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Multi-drug resistant bacteria isolates from lymphatic filariasis patients in the Ahanta West District, Ghana

BACKGROUND: Antimicrobial resistance is associated with increased morbidity in secondary infections and is a global threat owning to the ubiquitous nature of resistance genes in the environment. Recent estimate put the deaths associated with bacterial antimicrobial resistance in 2019 at 4.95 million...

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Autores principales: Aglomasa, Bill Clinton, Adu-Asiamah, Cynthia Kyerewaa, Asiedu, Samuel Opoku, Kini, Priscilla, Amewu, Emmanuel Kobla Atsu, Boahen, Kennedy Gyau, Wireko, Solomon, Amponsah, Isaac Kingsley, Boakye, Yaw Duah, Boamah, Vivian Etsiapa, Kwarteng, Alexander
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9552459/
https://www.ncbi.nlm.nih.gov/pubmed/36221074
http://dx.doi.org/10.1186/s12866-022-02624-9
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author Aglomasa, Bill Clinton
Adu-Asiamah, Cynthia Kyerewaa
Asiedu, Samuel Opoku
Kini, Priscilla
Amewu, Emmanuel Kobla Atsu
Boahen, Kennedy Gyau
Wireko, Solomon
Amponsah, Isaac Kingsley
Boakye, Yaw Duah
Boamah, Vivian Etsiapa
Kwarteng, Alexander
author_facet Aglomasa, Bill Clinton
Adu-Asiamah, Cynthia Kyerewaa
Asiedu, Samuel Opoku
Kini, Priscilla
Amewu, Emmanuel Kobla Atsu
Boahen, Kennedy Gyau
Wireko, Solomon
Amponsah, Isaac Kingsley
Boakye, Yaw Duah
Boamah, Vivian Etsiapa
Kwarteng, Alexander
author_sort Aglomasa, Bill Clinton
collection PubMed
description BACKGROUND: Antimicrobial resistance is associated with increased morbidity in secondary infections and is a global threat owning to the ubiquitous nature of resistance genes in the environment. Recent estimate put the deaths associated with bacterial antimicrobial resistance in 2019 at 4.95 million worldwide. Lymphatic filariasis (LF), a Neglected Tropical Disease (NTD), is associated with the poor living in the tropical regions of the world. LF patients are prone to developing acute dermatolymphangioadenitis (ADLA), a condition that puts them at risk of developing secondary bacterial infections due to skin peeling. ADLA particularly worsens the prognosis of patients leading to usage of antibiotics as a therapeutic intervention. This may result in inappropriate usage of antibiotics due to self-medication and non-compliance; exacerbating antimicrobial resistance in LF patients. In this perspective, we assessed the possibilities of antimicrobial resistance in LF patients. We focused on antibiotic usage, antibiotic resistance in Staphylococcus aureus, Escherichia coli and Pseudomonas aeruginosa isolates and looked at genes (mecA and Extended-spectrum beta-lactamase [blaCTX-M, blaSHV and blaTEM]) coding for resistance in multi-drug resistant (MDR) bacterial isolates. RESULTS: Of the sixty (60) participants, fifty-four (n = 54, 90%) were within 31–60 years of age, twenty (n = 20, 33.33%) were unemployed and thirty-eight (n = 38, 50.67%) had wounds aged (in months) seven (7) months and above. Amoxicillin (54%) and chloramphenicol (22%) were the most frequently used antibiotics for self-medication. Staphylococcus aureus isolates (n = 26) were mostly resistant to penicillin (n = 23, 88.46%) and least resistant to erythromycin (n = 2, 7.69%). Escherichia coli isolates (n = 5) were resistant to tetracycline (n = 5, 100%) and ampicillin (n = 5, 100%) but were sensitive to meropenem (n = 5, 100%). Pseudomonas aeruginosa isolates (n = 8) were most resistant to meropenem (n = 3, 37.50%) and to a lesser ciprofloxacin (n = 2, 25%), gentamicin (n = 2, 25%) and ceftazidime (n = 2, 25%). Multi-drug resistant methicillin resistant Staphylococcus aureus (MRSA), cephalosporin resistant Escherichia coli. and carbapenem resistant Pseudomonas aeruginosa were four (n = 4, 15.38%), two (n = 2, 40%) and two (n = 2, 25%) respectively. ESBL (blaCTX-M) and mecA genes were implicated in the resistance mechanism of Escherichia coli and MRSA, respectively. CONCLUSION: The findings show presence of MDR isolates from LF patients presenting with chronic wounds; thus, the need to prioritize resistance of MDR bacteria into treatment strategies optimizing morbidity management protocols. This could guide antibiotic selection for treating LF patients presenting with ADLA. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12866-022-02624-9.
