An Appropriate Cutoff Value for Determining the Colonization of Helicobacter pylori by the Pyrosequencing Method: Comparison with Conventional Methods. Issue 5 (9th February 2015)

• Record Type: Journal Article
• Authors: Kim, Jaeyeon; Kim, Nayoung; Jo, Hyun Jin; Park, Ji Hyun; Nam, Ryoung Hee; Seok, Yeong‐Jae; Kim, Yeon‐Ran; Kim, Joo Sung; Kim, Jung Mogg; Kim, Jung Min; Lee, Dong Ho; Jung, Hyun Chae
• Is Part Of: Helicobacter. Volume 20:Issue 5(2015:Oct.)
• Page Start: 370
• Page End: 380
• Publication Date: 2015-02-09
• Subjects: 16S ribosomal RNA -- gastric microbiota -- Helicobacter pylori -- stomach; Helicobacter -- Periodicals; Helicobacter infections -- Periodicals; Stomach -- Diseases -- Periodicals; 616.3301405
• DOI: 10.1111/hel.12214
• Languages: English
• ISSNs: 1083-4389

Abstract

Abstract: Background: Sequencing of 16S ribosomal RNA (rRNA) gene has improved the characterization of microbial communities. It enabled the detection of low abundance gastric Helicobacter pylori sequences even in subjects that were found to be H. pylori negative with conventional methods. The objective of this study was to obtain a cutoff value for H. pylori colonization in gastric mucosa samples by pyrosequencing method. Materials and Methods: Gastric mucosal biopsies were taken from 63 subjects whose H. pylori status was determined by a combination of serology, rapid urease test, culture, and histology. Microbial DNA from mucosal samples was amplified by PCR using universal bacterial primers. 16S rDNA amplicons were pyrosequenced. ROC curve analysis was performed to determine the cutoff value for H. pylori colonization by pyrosequencing. In addition, temporal changes in the stomach microbiota were observed in eight initially H. pylori ‐positive and eight H. pylori ‐negative subjects at a single time point 1–8 years later. Results: Of the 63 subjects, the presence of H. pylori sequences was detected in all (28/28) conventionally H. pylori ‐positive samples and in 60% (21/35) of H. pylori ‐negative samples. The average percent of H. pylori reads in each sample was 0.67 ± 1.09% in the H. pylori ‐negative group. Cutoff value for clinically positive H. pylori status was approximately 1.22% based on ROC curve analysis (AUC = 0.957; p < .001). Helicobacter pylori was successfully eradicated in five of seven treated H. pylori ‐positive subjects (71.4%), and the percentage of H. pylori reads in these five subjects dropped from 1.3–95.18% to 0–0.16% after eradication. Conclusion: These results suggest that the cutoff value of H. pylori sequence percentage for H. pylori colonization by pyrosequencing could be set at approximately 1%. It might be helpful to analyze gastric microbiota related to H. pylori sequence status.