Institutional members access full text with Ovid®

Group A Streptococcus Colonies From a Single Throat Swab Can Have Heterogeneous Antimicrobial Susceptibility Patterns

Vandevoorde, Aurélie MD*†; Ascenzo, Sabrina Bsc*; Deyi, Veronique Yvette Miendje MD, PhD; Mascart, Georges MD, PhD; Mansbach, Anne-Laure MD; Landsberg, Marguerite MD§; Dreze, Pierre BSc*; Steer, Andrew C. MD, PhD; Van Melderen, Laurence PhD*; Smeesters, Pierre R. MD, PhD*‖

Pediatric Infectious Disease Journal: March 2013 - Volume 32 - Issue 3 - p 296–298
doi: 10.1097/INF.0b013e31827c9796
Brief Reports

This study describes for the first time heterogeneity of antibiotic resistance profiles among group A Streptococcus isolates originating from a single throat swab in patients with acute pharyngitis. For each throat swab, 10 group A Streptococcus colonies were randomly selected from the primary plate and subcultured to a secondary plate. These isolates were characterized by various phenotypic and genotypic methods. Our results demonstrated that differing antibiotic resistance profiles were present in 19% of pediatric patients with acute pharyngitis before antimicrobial treatment. This heterogeneity likely resulted from horizontal gene transfer among streptococcal isolates sharing the same genetic background. As only a minority of colonies displayed antibiotic resistance among these heterogeneous samples, a classical diagnostic antibiogram would have classified them in most instances as “susceptible,” although therapeutic failure could be caused by the proliferation of resistant strains after initiation of antibiotic treatment.

From the *Bacterial Genetics and Physiology Laboratory, Institut de Biologie et de Médecine Moléculaires, Faculté des Sciences; ENT Department, University Children’s Hospital Reine Fabiola; Microbiology Department, Brugmann Hospital; §Paediatric Department, University Children’s Hospital Reine Fabiola, Université Libre de Bruxelles, Bruxelles, Belgium; Department of Paediatrics, Centre for International Child Health, University of Melbourne, Royal Children’s Hospital; and Murdoch Children Research Institute, Melbourne, Australia.

Accepted for publication October 25, 2012.

P.R.S. is a postdoctoral researcher from the Belgian research agency (Fonds National de Recherche Scientifique). The authors have no other funding or conflicts of interest to disclose.

Supplemental digital content is available for this article. Direct URL citations appear in the printed text and are provided in the HTML and PDF versions of this article on the journal’s website (www.pidj.com).

Address for correspondence: Pierre R. Smeesters, MD, PhD, Bacterial Genetics and Physiology Laboratory, Université Libre de Bruxelles, 12 Rue des Professeurs Jeener et Brachet, B: 6041 Gosselies, Belgium. E-mail: psmeeste@ulb.ac.be.

© 2013 Lippincott Williams & Wilkins, Inc.