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Flagella-mediated secretion of a novel Vibrio cholerae cytotoxin affecting both vertebrate and invertebrate hosts

Using Caenorhabditis elegans as an infection host model for Vibrio cholerae predator interactions, we discovered a bacterial cytotoxin, MakA, whose function as a virulence factor relies on secretion via the flagellum channel in a proton motive force-dependent manner. The MakA protein is expressed fr...

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Autores principales: Dongre, Mitesh, Singh, Bhupender, Aung, Kyaw Min, Larsson, Per, Miftakhova, Regina, Persson, Karina, Askarian, Fatemeh, Johannessen, Mona, von Hofsten, Jonas, Persson, Jenny L., Erhardt, Marc, Tuck, Simon, Uhlin, Bernt Eric, Wai, Sun Nyunt
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6123715/
https://www.ncbi.nlm.nih.gov/pubmed/30271941
http://dx.doi.org/10.1038/s42003-018-0065-z
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author Dongre, Mitesh
Singh, Bhupender
Aung, Kyaw Min
Larsson, Per
Miftakhova, Regina
Persson, Karina
Askarian, Fatemeh
Johannessen, Mona
von Hofsten, Jonas
Persson, Jenny L.
Erhardt, Marc
Tuck, Simon
Uhlin, Bernt Eric
Wai, Sun Nyunt
author_facet Dongre, Mitesh
Singh, Bhupender
Aung, Kyaw Min
Larsson, Per
Miftakhova, Regina
Persson, Karina
Askarian, Fatemeh
Johannessen, Mona
von Hofsten, Jonas
Persson, Jenny L.
Erhardt, Marc
Tuck, Simon
Uhlin, Bernt Eric
Wai, Sun Nyunt
author_sort Dongre, Mitesh
collection PubMed
description Using Caenorhabditis elegans as an infection host model for Vibrio cholerae predator interactions, we discovered a bacterial cytotoxin, MakA, whose function as a virulence factor relies on secretion via the flagellum channel in a proton motive force-dependent manner. The MakA protein is expressed from the polycistronic makDCBA (motility-associated killing factor) operon. Bacteria expressing makDCBA induced dramatic changes in intestinal morphology leading to a defecation defect, starvation and death in C. elegans. The Mak proteins also promoted V. cholerae colonization of the zebrafish gut causing lethal infection. A structural model of purified MakA at 1.9 Å resolution indicated similarities to members of a superfamily of bacterial toxins with unknown biological roles. Our findings reveal an unrecognized role for V. cholerae flagella in cytotoxin export that may contribute both to environmental spread of the bacteria by promoting survival and proliferation in encounters with predators, and to pathophysiological effects during infections.
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spelling pubmed-61237152018-09-28 Flagella-mediated secretion of a novel Vibrio cholerae cytotoxin affecting both vertebrate and invertebrate hosts Dongre, Mitesh Singh, Bhupender Aung, Kyaw Min Larsson, Per Miftakhova, Regina Persson, Karina Askarian, Fatemeh Johannessen, Mona von Hofsten, Jonas Persson, Jenny L. Erhardt, Marc Tuck, Simon Uhlin, Bernt Eric Wai, Sun Nyunt Commun Biol Article Using Caenorhabditis elegans as an infection host model for Vibrio cholerae predator interactions, we discovered a bacterial cytotoxin, MakA, whose function as a virulence factor relies on secretion via the flagellum channel in a proton motive force-dependent manner. The MakA protein is expressed from the polycistronic makDCBA (motility-associated killing factor) operon. Bacteria expressing makDCBA induced dramatic changes in intestinal morphology leading to a defecation defect, starvation and death in C. elegans. The Mak proteins also promoted V. cholerae colonization of the zebrafish gut causing lethal infection. A structural model of purified MakA at 1.9 Å resolution indicated similarities to members of a superfamily of bacterial toxins with unknown biological roles. Our findings reveal an unrecognized role for V. cholerae flagella in cytotoxin export that may contribute both to environmental spread of the bacteria by promoting survival and proliferation in encounters with predators, and to pathophysiological effects during infections. Nature Publishing Group UK 2018-06-07 /pmc/articles/PMC6123715/ /pubmed/30271941 http://dx.doi.org/10.1038/s42003-018-0065-z Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Dongre, Mitesh
Singh, Bhupender
Aung, Kyaw Min
Larsson, Per
Miftakhova, Regina
Persson, Karina
Askarian, Fatemeh
Johannessen, Mona
von Hofsten, Jonas
Persson, Jenny L.
Erhardt, Marc
Tuck, Simon
Uhlin, Bernt Eric
Wai, Sun Nyunt
Flagella-mediated secretion of a novel Vibrio cholerae cytotoxin affecting both vertebrate and invertebrate hosts
title Flagella-mediated secretion of a novel Vibrio cholerae cytotoxin affecting both vertebrate and invertebrate hosts
title_full Flagella-mediated secretion of a novel Vibrio cholerae cytotoxin affecting both vertebrate and invertebrate hosts
title_fullStr Flagella-mediated secretion of a novel Vibrio cholerae cytotoxin affecting both vertebrate and invertebrate hosts
title_full_unstemmed Flagella-mediated secretion of a novel Vibrio cholerae cytotoxin affecting both vertebrate and invertebrate hosts
title_short Flagella-mediated secretion of a novel Vibrio cholerae cytotoxin affecting both vertebrate and invertebrate hosts
title_sort flagella-mediated secretion of a novel vibrio cholerae cytotoxin affecting both vertebrate and invertebrate hosts
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6123715/
https://www.ncbi.nlm.nih.gov/pubmed/30271941
http://dx.doi.org/10.1038/s42003-018-0065-z
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