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Co-existence of bla(OXA-23) and bla(NDM-1) genes of Acinetobacter baumannii isolated from Nepal: antimicrobial resistance and clinical significance

BACKGROUND: Molecular analysis of carbapenem-resistant genes in Acinetobacter baumannii, an emerging pathogen, is less commonly reported from Nepal. In this study we determined the antibiotic susceptibility profile and genetic mechanism of carbapenem resistance in clinical isolates of A. baumannii....

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Autores principales: Joshi, Prabhu Raj, Acharya, Mahesh, Kakshapati, Trishna, Leungtongkam, Udomluk, Thummeepak, Rapee, Sitthisak, Sutthirat
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5297125/
https://www.ncbi.nlm.nih.gov/pubmed/28191309
http://dx.doi.org/10.1186/s13756-017-0180-5
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author Joshi, Prabhu Raj
Acharya, Mahesh
Kakshapati, Trishna
Leungtongkam, Udomluk
Thummeepak, Rapee
Sitthisak, Sutthirat
author_facet Joshi, Prabhu Raj
Acharya, Mahesh
Kakshapati, Trishna
Leungtongkam, Udomluk
Thummeepak, Rapee
Sitthisak, Sutthirat
author_sort Joshi, Prabhu Raj
collection PubMed
description BACKGROUND: Molecular analysis of carbapenem-resistant genes in Acinetobacter baumannii, an emerging pathogen, is less commonly reported from Nepal. In this study we determined the antibiotic susceptibility profile and genetic mechanism of carbapenem resistance in clinical isolates of A. baumannii. METHODS: A. baumannii were isolated from various clinical specimens and identified based on Gram staining, biochemical tests, and PCR amplification of organism specific 16S rRNA and bla (OXA-51) genes. The antibiotic susceptibility testing was performed using disc diffusion and E-test method. Multiplex PCR assays were used to detect the following β-lactamase genes: four class D carbapenem hydrolyzing oxacillinases (bla (OXA-51), bla (OXA-23), bla (OXA-24) and bla (OXA-58)). Uniplex PCRs were used to detect three class B metallo-β-lactamases genes (bla (IMP), bla (VIM) and bla (NDM-1)), class C cephalosporin resistance genes (bla (ADC)), aminoglycoside resistance gene (aphA6), and ISAba1 of all isolates. Insertion sequence ISAba125 among NDM-1 positive strains was detected. Clonal relatedness of all isolates were analyzed using repetitive sequence-based PCR (rep-PCR). RESULTS: Of total 44 analyzed isolates, 97.7% (n = 43) were carbapenem-resistant A. baumannii (CR-AB) and 97.7% (n = 43) were multidrug resistant A. baumannii (MDR-AB). One isolate was detected to be extremely drug resistant A. baumannii (XDR-AB). All the isolates were fully susceptible to colistin (MICs < 2 μg/ml). The bla (OXA-23) gene was detected in all isolates, while bla (NDM-1) was detected in 6 isolates (13.6%). Insertion sequence, ISAba1 was detected in all of bla (OXA-23) positive isolates. ISAba125 was detected in all bla (NDM-1) positive strains. The bla (ADC) and aphA6 genes were detected in 90.1 and 40.1%, respectively. The rep-PCR of all isolates represented 7 different genotypes. CONCLUSION: We found high prevalence of CR-AB and MDR-AB with bla (OXA-23) gene in a tertiary care hospital in Nepal. Systemic network surveillance should be established for monitoring and controlling the spread of these resistant strains. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13756-017-0180-5) contains supplementary material, which is available to authorized users.
