Nakata Masanobu, Kreikemeyer Bernd
Department of Oral Microbiology, Graduate School of Medical and Dental Sciences, Kagoshima University, Kagoshima, Japan.
Institute of Medical Microbiology, Virology and Hygiene, University of Rostock, Rostock, Germany.
Front Microbiol. 2021 Feb 9;12:616508. doi: 10.3389/fmicb.2021.616508. eCollection 2021.
(Group A ; GAS) is an exclusively human pathogen. This bacterial species is responsible for a large variety of infections, ranging from purulent but mostly self-limiting oropharynx/skin diseases to streptococcal sequelae, including glomerulonephritis and rheumatic fever, as well as life-threatening streptococcal toxic-shock syndrome. GAS displays a wide array of surface proteins, with antigenicity of the M protein and pili utilized for M- and T-serotyping, respectively. Since the discovery of GAS pili in 2005, their genetic features, including regulation of expression, and structural features, including assembly mechanisms and protein conformation, as well as their functional role in GAS pathogenesis have been intensively examined. Moreover, their potential as vaccine antigens has been studied in detail. Pilus biogenesis-related genes are located in a discrete section of the GAS genome encoding fibronectin and collagen binding proteins and trypsin-resistant antigens (FCT region). Based on the heterogeneity of genetic composition and DNA sequences, this region is currently classified into nine distinguishable forms. Pili and fibronectin-binding proteins encoded in the FCT region are known to be correlated with infection sites, such as the skin and throat, possibly contributing to tissue tropism. As also found for pili of other Gram-positive bacterial pathogens, GAS pilin proteins polymerize via isopeptide bonds, while intramolecular isopeptide bonds present in the pilin provide increased resistance to degradation by proteases. As supported by findings showing that the main subunit is primarily responsible for T-serotyping antigenicity, pilus functions and gene expression modes are divergent. GAS pili serve as adhesins for tonsillar tissues and keratinocyte cell lines. Of note, a minor subunit is considered to have a harpoon function by which covalent thioester bonds with host ligands are formed. Additionally, GAS pili participate in biofilm formation and evasion of the immune system in a serotype/strain-specific manner. These multiple functions highlight crucial roles of pili during the onset of GAS infection. This review summarizes the current state of the art regarding GAS pili, including a new mode of host-GAS interaction mediated by pili, along with insights into pilus expression in terms of tissue tropism.
A组链球菌(GAS)是一种专性人类病原体。该细菌物种可引发多种感染,从化脓性但大多为自限性的口咽/皮肤疾病到链球菌后遗症,包括肾小球肾炎和风湿热,以及危及生命的链球菌中毒性休克综合征。GAS表现出多种表面蛋白,M蛋白和菌毛的抗原性分别用于M分型和T分型。自2005年发现GAS菌毛以来,对其遗传特征(包括表达调控)、结构特征(包括组装机制和蛋白质构象)以及它们在GAS致病机制中的功能作用进行了深入研究。此外,还对它们作为疫苗抗原的潜力进行了详细研究。菌毛生物合成相关基因位于GAS基因组中编码纤连蛋白、胶原蛋白结合蛋白和抗胰蛋白酶抗原的离散区域(FCT区域)。基于遗传组成和DNA序列的异质性,该区域目前分为九种可区分的形式。已知FCT区域编码的菌毛和纤连蛋白结合蛋白与感染部位(如皮肤和喉咙)相关,可能有助于组织嗜性。正如在其他革兰氏阳性细菌病原体的菌毛中也发现的那样,GAS菌毛蛋白通过异肽键聚合,而菌毛蛋白中存在的分子内异肽键可增强对蛋白酶降解的抵抗力。有研究结果表明主要亚基主要负责T分型抗原性,菌毛功能和基因表达模式存在差异。GAS菌毛作为扁桃体组织和角质形成细胞系的黏附素。值得注意的是,一个小亚基被认为具有鱼叉功能,通过该功能可与宿主配体形成共价硫酯键。此外,GAS菌毛以血清型/菌株特异性方式参与生物膜形成和免疫系统逃避。这些多种功能突出了菌毛在GAS感染发病过程中的关键作用。本综述总结了关于GAS菌毛的当前研究现状,包括由菌毛介导的宿主与GAS相互作用新模式,以及对菌毛在组织嗜性方面表达的见解。