M protein typing of Thai group A streptococcal isolates by PCR-Restriction fragment length polymorphism analysis

Nonglak Yoonim1, Colleen Olive, Chulabhorn Pruksachatkunakorn

  • 1Department of Microbiology, Faculty of Medicine, Chiang Mai University, Chiang Mai, Thailand. amm_aon@yahoo.com

BMC Microbiology
|October 18, 2005
PubMed
Abstract

Insights

A new polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) assay effectively types Group A Streptococcus (GAS) M protein genes. This method is a valuable alternative for endemic developing countries, aiding in epidemiological analysis and vaccine development.

Area of Science:

  • Microbiology
  • Molecular Biology
  • Public Health

Background:

  • Group A Streptococcus (GAS) infections cause severe sequelae like rheumatic fever (RF) and rheumatic heart disease (RHD).
  • GAS typing is crucial for epidemiological analysis and vaccine development, but standard methods are limited.
  • M protein-nontypeable (MNT) GAS isolates are common, complicating typing efforts.

Purpose of the Study:

  • To develop a feasible molecular typing method for GAS M protein genes (emm).
  • To establish a Polymerase Chain Reaction-Restriction Fragment Length Polymorphism (PCR-RFLP) assay for M protein typing.
  • To assess the utility of PCR-RFLP for typing GAS isolates in resource-limited settings.

Main Methods:

  • Developed a PCR-RFLP assay using specific primers and Alu I digestion for GAS M protein gene (emm) typing.
  • Analyzed 106 GAS isolates from Thailand using the PCR-RFLP assay.
  • Utilized DNA sequencing to identify M types for isolates with atypical RFLP patterns.

Main Results:

  • The PCR-RFLP assay differentiated 13 known GAS M types based on unique band patterns.
  • 95 out of 106 isolates matched known M types via RFLP; 11 yielded novel patterns.
  • DNA sequencing identified six additional M types, with M93 GAS being the most prevalent in the study population.

Conclusions:

  • PCR-RFLP is a rapid and effective method for screening diverse GAS M types.
  • This assay offers a practical alternative for M typing in developing countries where GAS is endemic.
  • The findings support the use of PCR-RFLP for improved epidemiological surveillance and vaccine strategies against GAS.