Molecular Basis of TcdR-Dependent Promoter Activity for Toxin Production by Clostridioides difficile Studied by a Heterologous Reporter System

Author:

Zhang Xinyue12345,Li Jie2456,Chen Chao2456,Liu Ya-Jun2456ORCID,Cui Qiu2456,Hong Wei1,Chen Zhenghong13ORCID,Feng Yingang12456ORCID,Cui Guzhen13ORCID

Affiliation:

1. Key Laboratory of Microbiology and Parasitology of Education Department of Guizhou & Key Laboratory of Medical Molecular Biology of Guizhou Province, Guizhou Medical University, Guiyang 550025, China

2. CAS Key Laboratory of Biofuels, Shandong Provincial Key Laboratory of Synthetic Biology, Shandong Engineering Laboratory of Single Cell Oil, Qingdao Institute of Bioenergy and Bioprocess Technology, Chinese Academy of Sciences, Qingdao 266101, China

3. Joint Laboratory of Helicobacter Pylori and Intestinal Microecology of Affiliated Hospital of Guizhou Medical University, Guiyang 550025, China

4. Shandong Energy Institute, Qingdao 266101, China

5. Qingdao New Energy Shandong Laboratory, Qingdao 266101, China

6. University of Chinese Academy of Sciences, Beijing 100049, China

Abstract

The alternative σ factor TcdR controls the synthesis of two major enterotoxins: TcdA and TcdB in Clostridioides difficile. Four potential TcdR-dependent promoters in the pathogenicity locus of C. difficile showed different activities. In this study, we constructed a heterologous system in Bacillus subtilis to investigate the molecular basis of TcdR-dependent promoter activity. The promoters of the two major enterotoxins showed strong TcdR-dependent activity, while the two putative TcdR-dependent promoters in the upstream region of the tcdR gene did not show detectable activity, suggesting that the autoregulation of TcdR may need other unknown factors involved. Mutation analysis indicated that the divergent -10 region is the key determinant for different activities of the TcdR-dependent promoters. Analysis of the TcdR model predicted by AlphaFold2 suggested that TcdR should be classified into group 4, i.e., extracytoplasmic function, σ70 factors. The results of this study provide the molecular basis of the TcdR-dependent promoter recognition for toxin production. This study also suggests the feasibility of the heterologous system in analyzing σ factor functions and possibly in drug development targeting these factors.

Funder

National Natural Science Foundation of China

Shandong Energy Institute

Qingdao Independent Innovation Major Project

Strategic Priority Research Program of the Chinese Academy of Sciences

Foundation of Key Laboratory of Microbiology and Parasitology of Education Department, Guizhou

Innovation and Entrepreneurship Program for Overseas Talents in Guizhou

Excellent Young Talents Plan of Guizhou Medical University

Publisher

MDPI AG

Subject

Health, Toxicology and Mutagenesis,Toxicology

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