LEPTOSPIROSIS IN FREE-RANGING ENDANGERED EUROPEAN MINK (MUSTELA LUTREOLA) AND OTHER SMALL CARNIVORES (MUSTELIDAE, VIVERRIDAE) FROM SOUTHWESTERN FRANCE

To study the possible role of disease in the decline of endangered European mink (Mustela lutreola), we conducted a survey of antibody prevalence and renal carriage of pathogenic leptospira (Leptospira interrogans sensu lato) using serum and kidney samples collected from 1990 to 2007 from several free-ranging small carnivores and farmed American mink (Mustela vison) in southwestern France. An indirect microscopic agglutination test using a panel of 16 serovars belonging to 6 serogroups (Australis, Autumnalis, Icterohæmorrhagiæ, Grippotyphosa, Panama, Sejroe) revealed antibodies in all species, with significant differences in antibody prevalences: 74% in European mink (n=99), 65.4% in European polecats (Mustela putorius, n=133), 86% in American mink (n=74), 89% in stone martens (Martes foina, n=19), 74% in pine martens (Martes martes, n=19), 35% in common genets (Genetta genetta, n=79), and 31% in farmed American mink (n=51). Serogroups Australis and Icterohæmorragiæ were dominant in most free-ranging species; serogroup Grippotyphosa had high prevalences in European mink. Such high antibody prevalences have never been reported. They are probably related to the large number of known reservoirs, rats (Rattus spp.), muskrat (Ondatra zibethicus), and coypu (Myocastor coypu), in the study area. The polymerase chain reaction test specific for pathogenic leptospiral DNA detected renal carriage in 23% of 34 European mink, 22% of 18 polecats, and 15% of 33 free-ranging American mink, with no significant differences. Renal carriage shows that mustelids may shed leptospira for short periods, but their epidemiologic role is probably limited. High antibody prevalences suggest that the disease is unlikely to be highly pathogenic for these species; however, chronic forms of the disease (abortions, renal lesions) could reduce the reproductive success or life span of infected animals. Further studies on the pathogenicity of leptospirosis in these populations are needed to measure its impact on the population dynamics of these rodent predators.

[1]  S. Sourice,et al.  Reliability of stained placental scar counts in farmed American mink and application to free-ranging mustelids , 2010 .

[2]  S. Aulagnier,et al.  Spatial behaviour of European minkMustela lutreola and polecatMustela putorius in southwestern France , 2008, Mammal Research.

[3]  S. Aulagnier,et al.  Habitat utilization by sympatric European minkMustela lutreola and polecatsMustela putorius in south-western France , 2007, Acta Theriologica.

[4]  A. Kodjo,et al.  Leptospira exposure in the human environment in France: A survey in feral rodents and in fresh water. , 2009, Comparative immunology, microbiology and infectious diseases.

[5]  J. López‐Bao,et al.  Leptospirosis in wild and domestic carnivores in natural areas in Andalusia, Spain. , 2009, Vector borne and zoonotic diseases.

[6]  T. Kuiken,et al.  SEROLOGIC SURVEY FOR SELECTED VIRAL PATHOGENS IN FREE-RANGING ENDANGERED EUROPEAN MINK (MUSTELA LUTREOLA) AND OTHER MUSTELIDS FROM SOUTH-WESTERN FRANCE , 2008, Journal of wildlife diseases.

[7]  T. Maran Conservation biology of the European mink, Mustela lutreola (Linnaeus 1761): decline and causes of extinction , 2007 .

[8]  M. Ben‐David,et al.  Does Human Proximity Affect Antibody Prevalence in Marine-Foraging River Otters (Lontra canadensis)? , 2007, Journal of wildlife diseases.

[9]  G. R. Seamons,et al.  Mammal Species of the World: A Taxonomic and Geographic Reference (3rd edition) , 2006 .

[10]  A. Davison,et al.  Conservation genetics and population history of the threatened European mink Mustela lutreola, with an emphasis on the west European population , 2005, Molecular ecology.

[11]  C. Fillonneau,et al.  Polymerase chain reaction assay specific for pathogenic Leptospira based on the gene hap1 encoding the hemolysis-associated protein-1. , 2005, FEMS microbiology letters.

[12]  P. Berny,et al.  EVIDENCE OF SECONDARY POISONING OF FREE-RANGING RIPARIAN MUSTELIDS BY ANTICOAGULANT RODENTICIDES IN FRANCE: IMPLICATIONS FOR CONSERVATION OF EUROPEAN MINK (MUSTELA LUTREOLA) , 2004, Journal of wildlife diseases.

