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NADase as a target molecule of in vivo suppression of the toxicity in the invasive M-1 group A Streptococcal isolates

BACKGROUND: NAD-glycohydrolase (NADase) secreted by M-1 group A streptococcal (GAS) isolates are suspected as one of the virulence factors to cause severe invasive disease including streptococcal toxic shock-like syndrome (STSS). M-1 GAS strains were divided into three groups based on NADase activit...

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Detalles Bibliográficos
Autores principales: Tatsuno, Ichiro, Isaka, Masanori, Minami, Masaaki, Hasegawa, Tadao
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2887803/
https://www.ncbi.nlm.nih.gov/pubmed/20470439
http://dx.doi.org/10.1186/1471-2180-10-144
Descripción
Sumario:BACKGROUND: NAD-glycohydrolase (NADase) secreted by M-1 group A streptococcal (GAS) isolates are suspected as one of the virulence factors to cause severe invasive disease including streptococcal toxic shock-like syndrome (STSS). M-1 GAS strains were divided into three groups based on NADase activity: high activity, low activity and no activity in our previous report. RESULTS: The representative high activity isolates taken from STSS patients showed higher virulence compared with isolates from the low activity group, when used to infect mice. The knockout mutant of the nga gene, which encodes NADase also showed reduced virulence in a mouse infection study. The cloned nga gene was able to significantly complement the lost virulence. In addition, the solution containing purified recombinant IFS, which is an inhibitor of NADase, partially rescued mice infected with S. pyogenes. CONCLUSIONS: These results indicate that NADase is important for the virulence of S. pyogenes in vivo and is the potential target to suppress the virulence.