Gastric Microbiota in Helicobacter pylori-Negative and -Positive Gastritis Among High Incidence of Gastric Cancer Area

被引:59
作者
Gantuya, Boldbaatar [1 ,2 ]
El-Serag, Hashem B. [3 ]
Matsumoto, Takashi [1 ]
Ajami, Nadim J. [4 ]
Oyuntsetseg, Khasag [2 ]
Azzaya, Dashdorj [1 ,2 ]
Uchida, Tomohisa [5 ]
Yamaoka, Yoshio [1 ,3 ,6 ]
机构
[1] Oita Univ, Dept Environm & Prevent Med, Fac Med, 1-1 Idaigaoka, Yufu City, Oita 8795593, Japan
[2] Mongolian Natl Univ Med Sci, Dept Internal Med, Gastroenterol Unit, Zorig St, Ulaanbaatar 14210, Mongolia
[3] Baylor Coll Med, Dept Med, Gastroenterol & Hepatol Sect, 7200 Cambridge St, Houston, TX 77030 USA
[4] Baylor Coll Med, Alkek Ctr Metagen & Microbiome Res, Dept Mol Virol & Microbiol, Houston, TX 77030 USA
[5] Oita Univ, Dept Mol Pathol, Fac Med, 1-1 Idaigaoka, Yufu City, Oita 8795593, Japan
[6] Global Oita Med Adv Res Ctr Hlth, 1-1 Idaigaoka, Yufu City, Oita 8795593, Japan
来源
CANCERS | 2019年 / 11卷 / 04期
基金
美国国家卫生研究院;
关键词
Helicobacter pylori; non-Helicobacter pylori; gastritis; microbiota; 16S rRNA; INFECTION;
D O I
10.3390/cancers11040504
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Helicobacter pylori (H. pylori) related chronic gastritis is a well-known major etiological factor for gastric cancer development. However, H. pylori-negative gastritis (HpN) is not well described. We aimed to examine gastric mucosal microbiota in HpN compared to H. pylori-positive gastritis (HpP) and H. pylori-negative non-gastritis group (control). Here, we studied 11 subjects with HpN, 40 with HpP and 24 controls. We performed endoscopy with six gastric biopsies. Comparison groups were defined based on strict histological criteria for the disease and H. pylori diagnosis. We used 16S rRNA gene amplicon sequencing to profile the gastric microbiota according to comparison groups. These results demonstrate that the HpP group had significantly lower bacterial richness by the operational taxonomic unit (OTU) counts, and Shannon and Simpson indices as compared to HpN or controls. The linear discriminant analysis effect size analysis showed the enrichment of Firmicutes, Fusobacteria, Bacteroidetes and Actinobacteria at phylum level in the HpN group. In the age-adjusted multivariate analysis, Streptococcus sp. and Haemophilus parainfluenzae were at a significantly increased risk for HpN (odds ratio 18.9 and 12.3, respectively) based on abundance. Treponema sp. was uniquely found in HpN based on occurrence. In this paper, we conclude that Streptococcus sp., Haemophilus parainfluenzae and Treponema sp. are candidate pathogenic bacterial species for HpN. These results if confirmed may have important clinical implications.
引用
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页数:12
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