Serologic Survey and Results of Urinary PCR Testing for Leptospirosis in Captive Black-Tailed Prairie Dogs (Cynomys ludovicianus)
American Association of Zoo Veterinarians Conference 2015
June E. Olds1,2, DVM; David H. Baum3, MS, DVM, PhD; Phillip Gauger3, DVM, MS, PhD
1Department of Veterinary Clinical Sciences, College of Veterinary Medicine, Iowa State University, Ames, IA, USA; 2Blank Park Zoo, Des Moines, IA, USA; 3Veterinary Diagnostic Laboratory, College of Veterinary Medicine, Iowa State University, Ames, IA, USA

Abstract

Leptospirosis is an important zoonotic disease occurring clinically and subclinically in humans and a wide variety of mammalian species worldwide.1,7 Rodents and wild animals have been identified as important reservoirs for Leptospira bacteria.2,3,5,8,10,12-16 Twenty-two captive black-tailed prairie dogs (Cynomys ludovicianus) housed within a zoo were examined as part of a routine census and preventive medicine program. During examinations, blood and urine were collected to test for evidence of infection by Leptospira. All animals were apparently healthy at the time of examination. Leptospira microscopic agglutination test (MAT)6 identified twelve of 22 (54.5%) prairie dogs with Leptospira interrogans serovar Bratislava on initial serologic examination. All prairie dogs within this collection were serologically negative for Leptospira interrogans serovars Canicola, Hardjo, Icterohemorrhagiae, Pomona, and Leptospira kirschneri serovar Grippotyphosa. Leptospira PCR11 testing of urine was negative in all animals tested. A recent serologic survey of wild black-tailed prairie dogs in Mexico determined that almost 80% of wild prairie dog sera were positive for at least one L. interrogans serovar.9 This report suggests that these captive prairie dogs may have been exposed to Leptospira; however, low MAT results and lack of leptospire DNA detected by PCR indicate these animals are unlikely to be important reservoirs for the disease. We hypothesize the source of Leptospira exposure to be wild rodents.

Acknowledgments

The authors thank Yuxuan Sun, Department of Statistics, College of Liberal Arts and Sciences, Iowa State University, for statistical analysis. Heartfelt gratitude is also extended to the veterinary support team, small mammal team, and registrar of the Blank Park Zoo for excellent record keeping and tireless care for these wonderful animals.

Literature Cited

1.  Adler B, de la Pena Moctezuma A. Leptospira and leptospirosis. Vet Microbiol. 2010;140(3–4):287–296.

2.  Aviat F, Blanchard B, Michel V, Blanchet B, Branger C, Hars J, Mansotte F, et al. Leptospira exposure in the human environment in France: a survey in feral rodents and in fresh water. Comp Immunol Microbiol Infect Dis. 2009;32(6):463–476.

3.  Bronson E, Spiker H, Driscoll CP. Serosurvey for selected pathogens in free-ranging American black bears (Ursus americanus) in Maryland, USA. J Wildl Dis. 2014;50(4):829–836.

4.  Cole JR, Sulzer CR, Purcell AR. Improved microtechnique for leptospiral microscopic agglutination test. Appl Microbiol. 1973:25(6);976–980.

5.  Goyal SM, Mech LD, Nelson ME. Prevalence of antibody titers to Leptospira spp. in Minnesota white-tailed deer. J Wildl Dis. 1992;28(3):445–448.

6.  Hartskeerl RA, Terpstra WJ. Leptospirosis in wild animals. Vet Q. 1996;18 Suppl 3:S149–S150.

7.  Levett PN. Leptospirosis. Clin Microbiol Rev. 2001;14(2):296–326.

8.  Majetic ZS, Galloway R, Sabljic ER, Milas Z, Perko VM, Habus J, Margaletic J, et al. Epizootiological survey of small mammals as Leptospira spp. reservoirs in eastern Croatia. Acta Tropica. 2014;131:111–116.

9.  Montiel-Arteaga A, Atilano D, Ayanegui A, Ceballos G, Suzán G. Risk factors associated with prevalence of antibodies to Leptospira interrogans in a metapopulation of black-tailed prairie dogs in Mexico. J Wildl Dis. 2015;51:28–35.

10.  Smith KE, Zimmerman JJ, Bolin CA, Beran GW, Hill HT. A survey of house mice from Iowa swine farms for infection with Leptospira interrogans serovar Bratislava. Can Vet J. 1992;33(11):742–744.

11.  Stoddard RA, Gee JE, Wilkins PP, McCaustland K, Hoffmaster AR. Detection of pathogenic Leptospira spp. through TaqMan polymerase chain reaction targeting the LipL32 gene. Diagn Microbiol Infect Dis. 2009;64(3):247–255.

12.  Tan CG, Dharmarajan G, Beasley J, Rhodes O Jr, Moore G, Wu CC, Lin TL. Neglected leptospirosis in raccoons (Procyon lotor) in Indiana, USA. Vet Q. 2014;34(1):1–10.

13.  Tucunduva de Faria M, Calderwood MS, Athanazio DA, McBride AJA, Hartskeerl RA, Pereira MM, et al. Carriage of Leptospira interrogans among domestic rats from an urban setting highly endemic for leptospirosis in Brazil. Acta Trop. 2008;108(1):1–5.

14.  Webster JP, Ellis WA, Macdonald DW. Prevalence of Leptospira spp. in wild brown rats (Rattus norvegicus) on UK farms. Epidemiol Infect. 1995;114:195–201.

15.  World Health Organization. Leptospirosis worldwide, 1999. Wkly Epidemiol Rec. 1999;74(29):237–242.

16.  World Health Organization. Human leptospirosis: Guidance for diagnosis, surveillance, and control. World Health Organization, International Leptospirosis Society. Geneva: World Health Organization. 2003. www.who.int/csr/don/en/WHO_CDS_CSR_EPH_2002.23.pdf. Accessed January 19, 2015.

 

Speaker Information
(click the speaker's name to view other papers and abstracts submitted by this speaker)

June E. Olds, DVM
Department of Veterinary Clinical Sciences
College of Veterinary Medicine
Iowa State University
Ames, IA, USA


MAIN : Rodents, Marsupials, and Allometric Scaling : Serologic Survey & Urinary PCR Testing for Leptospirosis
Powered By VIN
SAID=27