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Comparative genomic and proteomic analyses of two Mycoplasma agalactiae strains: clues to the macro- and micro-events that are shaping mycoplasma diversity

BACKGROUND: While the genomic era is accumulating a tremendous amount of data, the question of how genomics can describe a bacterial species remains to be fully addressed. The recent sequencing of the genome of the Mycoplasma agalactiae type strain has challenged our general view on mycoplasmas by s...

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Autores principales: Nouvel, Laurent X, Sirand-Pugnet, Pascal, Marenda, Marc S, Sagné, Eveline, Barbe, Valérie, Mangenot, Sophie, Schenowitz, Chantal, Jacob, Daniel, Barré, Aurélien, Claverol, Stéphane, Blanchard, Alain, Citti, Christine
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2824730/
https://www.ncbi.nlm.nih.gov/pubmed/20122262
http://dx.doi.org/10.1186/1471-2164-11-86
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author Nouvel, Laurent X
Sirand-Pugnet, Pascal
Marenda, Marc S
Sagné, Eveline
Barbe, Valérie
Mangenot, Sophie
Schenowitz, Chantal
Jacob, Daniel
Barré, Aurélien
Claverol, Stéphane
Blanchard, Alain
Citti, Christine
author_facet Nouvel, Laurent X
Sirand-Pugnet, Pascal
Marenda, Marc S
Sagné, Eveline
Barbe, Valérie
Mangenot, Sophie
Schenowitz, Chantal
Jacob, Daniel
Barré, Aurélien
Claverol, Stéphane
Blanchard, Alain
Citti, Christine
author_sort Nouvel, Laurent X
collection PubMed
description BACKGROUND: While the genomic era is accumulating a tremendous amount of data, the question of how genomics can describe a bacterial species remains to be fully addressed. The recent sequencing of the genome of the Mycoplasma agalactiae type strain has challenged our general view on mycoplasmas by suggesting that these simple bacteria are able to exchange significant amount of genetic material via horizontal gene transfer. Yet, events that are shaping mycoplasma genomes and that are underlining diversity within this species have to be fully evaluated. For this purpose, we compared two strains that are representative of the genetic spectrum encountered in this species: the type strain PG2 which genome is already available and a field strain, 5632, which was fully sequenced and annotated in this study. RESULTS: The two genomes differ by ca. 130 kbp with that of 5632 being the largest (1006 kbp). The make up of this additional genetic material mainly corresponds (i) to mobile genetic elements and (ii) to expanded repertoire of gene families that encode putative surface proteins and display features of highly-variable systems. More specifically, three entire copies of a previously described integrative conjugative element are found in 5632 that accounts for ca. 80 kbp. Other mobile genetic elements, found in 5632 but not in PG2, are the more classical insertion sequences which are related to those found in two other ruminant pathogens, M. bovis and M. mycoides subsp. mycoides SC. In 5632, repertoires of gene families encoding surface proteins are larger due to gene duplication. Comparative proteomic analyses of the two strains indicate that the additional coding capacity of 5632 affects the overall architecture of the surface and suggests the occurrence of new phase variable systems based on single nucleotide polymorphisms. CONCLUSION: Overall, comparative analyses of two M. agalactiae strains revealed a very dynamic genome which structure has been shaped by gene flow among ruminant mycoplasmas and expansion-reduction of gene repertoires encoding surface proteins, the expression of which is driven by localized genetic micro-events.
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spelling pubmed-28247302010-02-20 Comparative genomic and proteomic analyses of two Mycoplasma agalactiae strains: clues to the macro- and micro-events that are shaping mycoplasma diversity Nouvel, Laurent X Sirand-Pugnet, Pascal Marenda, Marc S Sagné, Eveline Barbe, Valérie Mangenot, Sophie Schenowitz, Chantal Jacob, Daniel Barré, Aurélien Claverol, Stéphane Blanchard, Alain Citti, Christine BMC Genomics Research Article BACKGROUND: While the genomic era is accumulating a tremendous amount of data, the question of how genomics can describe a bacterial species remains to be fully addressed. The recent sequencing of the genome of the Mycoplasma agalactiae type strain has challenged our general view on mycoplasmas by suggesting that these simple bacteria are able to exchange significant amount of genetic material via horizontal gene transfer. Yet, events that are shaping mycoplasma genomes and that are underlining diversity within this species have to be fully evaluated. For this purpose, we compared two strains that are representative of the genetic spectrum encountered in this species: the type strain PG2 which genome is already available and a field strain, 5632, which was fully sequenced and annotated in this study. RESULTS: The two genomes differ by ca. 130 kbp with that of 5632 being the largest (1006 kbp). The make up of this additional genetic material mainly corresponds (i) to mobile genetic elements and (ii) to expanded repertoire of gene families that encode putative surface proteins and display features of highly-variable systems. More specifically, three entire copies of a previously described integrative conjugative element are found in 5632 that accounts for ca. 80 kbp. Other mobile genetic elements, found in 5632 but not in PG2, are the more classical insertion sequences which are related to those found in two other ruminant pathogens, M. bovis and M. mycoides subsp. mycoides SC. In 5632, repertoires of gene families encoding surface proteins are larger due to gene duplication. Comparative proteomic analyses of the two strains indicate that the additional coding capacity of 5632 affects the overall architecture of the surface and suggests the occurrence of new phase variable systems based on single nucleotide polymorphisms. CONCLUSION: Overall, comparative analyses of two M. agalactiae strains revealed a very dynamic genome which structure has been shaped by gene flow among ruminant mycoplasmas and expansion-reduction of gene repertoires encoding surface proteins, the expression of which is driven by localized genetic micro-events. BioMed Central 2010-02-02 /pmc/articles/PMC2824730/ /pubmed/20122262 http://dx.doi.org/10.1186/1471-2164-11-86 Text en Copyright ©2010 Nouvel et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Nouvel, Laurent X
Sirand-Pugnet, Pascal
Marenda, Marc S
Sagné, Eveline
Barbe, Valérie
Mangenot, Sophie
Schenowitz, Chantal
Jacob, Daniel
Barré, Aurélien
Claverol, Stéphane
Blanchard, Alain
Citti, Christine
Comparative genomic and proteomic analyses of two Mycoplasma agalactiae strains: clues to the macro- and micro-events that are shaping mycoplasma diversity
title Comparative genomic and proteomic analyses of two Mycoplasma agalactiae strains: clues to the macro- and micro-events that are shaping mycoplasma diversity
title_full Comparative genomic and proteomic analyses of two Mycoplasma agalactiae strains: clues to the macro- and micro-events that are shaping mycoplasma diversity
title_fullStr Comparative genomic and proteomic analyses of two Mycoplasma agalactiae strains: clues to the macro- and micro-events that are shaping mycoplasma diversity
title_full_unstemmed Comparative genomic and proteomic analyses of two Mycoplasma agalactiae strains: clues to the macro- and micro-events that are shaping mycoplasma diversity
title_short Comparative genomic and proteomic analyses of two Mycoplasma agalactiae strains: clues to the macro- and micro-events that are shaping mycoplasma diversity
title_sort comparative genomic and proteomic analyses of two mycoplasma agalactiae strains: clues to the macro- and micro-events that are shaping mycoplasma diversity
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2824730/
https://www.ncbi.nlm.nih.gov/pubmed/20122262
http://dx.doi.org/10.1186/1471-2164-11-86
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