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F 特异性亚基对 F 质粒编码的 IV 型分泌系统和 F 菌毛的贡献。

Contributions of F-specific subunits to the F plasmid-encoded type IV secretion system and F pilus.

机构信息

Department of Microbiology and Molecular Genetics, McGovern Medical School, Houston, Texas, USA.

Department of Biochemistry and Biophysics, Texas A&M University, College Station, Texas, USA.

出版信息

Mol Microbiol. 2022 May;117(5):1275-1290. doi: 10.1111/mmi.14908. Epub 2022 Apr 26.

Abstract

F plasmids circulate widely among the Enterobacteriaceae through encoded type IV secretion systems (T4SS s). Assembly of T4SS s and associated F pili requires 10 VirB/VirD4-like Tra subunits and eight or more F-specific subunits. Recently, we presented evidence using in situ cryoelectron tomography (cryoET) that T4SS s undergo structural transitions when activated for pilus production, and that assembled pili are deposited onto alternative basal platforms at the cell surface. Here, we deleted eight conserved F-specific genes from the MOBF12C plasmid pED208 and quantitated effects on plasmid transfer, pilus production by fluorescence microscopy, and elaboration of T4SS structures by in situ cryoET. Mutant phenotypes supported the assignment of F-specific subunits into three functional Classes: (i) TraF, TraH, and TraW are required for all T4SS -associated activities, (ii) TraU, TraN, and TrbC are nonessential but contribute significantly to distinct T4SS functions, and (iii) TrbB is essential for F pilus production but not for plasmid transfer. Equivalent mutations in a phylogenetically distantly related MOB12A F plasmid conferred similar phenotypes and generally supported these Class assignments. We present a new structure-driven model in which F-specific subunits contribute to distinct steps of T4SS assembly or activation to regulate DNA transfer and F pilus dynamics and deposition onto alternative platforms.

摘要

F 质粒通过编码的 IV 型分泌系统 (T4SSs) 在肠杆菌科中广泛传播。T4SSs 和相关的 F 菌毛的组装需要 10 个 VirB/VirD4 样 Tra 亚基和八个或更多的 F 特异性亚基。最近,我们使用原位冷冻电子断层扫描 (cryoET) 提供了证据,表明 T4SSs 在激活菌毛产生时会发生结构转变,并且组装好的菌毛会沉积在细胞表面的替代基底平台上。在这里,我们从 MOBF12C 质粒 pED208 中删除了八个保守的 F 特异性基因,并定量了它们对质粒转移、荧光显微镜下菌毛产生和原位 cryoET 中 T4SS 结构阐明的影响。突变表型支持将 F 特异性亚基分配到三个功能类中:(i) TraF、TraH 和 TraW 是所有 T4SS 相关活性所必需的,(ii) TraU、TraN 和 TrbC 是非必需的,但对不同的 T4SS 功能有重要贡献,(iii) TrbB 是 F 菌毛产生所必需的,但不是质粒转移所必需的。在系统发育上关系较远的 MOB12A F 质粒中的等效突变赋予了类似的表型,并且通常支持这些类别的分配。我们提出了一个新的结构驱动模型,其中 F 特异性亚基有助于 T4SS 组装或激活的不同步骤,以调节 DNA 转移和 F 菌毛的动力学以及沉积到替代平台上。

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