Skip Navigation


JAC Advance Access originally published online on October 16, 2009
Journal of Antimicrobial Chemotherapy 2009 64(6):1165-1169; doi:10.1093/jac/dkp364
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow All Versions of this Article:
64/6/1165    most recent
dkp364v1
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrowRequest Permissions
Right arrow Disclaimer
Google Scholar
Right arrow Articles by de la Pedrosa, E. G. G.
Right arrow Articles by Cantón, R.
PubMed
Right arrow PubMed Citation
Right arrow Articles by de la Pedrosa, E. G. G.
Right arrow Articles by Cantón, R.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

© The Author 2009. Published by Oxford University Press on behalf of the British Society for Antimicrobial Chemotherapy. All rights reserved. For Permissions, please e-mail: journals.permissions@oxfordjournals.org

Original research

High clonal diversity in erythromycin-resistant Streptococcus pneumoniae invasive isolates in Madrid, Spain (2000–07)

Elia Gómez G. de la Pedrosa1,2, Fernando Baquero1,2, Elena Loza1, José-María Nadal-Serrano1, Asunción Fenoll3, Rosa del Campo1,2 and Rafael Cantón1,2,*

1 Servicio de Microbiología, Hospital Ramón y Cajal y CIBER en Epidemiología y Salud Pública (CIBERESP), Madrid, Spain 2 Unidad de Resistencia a Antibióticos y Virulencia Bacteriana asociada al Consejo Superior de Investigaciones Científicas (CSIC), Madrid, Spain 3 Spanish Reference Laboratory for Pneumococci, Instituto de Salud Carlos III, Madrid, Spain

Received 23 May 2009; returned 24 June 2009; revised 12 September 2009; accepted 18 September 2009


* Corresponding author. Servicio de Microbiología, Hospital Ramón y Cajal, Madrid, Spain. Tel: +34-913368832; Fax: +34-913368809; E-mail: rcanton.hrc{at}salud.madrid.org

Objectives: Erythromycin resistance in Streptococcus pneumoniae is still increasing worldwide. All 78 erythromycin-resistant S. pneumoniae isolates collected from blood cultures in our hospital (2000–07) were studied and the population structure was analysed by using different mathematical diversity indexes.

Methods: Erythromycin resistance determinants were screened by PCR. The population structure, including multilocus sequence typing, was analysed by using quantitative clonal diversity (diversity ratio, Simpson, Selander–Levin and Shannon mathematical indexes).

Results: The leading resistance gene was erm(B) (74.3% of the isolates), followed by the erm(B) plus mef(A) combination (17.9%) and mef(A) alone (7.7%). The most frequent serotypes were 14 (18%), 19A (15.4%) and 6B (11.5%). A polyclonal structure was detected in resistant strains, including the Spain9V-3, Spain6B-2 and Denmark14-32 international clones. Both genetic diversity and genetic distribution were high, particularly among clones containing erm(B) and erm(B) plus mef(A) determinants.

Conclusions: The resistance determinants erm(B) and the combination of erm(B) plus mef(A) were observed within multiple S. pneumoniae bacteraemic clones. The preservation of a polyclonal structure might provide a suitable background for further evolution of antibiotic resistance.

Keywords: pneumococcal blood isolates , macrolide resistance , clonal diversity indexes


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?




Disclaimer: Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.