitered gazelles, Gazella subgutturosa (Güldenstaedt, 1780); roe deer, Capreolus capreolus (Linnaeus, 1758); and red deer, Cervus elaphus (Linnaeus, 1758) [8]. However, very little information is available regarding the lungworms of non-ruminant terrestrial mammals in the country.
In this article, we reviewed the available information about the status of nematode infections in the respiratory tract of equids, camels, wild boars, hedgehogs, hares, dogs, cats, and humans in Iran.

2. Materials and Methods

The search period for articles was from October 2018 to February 2023. In order to find related articles and studies, scientific resources and the Google Scholar search engine were used alongside IranDoc, Civilica, PubMed, and CAB Direct websites singularly and in combination, using English, Persian, and French language search strings “lungworm (s), mammals, carnivores, domestic, wild, wildlife; plus, common and scientific Latin names of the hosts and lungworms”. Searches were conducted in Persian (Farsi) and English languages. After the collection of the documents, the validity and accuracy of the studies were screened for clarity, originality, objectivity, sampling methods, diagnostic methods, and percentage of evaluation studies. An Excel file of the above information was prepared. Data were extracted as follows: study area, species of infected animal, species of helminths, prevalence of lungworms infecting animals, year of study, number of animals studied, and source of inspection (feces or carcass).

3. Results and Discussion

The collected documents were written in Persian and English, and all the reports were published after 1980. Among 31 publications, three studies were excluded since they did not match the validity and accuracy evaluation criteria. In the twenty-eight studies included in this review (i.e., twenty-six articles in peer-reviewed articles; twenty-three in English and three in Persian, one conference paper in Persian, and one D.V.M. thesis in Persian with an English abstract), 10 species of lungworms belonging to seven genera, e.g., Dictyocaulus (Railliet and Henry, 1907), Deraiophoronema (Romanovitch, 1916), Protostrongylus (Kamensky, 1905), Crenosoma (Molin, 1861), Eucoleus (Dujardin, 1845), Aelurostrongylus (Cameron, 1927), and Metastrongylus (Molin, 1861) have been reported in the respiratory system or feces of different domestic and wild terrestrial mammals namely, horse Equus caballus (Linnaeus, 1758), donkey Equus asinus (Linnaeus, 1758), mule (Equus asinus × Equus caballus), one-humped camel Camelus dromedarius (Linnaeus, 1758), dog Canis lupus subsp. Familiaris (Linnaeus, 1758), cat Felis catus (Linnaeus, 1758), Southern white-breasted hedgehog Erinaceus concolor (Martin, 1838), long-eared hedgehog Hemiechinus auritus (Gmelin, 1770), wild boar Sus scrofa (Linnaeus, 1758), and cape hare Lepus capensis (Linnaeus, 1758) (Figure 1). Most of the studies (22/28) were performed using post-mortem examination of animal carcasses.

3.1. Equid Lungworms

In Iran, horses, donkeys, and their hybrids, including male horse × female donkey (hinnies), female horse × male donkey (mules), are widely distributed across the country. Three publications reported eggs and larvae of Dictyocaulus arnfieldi (Cobbold, 1884) in horses, donkeys, and mules in Iran, including one research article, one case report, and one D.V.M. thesis [9,10,11]. So far, adult nematodes have not been isolated, and all of the conducted studies employed fecal flotation and the Baermann technique, with an overall prevalence of D. arnfieldi of 10.04% (50/498) in horses, 31.81% (21/66) in donkeys, and 24.32% (9/37) in mules, consistent with the literature stating that donkeys are more suitable definitive hosts of D. arnfieldi than horses as they can tolerate large numbers of parasites with few clinical signs of respiratory disease and are considered natural reservoirs [12]. Of note, the first-stage larvae of D. arnfieldi were recovered from the feces of two horses in a zoo in Mashhad, northeast of Iran, with a history of being co-housed with donkeys for a short time [9] (Table 1). However, in addition to domesticated equids, the IUCN red list includes endangered species [13]. The Persian onager, Equus hemionus subsp. Onager (Boddaert, 1785), is native to the deserts of Iran. No studies are available about Dictyocaulus sp. infection in onager populations, while in the only parasitological study available, Gasterophilus pecorum (Fabricius, 1794) and Habronema muscae (Carter, 1861) were isolated from the stomach of one dead animal [14]. Furthermore, although donkeys seem to play a more substantial role in the maintenance of this parasite than other horses [15], there is no information about their hybrids: hinnies and mules, which are commonly found in Iran and can be the subject of future research.

3.2. Nematodes of the Respiratory Tract of Camels

Nine publications reported lungworm infection in one-humped camels, including eight peer-reviewed articles [16,17,18,19,20,21,22,23] and one conference paper [24]. Approximately 152,000 Old World camels (OWCs), including one-humped (dromedary) and two-humped (Bactrian) camels (only 100–300 individuals), are scattered throughout 21 of the 31 Iranian provinces [25,26]. In Iran, D. filaria has been isolated from the lungs of examined dromedaries [18,27], implying cross-infection with ruminants. As the measurements have not been reported, it is not possible to assess the correct identification and differentiation from Dictyocaulus cameli (Boev, 1951). In general, compared with other livestock species, relatively few reports are available on the status of lungworm infections in camels, and a study on thirty-four camels in Kazakhstan over seven decades ago reported the infection of camels with D. cameli and a few D. filaria [28]. Although in the revision of the genus it was concluded that D. cameli is a valid species [29], there is not much known, especially about the epidemiology and molecular characterization of this nematode. So, the collection of Dictyocaulus from dromedaries and Bactrians in camel-rearing areas of the world through a multi-state study is advocated in order to increase our knowledge about this scantly known species. However, due to the fact that the life cycle of Dictyocaulus species requires moist conditions for the survival of the larvae, lungworm infection should not be a severe issue for dromedaries living in hot and dry climates. In addition to bronchial system-dwelling lungworms D. cameli, D. filaria, and D. viviparus [26], mature worms of the camel-specific filarioid nematode Deraiophoronema evansi (Lewis, 1882), commonly known as Dipetalonema evansi, inhabit various organs, including the pulmonary arteries, heart, testicles, epididymis, and spermatic cord [22,30]. In this article, we only considered documents reporting adult D. evansi worms from the respiratory system of dromedaries and pathological lesions associated with them; however, several other articles reported observation and/or molecular detection of the helminth microfilariae in the blood of 0.88–46.7% of dromedaries [26]. Studies reported in Table 2 examined the presence and pathology of lungworms postmortem. Overall, the prevalence of lungworm infections in tested camels in Iran was 16.9% (142/840) for D. evansi and 11.1% (10/90) for Dictyocaulus, reported as D. filaria. In neighboring Turkey, the prevalence of D. viviparus in wrestling hybrid camels (hybrids of female dromedary camels and male Bactrian camels) was 5.5% [31]. However, so far, this helminth species has not been reported in Iranian camels. Although there have been many coproscopy-based studies in Iran, the Baermann technique has not been applied in research to diagnose the L1 in feces. Hence, it is recommended to perform larvoscopy along with regular coproscopy in future studies.

