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Microbiology of secondary infections in Buruli ulcer lesions; implications for therapeutic interventions

BACKGROUND: Buruli ulcer (BU) is a skin disease caused by Mycobacterium ulcerans and is the second most common mycobacterial disease after tuberculosis in Ghana and Côte d’Ivoire. M. ulcerans produces mycolactone, an immunosuppressant macrolide toxin, responsible for the characteristic painless natu...

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Autores principales: Gyamfi, Elizabeth, Narh, Charles A, Quaye, Charles, Abbass, Adiza, Dzudzor, Bartholomew, Mosi, Lydia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7783985/
https://www.ncbi.nlm.nih.gov/pubmed/33402095
http://dx.doi.org/10.1186/s12866-020-02070-5
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author Gyamfi, Elizabeth
Narh, Charles A
Quaye, Charles
Abbass, Adiza
Dzudzor, Bartholomew
Mosi, Lydia
author_facet Gyamfi, Elizabeth
Narh, Charles A
Quaye, Charles
Abbass, Adiza
Dzudzor, Bartholomew
Mosi, Lydia
author_sort Gyamfi, Elizabeth
collection PubMed
description BACKGROUND: Buruli ulcer (BU) is a skin disease caused by Mycobacterium ulcerans and is the second most common mycobacterial disease after tuberculosis in Ghana and Côte d’Ivoire. M. ulcerans produces mycolactone, an immunosuppressant macrolide toxin, responsible for the characteristic painless nature of the infection. Secondary infection of ulcers before, during and after treatment has been associated with delayed wound healing and resistance to streptomycin and rifampicin. However, not much is known of the bacteria causing these infections as well as antimicrobial drugs for treating the secondary microorganism. This study sought to identify secondary microbial infections in BU lesions and to determine their levels of antibiotic resistance due to the prolonged antibiotic therapy required for Buruli ulcer. RESULTS: Swabs from fifty-one suspected BU cases were sampled in the Amansie Central District from St. Peters Hospital (Jacobu) and through an active case surveillance. Forty of the samples were M. ulcerans (BU) positive. Secondary bacteria were identified in all sampled lesions (N = 51). The predominant bacteria identified in both BU and Non-BU groups were Staphylococci spp and Bacilli spp. The most diverse secondary bacteria were detected among BU patients who were not yet on antibiotic treatment. Fungal species identified were Candida spp, Penicillium spp and Trichodema spp. Selected secondary bacteria isolates were all susceptible to clarithromycin and amikacin among both BU and Non-BU patients. Majority, however, had high resistance to streptomycin. CONCLUSIONS: Microorganisms other than M. ulcerans colonize and proliferate on BU lesions. Secondary microorganisms of BU wounds were mainly Staphylococcus spp, Bacillus spp and Pseudomonas spp. These secondary microorganisms were less predominant in BU patients under treatment compared to those without treatment. The delay in healing that are experienced by some BU patients could be as a result of these bacteria and fungi colonizing and proliferating in BU lesions. Clarithromycin and amikacin are likely suitable drugs for clearance of secondary infection of Buruli ulcer.
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spelling pubmed-77839852021-01-14 Microbiology of secondary infections in Buruli ulcer lesions; implications for therapeutic interventions Gyamfi, Elizabeth Narh, Charles A Quaye, Charles Abbass, Adiza Dzudzor, Bartholomew Mosi, Lydia BMC Microbiol Research Article BACKGROUND: Buruli ulcer (BU) is a skin disease caused by Mycobacterium ulcerans and is the second most common mycobacterial disease after tuberculosis in Ghana and Côte d’Ivoire. M. ulcerans produces mycolactone, an immunosuppressant macrolide toxin, responsible for the characteristic painless nature of the infection. Secondary infection of ulcers before, during and after treatment has been associated with delayed wound healing and resistance to streptomycin and rifampicin. However, not much is known of the bacteria causing these infections as well as antimicrobial drugs for treating the secondary microorganism. This study sought to identify secondary microbial infections in BU lesions and to determine their levels of antibiotic resistance due to the prolonged antibiotic therapy required for Buruli ulcer. RESULTS: Swabs from fifty-one suspected BU cases were sampled in the Amansie Central District from St. Peters Hospital (Jacobu) and through an active case surveillance. Forty of the samples were M. ulcerans (BU) positive. Secondary bacteria were identified in all sampled lesions (N = 51). The predominant bacteria identified in both BU and Non-BU groups were Staphylococci spp and Bacilli spp. The most diverse secondary bacteria were detected among BU patients who were not yet on antibiotic treatment. Fungal species identified were Candida spp, Penicillium spp and Trichodema spp. Selected secondary bacteria isolates were all susceptible to clarithromycin and amikacin among both BU and Non-BU patients. Majority, however, had high resistance to streptomycin. CONCLUSIONS: Microorganisms other than M. ulcerans colonize and proliferate on BU lesions. Secondary microorganisms of BU wounds were mainly Staphylococcus spp, Bacillus spp and Pseudomonas spp. These secondary microorganisms were less predominant in BU patients under treatment compared to those without treatment. The delay in healing that are experienced by some BU patients could be as a result of these bacteria and fungi colonizing and proliferating in BU lesions. Clarithromycin and amikacin are likely suitable drugs for clearance of secondary infection of Buruli ulcer. BioMed Central 2021-01-05 /pmc/articles/PMC7783985/ /pubmed/33402095 http://dx.doi.org/10.1186/s12866-020-02070-5 Text en © The Author(s) 2021 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research Article
Gyamfi, Elizabeth
Narh, Charles A
Quaye, Charles
Abbass, Adiza
Dzudzor, Bartholomew
Mosi, Lydia
Microbiology of secondary infections in Buruli ulcer lesions; implications for therapeutic interventions
title Microbiology of secondary infections in Buruli ulcer lesions; implications for therapeutic interventions
title_full Microbiology of secondary infections in Buruli ulcer lesions; implications for therapeutic interventions
title_fullStr Microbiology of secondary infections in Buruli ulcer lesions; implications for therapeutic interventions
title_full_unstemmed Microbiology of secondary infections in Buruli ulcer lesions; implications for therapeutic interventions
title_short Microbiology of secondary infections in Buruli ulcer lesions; implications for therapeutic interventions
title_sort microbiology of secondary infections in buruli ulcer lesions; implications for therapeutic interventions
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7783985/
https://www.ncbi.nlm.nih.gov/pubmed/33402095
http://dx.doi.org/10.1186/s12866-020-02070-5
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