Anti-S-layer monoclonal antibodies impact Clostridioides difficile physiology.
Lise HunaultEmile AuriaPatrick EnglandJulien DeschampsRomain BriandetVanessa KremerBruno IannascoliLéo Vidal-MaisonChunguang GuoLynn MacdonaldSéverine PéchinéCécile Denève-LarrazetBruno DupuyGuy GorochovPierre BruhnsDelphine SterlinPublished in: Gut microbes (2024)
Clostridioides difficile ( C. difficile ), a gram-positive anaerobic and spore-forming bacterium, is the leading cause of nosocomial antibiotic-associated diarrhea in adults which is characterized by high levels of recurrence and mortality. Surface (S)-layer Protein A (SlpA), the most abundantly expressed protein on the bacterial surface, plays a crucial role in the early stages of infection although the nature of its involvement in C. difficile physiology is yet to be fully understood. Anti-S-layer antibodies have been identified in the sera of convalescent patients and have been correlated with improved outcomes of C. difficile infection (CDI). However, the precise mechanisms by which anti-S-layer antibodies confer protection to the host remain unknown. In this study, we report the first monoclonal antibodies (mAbs) targeting the S-layer of reference strain 630. Characterization of these mAbs unraveled important roles for the S-layer protein in growth, toxin secretion, and biofilm formation by C. difficile , with differential and even opposite effects of various anti-SlpA mAbs on these functions. Moreover, one anti-SlpA mAb impaired C. difficile growth and conferred sensitivity to lysozyme-induced lysis. The results of this study show that anti-S-layer antibody responses can be beneficial or harmful for the course of CDI and provide important insights for the development of adequate S-layer-targeting therapeutics.
Keyphrases
- clostridium difficile
- biofilm formation
- end stage renal disease
- pseudomonas aeruginosa
- chronic kidney disease
- staphylococcus aureus
- newly diagnosed
- microbial community
- type diabetes
- binding protein
- candida albicans
- ejection fraction
- amino acid
- protein protein
- wastewater treatment
- oxidative stress
- peritoneal dialysis
- multidrug resistant
- drug resistant
- drug induced
- coronary artery disease
- free survival
- high glucose
- gram negative