人冠状病毒:先天免疫反应的激活和拮抗。

IF 8 1区 生物学 Q1 MICROBIOLOGY
Nikhila S Tanneti, Helen A Stillwell, Susan R Weiss
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引用次数: 0

摘要

人类冠状病毒可引起一系列呼吸道疾病,从普通感冒(HCoV-229E、HCoV-NL63、HCoV-OC43和SARS-CoV-2)到致死性肺炎(SARS-CoV、SARS-CoV-2和MERS-CoV)。冠状病毒与宿主先天免疫抗病毒反应的相互作用是疾病结局的重要决定因素。本综述比较了宿主对不同人类冠状病毒的先天反应。本文讨论的宿主抗病毒防御包括鼻上皮对呼吸道病毒的一线防御,先天免疫效应物对病毒感染的早期感知,双链RNA和应激诱导的抗病毒途径,以及保守的冠状病毒非结构蛋白和属特异性辅助蛋白介导的先天免疫应答的病毒拮抗。普通感冒冠状病毒HCoV-229E和-NL63诱导干扰素信号和相关先天免疫途径,SARS-CoV和SARS-CoV-2诱导中等水平的激活,MERS-CoV几乎完全关闭这些途径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Human coronaviruses: activation and antagonism of innate immune responses.

SUMMARYHuman coronaviruses cause a range of respiratory diseases, from the common cold (HCoV-229E, HCoV-NL63, HCoV-OC43, and SARS-CoV-2) to lethal pneumonia (SARS-CoV, SARS-CoV-2, and MERS-CoV). Coronavirus interactions with host innate immune antiviral responses are an important determinant of disease outcome. This review compares the host's innate response to different human coronaviruses. Host antiviral defenses discussed in this review include frontline defenses against respiratory viruses in the nasal epithelium, early sensing of viral infection by innate immune effectors, double-stranded RNA and stress-induced antiviral pathways, and viral antagonism of innate immune responses conferred by conserved coronavirus nonstructural proteins and genus-specific accessory proteins. The common cold coronaviruses HCoV-229E and -NL63 induce robust interferon signaling and related innate immune pathways, SARS-CoV and SARS-CoV-2 induce intermediate levels of activation, and MERS-CoV shuts down these pathways almost completely.

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来源期刊
CiteScore
18.80
自引率
0.80%
发文量
27
期刊介绍: Microbiology and Molecular Biology Reviews (MMBR), a journal that explores the significance and interrelationships of recent discoveries in various microbiology fields, publishes review articles that help both specialists and nonspecialists understand and apply the latest findings in their own research. MMBR covers a wide range of topics in microbiology, including microbial ecology, evolution, parasitology, biotechnology, and immunology. The journal caters to scientists with diverse interests in all areas of microbial science and encompasses viruses, bacteria, archaea, fungi, unicellular eukaryotes, and microbial parasites. MMBR primarily publishes authoritative and critical reviews that push the boundaries of knowledge, appealing to both specialists and generalists. The journal often includes descriptive figures and tables to enhance understanding. Indexed/Abstracted in various databases such as Agricola, BIOSIS Previews, CAB Abstracts, Cambridge Scientific Abstracts, Chemical Abstracts Service, Current Contents- Life Sciences, EMBASE, Food Science and Technology Abstracts, Illustrata, MEDLINE, Science Citation Index Expanded (Web of Science), Summon, and Scopus, among others.
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