Abstract
At the University Hospital Institute Méditerranée Infection (IHU, Marseille, France), for almost thirty years, veterinarians have been carrying out epidemiological investigations, together with doctors, on animals living near human cases of zoonoses, on the one hand, and on the other hand, transverse and longitudinal epidemiological surveillance studies on animals which are reservoirs, vectors or sentinels of potentially zoonotic infections,. This article presents the methods adopted and the results obtained from these studies. They have been the subject of 76 peer-reviewed publications relating to wild animals (37 publications) and/or domestic animals (48 publications). These studies were often carried out in the field with veterinarians from the French army's health service (39 publications). They were at the origin of the detection of some thirty zoonotic pathogens in the laboratories of the IHU (64 publications) and/or other French laboratories (18 publications). Our approach is an original embodiment of the “One Health” concept.
Keywords: Animal reservoir, Zoonoses, Epidemiosurveillance, One Health
Highlights
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At the University Hospital Institute Méditerranée Infection (Marseille, France), veterinarians have been carrying out epidemiological investigations on zoonotic pathogens in animals.
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The article presents the methods adopted and the results obtained which have been the subjects of 76 peer-reviewed publications relating to wild animals (37 papers) and/or domestic animals (48 papers).
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Our work is an original approach of the “One Health” concept.
1. Introduction
The most serious contemporary pandemics and epidemics with pandemic potential (HIV, influenza, SARS-2003, MERS-CoV, Covid-19) are due to RNA viruses that evolve from viruses naturally hosted by animals [1,2]. More than 60% of the infectious diseases known to humans have an animal reservoir. This is also the case for some 75% of emerging diseases and 80% of bioterrorism agents. It is clear that most human infectious diseases originate from animals [1,[3], [4], [5]]. In this context, it makes sense to have a veterinary component within the context of the University Hospital Institute (IHU for Institut Hospitalo-Universitaire) Méditerranée Infection (Marseille, France). It is a clear illustration of the relevance of the “One Health” concept. In this article, we shall explain how an operational epidemiological surveillance system for reservoir, vector and/or sentinel animals of human infections was developed from field to laboratory within the IHU. We shall then present an overview of all the studies carried out and published following this strategy.
2. Methodology
2.1. Field surveys
Several types of epidemiological surveillance surveys on infectious diseases in animals were carried out in a wide variety of contexts as a regular part of the IHU's research activities. The creation of a veterinary unit within a hospital establishment is a rare event and this multidisciplinary approach is one of the IHU's strengths. First, investigations were carried out on animals living in the environment of patients suspected of having zoonoses, at the request of physicians specialized in infectious diseases (Fig. 1). Domestic animals (dogs, cats, etc.) were the first to be sampled, soon followed by commensal animals (rats, birds, etc.) and others living in or near the environment of the patients. Surveys were thus performed out in localities where an outbreak of several grouped cases of zoonoses had been reported (e.g. Q fever). These field studies required material preparation to facilitate the representative sampling to be carried out according to the various opportunities and epidemiological contexts. If field samples are to be optimal, quantitatively and qualitatively, they must be collected in the right place, at the right time, on suitable species and matrices and using the most appropriate techniques. The epidemiological findings hit upon by the IHU using this method were inevitably serendipitous, but they are the results of more than forty years of field experience. The Veterinary Research Center (VRC), an annex of the IHU, is equipped to initiate or receive biological samples (blood, faeces, swabs, biopsies, etc.), endoparasites and ectoparasites of animal origin. For the ectoparasites, the VRC maintains close functional relations with the entomologists of the IHU insectarium. The VRC can also accommodate animals, domestic or wild, living or dead, suspected of zoonotic or unknown infectious diseases or likely to be asymptomatic carriers of pathogenic agents. Ante- or post-mortem diagnostic sampling can also be carried out on these animals there. The design of the VRC's facilities and the management of flows have been designed to carry out these activities in accordance with all the required biosafety rules, both within the IHU's premises and outside these premises. Another aspect of the veterinary epidemiosurveillance carried out at the IHU concerns cross-sectional and longitudinal studies carried out in targeted geographical areas at risk for certain zoonoses (e.g. African villages). Various samples (blood, rectal swabs) were taken from various domestic animals. These samples were then screened according to different screening techniques (serology, PCR, culture), in order to detect a pattern of infectious agents with zoonotic potential. The skills currently deployed within the IHU VRC in terms of epidemiological surveillance and field epidemiology are the fruit of many years of experience acquired in the context of epidemiological activities carried out on dogs and horses for the French Army and the National Gendarmerie. These latter sometimes acted as sentinels, making it possible to identify the animal or human disease agents circulating in certain ecosystems (e.g. Rift Valley fever, West Nile fever, dirofilariosis, leishmaniosis, trypanosomosis, etc.). Army veterinarians routinely drew the blood of military dogs, staying outside mainland France on missions, before their departure and on their return. These samples were fed into a sample bank, the use of which provided valuable information on exposure to certain pathogens in areas where the armed forces are deployed.
Fig. 1.
The variety of reservoir animals, sentinels or potential vectors in the entourage of a human person who is sick, suspected of and/or exposed to, zoonoses (Pictures: B. Davoust).
2.2. Ethical approval, biodiversity conservation, benefit-sharing obligations, and biosafety
All sampling of live animals (e.g. blood) is carried out in accordance with the international standards both for animal welfare [6] and for the preservation of protected species (CITES -Washington convention) [7], with European regulations [8] and the regulations of the country where the samples are collected. Where necessary, particularly with wild animals, chemical restraint techniques (teleanesthesia) are used, in accordance with the rules of good veterinary practice. This was the case for example, when for the first time in the history of research, sperm was collected from green monkeys by means of an electroejaculation technique using a rectal probe specially designed for our study. In addition, the IHU VRC's collaborative network with wildlife veterinarians provided access to samples (blood, swabs) collected from wild animals anaesthetised for various reasons: in zoological parks (for example, in the case of injuries) or during transport (in the case of bears from Slovenia introduced into the Pyrenees). The majority of animal samples collected in the course of the studies conducted by the IHU were collected in a non-invasive manner (e.g. faeces). Animals that had died recently, either in accidental circumstances (animals fatally injured on the road found during the mission) or as part of official operations carried out within the study area (hunting, slaughterhouse products, markets, campaigns to destroy pests such as rodents, etc.) were also frequently collected. Older remains (bones, teeth, coprolites, skins) could sometimes be collected in the wild (mass graves) or even in museums. Similarly, the concern to preserve biodiversity is increasingly taken into account, particularly since the adoption of the Convention on Biodiversity by the United Nations at a world conference in Nagoya (Japan) in 2010 [9]. France, as most of the countries of origin from which the animal samples were collected for studies carried out at the IHU, has ratified the Nagoya Protocol on access to genetic resources and fair and equitable sharing of the benefits arising out of their utilization. We are committed, on the one hand, never to participate in the destruction of endangered species of animals and, on the other hand, not to appropriate illegitimately any samples of animal origin (biopiracy). Whenever we conduct a study in a foreign country, we collaborate with the local scientists. These are partnerships that are rewarding for all parties involved. All animal samples collected within the framework of IHU activities are systematically subject to prior authorization from the competent national authorities (often the Ministry of the Environment), as well as from local authorities (e.g. village chiefs) and the owners of the animals collected, in the interests of transparency and good mutual relations. With regard to biosafety, we apply protocols to ensure that infectious diseases are not introduced from one country to another. Before shipment, official authorisation is obtained for the import of samples of animal origin for diagnosis and scientific research from the Bouches-du-Rhône (Marseille) prefecture in agreement with European regulations [10]. The samples are then transported to the IHU laboratories in accordance with current air transport standards [11]. Field staff working with the animals, as well as all those working on the samples, have received training in biosecurity. Several vaccinations (against rabies, leptospirosis …) and chemoprevention may be recommended.
