犬瘟热病毒在中食性动物中感染的系统发育结构和生态相关性。

IF 3.7 2区 生物学 Q2 MICROBIOLOGY
Microbiology spectrum Pub Date : 2025-04-01 Epub Date: 2025-03-03 DOI:10.1128/spectrum.01225-24
Jonathan Wilson, Samantha Rubio, Liliana C M Salvador, Nicole M Nemeth, Jillian D Fishburn, Nicole L Gottdenker
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引用次数: 0

摘要

人为土地利用通过改变宿主的空间分布、行为、密度和种群动态,影响野生动物-家庭-人类界面的传染病。犬瘟热病毒(CDV)是许多野生动物和家畜发病和死亡的重要原因。鉴于CDV对共生中食性动物的感染倾向,研究影响中食性动物CDV感染的宿主和环境因素具有重要意义。在这里,我们调查了CDV感染的模式,并建立了一个统计模型,以确定与常见感染的中食性动物CDV风险相关的环境变量。我们对2019年1月至2022年12月提交给东南野生动物合作疾病研究的尸体(N = 270)进行了采样,并对32只CDV阳性动物的CDV h基因进行了测序。总体而言,在13个州的270只中食肉动物中,有158只(58.5%)和4个物种(浣熊、红狐、灰狐和条纹臭鼬)被诊断出患有CDV。Ripley的K分析显示,由于偶然性,阳性病例在空间上聚集的距离比预期的要大。CDV感染动物的广义线性模型显示,地表不透水、降水和亚成年/成年年龄类别是显著的正解释变量,但海拔高度与CDV感染可能性存在显著的负相关。美国东南部野生中食肉动物的h基因序列多样性在地理上分为密西西比河以东和以西两个群体,只有两个东部样本与西部群体聚类。通过确定CDV风险最高的人类密集发展地区,有可能将监测工作重点放在这些地区,从而能够更早地发现疫情,从而有可能防止CDV的跨物种传播。重要性:人为的土地利用变化可以通过改变动物分布和行为影响传染病的传播。犬瘟热病毒(CDV)是野生和家养食肉动物发病和死亡的重要原因。这项研究通过检查2019年至2022年在美国东南部发现的死亡野生食肉动物的组织,调查了土地利用如何影响野生食肉动物的CDV感染。CDV菌株在地理上是不同的,在密西西比河东部和西部的人群之间存在差异。统计模型显示,人类发展程度高、降水量多的地区有较高的CDV风险;然而,海拔越高、动物越年轻,风险越低。这项研究的重要性在于它确定了CDV在美国南部的地理结构,并确定了CDV传播的潜在高风险地区的土地利用关系——这些信息对野生动物疾病监测和控制策略有用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Canine distemper virus phylogenetic structure and ecological correlates of infection in mesocarnivores across anthropogenic land use gradients.

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 (N = 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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来源期刊
Microbiology spectrum
Microbiology spectrum Biochemistry, Genetics and Molecular Biology-Genetics
CiteScore
3.20
自引率
5.40%
发文量
1800
期刊介绍: Microbiology Spectrum publishes commissioned review articles on topics in microbiology representing ten content areas: Archaea; Food Microbiology; Bacterial Genetics, Cell Biology, and Physiology; Clinical Microbiology; Environmental Microbiology and Ecology; Eukaryotic Microbes; Genomics, Computational, and Synthetic Microbiology; Immunology; Pathogenesis; and Virology. Reviews are interrelated, with each review linking to other related content. A large board of Microbiology Spectrum editors aids in the development of topics for potential reviews and in the identification of an editor, or editors, who shepherd each collection.
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