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血凝素亚型特异性与高致病性禽流感病毒起源的机制。

Hemagglutinin Subtype Specificity and Mechanisms of Highly Pathogenic Avian Influenza Virus Genesis.

机构信息

Department of Viroscience, Erasmus Medical Center, 3000 CA Rotterdam, The Netherlands.

Group Imaging and Bioinformatics, Leiden Institute of Advanced Computer Science (LIACS), Leiden University, 2300 RA Leiden, The Netherlands.

出版信息

Viruses. 2022 Jul 19;14(7):1566. doi: 10.3390/v14071566.

Abstract

Highly Pathogenic Avian Influenza Viruses (HPAIVs) arise from low pathogenic precursors following spillover from wild waterfowl into poultry populations. The main virulence determinant of HPAIVs is the presence of a multi-basic cleavage site (MBCS) in the hemagglutinin (HA) glycoprotein. The MBCS allows for HA cleavage and, consequently, activation by ubiquitous proteases, which results in systemic dissemination in terrestrial poultry. Since 1959, 51 independent MBCS acquisition events have been documented, virtually all in HA from the H5 and H7 subtypes. In the present article, data from natural LPAIV to HPAIV conversions and experimental in vitro and in vivo studies were reviewed in order to compile recent advances in understanding HA cleavage efficiency, protease usage, and MBCS acquisition mechanisms. Finally, recent hypotheses that might explain the unique predisposition of the H5 and H7 HA sequences to obtain an MBCS in nature are discussed.

摘要

高致病性禽流感病毒(HPAIVs)源自低致病性前体,通过从野生水禽溢出到家禽种群中而产生。HPAIV 的主要毒力决定因素是血凝素(HA)糖蛋白中存在多碱性切割位点(MBCS)。MBCS 允许 HA 切割,进而被普遍存在的蛋白酶激活,导致陆地家禽中的全身性传播。自 1959 年以来,已经记录了 51 次独立的 MBCS 获得事件,几乎所有事件都发生在 H5 和 H7 亚型的 HA 中。在本文中,回顾了来自自然 LPAIV 到 HPAIV 转化的以及体外和体内实验研究的数据,以总结对 HA 切割效率、蛋白酶使用和 MBCS 获得机制的最新理解进展。最后,讨论了最近的一些假说,这些假说可能解释了 H5 和 H7 HA 序列在自然界中获得 MBCS 的独特倾向性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/133c/9321182/e4423f0cce96/viruses-14-01566-g001.jpg

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