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Published on: September 5, 2013
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
Background:
Group A streptococcal (GAS) infections can lead to the development of severe post-infectious sequelae, such as rheumatic fever (RF) and rheumatic heart disease (RHD). RF and RHD are a major health concern in developing countries, and in indigenous populations of developed nations. The majority of GAS isolates are M protein-nontypeable (MNT) by standard serotyping. However, GAS typing is a necessary tool in the epidemiologically analysis of GAS and provides useful information for vaccine development. Although DNA sequencing is the most conclusive method for M protein typing, this is not a feasible approach especially in developing countries. To overcome this problem, we have developed a polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP)-based assay for molecular typing the M protein gene (emm) of GAS.
Results:
Using one pair of primers, 13 known GAS M types showed one to four bands of PCR products and after digestion with Alu I, they gave different RFLP patterns. Of 106 GAS isolates examined from the normal Thai population and from patients with GAS-associated complications including RHD, 95 isolates gave RFLP patterns that corresponded to the 13 known M types. Only 11 isolates gave RFLP patterns that differed from the 13 known M types. These were then analyzed by DNA sequencing and six additional M types were identified. In addition, we found that M93 GAS was the most common M type in the population studied, and is consistent with a previous study of Thai GAS isolates.
Conclusion:
PCR-RFLP analysis has the potential for the rapid screening of different GAS M types and is therefore considerably advantageous as an alternative M typing approach in developing countries in which GAS is endemic.
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.
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