ToxR represses the synthesis of c-di-GMP in <i>Vibrio parahaemolyticus</i>.

Miaomiao Zhang; Xingfan Xue; Junfang Sun; Qimin WU; Xue LI; Dongsheng Zhou; Bin NI; Renfei LU; Yiquan Zhang

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ToxR represses the synthesis of c-di-GMP in Vibrio parahaemolyticus.

Author: Miaomiao ZHANG ¹ ; Xingfan XUE ¹ ; Junfang SUN ² ; Qimin WU ² ; Xue LI ² ; Dongsheng ZHOU ³ ; Bin NI ¹ ; Renfei LU ² ; Yiquan ZHANG ¹
Author Information

1. School of Medicine, Jiangsu University, Zhenjiang 212013, Jiangsu, China.
2. Department of Clinical Laboratory, Affiliated Nantong Hospital of Nantong University, Nantong 226006, Jiangsu, China.
3. State Key Laboratory of Pathogen and Biosecurity, Beijing Institute of Microbiology and Epidemiology, Beijing 100071, China.
Publication Type:Journal Article
Keywords: ToxR; Vibrio parahaemolyticus; c-di-GMP; transcriptional regulation
MeSH: Vibrio parahaemolyticus/metabolism*; Escherichia coli/metabolism*; Bacterial Proteins/metabolism*; Transcription Factors/genetics*; Gene Expression Regulation, Bacterial
From: Chinese Journal of Biotechnology 2022;38(12):4719-4730
CountryChina
Language:Chinese
Abstract: Vibrio parahaemolyticus, the main pathogen causing seafood related food poisoning worldwide, has strong biofilm formation ability. ToxR is a membrane binding regulatory protein, which has regulatory effect on biofilm formation of V. parahaemolyticus, but the specific mechanism has not been reported. c-di-GMP is an important second messenger in bacteria and is involved in regulating a variety of bacterial behaviors including biofilm formation. In this study, we investigated the regulation of ToxR on c-di-GMP metabolism in V. parahaemolyticus. Intracellular c-di-GMP in the wild type (WT) and toxR mutant (ΔtoxR) strains were extracted by ultrasonication, and the concentrations of c-di-GMP were then determined by enzyme linked immunosorbent assay (ELISA). Three c-di-GMP metabolism-related genes scrA, scrG and vpa0198 were selected as the target genes. Quantitative real-time PCR (q-PCR) was employed to calculate the transcriptional variation of each target gene between WT and ΔtoxR strains. The regulatory DNA region of each target gene was cloned into the pHR309 plasmid harboring a promoterless lacZ gene. The recombinant plasmid was subsequently transferred into WT and ΔtoxR strains to detect the β-galactosidase activity in the cellular extracts. The recombinant lacZ plasmid containing each of the target gene was also transferred into E. coli 100λpir strain harboring the pBAD33 plasmid or the recombinant pBAD33-toxR to test whether ToxR could regulate the expression of the target gene in a heterologous host. The regulatory DNA region of each target gene was amplified by PCR, and the over-expressed His-ToxR was purified. The electrophoretic mobility shift assay (EMSA) was applied to verify whether His-ToxR directly bound to the target promoter region. ELISA results showed that the intracellular c-di-GMP level significantly enhanced in ΔtoxR strain relative to that in WT strain, suggesting that ToxR inhibited the production of c-di-GMP in V. parahaemolyticus. qPCR results showed that the mRNA levels of scrA, scrG and vpa0198 significantly increased in ΔtoxR strain relative to those in WT strain, suggesting that ToxR repressed the transcription of scrA, scrG and vpa0198. lacZ fusion assay showed that ToxR was able to repress the promoter activities of scrA, scrG and vpa0198 in both V. parahaemolyticus and E. coli 100λpir. EMSA results showed that His-ToxR was able to bind to the regulatory DNA regions of scrA and scrG, but not to the regulatory DNA region of vpa0198. In conclusion, ToxR inhibited the production of c-di-GMP in V. parahaemolyticus via directly regulating the transcription of enzyme genes associated with c-di-GMP metabolism, which would be beneficial for V. parahaemolyticus to precisely control bacterial behaviors including biofilm formation.