2.3. Collections
For more than twenty years, more than a hundred epidemiological surveys have been conducted in 25 countries on five continents, mainly in Africa. In total, more than 35,000 biological samples of animal origin, in addition to ectoparasite specimens, have been collected. An aliquot of each sample was preserved after analysis using various techniques (mainly freezing, alcohol, desiccation, etc.), thus constituting an important sample bank. Thousands of samples of faeces, sera, blood, internal organs (spleen, liver, kidneys, lungs, intestines, etc.), muscles, skin, teeth, etc. are also available in this bank. Samples from the domestic dog (Canis lupus) are the most represented. The bank also has nearly 17,000 blood samples from French military working dogs, collected over the last thirty years, particularly in the context of missions outside mainland France (Africa, Afghanistan, French Guiana, the Middle East, etc.). The other half of the samples were taken mainly from mammals of some 120 different species, both domestic (N = 30) and wild.
3. Investigations conducted on wild animals
3.1. Non-human primates
Non-human primates (NHPs), particularly the great apes (gorillas, chimpanzees, orangutans), are the animals that are phylogenetically closest to humans, with whom they share the greatest number of diseases. NHPs are wild animals that may have occasional contact with humans, for example in the course poaching activities, where pathogens may be transmitted to humans and can cause potential emerging diseases [12]. A synthesis of studies conducted at the IHU, using mainly faeces from great apes, has been published recently [13]. Thus, human adenovirus genotypes were discovered in gorillas from Congo-Brazzaville and, conversely, simian genotypes have been found in human beings sharing the same living area as the gorillas [14]. Again, a recombinant coxsackie/poliovirus has been found in wild gorillas and in the guardians of the reserve. One gorilla in fact presented sequelae of a central nervous system infection (muscular atrophies and flaccid paralysis) possibly due to this virus [15]. Work continues on the venereal infection of NHPs by the yaws agent (Treponema pallidum subsps. pertenue) [16,17] as well as on the detection of antibiotic-resistant bacteria in the faeces of these primates. NHPs share with humans many protozoan infections [18]. Table 1 provides additional information on the studies published within the framework of IHU activities [[19], [20], [21], [22], [23]]. They concern eleven NHPs species from Africa and French Guiana.
Table 1.
Zoonotic diseases the agents of which have been detected in reservoir (and/or sentinel) animals at, or in collaboration with, the IHU.
| Diseases | Pathogens and detection techniques | Animals | Countries | References |
|---|---|---|---|---|
| West Nile fever | West Nile virus (S) | Dog | France (Corsica), Hungary, Djibouti, Chad, RD Congo, Cote d'Ivoire, Senegal | [51,52] |
| Horse | France, Algeria, Senegal | [52,[73], [74], [75], [76]] | ||
| Goats | Senegal | [75] | ||
| Donkey | Senegal | [75] | ||
| Hepatitis E | Hepatitis E virus (S, PCR) | Pig | France, DR Congo | [89,90] |
| Hepatitis E virus (PCR) | Wild boar | France | [41] | |
| Rift Valley fever | Rift valley fever virus (S) | Goats | Chad | [81] |
| Sheep | ||||
| Cattle | ||||
| Crimean-Congo hemorrhagic fever | Crimean-Congo hemorrhagic fever virus (S) | Horse | Senegal | [77] |
| Cattle | ||||
| Sheep | ||||
| Goats | ||||
| Donkey | ||||
| Dog | ||||
| Toscana virus meningitis | Toscana virus (S) | Dog | France (Corsica), Algeria | [53,54] |
| Anaplasmosis | Anaplasma phagocytophilum (PCR) | Cattle | France, Algeria | [82,83] |
| Bartonellosis | Bartonella spp. (PCR) | Bat | French Guiana | [25] |
| Bartonella rattimassiliensis (PCR, C) | Brown rat | France | [35,36] | |
| Bartonella phoceensis (PCR, C) | Brown rat | France | [35,36] | |
| Bartonella clarridgeiae (PCR, M, C) | Cat, Dog | France, Gabon | [69–71] | |
| Bartonella henselae (PCR, M, C) | Cat, Dog | France, Gabon | [69–71] | |
| Bartonella tribocorum (PCR) Bartonella chomelii (PCR, C) | Various rodents Cattle | Senegal France (New Caledonia) | [30,87] | |
| Q fever | Coxiella burnetii (S, PCR) | Three-toed sloth | French Guiana | [47,48] |
| Coxiella burnetii (S) | Dog | France | [55] | |
| Lyme borreliosis | Borrelia burgdorferi (S) | Horse | France | [78] |
| West African tick-borne relapsing fever | Borrelia crocidurae (PCR) | Various rodents | Senegal | [30] |
| Leptospirosis | Leptospira interrogans serovar icterohaemorrhagiae (S, PCR) | Brown rat, Mice | France | [[36], [37], [38]] |
| Several serovars of pathogenic leptospires (S) | Rusa deer | France (New Caledonia) | 80 | |
| Cattle | France (New Caledonia) | [80] | ||
| Dog | France (New Caledonia), French Guiana, Gabon, Cote d'Ivoire, Senegal, Sudan | [[56], [57], [58],80] | ||
| Horse | France (New Caledonia) | [80] | ||
| Yaws | Treponema pallidum subsp. pertenue (S, PCR) | Green monkey, Baboon | Senegal | [16,17] |
| Hemolytic fever of megabats | Mycoplasma haemohominis | Bat | France (New Caledonia) | [28] |
| Buruli ulcer | Mycobacterium ulcerans (PCR, C) | Wild grasscutter | Cote d'Ivoire | [33] |
| Plague | Yersinia pestis (S) | Dog | DR Congo | [29] |
| Visceral leishmaniosis | Leishmania infantum (S, PCR) | Dog | France, French Guiana, Algeria, Cote d'Ivoire | [26,46,61,62] |
| Leishmania infantum (PCR) | Fox | France | [44,46] | |
| Horse | Algeria | [61] | ||
| Bat | French Guiana | [26] | ||
| Leishmania infantum (S, PCR) | Red howler monkey | French Guiana | [19] | |
| Cutaneous leishmaniosis | Leishmania guyanensis (PCR) | Red howler monkey | French Guiana | [19] |
| Toxoplasmosis | Toxoplasma gondii (S) | Wild boar | France | [42] |
| Pig | France (New Caledonia), Cote d'Ivoire | [60,91] | ||
| Dog | France (New Caledonia), Senegal, France | [59,60,91] | ||
| Horse | France (New Caledonia), France | [60] | ||
| Cattle | France (New Caledonia), France | [60] | ||
| Cat | France (New Caledonia) | [60] | ||
| Rusa deer | France (New Caledonia) | [60] | ||
| Sheep | Senegal | [59] | ||
| Goats | Senegal | [59] | ||
| Donkey | Senegal | [59] | ||
| Chagas disease | Trypanosoma cruzi (S, PCR) | Dog | French Guiana | [63] |
| Hepatic capillariosis | Calodium hepaticum (AP) | Brown rat, other rodents | France | [39] |
| Black rat | RD Congo | [40] | ||
| Gambian pouched rat | Senegal | [40] | ||
| Dirofilariosis | Dirofilaria immitis (DO, S, PCR) | Dog | France, French Guiana, France (New Caledonia), Algeria, Cote d'Ivoire, Gabon, Sudan | [[64], [65], [66], [67]] |
| Dirofilaria repens (PCR) | Dog | France | [65] | |
| Trichinellosis | Trichinella britovi (M, PCR) | Dog | Kosovo | [68] |
| Fox | France | [45] |
Abbrevations = DO: direct observation; S: serology; M: microscopy; AP: anatomic pathology; PCR: polymerase chain reaction; C: culture.
