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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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Autores principales: Yoonim, Nonglak, Olive, Colleen, Pruksachatkunakorn, Chulabhorn, Good, Michael F, Pruksakorn, Sumalee
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2005
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1274321/
https://www.ncbi.nlm.nih.gov/pubmed/16225702
http://dx.doi.org/10.1186/1471-2180-5-63
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author Yoonim, Nonglak
Olive, Colleen
Pruksachatkunakorn, Chulabhorn
Good, Michael F
Pruksakorn, Sumalee
author_facet Yoonim, Nonglak
Olive, Colleen
Pruksachatkunakorn, Chulabhorn
Good, Michael F
Pruksakorn, Sumalee
author_sort Yoonim, Nonglak
collection PubMed
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.
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spelling pubmed-12743212005-10-29 M protein typing of Thai group A streptococcal isolates by PCR-Restriction fragment length polymorphism analysis Yoonim, Nonglak Olive, Colleen Pruksachatkunakorn, Chulabhorn Good, Michael F Pruksakorn, Sumalee BMC Microbiol Research Article 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. BioMed Central 2005-10-16 /pmc/articles/PMC1274321/ /pubmed/16225702 http://dx.doi.org/10.1186/1471-2180-5-63 Text en Copyright © 2005 Yoonim et al; licensee BioMed Central Ltd.
spellingShingle Research Article
Yoonim, Nonglak
Olive, Colleen
Pruksachatkunakorn, Chulabhorn
Good, Michael F
Pruksakorn, Sumalee
M protein typing of Thai group A streptococcal isolates by PCR-Restriction fragment length polymorphism analysis
title 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_short 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
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1274321/
https://www.ncbi.nlm.nih.gov/pubmed/16225702
http://dx.doi.org/10.1186/1471-2180-5-63
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