Genotypic and Phenotypic Resistance to Clarithromycin inHelicobacter pyloriStrainsopen access
- Authors
- Gong, Eun Jeong; Ahn, Ji Yong; Kim, Jung Mogg; Lee, Sun Mi; Na, Hee Kyong; Lee, Jeong Hoon; Jung, Kee Wook; Choi, Kee Don; Kim, Do Hoon; Song, Ho June; Lee, Gin Hyug; Kim, So Won; Jung, Hwoon-Yong
- Issue Date
- Jun-2020
- Publisher
- MDPI
- Keywords
- antibiotic resistance; Helicobacter pylori; whole-genome sequencing
- Citation
- JOURNAL OF CLINICAL MEDICINE, v.9, no.6, pp.1 - 10
- Indexed
- SCIE
SCOPUS
- Journal Title
- JOURNAL OF CLINICAL MEDICINE
- Volume
- 9
- Number
- 6
- Start Page
- 1
- End Page
- 10
- URI
- https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/145602
- DOI
- 10.3390/jcm9061930
- ISSN
- 2077-0383
- Abstract
- Background: The increasing prevalence of antimicrobial resistance, together with the lack of novel treatment options, negatively affects successful eradication ofHelicobacter pylori. The aim of this study was to investigate genetic mutations in the 23S rRNA genes, which is associated with clarithromycin resistance, and to determine the clinical impact of genotype on phenotypic antimicrobial resistance. Methods: A total of 46H. pyloristrains were obtained from 13 patients, before and after unsuccessful eradication with clarithromycin-based triple therapy. The phenotypic resistance of eachH. pyloristrain was determined by minimum inhibitory concentration against clarithromycin using the serial two-fold agar dilution method. The genomic sequences of 23S rRNA genes were identified through next-generation sequencing, and nucleotide variants were determined based on comparison with genome sequences of the reference strainH. pylori26695. Results: Clarithromycin resistance was found in 9 of 13 subjects before treatment and all subjects after unsuccessful eradication. Whole-genome sequencing of the 23S rRNA genes detected 42 mutations on 40 nonidentical loci, including 2147A>G (formerly 2143A>G) and 2146A>G (formerly 2142A>G). All strains with clarithromycin-resistant phenotype had either 2147A>G or 2146A>G mutation. When comparing genotype and phenotype for clarithromycin resistance, there was a significant association between 2147A>G mutation and clarithromycin-resistant phenotype. Conclusions: All clarithromycin-resistant strains had either 2146A>G or 2147A>G mutation, suggesting that tests targeting these two mutations may be enough for the prediction of clarithromycin resistance in this population.
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