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Constructing Mutants in Serotype 1 Streptococcus pneumoniae strain 519/43
Published on: September 11, 2020
Rapid but Transient Microevolution with Minimal Recombination During High-Transmission Streptococcus pneumoniae
Tiago Touret1, Hermínia de Lencastre2,3, Raquel Sá-Leão1
1Laboratory of Molecular Microbiology of Human Pathogens, Instituto de Tecnologia Química e Biológica António Xavier, Universidade Nova de Lisboa, Oeiras, Portugal.
Insights
Pneumococcal evolution in children with asymptomatic carriage is rapid and transient, driven by short-term adaptations rather than recombination. Most mutations were unique, indicating limited long-term evolutionary impact during this study.
Area of Science:
- Microbiology
- Evolutionary Biology
- Genomics
Background:
- Asymptomatic carriage of Streptococcus pneumoniae (pneumococcus) is common, especially in high-transmission settings like day-care centers.
- Understanding within-host pneumococcal evolution during carriage is crucial for controlling transmission and disease.
Purpose of the Study:
- To investigate pneumococcal clonal dynamics, mutation accumulation, and the role of recombination during asymptomatic carriage in a high-transmission environment.
- To characterize the rate and patterns of microevolution in pneumococcal isolates from children over a 1-year period.
Main Methods:
- Whole-genome sequencing of 259 pneumococcal isolates collected monthly from 47 children over 1 year.
- Analysis of clonal lineages, single-nucleotide polymorphisms (SNPs), mutation rates, and evidence of recombination.
- Comparison of observed mutations with regional collections and assessment of antimicrobial exposure impact.
Main Results:
- 22 distinct pneumococcal lineages were identified, with most genomic changes being nonsynonymous SNPs.
- The mean mutation rate was 4.85 × 10-6 substitutions/site/year, with variations across clones.
- Recombination played a limited detectable role (≈4%), and most mutations were transient, with few persisting long-term or associated with antimicrobial use.
Conclusions:
- Pneumococcal microevolution during asymptomatic carriage in high-transmission settings is rapid but largely transient.
- Short-term adaptive responses to host or niche pressures dominate, with limited opportunity for long-term evolutionary change or significant recombination.
- Findings highlight the dynamic nature of pneumococcal populations during carriage and its implications for transmission dynamics.
Abstract:
Within-host pneumococcal evolution during asymptomatic carriage remains poorly characterized in high-transmission settings. We performed whole-genome sequencing of 259 isolates sampled monthly for 1 year from 47 children attending a single day-care to assess clonal dynamics, mutation accumulation, and the role of recombination. Isolates were resolved into 22 lineages based on serotype and multilocus sequence type. Most genomic changes were nonsynonymous single-nucleotide polymorphism, with only 30% of 357 mutations observed in more than 1 isolate. The mean mutation rate was 4.85 × 10-6 substitutions/site/year, with elevated rates in specific clones (notably 6B-176, 23F-81, and 19F-177). Outlier strains revealed co-circulating sublineages and room-structured divergence in a nontypeable lineage. Putative recombination accounted for ≈4% of mutations, indicating a limited detectable role during the study period. Parallel mutations occurred in genes linked to metabolism, regulation, and immune evasion (e.g., piaA, prtA, pspA, and ciaH). Antimicrobial exposure was not associated with increased mutational burden, and only a handful of mutations persisted when compared with a 2018-2019 regional collection. Overall, pneumococcal microevolution in this high-transmission setting was rapid but largely transient, with little contribution from recombination. These findings indicate that the dynamics captured over this 1-year period reflect rapid, short-term adaptive responses to host or niche pressures, with limited opportunity for longer-term evolutionary change.
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