3.3. Suid Lungworms

In six peer-reviewed articles, lungworm infections were reported in wild boars in Iran [32,33,34,35,36,37]. According to the Islamic Republic of Iran’s laws, which are based on Islamic precepts, retail and consumption of pork are illegal in the country, and subsequently, no industrial pig farming has been present since 1978. However, wild boars are widespread and occasionally get killed, mainly when they invade private farms and destroy crops. In Iran, three Metastrongylus species, including Metastrongylus apri (Gmelin, 1780) (syn. Metastrongylus elongatus), Metastrongylus pudendotectus (Wostokow, 1905) (syn. Metastrongylus brevivaginatus), and Metastrongylus salmi (Gedoelst, 1923), have been reported in wild boars (Table 3). In the studies above, the overall prevalence of lungworm infection in tested wild boars was 45.66% (58/127) using both fecal flotation (prevalence 23.62%; 30/127) and post-mortem examination (prevalence 76.38%; 97/127). Similarly, the same species composition and prevalence as in Iran were reported in Turkey, with M. apri (59%) being the most prevalent, followed by M. salmi and M. pudendotectus (both 52%) [38]. Suids are known to become infected with eight lungworm species, including M. apri, M. pudendotectus, and M. salmi, which have been reported from Iran, as well as M. confusus, M. asymmetricus, M. madagascariensis, M. pulmonalis, and M. tschiauricus [39,40], so understanding the possible presence of other Metastrongylus species in Iran needs future studies. In addition, from a public health point of view, human infection with suid lungworms rarely occurs, and five cases, four with M. elongatus and one with M. salmi, have been reported in Ecuador so far [39,41,42]. So, the role of Metastrongylus species as zoonotic pathogens must not be overlooked, and the environment and wildlife diseases sectors and researchers must be vigilant about the surveillance and occurrence of these helminths in swine alongside other known zoonotic parasites such as Ascaris suum (Goeze, 1782); Trichinella spiralis (Owen, 1835); and Balantidium coli (Malmsten, 1857).

3.4. Hedgehog Lungworms

In six peer-reviewed articles, the presence, prevalence, and pathology of lungworms were reported in hedgehogs in Iran [43,44,45,46,47,48]. Four species of hedgehogs, including the southern white-breasted hedgehog E. concolor, the long-eared hedgehog H. auratus, the Brandt’s hedgehog Paraechinus hypomelas (Brandt, 1836), and the desert hedgehog Paraechinus aethiopicus (Ehrenberg, 1832), occur in Iran [7]. Unfortunately, in some previous parasitology reports from Iran, species-level identification of hedgehogs was not performed correctly (discussed in Khodadadi et al., 2021 [49]); however, in this review article, we cross-matched the reports with the natural geographical habitats of each hedgehog species. In Iran, infection of southern white-breasted hedgehogs and long-eared hedgehogs with Crenosoma striatum (Zeder, 1800) has been recorded in Mazandaran, Kerman, Razavi Khorasan, and East Azerbaijan provinces (Figure 1). Furthermore, the southern white-breasted hedgehog has been reported to host Eucoleus aerophilus (Creplin, 1839) in the northwestern province of West Azarbaijan, which neighbors Turkey [48]. Overall, 38.61% (39/101) and 9.09% (4/44) of examined animals were found infected with C. striatum and E. aerophilus, respectively, after post-mortem examination (Table 4). These two nematodes were the only species reported in a study [50] on road-killed hedgehogs in neighboring Turkey, with C. striatum and E. aerophilus found in 55.5% and 22.2% of animals, respectively. Considering that E. aerophilus is potentially zoonotic and there has been a rising interest in keeping hedgehogs as exotic pets globally [51], it is suggested that Iranian veterinarians be watchful of the diagnostic, treatment, and management of parasitic infections in these playful animals.

