T3SS protein EsrC binds to the lacI -like operator of type 1 fimbrial operon to suppress adhesion of Edwardsiella piscicida

Author:

Sun Shan Shan12ORCID,He Tian Tian1,Zhang Shu Ya12,Yu Xiu-Jun3,Chen Chang4,Laghari Zubair Ahmed12,Nie Pin1ORCID,Xie Hai Xia1ORCID

Affiliation:

1. State Key Laboratory of Freshwater Ecology and Biotechnology, Institute of Hydrobiology, Chinese Academy of Sciences, Wuhan, China

2. College of Advanced Agricultural Sciences, University of Chinese Academy of Sciences, Beijing, China

3. MRC Center for Molecular Bacteriology and Infection, Imperial College London, London, United Kingdom

4. Key Laboratory of Tropical Marine Bio-Resources and Ecology, Guangdong Provincial Key Laboratory of Applied Marine Biology, South China Sea Institute of Oceanology, Chinese Academy of Sciences, Guangzhou, China

Abstract

ABSTRACT Type 1 fimbria, the short hair-like appendage assembled on the bacterial surface, plays a pivotal role in adhesion and invasion in Edwardsiella piscicida . The type III secretion system (T3SS), another bacterial surface appendage, facilitates E. piscicida ’s replication in vivo by delivering effectors into host cells. Our previous research demonstrated that E. piscicida T3SS protein EseJ inhibits adhesion and invasion of E. piscicida by suppressing type 1 fimbria. However, how EseJ suppresses type 1 fimbria remains elusive. In this study, a lacI -like operator (nt −245 to −1 of fimA ) upstream of type 1 fimbrial operon in E. piscicida was identified, and EseJ inhibits type 1 fimbria through the lacI -like operator. Moreover, through DNA pull-down and electrophoretic mobility shift assay, an AraC-type T3SS regulator, EsrC, was screened and verified to bind to nt −145 to −126 and nt −50 to −1 of fimA , suppressing type 1 fimbria. EseJ is almost abolished upon the depletion of EsrC. EsrC and EseJ impede type 1 fimbria expression. Intriguingly, nutrition and microbiota-derived indole activate type 1 fimbria through downregulating T3SS, alleviating EsrC or EseJ’s inhibitory effect on lacI -like operator of type 1 fimbrial operon. By this study, it is revealed that upon entering the gastrointestinal tract, rich nutrients and indole downregulate T3SS and thereof upregulate type 1 fimbria, stimulating efficient adhesion and invasion; upon being internalized into epithelium, the limit in indole and nutrition switches on T3SS and thereof switches off type 1 fimbria, facilitating effector delivery to guarantee E. piscicida ’s survival/replication in vivo . IMPORTANCE In this work, we identified the lacI -like operator of type 1 fimbrial operon in E. piscicida , which was suppressed by the repressors-T3SS protein EseJ and EsrC. We unveiled that E. piscicida upregulates type 1 fimbria upon sensing rich nutrition and the microbiota-derived indole, thereof promoting the adhesion of E. piscicida . The increase of indole and nutrition promotes type 1 fimbria by downregulating T3SS. The decrease in EseJ and EsrC alleviates their suppression on type 1 fimbria, and vice versa .

Funder

MOST | National Natural Science Foundation of China

the Key Research and Development Program of Hubei Province

Publisher

American Society for Microbiology

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