3.2. Bats
Bats are responsible for the transmission of many zoonoses, including the SARS-CoV-2 infection [2]. The ecology of numerous chiropteran species, in particular their extreme promiscuity within colonies often of several thousand bats, represents a major risk of transmission of pathogens to humans, either directly or via intermediate hosts [24]. These bat reservoirs are very effective because they are highly resistant to infection. A bat capture-release campaign was carried out as part of the IHU studies in French Guiana in search of the wild reservoir(s) of the causative agent of human Q fever (Coxiella burnetii). Blood samples and swabs were taken from 283 individuals from 21 species. Coxiella burnetii was not detected, but it was possible to culture two new species of Bartonella from the blood, to detect Leishmania infantum by PCR and to identify rickettsia in the soft ticks parasiting these bats [[25], [26], [27]]. Recently, in cooperation with the veterinary services of New Caledonia, the bacterial “Candidatus Mycoplasma haemohominis” species was recently detected in fruit bats of the Pteropus genus. This bacterium is responsible for haemolytic fever in humans, an emerging zoonosis [28].
3.3. Rodents
Rodents represent nearly 40% of mammalian species. They are reservoirs and vectors of many zoonoses. They have been studied as part of the IHU's work in the Democratic Republic of Congo (DRC) as a reservoir for the plague [29], in Senegal, Mali and Afghanistan as reservoirs of Bartonella [[30], [31], [32]]. In the Côte d'Ivoire, it has been shown that the cane rat (Thryonomys swinderianus) can carry mycobacteria, precisely the Mycobacterium ulcerans which is responsible in humans for Buruli ulcer and zoonotic leptospira [33,34]. Numerous bartonellae and leptospirae have been found in rats from the city of Marseille [[35], [36], [37], [38]]. Finally, hepatic capillariasis due to Calodium hepaticum has been identified in rodents from France Senegal and DRC [39,40].
3.4. Other mammalian species
A partnership concluded with two military hunting companies gave us access to wild boar (Sus scrofa) and red foxes (Vulpes vulpes) from the South-East of France. The hepatitis E virus genotype 3f in 2.5% (7/285) was thus detected by the PCR method in wild boar carcasses [41]. The seroprevalence of toxoplasmosis in these animals was 17% [42]. No tuberculous mycobacteria were detected in the faeces of these animals, but a new species of Nocardia was isolated [43]. Three zoonotic agents were detected in foxes: Coxiella burnetii, Trichinella britovi and Leishmania infantum [[44], [45], [46]]. For these last two agents, the fox acts as a reservoir. In addition, the haemoparasite Hepatozooncanis was detected in 92% of the 93 foxes tested [44]. This Apicomplexa is transmitted by ticks to canids. In French Guiana, our studies have shown that the three-toed sloth (Bradypus tridactylus) was a potential reservoir for Coxiella burnetii, the bacterium responsible for a serious human infection, Q fever, in this geographical area [47,48].
4. Screenings in domestic animals
4.1. Dogs
Dogs play a direct epidemiological role as a reservoir of pathogens [49]. They can also often act as asymptomatic sentinels for emerging infections [50]. The work carried out in the IHU on this species has focused on vector-borne diseases. This is the case for arboviruses, in particular the West Nile virus (WNV) infection and phlebovirus infections. Our studies have shown that the canine seroprevalence of the WNV is highly variable in different parts of Africa and Europe [51,52]. Military dogs, on their return from Africa, are good witnesses to the circulation of the virus in the ecosystems where they had been staying [49]. As for the Toscana virus, we have been able to identify seropositive dogs in Corsica and Algeria [53,54]. Canine seroprevalence surveys conducted in Africa, Corsica, French Guiana and New Caledonia have revealed the existence of risk areas for zoonoses, such as the plague [30], Q fever [54], leptospirosis [[55], [56], [57]] and toxoplasmosis [58,59]. Studies on canine leishmaniasis have been carried out in South-East France, but also in Algeria and, recently, the parasite Leishmania infantum has been detected (by positive PCR and sequencing) in autochthonous carrier dogs in French Guiana and Côte d'Ivoire [26,46,61,62]. In addition, for the first time, our work identified cases of asymptomatic infection by Trypanosoma cruzi, in dogs from French Guiana. This infection is the causal agent of Chagas disease in humans (screening of the parasite carried out by serology and PCR) [63]. Numerous studies have also been conducted on canine filariasis due to Dirofilaria immitis and D. repens [[64], [65], [66], [67]]. These are zoonotic parasitoses the range of which is now on the increase in Europe. Finally, the presence of Trichinella britovi has been detected in the muscles of stray dogs in Kosovo and these represent sentinels, a potential risk for human infestation with this parasite [68].
4.2. Cats
IHU research on stray cat populations has led to the cultivation of two bacteria, Bartonella henselae and B. clarridgeiae [69,70]. In an original way, our work has contributed to the demonstration of the persistence of Bartonellla spp. in the pulp of teeth extracted from the skeletons of cats [71]. During an investigation on animals present in the home of two patients suffering from spotted fever due to Rickettsia sibiricamongolotimonae, it was shown that the ticks (Rhipicephalus pusillus) of the patients' cat were the reservoir and vectors of this rickettsiosis [72].
4.3. Horses
Horses and donkeys are sentinels of WNV circulating in a given ecosystem. Our work confirmed this in Corsica, in various African countries, in particular in Djibouti, North-West Senegal and Algeria [52,[73], [74], [75], [76]]. Our work has made it possible to show, for the first time in Senegal, that horses were sentinels of the circulation of the Crimean-Congo haemorrhagic fever virus [77]. A seroprevalence survey of the Lyme disease conducted in France and Africa reported the absence of this disease south of the Sahara [78]. In France, our work contributed to the confirmatory diagnosis of the first described case of an equine infection with Anaplasma phagocytophilum, an agent of a rare zoonosis transmitted by ticks [79]. Finally, in New Caledonia, where leptospirosis is a public health problem, seroprevalence of this disease agent has been demonstrated, thus confirming the role of horses as sentinels of the infection [80]. In addition, leishmaniosis DNA was detected by PCR in the blood of a horse in Algeria [61].