[13]  C. Simon,et al.  ANTIBODIES TO ALEUTIAN MINK DISEASE PARVOVIRUS IN FREE-RANGING EUROPEAN MINK (MUSTELA LUTREOLA) AND OTHER SMALL CARNIVORES FROM SOUTHWESTERN FRANCE , 2004, Journal of wildlife diseases.

[14]  G. Andre-Fontaine,et al.  Occupational hazard of unnoticed leptospirosis in water ways maintenance staff , 1992, European Journal of Epidemiology.

[15]  C. Fillonneau,et al.  Role of the coypu (Myocastor coypus) in the epidemiology of leptospirosis in domestic animals and humans in France , 2004, European Journal of Epidemiology.

[16]  J. Estes,et al.  CLINICAL PATHOLOGY AND ASSESSMENT OF PATHOGEN EXPOSURE IN SOUTHERN AND ALASKAN SEA OTTERS , 2003, Journal of wildlife diseases.

[17]  C. Branger,et al.  Comparison of the efficacy of three commercial bacterins in preventing canine leptospirosis , 2003, Veterinary Record.

[18]  D. Richardson,et al.  A serosurvey of leptospirosis in Connecticut peridomestic wildlife. , 2003, Vector borne and zoonotic diseases.

[19]  A. Dobson,et al.  Disease, habitat fragmentation and conservation , 2002, Proceedings of the Royal Society of London. Series B: Biological Sciences.

[20]  R. Woodroffe Assessing the risks of intervention: immobilization, radio-collaring and vaccination of African wild dogs , 2001, Oryx.

[21]  A. Dobson,et al.  Detecting disease and parasite threats to endangered species and ecosystems. , 1995, Trends in ecology & evolution.

[22]  Daryl E. Wilson,et al.  Mammal Species of the World: A Taxonomic and Geographic Reference , 1993 .

[23]  F. Reinthaler,et al.  Results of serological examination for leptospirosis of domestic and wild animals in the Upper Nile province (Sudan). , 1989, Journal of hygiene, epidemiology, microbiology, and immunology.

[24]  S. O'Brien,et al.  Interactive influence of infectious disease and genetic diversity in natural populations , 1988, Trends in Ecology & Evolution.

[25]  A. E. Stevens,et al.  Infection of free-living carnivores with leptospires of the Australis serogroup , 1983, Veterinary Record.

[26]  C. Everard,et al.  LEPTOSPIRES IN WILDLIFE FROM TRINIDAD AND GRENADA , 1983, Journal of wildlife diseases.

[27]  S. Faine Guidelines for the control of leptospirosis. , 1982, WHO offset publication.

[28]  G. Heidt,et al.  SURVEY FOR RABIES, LEPTOSPIROSIS, TOXOPLASMOSIS AND TULAREMIA IN STRIPED SKUNKS (Mephitis mephitis) FROM THREE PUBLIC USE AREAS IN NORTHWESTERN ARKANSAS , 1981, Journal of wildlife diseases.

[29]  J. Gunson,et al.  A serological survey of Leptospira interrogans serotype pomona in Alberta and Saskatchewan striped skunks and possible transmission between cattle and skunks. , 1981, The Canadian veterinary journal = La revue veterinaire canadienne.

[30]  W. Adams,et al.  RENAL LESIONS IN STRIPED SKUNKS (Mephitis mephitis) FROM LOUISIANA , 1977, Journal of wildlife diseases.

[31]  K. L. Fennestad,et al.  LEPTOSPIROSIS IN DANISH WILD MAMMALS1 , 1972 .

[32]  J. R. Reilly The susceptibility of five species of wild animals to experimental infection with Leptospira grippotyphosa , 1970, Journal of wildlife diseases.

[33]  D. Ferris,et al.  Experimentally induced predator chain transmission of Leptospira grippotyphosa from rodents to wild marsupialia and carnivora. , 1970, American journal of veterinary research.

[34]  F. James Rohlf,et al.  Biometry: The Principles and Practice of Statistics in Biological Research , 1969 .

[35]  W. Adams,et al.  LEPTOSPIRURIA IN STRIPED SKUNKS. , 1963, Public health reports.

[36]  J. L. Harrison,et al.  Animal leptospirosis in Malaya: 1. Methods, zoogeographical background, and broad analysis of results. , 1961, Bulletin of the World Health Organization.