3.5. Lagomorph Lungworms

In the only documentation on lungworm infections in wild lagomorphs of Iran, Protostrongylus raillieti (Schulz, Orlow, and Kutass, 1933) was reported in 4 out of 420 (1.6%) cape hares collected from 24 provinces [52]. This nematode usually infects caprine ruminants such as Ovis aries subsp. Orientalis (Gmelin, 1774) [53]. In total, seven lungworm species belonging to the genus Protostrongylus (Nematoda, Protostrongylidae) are observed in lagomorphs worldwide: Protostrongylus pulmonalis (Frölich, 1802), Protostrongylus terminalis (Passerini, 1884); Protostrongylus kamenskyi (Schulz, 1930); Protostrongylus cuniculorum (Joyeux and Gaud, 1946); Protostrongylus tauricus (Schutz and Kadenatsii, 1949); Protostrongylus boughtoni (Goble and Dougherty, 1943); and Protostrongylus oryctolagi (Babo, 1955) [54]. However, according to a previous historical review on the morphological identification of Protostrongylus species isolated from Lagomorpha, there have been several confusions on the characterizations, for instance between P. terminalis and other species such as P. pulmonalis and P. rufescens, and also between P. cuniculorum and P. rufescens [55]. Similarly, Protostrongylus specimens isolated from L. capensis in Iran could potentially have been misidentified. Hence, the collection and reassessment of novel materials would be necessary to integrate morphological and molecular characterization. Furthermore, three other wild lagomorph species, namely the European hare Lepus europaeus (Pallas, 1778); the Tolai hare Lepus tolai (Pallas, 1778); and the Afghan pika Ochotona rufescens (Gray, 1842), occur in Iran [6], but despite their wide geographic distribution in the country [56], there have been no studies about their lungworm fauna. Therefore, further research on Lagomorpha in Iran is required to fill these many gaps.

3.6. Dog Lungworms

Only a single study reported eggs of the trichuroid nematode E. aerophilus during the fecal examination of 5 out of 100 domestic dogs in Mazandaran province [57], making our knowledge of the status of canine lungworms in Iran fragmentary. However, the eggs of E. aerophilus and Eucoleus boehmi (Supperer, 1953) are similar in morphological characteristics [58], so it is strongly recommended to perform multicenter epidemiological studies to shed light on the Eucoleus fauna of dogs in the country.
In this single Iranian study, fecal specimens were concentrated by the formalin-ether sedimentation method and flotation technique in a saturated zinc chloride solution [57]. Since cystic echinococcosis is hyper-endemic in the country and dogs are the main final hosts of Echinococcus granulosus (Batsch, 1786) sensu lato [59], handling and examining the canine fecal specimens require special care, and hence the Baermann technique for recovery of potentially present L1 larvae of metastrongyloid lungworms was not performed. Subsequently, information about the epidemiology of canid lungworms has remained limited in the country, though the infection can be diagnosed by other techniques such as imaging, and by examination of biological samples other than feces, including bronchoalveolar lavage, nasal secretions, and vomit [60].
Although E. aerophilus has been reported, it is known that dogs become infected mainly with Oslerus osleri (Cobbold, 1876) but also with Filaroides hirthi (Georgi and Anderson, 1975); Filaroides milksi (Whitlock, 1956); and Crenosoma vulpis (Dujardin, 1844), which are normally parasites of wild canids such as foxes, coyotes, and wolves [61]. However, despite the indispensable epidemiological roles of wild canids in lungworm infection of domestic dog populations, there is an absolute lack of information about the possible presence of lungworms in the various wild canid species widely present in Iran, such as the golden jackal Canis aureus (Linnaeus, 1758), the red fox Vulpes vulpes (Linnaeus, 1758), and the grey wolf Canis lupus (Linnaeus, 1758). It is worth mentioning that in recent years, the rocketing population of stray dogs has become a veterinary and public health concern in Iran. Hence, to raise scientific knowledge regarding the risk of lungworm infections in owned dogs, it is suggested to search for the lungworms infecting stray dog populations and wild canids in different regions of the country.
There has been an increasing habit of keeping dogs as pets in Iran in the past two decades. Considering that E. aerophilus is known to be potentially zoonotic (discussed in Section 3.8), it is strongly advisable to routinely include lungworms in the differential diagnosis of cardiorespiratory diseases in dogs.

3.7. Cat Lungworm

Only one paper in Iran has reported the presence of Aelurostrongylus abstrusus (Railliet, 1898) larvae circulating in the blood of a stray cat from Tehran [62]. In that study, researchers applied the Knott’s test to determine the presence of microfilariae in filarioid nematodes; therefore, the finding of A. abstrusus L1 was considered incidental [62]. Cats are the usual hosts of A. abstrusus, and feline aelurostrongylosis has been reported in different geographical regions with different prevalence rates [63], but there is limited information about West Asian countries. In a study in Qatar, aelurostrongylosis was reported in 7.5% of feline fecal samples [64], and the infection of cats in Iraq and Turkey was documented as case reports [65,66]. While A. abstrusus is considered to be the most prevalent lungworm of cats, other respiratory nematodes such as Troglostrongylus spp. (Vevers, 1923), Oslerus rostratus (Gerichter, 1945), and E. aerophilus have been reported from cats [60,67], none of which have been reported from Iran. However, a recent epidemiological study in Israel described Troglostrongylus brevior (Gerichter, 1949) as the dominant lungworm infecting feral cats in Jerusalem, Israel [68], suggesting that T. brevior is present in other Middle Eastern countries, including Iran. In the absence of information about lungworm infections in Iranian wild felids, including the Asiatic cheetah A. jubatus, the Persian leopard P. saxicolor, the caracal Caracal caracal (Schreber, 1776), Pallas’s cat Otocolobus manul (Pallas, 1776), and the Caucasian lynx Lynx lynx dinniki (Satunin, 1915), the wildcat Felis silvestris ornate (Gray, 1832), the jungle cat Felis chaus (Schreber, 1777), and the sand cat Felis margarita (Loche, 1858), conducting studies on these larger cats would be extremely informative considering that domestic and wild felids share several lungworm species, such as A. abstrusus, E. aerophilus, and T. brevior [60,69], and possibly additional lungworm species.

