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Differences in Gastric Mucosal Microbiota Profiling in Patients with Chronic Gastritis, Intestinal Metaplasia, and Gastric Cancer Using Pyrosequencing Methods

Authors
Eun, Chang SooKim, Byung KwonHan, Dong SooKim, Seon YoungKim, Kyung MoChoi, Bo YoulSong, Kyu SangKim, Yong SungKim, Jihyun F.
Issue Date
Dec-2014
Publisher
Blackwell Publishing Inc.
Keywords
gastric cancer; H; pylori; 16S ribosomal RNA; carcinogenesis
Citation
Helicobacter, v.19, no.6, pp 407 - 416
Pages
10
Indexed
SCI
SCIE
SCOPUS
Journal Title
Helicobacter
Volume
19
Number
6
Start Page
407
End Page
416
URI
https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/158519
DOI
10.1111/hel.12145
ISSN
1083-4389
1523-5378
Abstract
BackgroundHelicobacter pylori (H.pylori) infection plays an important role in the early stage of cancer development. However, various bacteria that promote the synthesis of reactive oxygen and nitrogen species may be involved in the later stages. We aimed to determine the microbial composition of gastric mucosa from the patients with chronic gastritis, intestinal metaplasia, and gastric cancer using 454 GS FLX Titanium. MethodsGastric mucosal biopsy samples were collected from 31 patients during endoscopy. After the extraction of genomic DNA, variable region V5 of the 16S rRNA gene was amplified. PCR products were sequenced using 454 high-throughput sequencer. The composition, diversity, and richness of microbial communities were compared between three groups. ResultsThe composition of H.pylori-containing Epsilonproteobacteria class appeared to be the most prevalent, but the relative increase in the Bacilli class in the gastric cancer group was noticed, resulting in a significant difference compared with the chronic gastritis group. By analyzing the Helicobacter-dominant group at a family level, the relative abundance of Helicobacteraceae family was significantly lower in the gastric cancer group compared with chronic gastritis and intestinal metaplasia groups, while the relative abundance of Streptococcaceae family significantly increased. In a UPGMA clustering of Helicobacter-dominant group based on UniFrac distance, the chronic gastritis group and gastric cancer group were clearly separated, while the intestinal metaplasia group was distributed in between the two groups. The evenness and diversity of gastric microbiota in the gastric cancer group was increased compared with other groups. ConclusionsIn Helicobacter predominant patients, the microbial compositions of gastric mucosa from gastric cancer patients are significantly different to chronic gastritis and intestinal metaplasia patients. These alterations of gastric microbial composition may play an important, as-yet-undetermined role in gastric carcinogenesis of Helicobacter predominant patients.
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