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胃部疾病患者中不同幽门螺杆菌菌株的ureB序列多样性、脲酶活性与基因型变异之间的关系

Relationship between ureB Sequence Diversity, Urease Activity and Genotypic Variations of Different Helicobacter pylori Strains in Patients with Gastric Disorders.

作者信息

Ghalehnoei Hossein, Ahmadzadeh Alireza, Farzi Nastaran, Alebouyeh Masoud, Aghdaei Hamid Asadzadeh, Azimzadeh Pendram, Molaei Mahsa, Zali Mohammad Reza

出版信息

Pol J Microbiol. 2016;65(2):153-9.

Abstract

Association of the severity of Helicobacter pylori induced diseases with virulence entity of the colonized strains was proven in some studies. Urease has been demonstrated as a potent virulence factor for H. pylori. The main aim of this study was investigation of the relationships of ureB sequence diversity, urease activity and virulence genotypes of different H. pylori strains with histopathological changes of gastric tissue in infected patients suffering from different gastric disorders. Analysis of the virulence genotypes in the isolated strains indicated significant associations between the presence of severe active gastritis and cagA+ (P = 0.039) or cagA/iceA1 genotypes (P = 0.026), and intestinal metaplasia and vacA m1 (P = 0.008) or vacA s1/m2 (P = 0.001) genotypes. Our results showed a 2.4-fold increased risk of peptic ulcer (95% CI: 0.483-11.93), compared with gastritis, in the infected patients who had dupA positive strains; however this association was not statistically significant. The results of urease activity showed a significant mean difference between the isolated strains from patients with PUD and NUD (P = 0.034). This activity was relatively higher among patients with intestinal metaplasia. Also a significant association was found between the lack of cagA and increased urease activity among the isolated strains (P = 0.036). While the greatest sequence variation of ureB was detected in a strain from a patient with intestinal metaplasia, the sole determined amino acid change in UreB sequence (Ala201Thr, 30%), showed no influence on urease activity. In conclusion, the supposed role of H. pylori urease to form peptic ulcer and advancing of intestinal metaplasia was postulated in this study. Higher urease activity in the colonizing H. pylori strains that present specific virulence factors was indicated as a risk factor for promotion of histopathological changes of gastric tissue that advance gastric malignancy.

摘要

一些研究证实了幽门螺杆菌所致疾病的严重程度与定植菌株的毒力实体之间的关联。脲酶已被证明是幽门螺杆菌的一种强效毒力因子。本研究的主要目的是调查不同幽门螺杆菌菌株的ureB序列多样性、脲酶活性和毒力基因型与患有不同胃部疾病的感染患者胃组织组织病理学变化之间的关系。对分离菌株的毒力基因型分析表明,严重活动性胃炎与cagA+(P = 0.039)或cagA/iceA1基因型(P = 0.026)之间,以及肠化生与vacA m1(P = 0.008)或vacA s1/m2(P = 0.001)基因型之间存在显著关联。我们的结果显示,与胃炎患者相比,感染了dupA阳性菌株的患者患消化性溃疡的风险增加了2.4倍(95%可信区间:0.483 - 11.93);然而,这种关联在统计学上并不显著。脲酶活性结果显示,来自消化性溃疡患者和非溃疡性消化不良患者的分离菌株之间存在显著的平均差异(P = 0.034)。这种活性在肠化生患者中相对较高。在分离菌株中还发现cagA缺失与脲酶活性增加之间存在显著关联(P = 0.036)。虽然在一名肠化生患者的菌株中检测到ureB的最大序列变异,但UreB序列中唯一确定的氨基酸变化(Ala201Thr,30%)对脲酶活性没有影响。总之,本研究推测了幽门螺杆菌脲酶在形成消化性溃疡和推进肠化生方面的作用。定植的幽门螺杆菌菌株中较高的脲酶活性,这些菌株具有特定的毒力因子,被表明是促进胃组织组织病理学变化从而推进胃癌发生的一个危险因素。

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