| Autor: |
Caulat LC; Institut Pasteur, Université de Paris, CNRS UMR6047, Laboratoire Pathogenèse des Bactéries Anaérobies, Paris, France., Lotoux A; Institut Pasteur, Université de Paris, CNRS UMR6047, Laboratoire Pathogenèse des Bactéries Anaérobies, Paris, France., Martins MC; Instituto de Tecnologia Química e Biológica António Xavier, Universidade Nova de Lisboa, Oeiras, Portugal., Kint N; Institut Pasteur, Université de Paris, CNRS UMR6047, Laboratoire Pathogenèse des Bactéries Anaérobies, Paris, France., Anjou C; Institut Pasteur, Université de Paris, CNRS UMR6047, Laboratoire Pathogenèse des Bactéries Anaérobies, Paris, France., Teixeira M; Instituto de Tecnologia Química e Biológica António Xavier, Universidade Nova de Lisboa, Oeiras, Portugal., Folgosa F; Instituto de Tecnologia Química e Biológica António Xavier, Universidade Nova de Lisboa, Oeiras, Portugal., Morvan C; Institut Pasteur, Université de Paris, CNRS UMR6047, Laboratoire Pathogenèse des Bactéries Anaérobies, Paris, France., Martin-Verstraete I; Institut Pasteur, Université de Paris, CNRS UMR6047, Laboratoire Pathogenèse des Bactéries Anaérobies, Paris, France.; Institut Universitaire de France, Paris, France. |
| Abstrakt: |
Clostridioides difficile , the major cause of antibiotic-associated diarrhea, is a strict anaerobic, sporulating Firmicutes. However, during its infectious cycle, this anaerobe is exposed to low oxygen (O 2 ) tensions, with a longitudinal decreasing gradient along the gastrointestinal tract and a second lateral gradient with higher O 2 tensions in the vicinity of the cells. A plethora of enzymes involved in oxidative stress detoxication has been identified in C. difficile , including four O 2 -reducing enzymes: two flavodiiron proteins (FdpA and FdpF) and two reverse rubrerythrins (revRbr1 and revRbr2). Here, we investigated the role of the four O 2 -reducing enzymes in the tolerance to increasing physiological O 2 tensions and air. The four enzymes have different, yet overlapping, spectra of activity. revRbr2 is specific to low O 2 tensions (<0.4%), FdpA to low and intermediate O 2 tensions (0.4%-1%), revRbr1 has a wider spectrum of activity (0.1%-4%), and finally FdpF is more specific to tensions > 4% and air. These different O 2 ranges of action partly arise from differences in regulation of expression of the genes encoding those enzymes. Indeed, we showed that revrbr2 is under the dual control of σ A and σ B . We also identified a regulator of the Spx family that plays a role in the induction of fdp and revrbr genes upon O 2 exposure. Finally, fdpF is regulated by Rex, a regulator sensing the NADH/NAD + ratio. Our results demonstrate that the multiplicity of O 2 -reducing enzymes of C. difficile is associated with different roles depending on the environmental conditions, stemming from a complex multi-leveled network of regulation.
Importance: The gastrointestinal tract is a hypoxic environment, with the existence of two gradients of O 2 along the gut, one longitudinal anteroposterior decreasing gradient and one proximodistal increasing from the lumen to the epithelial cells. O 2 is a major source of stress for an obligate anaerobe such as the enteropathogen C. difficile . This bacterium possesses a plethora of enzymes capable of scavenging O 2 and reducing it to H 2 O. In this work, we identified the role of the four O 2 -reducing enzymes in the tolerance to the physiological O 2 tensions faced by C. difficile during its infectious cycle. These four enzymes have different spectra of action and protect the vegetative cells over a large range of O 2 tensions. These differences are associated with a distinct regulation of each gene encoding those enzymes. The complex network of regulation is crucial for C. difficile to adapt to the various O 2 tensions encountered during infection.
Competing Interests: The authors declare no conflict of interest. |
