Abstract

Streptococcus pyogenes (Group A Streptococcus; 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.

Highlights

  • Several different types of pathogenic bacteria colonize distinct niches by adhering to host tissues via long filamentous appendages termed pili or fimbriae, which project from the cell surface

  • Combined with epidemiological and evolutionary studies, analyses of the diversity of the genetic organization of the FCT region indicate a relationship of its components with tissue tropism (Bessen, 2016)

  • In consideration of the positional advantage over other MSCRAMMs, primary contact with host molecules and interactions with host cells might be initiated by pili

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Summary

Introduction

Several different types of pathogenic bacteria colonize distinct niches by adhering to host tissues via long filamentous appendages termed pili or fimbriae, which project from the cell surface. Pilus-related genes constitute an operon and encode one major and one or two minor subunits, at least one pilinspecific SrtB or SrtC type sortase, and the FCT-form specific chaperone SipA/LepA (Barnett and Scott, 2002; Barnett et al, 2004; Zähner and Scott, 2008).

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