Type IV secretion systems: Advances in structure, function, and activation

被引:147
作者
Costa, Tiago R. D. [1 ]
Harb, Laith [2 ,3 ]
Khara, Pratick [4 ]
Zeng, Lanying [2 ,3 ]
Hu, Bo [4 ]
Christie, Peter J. [4 ]
机构
[1] Imperial Coll London, MRC Ctr Mol Bacteriol & Infect, Dept Life Sci, London, England
[2] Texas A&M Univ, Dept Biochem & Biophys, College Stn, TX 77843 USA
[3] Texas A&M Univ, Ctr Phage Technol, College Stn, TX 77843 USA
[4] UTHlth, Dept Microbiol & Mol Genet, McGovern Med Sch, 6431 Fannin St, Houston, TX 77030 USA
基金
英国惠康基金; 美国国家科学基金会; 英国医学研究理事会;
关键词
conjugation; cryoelectron microscopy; cryoelectron tomography; effector translocation; pilus; AGROBACTERIUM VIRB10; CORE COMPLEX; CONJUGATIVE TRANSFER; COUPLING PROTEINS; TRAFFIC ATPASE; GENE-TRANSFER; LEGIONELLA; DNA; TRANSLOCATION; DOMAIN;
D O I
10.1111/mmi.14670
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Bacterial type IV secretion systems (T4SSs) are a functionally diverse translocation superfamily. They consist mainly of two large subfamilies: (i) conjugation systems that mediate interbacterial DNA transfer and (ii) effector translocators that deliver effector macromolecules into prokaryotic or eukaryotic cells. A few other T4SSs export DNA or proteins to the milieu, or import exogenous DNA. The T4SSs are defined by 6 or 12 conserved "core" subunits that respectively elaborate "minimized" systems in Gram-positive or -negative bacteria. However, many "expanded" T4SSs are built from "core" subunits plus numerous others that are system-specific, which presumptively broadens functional capabilities. Recently, there has been exciting progress in defining T4SS assembly pathways and architectures using a combination of fluorescence and cryoelectron microscopy. This review will highlight advances in our knowledge of structure-function relationships for model Gram-negative bacterial T4SSs, including "minimized" systems resembling the Agrobacterium tumefaciens VirB/VirD4 T4SS and "expanded" systems represented by the Helicobacter pylori Cag, Legionella pneumophila Dot/Icm, and F plasmid-encoded Tra T4SSs. Detailed studies of these model systems are generating new insights, some at atomic resolution, to long-standing questions concerning mechanisms of substrate recruitment, T4SS channel architecture, conjugative pilus assembly, and machine adaptations contributing to T4SS functional versatility.
引用
收藏
页码:436 / 452
页数:17
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