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Updated: Jul 9, 2025

Genome-wide Gene Deletions in Streptococcus sanguinis by High Throughput PCR
Published on: November 23, 2012
A novel invasive Streptococcus pyogenes variant sublineage derived through recombinational replacement of the emm12
Yvette Unoarumhi1, Morgan L Davis1, Lori A Rowe1
1Centers for Disease Control and Prevention, Biotechnology Core Facility Branch, National Center for Emerging and Zoonotic Infectious Diseases, Division Scientific Resources, Atlanta, GA, USA.
Abstract:
Group A streptococcal strains potentially acquire new M protein gene types through genetic recombination (emm switching). To detect such variants, we screened 12,596 invasive GAS genomes for strains of differing emm types that shared the same multilocus sequence type (ST). Through this screening we detected a variant consisting of 16 serum opacity factor (SOF)-positive, emm pattern E, emm82 isolates that were ST36, previously only associated with SOF-negative, emm pattern A, emm12. The 16 emm82/ST36 isolates were closely interrelated (pairwise SNP distance of 0-43), and shared the same emm82-containing recombinational fragment. emm82/ST36 isolates carried the sof12 structural gene, however the sof12 indel characteristic of emm12 strains was corrected to confer the SOF-positive phenotype. Five independent emm82/ST36 invasive case isolates comprised two sets of genetically indistinguishable strains. The emm82/ST36 isolates were primarily macrolide resistant (12/16 isolates), displayed at least 4 different core genomic arrangements, and carried 11 different combinations of virulence and resistance determinants. Phylogenetic analysis revealed that emm82/ST36 was within a minor (non-clade 1) portion of ST36 that featured almost all ST36 antibiotic resistance. This work documents emergence of a rapidly diversifying variant that is the first confirmed example of an emm pattern A strain switched to a pattern E strain.
Insights
Group A Streptococcus (GAS) can acquire new M protein gene types via recombination. Researchers discovered a novel GAS variant (emm82/ST36) that switched from emm pattern A to E, showing increased diversity and antibiotic resistance.
Area of Science:
- Microbiology
- Genetics
- Epidemiology
Background:
- Group A Streptococcus (GAS) exhibits genetic variability, including M protein gene switching (emm switching), which can alter virulence and host adaptation.
- Understanding emm switching is crucial for tracking GAS evolution and predicting potential outbreaks.
Purpose of the Study:
- To detect and characterize novel variants of GAS that have undergone emm switching.
- To investigate the genetic makeup, virulence factors, and antibiotic resistance profiles of newly identified GAS variants.
Main Methods:
- Screening of 12,596 invasive GAS genomes for strains with differing emm types but identical multilocus sequence types (STs).
- Whole-genome sequencing and phylogenetic analysis of identified variants.
- Analysis of specific genes, including M protein (emm) and serum opacity factor (sof), and investigation of genetic recombination events.
Main Results:
- A novel variant of SOF-positive, emm pattern E, emm82 isolates belonging to ST36 was identified. This contrasts with the previously known SOF-negative, emm pattern A, emm12 association for ST36.
- The emm82/ST36 isolates were genetically related, sharing a common emm82-containing recombinational fragment and exhibiting a corrected sof12 gene for SOF-positive phenotype.
- These isolates demonstrated significant macrolide resistance (12/16), diverse core genomic arrangements, and multiple combinations of virulence and resistance determinants, with phylogenetic analysis placing them within an antibiotic-resistant lineage of ST36.
Conclusions:
- This study documents the emergence of a rapidly diversifying GAS variant, representing the first confirmed instance of an emm pattern A strain switching to an emm pattern E strain.
- The findings highlight the dynamic nature of GAS evolution through genetic recombination and the potential for new variants to acquire significant antibiotic resistance and virulence traits.
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