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DOI 10.1016/j.micpath.2013.04.001

Медицинская библиотека · Microbial pathogenesis · 2013

Distribution of Helicobacter pylori virulence markers in patients with gastroduodenal diseases in a region at high risk of gastric cancer.

Wang Ming-yi, Chen Cheng, Gao Xiao-zhong, Li Jie, Yue Jing, Ling Feng, Wang Xiao-chun, Shao Shi-he

СтатьяПоддержка исследования: вне правительства СШАПеревод пока не подготовлен

Аннотация

ABSTRACT

BACKGROUND

Helicobacter pylori (H. pylori) is a major human pathogen that is responsible for various gastroduodenal diseases. We investigated the prevalence of H. pylori virulence markers in a region at high risk of gastric cancer.

METHODS

One hundred and sixteen H. pylori strains were isolated from patients with gastroduodenal diseases. cagA, the cagA 3' variable region, cagPAI genes, vacA, and dupA genotypes were determined by PCR, and some amplicons of the cagA 3' variable region, cagPAI genes and dupA were sequenced.

RESULTS

cagA was detected in all strains. The cagA 3' variable region of 85 strains (73.3%) was amplified, and the sequences of 24 strains were obtained including 22 strains possessing the East Asian-type. The partial cagPAI presented at a higher frequency in chronic gastritis (44.4%) than that of the severe clinical outcomes (9.7%, p < 0.001). The most prevalent vacA genotypes were s1a/m2 (48.3%) and s1c/m2 (13.8%). Thirty-six strains (31.0%) possessed dupA and sequencing of dupA revealed an ORF of 2449-bp. The prevalence of dupA was significantly higher in strains from patients with the severe clinical outcomes (40.3%) than that from chronic gastritis (20.4%, p = 0.02).

CONCLUSION

The high rate of East Asian-type cagA, intact cagPAI, virulent vacA genotypes, and the intact long-type dupA may underlie the high risk of gastric cancer in the region.

Для цитирования: Wang Ming-yi, Chen Cheng, Gao Xiao-zhong, Li Jie, Yue Jing, Ling Feng, Wang Xiao-chun, Shao Shi-he. Distribution of Helicobacter pylori virulence markers in patients with gastroduodenal diseases in a region at high risk of gastric cancer.. Microbial pathogenesis. 2013. DOI: 10.1016/j.micpath.2013.04.001.

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