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结构和进化分析显示了艰难梭菌IV型菌毛中独特的稳定策略。

Structural and evolutionary analyses show unique stabilization strategies in the type IV pili of Clostridium difficile.

作者信息

Piepenbrink Kurt H, Maldarelli Grace A, Martinez de la Peña Claudia F, Dingle Tanis C, Mulvey George L, Lee Amanda, von Rosenvinge Erik, Armstrong Glen D, Donnenberg Michael S, Sundberg Eric J

机构信息

Institute of Human Virology, University of Maryland School of Medicine, Baltimore, MD 21201, USA.

Department of Medicine, University of Maryland School of Medicine, Baltimore, MD 21201, USA.

出版信息

Structure. 2015 Feb 3;23(2):385-96. doi: 10.1016/j.str.2014.11.018. Epub 2015 Jan 15.

Abstract

Type IV pili are produced by many pathogenic Gram-negative bacteria and are important for processes as diverse as twitching motility, biofilm formation, cellular adhesion, and horizontal gene transfer. However, many Gram-positive species, including Clostridium difficile, also produce type IV pili. Here, we identify the major subunit of the type IV pili of C. difficile, PilA1, and describe multiple 3D structures of PilA1, demonstrating the diversity found in three strains of C. difficile. We also model the incorporation of both PilA1 and a minor pilin, PilJ, into the pilus fiber. Although PilA1 contains no cysteine residues, and therefore cannot form the disulfide bonds found in all Gram-negative type IV pilins, it adopts unique strategies to achieve a typical pilin fold. The structures of PilA1 and PilJ exhibit similarities with the type IVb pilins from Gram-negative bacteria that suggest that the type IV pili of C. difficile are involved in microcolony formation.

摘要

IV型菌毛由许多致病性革兰氏阴性菌产生,对于诸如颤动运动、生物膜形成、细胞粘附和水平基因转移等多种过程都很重要。然而,许多革兰氏阳性菌,包括艰难梭菌,也会产生IV型菌毛。在此,我们鉴定出艰难梭菌IV型菌毛的主要亚基PilA1,并描述了PilA1的多个三维结构,展示了在三株艰难梭菌中发现的多样性。我们还模拟了PilA1和一个次要菌毛蛋白PilJ掺入菌毛纤维的过程。尽管PilA1不含半胱氨酸残基,因此无法形成在所有革兰氏阴性IV型菌毛蛋白中都存在的二硫键,但它采用独特策略来实现典型的菌毛蛋白折叠。PilA1和PilJ的结构与革兰氏阴性菌的IVb型菌毛蛋白相似,这表明艰难梭菌的IV型菌毛参与微菌落形成。

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