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S.G. Hennager

Publications and source records attributed to S.G. Hennager.

2 recordsLinked to original sources

Environmental and behavioral changes may influence the exposure of an Arctic apex predator to pathogens and contaminants

Recent decline of sea ice habitat has coincided with increased use of land by polar bears ( Ursus maritimus ) from the southern Beaufort Sea (SB), which may alter the risks of exposure to pathogens and contaminants. We assayed blood samples from SB polar bears to assess prior exposure to the pathogens Brucella spp ., Toxoplasma gondii , Coxiella burnetii , Francisella tularensis , and Neospora caninum , estimate concentrations of persistent organic pollutants (POPs), and evaluate risk factors associated with exposure to pathogens and POPs. We found that seroprevalence of Brucella spp . and T. gondii antibodies likely increased through time, and provide the first evidence of exposure of polar bears to C. burnetii , N. caninum , and F. tularensis . Additionally, the odds of exposure to T. gondii were greater for bears that used land than for bears that remained on the sea ice during summer and fall, while mean concentrations of the POP chlordane (ΣCHL) were lower for land-based bears. Changes in polar bear behavior brought about by climate-induced modifications to the Arctic marine ecosystem may increase exposure risk to certain pathogens and alter contaminant exposure pathways.

Alaska↗

Brucellosis in Yellowstone National Park bison: Quantitative serology and infection

We collected complete sets of tissues, fluids, and swabs (approx 30) from 37 Yellowstone National Park (YNP) female bison (Bison bison) killed as a result of management actions by the Montana Department of Livestock and YNP personnel. Our goal was to establish the relation between blood tests demonstrating an animal has antibody to Brucella and the potential of that animal to be infected during the second trimester of pregnancy, the time when most management actions are taken. Twenty-eight of the 37 bison were seropositive adults (27) or a seropositive calf (1). We cultured samples using macerated whole tissues plated onto 4 Brucella-selective media and incubated with added CO2 for 1 week. Specimens from 2 adult seropositive females were contaminated, thus eliminating them from our data. Twelve of the remaining 26 seropositive adult and calf female bison (46%) were culture positive for Brucella abortus from 1 or more tissues. Culture positive adult females had high serologic titers. All 11 adults measured <0.115 on the Particle Concentration Fluorescence Immunoassay (PCFIA), and 9 (82%) were <0.085. Complement fixation (CF) titers were >3+ at 1:40 for 10 of 11 (91%) animals. All culture positive female adults had either a PCFIA ???0.080 or a CF reaction ???4+ at 1:80. However 5 (36%) bison with high titers were culture negative for B. abortus. Our findings on the relation between Brucella serology and culture are similar to those reported from studies of chronically infected cattle herds.

Journal of Wildlife Management↗