Trends in Helicobacter pylori resistance to clarithromycin: from phenotypic to genomic approaches

Detalhes bibliográficos
Autor(a) principal: Marques, Andreia T.
Data de Publicação: 2020
Outros Autores: Vítor, Jorge M. B., Santos, Andrea, Oleastro, Mónica, Vale, Filipa
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10451/52327
Resumo: For a long time Helicobacter pylori infections have been treated using the macrolide antibiotic, clarithromycin. Clarithromycin resistance is increasing worldwide and is the most common cause of H. pylori treatment failure. Here we review the mechanisms of antibiotic resistance to clarithromycin, detailing the individual and combinations of point mutations found in the 23S rRNA gene associated with resistance. Additionally, we consider the methods used to detect clarithromycin resistance, emphasizing the use of high-throughput next-generation sequencing methods, which were applied to 17 newly sequenced pairs of H. pylori strains isolated from the antrum and corpus of a recent colonized paediatric population. This set of isolates was composed of six pairs of resistant strains whose phenotype was associated with two point mutations found in the 23S rRNA gene: A2142C and A2143G. Other point mutations were found simultaneously in the same gene, but, according to our results, it is unlikely that they contribute to resistance. Further, among susceptible isolates, genomic variations compatible with mutations previously associated with clarithromycin resistance were detected. Exposure to clarithromycin may select low-frequency variants, resulting in a progressive increase in the resistance rate due to selection pressure.
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spelling Trends in Helicobacter pylori resistance to clarithromycin: from phenotypic to genomic approachesHelicobacter pyloriclarithromycinresistance23S ribosomal RNA subunitnext-generation sequencingpoint mutationsFor a long time Helicobacter pylori infections have been treated using the macrolide antibiotic, clarithromycin. Clarithromycin resistance is increasing worldwide and is the most common cause of H. pylori treatment failure. Here we review the mechanisms of antibiotic resistance to clarithromycin, detailing the individual and combinations of point mutations found in the 23S rRNA gene associated with resistance. Additionally, we consider the methods used to detect clarithromycin resistance, emphasizing the use of high-throughput next-generation sequencing methods, which were applied to 17 newly sequenced pairs of H. pylori strains isolated from the antrum and corpus of a recent colonized paediatric population. This set of isolates was composed of six pairs of resistant strains whose phenotype was associated with two point mutations found in the 23S rRNA gene: A2142C and A2143G. Other point mutations were found simultaneously in the same gene, but, according to our results, it is unlikely that they contribute to resistance. Further, among susceptible isolates, genomic variations compatible with mutations previously associated with clarithromycin resistance were detected. Exposure to clarithromycin may select low-frequency variants, resulting in a progressive increase in the resistance rate due to selection pressure.F. F. V. is the recipient of a project grant (PTDC/BTM-SAL/28978/2017) from the Fundação para a Ciência e a Tecnologia (FCT), which supported this work. J. V.’s research group was financed by New England Biolabs, Inc. (USA).Microbiology Society [Society Publisher]Repositório da Universidade de LisboaMarques, Andreia T.Vítor, Jorge M. B.Santos, AndreaOleastro, MónicaVale, Filipa2022-04-13T11:05:52Z2020-03-022022-02-24T14:59:58Z2020-03-02T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/10451/52327engMarques AT, Vítor JMB, Santos A, Oleastro M, Vale FF. Trends in Helicobacter pylori resistance to clarithromycin: from phenotypic to genomic approaches. Microbial Genomics [Internet]. 2020;6(3). Disponível em: https://www.microbiologyresearch.org/content/journal/mgen/10.1099/mgen.0.0003442057-5858cv-prod-1216082https://doi.org/10.1099/mgen.0.000344info:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2023-07-14T15:38:26ZPortal AgregadorONG
dc.title.none.fl_str_mv Trends in Helicobacter pylori resistance to clarithromycin: from phenotypic to genomic approaches
title Trends in Helicobacter pylori resistance to clarithromycin: from phenotypic to genomic approaches
spellingShingle Trends in Helicobacter pylori resistance to clarithromycin: from phenotypic to genomic approaches
Marques, Andreia T.
