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Colonisation of antibiotic resistant bacteria in a cohort of HIV infected children in Ghana

Antibiotic use not only selects for resistance in pathogenic bacteria, but also in commensal flora of exposed individuals. Little is known epidemiologically about antibiotic resistance in relation to people with HIV infection in sub-Saharan Africa. This study investigated the carriage of antibiotic...

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Autores principales: Sampane-Donkor, Eric, Badoe, Ebenezer Vincent, Annan, Jennifer Adoley, Nii-Trebi, Nicholas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The African Field Epidemiology Network 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5398869/
https://www.ncbi.nlm.nih.gov/pubmed/28451037
http://dx.doi.org/10.11604/pamj.2017.26.60.10981
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author Sampane-Donkor, Eric
Badoe, Ebenezer Vincent
Annan, Jennifer Adoley
Nii-Trebi, Nicholas
author_facet Sampane-Donkor, Eric
Badoe, Ebenezer Vincent
Annan, Jennifer Adoley
Nii-Trebi, Nicholas
author_sort Sampane-Donkor, Eric
collection PubMed
description Antibiotic use not only selects for resistance in pathogenic bacteria, but also in commensal flora of exposed individuals. Little is known epidemiologically about antibiotic resistance in relation to people with HIV infection in sub-Saharan Africa. This study investigated the carriage of antibiotic resistant bacteria among HIV infected children at a tertiary hospital in Ghana. One hundred and eighteen HIV positive children were recruited at the Korle-Bu Teaching Hospital in Ghana and nasopharyngeal specimens were collected from them. The specimens were cultured for bacteria, and the isolates were identified by standard microbiological methods. Antibiotic susceptibility tests were carried out on selected bacterial organisms by the Kirby Bauer method. Bacteria isolated from the study subjects included Moraxella catarrhalis (39.8%), coagulase negative staphylococci (33.1%), Streptococcus pneumoniae (30.5%), diptheroids (29.7%), viridian streptococci (27.1%), Staphylococcus aureus (22.0%), Citrobacter spp. (4.2%) and Neisseria meningitidis (0.9%). Prevalence of antibiotic resistance of S. pneumoniae ranged from 5.6% (ceftriaxone) to 58.3% (cotrimoxazole), M. catarrhalis ranged from 2.1% (gentamicin) to 80.6% (ampicillin), and S. aureus ranged from 7.7% (cefoxitin) to 100% (penicillin). The prevalence of multiple drug resistance was 16.7% for S. pneumoniae, 57.4% for M. catarrhalis and 84.6% for S. aureus. HIV infected children in the study area commonly carry multi-drug resistant isolates of several pathogenic bacteria such as S. aureus and S. pneumoniae. Infections arising in these patients that are caused by S. aureus and S. pneumoniae could be treated with ceftriaxone and cefoxitin respectively.
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spelling pubmed-53988692017-04-27 Colonisation of antibiotic resistant bacteria in a cohort of HIV infected children in Ghana Sampane-Donkor, Eric Badoe, Ebenezer Vincent Annan, Jennifer Adoley Nii-Trebi, Nicholas Pan Afr Med J Research Antibiotic use not only selects for resistance in pathogenic bacteria, but also in commensal flora of exposed individuals. Little is known epidemiologically about antibiotic resistance in relation to people with HIV infection in sub-Saharan Africa. This study investigated the carriage of antibiotic resistant bacteria among HIV infected children at a tertiary hospital in Ghana. One hundred and eighteen HIV positive children were recruited at the Korle-Bu Teaching Hospital in Ghana and nasopharyngeal specimens were collected from them. The specimens were cultured for bacteria, and the isolates were identified by standard microbiological methods. Antibiotic susceptibility tests were carried out on selected bacterial organisms by the Kirby Bauer method. Bacteria isolated from the study subjects included Moraxella catarrhalis (39.8%), coagulase negative staphylococci (33.1%), Streptococcus pneumoniae (30.5%), diptheroids (29.7%), viridian streptococci (27.1%), Staphylococcus aureus (22.0%), Citrobacter spp. (4.2%) and Neisseria meningitidis (0.9%). Prevalence of antibiotic resistance of S. pneumoniae ranged from 5.6% (ceftriaxone) to 58.3% (cotrimoxazole), M. catarrhalis ranged from 2.1% (gentamicin) to 80.6% (ampicillin), and S. aureus ranged from 7.7% (cefoxitin) to 100% (penicillin). The prevalence of multiple drug resistance was 16.7% for S. pneumoniae, 57.4% for M. catarrhalis and 84.6% for S. aureus. HIV infected children in the study area commonly carry multi-drug resistant isolates of several pathogenic bacteria such as S. aureus and S. pneumoniae. Infections arising in these patients that are caused by S. aureus and S. pneumoniae could be treated with ceftriaxone and cefoxitin respectively. The African Field Epidemiology Network 2017-02-02 /pmc/articles/PMC5398869/ /pubmed/28451037 http://dx.doi.org/10.11604/pamj.2017.26.60.10981 Text en © Eric Sampane-Donkor et al. http://creativecommons.org/licenses/by/2.0/ The Pan African Medical Journal - ISSN 1937-8688. This is an Open Access article distributed under the terms of the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Sampane-Donkor, Eric
Badoe, Ebenezer Vincent
Annan, Jennifer Adoley
Nii-Trebi, Nicholas
Colonisation of antibiotic resistant bacteria in a cohort of HIV infected children in Ghana
title Colonisation of antibiotic resistant bacteria in a cohort of HIV infected children in Ghana
title_full Colonisation of antibiotic resistant bacteria in a cohort of HIV infected children in Ghana
title_fullStr Colonisation of antibiotic resistant bacteria in a cohort of HIV infected children in Ghana
title_full_unstemmed Colonisation of antibiotic resistant bacteria in a cohort of HIV infected children in Ghana
title_short Colonisation of antibiotic resistant bacteria in a cohort of HIV infected children in Ghana
title_sort colonisation of antibiotic resistant bacteria in a cohort of hiv infected children in ghana
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5398869/
https://www.ncbi.nlm.nih.gov/pubmed/28451037
http://dx.doi.org/10.11604/pamj.2017.26.60.10981
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