Genetic characterization of Helicobacter pylori vacA and cagA genes in Thai gastro-duodenal and hepatobiliary patients

Authors

  • Wongwarut Boonyanugomol Mahidol University, AmnatChareon Campus, Amnat Chareon, Thailand
  • Narong Khuntikeo Faculty of Medicine, Khon Kaen University, Khon Kaen, Thailand
  • Ake Pugkhem Faculty of Medicine, Khon Kaen University, Khon Kaen, Thailand
  • Kookwan Sawadpanich Faculty of Medicine, Khon Kaen University, Khon Kaen, Thailand
  • Chariya Hahnvajanawong Faculty of Medicine, Khon Kaen University, Khon Kaen, Thailand
  • Phattharaphon Wongphutorn Faculty of Medicine, Khon Kaen University, Khon Kaen, Thailand
  • Bandit Khampoosa King Mongkut’s University of Technology Thonburi, Bangkok, Thailand
  • Chariya Chomvarin Faculty of Medicine, Khon Kaen University, Khon Kaen, Thailand

DOI:

https://doi.org/10.3855/jidc.8126

Keywords:

H. pylori, vacA, cagA, gastro-duodenal diseases, hepatobiliary diseases

Abstract

Introduction: H. pylori has been detected in patients with hepatobiliary diseases. It is currently unclear whether the H. pylori detected in hepatobiliary patients are genetically similar to those in gastro-duodenal patients. The aim of this study was to determine H. pylori vacA and cagA genotypes in Thai patients with gastro-duodenal and hepatobiliary diseases.

Methodology: H. pylori DNA was extracted from samples from gastric biopsies of gastro-duodenal patients (n=100) and from bile samples of hepatobiliary patients (n=80). The vacA and cagA genotypes were performed via polymerase chain reaction (PCR) followed by DNA sequencing.

Results: The vacA m1 was found in Thai hepatobiliary patients (90%) at a higher rate compared with gastro-duodenal patients (50%).The combined vacA s1a+c/m1 were mostly found in Thai gastro-duodenal and hepatobiliary patients. The cagA gene was detected in 94% of patients with gastro-duodenal diseases compared with 28.8% in those with hepatobiliary diseases (p<0.05). On the other hand, the Western type cagA was more prominent among hepatobiliary patients (100%) than gastro-duodenal patients (57.4%), and this type was grouped into same cluster with Thai gastro-duodenal patients via phylogenetic analysis.

Conclusions: Based on vacA and cagA analysis, we conclude that infection with H. pylori in gastro-duodenal and hepatobiliary patients may be caused by the different H. pylori strains.

Author Biographies

Wongwarut Boonyanugomol, Mahidol University, AmnatChareon Campus, Amnat Chareon, Thailand

Mahidol University, Amnat Chareon Campus, Amnat Chareon, Thailand

Narong Khuntikeo, Faculty of Medicine, Khon Kaen University, Khon Kaen, Thailand

Department of Surgery, Faculty of Medicine, Khon Kaen University, Khon Kaen, Thailand

Ake Pugkhem, Faculty of Medicine, Khon Kaen University, Khon Kaen, Thailand

Department of Surgery, Faculty of Medicine, Khon Kaen University, Khon Kaen, Thailand

Kookwan Sawadpanich, Faculty of Medicine, Khon Kaen University, Khon Kaen, Thailand

Department of Medicine, Faculty of Medicine, Khon Kaen University, Khon Kaen, Thailand

Chariya Hahnvajanawong, Faculty of Medicine, Khon Kaen University, Khon Kaen, Thailand

Department of Microbiology, Faculty of Medicine, Khon Kaen University, Khon Kaen, Thailand

Phattharaphon Wongphutorn, Faculty of Medicine, Khon Kaen University, Khon Kaen, Thailand

Department of Microbiology, Faculty of Medicine, Khon Kaen University, Khon Kaen, Thailand

Bandit Khampoosa, King Mongkut’s University of Technology Thonburi, Bangkok, Thailand

School of Bioinformatics and Systems Biology, King Mongkut’s University of Technology Thonburi, Bangkok, Thailand

Chariya Chomvarin, Faculty of Medicine, Khon Kaen University, Khon Kaen, Thailand

Department of Microbiology, faculty of Medicine, Khon Kaen University, Khon Kaen, Thailand

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Published

2017-01-30

How to Cite

1.
Boonyanugomol W, Khuntikeo N, Pugkhem A, Sawadpanich K, Hahnvajanawong C, Wongphutorn P, Khampoosa B, Chomvarin C (2017) Genetic characterization of Helicobacter pylori vacA and cagA genes in Thai gastro-duodenal and hepatobiliary patients. J Infect Dev Ctries 11:42–50. doi: 10.3855/jidc.8126

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Section

Original Articles