T3SS chaperone of the CesT family is required for secretion of the anti-sigma factor BtrA in Bordetella pertussis

0578519 - MBÚ 2024 RIV GB eng J - Článek v odborném periodiku
Držmíšek, Jakub - Petráčková, Denisa - Dienstbier, Ana - Čurnová, Ivana - Večerek, Branislav
T3SS chaperone of the CesT family is required for secretion of the anti-sigma factor BtrA in Bordetella pertussis.
Emerging Microbes & Infections. Roč. 12, č. 2 (2023), č. článku 2272638. E-ISSN 2222-1751
Grant CEP: GA ČR(CZ) GA23-05634S
Institucionální podpora: RVO:61388971
Klíčová slova: enteropathogenic escherichia-coli * iii secretion * virulence * system * bronchiseptica * locus * pathogenesis * adaptation * motility * provides * Bordetella pertussis * t3ss * CesT chaperone * anti-sigma factor * biofilm
Obor OECD: Microbiology
Impakt faktor: 13.2, rok: 2022
Způsob publikování: Open access
https://www.tandfonline.com/doi/full/10.1080/22221751.2023.2272638

Bordetella pertussis is a Gram-negative, strictly human re-emerging respiratory pathogen and the causative agent of whooping cough. Similar to other Gram-negative pathogens, B. pertussis produces the type III secretion system, but its role in the pathogenesis of B. pertussis is enigmatic and yet to be elucidated. Here, we combined RNA-seq, LC-MS/MS, and co-immunoprecipitation techniques to identify and characterize the novel CesT family T3SS chaperone BP2265. We show that this chaperone specifically interacts with the secreted T3SS regulator BtrA and represents the first non-flagellar chaperone required for the secretion of an anti-sigma factor. In its absence, secretion but not production of BtrA and most T3SS substrates is severely impaired. It appears that the role of BtrA in regulating T3SS extends beyond its activity as an antagonist of the sigma factor BtrS. Predictions made by artificial intelligence system AlphaFold support the chaperone function of BP2265 towards BtrA and outline the structural basis for the interaction of BtrA with its target BtrS. We propose to rename BP2265 to BtcB for the Bordetella type III chaperone of BtrA.In addition, the absence of the BtcB chaperone results in increased expression of numerous flagellar genes and several virulence genes. While increased production of flagellar proteins and intimin BipA translated into increased biofilm formation by the mutant, enhanced production of virulence factors resulted in increased cytotoxicity towards human macrophages. We hypothesize that these phenotypic traits result indirectly from impaired secretion of BtrA and altered activity of the BtrA/BtrS regulatory node.
Trvalý link: https://hdl.handle.net/11104/0347509