Molecular characterization of rifabutin-resistance in refractory Helicobacter pylori infection in Taiwan

Objectives: To explore the molecular characteristics of rpoB, encoding β-subunit of DNA-directed RNA polymerase, and unravel the link to rifabutin-resistance in patients with refractory Helicobacter pylori infection. Methods: From January 2018-March 2021, a total of 1590 patients were screened for e...

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Main Authors: Chia-Jung Kuo, Ngoc-Niem Bui, Jun-Nong Ke, Cheng-Yu Lin, Wey-Ran Lin, Ming-Ling Chang, Hui-Yu Wu, Mei-Zi Huang, Cheng-Hsun Chiu, Cheng-Tang Chiu, Chih-Ho Lai
Format: Article
Language:English
Published: Elsevier 2024-01-01
Series:International Journal of Infectious Diseases
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S1201971223007622
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author Chia-Jung Kuo
Ngoc-Niem Bui
Jun-Nong Ke
Cheng-Yu Lin
Wey-Ran Lin
Ming-Ling Chang
Hui-Yu Wu
Mei-Zi Huang
Cheng-Hsun Chiu
Cheng-Tang Chiu
Chih-Ho Lai
author_facet Chia-Jung Kuo
Ngoc-Niem Bui
Jun-Nong Ke
Cheng-Yu Lin
Wey-Ran Lin
Ming-Ling Chang
Hui-Yu Wu
Mei-Zi Huang
Cheng-Hsun Chiu
Cheng-Tang Chiu
Chih-Ho Lai
author_sort Chia-Jung Kuo
collection DOAJ
description Objectives: To explore the molecular characteristics of rpoB, encoding β-subunit of DNA-directed RNA polymerase, and unravel the link to rifabutin-resistance in patients with refractory Helicobacter pylori infection. Methods: From January 2018-March 2021, a total of 1590 patients were screened for eligibility to participate in the study. Patients with refractory H. pylori infection were confirmed by using the (13C)-urea breath assay. All enrolled patients underwent esophagogastroduodenoscopy, and biopsies were taken for H. pylori culture and antibacterial susceptibility testing. Sequence analysis of rpoB was conducted for all rifabutin-resistant isolates. Results: In total, 70 patients were diagnosed with refractory H. pylori infection, and 39 isolates were successfully cultured. Amongst, 10 isolates were identified as rifabutin-resistance and nine isolates exhibited at least one amino acid substitution in RpoB. Isolates with a minimal inhibitory concentration >32 mg/l displayed a higher number of mutational changes in RpoB than the others. Additionally, more amino acid substitutions in RpoB correlated with developing a higher minimal inhibitory concentration for H. pylori rifabutin-resistance. Conclusion: Our findings highlight the relationship between rifabutin-resistance in refractory H. pylori infection and specific mutations in RpoB, which will aid the clinical selection of appropriate antibacterial agents with better therapeutic effects.
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spelling doaj.art-f98411d8054b4e5f8c9c2dcc23907b0f2023-12-15T07:22:47ZengElsevierInternational Journal of Infectious Diseases1201-97122024-01-011382528Molecular characterization of rifabutin-resistance in refractory Helicobacter pylori infection in TaiwanChia-Jung Kuo0Ngoc-Niem Bui1Jun-Nong Ke2Cheng-Yu Lin3Wey-Ran Lin4Ming-Ling Chang5Hui-Yu Wu6Mei-Zi Huang7Cheng-Hsun Chiu8Cheng-Tang Chiu9Chih-Ho Lai10Department of Gastroenterology and Hepatology, Chang Gung Memorial Hospital at Linkou, Taoyuan, Taiwan; School of Medicine, College of Medicine, Chang Gung University, Taoyuan, TaiwanGraduate Institute of Biomedical Sciences, College of Medicine, Chang Gung University, Taoyuan, Taiwan; Faculty of Medicine, Can Tho University of Medicine and Pharmacy, Can Tho, Viet NamGraduate Institute of Biomedical Sciences, College of Medicine, Chang Gung University, Taoyuan, Taiwan; Department of Laboratory Medicine, Chang Gung Memorial Hospital at Linkou, Taoyuan, TaiwanDepartment of Gastroenterology and Hepatology, Chang Gung Memorial Hospital at Linkou, Taoyuan, TaiwanDepartment of Gastroenterology and Hepatology, Chang Gung Memorial Hospital at Linkou, Taoyuan, Taiwan; School of Medicine, College of Medicine, Chang Gung University, Taoyuan, TaiwanDepartment of Gastroenterology and Hepatology, Chang Gung Memorial Hospital at Linkou, Taoyuan, Taiwan; School of Medicine, College of