3.8. Human Lungworm

In Iran, E. aerophilus was once recorded in a 9 year old boy with severe asthmatic symptoms, a productive cough, and moderate eosinophilia, whose symptoms were alleviated by prescribing diethylcarbamazine, thiabendazole, and steroids [70]. Human respiratory capillariasis caused by E. aerophilus is rare, with only 12 reported cases globally [71,72]. While the infection is more common in canine and feline medicine, one major issue in assessing the status of this complication is the lack of implementation of adequate diagnostic methods, and therefore many cases might go underdiagnosed [71]. In addition, human capillariosis is characterized by non-specific clinical signs such as fever, bronchitis, coughing, hemoptysis, and dyspnea and, importantly, may induce relevant damage resembling bronchial carcinoma [71]. Epidemiological information from the examination of dogs and cats throughout the country may help physicians assess the risk of human infections in each area.

4. Conclusions, Remarks, and Challenges for Future Research

The present review describes the considerable diversity of nematode species infecting the respiratory tract of wild and domesticated non-ruminant mammals in Iran, including humans. Although the relevance of nematodes infecting the respiratory tract of various mammalian hosts has been largely neglected when compared to other parasitic nematodes, they are considered important pathogens, causing significant complications in domestic and wild animals worldwide. In our previous review article, we highlighted the status quo of lungworms in pastoral livestock systems in Iran [8], and herein we noted the diversity of lungworms in non-ruminant mammals and humans. As previously mentioned, environmental conditions such as seasonal changes, rainfall, and temperature may directly influence the occurrence of lungworm infection in different host species and their epidemiology. Moreover, it should be noted that climate change, loss of biodiversity, animal trade, and a lack of large-scale surveillance can play key roles in fluctuations observed in the prevalence and diversity of species in different regions. The diversity of lungworms, their host associations, and prevalence have not received enough attention in the scientific community of Iran, and complementary studies are needed to describe the status of respiratory nematode species in Iran, especially in wild hosts. In the current study, it was shown that the majority of cases had been analyzed in post-mortem examinations, but it should be considered that finding carcasses of wild animals is difficult, so administering standard parasitological diagnostic tools on fresh biological specimens as well as developing robust and novel techniques to study older environmental samples could improve the diagnosis of parasites. Additionally, the use of classical and molecular techniques could boost the accuracy of diagnosis, especially in morphologically similar species.

Author Contributions

Conceptualization, A.S. and S.Z.; methodology, A.S. and S.Z.; investigation, S.Z., A.S. and S.M.; writing—original draft preparation, S.M., S.Z. and A.S.; writing—review and editing, A.S., D.O. and G.G.V.; supervision, A.S.; project administration, A.S. All authors have read and agreed to the published version of the manuscript.

Funding

This research did not receive any specific grant from funding agencies in the public, commercial, or not-for-profit sectors.

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

Not applicable.

Conflicts of Interest

The authors declare that they have no competing interest.

