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Transferable IncX3 plasmid harboring bla(NDM-1), ble(MBL), and aph(3’)-VI genes from Klebsiella pneumoniae conferring phenotypic carbapenem resistance in E. coli

BACKGROUND: The dissemination of carbapenem resistance via carbapenemases, such as the metallo-β-lactamase NDM, among Enterobacterales poses a public health threat. The aim of this study was to characterize a plasmid carrying the bla(NDM-1) gene, which was extracted from a clinical Klebsiella pneumo...

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Autores principales: Elshamy, Ann A., Saleh, Sarra E., Aboshanab, Khaled M., Aboulwafa, Mohammad M., Hassouna, Nadia A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Netherlands 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10209314/
https://www.ncbi.nlm.nih.gov/pubmed/37081308
http://dx.doi.org/10.1007/s11033-023-08401-9
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author Elshamy, Ann A.
Saleh, Sarra E.
Aboshanab, Khaled M.
Aboulwafa, Mohammad M.
Hassouna, Nadia A.
author_facet Elshamy, Ann A.
Saleh, Sarra E.
Aboshanab, Khaled M.
Aboulwafa, Mohammad M.
Hassouna, Nadia A.
author_sort Elshamy, Ann A.
collection PubMed
description BACKGROUND: The dissemination of carbapenem resistance via carbapenemases, such as the metallo-β-lactamase NDM, among Enterobacterales poses a public health threat. The aim of this study was to characterize a plasmid carrying the bla(NDM-1) gene, which was extracted from a clinical Klebsiella pneumoniae uropathogen from an Egyptian patient suffering from a urinary tract infection. METHODS AND RESULTS: The recovered plasmid was transformed into competent E. coli DH5α which acquired phenotypic resistance to cefoxitin, ceftazidime, and ampicillin/sulbactam, and intermediate sensitivity to ceftriaxone and imipenem (a carbapenem). Whole plasmid sequencing was performed on the extracted plasmid using the DNBSEQ™ platform. The obtained forward and reverse reads were assembled into contigs using the PRINSEQ and PLACNETw web tools. The obtained contigs were uploaded to PlasmidFinder and ResFinder for in silico plasmid typing and detection of antimicrobial resistance genes, respectively. The final consensus sequence was obtained using the Staden Package software. The plasmid (pNDMKP37, NCBI accession OK623716.1) was typed as an IncX3 plasmid with a size of 46,160 bp and harbored the antibiotic resistance genes bla(NDM-1), ble(MBL), and aph(3’)-VI. The plasmid also carried mobile genetic elements involved in the dissemination of antimicrobial resistance including insertion sequences IS30, IS630, and IS26. CONCLUSIONS: This is Egypt’s first report of a transmissible plasmid co-harboring bla(NDM-1) and aph(3’)-VI genes. Moreover, the respective plasmid is of great medical concern as it has caused the horizontal transmission of multidrug-resistant phenotypes to the transformant. Therefore, new guidelines should be implemented for the rational use of broad-spectrum antibiotics, particularly carbapenems. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s11033-023-08401-9.
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spelling pubmed-102093142023-05-26 Transferable IncX3 plasmid harboring bla(NDM-1), ble(MBL), and aph(3’)-VI genes from Klebsiella pneumoniae conferring phenotypic carbapenem resistance in E. coli Elshamy, Ann A. Saleh, Sarra E. Aboshanab, Khaled M. Aboulwafa, Mohammad M. Hassouna, Nadia A. Mol Biol Rep Original Article BACKGROUND: The dissemination of carbapenem resistance via carbapenemases, such as the metallo-β-lactamase NDM, among Enterobacterales poses a public health threat. The aim of this study was to characterize a plasmid carrying the bla(NDM-1) gene, which was extracted from a clinical Klebsiella pneumoniae uropathogen from an Egyptian patient suffering from a urinary tract infection. METHODS AND RESULTS: The recovered plasmid was transformed into competent E. coli DH5α which acquired phenotypic resistance to cefoxitin, ceftazidime, and ampicillin/sulbactam, and intermediate sensitivity to ceftriaxone and imipenem (a carbapenem). Whole plasmid sequencing was performed on the extracted plasmid using the DNBSEQ™ platform. The obtained forward and reverse reads were assembled into contigs using the PRINSEQ and PLACNETw web tools. The obtained contigs were uploaded to PlasmidFinder and ResFinder for in silico plasmid typing and detection of antimicrobial resistance genes, respectively. The final consensus sequence was obtained using the Staden Package software. The plasmid (pNDMKP37, NCBI accession OK623716.1) was typed as an IncX3 plasmid with a size of 46,160 bp and harbored the antibiotic resistance genes bla(NDM-1), ble(MBL), and aph(3’)-VI. The plasmid also carried mobile genetic elements involved in the dissemination of antimicrobial resistance including insertion sequences IS30, IS630, and IS26. CONCLUSIONS: This is Egypt’s first report of a transmissible plasmid co-harboring bla(NDM-1) and aph(3’)-VI genes. Moreover, the respective plasmid is of great medical concern as it has caused the horizontal transmission of multidrug-resistant phenotypes to the transformant. Therefore, new guidelines should be implemented for the rational use of broad-spectrum antibiotics, particularly carbapenems. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s11033-023-08401-9. Springer Netherlands 2023-04-20 2023 /pmc/articles/PMC10209314/ /pubmed/37081308 http://dx.doi.org/10.1007/s11033-023-08401-9 Text en © The Author(s) 2023, Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law. 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/) .
spellingShingle Original Article
Elshamy, Ann A.
Saleh, Sarra E.
Aboshanab, Khaled M.
Aboulwafa, Mohammad M.
Hassouna, Nadia A.
Transferable IncX3 plasmid harboring bla(NDM-1), ble(MBL), and aph(3’)-VI genes from Klebsiella pneumoniae conferring phenotypic carbapenem resistance in E. coli
title Transferable IncX3 plasmid harboring bla(NDM-1), ble(MBL), and aph(3’)-VI genes from Klebsiella pneumoniae conferring phenotypic carbapenem resistance in E. coli
title_full Transferable IncX3 plasmid harboring bla(NDM-1), ble(MBL), and aph(3’)-VI genes from Klebsiella pneumoniae conferring phenotypic carbapenem resistance in E. coli
title_fullStr Transferable IncX3 plasmid harboring bla(NDM-1), ble(MBL), and aph(3’)-VI genes from Klebsiella pneumoniae conferring phenotypic carbapenem resistance in E. coli
title_full_unstemmed Transferable IncX3 plasmid harboring bla(NDM-1), ble(MBL), and aph(3’)-VI genes from Klebsiella pneumoniae conferring phenotypic carbapenem resistance in E. coli
title_short Transferable IncX3 plasmid harboring bla(NDM-1), ble(MBL), and aph(3’)-VI genes from Klebsiella pneumoniae conferring phenotypic carbapenem resistance in E. coli
title_sort transferable incx3 plasmid harboring bla(ndm-1), ble(mbl), and aph(3’)-vi genes from klebsiella pneumoniae conferring phenotypic carbapenem resistance in e. coli
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10209314/
https://www.ncbi.nlm.nih.gov/pubmed/37081308
http://dx.doi.org/10.1007/s11033-023-08401-9
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