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本文引用的文献

1
Determination of Helicobacter pylori virulence by analysis of the cag pathogenicity island isolated from Iranian patients.通过分析从伊朗患者中分离出的cag致病岛来确定幽门螺杆菌的毒力。
Dig Liver Dis. 2009 Sep;41(9):634-8. doi: 10.1016/j.dld.2009.01.010. Epub 2009 Mar 3.
2
Helicobacter pylori cagA status and peptic ulcer disease in Iran.伊朗幽门螺杆菌cagA状态与消化性溃疡病
Dig Dis Sci. 2009 Mar;54(3):608-13. doi: 10.1007/s10620-008-0378-8. Epub 2008 Jul 10.
3
Clinical relevance of Helicobacter pylori cagA and vacA gene polymorphisms.幽门螺杆菌cagA和vacA基因多态性的临床相关性
Gastroenterology. 2008 Jul;135(1):91-9. doi: 10.1053/j.gastro.2008.03.041. Epub 2008 Mar 25.
4
Differences in virulence markers between Helicobacter pylori strains from Iraq and those from Iran: potential importance of regional differences in H. pylori-associated disease.伊拉克幽门螺杆菌菌株与伊朗幽门螺杆菌菌株毒力标志物的差异:幽门螺杆菌相关疾病区域差异的潜在重要性。
J Clin Microbiol. 2008 May;46(5):1774-9. doi: 10.1128/JCM.01737-07. Epub 2008 Mar 19.
5
A new Helicobacter pylori vacuolating cytotoxin determinant, the intermediate region, is associated with gastric cancer.一种新的幽门螺杆菌空泡毒素决定簇,即中间区域,与胃癌相关。
Gastroenterology. 2007 Sep;133(3):926-36. doi: 10.1053/j.gastro.2007.06.056. Epub 2007 Jul 3.
6
Strategy to characterize the number and type of repeating EPIYA phosphorylation motifs in the carboxyl terminus of CagA protein in Helicobacter pylori clinical isolates.鉴定幽门螺杆菌临床分离株中CagA蛋白羧基末端重复EPIYA磷酸化基序的数量和类型的策略。
J Clin Microbiol. 2007 Feb;45(2):488-95. doi: 10.1128/JCM.01616-06. Epub 2006 Dec 6.
7
The role of Helicobacter pylori CagA in gastric carcinogenesis.幽门螺杆菌细胞毒素相关基因A(CagA)在胃癌发生中的作用。
Int J Hematol. 2006 Nov;84(4):301-8. doi: 10.1532/IJH97.06166.
8
Association of H pylori cagA and vacA genotypes and IL-8 gene polymorphisms with clinical outcome of infection in Iranian patients with gastrointestinal diseases.幽门螺杆菌cagA和vacA基因型及IL-8基因多态性与伊朗胃肠疾病患者感染临床结局的关联
World J Gastroenterol. 2006 Aug 28;12(32):5205-10. doi: 10.3748/wjg.v12.i32.5205.
9
Influence of EPIYA-repeat polymorphism on the phosphorylation-dependent biological activity of Helicobacter pylori CagA.EPIYA重复多态性对幽门螺杆菌CagA磷酸化依赖性生物学活性的影响。
Gastroenterology. 2006 Apr;130(4):1181-90. doi: 10.1053/j.gastro.2005.12.038.
10
Helicobacter pylori CagA -- a bacterial intruder conspiring gastric carcinogenesis.幽门螺杆菌CagA——一种参与胃癌发生的细菌入侵者。
Int J Cancer. 2006 Sep 15;119(6):1217-23. doi: 10.1002/ijc.21831.

分析伊朗人群中分离的幽门螺杆菌 cagA 基因 3'-末端可变区。

Analysis of 3'-end variable region of the cagA gene in Helicobacter pylori isolated from Iranian population.

机构信息

Research Center of Gastroenterology and Liver Diseases, Shahid Beheshti University, MC, Tehran, Iran.

出版信息

J Gastroenterol Hepatol. 2010 Jan;25(1):172-7. doi: 10.1111/j.1440-1746.2009.05979.x. Epub 2009 Sep 27.

DOI:10.1111/j.1440-1746.2009.05979.x
PMID:19793167
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2818463/
Abstract

BACKGROUND AND AIMS

The 3' region of the cagA gene, the most well-known virulence factor of Helicobacter pylori, contains Glu-Pro-Ile-Tyr-Ala (EPIYA) motifs. Four segments flanking the EPIYA motifs, EPIYA-A, -B, -C, or -D, were reported to play important roles in H. pylori-related gastroduodenal pathogenesis. The aim was to determine the roles of EPIYA segments in gastroduodenal pathogenesis in an Iranian population.

METHODS

A total of 92 cagA-positive Iranian strains isolated from dyspepsia patients with non-ulcer dyspepsia (n = 77), peptic ulcer (n = 11) and gastric cancer (n = 4) were studied. The EPIYA motif genotyping was determined by polymerase chain reaction and sequencing.

RESULTS

A total of 86 (93.5%) strains had three copies of EPIYA (ABC type), three (3.3%) had four copies (ABCC type) and three (3.3%) had two copies (AB type). The alignment of the deduced protein sequences confirmed that there were no East Asian type EPIYA-D sequences (EPIYATIDFDEANQAG) in Iranian strains. When the prevalence of strains with multiple EPIYA-C segments in Iran was compared with previously published data, it was much lower than that in Colombia and Italy, but was higher than that of Iraq, and the patterns were parallel to the incidence of gastric cancer in these countries.

CONCLUSION

The structure of the 3' region of the cagA gene in Iranian strains was Western type. Although we could not find differences between EPIYA types and clinical outcomes, low prevalence of strains with multiple EPIYA-C segments might be reasons for low incidence of gastric cancer in Iran.

摘要

背景与目的

幽门螺杆菌(H. pylori)最著名的毒力因子 cagA 基因的 3' 区含有 Glu-Pro-Ile-Tyr-Ala(EPIYA)基序。EPIYA 基序侧翼的四个片段,EPIYA-A、-B、-C 或 -D,据报道在 H. pylori 相关的胃十二指肠发病机制中发挥重要作用。本研究旨在确定 EPIYA 片段在伊朗人群胃十二指肠发病机制中的作用。

方法

共研究了 92 株来自消化不良患者的 cagA 阳性伊朗菌株,其中非溃疡性消化不良(n = 77)、消化性溃疡(n = 11)和胃癌(n = 4)。通过聚合酶链反应和测序确定 EPIYA 基序基因分型。

结果

共有 86 株(93.5%)菌株具有三个 EPIYA 拷贝(ABC 型),3 株(3.3%)菌株具有四个拷贝(ABCC 型),3 株(3.3%)菌株具有两个拷贝(AB 型)。推导蛋白序列的比对证实伊朗菌株中没有东亚型 EPIYA-D 序列(EPIYATIDFDEANQAG)。与以前发表的数据相比,伊朗多拷贝 EPIYA-C 段菌株的流行率明显低于哥伦比亚和意大利,但高于伊拉克,与这些国家胃癌的发病率模式相似。

结论

伊朗菌株 cagA 基因 3' 区结构为西方型。尽管我们没有发现 EPIYA 类型与临床结果之间的差异,但多拷贝 EPIYA-C 段菌株的低流行率可能是伊朗胃癌发病率低的原因。