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Resistance of Klebsiella pneumoniae Strains Carrying bla(NDM–1) Gene and the Genetic Environment of bla(NDM–1)

OBJECTIVE: Regional dissemination is the major cause of the widespread prevalence of a plasmid-encoding NDM-1 enzyme. We investigated the drug resistance, joint efficiency, and gene environment of a Klebsiella pneumoniae strain carrying bla(NDM–1) gene. MATERIALS AND METHODS: Carbapenem-non-suscepti...

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Autores principales: Xiang, Tianxin, Chen, Chuanhui, Wen, Jiangxiong, Liu, Yang, Zhang, Qi, Cheng, Na, Wu, Xiaoping, Zhang, Wei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7203411/
https://www.ncbi.nlm.nih.gov/pubmed/32425903
http://dx.doi.org/10.3389/fmicb.2020.00700
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author Xiang, Tianxin
Chen, Chuanhui
Wen, Jiangxiong
Liu, Yang
Zhang, Qi
Cheng, Na
Wu, Xiaoping
Zhang, Wei
author_facet Xiang, Tianxin
Chen, Chuanhui
Wen, Jiangxiong
Liu, Yang
Zhang, Qi
Cheng, Na
Wu, Xiaoping
Zhang, Wei
author_sort Xiang, Tianxin
collection PubMed
description OBJECTIVE: Regional dissemination is the major cause of the widespread prevalence of a plasmid-encoding NDM-1 enzyme. We investigated the drug resistance, joint efficiency, and gene environment of a Klebsiella pneumoniae strain carrying bla(NDM–1) gene. MATERIALS AND METHODS: Carbapenem-non-susceptible strains were analyzed using the VITEK 2 Compact. Strains carrying bla(NDM–1) were identified using polymerase chain reaction and sequencing. Antimicrobial susceptibility testing and plasmid conjugation experiments were then conducted. Strains carrying bla(NDM–1) were subjected to Southern blot analysis. After the gene mapping of bla(NDM–1), library construction, and sequencing, plasmids were subsequently spliced and genotyped using the software Glimmer 3.0, and then analyzed using Mauve software. RESULTS: Among 1735 carbapenem-non-susceptible strains, 54 strains of bla(NDM–1)-positive bacteria were identified, which consisted of 44 strains of K. pneumoniae, 8 strains of Acinetobacter baumannii and 2 strains of Escherichia coli. Strains carrying bla(NDM–1) had a resistance rate of more than 50% in most antibiotics. Plasmid conjugation between strains carrying bla(NDM–1) and E. coli strain J53 had a success rate of 50%. Southern blot analysis indicated that each strain had multiple plasmids containing bla(NDM–1). Among the five plasmids containing bla(NDM–1) in K. pneumoniae for sequencing, two plasmids with complete sequences were obtained. The findings were as follows: (i) The p11106 and p12 plasmids were highly similar to pNDM-BTR; (ii) the p11106 and p12 plasmids showed differences in the 20–30 kb region (orf00032–orf00043) from the other six plasmids; and (iii) bla(NDM–1) was located at orf00037, while ble was found at orf00038. Two tnpA genes were located in the upstream region, and orf00052 (tnpA) in the 36 kb region was in the downstream sequence. CONCLUSION: bla(NDM–1)-containing bacteria exhibit multidrug resistance, which rapidly spreads and is transferred through efficient plasmid conjugation; the multidrug resistance of these bacteria may be determined by analyzing their drug-resistant plasmids. The presence of ble and tnpA genes suggests a possible hypothesis that bla(NDM–1) originates from A. baumannii, which is retained in K. pneumoniae over a long period by transposition of mobile elements.
