Plague Infection in Canadian Lynx Reintroduced to Colorado: Occurrence and Results of a Pilot Plague Vaccine Trial
American Association of Zoo Veterinarians Conference 2004
Lisa L. Wolfe1, MS, DVM; Tonie E. Rocke2, MS, PhD; S.M. Dieterich3; A.M. Friedlander4, MD; Tanya M. Shenk1, PhD; Gerard P. Andrews4, PhD; Laurie A. Baeten1, DVM; Terry R. Spraker5, DVM, PhD; Margaret A. Wild1,6, DVM, PhD; Michael W. Miller1, DVM, PhD
1Wildlife Research Center, Colorado Division of Wildlife, Fort Collins, CO, USA; 2National Wildlife Health Laboratory, Biological Resources Division, U.S. Geological Survey, Madison, WI, USA; 3Frisco Creek Wildlife Rehabilitation Center, Del Norte, CO, USA; 4Bacteriology Division, U.S. Army Medical Research Institute of Infectious Diseases, Fort Detrick, Frederick, MD, USA; 5Diagnostic Laboratory, Colorado State University, Fort Collins, CO, USA; 6Biological Resource Management Division, National Park Service, Fort Collins, CO, USA

Abstract

Plague appears to be a significant obstacle to successful reestablishment of lynx (Lynx canadensis) in Colorado. Yersinia pestis infections have been confirmed in six Canadian lynx reintroduced into Colorado as part of an ongoing species recovery program. Since 1999, plague was the primary cause in four of fifteen natural deaths, possibly contributed to one of six hit-by-vehicle deaths, and killed at least one kitten. In an attempt to minimize these impacts in future restoration efforts, we evaluated a recombinant capsular F1-V fusion protein vaccine that is safe and effective in black-footed ferrets. During January-April 2004, we vaccinated and serially bled 10 captive female lynx held in southwestern Colorado prior to their release in April 2004; 10 unvaccinated lynx served as controls. We observed no adverse effects of either the primary vaccine or booster doses on captive lynx. As of 15 March 2004, our study is still underway and serology results are pending. Based on observations to date, F1-V vaccine appears to be a safe vaccine in lynx; serologic responses and efficacy in reducing plague-related mortality remain to be determined.

 

Speaker Information
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Lisa L. Wolfe, MS, DVM
Division of Wildlife
Wildlife Research Center
Fort Collins, CO, USA


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