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Helicobacter pylori cagA and vacA genotypes in Cuban and Venezuelan populations
The aim of this study was to determine the presence of Helicobacter pylori cytotoxin-associated gene (cagA)/vacuolating cytotoxin gene (vacA) among patients with chronic gastritis in Cuba and Venezuela. Gastric antrum biopsies were taken for culture, DNA extraction and PCR analysis. Amplification of...
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Published in: | Memórias do Instituto Oswaldo Cruz 2010-05, Vol.105 (3), p.331-335 |
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Main Authors: | , , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | The aim of this study was to determine the presence of Helicobacter
pylori cytotoxin-associated gene (cagA)/vacuolating cytotoxin gene
(vacA) among patients with chronic gastritis in Cuba and Venezuela.
Gastric antrum biopsies were taken for culture, DNA extraction and PCR
analysis. Amplification of vacA and cagA segments was performed using
two regions of cagA: 349 bp were amplified with the F1/B1 primers and
the remaining 335 bp were amplified with the B7629/B7628 primers. The
VA1-F/VA1-R set of primers was used to amplify the 259-bp (s1) or
286-bp (s2) product and the VAG-R/VAG-F set of primers was used to
amplify the 567-bp (m1) or 642-bp (m2) regions of vacA. cagA was
detected in 87% of the antral samples from Cuban patients and 80.3% of
those from Venezuelan patients. All possible combinations of vacA
regions were found, with the exception of s2/m1. The predominant
combination found in both countries was s1/m1. The percentage of cagA+
strains was increased by the use of a second set of primers and a
greater number of strains was amplified with the B7629/B7628 primers in
the Cuban patients (p = 0.0001). There was no significant difference
between the presence of the allelic variants of vacA and cagA in both
populations. The predominant genotype was cagA+/s1m1 in both countries.
The results support the necessary investigation of isolates circulating
among the human population in each region. |
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ISSN: | 1678-8060 0074-0276 1678-8060 0074-0276 |
DOI: | 10.1590/S0074-02762010000300016 |