新型马冠状病毒基因组和恩贝科病毒亚属其他成员中的正向选择、基因重组和宿主内进化。

IF 3.7 2区 生物学 Q2 MICROBIOLOGY Microbiology spectrum Pub Date : 2024-11-05 Epub Date: 2024-10-07 DOI:10.1128/spectrum.00867-24
Jordan D Zehr, Sergei L Kosakovsky Pond, Stephen D Shank, Holly McQueary, Jennifer K Grenier, Gary R Whittaker, Michael J Stanhope, Laura B Goodman
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引用次数: 0

摘要

贝特克隆病毒亚属恩贝科病毒中有几例冠状病毒从动物宿主跳转到人类宿主。研究冠状病毒在非人类宿主中的进化因素可能有助于深入了解冠状病毒的宿主转换潜力。马和驴等马科动物容易感染马冠状病毒(ECoVs)。随着检测普及率的提高,一些马冠状病毒基因组序列已可用于分子进化分析,尤其是来自美利坚合众国(美国)的序列。迄今为止,尚未对 ECoV 基因组编码区内的进化特征进行分析。在这里,我们获得并描述了来自美国各地出现ECoV临床症状的受感染马的四个新的ECoV基因组序列,并推断出ECoV特异性和整个Embecovirus的分子进化模式。在分析的四组数据中,我们在其中两组数据中发现了核壳(N)基因内宿主内进化的证据,表明了类种的发展。我们还在ECoV基因组中发现了12个可能的基因重组事件,其中11个发生在ORF1ab中。最后,我们推断并比较了每个主要恩博科病毒成员支系的祖先分支上受到正选择的位点。具体来说,对于目前发现的两种从动物传染给人类的人类冠状病毒(HCoV)恩贝科病毒(HCoV-OC43 和 HCoV-HKU1),我们发现分别有 42 个和 2 个这样的位点,这或许反映了 HCoV-OC43 更复杂的祖先进化史,其中涉及多个不同的动物宿主。重要意义β冠状病毒亚属(Embecovirus)包含的冠状病毒不仅对动物和人类的健康构成威胁,而且还从动物宿主跳跃到人类宿主。马和驴等马科动物容易感染马冠状病毒(ECoV)。目前还没有研究系统地考察过 ECoV 基因组内的进化模式。我们的研究填补了这一空白,并深入了解了受感染马的宿主内ECoV进化情况。此外,我们还发现并报告了两种从动物跃迁到人类的栓状病毒[人类冠状病毒 OC43 和 HKU1(分别为 HCoV-OC43 和 HCoV-HKU1)]之间的自然选择模式差异,并假设所观察到的差异可能是由于每种病毒在跃迁到人类之前在不同的动物宿主中循环所致。最后,我们为科学界贡献了四个新的、高质量的ECoV基因组。
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Positive selection, genetic recombination, and intra-host evolution in novel equine coronavirus genomes and other members of the Embecovirus subgenus.

There are several examples of coronaviruses in the Betacoronavirus subgenus Embecovirus 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 Embecovirus-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 Embecovirus 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 Embecovirus 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.

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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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