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Updated: Jan 5, 2026

Constructing Mutants in Serotype 1 Streptococcus pneumoniae strain 519/43
Published on: September 11, 2020
Genomic epidemiology of penicillin-non-susceptible Streptococcus pneumoniae
Tamsin C M Dewé1, Joshua C D'Aeth1, Nicholas J Croucher1
1MRC Centre for Global Infectious Disease Analysis, Department of Infectious Disease Epidemiology, St. Mary's Campus, Imperial College London, London, W2 1PG, UK.
Abstract:
Penicillin-non-susceptible Streptococcus pneumoniae (PNSP) were first detected in the 1960s, and are now common worldwide, predominantly through the international spread of a limited number of strains. Extant PNSP are characterized by mosaic pbp2x, pbp2b and pbp1a genes generated by interspecies recombinations, with the extent of these alterations determining the range and concentrations of β-lactams to which the genotype is non-susceptible. The complexity of the genetics underlying these phenotypes has been the subject of both molecular microbiology and genome-wide association and epistasis analyses. Such studies can aid our understanding of PNSP evolution and help improve the already highly-performing bioinformatic methods capable of identifying PNSP from genomic surveillance data.
Insights
Penicillin-non-susceptible Streptococcus pneumoniae (PNSP) strains have evolved mosaic genes through recombination, leading to widespread resistance. Understanding PNSP genetics aids in tracking their evolution and improving detection methods.
Area of Science:
- Microbiology
- Genetics
- Evolutionary Biology
Background:
- Penicillin-non-susceptible Streptococcus pneumoniae (PNSP) emerged in the 1960s and are now globally prevalent.
- PNSP strains are characterized by mosaic pbp2x, pbp2b, and pbp1a genes resulting from interspecies recombination.
Purpose of the Study:
- To investigate the genetic basis of PNSP non-susceptibility.
- To enhance understanding of PNSP evolution and improve bioinformatic detection methods.
Main Methods:
- Molecular microbiology techniques.
- Genome-wide association studies (GWAS).
- Epistasis analyses.
Main Results:
- The extent of mosaic gene alterations correlates with the range and concentration of beta-lactam resistance.
- Genetic complexity underlies PNSP phenotypes.
Conclusions:
- Understanding PNSP genetic evolution is crucial for effective genomic surveillance.
- Improved bioinformatic tools can enhance the identification of PNSP from genomic data.
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