Molecular Mimicry by Bacterial Effector Proteins.

IF 3.5 4区 生物学 Q2 MICROBIOLOGY
Aakar Anshul, Pooja Kumari
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引用次数: 0

Abstract

Microorganisms have developed sophisticated mechanisms to invade the host and evade the host's immune surveillance while exploiting the host's resources for their establishment through co-evolution. Many pathogens employ specialized protein secretion systems to transport virulence factors from the bacterial cytosol into host cells. These bacterial protein secretion systems can generally be categorized into different classes based on their structures, functions, and specificity. Notably, some pathogens have evolved proteins that mimic specific eukaryotic cell proteins, enabling them to manipulate host cellular pathways. This phenomenon is known as molecular mimicry. These proteins either closely resemble eukaryotic proteins or possess domains typically found in eukaryotes but generally absent in prokaryotes. This mimicry allows pathogens to interfere with host functions and facilitate their survival and proliferation within the host. Here, we review the fundamental characteristics of these secretion pathways, delve into the remarkable diversity of effector proteins, and explore the molecular mechanisms by which different pathogens rewire cellular pathways. Additionally, we discuss recent findings on strategies to counteract pathogen mimicry and the insights gained for the discovery of new antimicrobials.

细菌效应蛋白的分子模拟。
微生物已经发展出复杂的机制来入侵宿主并逃避宿主的免疫监视,同时利用宿主的资源通过共同进化来建立自己。许多病原体利用专门的蛋白质分泌系统将毒力因子从细菌细胞质转运到宿主细胞中。这些细菌蛋白分泌系统一般可以根据其结构、功能和特异性分为不同的类别。值得注意的是,一些病原体已经进化出模仿特定真核细胞蛋白质的蛋白质,使它们能够操纵宿主细胞途径。这种现象被称为分子模仿。这些蛋白质要么与真核蛋白质非常相似,要么具有真核生物中通常存在但在原核生物中通常不存在的结构域。这种模仿使病原体能够干扰宿主的功能,促进它们在宿主内的生存和增殖。在此,我们回顾了这些分泌途径的基本特征,深入研究了效应蛋白的显著多样性,并探讨了不同病原体重新连接细胞途径的分子机制。此外,我们讨论了对抗病原体模仿的策略的最新发现以及为发现新的抗菌素所获得的见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Basic Microbiology
Journal of Basic Microbiology 生物-微生物学
CiteScore
6.10
自引率
0.00%
发文量
134
审稿时长
1.8 months
期刊介绍: The Journal of Basic Microbiology (JBM) publishes primary research papers on both procaryotic and eucaryotic microorganisms, including bacteria, archaea, fungi, algae, protozoans, phages, viruses, viroids and prions. Papers published deal with: microbial interactions (pathogenic, mutualistic, environmental), ecology, physiology, genetics and cell biology/development, new methodologies, i.e., new imaging technologies (e.g. video-fluorescence microscopy, modern TEM applications) novel molecular biology methods (e.g. PCR-based gene targeting or cassettes for cloning of GFP constructs).
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