4.7 Article

Autophagy Proteins Promote Repair of Endosomal Membranes Damaged by the Salmonella Type Three Secretion System 1

Journal

CELL HOST & MICROBE
Volume 18, Issue 5, Pages 527-537

Publisher

CELL PRESS
DOI: 10.1016/j.chom.2015.10.015

Keywords

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Funding

  1. SystemsX.ch
  2. Swiss Initiative in Systems Biology, RTD grants [51RT-0_126008, 51RTP0_151029]
  3. Swiss National Science Foundation [310030_153074/1]
  4. SyBIT
  5. IT project of SystemsX
  6. Institut Pasteur CARNOT-MIE programme
  7. ERC [261166]
  8. Pasteur Foundation
  9. Swiss National Science Foundation (SNF) [310030_153074] Funding Source: Swiss National Science Foundation (SNF)
  10. European Research Council (ERC) [261166] Funding Source: European Research Council (ERC)

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Salmonella Typhimurium (S.Tm) is an enteropathogen requiring multiple virulence factors, including two type three secretion systems (T1 and T2). T1 triggers epithelium invasion in which the bacteria are taken up into endosomes that mature into Salmonella-containing vacuoles (SCV) and trigger T2 induction upon acidification. Mechanisms controlling endosome membrane integrity or pathogen egress into the cytosol are incompletely understood. We screened for host factors affecting invasion and SCV maturation and identified a role for autophagy in sealing endosomal membranes damaged by T1 during host cell invasion. S.Tm-infected autophagy-deficient (atg5(-/-)) cells exhibit reduced SCV dye retention and lower T2 expression but no effects on steps preceding SCV maturation. However, in the absence of T1, autophagy is dispensable for T2 induction. These findings establish a role of autophagy at early stages of S.Tm infection and suggest that autophagy-mediated membrane repair might be generally important for invasive pathogens and endosomal membrane function.

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