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金黄色葡萄球菌感染中朊病毒蛋白的概述。

An overview of moonlighting proteins in Staphylococcus aureus infection.

机构信息

Department of Biological Sciences, Birla Institute of Technology and Science, BITS-Pilani, K. K. Birla Goa Campus, NH17B, Zuarinagar, Goa, 403726, India.

出版信息

Arch Microbiol. 2021 Mar;203(2):481-498. doi: 10.1007/s00203-020-02071-y. Epub 2020 Oct 13.

Abstract

Staphylococcus aureus is responsible for numerous instances of superficial, toxin-mediated, and invasive infections. The emergence of methicillin-resistant (MRSA), as well as vancomycin-resistant (VRSA) strains of S. aureus, poses a massive threat to human health. The tenacity of S. aureus to acquire resistance against numerous antibiotics in a very short duration makes the effort towards developing new antibiotics almost futile. S. aureus owes its destructive pathogenicity to the plethora of virulent factors it produces among which a majority of them are moonlighting proteins. Moonlighting proteins are the multifunctional proteins in which a single protein, with different oligomeric conformations, perform multiple independent functions in different cell compartments. Peculiarly, proteins involved in key ancestral functions and metabolic pathways typically exhibit moonlighting functions. Pathogens mainly employ those proteins as virulent factors which exhibit high structural conservation towards their host counterparts. Consequentially, the host immune system counteracts these invading bacterial virulent factors with minimal protective action. Additionally, many moonlighting proteins also play multiple roles in various stages of pathogenicity while augmenting the virulence of the bacterium. This has necessitated elaborative studies to be conducted on moonlighting proteins of S. aureus that can serve as drug targets. This review is a small effort towards understanding the role of various moonlighting proteins in the pathogenicity of S. aureus.

摘要

金黄色葡萄球菌可导致多种皮肤浅层感染、毒素介导感染和侵袭性感染。耐甲氧西林金黄色葡萄球菌(MRSA)和万古霉素耐药金黄色葡萄球菌(VRSA)菌株的出现,对人类健康构成了巨大威胁。金黄色葡萄球菌在短时间内对抗生素产生耐药性的顽强性使得开发新抗生素的努力几乎徒劳无功。金黄色葡萄球菌之所以具有极强的破坏性致病性,是因为它产生了大量的毒力因子,其中大多数是兼性蛋白。兼性蛋白是多功能蛋白,其中一种蛋白具有不同的寡聚构象,在不同的细胞区室中执行多个独立的功能。奇怪的是,参与关键祖先功能和代谢途径的蛋白质通常表现出兼性功能。病原体主要利用那些表现出与其宿主对应物高度结构保守性的蛋白质作为毒力因子。因此,宿主免疫系统对这些入侵的细菌毒力因子的反应很小,几乎没有保护作用。此外,许多兼性蛋白在致病性的各个阶段也发挥多种作用,同时增强了细菌的毒力。这就需要对金黄色葡萄球菌的兼性蛋白进行详细的研究,这些蛋白可以作为药物靶点。这篇综述是对理解金黄色葡萄球菌各种兼性蛋白在致病性中的作用的一个小小努力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2773/7551524/e1f214dee7af/203_2020_2071_Fig1_HTML.jpg

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