Cargando…
A Type IV Pilus Mediates DNA Binding during Natural Transformation in Streptococcus pneumoniae
Natural genetic transformation is widely distributed in bacteria and generally occurs during a genetically programmed differentiated state called competence. This process promotes genome plasticity and adaptability in Gram-negative and Gram-positive bacteria. Transformation requires the binding and...
Autores principales: | , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2013
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3694846/ https://www.ncbi.nlm.nih.gov/pubmed/23825953 http://dx.doi.org/10.1371/journal.ppat.1003473 |
_version_ | 1782274899487752192 |
---|---|
author | Laurenceau, Raphaël Péhau-Arnaudet, Gérard Baconnais, Sonia Gault, Joseph Malosse, Christian Dujeancourt, Annick Campo, Nathalie Chamot-Rooke, Julia Le Cam, Eric Claverys, Jean-Pierre Fronzes, Rémi |
author_facet | Laurenceau, Raphaël Péhau-Arnaudet, Gérard Baconnais, Sonia Gault, Joseph Malosse, Christian Dujeancourt, Annick Campo, Nathalie Chamot-Rooke, Julia Le Cam, Eric Claverys, Jean-Pierre Fronzes, Rémi |
author_sort | Laurenceau, Raphaël |
collection | PubMed |
description | Natural genetic transformation is widely distributed in bacteria and generally occurs during a genetically programmed differentiated state called competence. This process promotes genome plasticity and adaptability in Gram-negative and Gram-positive bacteria. Transformation requires the binding and internalization of exogenous DNA, the mechanisms of which are unclear. Here, we report the discovery of a transformation pilus at the surface of competent Streptococcus pneumoniae cells. This Type IV-like pilus, which is primarily composed of the ComGC pilin, is required for transformation. We provide evidence that it directly binds DNA and propose that the transformation pilus is the primary DNA receptor on the bacterial cell during transformation in S. pneumoniae. Being a central component of the transformation apparatus, the transformation pilus enables S. pneumoniae, a major Gram-positive human pathogen, to acquire resistance to antibiotics and to escape vaccines through the binding and incorporation of new genetic material. |
format | Online Article Text |
id | pubmed-3694846 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-36948462013-07-03 A Type IV Pilus Mediates DNA Binding during Natural Transformation in Streptococcus pneumoniae Laurenceau, Raphaël Péhau-Arnaudet, Gérard Baconnais, Sonia Gault, Joseph Malosse, Christian Dujeancourt, Annick Campo, Nathalie Chamot-Rooke, Julia Le Cam, Eric Claverys, Jean-Pierre Fronzes, Rémi PLoS Pathog Research Article Natural genetic transformation is widely distributed in bacteria and generally occurs during a genetically programmed differentiated state called competence. This process promotes genome plasticity and adaptability in Gram-negative and Gram-positive bacteria. Transformation requires the binding and internalization of exogenous DNA, the mechanisms of which are unclear. Here, we report the discovery of a transformation pilus at the surface of competent Streptococcus pneumoniae cells. This Type IV-like pilus, which is primarily composed of the ComGC pilin, is required for transformation. We provide evidence that it directly binds DNA and propose that the transformation pilus is the primary DNA receptor on the bacterial cell during transformation in S. pneumoniae. Being a central component of the transformation apparatus, the transformation pilus enables S. pneumoniae, a major Gram-positive human pathogen, to acquire resistance to antibiotics and to escape vaccines through the binding and incorporation of new genetic material. Public Library of Science 2013-06-27 /pmc/articles/PMC3694846/ /pubmed/23825953 http://dx.doi.org/10.1371/journal.ppat.1003473 Text en © 2013 Laurenceau et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Laurenceau, Raphaël Péhau-Arnaudet, Gérard Baconnais, Sonia Gault, Joseph Malosse, Christian Dujeancourt, Annick Campo, Nathalie Chamot-Rooke, Julia Le Cam, Eric Claverys, Jean-Pierre Fronzes, Rémi A Type IV Pilus Mediates DNA Binding during Natural Transformation in Streptococcus pneumoniae |
title | A Type IV Pilus Mediates DNA Binding during Natural Transformation in Streptococcus pneumoniae
|
title_full | A Type IV Pilus Mediates DNA Binding during Natural Transformation in Streptococcus pneumoniae
|
title_fullStr | A Type IV Pilus Mediates DNA Binding during Natural Transformation in Streptococcus pneumoniae
|
title_full_unstemmed | A Type IV Pilus Mediates DNA Binding during Natural Transformation in Streptococcus pneumoniae
|
title_short | A Type IV Pilus Mediates DNA Binding during Natural Transformation in Streptococcus pneumoniae
|
title_sort | type iv pilus mediates dna binding during natural transformation in streptococcus pneumoniae |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3694846/ https://www.ncbi.nlm.nih.gov/pubmed/23825953 http://dx.doi.org/10.1371/journal.ppat.1003473 |
work_keys_str_mv | AT laurenceauraphael atypeivpilusmediatesdnabindingduringnaturaltransformationinstreptococcuspneumoniae AT pehauarnaudetgerard atypeivpilusmediatesdnabindingduringnaturaltransformationinstreptococcuspneumoniae AT baconnaissonia atypeivpilusmediatesdnabindingduringnaturaltransformationinstreptococcuspneumoniae AT gaultjoseph atypeivpilusmediatesdnabindingduringnaturaltransformationinstreptococcuspneumoniae AT malossechristian atypeivpilusmediatesdnabindingduringnaturaltransformationinstreptococcuspneumoniae AT dujeancourtannick atypeivpilusmediatesdnabindingduringnaturaltransformationinstreptococcuspneumoniae AT camponathalie atypeivpilusmediatesdnabindingduringnaturaltransformationinstreptococcuspneumoniae AT chamotrookejulia atypeivpilusmediatesdnabindingduringnaturaltransformationinstreptococcuspneumoniae AT lecameric atypeivpilusmediatesdnabindingduringnaturaltransformationinstreptococcuspneumoniae AT claverysjeanpierre atypeivpilusmediatesdnabindingduringnaturaltransformationinstreptococcuspneumoniae AT fronzesremi atypeivpilusmediatesdnabindingduringnaturaltransformationinstreptococcuspneumoniae AT laurenceauraphael typeivpilusmediatesdnabindingduringnaturaltransformationinstreptococcuspneumoniae AT pehauarnaudetgerard typeivpilusmediatesdnabindingduringnaturaltransformationinstreptococcuspneumoniae AT baconnaissonia typeivpilusmediatesdnabindingduringnaturaltransformationinstreptococcuspneumoniae AT gaultjoseph typeivpilusmediatesdnabindingduringnaturaltransformationinstreptococcuspneumoniae AT malossechristian typeivpilusmediatesdnabindingduringnaturaltransformationinstreptococcuspneumoniae AT dujeancourtannick typeivpilusmediatesdnabindingduringnaturaltransformationinstreptococcuspneumoniae AT camponathalie typeivpilusmediatesdnabindingduringnaturaltransformationinstreptococcuspneumoniae AT chamotrookejulia typeivpilusmediatesdnabindingduringnaturaltransformationinstreptococcuspneumoniae AT lecameric typeivpilusmediatesdnabindingduringnaturaltransformationinstreptococcuspneumoniae AT claverysjeanpierre typeivpilusmediatesdnabindingduringnaturaltransformationinstreptococcuspneumoniae AT fronzesremi typeivpilusmediatesdnabindingduringnaturaltransformationinstreptococcuspneumoniae |