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spelling pubmed-72034112020-05-18 Resistance of Klebsiella pneumoniae Strains Carrying bla(NDM–1) Gene and the Genetic Environment of bla(NDM–1) Xiang, Tianxin Chen, Chuanhui Wen, Jiangxiong Liu, Yang Zhang, Qi Cheng, Na Wu, Xiaoping Zhang, Wei Front Microbiol Microbiology OBJECTIVE: Regional dissemination is the major cause of the widespread prevalence of a plasmid-encoding NDM-1 enzyme. We investigated the drug resistance, joint efficiency, and gene environment of a Klebsiella pneumoniae strain carrying bla(NDM–1) gene. MATERIALS AND METHODS: Carbapenem-non-susceptible strains were analyzed using the VITEK 2 Compact. Strains carrying bla(NDM–1) were identified using polymerase chain reaction and sequencing. Antimicrobial susceptibility testing and plasmid conjugation experiments were then conducted. Strains carrying bla(NDM–1) were subjected to Southern blot analysis. After the gene mapping of bla(NDM–1), library construction, and sequencing, plasmids were subsequently spliced and genotyped using the software Glimmer 3.0, and then analyzed using Mauve software. RESULTS: Among 1735 carbapenem-non-susceptible strains, 54 strains of bla(NDM–1)-positive bacteria were identified, which consisted of 44 strains of K. pneumoniae, 8 strains of Acinetobacter baumannii and 2 strains of Escherichia coli. Strains carrying bla(NDM–1) had a resistance rate of more than 50% in most antibiotics. Plasmid conjugation between strains carrying bla(NDM–1) and E. coli strain J53 had a success rate of 50%. Southern blot analysis indicated that each strain had multiple plasmids containing bla(NDM–1). Among the five plasmids containing bla(NDM–1) in K. pneumoniae for sequencing, two plasmids with complete sequences were obtained. The findings were as follows: (i) The p11106 and p12 plasmids were highly similar to pNDM-BTR; (ii) the p11106 and p12 plasmids showed differences in the 20–30 kb region (orf00032–orf00043) from the other six plasmids; and (iii) bla(NDM–1) was located at orf00037, while ble was found at orf00038. Two tnpA genes were located in the upstream region, and orf00052 (tnpA) in the 36 kb region was in the downstream sequence. CONCLUSION: bla(NDM–1)-containing bacteria exhibit multidrug resistance, which rapidly spreads and is transferred through efficient plasmid conjugation; the multidrug resistance of these bacteria may be determined by analyzing their drug-resistant plasmids. The presence of ble and tnpA genes suggests a possible hypothesis that bla(NDM–1) originates from A. baumannii, which is retained in K. pneumoniae over a long period by transposition of mobile elements. Frontiers Media S.A. 2020-04-30 /pmc/articles/PMC7203411/ /pubmed/32425903 http://dx.doi.org/10.3389/fmicb.2020.00700 Text en Copyright © 2020 Xiang, Chen, Wen, Liu, Zhang, Cheng, Wu and Zhang. http://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
Xiang, Tianxin
Chen, Chuanhui
Wen, Jiangxiong
Liu, Yang
Zhang, Qi
Cheng, Na
Wu, Xiaoping
Zhang, Wei
Resistance of Klebsiella pneumoniae Strains Carrying bla(NDM–1) Gene and the Genetic Environment of bla(NDM–1)
title Resistance of Klebsiella pneumoniae Strains Carrying bla(NDM–1) Gene and the Genetic Environment of bla(NDM–1)
title_full Resistance of Klebsiella pneumoniae Strains Carrying bla(NDM–1) Gene and the Genetic Environment of bla(NDM–1)
title_fullStr Resistance of Klebsiella pneumoniae Strains Carrying bla(NDM–1) Gene and the Genetic Environment of bla(NDM–1)
title_full_unstemmed Resistance of Klebsiella pneumoniae Strains Carrying bla(NDM–1) Gene and the Genetic Environment of bla(NDM–1)
title_short Resistance of Klebsiella pneumoniae Strains Carrying bla(NDM–1) Gene and the Genetic Environment of bla(NDM–1)
title_sort resistance of klebsiella pneumoniae strains carrying bla(ndm–1) gene and the genetic environment of bla(ndm–1)
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7203411/
https://www.ncbi.nlm.nih.gov/pubmed/32425903
http://dx.doi.org/10.3389/fmicb.2020.00700
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