Can aminoglycosides be used as a new treatment for Helicobacter pylori? In vitro activity of recently isolated isolated Helicobacter pylori

Kyoung Hwa Lee, Soon Young Park, Su Jin Jeong, Da Hyun Jung, Jie Hyun Kim, Seok Hoon Jeong, Il Mo Kang, Young Goo Song

Research output: Contribution to journalArticlepeer-review

3 Citations (Scopus)

Abstract

Background: Smectite can serve as a drug delivery system and gentamicin-intercalated smectite hybrids are expected to supersede the standard therapy for Helicobacter pylori eradication. The aim of this study was to confirm whether the minimum inhibitory concentration (MIC) of aminoglycosides applied as smectite hybrids remained low against recently isolated H. pylori strains. Materials and Methods: A total of 140 strains were collected for a minimum period of 3 years. Antimicrobial susceptibility tests were performed, and the MICs of eight antibiotics (amoxicillin, clarithromycin, metronidazole, tetracycline, levofloxacin, gentamicin, netilmicin, and tobramycin) were determined by using the Epsilometer test and following the European Committee on Antimicrobial Susceptibility Testing recommendations. Results: The resistance rate of clarithromycin was high, up to 30.7%, although it is a major antimicrobial agent used in standard therapy. The MIC50 and MIC90 of gentamicin (0.25 mg/L and 0.75 mg/L) and netilmicin (0.19 mg/L and 0.75 mg/L) were lower than other alternative therapies for H. pylori eradication. In clarithromycin-resistant strains, the MIC50 was 0.25 mg/L and the MIC90 was 1 mg/L for gentamicin; for netilmicin, the values were 0.25 mg/L and 0.75 mg/L, respectively. Conclusion: Through the use of gentamicin and netilmicin, which have low MICs for H. pylori, aminoglycoside-intercalated smectite hybrids are expected to emerge as a new standard therapy for H. pylori eradication.

Original languageEnglish
Pages (from-to)10-20
Number of pages11
JournalInfection and Chemotherapy
Volume51
Issue number1
DOIs
Publication statusPublished - 2019

Bibliographical note

Funding Information:
This work was supported by the Basic Research Project (Study No. GP2017-020) of the Korea Institute of Geoscience and Mineral Resources (KIGAM), funded by the Ministry of Science, ICT and Future Planning of Korea.

Publisher Copyright:
Copyright © 2019 by The Korean Society of Infectious Diseases and Korean Society for Antimicrobial Therapy.

All Science Journal Classification (ASJC) codes

  • Infectious Diseases
  • Pharmacology (medical)

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