Seven-year surveillance of emm types of pediatric Group A streptococcal pharyngitis isolates in Western Greece

An experimental 26-valent M protein Group A streptococcal (GAS) vaccine has entered clinical studies. Pharyngeal GAS emm type surveillances in different areas and time-periods enhance the understanding of the epidemiology of GAS pharyngitis. Moreover, these surveillances, combined with the data on G...

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Published inPloS one Vol. 8; no. 8; p. e71558
Main Authors Syrogiannopoulos, George A, Grivea, Ioanna N, Al-Lahham, Adnan, Panagiotou, Maria, Tsantouli, Alexandra G, Michoula Ralf René Reinert, Aspasia N, van der Linden, Mark
Format Journal Article
LanguageEnglish
Published United States Public Library of Science 19.08.2013
Public Library of Science (PLoS)
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Summary:An experimental 26-valent M protein Group A streptococcal (GAS) vaccine has entered clinical studies. Pharyngeal GAS emm type surveillances in different areas and time-periods enhance the understanding of the epidemiology of GAS pharyngitis. Moreover, these surveillances, combined with the data on GAS invasive disease, can play a significant role in the formulation of multivalent type-specific vaccines. During a 7-year period (1999-2005), 2408 GAS isolates were recovered from consecutive children with pharyngitis in Western Greece. The overall macrolide resistance rate was 22.8%. Along the study period we noted a tendency towards significantly decreased rates of resistance, with the lowest rates occurring in 2002 (15.3%), 2003 (15%) and 2004 (16.7%). A random sample of isolates from each year, 338 (61.7%) of the 548 macrolide-resistant and 205 (11%) of the macrolide-susceptible, underwent molecular analysis, including emm typing. The 543 typed isolates had 28 different emm types. A statistically significant association was found between macrolide resistance and emm4, emm22 and emm77, whereas emm1, emm3, emm6, emm12, emm87 and emm89 were associated with macrolide susceptibility. A significant yearly fluctuation was observed in emm4, emm28 and emm77. The most common macrolide-resistant GAS were emm77 isolates harboring erm(A), either alone or in combination with mef(A), emm4 carrying mef(A), emm28 possessing erm(B), emm75 carrying mef(A), emm12 harboring mef(A) and emm22 carrying erm(A). We estimated that 82.8% of the isolates belonged to emm types included in the novel 26-valent M protein vaccine. The vaccine coverage rate was determined mainly by the increased frequency of nonvaccine emm4 isolates. A limited number of emm types dominated among macrolide-susceptible and macrolide-resistant GAS isolates. We observed seasonal fluctuations, which were significant for emm4, emm28 and emm77. This type of data can serve as baseline information if the novel 26-valent M protein GAS vaccine is introduced into practice.
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Competing Interests: The authors have read the journal's policy and have the following conflicts: MvdL has received research grants from Wyeth/Pfizer and GSK and acts as a consultant for Wyeth/Pfizer, Sanofi-Aventis and GSK. RRR is currently an employee of Pfizer Pharmaceuticals. ING, GAS, AA-L, MP and AGT declare no competing interests. There are no patents, products in development or marketed products to declare. This does not alter the authors' adherence to all the PLOS ONE policies on sharing data and materials, as detailed online in the guide for authors.
Conceived and designed the experiments: GAS ING RRR MvdL. Performed the experiments: ING AA-L MP. Analyzed the data: MP AGT ANM. Contributed reagents/materials/analysis tools: GAS RRR MvdL. Wrote the paper: GAS ING AA-L MP AGT ANM RRR MvdL.
Current address: Pfizer Pharmaceuticals, Paris, France
ISSN:1932-6203
1932-6203
DOI:10.1371/journal.pone.0071558