Unlabelled: Anthropogenic land use impacts infectious diseases at the wildlife-domestic-human interface by changing host spatial distribution, behavior, density, and population dynamics. Canine distemper virus (CDV) is a significant cause of morbidity and mortality in many wild and domestic animals. Given the propensity of CDV to infect synanthropic mesocarnivores, it is important to investigate host and environmental factors affecting mesocarnivore CDV infection. Here, we investigated patterns of CDV infection and developed a statistical model to identify environmental variables related to CDV risk in commonly affected mesocarnivores. We sampled carcasses ( = 270) submitted to the Southeastern Cooperative Wildlife Disease Study from January 2019 to December 2022 and sequenced the CDV H-gene of 32 CDV-positive animals. Overall, 158 out of 270 mesocarnivores (58.5%) and four species (raccoon, red fox, gray fox, and striped skunk) were diagnosed with CDV across 13 states. Ripley's K analysis showed positive cases were more spatially clustered at larger distances than expected due to chance. A generalized linear model for CDV-infected animals showed surface imperviousness, precipitation, and subadult/adult age classes were significant positive explanatory variables, but elevation had a significant negative association with CDV infection likelihood. H-gene sequence diversity among wild mesocarnivores in the southeastern United States was geographically separated into groups east and west of the Mississippi River, with only two eastern samples clustering with western groups. By identifying areas of intense human development at the highest risk for CDV, it may be possible to focus surveillance efforts in these areas, allowing for earlier outbreak identification, potentially preventing cross-species CDV transmission.
Importance: Anthropogenic land use change can impact infectious disease spread by altering animal distribution and behavior. Canine distemper virus (CDV) is a significant cause of morbidity and mortality in wild and domestic carnivores. This study investigated how land use influences CDV infection in wild carnivores by examining tissues collected between 2019 and 2022 from wild carnivores found dead in the southeastern United States. CDV strains were geographically distinct, with differences between populations east and west of the Mississippi river. Statistical models showed areas with increased human development and higher precipitation had higher CDV risk; however, there was lower risk associated with higher elevations and younger animals. The importance of this study is that it identifies geographic structure of CDV in the southern United States, and identifies land-use associations with potential high-risk areas for CDV transmission-information that is useful for wildlife disease surveillance and control strategies.
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http://dx.doi.org/10.1128/spectrum.01225-24 | DOI Listing |
J Zoo Wildl Med
March 2025
Cheetah Conservation Fund, Otjiwarongo, Namibia,
Vaccinating African wild dogs () against canine distemper virus (CDV) using live attenuated vaccines (LAV) has been controversial because of limitations in the vaccines' effectiveness and safety. However, CDV is a significant pathogen for African wild dogs, and CDV LAV are currently the only vaccines readily available on the African continent, making them a crucial tool for conservation. There are few studies exploring immunogenicity of CDV LAV, and even less information pertaining to optimal vaccination protocols.
View Article and Find Full Text PDFMicrobiol Spectr
March 2025
Department of Pathology, College of Veterinary Medicine, University of Georgia, Athens, Georgia, USA.
Unlabelled: Anthropogenic land use impacts infectious diseases at the wildlife-domestic-human interface by changing host spatial distribution, behavior, density, and population dynamics. Canine distemper virus (CDV) is a significant cause of morbidity and mortality in many wild and domestic animals. Given the propensity of CDV to infect synanthropic mesocarnivores, it is important to investigate host and environmental factors affecting mesocarnivore CDV infection.
View Article and Find Full Text PDFFood Chem
February 2025
Ferdowsi University of Mashhad, Faculty of Agriculture, Department of Food Science and Technology, P.O. Box 917751163, Mashhad, Iran. Electronic address:
The study aimed to determine the relative contribution of peroxide value (PV), acid value (AV), conjugated diene value (CDV), carbonyl value (CV), saturated fatty acids (SFA) extent, the ratio between the extents of monounsaturated (MUFA) and polyunsaturated (PUFA) fatty acids, total tocopherols (TT, as mg of α-tocopherol per kg of oil) content, and total phenolic compounds (TP, as mg of gallic acid per kg of oil) content to the initiation (O) and propagation (r) oxidizabilities of vegetable oils (canola, soybean, sesame, corn, peanut, olive, and rice bran). The parameter O was a function of TT (24.6 %), MUFA/PUFA ratio (20.
View Article and Find Full Text PDFViruses
January 2025
Laboratory of Virology, Department of Translational Physiology, Infectiology and Public Health, Faculty of Veterinary Medicine, Ghent University, Salisburylaan 133, 9820 Merelbeke, Belgium.
Porcine reproductive and respiratory syndrome virus (PRRSV) and African swine fever virus (ASFV) cause serious economic losses to the swine industry worldwide. Both viruses show a tropism for macrophages, based on the use of specific entry mediators (e.g.
View Article and Find Full Text PDFViruses
January 2025
Department of Pathology, Microbiology, and Immunology, School of Veterinary Medicine, 4206 Vet Med 3A, University of California, Davis, CA 95616, USA.
Canine distemper is a severe and lethal viral disease of dogs and wild carnivores with an urgent need for the identification of effective antiviral agents against canine distemper virus (CDV). We assessed multiple agents for their ability to block the replication of three different lineages of CDV isolated from wild carnivores in the United States. Six antiviral compounds were selected after preliminary experiments that excluded ribavirin, hesperidin and rutin: a protease inhibitor (nirmatrelvir), a polymerase inhibitor (favipiravir) and four nucleoside analogs (remdesivir, GS-441524, EIDD2801 and EIDD1931).
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