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The twin arginine protein transport pathway exports multiple virulence proteins in the plant pathogen Streptomyces scabies
Authors:Madhumita V. Joshi  Stefan G. Mann  Haike Antelmann  David A. Widdick  Joanna K. Fyans  Govind Chandra  Matthew I. Hutchings  Ian Toth  Michael Hecker  Rosemary Loria  Tracy Palmer
Affiliation:1. Department of Plant Pathology and Plant‐Microbe Biology, Cornell University, Ithaca, NY 14853, USA.;2. Department of Molecular Microbiology, John Innes Centre, Norwich NR4 7UH, UK.;3. Institute for Microbiology, Ernst‐Moritz‐Arndt‐University of Greifswald, D‐17487 Greifswald, Germany.;4. Division of Molecular Microbiology, College of Life Sciences, University of Dundee, Dundee DD1 5EH, UK.;5. School of Biological Sciences, University of East Anglia, Norwich Research Park, Norwich, NR4 7TJ, UK.;6. Scottish Crop Research Institute, Invergowrie, Dundee, DD2 5DA, UK.
Abstract:Streptomyces scabies is one of a group of organisms that causes the economically important disease potato scab. Analysis of the S. scabies genome sequence indicates that it is likely to secrete many proteins via the twin arginine protein transport (Tat) pathway, including several proteins whose coding sequences may have been acquired through horizontal gene transfer and share a common ancestor with proteins in other plant pathogens. Inactivation of the S. scabies Tat pathway resulted in pleiotropic phenotypes including slower growth rate and increased permeability of the cell envelope. Comparison of the extracellular proteome of the wild type and ΔtatC strains identified 73 predicted secretory proteins that were present in reduced amounts in the tatC mutant strain, and 47 Tat substrates were verified using a Tat reporter assay. The ΔtatC strain was almost completely avirulent on Arabidopsis seedlings and was delayed in attaching to the root tip relative to the wild‐type strain. Genes encoding 14 candidate Tat substrates were individually inactivated, and seven of these mutants were reduced in virulence compared with the wild‐type strain. We conclude that the Tat pathway secretes multiple proteins that are required for full virulence.
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