Role of the global regulator Rex in control of NAD + ‐regeneration in Clostridioides (Clostridium) difficile - INRAE - Institut national de recherche pour l’agriculture, l’alimentation et l’environnement Access content directly
Journal Articles Molecular Microbiology Year : 2019

Role of the global regulator Rex in control of NAD + ‐regeneration in Clostridioides (Clostridium) difficile

Abstract

For the human pathogen Clostridioides (also known as Clostridium) difficile, the ability to adapt to nutrient availability is critical for its proliferation and production of toxins during infection. Synthesis of the toxins is regulated by the availability of certain carbon sources, fermentation products and amino acids (e.g. proline, cysteine, isoleucine, leucine and valine). The effect of proline is attributable at least in part to its role as an inducer and substrate of D-proline reductase (PR), a Stickland reaction that regenerates NAD+ from NADH. Many Clostridium spp. use Stickland metabolism (co-fermentation of pairs of amino acids) to generate ATP and NAD+ . Synthesis of PR is activated by PrdR, a proline-responsive regulatory protein. Here we report that PrdR, in the presence of proline, represses other NAD+ -generating pathways, such as the glycine reductase and succinate-acetyl CoA utilization pathways leading to butyrate production, but does so indirectly by affecting the activity of Rex, a global redox-sensing regulator that responds to the NAD+ /NADH ratio. Our results indicate that PR activity is the favored mechanism for NAD+ regeneration and that both Rex and PrdR influence toxin production. Using the hamster model of C. difficile infection, we revealed the importance of PrdR-regulated Stickland metabolism in the virulence of C. difficile.

Dates and versions

pasteur-02438283 , version 1 (14-01-2020)

Identifiers

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Laurent Bouillaut, Thomas Dubois, Michael Francis, Nadine Daou, Marc Monot, et al.. Role of the global regulator Rex in control of NAD + ‐regeneration in Clostridioides (Clostridium) difficile. Molecular Microbiology, 2019, 111 (6), pp.1671-1688. ⟨10.1111/mmi.14245⟩. ⟨pasteur-02438283⟩
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