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本文引用的文献

1
Alteration of the Helicobacter pylori membrane proteome in response to changes in environmental salt concentration.幽门螺杆菌膜蛋白质组对环境盐浓度变化的响应改变。
Proteomics Clin Appl. 2015 Dec;9(11-12):1021-34. doi: 10.1002/prca.201400176. Epub 2015 Sep 14.
2
Draft Genome Sequence of Gerbil-Adapted Carcinogenic Helicobacter pylori Strain 7.13.适应沙鼠的致癌幽门螺杆菌菌株7.13的基因组序列草图
Genome Announc. 2015 Jun 11;3(3):e00641-15. doi: 10.1128/genomeA.00641-15.
3
A mutation burst during the acute phase of Helicobacter pylori infection in humans and rhesus macaques.人类和恒河猴的幽门螺杆菌感染急性期发生突变爆发。
Nat Commun. 2014 Jun 13;5:4165. doi: 10.1038/ncomms5165.
4
Genes required for assembly of pili associated with the Helicobacter pylori cag type IV secretion system.与幽门螺杆菌cag IV型分泌系统相关的菌毛组装所需基因。
Infect Immun. 2014 Aug;82(8):3457-70. doi: 10.1128/IAI.01640-14. Epub 2014 Jun 2.
5
Analysis of surface-exposed outer membrane proteins in Helicobacter pylori.分析幽门螺杆菌表面暴露的外膜蛋白。
J Bacteriol. 2014 Jul;196(13):2455-71. doi: 10.1128/JB.01768-14. Epub 2014 Apr 25.
6
Helicobacter pylori CagA and gastric cancer: a paradigm for hit-and-run carcinogenesis.幽门螺杆菌 CagA 与胃癌:一个击中即跑致癌模式。
Cell Host Microbe. 2014 Mar 12;15(3):306-16. doi: 10.1016/j.chom.2014.02.008.
7
FeON-FeOFF: the Helicobacter pylori Fur regulator commutates iron-responsive transcription by discriminative readout of opposed DNA grooves.FeON-FeOFF:幽门螺杆菌 Fur 调控因子通过区分相反 DNA 沟槽的读取来调节铁反应性转录。
Nucleic Acids Res. 2014 Mar;42(5):3138-51. doi: 10.1093/nar/gkt1258. Epub 2013 Dec 9.
8
Diet, microbial virulence, and Helicobacter pylori-induced gastric cancer.饮食、微生物毒力和幽门螺杆菌引起的胃癌。
Gut Microbes. 2013 Nov-Dec;4(6):482-93. doi: 10.4161/gmic.26262. Epub 2013 Sep 3.
9
Random and site-specific mutagenesis of the Helicobacter pylori ferric uptake regulator provides insight into Fur structure-function relationships.随机和定点突变幽门螺杆菌的铁摄取调节蛋白,深入了解 Fur 结构与功能关系。
Mol Microbiol. 2013 Jul;89(2):304-23. doi: 10.1111/mmi.12278. Epub 2013 Jun 10.
10
Genome sequences of 65 Helicobacter pylori strains isolated from asymptomatic individuals and patients with gastric cancer, peptic ulcer disease, or gastritis.从无症状个体和胃癌、消化性溃疡病或胃炎患者中分离的 65 株幽门螺杆菌的基因组序列。
Pathog Dis. 2013 Jul;68(2):39-43. doi: 10.1111/2049-632X.12045. Epub 2013 May 23.

幽门螺杆菌在体内对高盐饮食的适应性。

Helicobacter pylori adaptation in vivo in response to a high-salt diet.

作者信息

Loh John T, Gaddy Jennifer A, Algood Holly M Scott, Gaudieri Silvana, Mallal Simon, Cover Timothy L

机构信息

Department of Medicine, Vanderbilt University School of Medicine, Nashville, Tennessee, USA.

Department of Medicine, Vanderbilt University School of Medicine, Nashville, Tennessee, USA Veterans Affairs Tennessee Valley Healthcare System, Nashville, Tennessee, USA.

出版信息

Infect Immun. 2015 Dec;83(12):4871-83. doi: 10.1128/IAI.00918-15. Epub 2015 Oct 5.

DOI:10.1128/IAI.00918-15
PMID:26438795
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4645402/
Abstract

Helicobacter pylori exhibits a high level of intraspecies genetic diversity. In this study, we investigated whether the diversification of H. pylori is influenced by the composition of the diet. Specifically, we investigated the effect of a high-salt diet (a known risk factor for gastric adenocarcinoma) on H. pylori diversification within a host. We analyzed H. pylori strains isolated from Mongolian gerbils fed either a high-salt diet or a regular diet for 4 months by proteomic and whole-genome sequencing methods. Compared to the input strain and output strains from animals fed a regular diet, the output strains from animals fed a high-salt diet produced higher levels of proteins involved in iron acquisition and oxidative-stress resistance. Several of these changes were attributable to a nonsynonymous mutation in fur (fur-R88H). Further experiments indicated that this mutation conferred increased resistance to high-salt conditions and oxidative stress. We propose a model in which a high-salt diet leads to high levels of gastric inflammation and associated oxidative stress in H. pylori-infected animals and that these conditions, along with the high intraluminal concentrations of sodium chloride, lead to selection of H. pylori strains that are most fit for growth in this environment.

摘要

幽门螺杆菌表现出高度的种内遗传多样性。在本研究中,我们调查了幽门螺杆菌的多样化是否受饮食组成的影响。具体而言,我们研究了高盐饮食(已知的胃腺癌风险因素)对宿主体内幽门螺杆菌多样化的影响。我们通过蛋白质组学和全基因组测序方法,分析了从喂食高盐饮食或常规饮食4个月的蒙古沙鼠中分离出的幽门螺杆菌菌株。与喂食常规饮食的动物的输入菌株和输出菌株相比,喂食高盐饮食的动物的输出菌株产生了更高水平的参与铁摄取和抗氧化应激的蛋白质。其中一些变化归因于fur基因(fur-R88H)中的一个非同义突变。进一步的实验表明,这种突变赋予了对高盐条件和氧化应激更强的抗性。我们提出了一个模型,即高盐饮食会导致幽门螺杆菌感染动物体内高水平的胃部炎症和相关的氧化应激,并且这些条件,连同管腔内高浓度的氯化钠,导致选择出最适合在这种环境中生长的幽门螺杆菌菌株。