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副溶血性弧菌中毒力基因及与生物膜形成相关操纵子的转录调控

Transcriptional regulation of the virulence genes and the biofilm formation associated operons in Vibrio parahaemolyticus.

作者信息

Zhang Yiquan, Qiu Yue, Xue Xingfan, Zhang Miaomiao, Sun Junfang, Li Xue, Hu Lingfei, Yin Zhe, Yang Wenhui, Lu Renfei, Zhou Dongsheng

机构信息

Wuxi School of Medicine, Jiangnan University, Wuxi, 214122, Jiangsu, China.

School of Medicine, Jiangsu University, Zhenjiang, 212013, Jiangsu, China.

出版信息

Gut Pathog. 2021 Mar 2;13(1):15. doi: 10.1186/s13099-021-00410-y.

Abstract

BACKGROUND

The membrane fusion protein (mfp) gene locus of Vibrio parahaemolyticus consists of two operons, cpsQ-mfpABC and mfpABC, which are both required for biofilm formation. ToxR and CalR are required for the full virulence of V. parahaemolyticus, and their mutual regulation has been demonstrated. Moreover, cell density-dependent expression of toxR was previously observed in V. parahaemolyticus, but details about the related mechanisms remained unclear. QsvR can work with the master quorum sensing (QS) regulators AphA and OpaR to regulate virulence expression and biofilm formation.

RESULTS

In the present work, we showed that QsvR bound to the promoter-proximal DNA regions of toxR and calR to repress their transcription as well as occupying the regulatory regions of cpsQ-mfpABC and mfpABC to activate their transcription. Thus, we reconstructed the QsvR-dependent promoter organization of toxR, calR, cpsQ-mfpABC, and mfpABC.

CONCLUSION

QsvR directly repressed toxR and calR transcription as well as directly activated cpsQ-mfpABC and mfpABC transcription. The data presented here promotes us to gain deeper knowledge of the regulatory network of the mfp locus in V. parahaemolyticus.

摘要

背景

副溶血性弧菌的膜融合蛋白(mfp)基因座由两个操纵子cpsQ-mfpABC和mfpABC组成,这两个操纵子对于生物膜形成都是必需的。ToxR和CalR对于副溶血性弧菌的完全毒力是必需的,并且它们之间的相互调节已经得到证实。此外,先前在副溶血性弧菌中观察到toxR的细胞密度依赖性表达,但其相关机制的细节仍不清楚。QsvR可以与群体感应(QS)主调节因子AphA和OpaR共同作用,以调节毒力表达和生物膜形成。

结果

在本研究中,我们表明QsvR与toxR和calR的启动子近端DNA区域结合以抑制它们的转录,同时占据cpsQ-mfpABC和mfpABC的调节区域以激活它们的转录。因此,我们重建了toxR、calR、cpsQ-mfpABC和mfpABC的QsvR依赖性启动子组织。

结论

QsvR直接抑制toxR和calR的转录,并直接激活cpsQ-mfpABC和mfpABC的转录。本文提供的数据促使我们对副溶血性弧菌中mfp基因座的调控网络有更深入的了解。

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