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Increase in antibiotic resistant Helicobacter pylori in a University Hospital in Japan
BACKGROUND: Eradication effectively prevents Helicobacter pylori-associated diseases; however, H. pylori antibiotic resistance has increased throughout Japan and worldwide. This study aimed to assess rates of resistance to antibiotics; amoxicillin, clarithromycin and metronidazole in a University Ho...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6419596/ https://www.ncbi.nlm.nih.gov/pubmed/30881065 http://dx.doi.org/10.2147/IDR.S196452 |
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author | Kageyama, Chihiro Sato, Mayu Sakae, Hiroyuki Obayashi, Yuka Kawahara, Yoshiro Mima, Takehiko Matsushita, Osamu Yokota, Kenji Mizuno, Motowo Okada, Hiroyuki |
author_facet | Kageyama, Chihiro Sato, Mayu Sakae, Hiroyuki Obayashi, Yuka Kawahara, Yoshiro Mima, Takehiko Matsushita, Osamu Yokota, Kenji Mizuno, Motowo Okada, Hiroyuki |
author_sort | Kageyama, Chihiro |
collection | PubMed |
description | BACKGROUND: Eradication effectively prevents Helicobacter pylori-associated diseases; however, H. pylori antibiotic resistance has increased throughout Japan and worldwide. This study aimed to assess rates of resistance to antibiotics; amoxicillin, clarithromycin and metronidazole in a University Hospital in Japan. MATERIALS AND METHODS: H. pylori (208 strains) were isolated from patients at the Okayama University Hospital in Japan. The minimum inhibitory concentrations (MIC) were determined using the mean values of the E-test to determine the antimicrobial susceptibilities of the strains. Sequencing and gene analysis were performed to analyze resistance genes to clarithromycin and amoxicillin. RESULTS: Rates of amoxicillin, clarithromycin, and metronidazole resistance were 13%, 48%, and 49%, respectively. Genetic analysis indicated that the A2143G point mutation in 23S rDNA is closely associated with the MIC of clarithromycin. The MIC in amoxicillin-resistant strains increased with an increase in the number of PBP1A amino acids mutations. CONCLUSION: Genetic analysis for resistant strains is not clinically effective in cases of amoxicillin resistance. Numerous bacteria with already high antibiotic resistance rates have been isolated in large hospitals such as a University Hospital. For effective eradication therapy, MIC measurement should be considered via several methods. |
format | Online Article Text |
id | pubmed-6419596 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-64195962019-03-16 Increase in antibiotic resistant Helicobacter pylori in a University Hospital in Japan Kageyama, Chihiro Sato, Mayu Sakae, Hiroyuki Obayashi, Yuka Kawahara, Yoshiro Mima, Takehiko Matsushita, Osamu Yokota, Kenji Mizuno, Motowo Okada, Hiroyuki Infect Drug Resist Original Research BACKGROUND: Eradication effectively prevents Helicobacter pylori-associated diseases; however, H. pylori antibiotic resistance has increased throughout Japan and worldwide. This study aimed to assess rates of resistance to antibiotics; amoxicillin, clarithromycin and metronidazole in a University Hospital in Japan. MATERIALS AND METHODS: H. pylori (208 strains) were isolated from patients at the Okayama University Hospital in Japan. The minimum inhibitory concentrations (MIC) were determined using the mean values of the E-test to determine the antimicrobial susceptibilities of the strains. Sequencing and gene analysis were performed to analyze resistance genes to clarithromycin and amoxicillin. RESULTS: Rates of amoxicillin, clarithromycin, and metronidazole resistance were 13%, 48%, and 49%, respectively. Genetic analysis indicated that the A2143G point mutation in 23S rDNA is closely associated with the MIC of clarithromycin. The MIC in amoxicillin-resistant strains increased with an increase in the number of PBP1A amino acids mutations. CONCLUSION: Genetic analysis for resistant strains is not clinically effective in cases of amoxicillin resistance. Numerous bacteria with already high antibiotic resistance rates have been isolated in large hospitals such as a University Hospital. For effective eradication therapy, MIC measurement should be considered via several methods. Dove Medical Press 2019-03-12 /pmc/articles/PMC6419596/ /pubmed/30881065 http://dx.doi.org/10.2147/IDR.S196452 Text en © 2019 Kageyama et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Original Research Kageyama, Chihiro Sato, Mayu Sakae, Hiroyuki Obayashi, Yuka Kawahara, Yoshiro Mima, Takehiko Matsushita, Osamu Yokota, Kenji Mizuno, Motowo Okada, Hiroyuki Increase in antibiotic resistant Helicobacter pylori in a University Hospital in Japan |
title | Increase in antibiotic resistant Helicobacter pylori in a University Hospital in Japan |
title_full | Increase in antibiotic resistant Helicobacter pylori in a University Hospital in Japan |
title_fullStr | Increase in antibiotic resistant Helicobacter pylori in a University Hospital in Japan |
title_full_unstemmed | Increase in antibiotic resistant Helicobacter pylori in a University Hospital in Japan |
title_short | Increase in antibiotic resistant Helicobacter pylori in a University Hospital in Japan |
title_sort | increase in antibiotic resistant helicobacter pylori in a university hospital in japan |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6419596/ https://www.ncbi.nlm.nih.gov/pubmed/30881065 http://dx.doi.org/10.2147/IDR.S196452 |
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