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Implementation of a Permeable Membrane Insert-based Infection System to Study the Effects of Secreted Bacterial Toxins on Mammalian Host Cells
Published on: August 19, 2016
Genetic diversity and exotoxin A production of group A streptococci causing sepsis
Eun Ha Koh1, Nam Yong Lee, Eui Chong Kim
1Department of Laboratory Medicine, Institute of Health Sciences, Gyeongsang National University School of Medicine, Chilamdong, Jinju, Korea.
Abstract:
The M protein and streptococcus pyrogenic exotoxin (SPE A) are important virulence factors in group A streptococci (GAS) infections. The emm types of GAS strains isolated from patients with sepsis were determined by sequencing the 5' N-terminus of the emm gene, encoding the M protein, and clonality analysis using pulsed-field gel electrophoresis. The presence of speA and production of SPE A were also examined. There were no predominant GAS clones. The emm genotypes were variable, and the most common genotype was emm13 (17.9%). The production prevalence of SPE A was 21.4%. The low mortality rate (7.1%) of GAS sepsis might be attributable to the low incidence of virulent strains such as emm1 (10.7%) and emm3 (7.1%), as well as to low production rate of SPE A.
Insights
Group A Streptococcus (GAS) sepsis virulence factors, M protein (emm types) and streptococcus pyrogenic exotoxin A (SPE A), were analyzed. Low mortality may be linked to less common virulent strains and lower SPE A production.
Area of Science:
- Microbiology
- Infectious Diseases
- Genetics
Background:
- Group A Streptococcus (GAS) causes various infections, with M protein and streptococcus pyrogenic exotoxin A (SPE A) being key virulence factors.
- Understanding the genetic diversity and toxin production of GAS strains is crucial for managing infections like sepsis.
Purpose of the Study:
- To characterize the emm types and SPE A production in GAS strains isolated from sepsis patients.
- To investigate the clonal structure of these GAS isolates.
- To correlate strain characteristics with the observed low mortality rate of GAS sepsis.
Main Methods:
- emm gene sequencing to determine M protein types.
- Pulsed-field gel electrophoresis (PFGE) for clonality analysis.
- Assays to detect the presence and production of SPE A.
Main Results:
- No predominant GAS clones were identified among the isolates.
- emm genotypes were diverse, with emm13 being the most common (17.9%).
- SPE A production was observed in 21.4% of the isolates.
Conclusions:
- The genetic variability of GAS strains and the relatively low prevalence of highly virulent emm types (emm1, emm3) may contribute to the low mortality rate in GAS sepsis.
- Low production rates of SPE A might also play a role in reduced disease severity.
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