Gastric microbial community profiling reveals a dysbiotic cancer-associated microbiota.
Gastric microbial community profiling reveals a dysbiotic cancer-associated microbiota.
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DOI:
10.1136/gutjnl-2017-314205
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发表时间:
2018-03
期刊:
影响因子:
24.5
通讯作者:
Figueiredo C
中科院分区:
文献类型:
--
作者:
Ferreira RM;Pereira-Marques J;Pinto-Ribeiro I;Costa JL;Carneiro F;Machado JC;Figueiredo C
Gastric carcinoma development is triggered by Helicobacter pylori. Chronic H. pylori infection leads to reduced acid secretion, which may allow the growth of a different gastric bacterial community. This change in the microbiome may increase aggression to the gastric mucosa and contribute to malignancy. Our aim was to evaluate the composition of the gastric microbiota in chronic gastritis and in gastric carcinoma. The gastric microbiota was retrospectively investigated in 54 patients with gastric carcinoma and 81 patients with chronic gastritis by 16S rRNA gene profiling, using next-generation sequencing. Differences in microbial composition of the two patient groups were assessed using linear discriminant analysis effect size. Associations between the most relevant taxa and clinical diagnosis were validated by real-time quantitative PCR. Predictive functional profiling of microbial communities was obtained with PICRUSt. The gastric carcinoma microbiota was characterised by reduced microbial diversity, by decreased abundance of Helicobacter and by the enrichment of other bacterial genera, mostly represented by intestinal commensals. The combination of these taxa into a microbial dysbiosis index revealed that dysbiosis has excellent capacity to discriminate between gastritis and gastric carcinoma. Analysis of the functional features of the microbiota was compatible with the presence of a nitrosating microbial community in carcinoma. The major observations were confirmed in validation cohorts from different geographic origins. Detailed analysis of the gastric microbiota revealed for the first time that patients with gastric carcinoma exhibit a dysbiotic microbial community with genotoxic potential, which is distinct from that of patients with chronic gastritis.
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影响因子:
4.6
作者:
Aviles-Jimenez F;Vazquez-Jimenez F;Medrano-Guzman R;Mantilla A;Torres J
通讯作者:
Torres J
影响因子:
3.7
作者:
Li XX;Wong GL;To KF;Wong VW;Lai LH;Chow DK;Lau JY;Sung JJ;Ding C
通讯作者:
Ding C
DOI:
10.1099/ijs.0.067017-0
发表时间:
2015-02-01
影响因子:
2.8
作者:
Jiao, Yin Shan;Yan, Hui;Chen, Wen Feng
通讯作者:
Chen, Wen Feng
DOI:
10.1056/nejmra0707500
发表时间:
2008-10-30
期刊:
The New England journal of medicine
影响因子:
--
作者:
Kelly, Ciaran P;LaMont, J Thomas
通讯作者:
LaMont, J Thomas
影响因子:
3.7
作者:
Andersson, Anders F.;Lindberg, Mathilda;Jakobsson, Hedvig;Backhed, Fredrik;Nyren, Pal;Engstrand, Lars
通讯作者:
Engstrand, Lars