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Discovery of a Novel Inner Membrane-Associated Bacterial Structure Related to the Flagellar Type III Secretion System.
Kaplan, Mohammed; Oikonomou, Catherine M; Wood, Cecily R; Chreifi, Georges; Ghosal, Debnath; Dobro, Megan J; Yao, Qing; Pal, Ritesh Ranjan; Baidya, Amit K; Liu, Yuxi; Maggi, Stefano; McDowall, Alasdair W; Ben-Yehuda, Sigal; Rosenshine, Ilan; Briegel, Ariane; Beeby, Morgan; Chang, Yi-Wei; Shaffer, Carrie L; Jensen, Grant J.
Afiliação
  • Kaplan M; Division of Biology and Biological Engineering, California Institute of Technologygrid.20861.3d, Pasadena, California, USA.
  • Oikonomou CM; Division of Biology and Biological Engineering, California Institute of Technologygrid.20861.3d, Pasadena, California, USA.
  • Wood CR; Department of Veterinary Sciences, University of Kentucky College of Agriculture, Lexington, Kentucky, USA.
  • Chreifi G; Division of Biology and Biological Engineering, California Institute of Technologygrid.20861.3d, Pasadena, California, USA.
  • Ghosal D; Division of Medicine, Dentistry and Health Sciences, University of Melbourne, Parkville, Victoria, Australia.
  • Dobro MJ; Hampshire College, Amherst, Massachusetts, USA.
  • Yao Q; Division of Biology and Biological Engineering, California Institute of Technologygrid.20861.3d, Pasadena, California, USA.
  • Pal RR; Department of Microbiology and Molecular Genetics, Institute of Medical Research Israel-Canada, Faculty of Medicine, The Hebrew University of Jerusalem,grid.9619.7 Jerusalem, Israel.
  • Baidya AK; School of Biological Sciences, Indian Association for the Cultivation of Science, Kolkata, West Bengal, India.
  • Liu Y; Department of Microbiology and Molecular Genetics, Institute of Medical Research Israel-Canada, Faculty of Medicine, The Hebrew University of Jerusalem,grid.9619.7 Jerusalem, Israel.
  • Maggi S; Molecular Biophysics Unit, Indian Institute of Science, Bangalore, Karnataka, India.
  • McDowall AW; Division of Biology and Biological Engineering, California Institute of Technologygrid.20861.3d, Pasadena, California, USA.
  • Ben-Yehuda S; Division of Biology and Biological Engineering, California Institute of Technologygrid.20861.3d, Pasadena, California, USA.
  • Rosenshine I; Division of Biology and Biological Engineering, California Institute of Technologygrid.20861.3d, Pasadena, California, USA.
  • Briegel A; Department of Microbiology and Molecular Genetics, Institute of Medical Research Israel-Canada, Faculty of Medicine, The Hebrew University of Jerusalem,grid.9619.7 Jerusalem, Israel.
  • Beeby M; Department of Microbiology and Molecular Genetics, Institute of Medical Research Israel-Canada, Faculty of Medicine, The Hebrew University of Jerusalem,grid.9619.7 Jerusalem, Israel.
  • Chang YW; Leiden Universitygrid.5132.5, Institute of Biology, Leiden, The Netherlands.
  • Shaffer CL; Department of Life Sciences, Imperial College Londongrid.7445.2, South Kensington Campus, London, United Kingdom.
  • Jensen GJ; Department of Biochemistry and Biophysics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, USA.
J Bacteriol ; 204(8): e0014422, 2022 08 16.
Article em En | MEDLINE | ID: mdl-35862756
ABSTRACT
The bacterial flagellar type III secretion system (fT3SS) is a suite of membrane-embedded and cytoplasmic proteins responsible for building the flagellar motility machinery. Homologous nonflagellar (NF-T3SS) proteins form the injectisome machinery that bacteria use to deliver effector proteins into eukaryotic cells, and other family members were recently reported to be involved in the formation of membrane nanotubes. Here, we describe a novel, evolutionarily widespread, hat-shaped structure embedded in the inner membranes of bacteria, of yet-unidentified function, that is present in species containing fT3SS. Mutant analysis suggests a relationship between this novel structure and the fT3SS, but not the NF-T3SS. While the function of this novel structure remains unknown, we hypothesize that either some of the fT3SS proteins assemble within the hat-like structure, perhaps including the fT3SS core complex, or that fT3SS components regulate other proteins that form part of this novel structure. IMPORTANCE The type III secretion system (T3SS) is a fascinating suite of proteins involved in building diverse macromolecular systems, including the bacterial flagellar motility machine, the injectisome machinery that bacteria use to inject effector proteins into host cells, and probably membrane nanotubes which connect bacterial cells. Here, we accidentally discovered a novel inner membrane-associated complex related to the flagellar T3SS. Examining our lab database, which is comprised of more than 40,000 cryo-tomograms of dozens of species, we discovered that this novel structure is both ubiquitous and ancient, being present in highly divergent classes of bacteria. Discovering a novel, widespread structure related to what are among the best-studied molecular machines in bacteria will open new venues for research aiming at understanding the function and evolution of T3SS proteins.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Flagelos / Sistemas de Secreção Tipo III Tipo de estudo: Risk_factors_studies Idioma: En Revista: J Bacteriol Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Flagelos / Sistemas de Secreção Tipo III Tipo de estudo: Risk_factors_studies Idioma: En Revista: J Bacteriol Ano de publicação: 2022 Tipo de documento: Article