Volume 19, Issue 6 p. 407-416
Original Article

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

Chang Soo Eun

Chang Soo Eun

Department of Internal Medicine, Hanyang University Guri Hospital, Gyeonggi-Do, Korea

These authors contributed equally to this work.Search for more papers by this author
Byung Kwon Kim

Byung Kwon Kim

Bionano Health Guard Research Center, Korea Research Institute of Bioscience and Biotechnology, Daejeon, Korea

These authors contributed equally to this work.Search for more papers by this author
Dong Soo Han

Corresponding Author

Dong Soo Han

Department of Internal Medicine, Hanyang University Guri Hospital, Gyeonggi-Do, Korea

Reprint requests to: Dong Soo Han, Department of Internal Medicine, Hanyang University Guri Hospital, 249-1, Gyomoon-Dong, Guri-Si, Gyeonggi-Do 471-701, Korea. E-mail: hands@hanyang.ac.krSearch for more papers by this author
Seon Young Kim

Seon Young Kim

Medical Genomics Research Center, Korea Research Institute of Bioscience and Biotechnology, Daejeon, Korea

Search for more papers by this author
Kyung Mo Kim

Kyung Mo Kim

Biological Resource Center, Korea Research Institute of Bioscience and Biotechnology, Daejeon, Korea

Search for more papers by this author
Bo Youl Choi

Bo Youl Choi

Department of Preventive Medicine, Hanyang University College of Medicine, Seoul, Korea

Search for more papers by this author
Kyu Sang Song

Kyu Sang Song

Department of Pathology, Chungnam National University, College of Medicine, Daejeon, Korea

Search for more papers by this author
Yong Sung Kim

Yong Sung Kim

Medical Genomics Research Center, Korea Research Institute of Bioscience and Biotechnology, Daejeon, Korea

Search for more papers by this author
Jihyun F. Kim

Jihyun F. Kim

Department of Systems Biology and Division of Life Sciences, Yonsei University, Seoul, Korea

Search for more papers by this author
First published: 23 July 2014
Citations: 215

Abstract

Background

Helicobacter 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.

Methods

Gastric 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.

Results

The 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.

Conclusions

In 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.

The full text of this article hosted at iucr.org is unavailable due to technical difficulties.