2010
DOI: 10.1186/1476-0711-9-10
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Prevalence of Helicobacter pylori vacA, cagA, iceA and oipA genotypes in Tunisian patients

Abstract: BackgroundDistinct virulence factors of H. pylori have been described: the vaculating cytotoxin (vacA), the cytotoxin associated gene (cagA), the induced by contact with epithelium factor Antigen (iceA gene) and the outer membrane protein oipA. In Tunisia, there are no data regarding the pattern of H. pylori genotypes; therefore, this prospective and multicentre study was the first to be done in Tunisia and aimed to investigate the prevalence of the vacA, cagA, iceA and oipA genotypes of H. pylori isolates fro… Show more

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Cited by 71 publications
(63 citation statements)
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“…H. pylori strains from human biopsy specimens were cultured, and 24-h cultures were used for DNA extraction using a MagNA Pure compact system and DNA isolation kit (Roche) according to the manufacturer's instructions. A PCR was then performed to determine cagA and cagM status as previously described (18,19). In clinical isolates, the presence of cagA and cagM was used as a marker of the presence of the cag PAI.…”
Section: Methodsmentioning
confidence: 99%
“…H. pylori strains from human biopsy specimens were cultured, and 24-h cultures were used for DNA extraction using a MagNA Pure compact system and DNA isolation kit (Roche) according to the manufacturer's instructions. A PCR was then performed to determine cagA and cagM status as previously described (18,19). In clinical isolates, the presence of cagA and cagM was used as a marker of the presence of the cag PAI.…”
Section: Methodsmentioning
confidence: 99%
“…In a study conducted by Mansour and colleagues (17), there was no significant association between cagA gene and sex, but the association was statistically significant among the vacA, iceA and oipA genes (17). …”
Section: H Pylori Genotypesmentioning
confidence: 99%
“…Multiplex PCR was used to study the distribution of vacA (s1a, s1b, s1c, s2, m1a, m1b and m2) and cagA genotypes. List of primers and PCR condition is shown in Table 1 (14,15). All runs were done using a programmable thermal cycler (Eppendorf-Netheler-Hinz GmbH, Germany) PCR device.…”
Section: Genotyping Of Vaca and Caga Genotypesmentioning
confidence: 99%