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Distribution, Function and Regulation of Type 6 Secretion Systems of Xanthomonadales
Members of the Xanthomonadales order include several plant pathogens of significant economic and agricultural impact, such as Xanthomonas spp. Type 6 secretion systems (T6SSs) are contractile nanomachines used by many bacterial species to inject protein effectors into target prokaryotic and eukaryot...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2019
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6653060/ https://www.ncbi.nlm.nih.gov/pubmed/31379785 http://dx.doi.org/10.3389/fmicb.2019.01635 |
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author | Bayer-Santos, Ethel Ceseti, Lucas de Moraes Farah, Chuck Shaker Alvarez-Martinez, Cristina Elisa |
author_facet | Bayer-Santos, Ethel Ceseti, Lucas de Moraes Farah, Chuck Shaker Alvarez-Martinez, Cristina Elisa |
author_sort | Bayer-Santos, Ethel |
collection | PubMed |
description | Members of the Xanthomonadales order include several plant pathogens of significant economic and agricultural impact, such as Xanthomonas spp. Type 6 secretion systems (T6SSs) are contractile nanomachines used by many bacterial species to inject protein effectors into target prokaryotic and eukaryotic cells and provide a competitive advantage for bacteria in different environments. Effectors with antibacterial properties include peptidoglycan hydrolases, lipases and phospholipases that break down structural components of the cell envelope, promoting target-cell lysis; and RNases, DNAses, and NADases that affect target-cell metabolism, arresting growth. Effectors with anti-eukaryotic properties are functionally more diverse. The T6SS of Xanthomonas citri is the only example experimentally characterized so far within the Xanthomonadales order and displays anti-eukaryotic function by providing resistance to predation by amoeba. This T6SS is regulated at the transcriptional level by a signaling cascade involving a Ser/Thr kinase and an extracytoplasmic function (ECF) sigma factor. In this review, we performed in silico analyses of 35 genomes of Xanthomonadales and showed that T6SSs are widely distributed and phylogenetically classified into three major groups. In silico predictions identified a series of proteins with known toxic domains as putative T6SS effectors, suggesting that the T6SSs of Xanthomonadales display both anti-prokaryotic and anti-eukaryotic properties depending on the phylogenetic group and bacterial species. |
format | Online Article Text |
id | pubmed-6653060 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-66530602019-08-02 Distribution, Function and Regulation of Type 6 Secretion Systems of Xanthomonadales Bayer-Santos, Ethel Ceseti, Lucas de Moraes Farah, Chuck Shaker Alvarez-Martinez, Cristina Elisa Front Microbiol Microbiology Members of the Xanthomonadales order include several plant pathogens of significant economic and agricultural impact, such as Xanthomonas spp. Type 6 secretion systems (T6SSs) are contractile nanomachines used by many bacterial species to inject protein effectors into target prokaryotic and eukaryotic cells and provide a competitive advantage for bacteria in different environments. Effectors with antibacterial properties include peptidoglycan hydrolases, lipases and phospholipases that break down structural components of the cell envelope, promoting target-cell lysis; and RNases, DNAses, and NADases that affect target-cell metabolism, arresting growth. Effectors with anti-eukaryotic properties are functionally more diverse. The T6SS of Xanthomonas citri is the only example experimentally characterized so far within the Xanthomonadales order and displays anti-eukaryotic function by providing resistance to predation by amoeba. This T6SS is regulated at the transcriptional level by a signaling cascade involving a Ser/Thr kinase and an extracytoplasmic function (ECF) sigma factor. In this review, we performed in silico analyses of 35 genomes of Xanthomonadales and showed that T6SSs are widely distributed and phylogenetically classified into three major groups. In silico predictions identified a series of proteins with known toxic domains as putative T6SS effectors, suggesting that the T6SSs of Xanthomonadales display both anti-prokaryotic and anti-eukaryotic properties depending on the phylogenetic group and bacterial species. Frontiers Media S.A. 2019-07-17 /pmc/articles/PMC6653060/ /pubmed/31379785 http://dx.doi.org/10.3389/fmicb.2019.01635 Text en Copyright © 2019 Bayer-Santos, Ceseti, Farah and Alvarez-Martinez. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Microbiology Bayer-Santos, Ethel Ceseti, Lucas de Moraes Farah, Chuck Shaker Alvarez-Martinez, Cristina Elisa Distribution, Function and Regulation of Type 6 Secretion Systems of Xanthomonadales |
title | Distribution, Function and Regulation of Type 6 Secretion Systems of Xanthomonadales |
title_full | Distribution, Function and Regulation of Type 6 Secretion Systems of Xanthomonadales |
title_fullStr | Distribution, Function and Regulation of Type 6 Secretion Systems of Xanthomonadales |
title_full_unstemmed | Distribution, Function and Regulation of Type 6 Secretion Systems of Xanthomonadales |
title_short | Distribution, Function and Regulation of Type 6 Secretion Systems of Xanthomonadales |
title_sort | distribution, function and regulation of type 6 secretion systems of xanthomonadales |
topic | Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6653060/ https://www.ncbi.nlm.nih.gov/pubmed/31379785 http://dx.doi.org/10.3389/fmicb.2019.01635 |
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