Interactions between the AraC/XylS-like transcriptional activator InvF of Salmonella Typhimurium, the RNA polymerase alpha subunit and the chaperone SicA

Salmonella enterica serovar Typhimurium causes gastroenteritis and systemic infections in humans. For this bacterium the expression of a type III secretion system (T3SS) and effector proteins encoded in the Salmonella pathogenicity island-1 (SPI-1), is keystone for the virulence of this bacterium. E...

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Veröffentlicht in:Scientific reports 2024-01, Vol.14 (1), p.156-12, Article 156
Hauptverfasser: Cortés-Avalos, Daniel, Borges Farias, André, Romero-González, Luis E., Lara-Ochoa, Cristina, Villa-Tanaca, Lourdes, García-del Portillo, Francisco, López-Guerrero, Vanessa, Bustamante, Víctor H., Pérez-Rueda, Ernesto, Ibarra, J. Antonio
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Sprache:eng
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Zusammenfassung:Salmonella enterica serovar Typhimurium causes gastroenteritis and systemic infections in humans. For this bacterium the expression of a type III secretion system (T3SS) and effector proteins encoded in the Salmonella pathogenicity island-1 (SPI-1), is keystone for the virulence of this bacterium. Expression of these is controlled by a regulatory cascade starting with the transcriptional regulators HilD, HilC and RtsA that induce the expression of HilA, which then activates expression of the regulator InvF, a transcriptional regulator of the AraC/XylS family. InvF needs to interact with the chaperone SicA to activate transcription of SPI-1 genes including sicA, sopB, sptP, sopE, sopE2 , and STM1239 . InvF very likely acts as a classical activator; however, whether InvF interacts with the RNA polymerase alpha subunit RpoA has not been determined. Results from this study confirm the interaction between InvF with SicA and reveal that both proteins interact with the RNAP alpha subunit. Thus, our study further supports that the InvF/SicA complex acts as a classical activator. Additionally, we showed for the first time an interaction between a chaperone of T3SS effectors (SicA) and the RNAP.
ISSN:2045-2322
2045-2322
DOI:10.1038/s41598-023-50636-w