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奥密克戎亚变种非刺突蛋白中的独特突变:对病毒发病机制和宿主免疫逃逸的潜在影响。

Unique mutations in SARS-CoV-2 Omicron subvariants' non-spike proteins: Potential impacts on viral pathogenesis and host immune evasion.

机构信息

Department of Microbiology, University of Dhaka, Dhaka, 1000, Bangladesh.

Department of Microbiology, Jashore University of Science and Technology, Jashore, 7408, Bangladesh.

出版信息

Microb Pathog. 2022 Sep;170:105699. doi: 10.1016/j.micpath.2022.105699. Epub 2022 Aug 6.

Abstract

SARS-CoV-2 is the causative agent behind the ongoing COVID-19 pandemic. This virus is a cumulative outcome of mutations, leading to frequent emergence of new variants and their subvariants. Some of them are a matter of high concern, while others are variants of interest for studying the mutational effect. The major five variants of concern (VOCs) are Alpha (B.1.1.7), Beta (B.1.315), Gamma (P.1), Delta (B.1.617.2), and Omicron (B.1.1.529./BA.). Omicron itself has >100 subvariants at present, among which BA.1 (21K), BA.2 (21L), BA.4 (22A), BA.5 (22B), and BA.2.12.1 (22C) are the dominant ones. Undoubtedly, these variants and sometimes their progeny subvariants have significant differences in their spike region that impart them the unique properties they harbor. But alongside, the mutations in their non-spike regions could also be responsible elements behind their characteristics, such as replication time, virulence, survival, host immune evasion, and such. There exists a probability that these mutations of non-spike proteins may also impart epistatic effects that are yet to be brought to light. The focus of this review encompasses the non-spike mutations of Omicron, especially in its widely circulating subvariants (BA.1, BA.2, BA.4, BA.5, and BA.2.12.1). The mutations such as in NSP3, NSP6, NSP13, M protein, ORF7b, and ORF9b are mentioned few of all, which might have led to the varying properties, including growth advantages, higher transmission rate, lower infectivity, and most importantly better host immune evasion through natural killer cell inactivation, autophagosome-lysosome fusion prevention, host protein synthesis disruption, and so on. This aspect of Omicron subvariants has not yet been explored. Further study of alteration of expression or interaction profile of these non-spike mutations bearing proteins, if present, can add a great deal of knowledge to the current understanding of the viral properties and thus effective prevention strategies.

摘要

SARS-CoV-2 是导致当前 COVID-19 大流行的病原体。这种病毒是突变的累积结果,导致新变体及其亚变体频繁出现。其中一些变体引起了高度关注,而另一些变体则是研究突变影响的研究对象。主要的五个关切变体 (VOC) 是 Alpha (B.1.1.7)、Beta (B.1.315)、Gamma (P.1)、Delta (B.1.617.2) 和 Omicron (B.1.1.529./BA.)。Omicron 目前本身有超过 100 个亚变体,其中 BA.1 (21K)、BA.2 (21L)、BA.4 (22A)、BA.5 (22B) 和 BA.2.12.1 (22C) 是主要的亚变体。毫无疑问,这些变体及其后代亚变体在其刺突区域存在显著差异,赋予了它们独特的特性。但与此同时,其非刺突区域的突变也可能是其复制时间、毒力、存活、宿主免疫逃避等特性的关键因素。这些非刺突蛋白的突变也可能产生尚未被发现的上位效应。本综述的重点是 Omicron 的非刺突突变,特别是其广泛传播的亚变体 (BA.1、BA.2、BA.4、BA.5 和 BA.2.12.1)。提及了 NSP3、NSP6、NSP13、M 蛋白、ORF7b 和 ORF9b 等突变,这些突变可能导致了不同的特性,包括生长优势、更高的传播率、更低的感染力,以及最重要的是通过自然杀伤细胞失活、自噬体-溶酶体融合预防、宿主蛋白合成中断等更好地逃避宿主免疫。Omicron 亚变体的这一方面尚未得到探索。如果存在这些非刺突突变携带蛋白的表达或相互作用谱的改变的进一步研究,可以为当前对病毒特性的理解和因此有效的预防策略增加大量知识。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8dc3/9356572/297767c7a72f/gr1_lrg.jpg

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