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Updated: Jun 16, 2026

Constructing Mutants in Serotype 1 Streptococcus pneumoniae strain 519/43
Published on: September 11, 2020
Mutation frequency in antibiotic-resistant and -susceptible isolates of Streptococcus pneumoniae
Stephanie K Henderson-Begg1, Carmen L Sheppard, Robert C George
1Queen Mary University of London, Barts and The London School of Medicine and Dentistry, Centre for Immunology and Infectious Disease, Blizard Institute of Cell and Molecular Science, 4 Newark Street, London E1 2AT, UK.
Abstract:
Development of multiple antibiotic resistance in Streptococcus pneumoniae typically involves either mutation or transformation at several well-separated chromosomal loci. We postulated that this series of genetic events would be more likely to occur in organisms with deficient DNA repair mechanisms. Investigation of 27 antibiotic-resistant or -susceptible clinical isolates of S. pneumoniae revealed a broad range of mutation frequencies, but no isolate was as mutable as a mismatch repair (MMR)-deficient laboratory isolate. No correlation was observed between antibiotic resistance and higher mutation frequency. Examination of a further 180 clinical isolates using a newly developed rapid screen method also failed to identify any isolates with a mutation frequency as high as the MMR-deficient control strain. We argue that there is currently no clear evidence of a distinct population of mutators among clinical pneumococci.
Insights
This study investigated antibiotic resistance in Streptococcus pneumoniae, finding no evidence of a distinct "mutator" population among clinical isolates. Higher mutation frequencies were not linked to increased antibiotic resistance in the examined strains.
Area of Science:
- Microbiology
- Genetics
- Molecular Biology
Background:
- Multiple antibiotic resistance in Streptococcus pneumoniae develops through genetic mutations or transformations at various chromosomal locations.
- Deficient DNA repair mechanisms are hypothesized to facilitate the accumulation of these genetic events, leading to increased mutability.
Purpose of the Study:
- To investigate whether clinical isolates of Streptococcus pneumoniae exhibit a higher mutation frequency, particularly those with deficient DNA repair mechanisms.
- To determine if a distinct population of
Main Methods:
- Analysis of mutation frequencies in 27 clinical isolates of Streptococcus pneumoniae, comparing them to a mismatch repair (MMR)-deficient laboratory strain.
- Screening of an additional 180 clinical isolates using a novel rapid method to assess mutation rates.
Main Results:
- A wide spectrum of mutation frequencies was observed across clinical isolates, but none matched the high mutability of the MMR-deficient control.
- No correlation was found between the level of antibiotic resistance and increased mutation frequency in the clinical isolates.
- The rapid screening of 180 isolates did not identify any with mutation frequencies comparable to the MMR-deficient strain.
Conclusions:
- Current evidence does not support the existence of a distinct population of hypermutable strains (mutators) among clinical isolates of Streptococcus pneumoniae.
- The development of multiple antibiotic resistance in S. pneumoniae may not be primarily driven by a subset of highly mutable organisms.
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