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1.
J Wildl Dis ; 55(3): 576-588, 2019 07.
Artigo em Inglês | MEDLINE | ID: mdl-30557123

RESUMO

We collected blood and serum from 155 brown bears (Ursus arctos) inhabiting five locations in Alaska, US during 2013-16 and tested samples for evidence of prior exposure to a suite of bacterial, viral, and parasitic agents. Antibody seroprevalence among Alaska brown bears was estimated to be 15% for Brucella spp., 10% for Francisella tularensis, 7% for Leptospira spp., 18% for canine adenovirus type 1 (CAV-1), 5% for canine distemper virus (CDV), 5% for canine parvovirus, 5% for influenza A virus (IAV), and 44% for Toxoplasma gondii. No samples were seropositive for antibodies to Trichinella spp. Point estimates of prior exposure to pathogens among brown bears at previously unsampled locations generally fell within the range of estimates for previously or contemporaneously sampled bears in Alaska. Statistical support was found for variation in antibody seroprevalence among bears by location or age cohort for CAV-1, CDV, IAV, and T. gondii. There was limited concordance in comparisons between our results and previous serosurveys regarding spatial and age-related trends in antibody seroprevalence among Alaska brown bears suggestive of temporal variation. However, we found evidence that the seroprevalence of CAV-1 antibodies is consistently high in bears inhabiting southwest Alaska and the cumulative probability of exposure may increase with age. We found evidence for seroconversion or seroreversion to six different infectious agents in one or more bears. Results of this study increase our collective understanding of disease risk to both Alaska brown bear populations and humans that utilize this resource.


Assuntos
Envelhecimento , Infecções Bacterianas/veterinária , Toxoplasmose Animal/imunologia , Triquinelose/veterinária , Ursidae , Viroses/veterinária , Alaska/epidemiologia , Animais , Anticorpos Antibacterianos/sangue , Anticorpos Anti-Helmínticos/sangue , Anticorpos Antiprotozoários/sangue , Anticorpos Antivirais/sangue , Infecções Bacterianas/sangue , Infecções Bacterianas/epidemiologia , Infecções Bacterianas/imunologia , Estudos Soroepidemiológicos , Toxoplasmose Animal/sangue , Toxoplasmose Animal/epidemiologia , Triquinelose/sangue , Triquinelose/epidemiologia , Triquinelose/imunologia , Viroses/sangue , Viroses/epidemiologia , Viroses/imunologia
2.
Ecohealth ; 15(1): 121-131, 2018 03.
Artigo em Inglês | MEDLINE | ID: mdl-29168050

RESUMO

Increasingly, population- and ecosystem-level health assessments are performed using sophisticated molecular tools. Advances in molecular technology enable the identification of synergistic effects of multiple stressors on the individual physiology of different species. Brown bears (Ursus arctos) are an apex predator; thus, they are ideal candidates for detecting potentially ecosystem-level systemic perturbations using molecular-based tools. We used gene transcription to analyze 130 brown bear samples from three National Parks and Preserves in Alaska. Although the populations we studied are apparently stable in abundance and exist within protected and intact environments, differences in transcript profiles were noted. The most prevalent differences were among locations. The transcript patterns among groups reflect the influence of environmental factors, such as nutritional status, disease, and xenobiotic exposure. However, these profiles also likely represent baselines for each unique environment by which future measures can be made to identify early indication of population-level changes due to, for example, increasing Arctic temperatures. Some of those environmental changes are predicted to be potentially positive for brown bears, but other effects such as the manifestation of disease or indirect effects of oceanic acidification may produce negative impacts.


Assuntos
Doenças dos Animais/genética , Estado Nutricional/genética , Transcrição Gênica , Ursidae/genética , Alaska , Animais , Antioxidantes/metabolismo , Regiões Árticas , Feminino , Genes Supressores de Tumor , Inflamação/genética , Masculino , Reação em Cadeia da Polimerase , Análise de Sequência de DNA , Estresse Fisiológico/genética , Xenobióticos/metabolismo
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