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Genomic Characteristics of a Multidrug-Resistant ST648 Escherichia coli Isolate Co-Carrying bla(KPC-2) and bla(CTX-M-15) Genes Recovered from a Respiratory Infection in China
BACKGROUND: The transmission of carbapenem-resistant Enterobacterales pose a significant threat to global public health, which weakens the effectiveness of most antimicrobial agents. The aim of this study is to present the genomic characteristics of a multidrug-resistant Escherichia coli, which cont...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10246572/ https://www.ncbi.nlm.nih.gov/pubmed/37293536 http://dx.doi.org/10.2147/IDR.S415846 |
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author | He, Xianhong Xu, Liwei Dai, Hangdong Ge, Minxia Zhu, Jufang Fu, Hangyu Zhu, Shuilong Shao, Jiayu |
author_facet | He, Xianhong Xu, Liwei Dai, Hangdong Ge, Minxia Zhu, Jufang Fu, Hangyu Zhu, Shuilong Shao, Jiayu |
author_sort | He, Xianhong |
collection | PubMed |
description | BACKGROUND: The transmission of carbapenem-resistant Enterobacterales pose a significant threat to global public health, which weakens the effectiveness of most antimicrobial agents. The aim of this study is to present the genomic characteristics of a multidrug-resistant Escherichia coli, which contains both bla(KPC-2) and bla(CTX-M-15) genes, discovered from a respiratory infection in China. METHODS: The antimicrobial susceptibility of E. coli isolate 488 was measured by using the broth microdilution method. The Oxford Nanopore MinION and Illumina NovaSeq 6000 platforms were applied to determine the whole-genome sequence of this isolate. De novo assembly of short Illumina reads and long MinION reads were performed by Unicycler. In silico multilocus sequence typing (MLST), antimicrobial resistance genes and plasmid replicon types were determined using the genome sequencing data. Additionally, a pairwise core genome single nucleotide polymorphism (cgSNP) comparison between E. coli 488 and all ST648 E. coli strains retrieved from NCBI GenBank database were conducted using the BacWGSTdb 2.0 server. RESULTS: E. coli 488 was resistant to aztreonam, levofloxacin, cefepime, fosfomycin, amikacin, imipenem, cefotaxime, and meropenem. The complete genome sequence of E. coli 488 (belong to ST648) is made up of eleven contigs totaling 5,573,915 bp, including one chromosome and ten plasmids. Eight antimicrobial resistance genes were identified, including bla(KPC-2) located in a 46,161 bp IncI1-type plasmid and the bla(CTX-M-15) gene situated in the chromosome. Other two E. coli S617-2 and R616-1 isolates, recovered from China in 2018, are the closest relatives of E. coli 488, with only 52 SNPs difference. The genome also contains at least 57 genomic islands and several IS elements. CONCLUSION: Our study reveals the first ST648 E. coli isolate containing both bla(KPC-2) and bla(CTX-M-15) in China. These results could provide valuable insights into the genetic characteristics, antimicrobial resistance mechanisms, and transmission dynamics of carbapenem-resistant Enterobacterales in clinical settings. |
format | Online Article Text |
id | pubmed-10246572 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Dove |
record_format | MEDLINE/PubMed |
spelling | pubmed-102465722023-06-08 Genomic Characteristics of a Multidrug-Resistant ST648 Escherichia coli Isolate Co-Carrying bla(KPC-2) and bla(CTX-M-15) Genes Recovered from a Respiratory Infection in China He, Xianhong Xu, Liwei Dai, Hangdong Ge, Minxia Zhu, Jufang Fu, Hangyu Zhu, Shuilong Shao, Jiayu Infect Drug Resist Original Research BACKGROUND: The transmission of carbapenem-resistant Enterobacterales pose a significant threat to global public health, which weakens the effectiveness of most antimicrobial agents. The aim of this study is to present the genomic characteristics