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Journal of Clinical Microbiology, September 2007, p. 2909-2916, Vol. 45, No. 9
0095-1137/07/$08.00+0     doi:10.1128/JCM.00999-07
Copyright © 2007, American Society for Microbiology. All Rights Reserved.

Molecular Epidemiology and Distribution of Serotypes, Surface Proteins, and Antibiotic Resistance among Group B Streptococci in Italy{triangledown}

Giovanni Gherardi,1 Monica Imperi,2 Lucilla Baldassarri,2 Marco Pataracchia,2 Giovanna Alfarone,2 Simona Recchia,2 Graziella Orefici,2 Giordano Dicuonzo,1 and Roberta Creti2*

Dipartimento di Medicina di Laboratorio e Microbiologia, Università Campus Bio-Medico,1 Dipartimento di Malattie Infettive, Parassitarie ed Immunomediate, Istituto Superiore di Sanità, Rome, Italy2

Received 14 May 2007/ Returned for modification 11 June 2007/ Accepted 9 July 2007

Group B streptococci (GBS) comprising three different sets of isolates (31 invasive, 36 noninvasive, and 24 colonizing isolates) were collected in Italy during the years 2002 to 2005. Clonal groups were established by pulsed-field gel electrophoresis (PFGE), and selected isolates were studied by multilocus sequence typing (MLST). GBS isolates were also characterized by classical and molecular techniques for serotyping and protein gene and antibiotic resistance profiling. Some serotypes were significantly associated with a particular isolate population: serotype Ia more frequently corresponded to invasive strains than other strains, serotype V was more frequently encountered among noninvasive strains, and nontypeable strains were more common among isolates from carriers. Four major clonal groups accounted for 52.7% of all isolates: PFGE type 1/clonal complex 1 (CC1) comprised mainly serotype V isolates carrying the alp3 gene, PFGE type 2/CC23 encompassed serotype Ia isolates with the alp1 or alpha gene, PFGE type 3/CC17 comprised serotype III isolates carrying the rib gene, and PFGE type 4/CC19 consisted mainly of serotype II isolates possessing the rib gene. The same serotypes were shared by isolates of different clonal groups, and conversely, isolates belonging to the same clonal groups were found to be of different serotypes, presumably due to capsular switching by the horizontal transfer of capsular genes. Erythromycin resistance (prevalence, 16.5%; 15 resistant isolates of 91) was restricted to strains isolated from patients with noninvasive infections and carriers, while tetracycline resistance was evenly distributed (prevalence, 68.1%; 62 resistant isolates of 91). Most erythromycin-resistant GBS strains were of serotype V, were erm(B) positive, and belonged to the PFGE type 1/CC1 group, suggesting that macrolide resistance may have arisen both by clonal dissemination and by the horizontal transfer of resistance genes.

* Corresponding author. Mailing address: Reparto di Malattie Batteriche Respiratorie e Sistemiche, Dipartimento di Malattie Infettive, Parassitarie ed Immunomediate, Istituto Superiore di Sanità, Viale Regina Elena, 299, 00161 Rome, Italy. Phone: 39-06-49902116. Fax: 39-06-49902886. E-mail: roberta.creti{at}iss.it

{triangledown} Published ahead of print on 18 July 2007.

Journal of Clinical Microbiology, September 2007, p. 2909-2916, Vol. 45, No. 9
0095-1137/07/$08.00+0     doi:10.1128/JCM.00999-07
Copyright © 2007, American Society for Microbiology. All Rights Reserved.



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