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γ-谷氨酰转肽酶在幽门螺杆菌属中的保守功能证据。

Evidence for conserved function of γ-glutamyltranspeptidase in Helicobacter genus.

机构信息

Department of Food Hygiene and Environmental Health, Faculty of Veterinary Medicine, University of Helsinki, Helsinki, Finland.

出版信息

PLoS One. 2012;7(2):e30543. doi: 10.1371/journal.pone.0030543. Epub 2012 Feb 14.

Abstract

The confounding consequences of Helicobacter bilis infection in experimental mice populations are well recognized, but the role of this bacterium in human diseases is less known. Limited data are available on virulence determinants of this species. In Helicobacter pylori, γ-glutamyltranspeptidase (γGT) contributes to the colonization of the gastric mucosa and to the pathogenesis of peptic ulcer. The role of γGT in H. bilis infections remains unknown. The annotated genome sequence of H. bilis revealed two putative ggt genes and our aim was to characterize these H. bilis γGT paralogues. We performed a phylogenetic analysis to understand the evolution of Helicobacter γGTs and to predict functional activities of these two genes. In addition, both copies of H. bilis γGTs were expressed as recombinant proteins and their biochemical characteristics were analysed. Functional complementation of Esherichia coli deficient in γGT activity and deletion of γGT in H. bilis were performed. Finally, the inhibitory effect of T-cell and gastric cell proliferation by H. bilis γGT was assessed. Our results indicated that one gene is responsible for γGT activity, while the other showed no γGT activity due to lack of autoprocessing. Although both H. bilis and H. pylori γGTs exhibited a similar affinity to L-Glutamine and γ-Glutamyl-p-nitroanilide, the H. bilis γGT was significantly less active. Nevertheless, H. bilis γGT inhibited T-cell proliferation at a similar level to that observed for H. pylori. Finally, we showed a similar suppressive influence of both H. bilis and H. pylori γGTs on AGS cell proliferation mediated by an apoptosis-independent mechanism. Our data suggest a conserved function of γGT in the Helicobacter genus. Since γGT is present only in a few enterohepatic Helicobacter species, its expression appears not to be essential for colonization of the lower gastrointestinal tract, but it could provide metabolic advantages in colonization capability of different niches.

摘要

胆汁螺旋杆菌感染实验鼠所带来的复杂后果已被广泛认知,但这种细菌在人类疾病中的作用却知之甚少。目前仅有少量关于该物种毒力决定因子的相关数据。在幽门螺旋杆菌中,γ-谷氨酰转移酶(γGT)有助于胃黏膜的定植和消化性溃疡的发病机制。γGT 在胆汁螺旋杆菌感染中的作用尚不清楚。胆汁螺旋杆菌的基因组序列注释显示存在两个推定的 ggt 基因,我们的目的是对这两种胆汁螺旋杆菌 γGT 同工酶进行特征描述。我们进行了系统发育分析,以了解幽门螺旋杆菌 γGT 的进化并预测这两个基因的功能活性。此外,我们还表达了两种重组蛋白并对其生化特性进行了分析。我们还对缺乏 γGT 活性的大肠杆菌进行了功能互补和胆汁螺旋杆菌中 γGT 的缺失实验。最后,我们评估了胆汁螺旋杆菌 γGT 对 T 细胞和胃细胞增殖的抑制作用。我们的研究结果表明,一个基因负责 γGT 的活性,而另一个由于缺乏自加工而不具有 γGT 活性。尽管胆汁螺旋杆菌和幽门螺旋杆菌的 γGT 都对 L-谷氨酰胺和 γ-谷氨酰对硝基苯胺表现出相似的亲和力,但胆汁螺旋杆菌的 γGT 活性明显较低。尽管如此,胆汁螺旋杆菌 γGT 对 T 细胞增殖的抑制作用与观察到的幽门螺旋杆菌 γGT 相似。最后,我们发现,无论是胆汁螺旋杆菌还是幽门螺旋杆菌的 γGT,都通过一种非凋亡机制对 AGS 细胞增殖具有相似的抑制作用。我们的数据表明,γGT 在螺旋杆菌属中具有保守功能。由于 γGT 仅存在于少数肠肝螺旋杆菌物种中,其表达似乎不是定植下消化道所必需的,但它可能为不同生态位的定植能力提供代谢优势。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f0dc/3279353/86f0648c93f7/pone.0030543.g001.jpg

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