References

  1. Poulin, R.; Morand, S. Parasite biodiversity; Smithsonian Institution: Washington, DC, USA, 2005. [Google Scholar]
  2. de Macedo, L.O.; Lima, T.A.; Verocai, G.G.; Alves, L.C.; de Carvalho, G.A.; Ramos, R.A. Lungworms in ruminants from Brazil: A retrospective epidemiological study over four decades. Vet. Parasitol. Reg. Stud. Rep. 2021, 26, 100645. [Google Scholar] [CrossRef] [PubMed]
  3. Verocai, G.G.; Kutz, S.J.; Simard, M.; Hoberg, E.P. Varestrongylus eleguneniensis sp. n. (Nematoda: Protostrongylidae): A widespread, multi-host lungworm of wild North American ungulates, with an emended diagnosis for the genus and explorations of biogeography. Parasit. Vectors. 2014, 7, 556. [Google Scholar] [CrossRef] [PubMed]
  4. Holzhauer, M.; Van Schaik, G.; Saatkamp, H.; Ploeger, H. Lungworm outbreaks in adult dairy cows: Estimating economic losses and lessons to be learned. Vet. Rec. 2011, 169, 494. [Google Scholar] [CrossRef] [PubMed]
  5. Firouz, E. The Complete Fauna of Iran; IB Tauris: New York, NY, USA, 2005. [Google Scholar]
  6. Yusefi, G.H.; Faizolahi, K.; Darvish, J.; Safi, K.; Brito, J.C. The species diversity, distribution, and conservation status of the terrestrial mammals of Iran. J. Mammal. 2019, 100, 55–71. [Google Scholar] [CrossRef]
  7. Karami, M.; Ghadirian, T.; Faizolahi, K. The atlas of Mammals of Iran; Jahad Daneshgahi, Kharazmi Branch: Karaj, Iran, 2016. [Google Scholar]
  8. Zafari, S.; Mohtasebi, S.; Sazmand, A.; Bahari, A.; Sargison, N.D.; Verocai, G.G. The prevalence and control of lungworms of pastoral ruminants in Iran. Pathogens 2022, 11, 1392. [Google Scholar] [CrossRef] [PubMed]
  9. Sharifi, K.; Borji, H.; Milani, P. First report of Dictyocaulus arnfieldi infestation in a horse in Mashhad, Iran. Iran. J. Vet. Sci. Tech. 2010, 2, 45–50. [Google Scholar]
  10. Saadi, A.; Tavassoli, M.; Dalir-Naghadeh, B.; Samiei, A. A survey of Dictyocaulus arnfieldi (Nematoda) infections in equids in Urmia region, Iran. Ann. Parasitol. 2018, 64, 235–240. [Google Scholar] [CrossRef]
  11. Seif, P. Prevalence of gastrointestinal parasitic helminthes in horses in Kermanshah city via stool examination. DVM Thesis, Razi University, Kermanshah, Iran, 2016. [Google Scholar]
  12. Nicholls, J.; Clayton, H.; Duncan, J.; Buntain, B. Lungworm (Dictyocaulus arnfieldi) infection in donkeys. Vet. Rec. 1979, 104, 567–570. [Google Scholar] [CrossRef]
  13. Kaczensky, P.; Lkhagvasuren, B.; Pereladova, O.; Hemami, M.; Bouskila, A. Equus hemionus. The IUCN Red List of Threatened Species; e. T7951A45171204; IUCN: Gland, Switzerland, 2015. [Google Scholar]
  14. Zaheri, B.A.; Ronaghi, H.; Youssefi, M.R.; Hoseini, S.M.; Omidzahir, S.; Dozouri, R.; Ramezanpour Eshkevari, S.; Mousapour, A. Gasterophilus pecorum and Habronema muscae in Persian onager (Equus hemionus onager), histopathology and parasitology survey. Comp. Clin. Pathol. 2015, 24, 1009–1013. [Google Scholar] [CrossRef]
  15. Lyons, E.; Tolliver, S.; Drudge, J.; Swerczek, T.; Crowe, M. Lungworms (Dictyocaulus arnfieldi): Prevalence in live equids in Kentucky. Am. J. Vet. Res. 1985, 46, 921–923. [Google Scholar]
  16. Mirzayans, A.; Halim, R. Parasitic infection of Camelus dromedarius from Iran. Bull. Soc. Pathol. Exot. Filiales. 1980, 73, 442–445. [Google Scholar] [PubMed]
  17. Jamshidi, K. Slaughterhouse study of the relative prevalence of histopathological lesions of camel lung (Camelus deromedarius). J. Comp. Pathobiol. 2012, 8, 651–656. (In Persian) [Google Scholar]
  18. Radfar, M.H.; Ebrahimy Maimand, A.; Sharify, A. A report on parasitic infections in camel (Camelus dromedarius) of Kerman slaughterhouse. J. Fac. Vet. Med. Univ. Tehran. 2006, 61, 165–168. [Google Scholar]
  19. Moghaddar, N.; Oryan, A.; Hanipour, M.R. Helminths recovered from the liver and lungs of camel with special reference to their incidence and pathogenesis in Shiraz, Islamic Republic of Iran. Indian J. Anim. Sci. 1992, 62, 1018–1023. [Google Scholar]
  20. Nourollahi-Fard, S.R.; Kheirandish, R.; Fathi, S.; Norouzi-Asl, E. Prevalence of Dipetalonema evansi infection in Camelus dromedaries. J. Vet. Res. 2011, 15, 261–269. [Google Scholar]
  21. Khodakaram-Tafti, A.; Mansourian, M. Pulmonary lesions of slaughtered camels (Camelus dromedarius) in Southern Iran. J. Camel. Pract. Res. 2010, 17, 21–24. [Google Scholar]
  22. Sazmand, A.; Anvari-Tafti, M.H.; Hekmatimoghaddam, S.; Moobedi, I. Dipetalonema evansi infection in camels of Iran's central area. Pak. J. Biol. Sci. 2013, 16, 647–650. [Google Scholar] [CrossRef]
  23. Oryan, A.; Valinezhad, A.; Bahrami, S. Prevalence and pathology of camel filariasis in Iran. Parasitol. Res. 2008, 103, 1125–1131. [Google Scholar] [CrossRef]
  24. Araghi, M.; Gheisari-Ramezanian, B.; Borji, H. A slaughterhouse study of camel lung parasites in Mashhad. In Proceedings of the The Regional Conference of Camel Research Priorities, Mashhad, Iran, 15–16 April 2009. (In Persian). [Google Scholar]
  25. FAOSTAT. Statistics division of food and agriculture organization of the United Nations. 2022. Available online: https://www.fao.org/faostat/en/#data (accessed on 17 January 2023).
