Rachel C. Abbott
United States Geological Survey
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Publication
Featured researches published by Rachel C. Abbott.
Journal of Wildlife Diseases | 2015
Daniel W. Tripp; Tonie E. Rocke; Sean P. Streich; Rachel C. Abbott; Jorge E. Osorio; Michael W. Miller
Abstract Prairie dogs (Cynomys spp.) suffer high rates of mortality from plague. An oral sylvatic plague vaccine using the raccoon poxvirus vector (designated RCN-F1/V307) has been developed for prairie dogs. This vaccine is incorporated into palatable bait along with rhodamine B as a biomarker. We conducted trials in August and September 2012 to demonstrate uptake and apparent safety of the RCN-F1/V307 vaccine in two prairie dog species under field conditions. Free-ranging prairie dogs and other associated small rodents readily consumed vaccine-laden baits during field trials with no apparent adverse effects; most sampled prairie dogs (90%) and associated small rodents (78%) had consumed baits. Visual counts of prairie dogs and their burrows revealed no evidence of prairie dog decline after vaccine exposure. No vaccine-related morbidity, mortality, or gross or microscopic lesions were observed. Poxviruses were not isolated from any animal sampled prior to bait distribution or on sites that received placebo baits. We isolated RCN-F1/V307 from 17 prairie dogs and two deer mice (Peromyscus maniculatus) captured on sites where vaccine-laden baits were distributed. Based on these findings, studies examining the utility and effectiveness of oral vaccination to prevent plague-induced mortality in prairie dogs and associated species are underway.
Journal of Wildlife Diseases | 2014
Rachel C. Abbott; Robert Hudak; Roy Mondesire; Laurie A. Baeten; Robin E. Russell; Tonie E. Rocke
Abstract Plague surveillance is routinely conducted to predict future epizootics in wildlife and exposure risk for humans. The most common surveillance method for sylvatic plague is detection of antibodies to Yersinia pestis F1 capsular antigen in sentinel animals, such as coyotes (Canis latrans). Current serologic tests for Y. pestis, hemagglutination (HA) test and enzyme-linked immunosorbent assay (ELISA), are expensive and labor intensive. To address this need, we developed a complete lateral flow device for the detection of specific antibodies to Y. pestis F1 and V antigens. Our test detected anti-F1 and anti-V antibodies in serum and Nobuto filter paper samples from coyotes, and in serum samples from prairie dogs (Cynomys ludovicianus), lynx (Lynx canadensis), and black-footed ferrets (Mustela nigripes). Comparison of cassette results for anti-F1 and anti-V antibodies with results of ELISA or HA tests showed correlations ranging from 0.68 to 0.98. This device provides an affordable, user-friendly tool that may be useful in plague surveillance programs and as a research tool.
Journal of Wildlife Diseases | 2017
Elsa M. Cárdenas-Canales; Lisa L. Wolfe; Daniel W. Tripp; Tonie E. Rocke; Rachel C. Abbott; Michael W. Miller
Abstract We confirmed safety and immunogenicity of mass-produced vaccine baits carrying an experimental, commercial-source plague vaccine (RCN-F1/V307) expressing Yersinia pestis V and F1 antigens. Forty-five juvenile black-tailed prairie dogs (Cynomys ludovicianus) were randomly divided into three treatment groups (n=15 animals/group). Animals in the first group received one standard-dose vaccine bait (5×107 plaque-forming units [pfu]; STD). The second group received a lower-dose bait (1×107 pfu; LOW). In the third group, five animals received two standard-dose baits and 10 were left untreated but in contact. Two vaccine-treated and one untreated prairie dogs died during the study, but laboratory analyses ruled out vaccine involvement. Overall, 17 of 33 (52%; 95% confidence interval for binomial proportion [bCI] 34−69%) prairie dogs receiving vaccine-laden bait showed a positive anti-V antibody response on at least one sampling occasion after bait consumption, and eight (24%; bCI 11–42%) showed sustained antibody responses. The STD and LOW groups did not differ (P≥0.78) in their proportions of overall or sustained antibody responses after vaccine bait consumption. Serum from one of the nine (11%; bCI 0.3–48%) surviving untreated, in-contact prairie dogs also had detectable antibody on one sampling occasion. We did not observe any adverse effects related to oral vaccination.
Ecology and Evolution | 2018
Robin E. Russell; Rachel C. Abbott; Daniel W. Tripp; Tonie E. Rocke
Abstract Outbreaks of plague, a flea‐vectored bacterial disease, occur periodically in prairie dog populations in the western United States. In order to understand the conditions that are conducive to plague outbreaks and potentially predict spatial and temporal variations in risk, it is important to understand the factors associated with flea abundance and distribution that may lead to plague outbreaks. We collected and identified 20,041 fleas from 6,542 individual prairie dogs of four different species over a 4‐year period along a latitudinal gradient from Texas to Montana. We assessed local climate and other factors associated with flea prevalence and abundance, as well as the incidence of plague outbreaks. Oropsylla hirsuta, a prairie dog specialist flea, and Pulex simulans, a generalist flea species, were the most common fleas found on our pairs. High elevation pairs in Wyoming and Utah had distinct flea communities compared with the rest of the study pairs. The incidence of prairie dogs with Yersinia pestis detections in fleas was low (n = 64 prairie dogs with positive fleas out of 5,024 samples from 4,218 individual prairie dogs). The results of our regression models indicate that many factors are associated with the presence of fleas. In general, flea abundance (number of fleas on hosts) is higher during plague outbreaks, lower when prairie dogs are more abundant, and reaches peak levels when climate and weather variables are at intermediate levels. Changing climate conditions will likely affect aspects of both flea and host communities, including population densities and species composition, which may lead to changes in plague dynamics. Our results support the hypothesis that local conditions, including host, vector, and environmental factors, influence the likelihood of plague outbreaks, and that predicting changes to plague dynamics under climate change scenarios will have to consider both host and vector responses to local factors.
Ecohealth | 2012
Rachel C. Abbott; Jorge E. Osorio; Christine M. Bunck; Tonie E. Rocke
Ecotoxicology | 2011
Julia Rodriguez-Ramos Fernandez; Ursula Höfle; Rafael Mateo; Olga Nicolas de Francisco; Rachel C. Abbott; Pelayo Acevedo; Juan Manuel Blanco
Ecohealth | 2017
Tonie E. Rocke; Daniel W. Tripp; Robin E. Russell; Rachel C. Abbott; Katherine L. D. Richgels; Marc R. Matchett; Dean E. Biggins; Randall L. Griebel; Greg Schroeder; Shaun M. Grassel; David R. Pipkin; Jennifer Cordova; Adam Kavalunas; Brian D. Maxfield; Jesse T. Boulerice; Michael W. Miller
Ecohealth | 2015
Tonie E. Rocke; Daniel W. Tripp; Faye Lorenzsonn; Elizabeth A. Falendysz; Susan R. Smith; Judy L. Williamson; Rachel C. Abbott
Ecohealth | 2017
Daniel W. Tripp; Tonie E. Rocke; Jonathan P. Runge; Rachel C. Abbott; Michael W. Miller
Ecohealth | 2018
Rachel C. Abbott; Robin E. Russell; Katherine L. D. Richgels; Daniel W. Tripp; Marc R. Matchett; Dean E. Biggins; Tonie E. Rocke