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: Nonglak Yoonim, Colleen Olive, Chulabhorn Pruksachatkunakorn, Michael F. Good, Sumalee Pruksakorn
Format: Journal
Published: 2018
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spelling th-cmuir.6653943832-622472018-09-11T09:25:47Z M protein typing of Thai group A streptococcal isolates by PCR-restriction fragment length polymorphism analysis Nonglak Yoonim Colleen Olive Chulabhorn Pruksachatkunakorn Michael F. Good Sumalee Pruksakorn Immunology and Microbiology Medicine 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. 2018-09-11T09:24:20Z 2018-09-11T09:24:20Z 2005-10-16 Journal 14712180 14712180 2-s2.0-27744601711 10.1186/1471-2180-5-63 https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=27744601711&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/62247
institution Chiang Mai University
building Chiang Mai University Library
country Thailand
collection CMU Intellectual Repository
topic Immunology and Microbiology
Medicine
spellingShingle Immunology and Microbiology
Medicine
Nonglak Yoonim
Colleen Olive
Chulabhorn Pruksachatkunakorn
Michael F. Good
Sumalee Pruksakorn
M protein typing of Thai group A streptococcal isolates by PCR-restriction fragment length polymorphism analysis
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 Journal
author Nonglak Yoonim
Colleen Olive
Chulabhorn Pruksachatkunakorn
Michael F. Good
Sumalee Pruksakorn
author_facet Nonglak Yoonim
Colleen Olive
Chulabhorn Pruksachatkunakorn
Michael F. Good
Sumalee Pruksakorn
author_sort Nonglak Yoonim
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 2018
url https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=27744601711&origin=inward
http://cmuir.cmu.ac.th/jspui/handle/6653943832/62247
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