  26. Sazmand, A.; Joachim, A. Parasitic diseases of camels in Iran (1931–2017)–a literature review. Parasite 2017, 24, 21. [Google Scholar] [CrossRef]
  27. Mizan Zadeh, H. Study of diversity and prevalence of occurance of diseases in slaughtered camels in Najaf-Abad slaughterhouse. D.V.M. Thesis, University of Tehran, Tehran, Iran, 1995. [Google Scholar]
  28. Shumilina, Z.V. A Study of Dictyocaulus Disease in Camels. Papers on Helminthology Presented to Academician, K.I. Skrjabin on His 75th Birthday; Akademii Nauk SSSR: Moscow, Russia, 1953. [Google Scholar]
  29. Gibbons, L.M.; Khalil, L.F. A revision of the genus Dictyocaulus Railliet & Henry, 1907 (Nematoda: Trichostrongyloidea) with the description of D. africanus n. sp from African artiodactylids. J. Afr. Zool. 1988, 102, 151–175. [Google Scholar]
  30. Sazmand, A.; Eigner, B.; Mirzaei, M.; Hekmatimoghaddam, S.; Harl, J.; Duscher, G.G.; Fuehrer, H.P.; Joachim, A. Molecular identification and phylogenetic analysis of Dipetalonema evansi (Lewis, 1882) in camels (Camelus dromedarius) of Iran. Parasitol. Res. 2016, 115, 1605–1610. [Google Scholar] [CrossRef] [PubMed]
  31. Aypak, S.; Eren, H.; Bakirci, S.; Uner, S.; Simsek, E.; Boga, B. Parasites detected by examination of fecal samples in wrestling camels. Kafkas. Univ. Vet. Fak. Derg. 2013, 19, 371–374. [Google Scholar]
  32. Garedaghi, Y.; Mojallal, S.; Ouzbandi, A. Helminth parasites of a hunted-wild boar (Sus scrofa) in the Talesh city, North of Iran. Bull. Environ. Pharmacol. Life. Sci. 2014, 3, 247–250. [Google Scholar]
  33. Solaymani-Mohammadi, S.; Mobedi, I.; Rezaian, M.; Massoud, J.; Mohebali, M.; Hooshyar, H.; Ashrafi, K.; Rokni, M.B. Helminth parasites of the wild boar, Sus scrofa, in Luristan province, western Iran and their public health significance. J. Helminthol. 2003, 77, 263–267. [Google Scholar] [CrossRef] [PubMed]
  34. Norouzi, R.; Ouzbandi, A. Survey of gastrointestinal parasite in wild boar (Sus scrofa), wild goat (Capra aegagrus) and red deer (Cervus elaphus) in the Aynaloo protected area, East Azerbaijan. J. Vet. Clin. Path. 2017, 11, 107–117. [Google Scholar]
  35. Farahnak, A.; Mobedi, I.; Mohamadi, F. Study of zoonotic helminths of carnivores in Khuzestan, Iran. Iran. J. Publ. Health. 1998, 27, 3–4. [Google Scholar]
  36. Mansouri, M.; Sarkari, B.; Mowlavi, G.R. Helminth parasites of wild boars, Sus scrofa, in Bushehr province, southwestern Iran. Iran. J. Parasitol. 2016, 11, 377–382. [Google Scholar] [PubMed]
  37. Eslami, A.; Farsad-Hamdi, S. Helminth parasites of wild boar, Sus scrofa, in Iran. J. Wildl. Dis. 1992, 28, 316–318. [Google Scholar] [CrossRef]
  38. García-González, Á.M.; Pérez-Martín, J.E.; Gamito-Santos, J.A.; Calero-Bernal, R.; Alonso, M.A.; Carrión, E.M.F. Epidemiologic study of lung parasites (Metastrongylus spp.) in wild boar (Sus scrofa) in southwestern Spain. J. Wildl. Dis. 2013, 49, 157–162. [Google Scholar] [CrossRef]
  39. Calvopina, M.; Caballero, H.; Morita, T.; Korenaga, M. Human pulmonary infection by the zoonotic Metastrongylus salmi nematode. The first reported case in the Americas. Am. J. Trop. Med. Hyg. 2016, 95, 871–873. [Google Scholar] [CrossRef] [PubMed]
  40. Gassó, D.; Rossi, L.; Mentaberre, G.; Casas, E.; Velarde, R.; Nosal, P.; Serrano, E.; Segales, J.; Fernandez-Llario, P.; Feliu, C. An identification key for the five most common species of Metastrongylus. Parasitol. Res. 2014, 113, 3495–3500. [Google Scholar] [CrossRef]
  41. Miloshev, B. Case of triple infection with Metastrongylus elongatus, Thaeniarhynchus saginatus and Enterobius vermicularis. Suvr. Med. 1956, 7, 94–97. [Google Scholar]
  42. Mathison, B.A.; Sapp, S.G.H. An annotated checklist of the eukaryotic parasites of humans, exclusive of fungi and algae. Zookeys 2021, 1069, 67403. [Google Scholar] [CrossRef]
  43. Youssefi, M.R.; Rahimi, M.T.; Halajian, A.; Moosapour, A.A.; Nikzad, R.; Nikzad, M.; Ramezanpour, S.; Ebrahimpour, S. Helminth parasites of eastern European hedgehog (Erinaceus concolor) in Northern Iran. Iran. J. Parasitol. 2013, 8, 645–650. [Google Scholar]
  44. Hoseini, S.M.; Youssefi, M.R.; Mousapour, A.; Dozouri, R.; Eshkevari-Ramezanpour, S.; Nikzad, M.; Nikzad, R.; Omidzahir, S. Histopathologic study of eosinophilic bronchointerstitial pneumonia caused by Crenosoma striatum in the hedgehog. J. Zoo. Wildl. Med. 2014, 45, 335–338. [Google Scholar] [CrossRef] [PubMed]
  45. Moshaverinia, A.; Borji, H.; Kameli, M.; Ghabdian, S.; Ghanei, R. A survey on parasites of long-eared hedgehog (Hemiechinus auritus) in Northeast of Iran. J. Parasit. Dis. 2016, 40, 1355–1358. [Google Scholar] [CrossRef]
  46. Mirzaei, M. Infection with Crenosoma striatum lungworm in long-eared hedgehog (Hemiechinus auritus) in Kerman province Southeast of Iran. Turkiye. Parazitol. Derg. 2014, 38, 255–257. [Google Scholar] [CrossRef]
  47. Naem, S.; Tavakoli, M.; Javanbakht, J.; Ali-Mohammadi, S.; Farshid, A.A.; Mohammad-Hassan, M.A. Macroscopic and microscopic examination of pulmonary Crenosoma striatum in hedgehog. J. Parasit. Dis. 2014, 38, 185–189. [Google Scholar] [CrossRef]
