Highly Frequent Mutations in Negative Regulators of Multiple Virulence Genes in Group A Streptococcal Toxic Shock Syndrome Isolates
Adult
Gene Expression Regulation, Viral
Male
Adolescent
QH301-705.5
Blotting, Western
Gene Expression
Mice, Nude
Mice
03 medical and health sciences
Bacterial Proteins
Animals
Humans
Biology (General)
Child
Aged
Aged, 80 and over
Comparative Genomic Hybridization
0303 health sciences
Infant, Newborn
Infant
RC581-607
Middle Aged
3. Good health
Child, Preschool
Mutation
Immunologic diseases. Allergy
Research Article
DOI:
10.1371/journal.ppat.1000832
Publication Date:
2010-04-01T19:22:45Z
AUTHORS (7)
ABSTRACT
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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