Cargando…

Midcell Recruitment of the DNA Uptake and Virulence Nuclease, EndA, for Pneumococcal Transformation

Genetic transformation, in which cells internalize exogenous DNA and integrate it into their chromosome, is widespread in the bacterial kingdom. It involves a specialized membrane-associated machinery for binding double-stranded (ds) DNA and uptake of single-stranded (ss) fragments. In the human pat...

Descripción completa

Detalles Bibliográficos
Autores principales: Bergé, Matthieu J., Kamgoué, Alain, Martin, Bernard, Polard, Patrice, Campo, Nathalie, Claverys, Jean-Pierre
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3764208/
https://www.ncbi.nlm.nih.gov/pubmed/24039578
http://dx.doi.org/10.1371/journal.ppat.1003596
_version_ 1782283118910111744
author Bergé, Matthieu J.
Kamgoué, Alain
Martin, Bernard
Polard, Patrice
Campo, Nathalie
Claverys, Jean-Pierre
author_facet Bergé, Matthieu J.
Kamgoué, Alain
Martin, Bernard
Polard, Patrice
Campo, Nathalie
Claverys, Jean-Pierre
author_sort Bergé, Matthieu J.
collection PubMed
description Genetic transformation, in which cells internalize exogenous DNA and integrate it into their chromosome, is widespread in the bacterial kingdom. It involves a specialized membrane-associated machinery for binding double-stranded (ds) DNA and uptake of single-stranded (ss) fragments. In the human pathogen Streptococcus pneumoniae, this machinery is specifically assembled at competence. The EndA nuclease, a constitutively expressed virulence factor, is recruited during competence to play the key role of converting dsDNA into ssDNA for uptake. Here we use fluorescence microscopy to show that EndA is uniformly distributed in the membrane of noncompetent cells and relocalizes at midcell during competence. This recruitment requires the dsDNA receptor ComEA. We also show that under ‘static’ binding conditions, i.e., in cells impaired for uptake, EndA and ComEA colocalize at midcell, together with fluorescent end-labelled dsDNA (Cy3-dsDNA). We conclude that midcell clustering of EndA reflects its recruitment to the DNA uptake machinery rather than its sequestration away from this machinery to protect transforming DNA from extensive degradation. In contrast, a fraction of ComEA molecules were located at cell poles post-competence, suggesting the pole as the site of degradation of the dsDNA receptor. In uptake-proficient cells, we used Cy3-dsDNA molecules enabling expression of a GFP fusion upon chromosomal integration to identify transformed cells as GFP producers 60–70 min after initial contact between DNA and competent cells. Recording of images since initial cell-DNA contact allowed us to look back to the uptake period for these transformed cells. Cy3-DNA foci were thus detected at the cell surface 10–11 min post-initial contact, all exclusively found at midcell, strongly suggesting that active uptake of transforming DNA takes place at this position in pneumococci. We discuss how midcell uptake could influence homology search, and the likelihood that midcell uptake is characteristic of cocci and/or the growth phase-dependency of competence.
format Online
Article
Text
id pubmed-3764208
institution National Center for Biotechnology Information
language English
publishDate 2013
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-37642082013-09-13 Midcell Recruitment of the DNA Uptake and Virulence Nuclease, EndA, for Pneumococcal Transformation Bergé, Matthieu J. Kamgoué, Alain Martin, Bernard Polard, Patrice Campo, Nathalie Claverys, Jean-Pierre PLoS Pathog Research Article Genetic transformation, in which cells internalize exogenous DNA and integrate it into their chromosome, is widespread in the bacterial kingdom. It involves a specialized membrane-associated machinery for binding double-stranded (ds) DNA and uptake of single-stranded (ss) fragments. In the human pathogen Streptococcus pneumoniae, this machinery is specifically assembled at competence. The EndA nuclease, a constitutively expressed virulence factor, is recruited during competence to play the key role of converting dsDNA into ssDNA for uptake. Here we use fluorescence microscopy to show that EndA is uniformly distributed in the membrane of noncompetent cells and relocalizes at midcell during competence. This recruitment requires the dsDNA receptor ComEA. We also show that under ‘static’ binding conditions, i.e., in cells impaired for uptake, EndA and ComEA colocalize at midcell, together with fluorescent end-labelled dsDNA (Cy3-dsDNA). We conclude that midcell clustering of EndA reflects its recruitment to the DNA uptake machinery rather than its sequestration away from this machinery to protect transforming DNA from extensive degradation. In contrast, a fraction of ComEA molecules were located at cell poles post-competence, suggesting the pole as the site of degradation of the dsDNA receptor. In uptake-proficient cells, we used Cy3-dsDNA molecules enabling expression of a GFP fusion upon chromosomal integration to identify transformed cells as GFP producers 60–70 min after initial contact between DNA and competent cells. Recording of images since initial cell-DNA contact allowed us to look back to the uptake period for these transformed cells. Cy3-DNA foci were thus detected at the cell surface 10–11 min post-initial contact, all exclusively found at midcell, strongly suggesting that active uptake of transforming DNA takes place at this position in pneumococci. We discuss how midcell uptake could influence homology search, and the likelihood that midcell uptake is characteristic of cocci and/or the growth phase-dependency of competence. Public Library of Science 2013-09-05 /pmc/articles/PMC3764208/ /pubmed/24039578 http://dx.doi.org/10.1371/journal.ppat.1003596 Text en © 2013 Bergé 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
Bergé, Matthieu J.
Kamgoué, Alain
Martin, Bernard
Polard, Patrice
Campo, Nathalie
Claverys, Jean-Pierre
Midcell Recruitment of the DNA Uptake and Virulence Nuclease, EndA, for Pneumococcal Transformation
title Midcell Recruitment of the DNA Uptake and Virulence Nuclease, EndA, for Pneumococcal Transformation
title_full Midcell Recruitment of the DNA Uptake and Virulence Nuclease, EndA, for Pneumococcal Transformation
title_fullStr Midcell Recruitment of the DNA Uptake and Virulence Nuclease, EndA, for Pneumococcal Transformation
title_full_unstemmed Midcell Recruitment of the DNA Uptake and Virulence Nuclease, EndA, for Pneumococcal Transformation
title_short Midcell Recruitment of the DNA Uptake and Virulence Nuclease, EndA, for Pneumococcal Transformation
title_sort midcell recruitment of the dna uptake and virulence nuclease, enda, for pneumococcal transformation
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3764208/
https://www.ncbi.nlm.nih.gov/pubmed/24039578
http://dx.doi.org/10.1371/journal.ppat.1003596
work_keys_str_mv AT bergematthieuj midcellrecruitmentofthednauptakeandvirulencenucleaseendaforpneumococcaltransformation
AT kamgouealain midcellrecruitmentofthednauptakeandvirulencenucleaseendaforpneumococcaltransformation
AT martinbernard midcellrecruitmentofthednauptakeandvirulencenucleaseendaforpneumococcaltransformation
AT polardpatrice midcellrecruitmentofthednauptakeandvirulencenucleaseendaforpneumococcaltransformation
AT camponathalie midcellrecruitmentofthednauptakeandvirulencenucleaseendaforpneumococcaltransformation
AT claverysjeanpierre midcellrecruitmentofthednauptakeandvirulencenucleaseendaforpneumococcaltransformation