Your browser doesn't support javascript.
loading
An AraC/XylS Family Transcriptional Regulator Modulates the Oxidative Stress Response of Francisella tularensis.
Marghani, Dina; Ma, Zhuo; Centone, Anthony J; Huang, Weihua; Malik, Meenakshi; Bakshi, Chandra Shekhar.
Afiliação
  • Marghani D; Department of Pathology, Microbiology, and Immunology, New York Medical Collegegrid.260917.b, Valhalla, New York, USA.
  • Ma Z; Department of Basic and Clinical Sciences, Albany College of Pharmacy and Health Sciencesgrid.413555.3, Albany, New York, USA.
  • Centone AJ; Department of Pathology, Microbiology, and Immunology, New York Medical Collegegrid.260917.b, Valhalla, New York, USA.
  • Huang W; Department of Pathology, Microbiology, and Immunology, New York Medical Collegegrid.260917.b, Valhalla, New York, USA.
  • Malik M; Department of Basic and Clinical Sciences, Albany College of Pharmacy and Health Sciencesgrid.413555.3, Albany, New York, USA.
  • Bakshi CS; Department of Pathology, Microbiology, and Immunology, New York Medical Collegegrid.260917.b, Valhalla, New York, USA.
J Bacteriol ; 203(23): e0018521, 2021 11 05.
Article em En | MEDLINE | ID: mdl-34543107
ABSTRACT
Francisella tularensis is a Gram-negative bacterium that causes a fatal human disease known as tularemia. The Centers for Disease Control and Prevention have classified F. tularensis as a category A tier 1 select agent. The virulence mechanisms of Francisella are not entirely understood. Francisella possesses very few transcription regulators, and most of these regulate the expression of genes involved in intracellular survival and virulence. The F. tularensis genome sequence analysis reveals an AraC (FTL_0689) transcriptional regulator homologous to the AraC/XylS family of transcriptional regulators. In Gram-negative bacteria, AraC activates genes required for l-arabinose utilization and catabolism. The role of the FTL_0689 regulator in F. tularensis is not known. In this study, we characterized the role of FTL_0689 in the gene regulation of F. tularensis and investigated its contribution to intracellular survival and virulence. The results demonstrate that FTL_0689 in Francisella is not required for l-arabinose utilization. Instead, FTL_0689 specifically regulates the expression of the oxidative and global stress response, virulence, metabolism, and other key pathways genes required by Francisella when exposed to oxidative stress. The FTL_0689 mutant is attenuated for intramacrophage growth and virulence in mice. Based on the deletion mutant phenotype, FTL_0689 was termed osrR (oxidative stress response regulator). Altogether, this study elucidates the role of the osrR transcriptional regulator in tularemia pathogenesis. IMPORTANCE The virulence mechanisms of category A select agent Francisella tularensis, the causative agent of a fatal human disease known as tularemia, remain largely undefined. The present study investigated the role of a transcriptional regulator and its overall contribution to the oxidative stress resistance of F. tularensis. The results provide an insight into a novel gene regulatory mechanism, especially when Francisella is exposed to oxidative stress conditions. Understanding such Francisella- specific regulatory mechanisms will help identify potential targets for developing effective therapies and vaccines to prevent tularemia.
Assuntos
Palavras-chave

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Regulação Bacteriana da Expressão Gênica / Estresse Oxidativo / Fator de Transcrição AraC / Francisella tularensis Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Revista: J Bacteriol Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Regulação Bacteriana da Expressão Gênica / Estresse Oxidativo / Fator de Transcrição AraC / Francisella tularensis Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Revista: J Bacteriol Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Estados Unidos