Medicine, Chang Gung University, Taoyuan, TaiwanGraduate Institute of Biomedical Sciences, College of Medicine, Chang Gung University, Taoyuan, TaiwanGraduate Institute of Biomedical Sciences, College of Medicine, Chang Gung University, Taoyuan, TaiwanSchool of Medicine, College of Medicine, Chang Gung University, Taoyuan, Taiwan; Graduate Institute of Biomedical Sciences, College of Medicine, Chang Gung University, Taoyuan, Taiwan; Molecular Infectious Disease Research Center, Department of Pediatrics, Chang Gung Memorial Hospital at Linkou, Taoyuan, TaiwanDepartment of Gastroenterology and Hepatology, Chang Gung Memorial Hospital at Linkou, Taoyuan, Taiwan; School of Medicine, College of Medicine, Chang Gung University, Taoyuan, TaiwanGraduate Institute of Biomedical Sciences, College of Medicine, Chang Gung University, Taoyuan, Taiwan; Molecular Infectious Disease Research Center, Department of Pediatrics, Chang Gung Memorial Hospital at Linkou, Taoyuan, Taiwan; Department of Medical Research, School of Medicine, China Medical University and Hospital, Taichung, Taiwan; Department of Nursing, Asia University, Taichung, Taiwan; Department of Microbiology and Immunology, Chang Gung University, Taoyuan, Taiwan; Corresponding author.Objectives: To explore the molecular characteristics of rpoB, encoding β-subunit of DNA-directed RNA polymerase, and unravel the link to rifabutin-resistance in patients with refractory Helicobacter pylori infection. Methods: From January 2018-March 2021, a total of 1590 patients were screened for eligibility to participate in the study. Patients with refractory H. pylori infection were confirmed by using the (13C)-urea breath assay. All enrolled patients underwent esophagogastroduodenoscopy, and biopsies were taken for H. pylori culture and antibacterial susceptibility testing. Sequence analysis of rpoB was conducted for all rifabutin-resistant isolates. Results: In total, 70 patients were diagnosed with refractory H. pylori infection, and 39 isolates were successfully cultured. Amongst, 10 isolates were identified as rifabutin-resistance and nine isolates exhibited at least one amino acid substitution in RpoB. Isolates with a minimal inhibitory concentration >32 mg/l displayed a higher number of mutational changes in RpoB than the others. Additionally, more amino acid substitutions in RpoB correlated with developing a higher minimal inhibitory concentration for H. pylori rifabutin-resistance. Conclusion: Our findings highlight the relationship between rifabutin-resistance in refractory H. pylori infection and specific mutations in RpoB, which will aid the clinical selection of appropriate antibacterial agents with better therapeutic effects.http://www.sciencedirect.com/science/article/pii/S1201971223007622Helicobacter pyloriRefractory infectionRifabutin-resistanceRpoBMutation
spellingShingle Chia-Jung Kuo
Ngoc-Niem Bui
Jun-Nong Ke
Cheng-Yu Lin
Wey-Ran Lin
Ming-Ling Chang
Hui-Yu Wu
Mei-Zi Huang
Cheng-Hsun Chiu
Cheng-Tang Chiu
Chih-Ho Lai
Molecular characterization of rifabutin-resistance in refractory Helicobacter pylori infection in Taiwan
International Journal of Infectious Diseases
Helicobacter pylori
Refractory infection
Rifabutin-resistance
RpoB
Mutation
title Molecular characterization of rifabutin-resistance in refractory Helicobacter pylori infection in Taiwan
title_full Molecular characterization of rifabutin-resistance in refractory Helicobacter pylori infection in Taiwan
title_fullStr Molecular characterization of rifabutin-resistance in refractory Helicobacter pylori infection in Taiwan
title_full_unstemmed Molecular characterization of rifabutin-resistance in refractory Helicobacter pylori infection in Taiwan
title_short Molecular characterization of rifabutin-resistance in refractory Helicobacter pylori infection in Taiwan
title_sort molecular characterization of rifabutin resistance in refractory helicobacter pylori infection in taiwan
topic Helicobacter pylori
Refractory infection
Rifabutin-resistance
RpoB
Mutation
url http://www.sciencedirect.com/science/article/pii/S1201971223007622
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