4.4. Livestock
In cattle in Chad, seroprevalence surveys made it possible for us to highlight for the first time the circulation of an arbovirosis, namely Rift Valley Fever which is potentially serious in humans, [81]. In France and Algeria, clinical bovine infections due to A. phagocytophilum were diagnosed [82,83]. We have also shown the frequency of cattle infections with bartonelles in Africa [[84], [85], [86]]. In New Caledonia, six strains of bartonelles isolated from cattle were close to the reference strain of Bartonella chomelii and, in all probability, were imported from France along with cattle of the Limousin race [87]. In south-eastern France, an investigation was carried out demonstrating how ewes infected with Coxiella burnetii, the agent of Q fever, transmitted the infection to the owner of these animals [88]. Our studies have also highlighted the role of pigs as a reservoir for the hepatitis E virus [89,90] and toxoplasms [91]. Finally, in poultry, we have studied how the carriage of extended-spectrum beta-lactamases in faeces, are responsible for antibiotic resistance in human medicine [92].
5. Conclusion
The work carried out by the IHU on zoonotic agents and animal reservoirs has led to scientific discoveries and advances in epidemiological knowledge in this field. These results illustrate the need to continue this cross-cutting and integrated research approach (One Health) within the framework of the activities carried out within the IHU and, more generally, in the scientific programmes on zoonoses. Improving the identification of the agents of zoonoses and the assessment of the risk factors related to these agents will make it possible to implement better responses for the benefit of human and animal health and to contribute to a more conservation of biodiversity [[93], [94], [95]].
Authors' contributions
BD conceived the original paper and wrote the initial draft. SWG, CD, DR and OM extensively revised and approved the final version of the manuscript.
Ethics approval and consent to participate
Not applicable.
Funding
This study was supported by the Health Service of the French Army and the Institut Hospitalo-Universitaire (IHU) Méditerranée Infection, the National Research Agency under the program “Investissements d'avenir”, reference ANR-10-IAHU-03, the Region Provence-Alpes-Côte d'Azur and European funding FEDER PRIMI.
Declaration of Competing Interest
There are no competing interests.
References
- 1.Jones K.E., Patel N.G., Levy M.A., Storeygard A., Balk D., Gittleman J.L., Daszak P. Global trends in emerging infectious diseases. Nature. 2008;451:990–993. doi: 10.1038/nature06536. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 2.Zhou P., Lou Yang X., Wang X.G., Hu B., Zhang L., Zhang W., Si H.R., Zhu Y., Li B., Huang C.L., Chen H.D., Chen J., Luo Y., Guo H., Di Jiang R., Liu M.Q., Chen Y., Shen X.R., Wang X., Zheng X.S., Zhao K., Chen Q.J., Deng F., Liu L.L., Yan B., Zhan F.X., Wang Y.Y., Xiao G.F., Shi Z.L. A pneumonia outbreak associated with a new coronavirus of probable bat origin. Nature. 2020;579:270–273. doi: 10.1038/s41586-020-2012-7. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 3.Taylor L.H., Latham S.M., Woolhouse M.E.J. Risk factors for human disease emergence. Philos. Trans. R. Soc. B Biol. Sci. 2001;356:983–989. doi: 10.1098/rstb.2001.0888. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 4.Cunningham A.A., Daszak P., Wood J.L.N. One health, emerging infectious diseases and wildlife: Two decades of progress? Philos. Trans. R. Soc. B Biol. Sci. 2017;372 doi: 10.1098/rstb.2016.0167. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 5.World organisation for animal health (OIE) Biological Threat Reduction Strategy. Strenghtening Global Biological Security. 2015. https://www.oie.int/fileadmin/Home/eng/Our_scientific_expertise/docs/pdf/EN_FINAL_Biothreat_Reduction_Strategy_OCT2015.pdf
- 6.World Organisation for Animal Health (OIE) Terrestrial Animal Health Code. 2019. https://www.oie.int/en/standard-setting/terrestrial-code/access-online/
- 7.Convention on International Trade in Endangered Species of Wild Fauna and Flora, also known as the Washington Convention. 1975. https://www.cites.org/ [DOI] [PubMed]
- 8.European Commission European Convention for the Protection of Vertebrate Animals Used for Experimental and Other Scientific Purposes. 1986. https://www.coe.int/fr/web/conventions/full-list/-/conventions/rms/090000168007a67b
- 9.United Nations Convention on Biological Diversity, Nagoya Protocol on Access and Benefit-Sharing. 2014. https://www.cbd.int/abs/doc/protocol/nagoya-protocol-en.pdf
- 10.Journal officiel de la République Française . 2013. Avis aux importateurs relatif aux importations d’échantillons de recherche et de diagnostic d’origine animale en provenance de pays tiers à l’Union européenne. n°0036 du 12 février 2013, page 2443, texte n°76. NOR: AGRG1303516V, (2013) [Google Scholar]
- 11.World health organisation Guidance on Regulations for the Transport of Infectious Substances the Transport of Infectious Substances. 2019. http://apps.who.int/iris/bitstream/10665/149288/1/WHO_HSE_GCR_2015.2_eng.pdf?ua=1&ua=1
