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

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 ma...

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Main Authors: Yoonim N., Olive C., Pruksachatkunakorn C., Good M.F., Pruksakorn S.
Format: Article
Language:English
Published: 2014
Online Access:http://www.scopus.com/inward/record.url?eid=2-s2.0-27744601711&partnerID=40&md5=ad4cd9ae78b09a6be5a3289eacd5e799
http://www.ncbi.nlm.nih.gov/pubmed/16225702
http://cmuir.cmu.ac.th/handle/6653943832/1825
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spelling th-cmuir.6653943832-18252014-08-30T02:00:09Z M protein typing of Thai group A streptococcal isolates by PCR-restriction fragment length polymorphism analysis Yoonim N. Olive C. Pruksachatkunakorn C. Good M.F. Pruksakorn S. 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. © 2005 Yoonim et al; licensee BioMed Central Ltd. 2014-08-30T02:00:09Z 2014-08-30T02:00:09Z 2005 Article 14712180 10.1186/1471-2180-5-63 16225702 http://www.scopus.com/inward/record.url?eid=2-s2.0-27744601711&partnerID=40&md5=ad4cd9ae78b09a6be5a3289eacd5e799 http://www.ncbi.nlm.nih.gov/pubmed/16225702 http://cmuir.cmu.ac.th/handle/6653943832/1825 English
institution Chiang Mai University
building Chiang Mai University Library
country Thailand
collection CMU Intellectual Repository
language English
description 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. © 2005 Yoonim et al; licensee BioMed Central Ltd.
format Article
author Yoonim N.
Olive C.
Pruksachatkunakorn C.
Good M.F.
Pruksakorn S.
spellingShingle Yoonim N.
Olive C.
Pruksachatkunakorn C.
Good M.F.
Pruksakorn S.
M protein typing of Thai group A streptococcal isolates by PCR-restriction fragment length polymorphism analysis
author_facet Yoonim N.
Olive C.
Pruksachatkunakorn C.
Good M.F.
Pruksakorn S.
author_sort Yoonim N.
title M protein typing of Thai group A streptococcal isolates by PCR-restriction fragment length polymorphism analysis
title_short M protein typing of Thai group A streptococcal isolates by PCR-restriction fragment length polymorphism analysis
title_full M protein typing of Thai group A streptococcal isolates by PCR-restriction fragment length polymorphism analysis
title_fullStr M protein typing of Thai group A streptococcal isolates by PCR-restriction fragment length polymorphism analysis
title_full_unstemmed M protein typing of Thai group A streptococcal isolates by PCR-restriction fragment length polymorphism analysis
title_sort m protein typing of thai group a streptococcal isolates by pcr-restriction fragment length polymorphism analysis
publishDate 2014
url http://www.scopus.com/inward/record.url?eid=2-s2.0-27744601711&partnerID=40&md5=ad4cd9ae78b09a6be5a3289eacd5e799
http://www.ncbi.nlm.nih.gov/pubmed/16225702
http://cmuir.cmu.ac.th/handle/6653943832/1825
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