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spelling pubmed-52971252017-02-10 Co-existence of bla(OXA-23) and bla(NDM-1) genes of Acinetobacter baumannii isolated from Nepal: antimicrobial resistance and clinical significance Joshi, Prabhu Raj Acharya, Mahesh Kakshapati, Trishna Leungtongkam, Udomluk Thummeepak, Rapee Sitthisak, Sutthirat Antimicrob Resist Infect Control Research BACKGROUND: Molecular analysis of carbapenem-resistant genes in Acinetobacter baumannii, an emerging pathogen, is less commonly reported from Nepal. In this study we determined the antibiotic susceptibility profile and genetic mechanism of carbapenem resistance in clinical isolates of A. baumannii. METHODS: A. baumannii were isolated from various clinical specimens and identified based on Gram staining, biochemical tests, and PCR amplification of organism specific 16S rRNA and bla (OXA-51) genes. The antibiotic susceptibility testing was performed using disc diffusion and E-test method. Multiplex PCR assays were used to detect the following β-lactamase genes: four class D carbapenem hydrolyzing oxacillinases (bla (OXA-51), bla (OXA-23), bla (OXA-24) and bla (OXA-58)). Uniplex PCRs were used to detect three class B metallo-β-lactamases genes (bla (IMP), bla (VIM) and bla (NDM-1)), class C cephalosporin resistance genes (bla (ADC)), aminoglycoside resistance gene (aphA6), and ISAba1 of all isolates. Insertion sequence ISAba125 among NDM-1 positive strains was detected. Clonal relatedness of all isolates were analyzed using repetitive sequence-based PCR (rep-PCR). RESULTS: Of total 44 analyzed isolates, 97.7% (n = 43) were carbapenem-resistant A. baumannii (CR-AB) and 97.7% (n = 43) were multidrug resistant A. baumannii (MDR-AB). One isolate was detected to be extremely drug resistant A. baumannii (XDR-AB). All the isolates were fully susceptible to colistin (MICs < 2 μg/ml). The bla (OXA-23) gene was detected in all isolates, while bla (NDM-1) was detected in 6 isolates (13.6%). Insertion sequence, ISAba1 was detected in all of bla (OXA-23) positive isolates. ISAba125 was detected in all bla (NDM-1) positive strains. The bla (ADC) and aphA6 genes were detected in 90.1 and 40.1%, respectively. The rep-PCR of all isolates represented 7 different genotypes. CONCLUSION: We found high prevalence of CR-AB and MDR-AB with bla (OXA-23) gene in a tertiary care hospital in Nepal. Systemic network surveillance should be established for monitoring and controlling the spread of these resistant strains. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13756-017-0180-5) contains supplementary material, which is available to authorized users. BioMed Central 2017-02-07 /pmc/articles/PMC5297125/ /pubmed/28191309 http://dx.doi.org/10.1186/s13756-017-0180-5 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. 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.
spellingShingle Research
Joshi, Prabhu Raj
Acharya, Mahesh
Kakshapati, Trishna
Leungtongkam, Udomluk
Thummeepak, Rapee
Sitthisak, Sutthirat
Co-existence of bla(OXA-23) and bla(NDM-1) genes of Acinetobacter baumannii isolated from Nepal: antimicrobial resistance and clinical significance
title Co-existence of bla(OXA-23) and bla(NDM-1) genes of Acinetobacter baumannii isolated from Nepal: antimicrobial resistance and clinical significance
title_full Co-existence of bla(OXA-23) and bla(NDM-1) genes of Acinetobacter baumannii isolated from Nepal: antimicrobial resistance and clinical significance
title_fullStr Co-existence of bla(OXA-23) and bla(NDM-1) genes of Acinetobacter baumannii isolated from Nepal: antimicrobial resistance and clinical significance
title_full_unstemmed Co-existence of bla(OXA-23) and bla(NDM-1) genes of Acinetobacter baumannii isolated from Nepal: antimicrobial resistance and clinical significance
title_short Co-existence of bla(OXA-23) and bla(NDM-1) genes of Acinetobacter baumannii isolated from Nepal: antimicrobial resistance and clinical significance
title_sort co-existence of bla(oxa-23) and bla(ndm-1) genes of acinetobacter baumannii isolated from nepal: antimicrobial resistance and clinical significance
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5297125/
https://www.ncbi.nlm.nih.gov/pubmed/28191309
http://dx.doi.org/10.1186/s13756-017-0180-5
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