RopB represses the transcription ofspeBin the absence of SIP in group AStreptococcus

Author:

Chiang-Ni Chuan1234ORCID,Chen Yan-Wen1,Chen Kai-Lin3,Jiang Jian-Xian2,Shi Yong-An2ORCID,Hsu Chih-Yun1,Chen Yi-Ywan M124ORCID,Lai Chih-Ho124,Chiu Cheng-Hsun24

Affiliation:

1. Department of Microbiology and Immunology, College of Medicine, Chang Gung University

2. Graduate Institute of Biomedical Sciences, College of Medicine, Chang Gung University

3. Department of Orthopedic Surgery, Chang Gung Memorial Hospital at Linkou

4. Molecular Infectious Disease Research Center, Chang Gung Memorial Hospital at Linkou

Abstract

RopB is a quorum-sensing regulator that binds to the SpeB-inducing peptide (SIP) under acidic conditions. SIP is known to be degraded by the endopeptidase PepO, whose transcription is repressed by the CovR/CovS two-component regulatory system. Both SIP-bound RopB (RopB-SIP) and SIP-free RopB (apo-RopB) can bind to thespeBpromoter; however, only RopB-SIP activatesspeBtranscription. In this study, we found that the SpeB expression was higher in theropBmutant than in the SIP-inactivated (SIP*) mutant. Furthermore, the deletion ofropBin theSIP* mutant derepressedspeBexpression, suggesting that apo-RopB is a transcriptional repressor ofspeB. Up-regulation of PepO in thecovSmutant degraded SIP, resulting in the down-regulation ofspeB. We demonstrate that deletingropBin thecovSmutant derepressed thespeBexpression, suggesting that thespeBrepression in this mutant was mediated not only by PepO-dependent SIP degradation but also by apo-RopB. These findings reveal a crosstalk between the CovR/CovS and RopB-SIP systems and redefine the role of RopB in regulatingspeBexpression in group AStreptococcus.

Funder

Ministry of Science and Technology, Taiwan

Chang Gung Memorial Hospital, Linkou

Publisher

Life Science Alliance, LLC

Subject

Health, Toxicology and Mutagenesis,Plant Science,Biochemistry, Genetics and Molecular Biology (miscellaneous),Ecology

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