Helicobacter macacaeMazF interplays with Escherichia coli homologs and enhances antibiotic tolerance

Author:

Zeng Xi12,Hu Limiao1,Ai Qi1,Liu Cai‐Juan1,Xiong Lu‐Xi1,Yang Wei‐Wei1,Zhang Xiaotuan3,Liu Logen45ORCID,Li Guo‐Qing15ORCID

Affiliation:

1. Department of Gastroenterology, The Second Affiliated Hospital, Hengyang Medical School University of South China Hengyang China

2. Department of Gastroenterology The First Affiliated Hospital of Shaoyang University Shaoyang China

3. Department of Clinical Laboratory The First Affiliated Hospital of Wenzhou Medical University Wenzhou China

4. Clinical Research Center, The Second Affiliated Hospital, Hengyang Medical School University of South China Hengyang China

5. Hunan Provincial Key Laboratory of Basic and Clinical Pharmacological Research on Gastrointestinal Tumors University of South China Hengyang China

Abstract

AbstractBackgroundToxin‐antitoxin systems are highly variable, even among strains of the same bacterial species. The MazEF toxin‐antitoxin system is found in many bacteria and plays important roles in various biological processes such as antibiotic tolerance and phage defense. However, no interplay of MazEF systems between different species was reported.Materials and MethodsMazEF toxin‐antitoxin system of Helicobacter macacae was examined in three Escherichia coli strains with and without endogenous MazEF knockout. In vivo toxicity, antibiotic tolerance, and live/dead staining followed by flowcytometry analysis were performed to evaluate the functionality and interplay of the toxin‐antitoxin system between the two species.ResultsControlled ectopic expression of MazF of H. macacae (MazFhm) in E. coli did not affect its growth. However, in endogenous MazEF knockout E. coli strains, MazFhm expression caused a sharp growth arrest. The toxicity of MazFhm could be neutralized by both the antitoxin of MazE homolog of H.macacae and the antitoxin of MazE of E. coli, indicating interplay of MazEF toxin‐antitoxin systems between the two species. Induced expression of MazFhm enhanced tolerance to a lethal dose of levofloxacin, suggesting enhanced persister formation, which was further confirmed by live/dead cell staining.ConclusionsThe MazEF toxin‐antitoxin system of H. macace enhances persister formation and thus antibiotic tolerance in E. coli. Our findings reveal an interplay between the MazEF systems of H. macacae and E. coli, emphasizing the need to consider this interaction while evaluating the toxicity and functionality of MazF homologs from different species in future studies.

Funder

Natural Science Foundation of Hunan Province

Publisher

Wiley

Subject

Infectious Diseases,Gastroenterology,General Medicine

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