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Primary antibiotic resistance and associated mechanisms in Helicobacter pylori isolates from Senegalese patients

BACKGROUND: Antibiotic combination therapy for Helicobacter pylori eradication must be adapted to local resistance patterns, but the epidemiology of H. pylori resistance to antibiotics is poorly documented in Africa. The aim was to determine the antibiotic resistance rates, as well as the associated...

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Autores principales: Seck, Abdoulaye, Burucoa, Christophe, Dia, Daouda, Mbengue, Mouhamadou, Onambele, Manuella, Raymond, Josette, Breurec, Sebastien
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3552979/
https://www.ncbi.nlm.nih.gov/pubmed/23298145
http://dx.doi.org/10.1186/1476-0711-12-3
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author Seck, Abdoulaye
Burucoa, Christophe
Dia, Daouda
Mbengue, Mouhamadou
Onambele, Manuella
Raymond, Josette
Breurec, Sebastien
author_facet Seck, Abdoulaye
Burucoa, Christophe
Dia, Daouda
Mbengue, Mouhamadou
Onambele, Manuella
Raymond, Josette
Breurec, Sebastien
author_sort Seck, Abdoulaye
collection PubMed
description BACKGROUND: Antibiotic combination therapy for Helicobacter pylori eradication must be adapted to local resistance patterns, but the epidemiology of H. pylori resistance to antibiotics is poorly documented in Africa. The aim was to determine the antibiotic resistance rates, as well as the associated molecular mechanisms, of strains isolated in Dakar, Senegal. METHODS: One hundred and eight H. pylori strains were isolated between 2007 and 2009 from 108 patients presenting with upper abdominal pain to the Gastroenterology Department of Le Dantec Hospital. Antimicrobial susceptibility testing was performed for amoxicillin, clarithromycin, metronidazole, levofloxacin and tetracyclin using the E-test method. Mutations in the 23S rRNA gene of clarithromycin-resistant strains and in gyrA and gyrB of levofloxacin-resistant strains were investigated. RESULTS: Isolates were characterized by no resistance to amoxicillin (0%), tetracycline (0%), and very low rate of resistance to clarithromycin (1%), but a high rate of resistance to metronidazole (85%). The clarithromycin-resistant strain displayed the A2143G mutation. A worrying rate of levofloxacin resistance was detected (15%). N87I and D91N were the most common mutations in the quinolone-resistance-determining region of gyrA. CONCLUSIONS: The first-line empirical regimen for H. pylori eradication in Senegal should include clarithromycin. Increasing rates of fluoroquinolone resistance detected should discourage the use of levofloxacin-containing regimens without prior antimicrobial susceptibility testing.
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spelling pubmed-35529792013-01-28 Primary antibiotic resistance and associated mechanisms in Helicobacter pylori isolates from Senegalese patients Seck, Abdoulaye Burucoa, Christophe Dia, Daouda Mbengue, Mouhamadou Onambele, Manuella Raymond, Josette Breurec, Sebastien Ann Clin Microbiol Antimicrob Research BACKGROUND: Antibiotic combination therapy for Helicobacter pylori eradication must be adapted to local resistance patterns, but the epidemiology of H. pylori resistance to antibiotics is poorly documented in Africa. The aim was to determine the antibiotic resistance rates, as well as the associated molecular mechanisms, of strains isolated in Dakar, Senegal. METHODS: One hundred and eight H. pylori strains were isolated between 2007 and 2009 from 108 patients presenting with upper abdominal pain to the Gastroenterology Department of Le Dantec Hospital. Antimicrobial susceptibility testing was performed for amoxicillin, clarithromycin, metronidazole, levofloxacin and tetracyclin using the E-test method. Mutations in the 23S rRNA gene of clarithromycin-resistant strains and in gyrA and gyrB of levofloxacin-resistant strains were investigated. RESULTS: Isolates were characterized by no resistance to amoxicillin (0%), tetracycline (0%), and very low rate of resistance to clarithromycin (1%), but a high rate of resistance to metronidazole (85%). The clarithromycin-resistant strain displayed the A2143G mutation. A worrying rate of levofloxacin resistance was detected (15%). N87I and D91N were the most common mutations in the quinolone-resistance-determining region of gyrA. CONCLUSIONS: The first-line empirical regimen for H. pylori eradication in Senegal should include clarithromycin. Increasing rates of fluoroquinolone resistance detected should discourage the use of levofloxacin-containing regimens without prior antimicrobial susceptibility testing. BioMed Central 2013-01-08 /pmc/articles/PMC3552979/ /pubmed/23298145 http://dx.doi.org/10.1186/1476-0711-12-3 Text en Copyright ©2013 Seck et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Seck, Abdoulaye
Burucoa, Christophe
Dia, Daouda
Mbengue, Mouhamadou
Onambele, Manuella
Raymond, Josette
Breurec, Sebastien
Primary antibiotic resistance and associated mechanisms in Helicobacter pylori isolates from Senegalese patients
title Primary antibiotic resistance and associated mechanisms in Helicobacter pylori isolates from Senegalese patients
title_full Primary antibiotic resistance and associated mechanisms in Helicobacter pylori isolates from Senegalese patients
title_fullStr Primary antibiotic resistance and associated mechanisms in Helicobacter pylori isolates from Senegalese patients
title_full_unstemmed Primary antibiotic resistance and associated mechanisms in Helicobacter pylori isolates from Senegalese patients
title_short Primary antibiotic resistance and associated mechanisms in Helicobacter pylori isolates from Senegalese patients
title_sort primary antibiotic resistance and associated mechanisms in helicobacter pylori isolates from senegalese patients
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3552979/
https://www.ncbi.nlm.nih.gov/pubmed/23298145
http://dx.doi.org/10.1186/1476-0711-12-3
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