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Life on Arginine for Mycoplasma hominis: Clues from Its Minimal Genome and Comparison with Other Human Urogenital Mycoplasmas

Mycoplasma hominis is an opportunistic human mycoplasma. Two other pathogenic human species, M. genitalium and Ureaplasma parvum, reside within the same natural niche as M. hominis: the urogenital tract. These three species have overlapping, but distinct, pathogenic roles. They have minimal genomes...

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Autores principales: Pereyre, Sabine, Sirand-Pugnet, Pascal, Beven, Laure, Charron, Alain, Renaudin, Hélène, Barré, Aurélien, Avenaud, Philippe, Jacob, Daniel, Couloux, Arnaud, Barbe, Valérie, de Daruvar, Antoine, Blanchard, Alain, Bébéar, Cécile
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2751442/
https://www.ncbi.nlm.nih.gov/pubmed/19816563
http://dx.doi.org/10.1371/journal.pgen.1000677
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author Pereyre, Sabine
Sirand-Pugnet, Pascal
Beven, Laure
Charron, Alain
Renaudin, Hélène
Barré, Aurélien
Avenaud, Philippe
Jacob, Daniel
Couloux, Arnaud
Barbe, Valérie
de Daruvar, Antoine
Blanchard, Alain
Bébéar, Cécile
author_facet Pereyre, Sabine
Sirand-Pugnet, Pascal
Beven, Laure
Charron, Alain
Renaudin, Hélène
Barré, Aurélien
Avenaud, Philippe
Jacob, Daniel
Couloux, Arnaud
Barbe, Valérie
de Daruvar, Antoine
Blanchard, Alain
Bébéar, Cécile
author_sort Pereyre, Sabine
collection PubMed
description Mycoplasma hominis is an opportunistic human mycoplasma. Two other pathogenic human species, M. genitalium and Ureaplasma parvum, reside within the same natural niche as M. hominis: the urogenital tract. These three species have overlapping, but distinct, pathogenic roles. They have minimal genomes and, thus, reduced metabolic capabilities characterized by distinct energy-generating pathways. Analysis of the M. hominis PG21 genome sequence revealed that it is the second smallest genome among self-replicating free living organisms (665,445 bp, 537 coding sequences (CDSs)). Five clusters of genes were predicted to have undergone horizontal gene transfer (HGT) between M. hominis and the phylogenetically distant U. parvum species. We reconstructed M. hominis metabolic pathways from the predicted genes, with particular emphasis on energy-generating pathways. The Embden–Meyerhoff–Parnas pathway was incomplete, with a single enzyme absent. We identified the three proteins constituting the arginine dihydrolase pathway. This pathway was found essential to promote growth in vivo. The predicted presence of dimethylarginine dimethylaminohydrolase suggested that arginine catabolism is more complex than initially described. This enzyme may have been acquired by HGT from non-mollicute bacteria. Comparison of the three minimal mollicute genomes showed that 247 CDSs were common to all three genomes, whereas 220 CDSs were specific to M. hominis, 172 CDSs were specific to M. genitalium, and 280 CDSs were specific to U. parvum. Within these species-specific genes, two major sets of genes could be identified: one including genes involved in various energy-generating pathways, depending on the energy source used (glucose, urea, or arginine) and another involved in cytadherence and virulence. Therefore, a minimal mycoplasma cell, not including cytadherence and virulence-related genes, could be envisaged containing a core genome (247 genes), plus a set of genes required for providing energy. For M. hominis, this set would include 247+9 genes, resulting in a theoretical minimal genome of 256 genes.
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spelling pubmed-27514422009-10-09 Life on Arginine for Mycoplasma hominis: Clues from Its Minimal Genome and Comparison with Other Human Urogenital Mycoplasmas Pereyre, Sabine Sirand-Pugnet, Pascal Beven, Laure Charron, Alain Renaudin, Hélène Barré, Aurélien Avenaud, Philippe Jacob, Daniel Couloux, Arnaud Barbe, Valérie de Daruvar, Antoine Blanchard, Alain Bébéar, Cécile PLoS Genet Research Article Mycoplasma hominis is an opportunistic human mycoplasma. Two other pathogenic human species, M. genitalium and Ureaplasma parvum, reside within the same natural niche as M. hominis: the urogenital tract. These three species have overlapping, but distinct, pathogenic roles. They have minimal genomes and, thus, reduced metabolic capabilities characterized by distinct energy-generating pathways. Analysis of the M. hominis PG21 genome sequence revealed that it is the second smallest genome among self-replicating free living organisms (665,445 bp, 537 coding sequences (CDSs)). Five clusters of genes were predicted to have undergone horizontal gene transfer (HGT) between M. hominis and the phylogenetically distant U. parvum species. We reconstructed M. hominis metabolic pathways from the predicted genes, with particular emphasis on energy-generating pathways. The Embden–Meyerhoff–Parnas pathway was incomplete, with a single enzyme absent. We identified the three proteins constituting the arginine dihydrolase pathway. This pathway was found essential to promote growth in vivo. The predicted presence of dimethylarginine dimethylaminohydrolase suggested that arginine catabolism is more complex than initially described. This enzyme may have been acquired by HGT from non-mollicute bacteria. Comparison of the three minimal mollicute genomes showed that 247 CDSs were common to all three genomes, whereas 220 CDSs were specific to M. hominis, 172 CDSs were specific to M. genitalium, and 280 CDSs were specific to U. parvum. Within these species-specific genes, two major sets of genes could be identified: one including genes involved in various energy-generating pathways, depending on the energy source used (glucose, urea, or arginine) and another involved in cytadherence and virulence. Therefore, a minimal mycoplasma cell, not including cytadherence and virulence-related genes, could be envisaged containing a core genome (247 genes), plus a set of genes required for providing energy. For M. hominis, this set would include 247+9 genes, resulting in a theoretical minimal genome of 256 genes. Public Library of Science 2009-10-09 /pmc/articles/PMC2751442/ /pubmed/19816563 http://dx.doi.org/10.1371/journal.pgen.1000677 Text en Pereyre 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
Pereyre, Sabine
Sirand-Pugnet, Pascal
Beven, Laure
Charron, Alain
Renaudin, Hélène
Barré, Aurélien
Avenaud, Philippe
Jacob, Daniel
Couloux, Arnaud
Barbe, Valérie
de Daruvar, Antoine
Blanchard, Alain
Bébéar, Cécile
Life on Arginine for Mycoplasma hominis: Clues from Its Minimal Genome and Comparison with Other Human Urogenital Mycoplasmas
title Life on Arginine for Mycoplasma hominis: Clues from Its Minimal Genome and Comparison with Other Human Urogenital Mycoplasmas
title_full Life on Arginine for Mycoplasma hominis: Clues from Its Minimal Genome and Comparison with Other Human Urogenital Mycoplasmas
title_fullStr Life on Arginine for Mycoplasma hominis: Clues from Its Minimal Genome and Comparison with Other Human Urogenital Mycoplasmas
title_full_unstemmed Life on Arginine for Mycoplasma hominis: Clues from Its Minimal Genome and Comparison with Other Human Urogenital Mycoplasmas
title_short Life on Arginine for Mycoplasma hominis: Clues from Its Minimal Genome and Comparison with Other Human Urogenital Mycoplasmas
title_sort life on arginine for mycoplasma hominis: clues from its minimal genome and comparison with other human urogenital mycoplasmas
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2751442/
https://www.ncbi.nlm.nih.gov/pubmed/19816563
http://dx.doi.org/10.1371/journal.pgen.1000677
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