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Klebsiella grimontii, a New Species Acquired Carbapenem Resistance

Klebsiella grimontii is a newly identified species closely related to Klebsiella oxytoca, but carbapenem resistance was not identified in the species before. We found a carbapenem-resistant K. oxytoca-like clinical strain, WCHKG020121. The strain was subjected to whole genome sequencing using Illumi...

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Autores principales: Liu, Lu, Feng, Yu, Hu, Yiyi, Kang, Mei, Xie, Yi, Zong, Zhiyong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6142883/
https://www.ncbi.nlm.nih.gov/pubmed/30271396
http://dx.doi.org/10.3389/fmicb.2018.02170
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author Liu, Lu
Feng, Yu
Hu, Yiyi
Kang, Mei
Xie, Yi
Zong, Zhiyong
author_facet Liu, Lu
Feng, Yu
Hu, Yiyi
Kang, Mei
Xie, Yi
Zong, Zhiyong
author_sort Liu, Lu
collection PubMed
description Klebsiella grimontii is a newly identified species closely related to Klebsiella oxytoca, but carbapenem resistance was not identified in the species before. We found a carbapenem-resistant K. oxytoca-like clinical strain, WCHKG020121. The strain was subjected to whole genome sequencing using Illumina HiSeq X10. The precise species identification was established based on average nucleotide identity (ANI) and in silico DNA–DNA hybridization (isDDH) between strain WCHKG020121 and type strains of Klebsiella species. Antimicrobial resistance genes were identified from the genome sequence. The sequence of the bla(KPC-2)-carrying plasmid was completed using PCR and Sanger sequencing. Conjugation experiments were performed to obtain the plasmid carrying bla(KPC-2). All K. grimontii genomes were retrieved from GenBank and were analyzed for antimicrobial resistance genes. Strain WCHKG020121 was resistant to imipenem and meropenem (MIC for both, 32 μg/ml) but was susceptible to colistin (1 μg/ml). Strain WCHKG020121 was initially identified as K. oxytoca using Vitek II but it actually belongs to K. grimontii as it had a 98.81% ANI and 83.4% isDDH value with K. grimontii type strain. Strain WCHKG020121 had bla(KPC-2); by contrast, none of other K. grimontii genomes carry any known carbapenemase genes. bla(KPC-2) was carried by a 95,734-bp plasmid, designated pKPC2_020121, which contained two different FII(Y) replicons. pKPC2_020121 was closest (93% coverage, 99% identity) to bla(KPC-2)-carrying plasmids from Enterobacter hormaechei recovered in 2014 at the same hospital. pKPC2_020121 was not self-transmissible, which could be explained by the absence of a conjugation essential gene, traY. In conclusion, we reported the first K. grimontii strain that produced the KPC carbapenemase. Carbapenem resistant K. grimontii may represent a new threat.
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spelling pubmed-61428832018-09-28 Klebsiella grimontii, a New Species Acquired Carbapenem Resistance Liu, Lu Feng, Yu Hu, Yiyi Kang, Mei Xie, Yi Zong, Zhiyong Front Microbiol Microbiology Klebsiella grimontii is a newly identified species closely related to Klebsiella oxytoca, but carbapenem resistance was not identified in the species before. We found a carbapenem-resistant K. oxytoca-like clinical strain, WCHKG020121. The strain was subjected to whole genome sequencing using Illumina HiSeq X10. The precise species identification was established based on average nucleotide identity (ANI) and in silico DNA–DNA hybridization (isDDH) between strain WCHKG020121 and type strains of Klebsiella species. Antimicrobial resistance genes were identified from the genome sequence. The sequence of the bla(KPC-2)-carrying plasmid was completed using PCR and Sanger sequencing. Conjugation experiments were performed to obtain the plasmid carrying bla(KPC-2). All K. grimontii genomes were retrieved from GenBank and were analyzed for antimicrobial resistance genes. Strain WCHKG020121 was resistant to imipenem and meropenem (MIC for both, 32 μg/ml) but was susceptible to colistin (1 μg/ml). Strain WCHKG020121 was initially identified as K. oxytoca using Vitek II but it actually belongs to K. grimontii as it had a 98.81% ANI and 83.4% isDDH value with K. grimontii type strain. Strain WCHKG020121 had bla(KPC-2); by contrast, none of other K. grimontii genomes carry any known carbapenemase genes. bla(KPC-2) was carried by a 95,734-bp plasmid, designated pKPC2_020121, which contained two different FII(Y) replicons. pKPC2_020121 was closest (93% coverage, 99% identity) to bla(KPC-2)-carrying plasmids from Enterobacter hormaechei recovered in 2014 at the same hospital. pKPC2_020121 was not self-transmissible, which could be explained by the absence of a conjugation essential gene, traY. In conclusion, we reported the first K. grimontii strain that produced the KPC carbapenemase. Carbapenem resistant K. grimontii may represent a new threat. Frontiers Media S.A. 2018-09-11 /pmc/articles/PMC6142883/ /pubmed/30271396 http://dx.doi.org/10.3389/fmicb.2018.02170 Text en Copyright © 2018 Liu, Feng, Hu, Kang, Xie and Zong. 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
Liu, Lu
Feng, Yu
Hu, Yiyi
Kang, Mei
Xie, Yi
Zong, Zhiyong
Klebsiella grimontii, a New Species Acquired Carbapenem Resistance
title Klebsiella grimontii, a New Species Acquired Carbapenem Resistance
title_full Klebsiella grimontii, a New Species Acquired Carbapenem Resistance
title_fullStr Klebsiella grimontii, a New Species Acquired Carbapenem Resistance
title_full_unstemmed Klebsiella grimontii, a New Species Acquired Carbapenem Resistance
title_short Klebsiella grimontii, a New Species Acquired Carbapenem Resistance
title_sort klebsiella grimontii, a new species acquired carbapenem resistance
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6142883/
https://www.ncbi.nlm.nih.gov/pubmed/30271396
http://dx.doi.org/10.3389/fmicb.2018.02170
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