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spelling pubmed-95524592022-10-12 Multi-drug resistant bacteria isolates from lymphatic filariasis patients in the Ahanta West District, Ghana Aglomasa, Bill Clinton Adu-Asiamah, Cynthia Kyerewaa Asiedu, Samuel Opoku Kini, Priscilla Amewu, Emmanuel Kobla Atsu Boahen, Kennedy Gyau Wireko, Solomon Amponsah, Isaac Kingsley Boakye, Yaw Duah Boamah, Vivian Etsiapa Kwarteng, Alexander BMC Microbiol Research BACKGROUND: Antimicrobial resistance is associated with increased morbidity in secondary infections and is a global threat owning to the ubiquitous nature of resistance genes in the environment. Recent estimate put the deaths associated with bacterial antimicrobial resistance in 2019 at 4.95 million worldwide. Lymphatic filariasis (LF), a Neglected Tropical Disease (NTD), is associated with the poor living in the tropical regions of the world. LF patients are prone to developing acute dermatolymphangioadenitis (ADLA), a condition that puts them at risk of developing secondary bacterial infections due to skin peeling. ADLA particularly worsens the prognosis of patients leading to usage of antibiotics as a therapeutic intervention. This may result in inappropriate usage of antibiotics due to self-medication and non-compliance; exacerbating antimicrobial resistance in LF patients. In this perspective, we assessed the possibilities of antimicrobial resistance in LF patients. We focused on antibiotic usage, antibiotic resistance in Staphylococcus aureus, Escherichia coli and Pseudomonas aeruginosa isolates and looked at genes (mecA and Extended-spectrum beta-lactamase [blaCTX-M, blaSHV and blaTEM]) coding for resistance in multi-drug resistant (MDR) bacterial isolates. RESULTS: Of the sixty (60) participants, fifty-four (n = 54, 90%) were within 31–60 years of age, twenty (n = 20, 33.33%) were unemployed and thirty-eight (n = 38, 50.67%) had wounds aged (in months) seven (7) months and above. Amoxicillin (54%) and chloramphenicol (22%) were the most frequently used antibiotics for self-medication. Staphylococcus aureus isolates (n = 26) were mostly resistant to penicillin (n = 23, 88.46%) and least resistant to erythromycin (n = 2, 7.69%). Escherichia coli isolates (n = 5) were resistant to tetracycline (n = 5, 100%) and ampicillin (n = 5, 100%) but were sensitive to meropenem (n = 5, 100%). Pseudomonas aeruginosa isolates (n = 8) were most resistant to meropenem (n = 3, 37.50%) and to a lesser ciprofloxacin (n = 2, 25%), gentamicin (n = 2, 25%) and ceftazidime (n = 2, 25%). Multi-drug resistant methicillin resistant Staphylococcus aureus (MRSA), cephalosporin resistant Escherichia coli. and carbapenem resistant Pseudomonas aeruginosa were four (n = 4, 15.38%), two (n = 2, 40%) and two (n = 2, 25%) respectively. ESBL (blaCTX-M) and mecA genes were implicated in the resistance mechanism of Escherichia coli and MRSA, respectively. CONCLUSION: The findings show presence of MDR isolates from LF patients presenting with chronic wounds; thus, the need to prioritize resistance of MDR bacteria into treatment strategies optimizing morbidity management protocols. This could guide antibiotic selection for treating LF patients presenting with ADLA. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12866-022-02624-9. BioMed Central 2022-10-11 /pmc/articles/PMC9552459/ /pubmed/36221074 http://dx.doi.org/10.1186/s12866-022-02624-9 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://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
Aglomasa, Bill Clinton
Adu-Asiamah, Cynthia Kyerewaa
Asiedu, Samuel Opoku
Kini, Priscilla
Amewu, Emmanuel Kobla Atsu
Boahen, Kennedy Gyau
Wireko, Solomon
Amponsah, Isaac Kingsley
Boakye, Yaw Duah
Boamah, Vivian Etsiapa
Kwarteng, Alexander
Multi-drug resistant bacteria isolates from lymphatic filariasis patients in the Ahanta West District, Ghana
title Multi-drug resistant bacteria isolates from lymphatic filariasis patients in the Ahanta West District, Ghana
title_full Multi-drug resistant bacteria isolates from lymphatic filariasis patients in the Ahanta West District, Ghana
title_fullStr Multi-drug resistant bacteria isolates from lymphatic filariasis patients in the Ahanta West District, Ghana
title_full_unstemmed Multi-drug resistant bacteria isolates from lymphatic filariasis patients in the Ahanta West District, Ghana
title_short Multi-drug resistant bacteria isolates from lymphatic filariasis patients in the Ahanta West District, Ghana
title_sort multi-drug resistant bacteria isolates from lymphatic filariasis patients in the ahanta west district, ghana
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9552459/
https://www.ncbi.nlm.nih.gov/pubmed/36221074
http://dx.doi.org/10.1186/s12866-022-02624-9
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