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The metabolic enzyme fructose-1,6-bisphosphate aldolase acts as a transcriptional regulator in pathogenic Francisella.
Ziveri, Jason; Tros, Fabiola; Guerrera, Ida Chiara; Chhuon, Cerina; Audry, Mathilde; Dupuis, Marion; Barel, Monique; Korniotis, Sarantis; Fillatreau, Simon; Gales, Lara; Cahoreau, Edern; Charbit, Alain.
Afiliação
  • Ziveri J; Université Paris Descartes, Sorbonne Paris Cité, Bâtiment Leriche, Paris, 75993, France.
  • Tros F; INSERM U1151 - CNRS UMR 8253, Institut Necker-Enfants Malades, Team 11: Pathogenesis of Systemic Infections, Paris, 75993, France.
  • Guerrera IC; Université Paris Descartes, Sorbonne Paris Cité, Bâtiment Leriche, Paris, 75993, France.
  • Chhuon C; INSERM U1151 - CNRS UMR 8253, Institut Necker-Enfants Malades, Team 11: Pathogenesis of Systemic Infections, Paris, 75993, France.
  • Audry M; Université Paris Descartes, Sorbonne Paris Cité, Bâtiment Leriche, Paris, 75993, France.
  • Dupuis M; Plateforme Protéomique 3P5-Necker, Structure Fédérative de Recherche Necker and Université Paris Descartes, INSERM US24/CNRS UMS3633, Paris, 75993, France.
  • Barel M; Université Paris Descartes, Sorbonne Paris Cité, Bâtiment Leriche, Paris, 75993, France.
  • Korniotis S; Plateforme Protéomique 3P5-Necker, Structure Fédérative de Recherche Necker and Université Paris Descartes, INSERM US24/CNRS UMS3633, Paris, 75993, France.
  • Fillatreau S; Université Paris Descartes, Sorbonne Paris Cité, Bâtiment Leriche, Paris, 75993, France.
  • Gales L; INSERM U1151 - CNRS UMR 8253, Institut Necker-Enfants Malades, Team 11: Pathogenesis of Systemic Infections, Paris, 75993, France.
  • Cahoreau E; Université Paris Descartes, Sorbonne Paris Cité, Bâtiment Leriche, Paris, 75993, France.
  • Charbit A; INSERM U1151 - CNRS UMR 8253, Institut Necker-Enfants Malades, Team 11: Pathogenesis of Systemic Infections, Paris, 75993, France.
Nat Commun ; 8(1): 853, 2017 10 11.
Article em En | MEDLINE | ID: mdl-29021545
ABSTRACT
The enzyme fructose-bisphosphate aldolase occupies a central position in glycolysis and gluconeogenesis pathways. Beyond its housekeeping role in metabolism, fructose-bisphosphate aldolase has been involved in additional functions and is considered as a potential target for drug development against pathogenic bacteria. Here, we address the role of fructose-bisphosphate aldolase in the bacterial pathogen Francisella novicida. We demonstrate that fructose-bisphosphate aldolase is important for bacterial multiplication in macrophages in the presence of gluconeogenic substrates. In addition, we unravel a direct role of this metabolic enzyme in transcription regulation of genes katG and rpoA, encoding catalase and an RNA polymerase subunit, respectively. We propose a model in which fructose-bisphosphate aldolase participates in the control of host redox homeostasis and the inflammatory immune response.The enzyme fructose-bisphosphate aldolase (FBA) plays central roles in glycolysis and gluconeogenesis. Here, Ziveri et al. show that FBA of the pathogen Francisella novicida acts, in addition, as a transcriptional regulator and is important for bacterial multiplication in macrophages.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Regulação Bacteriana da Expressão Gênica / Francisella tularensis / Frutose-Bifosfato Aldolase Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Regulação Bacteriana da Expressão Gênica / Francisella tularensis / Frutose-Bifosfato Aldolase Idioma: En Ano de publicação: 2017 Tipo de documento: Article