  48. Naem, S.; Pourreza, B.; Gorgani-Firouzjaei, T. The European hedgehog (Erinaceus europaeus), as a reservoir for helminth parasites in Iran. Vet. Res. Forum. 2015, 6, 149–153. [Google Scholar] [PubMed]
  49. Khodadadi, N.; Nabavi, R.; Sarani, A.; Saadati, D.; Ganjali, M.; Mihalca, A.D.; Otranto, D.; Sazmand, A. Identification of Anaplasma marginale in long-eared hedgehogs (Hemiechinus auritus) and their Rhipicephalus turanicus ticks in Iran. Ticks Tick. Borne. Dis. 2021, 12, 101641. [Google Scholar] [CrossRef] [PubMed]
  50. Cirak, V.Y.; Senlik, B.; Aydogdu, A.; Selver, M.; Akyol, V. Helminth parasites found in hedgehogs (Erinaceus concolor) from Turkey. Prev. Vet. Med. 2010, 97, 64–66. [Google Scholar] [CrossRef]
  51. Simone-Freilicher, E.A.; Hoefer, H.L. Hedgehog care and husbandry. Vet. Clin. N. Am. Exot. Anim. Pract. 2004, 7, 257–267. [Google Scholar] [CrossRef]
  52. Eslami, A.; Changizy, E.; Moghadam, M. Prevalence of helminth infections in the cape hare (Lepus capensis) in Iran. Vet. Res. Commun. 2000, 24, 455. [Google Scholar] [CrossRef]
  53. Eslami, A.; Nikbin, S.; Rahbari, S. Lugworm infection of wild sheep (Ovis ammon orientalis) and gazelle (Gazella subgutturosa) in Iran. J. Fac. Vet. Med. Univ. Tehran. 1980, 35, 11–16. (In Persian) [Google Scholar]
  54. Boev, S.N. Protostrongylidi. In Osnovy Nematodologii; Rijikov, K., Ed.; Izdatelstvo Nauka: Moskva, Russia, 1975; 264p. (In Russian) [Google Scholar]
  55. Lesage, C.; Jouet, D.; Patrelle, C.; Guitton, J.-S.; Decors, A.; Ferté, H. Protostrongylus pulmonalis (Frölich, 1802) and P. oryctolagi Baboš, 1955 (Nematoda: Protostrongylidae), parasites of the lungs of European hare (Lepus europaeus L.) in France: Morphological and molecular approaches. Parasitol. Res. 2014, 113, 2103–2111. [Google Scholar] [CrossRef] [PubMed]
  56. Aliabadian, M. A survey on ecto- and endoparasites of Lagomorphs in Iran. In Proceedings of the The Second International Congress of Vector-Borne Diseases and Climate Change and the Fourth National Congress of Medical Entomology of Iran, Mashhad, Iran, 13 December 2019. [Google Scholar]
  57. Sarvi, S.; Daryani, A.; Sharif, M.; Rahimi, M.T.; Azami, D.; Marhaba, Z.; Ahmadpour, E.; Mizani, A. Domestic dog as a human health hazard in north of Iran. J. Parasit. Dis. 2016, 40, 930–934. [Google Scholar] [CrossRef]
  58. Di Cesare, A.; Castagna, G.; Meloni, S.; Otranto, D.; Traversa, D. Mixed trichuroid infestation in a dog from Italy. Parasit. Vectors 2012, 5, 128. [Google Scholar] [CrossRef]
  59. Shariatzadeh, S.A.; Spotin, A.; Gholami, S.; Fallah, E.; Hazratian, T.; Mahami-Oskouei, M.; Montazeri, F.; Moslemzadeh, H.R.; Shahbazi, A. The first morphometric and phylogenetic perspective on molecular epidemiology of Echinococcus granulosus sensu lato in stray dogs in a hyperendemic Middle East focus, northwestern Iran. Parasit. Vectors. 2015, 8, 409. [Google Scholar] [CrossRef] [PubMed]
  60. Conboy, G. Helminth parasites of the canine and feline respiratory tract. Vet. Clin. North. Am. Small. Anim. 2009, 39, 1109–1126. [Google Scholar] [CrossRef]
  61. Beugnet, F.; Halos, L.; Guillot, J. Textbook of Clinical Parasitology in Dogs and Cats. Servet editorial-Grupo Asís Biomedia, SL: Zaragoza, Spain, 2018. [Google Scholar]
  62. Rassouli, M.; Ghaderi, J.; Goudarzi, A.; Sabouri, S. Aelurostrongylus abstrusus in a stray cat’s blood stream. Comp. Clin. Path. 2015, 24, 773–775. [Google Scholar] [CrossRef]
  63. 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]
  64. Abu-Madi, M.; Al-Ahbabi, D.; Al-Mashhadani, M.; Al-Ibrahim, R.; Pal, P.; Lewis, J. Patterns of parasitic infections in faecal samples from stray cat populations in Qatar. J. Helminthol. 2007, 81, 281–286. [Google Scholar] [CrossRef]
  65. Al-Tae, A.R.; Al-Rubaie, A.R. Checklists of parasites stray cats Felis catus of Iraq. Ibn al-Haitham J. Pure Appl. Sci. 2018, 2017, 143–151. [Google Scholar] [CrossRef]
  66. Burgu, A.; Sarimehmetoğlu, O. Aelurostrongylus abstrusus infection in two cats. Vet. Rec. 2004, 154, 602–604. [Google Scholar] [CrossRef] [PubMed]
  67. Brianti, E.; Gaglio, G.; Anile, S.; Arrabito, C.; Mazzamuto, M.V.; Scornavacca, D.; Ragni, B.; Mallia, E.; Randi, E.; Mattucci, F. Helminthic fauna of wildcats (Felis silvestris silvestris) in Southern Italy. Hystrix It. J. Mamm. 2012, 44. [Google Scholar]
  68. Salant, H.; Yasur-Landau, D.; Rojas, A.; Otranto, D.; Mazuz, M.; Baneth, G. Troglostrongylus brevior is the dominant lungworm infecting feral cats in Jerusalem. Parasitol. Res. 2020, 119, 3443–3450. [Google Scholar] [CrossRef]
  69. Falsone, L.; Brianti, E.; Gaglio, G.; Napoli, E.; Anile, S.; Mallia, E.; Giannelli, A.; Poglayen, G.; Giannetto, S.; Otranto, D. The European wildcats (Felis silvestris silvestris) as reservoir hosts of Troglostrongylus brevior (Strongylida: Crenosomatidae) lungworms. Vet. Parasitol. 2014, 205, 193–198. [Google Scholar] [CrossRef]
  70. Aftandelians, R.; Raafat, F.; Taffazoli, M.; Beaver, P.C. Pulmonary capillariasis in a child in Iran. Am. J. Trop. Med. Hyg. 1977, 26, 64–71. [Google Scholar] [CrossRef]
  71. Di Cesare, A.; Castagna, G.; Otranto, D.; Meloni, S.; Milillo, P.; Latrofa, M.S.; Paoletti, B.; Bartolini, R.; Traversa, D. Molecular detection of Capillaria aerophila, an agent of canine and feline pulmonary capillariosis. J. Clin. Microbiol. 2012, 50, 1958–1963. [Google Scholar] [CrossRef] [PubMed]