Helicobacter pylori
clarithromycin
resistance
23S ribosomal RNA subunit
next-generation sequencing
point mutations
title_short Trends in Helicobacter pylori resistance to clarithromycin: from phenotypic to genomic approaches
title_full Trends in Helicobacter pylori resistance to clarithromycin: from phenotypic to genomic approaches
title_fullStr Trends in Helicobacter pylori resistance to clarithromycin: from phenotypic to genomic approaches
title_full_unstemmed Trends in Helicobacter pylori resistance to clarithromycin: from phenotypic to genomic approaches
title_sort Trends in Helicobacter pylori resistance to clarithromycin: from phenotypic to genomic approaches
author Marques, Andreia T.
author_facet Marques, Andreia T.
Vítor, Jorge M. B.
Santos, Andrea
Oleastro, Mónica
Vale, Filipa
author_role author
author2 Vítor, Jorge M. B.
Santos, Andrea
Oleastro, Mónica
Vale, Filipa
author2_role author
author
author
author
dc.contributor.none.fl_str_mv Repositório da Universidade de Lisboa
dc.contributor.author.fl_str_mv Marques, Andreia T.
Vítor, Jorge M. B.
Santos, Andrea
Oleastro, Mónica
Vale, Filipa
dc.subject.por.fl_str_mv Helicobacter pylori
clarithromycin
resistance
23S ribosomal RNA subunit
next-generation sequencing
point mutations
topic Helicobacter pylori
clarithromycin
resistance
23S ribosomal RNA subunit
next-generation sequencing
point mutations
description For a long time Helicobacter pylori infections have been treated using the macrolide antibiotic, clarithromycin. Clarithromycin resistance is increasing worldwide and is the most common cause of H. pylori treatment failure. Here we review the mechanisms of antibiotic resistance to clarithromycin, detailing the individual and combinations of point mutations found in the 23S rRNA gene associated with resistance. Additionally, we consider the methods used to detect clarithromycin resistance, emphasizing the use of high-throughput next-generation sequencing methods, which were applied to 17 newly sequenced pairs of H. pylori strains isolated from the antrum and corpus of a recent colonized paediatric population. This set of isolates was composed of six pairs of resistant strains whose phenotype was associated with two point mutations found in the 23S rRNA gene: A2142C and A2143G. Other point mutations were found simultaneously in the same gene, but, according to our results, it is unlikely that they contribute to resistance. Further, among susceptible isolates, genomic variations compatible with mutations previously associated with clarithromycin resistance were detected. Exposure to clarithromycin may select low-frequency variants, resulting in a progressive increase in the resistance rate due to selection pressure.
publishDate 2020
dc.date.none.fl_str_mv 2020-03-02
2020-03-02T00:00:00Z
2022-04-13T11:05:52Z
2022-02-24T14:59:58Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://hdl.handle.net/10451/52327
url http://hdl.handle.net/10451/52327
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Marques AT, Vítor JMB, Santos A, Oleastro M, Vale FF. Trends in Helicobacter pylori resistance to clarithromycin: from phenotypic to genomic approaches. Microbial Genomics [Internet]. 2020;6(3). Disponível em: https://www.microbiologyresearch.org/content/journal/mgen/10.1099/mgen.0.000344
2057-5858
cv-prod-1216082
https://doi.org/10.1099/mgen.0.000344
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Microbiology Society [Society Publisher]
publisher.none.fl_str_mv Microbiology Society [Society Publisher]
dc.source.none.fl_str_mv reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
instacron:RCAAP
instname_str Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
instacron_str RCAAP
institution RCAAP
reponame_str Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
collection Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
repository.name.fl_str_mv
repository.mail.fl_str_mv
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