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Novel Flp pilus biogenesis-dependent natural transformation
Natural transformation has been described in bacterial species spread through nearly all major taxonomic groups. However, the current understanding of the structural components and the regulation of competence development is derived from only a few model organisms. Although natural transformation wa...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4322843/ https://www.ncbi.nlm.nih.gov/pubmed/25713572 http://dx.doi.org/10.3389/fmicb.2015.00084 |
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author | Angelov, Angel Bergen, Paul Nadler, Florian Hornburg, Philipp Lichev, Antoni Übelacker, Maria Pachl, Fiona Kuster, Bernhard Liebl, Wolfgang |
author_facet | Angelov, Angel Bergen, Paul Nadler, Florian Hornburg, Philipp Lichev, Antoni Übelacker, Maria Pachl, Fiona Kuster, Bernhard Liebl, Wolfgang |
author_sort | Angelov, Angel |
collection | PubMed |
description | Natural transformation has been described in bacterial species spread through nearly all major taxonomic groups. However, the current understanding of the structural components and the regulation of competence development is derived from only a few model organisms. Although natural transformation was discovered in members of the Actinobacteria (high GC Gram-positive bacteria) more than four decades ago, the structural components or the regulation of the competence system have not been studied in any representative of the entire phylum. In this report we identify a new role for a distinct type of pilus biogenesis genes (tad genes, for tight adherence), which so far have been connected only with biofilm formation, adherence and virulence traits. The tad-like genes found in the genome of Micrococcus luteus were shown to be required for genetic transformation in this actinobacterial species. We generated and analyzed individual knockout mutants for every open reading frame of the two predicted tad gene clusters as well as for a potential prepilin processing peptidase and identified the major component of the putative pili. By expressing a tagged variant of the major prepilin subunit and immunofluorescence microscopy we visualized filamentous structures extending from the cell surface. Our data indicate that the two tad gene islands complementarily contribute to the formation of a functional competence pilus in this organism. It seems likely that the involvement of tad genes in natural transformation is not unique only for M. luteus but may also prove to be the case in other representatives of the Actinobacteria, which contains important medically and biotechnologically relevant species. |
format | Online Article Text |
id | pubmed-4322843 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-43228432015-02-24 Novel Flp pilus biogenesis-dependent natural transformation Angelov, Angel Bergen, Paul Nadler, Florian Hornburg, Philipp Lichev, Antoni Übelacker, Maria Pachl, Fiona Kuster, Bernhard Liebl, Wolfgang Front Microbiol Microbiology Natural transformation has been described in bacterial species spread through nearly all major taxonomic groups. However, the current understanding of the structural components and the regulation of competence development is derived from only a few model organisms. Although natural transformation was discovered in members of the Actinobacteria (high GC Gram-positive bacteria) more than four decades ago, the structural components or the regulation of the competence system have not been studied in any representative of the entire phylum. In this report we identify a new role for a distinct type of pilus biogenesis genes (tad genes, for tight adherence), which so far have been connected only with biofilm formation, adherence and virulence traits. The tad-like genes found in the genome of Micrococcus luteus were shown to be required for genetic transformation in this actinobacterial species. We generated and analyzed individual knockout mutants for every open reading frame of the two predicted tad gene clusters as well as for a potential prepilin processing peptidase and identified the major component of the putative pili. By expressing a tagged variant of the major prepilin subunit and immunofluorescence microscopy we visualized filamentous structures extending from the cell surface. Our data indicate that the two tad gene islands complementarily contribute to the formation of a functional competence pilus in this organism. It seems likely that the involvement of tad genes in natural transformation is not unique only for M. luteus but may also prove to be the case in other representatives of the Actinobacteria, which contains important medically and biotechnologically relevant species. Frontiers Media S.A. 2015-02-10 /pmc/articles/PMC4322843/ /pubmed/25713572 http://dx.doi.org/10.3389/fmicb.2015.00084 Text en Copyright © 2015 Angelov, Bergen, Nadler, Hornburg, Lichev, Übelacker, Pachl, Kuster and Liebl. 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) or licensor 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 Angelov, Angel Bergen, Paul Nadler, Florian Hornburg, Philipp Lichev, Antoni Übelacker, Maria Pachl, Fiona Kuster, Bernhard Liebl, Wolfgang Novel Flp pilus biogenesis-dependent natural transformation |
title | Novel Flp pilus biogenesis-dependent natural transformation |
title_full | Novel Flp pilus biogenesis-dependent natural transformation |
title_fullStr | Novel Flp pilus biogenesis-dependent natural transformation |
title_full_unstemmed | Novel Flp pilus biogenesis-dependent natural transformation |
title_short | Novel Flp pilus biogenesis-dependent natural transformation |
title_sort | novel flp pilus biogenesis-dependent natural transformation |
topic | Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4322843/ https://www.ncbi.nlm.nih.gov/pubmed/25713572 http://dx.doi.org/10.3389/fmicb.2015.00084 |
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