- 12.Devaux C.A., Mediannikov O., Medkour H., Raoult D. Infectious disease risk across the growing human-non human primate interface: a review of the evidence. Front. Public Health. 2019;7:1–22. doi: 10.3389/fpubh.2019.00305. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 13.Davoust B., Levasseur A., Mediannikov O. Studies of nonhuman primates: key sources of data on zoonoses and microbiota. New Microbes New Infect. 2018;26:S104–S108. doi: 10.1016/j.nmni.2018.08.014. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 14.Medkour H., Amona I., Akiana J., Davoust B., Bitam I., Levasseur A., Tall M.L., Diatta G., Sokhna C., Hernandez-Aguilar R.A., Barciela A., Gorsane S., La Scola B., Raoult D., Fenollar F., Mediannikov O. Adenovirus infections in African humans and wild non-human primates: great diversity and cross-species transmission. Viruses. 2020;12(6):657. doi: 10.3390/v12060657. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 15.Amona I., Medkour H., Akiana J., Davoust B., Tall M.L., Grimaldier C., Gazin C., Zandotti C., Levasseur A., La Scola B., Raoult D., Fenollar F., Banga-Mboko H., Mediannikov O. Isolation and molecular characterization of Enteroviruses from great apes and humans in the Republic of Congo: recombination within Enterovirus C serotypes. Microorganisms. 2020;8(11):1779. doi: 10.20944/preprints202009.0035.v1. 2020090035. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 16.Knauf S., Gogarten J.F., Schuenemann V.J., De Nys H.M., Düx A., Strouhal M., Mikalová L., Bos K.I., Armstrong R., Batamuzi E.K., Chuma I.S., Davoust B., Diatta G., Fyumagwa R.D., Kazwala R.R., Keyyu J.D., Lejora I.A.V., Levasseur A., Liu H., Mayhew M.A., Mediannikov O., Raoult D., Wittig R.M., Roos C., Leendertz F.H., Šmajs D., Nieselt K., Krause J., Calvignac-Spencer S. Nonhuman primates across sub-Saharan Africa are infected with the yaws bacterium Treponema pallidum subsp. pertenue. Emerg. Microbes Infect. 2018;7 doi: 10.1038/s41426-018-0156-4. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 17.Mediannikov O., Fenollar F., Davoust B., Amanzougaghene N., Lepidi H., Arzouni J.P., Diatta G., Sokhna C., Delerce J., Levasseur A., Raoult D. Epidemic of venereal treponematosis in wild monkeys: a paradigm for syphilis origin. New Microbes New Infect. 2020;35:100670. doi: 10.1016/j.nmni.2020.100670. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 18.Medkour H., Amona I., Laidoudi Y., Davoust B., Bitam I., Levasseur A., Akiana J., Diatta G., Pacheco L., Gorsane S., Sokhna C., Hernandez-Aguilar R.A., Barciela A., Fenollar F., Raoult D., Mediannikov O. Parasitic infections in African humans and non-human primates. Pathogens. 2020;9:1–20. doi: 10.3390/pathogens9070561. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 19.Laidoudi Y., Medkour H., Latrofa M.S., Davoust B., Sokhna C., Barciela A., Hernandez-Aguilar R.A., Raoult D., Otranto D., Mediannikov O. Zoonotic Abbreviata caucasica in wild chimpanzees (Pan troglodytes verus) from Senegal. Pathogens. 2020;9(7):517. doi: 10.3390/pathogens9070517. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 20.Medkour H., Davoust B., Levasseur A., Mediannikov O. Molecular evidence of Leishmania infantum and Leishmania guyanensis in red howler monkey (Alouatta seniculus) from French Guiana. Vector-Borne Zoonotic Dis. 2019;19(12):896–900. doi: 10.1089/vbz.2019.2459. [DOI] [PubMed] [Google Scholar]
- 21.Duraisamy R., Akiana J., Davoust B., Mediannikov O., Michelle C., Robert C., Parra H.J., Raoult D., Biagini P., Desnues C. Detection of novel RNA viruses from free-living gorillas, Republic of the Congo: genetic diversity of picobirnaviruses. Virus Genes. 2018;54:256–271. doi: 10.1007/s11262-018-1543-6. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 22.Temmam S., Davoust B., Chaber A.L., Lignereux Y., Michelle C., Monteil-Bouchard S., Raoult D., Desnues C. Screening for viral pathogens in African simian bushmeat seized at a French airport. Transbound. Emerg. Dis. 2017;64:1159–1167. doi: 10.1111/tbed.12481. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 23.Fenollar F., Trani M., Davoust B., Salle B., Birg M.L., Rolain J.M., Raoult D. Prevalence of asymptomatic Tropheryma whipplei carriage among humans and non-human primates. J. Infect. Dis. 2008;197:880–887. doi: 10.1086/528693. [DOI] [PubMed] [Google Scholar]
- 24.Hayman D.T.S., Bowen R.A., Cryan P.M., Mccracken G.F., O’Shea T.J., Peel A.J., Gilbert A., Webb C.T., Wood J.L.N. Ecology of zoonotic infectious diseases in bats: current knowledge and future directions. Zoonoses Public Health. 2013;60:2–21. doi: 10.1111/zph.12000. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 25.Davoust B., Marié J.L., Dahmani M., Berenger J.M., Bompar J.M., Blanchet D., Cheuret M., Raoult D., Mediannikov O. Evidence of Bartonella spp. in blood and ticks (Ornithodoros hasei) of bats, in French Guiana. Vector Borne Zoonotic Dis. 2016;16(8):516–519. doi: 10.1089/vbz.2015.1918. [DOI] [PubMed] [Google Scholar]
- 26.Medkour H., Davoust B., Dulieu F., Maurizi L., Lamour T., Lou Marié J., Mediannikov O. Potential animal reservoirs (dogs and bats) of human visceral leishmaniasis due to Leishmania infantum in French Guiana. PLoS Negl. Trop. Dis. 2019;13:1–15. doi: 10.1371/journal.pntd.0007456. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 27.Tahir D., Socolovschi C., Marié J.L., Ganay G., Berenger J.M., Bompar J.M., Blanchet D., Cheuret M., Mediannikov O., Raoult D., Davoust B., Parola P. New Rickettsia species in soft ticks Ornithodoros hasei collected from bats in French Guiana. Ticks Tick. Borne. Dis. 2016;7:1089–1096. doi: 10.1016/j.ttbdis.2016.09.004. [DOI] [PubMed] [Google Scholar]
- 28.Descloux E., Mediannikov O., Gourinat A.C., Colot J., Chauvet M., Mermoud I., Desoutter D., Cazorla C., Klement-Frutos E., Antonini L., Levasseur A., Bossi V., Davoust B., Merlet A., Goujart M.A., Oedin M., Brescia F., Laumond S., Fournier P.E., Raoult D. Flying fox haemolytic fever, description of a new zoonosis caused by "Candidatus Mycoplasma haemohominis". Clin. Infect. Dis. 2020 doi: 10.1093/cid/ciaa1648. [DOI] [PubMed] [Google Scholar]
- 29.Davoust B., Diatta G., Shako J.C., Rajerison M., Abedi A.A., Karhemere S., Piarroux R., Raoult D. Seroprevalence of Yersinia pestis in dogs and small rodents in one hyperendemic plague focus of Democratic Republic of Congo. Afr. J. Microbiol. Res. 2013;7:1622–1624. doi: 10.5897/ajmr12.1689. [DOI] [Google Scholar]
- 30.Dahmana H., Granjon L., Diagne C., Davoust B., Fenollar F., Mediannikov O. Rodents as hosts of pathogens and related zoonotic disease risk. Pathogens. 2020;9(3):202. doi: 10.3390/pathogens9030202. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 31.Diarra A.K., Kone A.K., Niare D.S., Laroche M., Diatta G., Atteynine S.A., Coulibaly M., Sangare A.K., Kouriba B., Djimde A., Dabo A., Sagara I., Davoust B., Ranque S., Thera M.A., Raoult D., Doumbo O.K., Parola P. Molecular detection of microorganisms associated with small mammals and their ectoparasites in Mali. Am. J. Trop. Med. Hyg. 2020 doi: 10.4269/ajtmh.19-0727. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 32.Marié J.L., Fournier P.E., Rolain J.M., Briolant S., Davoust B., Raoult D. Molecular detection of Bartonella quintana, B. elizabethae, B. koehlerae, B. doshiae, B. taylorii, and Rickettsia felis in rodent fleas collected in Kabul, Afghanistan. Am. J. Trop. Med. Hyg. 2006;74:436–439. doi: 10.4269/ajtmh.2006.74.436. [DOI] [PubMed] [Google Scholar]