of a multidrug-resistant Escherichia coli, which contains both bla(KPC-2) and bla(CTX-M-15) genes, discovered from a respiratory infection in China. METHODS: The antimicrobial susceptibility of E. coli isolate 488 was measured by using the broth microdilution method. The Oxford Nanopore MinION and Illumina NovaSeq 6000 platforms were applied to determine the whole-genome sequence of this isolate. De novo assembly of short Illumina reads and long MinION reads were performed by Unicycler. In silico multilocus sequence typing (MLST), antimicrobial resistance genes and plasmid replicon types were determined using the genome sequencing data. Additionally, a pairwise core genome single nucleotide polymorphism (cgSNP) comparison between E. coli 488 and all ST648 E. coli strains retrieved from NCBI GenBank database were conducted using the BacWGSTdb 2.0 server. RESULTS: E. coli 488 was resistant to aztreonam, levofloxacin, cefepime, fosfomycin, amikacin, imipenem, cefotaxime, and meropenem. The complete genome sequence of E. coli 488 (belong to ST648) is made up of eleven contigs totaling 5,573,915 bp, including one chromosome and ten plasmids. Eight antimicrobial resistance genes were identified, including bla(KPC-2) located in a 46,161 bp IncI1-type plasmid and the bla(CTX-M-15) gene situated in the chromosome. Other two E. coli S617-2 and R616-1 isolates, recovered from China in 2018, are the closest relatives of E. coli 488, with only 52 SNPs difference. The genome also contains at least 57 genomic islands and several IS elements. CONCLUSION: Our study reveals the first ST648 E. coli isolate containing both bla(KPC-2) and bla(CTX-M-15) in China. These results could provide valuable insights into the genetic characteristics, antimicrobial resistance mechanisms, and transmission dynamics of carbapenem-resistant Enterobacterales in clinical settings. Dove 2023-06-03 /pmc/articles/PMC10246572/ /pubmed/37293536 http://dx.doi.org/10.2147/IDR.S415846 Text en © 2023 He et al. https://creativecommons.org/licenses/by-nc/3.0/This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/ (https://creativecommons.org/licenses/by-nc/3.0/) ). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php). |
spellingShingle | Original Research He, Xianhong Xu, Liwei Dai, Hangdong Ge, Minxia Zhu, Jufang Fu, Hangyu Zhu, Shuilong Shao, Jiayu Genomic Characteristics of a Multidrug-Resistant ST648 Escherichia coli Isolate Co-Carrying bla(KPC-2) and bla(CTX-M-15) Genes Recovered from a Respiratory Infection in China |
title | Genomic Characteristics of a Multidrug-Resistant ST648 Escherichia coli Isolate Co-Carrying bla(KPC-2) and bla(CTX-M-15) Genes Recovered from a Respiratory Infection in China |
title_full | Genomic Characteristics of a Multidrug-Resistant ST648 Escherichia coli Isolate Co-Carrying bla(KPC-2) and bla(CTX-M-15) Genes Recovered from a Respiratory Infection in China |
title_fullStr | Genomic Characteristics of a Multidrug-Resistant ST648 Escherichia coli Isolate Co-Carrying bla(KPC-2) and bla(CTX-M-15) Genes Recovered from a Respiratory Infection in China |
title_full_unstemmed | Genomic Characteristics of a Multidrug-Resistant ST648 Escherichia coli Isolate Co-Carrying bla(KPC-2) and bla(CTX-M-15) Genes Recovered from a Respiratory Infection in China |
title_short | Genomic Characteristics of a Multidrug-Resistant ST648 Escherichia coli Isolate Co-Carrying bla(KPC-2) and bla(CTX-M-15) Genes Recovered from a Respiratory Infection in China |
title_sort | genomic characteristics of a multidrug-resistant st648 escherichia coli isolate co-carrying bla(kpc-2) and bla(ctx-m-15) genes recovered from a respiratory infection in china |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10246572/ https://www.ncbi.nlm.nih.gov/pubmed/37293536 http://dx.doi.org/10.2147/IDR.S415846 |
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