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Helicobacter pylori cagA gene variants in Malaysians of different ethnicity
We have defined DNA repeat variability in the 3′-terminus of the cagA gene of Helicobacter pylori strains from Malaysian patients of different ethnicities. We identified different alleles based on the EPIYA repeats. cagA types A-B-D and A-B-B-D are more similar to the sequence of Japanese strains, w...
Autores principales: | , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Springer-Verlag
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2693772/ https://www.ncbi.nlm.nih.gov/pubmed/19247698 http://dx.doi.org/10.1007/s10096-009-0712-x |
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author | Mohamed, Ramelah Hanafiah, Alfizah Rose, Isa M. Manaf, Mohd Rizal A. Abdullah, Shiekh Anwar Sagap, Ismail van Belkum, A. Yaacob, Jasmi A. |
author_facet | Mohamed, Ramelah Hanafiah, Alfizah Rose, Isa M. Manaf, Mohd Rizal A. Abdullah, Shiekh Anwar Sagap, Ismail van Belkum, A. Yaacob, Jasmi A. |
author_sort | Mohamed, Ramelah |
collection | PubMed |
description | We have defined DNA repeat variability in the 3′-terminus of the cagA gene of Helicobacter pylori strains from Malaysian patients of different ethnicities. We identified different alleles based on the EPIYA repeats. cagA types A-B-D and A-B-B-D are more similar to the sequence of Japanese strains, whereas cagA types A-B-C, A-B-C-C, A-B and A-C displayed similarity to strain 26695 sequences. A significant association was found between cagA genotypes and patients’ ethnicity, with cagA type A-B-D being predominantly isolated from Chinese patients and cagA type A-B-C from Malays and Indians. Our data further corroborate the possibility that variant biological activity of CagA may affect the host specificity and/or pathogenicity of H. pylori. |
format | Text |
id | pubmed-2693772 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | Springer-Verlag |
record_format | MEDLINE/PubMed |
spelling | pubmed-26937722009-06-09 Helicobacter pylori cagA gene variants in Malaysians of different ethnicity Mohamed, Ramelah Hanafiah, Alfizah Rose, Isa M. Manaf, Mohd Rizal A. Abdullah, Shiekh Anwar Sagap, Ismail van Belkum, A. Yaacob, Jasmi A. Eur J Clin Microbiol Infect Dis Brief Report We have defined DNA repeat variability in the 3′-terminus of the cagA gene of Helicobacter pylori strains from Malaysian patients of different ethnicities. We identified different alleles based on the EPIYA repeats. cagA types A-B-D and A-B-B-D are more similar to the sequence of Japanese strains, whereas cagA types A-B-C, A-B-C-C, A-B and A-C displayed similarity to strain 26695 sequences. A significant association was found between cagA genotypes and patients’ ethnicity, with cagA type A-B-D being predominantly isolated from Chinese patients and cagA type A-B-C from Malays and Indians. Our data further corroborate the possibility that variant biological activity of CagA may affect the host specificity and/or pathogenicity of H. pylori. Springer-Verlag 2009-02-27 2009-07 /pmc/articles/PMC2693772/ /pubmed/19247698 http://dx.doi.org/10.1007/s10096-009-0712-x Text en © The Author(s) 2009 |
spellingShingle | Brief Report Mohamed, Ramelah Hanafiah, Alfizah Rose, Isa M. Manaf, Mohd Rizal A. Abdullah, Shiekh Anwar Sagap, Ismail van Belkum, A. Yaacob, Jasmi A. Helicobacter pylori cagA gene variants in Malaysians of different ethnicity |
title | Helicobacter pylori cagA gene variants in Malaysians of different ethnicity |
title_full | Helicobacter pylori cagA gene variants in Malaysians of different ethnicity |
title_fullStr | Helicobacter pylori cagA gene variants in Malaysians of different ethnicity |
title_full_unstemmed | Helicobacter pylori cagA gene variants in Malaysians of different ethnicity |
title_short | Helicobacter pylori cagA gene variants in Malaysians of different ethnicity |
title_sort | helicobacter pylori caga gene variants in malaysians of different ethnicity |
topic | Brief Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2693772/ https://www.ncbi.nlm.nih.gov/pubmed/19247698 http://dx.doi.org/10.1007/s10096-009-0712-x |
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