- 33.Hammoudi N., Dizoé A.S., Regoui S., Davoust B., Drancourt M., Bouam A. Disseminated Mycobacterium ulcerans infection in wild grasscutters (Thryonomys swinderianus), Côte d’Ivoire. Am. J. Trop. Med. Hyg. 2019;101:491–493. doi: 10.4269/ajtmh.19-0137. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 34.Hammoudi N., Davoust B., Dizoé S., Le Guyader M., Drancourt M., Bouam A., Kodjo A. 2020. Molecular Detection of Pathogenic Leptospira in Grasscutters (Thryonomys swinderianus) from Côte d’Ivoire, Vector-Borne Zoonotic Dis. [DOI] [PubMed] [Google Scholar]
- 35.Gundi V.A.K.B., Davoust B., Khamis A., Raoult D., La Scola B. Isolation of Bartonella rattimassiliensis sp. nov. and Bartonella phoceensis sp. nov. from European Rattus norvegicus. J. Clin. Microbiol. 2004;42:3816–3818. doi: 10.1128/JCM.42.8.3816. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 36.Levieuge A., Aboubaker M.H., Terrier O., Drancourt M., Davoust B. Real-time PCR detection of Leptospira sp. in rodents from Toulon harbour (France) Rev. Med. Vet. (Toulouse) 2010;161:264–266. [Google Scholar]
- 37.Dupouey J., Faucher B., Edouard S., Richet H., de Broucker C.A., Marié J.L., Kodjo A., Davoust B. Epidemiological investigation of a human leptospirosis case reported in a suburban area near Marseille. New Microbes New Infect. 2014;2:82–83. doi: 10.1002/nmi2.45. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 38.Sanchez Fernandez P., Kodjo A., Medkour H., Laidoudi Y., Dubourg G., Eldin C., Parola P., Davoust B., Lagier J.C. Autochthonous human and animal leptospirosis, Marseille, France. IDCases. 2020;21 doi: 10.1016/j.idcr.2020.e00899. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 39.Scandola P., de Biasi C., Davoust B., Marié J.L. Prevalence of Capillaria hepatica in non-commensal rodents from a forest area near Dijon, France. Parasitol. Res. 2013;112:2741–2744. doi: 10.1007/s00436-013-3369-4. [DOI] [PubMed] [Google Scholar]
- 40.Davoust B., de Biasi C., Demoncheaux J.P., Diatta G., Pasqualini C., Piarroux R. Capillariose hépatique (Calodium hepaticum) chez des rongeurs en Ituri (République démocratique du Congo) et à Dakar (Sénégal) Bull. La Soc. Pathol. Exot. 2014;107:7–9. doi: 10.1007/s13149-014-0326-5. [DOI] [PubMed] [Google Scholar]
- 41.Kaba M., Davoust B., Marié J.L., Colson P. Detection of hepatitis E virus in wild boar (Sus scrofa) livers. Vet. J. 2010;186:259–261. doi: 10.1016/j.tvjl.2009.08.008. [DOI] [PubMed] [Google Scholar]
- 42.Roqueplo C., Blaga R., Marié J.L., Vallée I., Davoust B. Seroprevalence of Toxoplasma gondii in hunted wild boars (Sus scrofa) from southeastern France. Folia Parasitol. 2017;64:19–21. doi: 10.14411/fp.2017.003. [DOI] [PubMed] [Google Scholar]
- 43.Fellag M., Levasseur A., Delerce J., Bittar F., Marié J.L., Davoust B., Drancourt M. Draft genome sequence of “Nocardia suismassiliense” strain S-137 (CSUR P4007) Genome Announc. 2018;6(16):e00212–e00218. doi: 10.1128/genomeA.00212-18. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 44.Medkour H., Laidoudi Y., Marié J.L., Fenollar F., Davoust B., Mediannikov O. Molecular investigation of vector-borne pathogens in red foxes (Vulpes vulpes) from Southern France. J. Wildl. Dis. 2020;56 doi: 10.7589/2019-09-234. [DOI] [PubMed] [Google Scholar]
- 45.Aoun O., Lacour S.A., Levieuge A., Marié J.L., Vallée I., Davoust B. Screening for Trichinella britovi infection in red fox (Vulpes vulpes) and wild boar (Sus scrofa) in southeastern France. J. Wildl. Dis. 2012;48(1):223–225. doi: 10.7589/0090-3558-48.1.223. [DOI] [PubMed] [Google Scholar]
- 46.Aoun O., Mary C., Roqueplo C., Marié J.L., Terrier O., Levieuge A., Davoust B. Canine leishmaniasis in south-east of France: screening of Leishmania infantum antibodies (western blotting, ELISA) and parasitaemia levels by PCR quantification. Vet. Parasitol. 2009;166:27–31. doi: 10.1016/j.vetpar.2009.08.006. [DOI] [PubMed] [Google Scholar]
- 47.Davoust B., Marié J.L., Pommier de Santi V., Berenger J.M., Edouard S., Raoult D. Three-toed sloth as putative reservoir of Coxiella burnetii, Cayenne, French Guiana. Emerg. Infect. Dis. 2014;20:1760–1761. doi: 10.3201/eid2010.140694. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 48.Pommier de Santi V., Briolant S., Mahamat A., Ilcinkas C., Blanchet D., de Thoisy B., Reynaud Y., Hyvert G., Marié J.L., Edouard S., Davoust B., Raoult D. Q fever epidemic in Cayenne, French Guiana, epidemiologically linked to three-toed sloth. Comp. Immunol. Microbiol. Infect. Dis. 2018;56:34–38. doi: 10.1016/j.cimid.2017.12.004. [DOI] [PubMed] [Google Scholar]
- 49.Ellwanger J.H., Chies J.A.B. The triad “dogs, conservation and zoonotic diseases” - an old and still neglected problem in Brazil. Perspect. Ecol. Conserv. 2019;17(3):157–161. doi: 10.1016/j.pecon.2019.06.003. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 50.Bowser N.H., Anderson N.E. Dogs (Canis familiaris) as sentinels for human infectious disease and application to Canadian populations: A systematic review. Vet. Sci. 2018;5 doi: 10.3390/vetsci5040083. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 51.Davoust B., Leparc-Goffart I., Demoncheaux J.P., Tine R., Diarra M., Trombini G., Mediannikov O., Marié J.L. Serologic surveillance for West Nile virus in dogs, Africa. Emerg. Infect. Dis. 2014;20:1415–1417. doi: 10.3201/eid2008.130691. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 52.Maquart M., Dahmani M., Marié J.L., Gravier P., Leparc-Goffart I., Davoust B. First serological evidence of West Nile virus in horses and dogs from Corsica Island, France. Vector-Borne Zoonotic Dis. 2017;17:275–277. doi: 10.1089/vbz.2016.2024. [DOI] [PubMed] [Google Scholar]
