Koma Takaaki, Adachi Shun, Doi Naoya, Adachi Akio, Nomaguchi Masako
Department of Microbiology, Tokushima University Graduate School of Medical Science, Tokushima, Japan.
Department of Microbiology, Kansai Medical University, Osaka, Japan.
Front Microbiol. 2020 Aug 25;11:2016. doi: 10.3389/fmicb.2020.02016. eCollection 2020.
Human coronaviruses (HCoVs) are of zoonotic origins, and seven distinct HCoVs are currently known to infect humans. While the four seasonal HCoVs appear to be mildly pathogenic and circulate among human populations, the other three designated SARS-CoV, MERS-CoV, and SARS-CoV-2 can cause severe diseases in some cases. The newly identified SARS-CoV-2, a causative virus of COVID-19 that can be deadly, is now spreading worldwide much more efficiently than the other two pathogenic viruses. Despite evident differences in these properties, all HCoVs commonly have an exceptionally large genomic RNA with a rather peculiar gene organization and have the potential to readily alter their biological properties. CoVs are characterized by their biological diversifications, high recombination, and efficient adaptive evolution. We are particularly concerned about the high replication and transmission nature of SARS-CoV-2, which may lead to the emergence of more transmissible and/or pathogenic viruses than ever before. Furthermore, novel variant viruses may appear at any time from the CoV pools actively circulating or persistently being maintained in the animal reservoirs, and from the CoVs in infected human individuals. In this review, we describe knowns of the CoVs and then mention their unknowns to clarify the major issues to be addressed. Genome organizations and sequences of numerous CoVs have been determined, and the viruses are presently classified into separate phylogenetic groups. Functional roles in the viral replication cycle of non-structural and structural proteins are also quite well understood or suggested. In contrast, those in the and replication for various accessory proteins encoded by the variable 3' one-third portion of the CoV genome mostly remain to be determined. Importantly, the genomic sequences/structures closely linked to the high CoV recombination are poorly investigated and elucidated. Also, determinants for adaptation and pathogenicity have not been systematically investigated. We summarize here these research situations. Among conceivable projects, we are especially interested in the underlying molecular mechanism by which the observed CoV diversification is generated. Finally, as virologists, we discuss how we handle the present difficulties and propose possible research directions in the medium or long term.
人类冠状病毒(HCoVs)起源于动物,目前已知有七种不同的HCoV可感染人类。虽然四种季节性HCoV似乎致病性较弱且在人群中传播,但另外三种分别为严重急性呼吸综合征冠状病毒(SARS-CoV)、中东呼吸综合征冠状病毒(MERS-CoV)和严重急性呼吸综合征冠状病毒2(SARS-CoV-2),在某些情况下可导致严重疾病。新发现的SARS-CoV-2是导致 COVID-19的致病病毒,可能致命,目前在全球传播的效率比其他两种致病病毒高得多。尽管这些特性存在明显差异,但所有HCoV通常都有一个异常大的基因组RNA,其基因组织相当奇特,并且有可能轻易改变其生物学特性。冠状病毒的特点是具有生物学多样性、高重组率和高效的适应性进化。我们特别关注SARS-CoV-2的高复制和传播特性,这可能导致出现比以往更具传播性和/或致病性的病毒。此外,新型变异病毒可能随时出现在动物宿主中活跃循环或持续存在的冠状病毒库中,以及受感染人类个体中的冠状病毒中。在这篇综述中,我们描述了冠状病毒的已知情况,然后提及它们的未知情况,以阐明需要解决的主要问题。许多冠状病毒的基因组组织和序列已经确定,目前这些病毒被分为不同的系统发育组。非结构蛋白和结构蛋白在病毒复制周期中的功能作用也得到了很好的理解或推测。相比之下,冠状病毒基因组可变3'三分之一部分编码的各种辅助蛋白在病毒复制和致病中的作用大多仍有待确定。重要的是,与冠状病毒高重组密切相关的基因组序列/结构研究和阐明不足。此外,适应性和致病性的决定因素尚未得到系统研究。我们在此总结这些研究情况。在可设想的项目中,我们特别感兴趣的是观察到的冠状病毒多样化产生的潜在分子机制。最后,作为病毒学家,我们讨论如何应对当前的困难,并提出中长期可能的研究方向。