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Mycobacterial ESX-1 secretion system mediates host cell lysis through bacterium contact-dependent gross membrane disruptions.
Conrad, William H; Osman, Morwan M; Shanahan, Jonathan K; Chu, Frances; Takaki, Kevin K; Cameron, James; Hopkinson-Woolley, Digby; Brosch, Roland; Ramakrishnan, Lalita.
Afiliação
  • Conrad WH; Department of Medicine, University of Cambridge, Cambridge CB2 0QH, United Kingdom.
  • Osman MM; Department of Medicine, University of Cambridge, Cambridge CB2 0QH, United Kingdom.
  • Shanahan JK; Molecular and Cellular Biology Graduate Program, University of Washington, Seattle, WA 98105.
  • Chu F; Department of Medicine, University of Cambridge, Cambridge CB2 0QH, United Kingdom.
  • Takaki KK; Wellcome Trust PhD Program in Infection, Immunity, and Inflammation, University of Cambridge, Cambridge CB2 0XY, United Kingdom.
  • Cameron J; Department of Microbiology, University of Washington, Seattle, WA 98105.
  • Hopkinson-Woolley D; Department of Medicine, University of Cambridge, Cambridge CB2 0QH, United Kingdom.
  • Brosch R; Department of Microbiology, University of Washington, Seattle, WA 98105.
  • Ramakrishnan L; Department of Biology, Eton College, Windsor SL4 6DW, United Kingdom.
Proc Natl Acad Sci U S A ; 114(6): 1371-1376, 2017 02 07.
Article em En | MEDLINE | ID: mdl-28119503
ABSTRACT
Mycobacterium tuberculosis and Mycobacterium marinum are thought to exert virulence, in part, through their ability to lyse host cell membranes. The type VII secretion system ESX-1 [6-kDa early secretory antigenic target (ESAT-6) secretion system 1] is required for both virulence and host cell membrane lysis. Both activities are attributed to the pore-forming activity of the ESX-1-secreted substrate ESAT-6 because multiple studies have reported that recombinant ESAT-6 lyses eukaryotic membranes. We too find ESX-1 of M. tuberculosis and M. marinum lyses host cell membranes. However, we find that recombinant ESAT-6 does not lyse cell membranes. The lytic activity previously attributed to ESAT-6 is due to residual detergent in the preparations. We report here that ESX-1-dependent cell membrane lysis is contact dependent and accompanied by gross membrane disruptions rather than discrete pores. ESX-1-mediated lysis is also morphologically distinct from the contact-dependent lysis of other bacterial secretion systems. Our findings suggest redirection of research to understand the mechanism of ESX-1-mediated lysis.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Proteínas de Bactérias / Membrana Eritrocítica / Eritrócitos / Hemólise / Antígenos de Bactérias Limite: Animals / Humans Idioma: En Revista: Proc Natl Acad Sci U S A Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Reino Unido

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Proteínas de Bactérias / Membrana Eritrocítica / Eritrócitos / Hemólise / Antígenos de Bactérias Limite: Animals / Humans Idioma: En Revista: Proc Natl Acad Sci U S A Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Reino Unido