Proteomic biomarkers associated with Streptococcus agalactiae invasive genogroups.

Group B streptococcus (GBS, Streptococcus agalactiae) is a leading cause of meningitis and sepsis in newborns and an etiological agent of meningitis, endocarditis, osteoarticular and soft tissue infections in adults. GBS isolates are routinely clustered in serotypes and in genotypes. At present one...

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Main Authors: Philippe Lanotte, Marylise Perivier, Eve Haguenoer, Laurent Mereghetti, Christophe Burucoa, Stéphane Claverol, Christo Atanassov
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2013-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3553121?pdf=render
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author Philippe Lanotte
Marylise Perivier
Eve Haguenoer
Laurent Mereghetti
Christophe Burucoa
Stéphane Claverol
Christo Atanassov
author_facet Philippe Lanotte
Marylise Perivier
Eve Haguenoer
Laurent Mereghetti
Christophe Burucoa
Stéphane Claverol
Christo Atanassov
author_sort Philippe Lanotte
collection DOAJ
description Group B streptococcus (GBS, Streptococcus agalactiae) is a leading cause of meningitis and sepsis in newborns and an etiological agent of meningitis, endocarditis, osteoarticular and soft tissue infections in adults. GBS isolates are routinely clustered in serotypes and in genotypes. At present one GBS sequence type (i.e. ST17) is considered to be closely associated with bacterial invasiveness and novel proteomic biomarkers could make a valuable contribution to currently available GBS typing data. For that purpose we analyzed the protein profiles of 170 genotyped GBS isolates by Surface-Enhanced Laser Desorption/Ionization Time-of-Flight Mass Spectrometry (SELDI). Univariate statistical analysis of the SELDI profiles identified four protein biomarkers significantly discriminating ST17 isolates from those of the other sequence types. Two of these biomarkers (MW of 7878 Da and 12200 Da) were overexpressed and the other two (MW of 6258 Da and 10463 Da) were underexpressed in ST17. The four proteins were isolated by mass spectrometry-assisted purification and their tryptic peptides analyzed by LC-MS/MS. They were thereby identified as the small subunit of exodeoxyribonuclease VII, the 50S ribosomal protein L7/L12, a CsbD-like protein and thioredoxin, respectively. In conclusion, we identified four candidate biomarkers of ST17 by SELDI for high-throughput screening. These markers may serve as a basis for further studies on the pathophysiology of GBS infection, and for the development of novel vaccines.
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spelling doaj.art-cf0345dbfc884e8dac3fded53f98ce042022-12-21T22:52:07ZengPublic Library of Science (PLoS)PLoS ONE1932-62032013-01-0181e5439310.1371/journal.pone.0054393Proteomic biomarkers associated with Streptococcus agalactiae invasive genogroups.Philippe LanotteMarylise PerivierEve HaguenoerLaurent MereghettiChristophe BurucoaStéphane ClaverolChristo AtanassovGroup B streptococcus (GBS, Streptococcus agalactiae) is a leading cause of meningitis and sepsis in newborns and an etiological agent of meningitis, endocarditis, osteoarticular and soft tissue infections in adults. GBS isolates are routinely clustered in serotypes and in genotypes. At present one GBS sequence type (i.e. ST17) is considered to be closely associated with bacterial invasiveness and novel proteomic biomarkers could make a valuable contribution to currently available GBS typing data. For that purpose we analyzed the protein profiles of 170 genotyped GBS isolates by Surface-Enhanced Laser Desorption/Ionization Time-of-Flight Mass Spectrometry (SELDI). Univariate statistical analysis of the SELDI profiles identified four protein biomarkers significantly discriminating ST17 isolates from those of the other sequence types. Two of these biomarkers (MW of 7878 Da and 12200 Da) were overexpressed and the other two (MW of 6258 Da and 10463 Da) were underexpressed in ST17. The four proteins were isolated by mass spectrometry-assisted purification and their tryptic peptides analyzed by LC-MS/MS. They were thereby identified as the small subunit of exodeoxyribonuclease VII, the 50S ribosomal protein L7/L12, a CsbD-like protein and thioredoxin, respectively. In conclusion, we identified four candidate biomarkers of ST17 by SELDI for high-throughput screening. These markers may serve as a basis for further studies on the pathophysiology of GBS infection, and for the development of novel vaccines.http://europepmc.org/articles/PMC3553121?pdf=render
spellingShingle Philippe Lanotte
Marylise Perivier
Eve Haguenoer
Laurent Mereghetti
Christophe Burucoa
Stéphane Claverol
Christo Atanassov
Proteomic biomarkers associated with Streptococcus agalactiae invasive genogroups.
PLoS ONE
title Proteomic biomarkers associated with Streptococcus agalactiae invasive genogroups.
title_full Proteomic biomarkers associated with Streptococcus agalactiae invasive genogroups.
title_fullStr Proteomic biomarkers associated with Streptococcus agalactiae invasive genogroups.
title_full_unstemmed Proteomic biomarkers associated with Streptococcus agalactiae invasive genogroups.
title_short Proteomic biomarkers associated with Streptococcus agalactiae invasive genogroups.
title_sort proteomic biomarkers associated with streptococcus agalactiae invasive genogroups
url http://europepmc.org/articles/PMC3553121?pdf=render
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