- 53.Dahmani M., Alwassouf S., Grech-Angelini S., Marié J.L., Davoust B., Charrel R.N. Seroprevalence of Toscana virus in dogs from Corsica, France. Parasit. Vectors. 2016;9:1–4. doi: 10.1186/s13071-016-1665-4. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 54.Tahir D., Alwassouf S., Loudahi A., Davoust B., Charrel R.N. Seroprevalence of Toscana virus in dogs from Kabylia (Algeria) Clin. Microbiol. Infect. 2016;22:e16–e17. doi: 10.1016/j.cmi.2015.10.029. [DOI] [PubMed] [Google Scholar]
- 55.Davoust B., Marié J.L., Tahir D., Dahmani M., Dufour P., Thiéry R., Rousset E. Seroprevalence of Coxiella burnetii infection in dogs from southeastern France. Int. J. Infect. Dis. 2019;79:122. doi: 10.1016/j.ijid.2018.11.300. [DOI] [Google Scholar]
- 56.Roqueplo C., Davoust B., Marié J.L., Kodjo A. Serological study of leptospirosis in dogs from French Guiana. Int. J. Infect. Dis. 2019;79:121–122. doi: 10.1016/j.ijid.2018.11.298. [DOI] [Google Scholar]
- 57.Roqueplo C., Kodjo A., Demoncheaux J.P., Scandola P., Bassene H., Diatta G., Sokhna C., Raoult D., Davoust B., Mediannikov O. Leptospirosis, one neglected disease in rural Senegal. Vet. Med. Sci. 2019;5:536–544. doi: 10.1002/vms3.186. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 58.Roqueplo C., Marié J.L., André-Fontaine G., Kodjo A., Davoust B. Serological survey of canine leptospirosis in three countries of tropical Africa: Sudan, Gabon and Ivory Coast. Comp. Immunol. Microbiol. Infect. Dis. 2015;38:57–61. doi: 10.1016/j.cimid.2014.10.006. [DOI] [PubMed] [Google Scholar]
- 59.Davoust B., Mediannikov O., Roqueplo C., Perret C., Demoncheaux J.P., Sambou M., Guillot J., Blaga R. Enquête de séroprévalence de la toxoplasmose animale au Sénégal. Bull. Soc. Pathol. Exot. 2014;108:73–77. doi: 10.1007/s13149-014-0403-4. [DOI] [PubMed] [Google Scholar]
- 60.Roqueplo C., Halos L., Cabre O., Davoust B. Toxoplasma gondii in wild and domestic animals from New Caledonia. Parasite. 2011;18(4):345–348. doi: 10.1051/parasite/2011184345. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 61.Medkour H., Laidoudi Y., Lafri I., Bitam I., Mediannikov O., Davoust B. Canine leishmaniosis and first report of Leishmania infantum in the blood of equids in Kabylia (Algeria) Int. J. Infect. Dis. 2019;79:117–118. doi: 10.1016/j.ijid.2018.11.290. [DOI] [Google Scholar]
- 62.Medkour H., Laidoudi Y., Athias E., Bouam A., Dizoé S., Davoust B., Mediannikov O. Molecular and serological detection of animal and human vector-borne pathogens in the blood of dogs from Côte d’Ivoire. Comp. Immunol. Microbiol. Infect. Dis. 2020;69:101412. doi: 10.1016/j.cimid.2019.101412. [DOI] [PubMed] [Google Scholar]
- 63.Tahir D., Davoust B., Heu K., Lamour T., Demar M., Marié J.L., Blanchet D. Molecular and serological investigation of Trypanosoma cruzi infection in dogs in French Guiana. Vet. Parasitol. Reg. Stud. Rep. 2018;12:106–109. doi: 10.1016/j.vprsr.2017.06.004. [DOI] [PubMed] [Google Scholar]
- 64.Watier-Grillot S., Marié J.L., Cabre O., Davoust B. Survey of canine Dirofilaria immitis infection in New Caledonia. Vet. Med. Int. 2011;380680 doi: 10.4061/2011/380680. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 65.Tahir D., Bittar F., Barré-Cardi H., Sow D., Dahmani M., Mediannikov O., Raoult D., Davoust B., Parola P. Molecular survey of Dirofilaria immitis and Dirofilaria repens by new real-time TaqMan® PCR assay in dogs and mosquitoes (Diptera: Culicidae) in Corsica (France) Vet. Parasitol. 2017;235:1–7. doi: 10.1016/j.vetpar.2017.01.002. [DOI] [PubMed] [Google Scholar]
- 66.Tahir D., Damene H., Davoust B., Parola P. First molecular detection of Dirofilaria immitis (Spirurida: Onchocercidae) infection in dogs from Northern Algeria. Comp. Immunol. Microbiol. Infect. Dis. 2017;51:66–68. doi: 10.1016/j.cimid.2017.04.001. [DOI] [PubMed] [Google Scholar]
- 67.Laidoudi Y., Marié J.L., Tahir D., Watier-Grillot S., Mediannikov O., Davoust B. Detection of canine vector-borne filariasis and their wolbachia endosymbionts in French Guiana. Microorganisms. 2020;8 doi: 10.3390/microorganisms8050770. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 68.Watier-Grillot S., Vallée I., Lacour S.A., Cana A., Davoust B., Marié J.L. Strayed dogs sentinels of Trichinella britovi infection in Kosovo. Parasite. 2011;18(3):281–283. doi: 10.1051/parasite/2011183281. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 69.Rolain J.M., La Scola B., Liang Z., Davoust B., Raoult D. Immunofluorescent detection of intraerythrocytic Bartonella henselae in naturally infected cats. J. Clin. Microbiol. 2001;39(8):2978–2980. doi: 10.1128/JCM.39.8.2978-2980.2001. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 70.Rolain J.M., Locatelli C., Chabanne L., Davoust B., Raoult D. Prevalence of Bartonella clarridgeiae and Bartonella henselae in domestic cats from France and detection of the organisms in erythrocytes by immunofluorescence. Clin. Diagn. Lab. Immunol. 2004;11:423–425. doi: 10.1128/CDLI.11.2.423-425.2003. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 71.Aboudharam G., Vu D.L., La B. Davoust, Drancourt M., Raoult D. Molecular detection of Bartonella spp. in the dental pulp of stray cats buried for a year. Microb. Pathog. 2005;38:47–51. doi: 10.1016/j.micpath.2004.10.004. [DOI] [PubMed] [Google Scholar]
- 72.Edouard S., Parola P., Socolovschi C., Davoust B., la Scola B., Raoult D. Clustered cases of Rickettsia sibirica mongolitimonae infection, France. Emerg. Infect. Dis. 2013;19:337–338. doi: 10.3201/eid1902.120863. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 73.Cabre O., Grandadam M., Marié J.L., Gravier P., Prangé A., Santinelli Y., Rous V., Bourry O., Durand J.P., Tolou H., Davoust B. West Nile virus in horses, sub-Saharan Africa. Emerg. Infect. Dis. 2006;12:1958–1960. doi: 10.3201/eid1212.060042. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 74.Marié J.L., Lafrance B., Maquart M., Mulot B., Leclerc A., Davoust B., Leparc-Goffart I. West Nile virus circulation in Djibouti. Int. J. Infect. Dis. 2016;53:158. doi: 10.1016/j.ijid.2016.11.385. [DOI] [Google Scholar]
