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环二鸟苷酸和VpsR诱导霍乱弧菌II型分泌的表达。

Cyclic Di-GMP and VpsR Induce the Expression of Type II Secretion in Vibrio cholerae.

作者信息

Sloup Rudolph E, Konal Ashley E, Severin Geoffrey B, Korir Michelle L, Bagdasarian Mira M, Bagdasarian Michael, Waters Christopher M

机构信息

Department of Microbiology and Molecular Genetics, Michigan State University, East Lansing, Michigan, USA.

Department of Microbiology and Molecular Genetics, Michigan State University, East Lansing, Michigan, USA

出版信息

J Bacteriol. 2017 Sep 5;199(19). doi: 10.1128/JB.00106-17. Print 2017 Oct 1.

DOI:10.1128/JB.00106-17
PMID:28674069
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5585705/
Abstract

is a human pathogen that alternates between growth in environmental reservoirs and infection of human hosts, causing severe diarrhea. The second messenger cyclic di-GMP (c-di-GMP) mediates this transition by controlling a wide range of functions, such as biofilms, virulence, and motility. Here, we report that c-di-GMP induces expression of the extracellular protein secretion () gene cluster, which encodes the type II secretion system (T2SS) in Analysis of the genes confirmed the presence of two promoters located upstream of , the first gene in the operon, one of which is induced by c-di-GMP. This induction is directly mediated by the c-di-GMP-binding transcriptional activator VpsR. Increased expression of the operon did not impact secretion of extracellular toxin or biofilm formation but did increase expression of the pseudopilin protein EpsG on the cell surface. Type II secretion systems (T2SSs) are the primary molecular machines by which Gram-negative bacteria secrete proteins and protein complexes that are folded and assembled in the periplasm. The substrates of T2SSs include extracellular factors, such as proteases and toxins. Here, we show that the widely conserved second messenger cyclic di-GMP (c-di-GMP) upregulates expression of the genes encoding the T2SS in the pathogen via the c-di-GMP-dependent transcription factor VpsR.

摘要

是一种人类病原体,在环境储库中的生长与人类宿主的感染之间交替,导致严重腹泻。第二信使环二鸟苷酸(c-di-GMP)通过控制多种功能,如生物膜、毒力和运动性,介导这种转变。在这里,我们报告c-di-GMP诱导细胞外蛋白分泌()基因簇的表达,该基因簇在中编码II型分泌系统(T2SS)。对基因的分析证实,在操纵子的第一个基因上游存在两个启动子,其中一个由c-di-GMP诱导。这种诱导直接由c-di-GMP结合转录激活因子VpsR介导。操纵子表达的增加对细胞外毒素的分泌或生物膜形成没有影响,但确实增加了细胞表面假菌毛蛋白EpsG的表达。II型分泌系统(T2SSs)是革兰氏阴性菌分泌在外周质中折叠和组装的蛋白质和蛋白质复合物的主要分子机器。T2SSs的底物包括细胞外因子,如蛋白酶和毒素。在这里,我们表明,广泛保守的第二信使环二鸟苷酸(c-di-GMP)通过c-di-GMP依赖性转录因子VpsR上调病原体中编码T2SS的基因的表达。

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本文引用的文献

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Identification and characterization of VpsR and VpsT binding sites in Vibrio cholerae.霍乱弧菌中VpsR和VpsT结合位点的鉴定与表征
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The Type II secretion system delivers matrix proteins for biofilm formation by Vibrio cholerae.II型分泌系统为霍乱弧菌生物膜形成输送基质蛋白。
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The type II secretion pathway in Vibrio cholerae is characterized by growth phase-dependent expression of exoprotein genes and is positively regulated by σE.霍乱弧菌的 II 型分泌途径的特点是外蛋白基因的表达与生长阶段相关,并且受到 σE 的正向调节。
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Cyclic di-GMP inhibits Vibrio cholerae motility by repressing induction of transcription and inducing extracellular polysaccharide production.环二鸟苷酸通过抑制转录诱导和诱导细胞外多糖产生来抑制霍乱弧菌的运动性。
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The type II secretion system and its ubiquitous lipoprotein substrate, SslE, are required for biofilm formation and virulence of enteropathogenic Escherichia coli.II 型分泌系统及其普遍存在的脂蛋白底物 SslE,是肠致病性大肠杆菌生物膜形成和毒力所必需的。
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