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新型马冠状病毒基因组和亚科其他成员中的正选择、遗传重组和宿主内进化。

Positive selection, genetic recombination, and intra-host evolution in novel equine coronavirus genomes and other members of the subgenus.

机构信息

Department of Biology, Institute for Genomics and Evolutionary Medicine, Temple University, Philadelphia, Pennsylvania, USA.

James A. Baker Institute for Animal Health, College of Veterinary Medicine, Cornell University, Ithaca, New York, USA.

出版信息

Microbiol Spectr. 2024 Nov 5;12(11):e0086724. doi: 10.1128/spectrum.00867-24. Epub 2024 Oct 7.

DOI:10.1128/spectrum.00867-24
PMID:39373506
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11542594/
Abstract

There are several examples of coronaviruses in the Betacoronavirus subgenus that have jumped from an animal to the human host. Studying how evolutionary factors shape coronaviruses in non-human hosts may provide insight into the coronavirus host-switching potential. Equids, such as horses and donkeys, are susceptible to equine coronaviruses (ECoVs). With increased testing prevalence, several ECoV genome sequences have become available for molecular evolutionary analyses, especially those from the United States of America (USA). To date, no analyses have been performed to characterize evolution within coding regions of the ECoV genome. Here, we obtain and describe four new ECoV genome sequences from infected equines from across the USA presenting clinical symptoms of ECoV, and infer ECoV-specific and -wide patterns of molecular evolution. Within two of the four data sets analyzed, we find evidence of intra-host evolution within the nucleocapsid (N) gene, suggestive of quasispecies development. We also identify 12 putative genetic recombination events within the ECoV genome, 11 of which fall in ORF1ab. Finally, we infer and compare sites subject to positive selection on the ancestral branch of each major member clade. Specifically, for the two currently identified human coronavirus (HCoV) embecoviruses that have spilled from animals to humans (HCoV-OC43 and HCoV-HKU1), we find that there are 42 and 2 such sites, respectively, perhaps reflective of the more complex ancestral evolutionary history of HCoV-OC43, which involves several different animal hosts.IMPORTANCEThe Betacoronavirus subgenus contains coronaviruses that not only pose a health threat to animals and humans, but also have jumped from animal to human host. Equids, such as horses and donkeys are susceptible to equine coronavirus (ECoV) infections. No studies have systematically examined evolutionary patterns within ECoV genomes. Our study addresses this gap and provides insight into intra-host ECoV evolution from infected horses. Further, we identify and report natural selection pattern differences between two embecoviruses that have jumped from animals to humans [human coronavirus OC43 and HKU1 (HCoV-OC43 and HCoV-HKU1, respectively)], and hypothesize that the differences observed may be due to the different animal host(s) that each virus circulated in prior to its jump into humans. Finally, we contribute four novel, high-quality ECoV genomes to the scientific community.

摘要

有几种贝塔冠状病毒亚属的冠状病毒已经从动物宿主跳跃到人类宿主。研究进化因素如何塑造非人类宿主中的冠状病毒,可能有助于了解冠状病毒的宿主转换潜力。马属动物(如马和驴)易感染马冠状病毒(ECoV)。随着检测流行率的增加,已经获得了几种 ECoV 基因组序列,可用于分子进化分析,特别是来自美利坚合众国(USA)的序列。迄今为止,尚未进行分析以描述 ECoV 基因组编码区内部的进化。在这里,我们从美国各地出现 ECoV 临床症状的感染马属动物中获得并描述了四个新的 ECoV 基因组序列,并推断了 ECoV 特异性和广泛的分子进化模式。在所分析的四个数据集的两个数据集中,我们发现核衣壳(N)基因内存在宿主内进化的证据,提示准种的发展。我们还在 ECoV 基因组内鉴定了 12 个推定的遗传重组事件,其中 11 个发生在 ORF1ab 内。最后,我们推断并比较了每个主要成员分支的祖先分支上受正选择影响的位点。具体而言,对于从动物传播到人类的两种目前已确定的人类冠状病毒(HCoV)嵌杯病毒(HCoV-OC43 和 HCoV-HKU1),我们发现分别有 42 个和 2 个这样的位点,这可能反映了 HCoV-OC43 更复杂的祖先进化历史,其中涉及几种不同的动物宿主。

重要性

贝塔冠状病毒亚属包含不仅对动物和人类构成健康威胁,而且还从动物宿主跳跃到人类宿主的冠状病毒。马属动物(如马和驴)易感染马冠状病毒(ECoV)。尚无研究系统地检查 ECoV 基因组内的进化模式。我们的研究解决了这一空白,并深入了解了受感染马属动物的 ECoV 宿主内进化。此外,我们确定并报告了两种从动物跳跃到人类的嵌杯病毒(人类冠状病毒 OC43 和 HKU1(分别为 HCoV-OC43 和 HCoV-HKU1))之间自然选择模式的差异,并假设观察到的差异可能是由于每种病毒在跳跃到人类之前在不同的动物宿主中循环。最后,我们为科学界贡献了四个新的高质量 ECoV 基因组。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c79/11542594/10e56f46d1d5/spectrum.00867-24.f006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c79/11542594/c62b29cc40c0/spectrum.00867-24.f001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c79/11542594/8f0c187ed8a6/spectrum.00867-24.f002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c79/11542594/4c2e974267db/spectrum.00867-24.f003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c79/11542594/26798b316125/spectrum.00867-24.f004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c79/11542594/d88efe6a6ced/spectrum.00867-24.f005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c79/11542594/10e56f46d1d5/spectrum.00867-24.f006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c79/11542594/c62b29cc40c0/spectrum.00867-24.f001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c79/11542594/8f0c187ed8a6/spectrum.00867-24.f002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c79/11542594/4c2e974267db/spectrum.00867-24.f003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c79/11542594/26798b316125/spectrum.00867-24.f004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c79/11542594/d88efe6a6ced/spectrum.00867-24.f005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c79/11542594/10e56f46d1d5/spectrum.00867-24.f006.jpg

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