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Serotype-Switch Variant of Multidrug-Resistant Streptococcus pneumoniae Sequence Type 271
Emerging Infectious Diseases
|April 29, 2021
Summary
Three invasive, multidrug-resistant Streptococcus pneumoniae strains with vaccine-refractory serotype 3 emerged via recombination. Genomic analysis identified a 55.9-kb fragment responsible for this serotype switch in the successful sequence type 271 complex.
Area of Science:
- Microbiology
- Genomics
- Infectious Diseases
Background:
- Streptococcus pneumoniae is a leading cause of bacterial infections worldwide.
- The emergence of multidrug-resistant (MDR) strains poses a significant public health threat.
- Vaccine-refractory serotypes can evade existing immunization strategies.
Purpose of the Study:
- To investigate the genomic basis of newly emerged invasive, multidrug-resistant Streptococcus pneumoniae isolates.
- To characterize the recombination event responsible for a serotype switch to vaccine-refractory capsular serotype 3.
- To identify the genetic elements within the donated fragment.
Main Methods:
- Whole-genome sequencing of three invasive Streptococcus pneumoniae isolates.
- Comparative genomic analysis to identify recombination events.
- Mapping of recombination sites and characterization of the donated DNA fragment.
Main Results:
- Discovery of three invasive, MDR Streptococcus pneumoniae isolates belonging to the successful sequence type 271 complex.
- Identification of a serotype switch to capsular serotype 3, a known vaccine-refractory type.
- Mapping revealed a 55.9-kb donated fragment containing the capsular polysaccharide synthesis locus (cps3), pbp1a, and other virulence factors.
Conclusions:
- A recombination event involving a large DNA fragment led to the emergence of vaccine-refractory, MDR Streptococcus pneumoniae serotype 3.
- This event highlights the dynamic nature of Streptococcus pneumoniae evolution and the potential for rapid adaptation.
- Understanding these recombination mechanisms is crucial for developing effective control strategies against invasive pneumococcal disease.

