Publication

Composite mobile genetic elements disseminating macrolide resistance in Streptococcus pneumoniae

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Last modified
  • 02/20/2025
Type of Material
Authors
    Scott Chancey, Emory UniversitySonia Agrawal, University of MarylandMax R. Schroeder, Emory UniversityMonica Farley, Emory UniversityHervé Tettelin, University of MarylandDavid S Stephens, Emory University
Language
  • English
Date
  • 2015-02-09
Publisher
  • Frontiers
Publication Version
Copyright Statement
  • © 2015 Chancey, Agrawal, Schroeder, Farley, Tettelin and Stephens.
License
Final Published Version (URL)
Title of Journal or Parent Work
ISSN
  • 1664-302X
Volume
  • 6
Start Page
  • 26
End Page
  • 26
Grant/Funding Information
  • his study was funded in part with an R01 grant from the National Institutes of Health (R01 AI070829 (to David S. Stephens) and with federal funds from the National Institute of Allergy and Infectious Diseases, National Institutes of Health, Department of Health and Human Services under contract number HHSN272200900009C.
  • The funders had no role in study design, data collection and analysis, or preparation of the manuscript, but signed off on the publication after we sent them a copy for review.
Supplemental Material (URL)
Abstract
  • Macrolide resistance in Streptococcus pneumoniae emerged in the U.S. and globally during the early 1990's. The RNA methylase encoded by erm(B) and the macrolide efflux genes mef(E) and mel were identified as the resistance determining factors. These genes are disseminated in the pneumococcus on mobile, often chimeric elements consisting of multiple smaller elements. To better understand the variety of elements encoding macrolide resistance and how they have evolved in the pre- and post-conjugate vaccine eras, the genomes of 121 invasive and ten carriage isolates from Atlanta from 1994 to 2011 were analyzed for mobile elements involved in the dissemination of macrolide resistance. The isolates were selected to provide broad coverage of the genetic variability of antibiotic resistant pneumococci and included 100 invasive isolates resistant to macrolides. Tn916-like elements carrying mef(E) and mel on the Macrolide Genetic Assembly (Mega) and erm(B) on the erm(B) element and Tn917 were integrated into the pneumococcal chromosome backbone and into larger Tn5253-like composite elements. The results reported here include identification of novel insertion sites for Mega and characterization of the insertion sites of Tn916-like elements in the pneumococcal chromosome and in larger composite elements. The data indicate that integration of elements by conjugation was infrequent compared to recombination. Thus, it appears that conjugative mobile elements allow the pneumococcus to acquire DNA from distantly related bacteria, but once integrated into a pneumococcal genome, transformation and recombination is the primary mechanism for transmission of novel DNA throughout the pneumococcal population.
Author Notes
  • David S. Stephens, Division of Infectious Diseases, Department of Medicine, Emory University School of Medicine, Atlanta, GA, USA; Laboratories of Microbial Pathogenesis, Department of Veterans Affairs Medical Center, Atlanta, GA, USA e-mail: dstep01@emory.edu
Keywords
Research Categories
  • Health Sciences, General
  • Health Sciences, Immunology
  • Health Sciences, Pathology

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