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Molecular epidemiology and antimicrobial susceptibility of Pseudomonas spp. and Acinetobacter spp. from clinical samples at Jimma medical center, Ethiopia

INTRODUCTION: Pseudomonas aeruginosa (P. aeruginosa) and Acinetobacter baumannii (A. baumannii) can cause difficult-to-treat infections. We characterized molecular epidemiology of ceftazidime-resistant P. aeruginosa and carbapenem-resistant A. baumannii at a tertiary hospital in Ethiopia. MATERIALS...

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Autores principales: Sewunet, Tsegaye, Asrat, Daniel, Woldeamanuel, Yimtubezinash, Aseffa, Abraham, Giske, Christian G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9530197/
https://www.ncbi.nlm.nih.gov/pubmed/36204631
http://dx.doi.org/10.3389/fmicb.2022.951857
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author Sewunet, Tsegaye
Asrat, Daniel
Woldeamanuel, Yimtubezinash
Aseffa, Abraham
Giske, Christian G.
author_facet Sewunet, Tsegaye
Asrat, Daniel
Woldeamanuel, Yimtubezinash
Aseffa, Abraham
Giske, Christian G.
author_sort Sewunet, Tsegaye
collection PubMed
description INTRODUCTION: Pseudomonas aeruginosa (P. aeruginosa) and Acinetobacter baumannii (A. baumannii) can cause difficult-to-treat infections. We characterized molecular epidemiology of ceftazidime-resistant P. aeruginosa and carbapenem-resistant A. baumannii at a tertiary hospital in Ethiopia. MATERIALS AND METHODS: Non-fermenting gram-negative bacilli (n = 80) isolated from admitted patients were subjected for species identification by MALDI-TOF. Pseudomonas species resistant to ceftazidime or meropenem, and Acinetobacter species resistant to meropenem, or imipenem were selected for whole genome sequencing. DNA extracted with EZ1 Advanced XL instrument (Qiagen, Hilden, Germany) was sequenced on Illumina (HiSeq2500) using libraries prepared by NEXTRA-kits (Illumina). Raw reads were assembled using SPAdes 3.13.0, and assembled genomes were used to query databases for resistome profile and sequence types. RESULT: Among Pseudomonas species isolated, 31.7% (13/41), and 7.3% (3/41) were non-susceptible to ceftazidime, and meropenem, respectively. Carbapenem-resistance was 56.4% (22/39) among Acinetobacter species. Moreover, 92% (12/13) of Pseudomonas species non-susceptible to ceftazidime and/or meropenem, and 89.4% (17/19) of Acinetobacter species encoded multiple resistance genes for at least three classes of antimicrobials. The prevalent β - lactamase genes were bla(OXA–486) (53.8%, 7/13), bla(CTX–M–15) (23.0%, 3/13) among Pseudomonas, and bla(GES–11) (57.8%, 11/19) among Acinetobacter. The bla(OXA–51)-like β - lactamase, bla(OXA–69) (63.1%, 12/19) was the most prevalent carbapenemase gene among Acinetobacter isolates. Single isolates from both P. aeruginosa, and A. baumannii were detected with the bla(NDM–1). Sequence type (ST)1 A. baumannii and ST274 P. aeruginosa were the prevalent sequence types. A cgMLST analysis of the ST1 A. baumannii isolates showed that they were closely related and belonged to the international clonal complex one (ICC1). Similarly, ST274 P. aeruginosa isolates were clonally related. CONCLUSION: The prevalence of MDR isolates of Pseudomonas and Acinetobacter spp. was high. A. baumannii isolates were clonally spreading in the admission wards at the hospital. Emergence of bla(NDM–1) in the intensive care, and surgical wards of the hospital is a severe threat that requires urgent intervention.
