Author/Authors :
Haddadi, Mohammad Hossein Department of Bacteriology and Virology - Shiraz Medical School - Shiraz University of Medical Sciences, Iran , Bazargani, Abdollah Department of Bacteriology and Virology - Shiraz Medical School - Shiraz University of Medical Sciences, Iran , Khashei, Reza Department of Bacteriology and Virology - Shiraz Medical School - Shiraz University of Medical Sciences, Iran , Fattahi, Mohammad Reza Department of Internal Medicine - Gastroenterohepatology Research Center - Shiraz University of Medical Sciences, Iran , Bagheri Lankarani, Kamran Department of Internal Medicine - Gastroenterohepatology Research Center - Shiraz University of Medical Sciences, Iran , Moini, Maryam Department of Internal Medicine - Gastroenterohepatology Research Center - Shiraz University of Medical Sciences, Iran , Rokni Hosseini, Mohammad Hossein Department of Bacteriology and Virology - Shiraz Medical School - Shiraz University of Medical Sciences, Iran
Abstract :
Aim: Our aim was to determine the EPIYA-cagA Phosphorylation sites and dupA gene in H. pylori isolates among
patients with upper gastrointestinal diseases.
Background: Pathogenicity of the cagA-positive Helicobacter pylori is associated with EPIYA motifs and higher
number of EPIYA-C segments is a risk factor of gastric cancer, while duodenal ulcer-promoting gene (dupA) is
determined as a protective factor against gastric cancer.
Patients and methods: A total of 280 non-repeated gastric biopsies obtained from patients undergoing endoscopy from
January 2013 till July 2013. Samples were cultured on selective horse blood agar and incubated in microaerophilic
atmosphere. The isolated organisms were identified as H. pylori by Gram staining and positive oxidase, catalase, and
urease tests. Various motif types of cagA and the prevalence of dupA were determined by PCR method.
Results: Out of 280 specimens, 128 (54.7%) isolated organisms were identified as H. pylori. Of 120 H. pylori isolates,
35.9% were dupA positive and 56.26% were cagA positive, while cagA with ABC and ABCC motifs were 55.5% and
44.5%, respectively. Fifty six percent of the isolates with the ABCC motif have had dupA genes. We also found a
significant association between strains with genotypes of dupA-ABC and duodenal ulcer disease (p = 0.007).
Conclusion: The results of this study showed that the prevalence of cagA-positive H. pylori in Shiraz was as high as in
western countries and higher numbers of EPIYA-C segments were seen in gastric cancer patients. We may also use
dupA as a prognostic and pathogenic marker for duodenal ulcer disease and cagA with the segment C for gastric cancer
and gastric ulcer disease in this region.
Keywords :
Helicobacter pylori , Gastric Cancer , cagA motifs , dupA , gastrointestinal disease