Azuma Takeshi, Yamakawa Akiyo, Yamazaki Shiho, Fukuta Kanako, Ohtani Masahiro, Ito Yoshiyuki, Dojo Manabu, Yamazaki Yukinao, Kuriyama Masaru
Second Department of Internal Medicine, Fukui Medical University, Japan.
J Infect Dis. 2002 Dec 1;186(11):1621-30. doi: 10.1086/345374. Epub 2002 Nov 11.
Genetic diversity within the cag pathogenicity island (PAI) of Helicobacter pylori may have a modifying effect on the pathogenic potential of the infecting strain. The genetic structure of the cag PAI was examined in Japanese isolates. The composition and nucleotide sequences of the cag PAI were quite similar among strains; however, diversity between 2 cag genes (virB10 and cagA) was observed. The variety in the number of repetition of the 5-amino acid sequence R1 (EPIYA) in the 3' region of the cagA gene was identified. The frequencies of the genotypes that contained >4 R1 sequences were significantly higher in atrophic gastritis-causing strains than in duodenal ulcer-causing strains. One-third of strains with >4 R1 sequences were gastric cancer-causing strains. Although the cag PAI is conserved in H. pylori isolates in Japan, H. pylori infection with the cagA genotype with >4 R1 sequences may correlate with the pathogenesis of atrophic gastritis and gastric cancer.
幽门螺杆菌细胞毒素相关基因(cag)致病岛(PAI)内的遗传多样性可能会对感染菌株的致病潜力产生修饰作用。对日本分离株的cag致病岛的遗传结构进行了检测。cag致病岛的组成和核苷酸序列在菌株之间相当相似;然而,观察到两个cag基因(virB10和cagA)之间存在多样性。鉴定出cagA基因3'区域中5个氨基酸序列R1(EPIYA)重复次数的差异。在萎缩性胃炎致病菌株中,包含>4个R1序列的基因型频率显著高于十二指肠溃疡致病菌株。三分之一具有>4个R1序列的菌株是胃癌致病菌株。尽管cag致病岛在日本的幽门螺杆菌分离株中是保守的,但感染具有>4个R1序列的cagA基因型的幽门螺杆菌可能与萎缩性胃炎和胃癌的发病机制相关。