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spelling pubmed-95301972022-10-05 Molecular epidemiology and antimicrobial susceptibility of Pseudomonas spp. and Acinetobacter spp. from clinical samples at Jimma medical center, Ethiopia Sewunet, Tsegaye Asrat, Daniel Woldeamanuel, Yimtubezinash Aseffa, Abraham Giske, Christian G. Front Microbiol Microbiology INTRODUCTION: Pseudomonas aeruginosa (P. aeruginosa) and Acinetobacter baumannii (A. baumannii) can cause difficult-to-treat infections. We characterized molecular epidemiology of ceftazidime-resistant P. aeruginosa and carbapenem-resistant A. baumannii at a tertiary hospital in Ethiopia. MATERIALS AND METHODS: Non-fermenting gram-negative bacilli (n = 80) isolated from admitted patients were subjected for species identification by MALDI-TOF. Pseudomonas species resistant to ceftazidime or meropenem, and Acinetobacter species resistant to meropenem, or imipenem were selected for whole genome sequencing. DNA extracted with EZ1 Advanced XL instrument (Qiagen, Hilden, Germany) was sequenced on Illumina (HiSeq2500) using libraries prepared by NEXTRA-kits (Illumina). Raw reads were assembled using SPAdes 3.13.0, and assembled genomes were used to query databases for resistome profile and sequence types. RESULT: Among Pseudomonas species isolated, 31.7% (13/41), and 7.3% (3/41) were non-susceptible to ceftazidime, and meropenem, respectively. Carbapenem-resistance was 56.4% (22/39) among Acinetobacter species. Moreover, 92% (12/13) of Pseudomonas species non-susceptible to ceftazidime and/or meropenem, and 89.4% (17/19) of Acinetobacter species encoded multiple resistance genes for at least three classes of antimicrobials. The prevalent β - lactamase genes were bla(OXA–486) (53.8%, 7/13), bla(CTX–M–15) (23.0%, 3/13) among Pseudomonas, and bla(GES–11) (57.8%, 11/19) among Acinetobacter. The bla(OXA–51)-like β - lactamase, bla(OXA–69) (63.1%, 12/19) was the most prevalent carbapenemase gene among Acinetobacter isolates. Single isolates from both P. aeruginosa, and A. baumannii were detected with the bla(NDM–1). Sequence type (ST)1 A. baumannii and ST274 P. aeruginosa were the prevalent sequence types. A cgMLST analysis of the ST1 A. baumannii isolates showed that they were closely related and belonged to the international clonal complex one (ICC1). Similarly, ST274 P. aeruginosa isolates were clonally related. CONCLUSION: The prevalence of MDR isolates of Pseudomonas and Acinetobacter spp. was high. A. baumannii isolates were clonally spreading in the admission wards at the hospital. Emergence of bla(NDM–1) in the intensive care, and surgical wards of the hospital is a severe threat that requires urgent intervention. Frontiers Media S.A. 2022-09-20 /pmc/articles/PMC9530197/ /pubmed/36204631 http://dx.doi.org/10.3389/fmicb.2022.951857 Text en Copyright © 2022 Sewunet, Asrat, Woldeamanuel, Aseffa and Giske. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Sewunet, Tsegaye
Asrat, Daniel
Woldeamanuel, Yimtubezinash
Aseffa, Abraham
Giske, Christian G.
Molecular epidemiology and antimicrobial susceptibility of Pseudomonas spp. and Acinetobacter spp. from clinical samples at Jimma medical center, Ethiopia
title Molecular epidemiology and antimicrobial susceptibility of Pseudomonas spp. and Acinetobacter spp. from clinical samples at Jimma medical center, Ethiopia
title_full Molecular epidemiology and antimicrobial susceptibility of Pseudomonas spp. and Acinetobacter spp. from clinical samples at Jimma medical center, Ethiopia
title_fullStr Molecular epidemiology and antimicrobial susceptibility of Pseudomonas spp. and Acinetobacter spp. from clinical samples at Jimma medical center, Ethiopia
title_full_unstemmed Molecular epidemiology and antimicrobial susceptibility of Pseudomonas spp. and Acinetobacter spp. from clinical samples at Jimma medical center, Ethiopia
title_short Molecular epidemiology and antimicrobial susceptibility of Pseudomonas spp. and Acinetobacter spp. from clinical samples at Jimma medical center, Ethiopia
title_sort molecular epidemiology and antimicrobial susceptibility of pseudomonas spp. and acinetobacter spp. from clinical samples at jimma medical center, ethiopia
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9530197/
https://www.ncbi.nlm.nih.gov/pubmed/36204631
http://dx.doi.org/10.3389/fmicb.2022.951857
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