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The interplay between mutations in cagA, 23S rRNA, gyrA and drug resistance in Helicobacter pylori

In this study, we evaluated the mutations of Helicobacter pylori associated with resistance to clarithromycin and levofloxacin. Furthermore, based on the proposed interaction between antimicrobial resistance and pathogenicity, we correlated the mutation profiles of the strains with the presence of t...

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Autores principales: Vianna, Júlia Silveira, Ramis, Ivy Bastos, Ramos, Daniela Fernandes, Gastal, Otávio Leite, da Silva, Renato Azevedo, Gonçalves, Carla Vitola, da Silva, Pedro Eduardo Almeida
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Instituto de Medicina Tropical 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6029892/
https://www.ncbi.nlm.nih.gov/pubmed/29972462
http://dx.doi.org/10.1590/S1678-9946201860025
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author Vianna, Júlia Silveira
Ramis, Ivy Bastos
Ramos, Daniela Fernandes
Gastal, Otávio Leite
da Silva, Renato Azevedo
Gonçalves, Carla Vitola
da Silva, Pedro Eduardo Almeida
author_facet Vianna, Júlia Silveira
Ramis, Ivy Bastos
Ramos, Daniela Fernandes
Gastal, Otávio Leite
da Silva, Renato Azevedo
Gonçalves, Carla Vitola
da Silva, Pedro Eduardo Almeida
author_sort Vianna, Júlia Silveira
collection PubMed
description In this study, we evaluated the mutations of Helicobacter pylori associated with resistance to clarithromycin and levofloxacin. Furthermore, based on the proposed interaction between antimicrobial resistance and pathogenicity, we correlated the mutation profiles of the strains with the presence of the pathogenicity gene cagA. We analyzed 80 gastric biopsy specimens from H. pylori-infected patients for point mutations in the 23S rRNA gene region and in the gyrA gene, which are related to clarithromycin and levofloxacin resistance, respectively, and investigated the presence of the cagA gene in these strains. We observed that in the assayed biopsies, 8.7% (7/80) had mutations in the 23S rRNA gene region at positions 2143 and 2142, while 22.5% (18/80) had mutations in gyrA at codons 87 and 91. Moreover, absence of the CagA-EPIYA pathogenicity factor was observed in 68% (17/25) of resistant samples. The knowledge of the local profile of antimicrobial resistance and the complex interplay involving resistance and pathogenicity can contribute to an appropriate clinical approach.
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spelling pubmed-60298922018-07-05 The interplay between mutations in cagA, 23S rRNA, gyrA and drug resistance in Helicobacter pylori Vianna, Júlia Silveira Ramis, Ivy Bastos Ramos, Daniela Fernandes Gastal, Otávio Leite da Silva, Renato Azevedo Gonçalves, Carla Vitola da Silva, Pedro Eduardo Almeida Rev Inst Med Trop Sao Paulo Brief Communication In this study, we evaluated the mutations of Helicobacter pylori associated with resistance to clarithromycin and levofloxacin. Furthermore, based on the proposed interaction between antimicrobial resistance and pathogenicity, we correlated the mutation profiles of the strains with the presence of the pathogenicity gene cagA. We analyzed 80 gastric biopsy specimens from H. pylori-infected patients for point mutations in the 23S rRNA gene region and in the gyrA gene, which are related to clarithromycin and levofloxacin resistance, respectively, and investigated the presence of the cagA gene in these strains. We observed that in the assayed biopsies, 8.7% (7/80) had mutations in the 23S rRNA gene region at positions 2143 and 2142, while 22.5% (18/80) had mutations in gyrA at codons 87 and 91. Moreover, absence of the CagA-EPIYA pathogenicity factor was observed in 68% (17/25) of resistant samples. The knowledge of the local profile of antimicrobial resistance and the complex interplay involving resistance and pathogenicity can contribute to an appropriate clinical approach. Instituto de Medicina Tropical 2018-06-28 /pmc/articles/PMC6029892/ /pubmed/29972462 http://dx.doi.org/10.1590/S1678-9946201860025 Text en https://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License, which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Brief Communication
Vianna, Júlia Silveira
Ramis, Ivy Bastos
Ramos, Daniela Fernandes
Gastal, Otávio Leite
da Silva, Renato Azevedo
Gonçalves, Carla Vitola
da Silva, Pedro Eduardo Almeida
The interplay between mutations in cagA, 23S rRNA, gyrA and drug resistance in Helicobacter pylori
title The interplay between mutations in cagA, 23S rRNA, gyrA and drug resistance in Helicobacter pylori
title_full The interplay between mutations in cagA, 23S rRNA, gyrA and drug resistance in Helicobacter pylori
title_fullStr The interplay between mutations in cagA, 23S rRNA, gyrA and drug resistance in Helicobacter pylori
title_full_unstemmed The interplay between mutations in cagA, 23S rRNA, gyrA and drug resistance in Helicobacter pylori
title_short The interplay between mutations in cagA, 23S rRNA, gyrA and drug resistance in Helicobacter pylori
title_sort interplay between mutations in caga, 23s rrna, gyra and drug resistance in helicobacter pylori
topic Brief Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6029892/
https://www.ncbi.nlm.nih.gov/pubmed/29972462
http://dx.doi.org/10.1590/S1678-9946201860025
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