20
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: not found

      A type VI secretion-related pathway in Bacteroidetes mediates interbacterial antagonism.

      Read this article at

      ScienceOpenPublisherPMC
      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          Bacteroidetes are a phylum of Gram-negative bacteria abundant in mammalian-associated polymicrobial communities, where they impact digestion, immunity, and resistance to infection. Despite the extensive competition at high cell density that occurs in these settings, cell contact-dependent mechanisms of interbacterial antagonism, such as the type VI secretion system (T6SS), have not been defined in this group of organisms. Herein we report the bioinformatic and functional characterization of a T6SS-like pathway in diverse Bacteroidetes. Using prominent human gut commensal and soil-associated species, we demonstrate that these systems localize dynamically within the cell, export antibacterial proteins, and target competitor bacteria. The Bacteroidetes system is a distinct pathway with marked differences in gene content and high evolutionary divergence from the canonical T6S pathway. Our findings offer a potential molecular explanation for the abundance of Bacteroidetes in polymicrobial environments, the observed stability of Bacteroidetes in healthy humans, and the barrier presented by the microbiota against pathogens.

          Related collections

          Author and article information

          Journal
          Cell Host Microbe
          Cell host & microbe
          1934-6069
          1931-3128
          Aug 13 2014
          : 16
          : 2
          Affiliations
          [1 ] Department of Microbiology, University of Washington, Seattle, WA 98195, USA.
          [2 ] Department of Microbial Pathogenesis and Microbial Diversity Institute, Yale University School of Medicine, New Haven, CT 06536, USA.
          [3 ] Department of Pharmaceutical Sciences, School of Pharmacy, University of Maryland, Baltimore, MD 21201, USA.
          [4 ] Janelia Research Campus, Howard Hughes Medical Institute, Ashburn, VA 20147, USA.
          [5 ] Department of Microbial Pathogenesis and Microbial Diversity Institute, Yale University School of Medicine, New Haven, CT 06536, USA. Electronic address: andrew.goodman@yale.edu.
          [6 ] Department of Microbiology, University of Washington, Seattle, WA 98195, USA. Electronic address: mougous@u.washington.edu.
          Article
          S1931-3128(14)00261-3 NIHMS613784
          10.1016/j.chom.2014.07.007
          4136423
          25070807
          1e3a358a-9b16-40a6-ba02-caebab7b2478
          Copyright © 2014 Elsevier Inc. All rights reserved.
          History

          Comments

          Comment on this article