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Highly Frequent Mutations in Negative Regulators of Multiple Virulence Genes in Group A Streptococcal Toxic Shock Syndrome Isolates

Streptococcal toxic shock syndrome (STSS) is a severe invasive infection characterized by the sudden onset of shock and multiorgan failure; it has a high mortality rate. Although a number of studies have attempted to determine the crucial factors behind the onset of STSS, the responsible genes in gr...

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Autores principales: Ikebe, Tadayoshi, Ato, Manabu, Matsumura, Takayuki, Hasegawa, Hideki, Sata, Tetsutaro, Kobayashi, Kazuo, Watanabe, Haruo
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2848555/
https://www.ncbi.nlm.nih.gov/pubmed/20368967
http://dx.doi.org/10.1371/journal.ppat.1000832
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author Ikebe, Tadayoshi
Ato, Manabu
Matsumura, Takayuki
Hasegawa, Hideki
Sata, Tetsutaro
Kobayashi, Kazuo
Watanabe, Haruo
author_facet Ikebe, Tadayoshi
Ato, Manabu
Matsumura, Takayuki
Hasegawa, Hideki
Sata, Tetsutaro
Kobayashi, Kazuo
Watanabe, Haruo
author_sort Ikebe, Tadayoshi
collection PubMed
description Streptococcal toxic shock syndrome (STSS) is a severe invasive infection characterized by the sudden onset of shock and multiorgan failure; it has a high mortality rate. Although a number of studies have attempted to determine the crucial factors behind the onset of STSS, the responsible genes in group A Streptococcus have not been clarified. We previously reported that mutations of csrS/csrR genes, a two-component negative regulator system for multiple virulence genes of Streptococcus pyogenes, are found among the isolates from STSS patients. In the present study, mutations of another negative regulator, rgg, were also found in clinical isolates of STSS patients. The rgg mutants from STSS clinical isolates enhanced lethality and impaired various organs in the mouse models, similar to the csrS mutants, and precluded their being killed by human neutrophils, mainly due to an overproduction of SLO. When we assessed the mutation frequency of csrS, csrR, and rgg genes among S. pyogenes isolates from STSS (164 isolates) and non-invasive infections (59 isolates), 57.3% of the STSS isolates had mutations of one or more genes among three genes, while isolates from patients with non-invasive disease had significantly fewer mutations in these genes (1.7%). The results of the present study suggest that mutations in the negative regulators csrS/csrR and rgg of S. pyogenes are crucial factors in the pathogenesis of STSS, as they lead to the overproduction of multiple virulence factors.
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spelling pubmed-28485552010-04-05 Highly Frequent Mutations in Negative Regulators of Multiple Virulence Genes in Group A Streptococcal Toxic Shock Syndrome Isolates Ikebe, Tadayoshi Ato, Manabu Matsumura, Takayuki Hasegawa, Hideki Sata, Tetsutaro Kobayashi, Kazuo Watanabe, Haruo PLoS Pathog Research Article Streptococcal toxic shock syndrome (STSS) is a severe invasive infection characterized by the sudden onset of shock and multiorgan failure; it has a high mortality rate. Although a number of studies have attempted to determine the crucial factors behind the onset of STSS, the responsible genes in group A Streptococcus have not been clarified. We previously reported that mutations of csrS/csrR genes, a two-component negative regulator system for multiple virulence genes of Streptococcus pyogenes, are found among the isolates from STSS patients. In the present study, mutations of another negative regulator, rgg, were also found in clinical isolates of STSS patients. The rgg mutants from STSS clinical isolates enhanced lethality and impaired various organs in the mouse models, similar to the csrS mutants, and precluded their being killed by human neutrophils, mainly due to an overproduction of SLO. When we assessed the mutation frequency of csrS, csrR, and rgg genes among S. pyogenes isolates from STSS (164 isolates) and non-invasive infections (59 isolates), 57.3% of the STSS isolates had mutations of one or more genes among three genes, while isolates from patients with non-invasive disease had significantly fewer mutations in these genes (1.7%). The results of the present study suggest that mutations in the negative regulators csrS/csrR and rgg of S. pyogenes are crucial factors in the pathogenesis of STSS, as they lead to the overproduction of multiple virulence factors. Public Library of Science 2010-04-01 /pmc/articles/PMC2848555/ /pubmed/20368967 http://dx.doi.org/10.1371/journal.ppat.1000832 Text en Ikebe 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
Ikebe, Tadayoshi
Ato, Manabu
Matsumura, Takayuki
Hasegawa, Hideki
Sata, Tetsutaro
Kobayashi, Kazuo
Watanabe, Haruo
Highly Frequent Mutations in Negative Regulators of Multiple Virulence Genes in Group A Streptococcal Toxic Shock Syndrome Isolates
title Highly Frequent Mutations in Negative Regulators of Multiple Virulence Genes in Group A Streptococcal Toxic Shock Syndrome Isolates
title_full Highly Frequent Mutations in Negative Regulators of Multiple Virulence Genes in Group A Streptococcal Toxic Shock Syndrome Isolates
title_fullStr Highly Frequent Mutations in Negative Regulators of Multiple Virulence Genes in Group A Streptococcal Toxic Shock Syndrome Isolates
title_full_unstemmed Highly Frequent Mutations in Negative Regulators of Multiple Virulence Genes in Group A Streptococcal Toxic Shock Syndrome Isolates
title_short Highly Frequent Mutations in Negative Regulators of Multiple Virulence Genes in Group A Streptococcal Toxic Shock Syndrome Isolates
title_sort highly frequent mutations in negative regulators of multiple virulence genes in group a streptococcal toxic shock syndrome isolates
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2848555/
https://www.ncbi.nlm.nih.gov/pubmed/20368967
http://dx.doi.org/10.1371/journal.ppat.1000832
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