  72. Lalošević, D.; Stanojev-Jovanović, D.; Lalošević, V.; Pozio, E.; Klem, I. Pulmonary capillariasis miming bronchial carcinoma. Am. J. Trop. Med. Hyg 2008, 78, 14–16. [Google Scholar] [CrossRef] [PubMed]
Figure 1. Map of Iran showing the distribution of reports of non-ruminant terrestrial mammals and humans.
Figure 1. Map of Iran showing the distribution of reports of non-ruminant terrestrial mammals and humans.
Pathogens 12 00759 g001
Table 1. Lungworm Dictyocaulus arnfieldi in equids from Iran according to geographical area.
Table 1. Lungworm Dictyocaulus arnfieldi in equids from Iran according to geographical area.
Host% PrevalenceNumber of Examined HostGeographical RegionStudy AreaYear of StudyReferences
HorseCase report2Eastern provincesMashhad2008[9]
Horse1.4140Western provincesKermanshahNot stated[11]
Horse13.2356Northwestern provincesUrmia2014–2016[10]
Donkey31.866 Urmia2014–2016[10]
Mule24.337 Urmia2014–2016[10]
All of the studies used the Baermann technique, except one [11] that employed fecal flotation for the diagnosis.
Table 2. Nematodes affecting the respiratory tract of camels (Camelus dromedarius) in Iran according to geographic area and nematode species.
Table 2. Nematodes affecting the respiratory tract of camels (Camelus dromedarius) in Iran according to geographic area and nematode species.
Nematode Species% PrevalenceNumber of Examined HostGeographical RegionStudy AreaYear of StudyReferences
Dictyocaulus filaria3.330Northern provincesTehranNot stated[16]
Deraiophoronema evansi9.930 TehranNot stated[16]
Verminous pneumonia (Dictyocaulus viviparus)1.0100 Semnan2011[17]
Dictyocaulus filaria10.060Southern provincesKermanNot stated[18]
Deraiophoronema evansi17.540 ShirazNot stated[19]
Deraiophoronema evansi8.4309 Kerman2009–2010[20]
Deraiophoronema evansi27.0100 Fars and YazdNot stated[21]
Deraiophoronema evansi2.8144 Yazd, Najaf-Abad, and RafsanjanNot stated[22]
Deraiophoronema evansi34.5197Eastern provincesMashhad, Afghanistan, and Pakistan2003–2006[23]
Deraiophoronema evansi18.050 Mashhad2008–2009[24]
All these studies used post-mortem examinations of carcasses at an abattoir.
Table 3. Lungworms of wild boars (Sus scrofa) in Iran according to geographical area and nematode species.
Table 3. Lungworms of wild boars (Sus scrofa) in Iran according to geographical area and nematode species.
Nematode Species% PrevalenceNumber of Examined Host Geographical RegionStudy AreaYear of StudyReferences
Metastrongylus apriCase report1Northern provincesTalesh2013[32]
Metastrongylus apri41.612Western provincesLorestan2000–2001[33]
Metastrongylus pudendotectus16.612 Lorestan2000–2001[33]
Metastrongylus salmi8.312 Lorestan2000–2001[33]
Metastrongylus apri16.730Northwestern provincesEast Azarbaijan2015[34]
Metastrongylus sp.Case report2Southwestern provincesKhuzestanNot stated[35]
Metastrongylus sp.68.025 Bushehr2013[36]
Metastrongylus apri16.057National parks and protected regions of Iran Not stated[37]
Metastrongylus pudendotectus14.057 Not stated[37]
Metastrongylus salmi14.057 Not stated[37]
All the studies except one [34], which employed direct smears and fecal flotation for the diagnosis, studied the carcasses postmortem.
Table 4. Lungworms of hedgehogs in Iran according to geographical area and nematode species.
Table 4. Lungworms of hedgehogs in Iran according to geographical area and nematode species.
Nematode Species% PrevalenceHostNumber of Examined Host Geographical RegionStudy AreaYear of StudyReferences
Crenosoma striatum20.0Erinaceus concolor10Northern provincesBabol2011[43]
Crenosoma striatum37.5Erinaceus concolor8 Mazandaran2010–2011[44]
Crenosoma striatum4.3Hemiechinus auritus23Eastern provincesMashhad2010–2014[45]
Crenosoma striatum100Hemiechinus auritus6Southern provincesKermanNot stated[46]
Crenosoma striatum61.0Erinaceus concolor44Northwestern provincesUrmia2009–2011[48]
Crenosoma striatumNot statedNot stated10 Urmia2012[47]
Eucoleus aerophilus9.0Erinaceus concolor44 Urmia2009–2011[48]
All animals were studied postmortem.
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

Mohtasebi, S.; Sazmand, A.; Zafari, S.; Verocai, G.G.; Otranto, D. Lungworms of Non-Ruminant Terrestrial Mammals and Humans in Iran. Pathogens 2023, 12, 759. https://doi.org/10.3390/pathogens12060759

AMA Style

Mohtasebi S, Sazmand A, Zafari S, Verocai GG, Otranto D. Lungworms of Non-Ruminant Terrestrial Mammals and Humans in Iran. Pathogens. 2023; 12(6):759. https://doi.org/10.3390/pathogens12060759

Chicago/Turabian Style

Mohtasebi, Sina, Alireza Sazmand, Salman Zafari, Guilherme G. Verocai, and Domenico Otranto. 2023. "Lungworms of Non-Ruminant Terrestrial Mammals and Humans in Iran" Pathogens 12, no. 6: 759. https://doi.org/10.3390/pathogens12060759

APA Style

Mohtasebi, S., Sazmand, A., Zafari, S., Verocai, G. G., & Otranto, D. (2023). Lungworms of Non-Ruminant Terrestrial Mammals and Humans in Iran. Pathogens, 12(6), 759. https://doi.org/10.3390/pathogens12060759

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