- 75.Davoust B., Maquart M., Roqueplo C., Gravier P., Sambou M., Mediannikov O., Leparc-Goffart I. Serological survey of West Nile virus in domestic animals from Northwest Senegal. Vector-Borne Zoonotic Dis. 2016;16:359–361. doi: 10.1089/vbz.2015.1881. [DOI] [PubMed] [Google Scholar]
- 76.Lafri I., Prat C.M., Bitam I., Gravier P., Besbaci M., Zeroual F., Ben-Mahdi M.H., Davoust B., Leparc-Goffart I. Seroprevalence of West Nile virus antibodies in equids in the North-East of Algeria and detection of virus circulation in 2014. Comp. Immunol. Microbiol. Infect. Dis. 2017;50:8–12. doi: 10.1016/j.cimid.2016.11.005. [DOI] [PubMed] [Google Scholar]
- 77.Mangombi J.B., Roqueplo C., Sambou M., Dahmani M., Mediannikov O., Comtet L., Davoust B. Seroprevalence of Crimean-Congo hemorrhagic fever in domesticated animals in Northwestern Senegal. Vector-Borne Zoonotic Dis. 2020 doi: 10.1089/vbz.2019.2592. [DOI] [PubMed] [Google Scholar]
- 78.Maurizi L., Marié J.L., Aoun O., Courtin C., Gorsane S., Chal D., Davoust B. Seroprevalence survey of equine Lyme borreliosis in France and in sub-Saharan Africa. Vector-Borne Zoonotic Dis. 2010;10:535–537. doi: 10.1089/vbz.2009.0083. [DOI] [PubMed] [Google Scholar]
- 79.Bermann F., Davoust B., Fournier P.E., Brisou-Lapointe A.V., Brouqui P. Ehrlichia equi (Anaplasma phagocytophila) infection in an adult horse in France. Vet. Rec. 2002;150(25):787–788. doi: 10.1136/vr.150.25.787. [DOI] [PubMed] [Google Scholar]
- 80.Roqueplo C., Cabre O., Davoust B., Kodjo A. Epidemiological study of animal leptospirosis in New Caledonia. Vet. Med. Int. 2013;826834 doi: 10.1155/2013/826834. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 81.Ringot D., Durand J.P., Tolou H., Boutin J.P., Davoust B. Rift Valley fever in Chad. Emerg. Infect. Dis. 2004;10:945–947. doi: 10.3201/eid1005.030621. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 82.Matsumoto K., Joncour G., Davoust B., Pitel P.H., Chauzy A., Collin E., Morvan H., Vassallo N., Brouqui P. Anaplasma phagocytophilum infection in cattle in France. Ann. N. Y. Acad. Sci. 2006;1078:491–494. doi: 10.1196/annals.1374.092. [DOI] [PubMed] [Google Scholar]
- 83.Dahmani M., Davoust B., Benterki M.S., Fenollar F., Raoult D., Mediannikov O. Development of a new PCR-based assay to detect Anaplasmataceae and the first report of Anaplasma phagocytophilum and Anaplasma platys in cattle from Algeria. Comp. Immunol. Microbiol. Infect. Dis. 2015;39:39–45. doi: 10.1016/j.cimid.2015.02.002. [DOI] [PubMed] [Google Scholar]
- 84.Dahmani M., Sambou M., Scandola P., Raoult D., Fenollar F., Mediannikov O. Bartonella bovis and Candidatus Bartonella davousti in cattle from Senegal. Comp. Immunol. Microbiol. Infect. Dis. 2017;50:63–69. doi: 10.1016/j.cimid.2016.11.010. [DOI] [PubMed] [Google Scholar]
- 85.Raoult D., La Scola B., Kelly P.J., Davoust B., Gomez J. Bartonella bovis in cattle in Africa. Vet. Microbiol. 2005;105(2):155–156. doi: 10.1016/j.vetmic.2004.10.013. [DOI] [PubMed] [Google Scholar]
- 86.Saisongkorh W., Barrassi L., Davoust B., de Broucker C.A., Raoult D., Rolain J.M. First isolation of Bartonella bovis from animals in French Guyana, South America. Clin. Microbiol. Infect. 2009;15:124–126. doi: 10.1111/j.1469-0691.2008.02198.x. [DOI] [PubMed] [Google Scholar]
- 87.Mediannikov O., Davoust B., Cabre O., Rolain J.M., Raoult D. Bartonellae in animals and vectors in New Caledonia. Comp. Immunol. Microbiol. Infect. Dis. 2011;34:497–501. doi: 10.1016/j.cimid.2011.09.002. [DOI] [PubMed] [Google Scholar]
- 88.Medkour H., Davoust B., Angelakis M., Thiéry R., Raoult D., Rousset E., Parola P., Eldin C. A sporadic case of acute Q fever and identification of the animal source of the infection. Folia Microbiol. (Praha) 2020;65:797–800. doi: 10.1007/s12223-020-00788-3. [DOI] [PubMed] [Google Scholar]
- 89.Colson P., Saint-Jacques P., Ferretti A., Davoust B. Hepatitis E virus of subtype 3a in a pig farm, South-Eastern France. Zoonoses Public Health. 2015;62:593–598. doi: 10.1111/zph.12211. [DOI] [PubMed] [Google Scholar]
- 90.Kaba M., Colson P., Musongela J.P., Tshilolo L., Davoust B. Detection of hepatitis E virus of genotype 3 in a farm pig in Kinshasa (Democratic Republic of the Congo) Infect. Genet. Evol. 2010;10:154–157. doi: 10.1016/j.meegid.2009.09.011. [DOI] [PubMed] [Google Scholar]
- 91.Prangé A., Perret C., Marié J.L., Calvet F., Halos L., Boireau P., Davoust B. Toxoplasmose: À propos d’une enquête sur la viande en Côte d’Ivoire. Med. Trop. 2009;69:629–630. [PubMed] [Google Scholar]
- 92.Chabou S., Leulmi H., Davoust B., Aouadi A., Rolain J.M. Prevalence of extended-spectrum β-lactamase and carbapenemase-encoding genes in poultry faeces from Algeria and Marseille, France. J. Glob. Antimicrob. Resist. 2018;13:28–32. doi: 10.1016/j.jgar.2017.11.002. [DOI] [PubMed] [Google Scholar]
- 93.Kelly T.R., Karesh W.B., Johnson C.K., Gilardi K.V., Anthony S.J., Goldstein T., Olson S.H., Machalaba C., PREDICT Consortium, Mazet J.A. One Health proof of concept: Bringing a transdisciplinary approach to surveillance for zoonotic viruses at the human-wild animal interface. Prev. Vet. Med. 2017;137:112–118. doi: 10.1016/j.prevetmed.2016.11.023. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 94.Hosseini P.R., Mills J.N., Prieur-Richard A.H., Ezenwa V.O., Bailly X., Rizzoli A., Suzán G., Vittecoq M., García-Penã G.E., Daszak P., Guégan J.F., Roche B. Does the impact of biodiversity differ between emerging and endemic pathogens? The need to separate the concepts of hazard and risk. Philos. Trans. R. Soc. B. Biol. Sci. 2017;372 doi: 10.1098/rstb.2016.0129. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 95.Berg S.S., Forester J.D., Craft M.E. Infectious disease in wild animal populations: Examining transmission and control with mathematical models. In: Hurst C., editor. The Connections between Ecology and Infectious Disease. Advances in Environmental Microbiology. vol. 5. Springer; Cham: 2018. pp. 231–266. [DOI] [Google Scholar]

