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M-protein and other intrinsic virulence factors of Streptococcus pyogenes are encoded on an ancient pathogenicity island

BACKGROUND: The increasing number of completely sequenced bacterial genomes allows comparing their architecture and genetic makeup. Such new information highlights the crucial role of lateral genetic exchanges in bacterial evolution and speciation. RESULTS: Here we analyzed the twelve sequenced geno...

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Autores principales: Panchaud, Alexandre, Guy, Lionel, Collyn, François, Haenni, Marisa, Nakata, Masanobu, Podbielski, Andreas, Moreillon, Philippe, Roten, Claude-Alain H
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2683870/
https://www.ncbi.nlm.nih.gov/pubmed/19397826
http://dx.doi.org/10.1186/1471-2164-10-198
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author Panchaud, Alexandre
Guy, Lionel
Collyn, François
Haenni, Marisa
Nakata, Masanobu
Podbielski, Andreas
Moreillon, Philippe
Roten, Claude-Alain H
author_facet Panchaud, Alexandre
Guy, Lionel
Collyn, François
Haenni, Marisa
Nakata, Masanobu
Podbielski, Andreas
Moreillon, Philippe
Roten, Claude-Alain H
author_sort Panchaud, Alexandre
collection PubMed
description BACKGROUND: The increasing number of completely sequenced bacterial genomes allows comparing their architecture and genetic makeup. Such new information highlights the crucial role of lateral genetic exchanges in bacterial evolution and speciation. RESULTS: Here we analyzed the twelve sequenced genomes of Streptococcus pyogenes by a naïve approach that examines the preferential nucleotide usage along the chromosome, namely the usage of G versus C (GC-skew) and T versus A (TA-skew). The cumulative GC-skew plot presented an inverted V-shape composed of two symmetrical linear segments, where the minimum and maximum corresponded to the origin and terminus of DNA replication. In contrast, the cumulative TA-skew presented a V-shape, which segments were interrupted by several steep slopes regions (SSRs), indicative of a different nucleotide composition bias. Each S. pyogenes genome contained up to nine individual SSRs, encompassing all described strain-specific prophages. In addition, each genome contained a similar unique non-phage SSR, the core of which consisted of 31 highly homologous genes. This core includes the M-protein, other mga-related factors and other virulence genes, totaling ten intrinsic virulence genes. In addition to a high content in virulence-related genes and to a peculiar nucleotide bias, this SSR, which is 47 kb-long in a M1GAS strain, harbors direct repeats and a tRNA gene, suggesting a mobile element. Moreover, its complete absence in a M-protein negative group A Streptococcus natural isolate demonstrates that it could be spontaneously lost, but in vitro deletion experiments indicates that its excision occurred at very low rate. The stability of this SSR, combined to its presence in all sequenced S. pyogenes sequenced genome, suggests that it results from an ancient acquisition. CONCLUSION: Thus, this non-phagic SSR is compatible with a pathogenicity island, acquired before S. pyogenes speciation. Its potential excision might bear relevance for vaccine development, because vaccines targeting M-protein might select for M-protein-negative variants that still carry other virulence determinants.
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spelling pubmed-26838702009-05-19 M-protein and other intrinsic virulence factors of Streptococcus pyogenes are encoded on an ancient pathogenicity island Panchaud, Alexandre Guy, Lionel Collyn, François Haenni, Marisa Nakata, Masanobu Podbielski, Andreas Moreillon, Philippe Roten, Claude-Alain H BMC Genomics Research Article BACKGROUND: The increasing number of completely sequenced bacterial genomes allows comparing their architecture and genetic makeup. Such new information highlights the crucial role of lateral genetic exchanges in bacterial evolution and speciation. RESULTS: Here we analyzed the twelve sequenced genomes of Streptococcus pyogenes by a naïve approach that examines the preferential nucleotide usage along the chromosome, namely the usage of G versus C (GC-skew) and T versus A (TA-skew). The cumulative GC-skew plot presented an inverted V-shape composed of two symmetrical linear segments, where the minimum and maximum corresponded to the origin and terminus of DNA replication. In contrast, the cumulative TA-skew presented a V-shape, which segments were interrupted by several steep slopes regions (SSRs), indicative of a different nucleotide composition bias. Each S. pyogenes genome contained up to nine individual SSRs, encompassing all described strain-specific prophages. In addition, each genome contained a similar unique non-phage SSR, the core of which consisted of 31 highly homologous genes. This core includes the M-protein, other mga-related factors and other virulence genes, totaling ten intrinsic virulence genes. In addition to a high content in virulence-related genes and to a peculiar nucleotide bias, this SSR, which is 47 kb-long in a M1GAS strain, harbors direct repeats and a tRNA gene, suggesting a mobile element. Moreover, its complete absence in a M-protein negative group A Streptococcus natural isolate demonstrates that it could be spontaneously lost, but in vitro deletion experiments indicates that its excision occurred at very low rate. The stability of this SSR, combined to its presence in all sequenced S. pyogenes sequenced genome, suggests that it results from an ancient acquisition. CONCLUSION: Thus, this non-phagic SSR is compatible with a pathogenicity island, acquired before S. pyogenes speciation. Its potential excision might bear relevance for vaccine development, because vaccines targeting M-protein might select for M-protein-negative variants that still carry other virulence determinants. BioMed Central 2009-04-27 /pmc/articles/PMC2683870/ /pubmed/19397826 http://dx.doi.org/10.1186/1471-2164-10-198 Text en Copyright © 2009 Panchaud 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
Panchaud, Alexandre
Guy, Lionel
Collyn, François
Haenni, Marisa
Nakata, Masanobu
Podbielski, Andreas
Moreillon, Philippe
Roten, Claude-Alain H
M-protein and other intrinsic virulence factors of Streptococcus pyogenes are encoded on an ancient pathogenicity island
title M-protein and other intrinsic virulence factors of Streptococcus pyogenes are encoded on an ancient pathogenicity island
title_full M-protein and other intrinsic virulence factors of Streptococcus pyogenes are encoded on an ancient pathogenicity island
title_fullStr M-protein and other intrinsic virulence factors of Streptococcus pyogenes are encoded on an ancient pathogenicity island
title_full_unstemmed M-protein and other intrinsic virulence factors of Streptococcus pyogenes are encoded on an ancient pathogenicity island
title_short M-protein and other intrinsic virulence factors of Streptococcus pyogenes are encoded on an ancient pathogenicity island
title_sort m-protein and other intrinsic virulence factors of streptococcus pyogenes are encoded on an ancient pathogenicity island
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2683870/
https://www.ncbi.nlm.nih.gov/pubmed/19397826
http://dx.doi.org/10.1186/1471-2164-10-198
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