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Multiple factors contribute to bimodal toxin gene expression in Clostridioides ( Clostridium) difficile
Author(s) -
Ransom Eric M.,
Kaus Gabriela M.,
Tran Phuong M.,
Ellermeier Craig D.,
Weiss David S.
Publication year - 2018
Publication title -
molecular microbiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.857
H-Index - 247
eISSN - 1365-2958
pISSN - 0950-382X
DOI - 10.1111/mmi.14107
Subject(s) - biology , clostridium difficile toxin a , toxin , clostridium difficile toxin b , gene expression , gene , clostridium , microbiology and biotechnology , population , clostridium difficile , regulation of gene expression , genetics , bacteria , demography , sociology , antibiotics
Summary Clostridioides (formerly Clostridium ) difficile produces two major toxins, TcdA and TcdB, upon entry into stationary phase. Transcription of tcdA and tcdB requires the specialized sigma factor, σ TcdR , which also directs RNA Polymerase to transcribe tcdR itself. We fused a gene for a red fluorescent protein to the tcdA promoter to study toxin gene expression at the level of individual C. difficile cells. Surprisingly, only a subset of cells became red fluorescent upon entry into stationary phase. Breaking the positive feedback loop that controls σ TcdR production by engineering cells to express tcdR from a tetracycline‐inducible promoter resulted in uniform fluorescence across the population. Experiments with two regulators of tcdR expression, σ D and CodY, revealed neither is required for bimodal toxin gene expression. However, σ D biased cells toward the Toxin‐ON state, while CodY biased cells toward the Toxin‐OFF state. Finally, toxin gene expression was observed in sporulating cells. We conclude that (i) toxin production is regulated by a bistable switch governed by σ TcdR , which only accumulates to high enough levels to trigger toxin gene expression in a subset of cells, and (ii) toxin production and sporulation are not mutually exclusive developmental programs.