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Constructing Mutants in Serotype 1 Streptococcus pneumoniae strain 519/43
Published on: September 11, 2020
Composite mobile genetic elements disseminating macrolide resistance in Streptococcus pneumoniae
Scott T Chancey1, Sonia Agrawal2, Max R Schroeder1
1Division 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.
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.
Insights
Macrolide resistance in Streptococcus pneumoniae is driven by erm(B) and mef(E)/mel genes on mobile elements. Recombination, not conjugation, is the primary driver for spreading these resistance genes within pneumococcal populations.
Area of Science:
- Microbiology
- Genetics
- Molecular Biology
Background:
- Macrolide resistance in Streptococcus pneumoniae emerged globally in the early 1990s.
- Key resistance factors include erm(B) and macrolide efflux genes mef(E)/mel.
- These genes are found on mobile genetic elements within pneumococci.
Purpose of the Study:
- To investigate the diversity and evolution of mobile elements conferring macrolide resistance.
- To analyze these elements in pneumococcal isolates from pre- and post-conjugate vaccine eras.
- To characterize novel insertion sites and understand dissemination mechanisms.
Main Methods:
- Genomic analysis of 131 Streptococcus pneumoniae isolates (121 invasive, 10 carriage) from Atlanta (1994-2011).
- Focus on 100 macrolide-resistant invasive isolates to identify mobile elements.
- Characterization of insertion sites for Mega, erm(B) element, Tn917, and Tn916-like elements.
Main Results:
- Tn916-like elements with mef(E)/mel (on Mega) and erm(B) (on erm(B) element/Tn917) were identified.
- Elements integrated into the pneumococcal chromosome and larger Tn5253-like composite elements.
- Novel insertion sites for Mega were found, and Tn916-like element insertion sites were characterized.
Conclusions:
- Conjugative mobile elements facilitate acquisition of DNA from diverse bacteria.
- Recombination is the predominant mechanism for transmitting novel DNA within pneumococcal populations post-integration.
- Understanding these mechanisms is crucial for tracking antibiotic resistance evolution.
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