Cargando…
Phenotypic and Enzymatic Comparative Analysis of the KPC Variants, KPC-2 and Its Recently Discovered Variant KPC-15
Sixteen different variants (KPC-2 to KPC-17) in the KPC family have been reported, and most current studies are focusing on KPC-2 and KPC-3. The KPC-15 variant, which isolated from Klebsiella pneumoniae in a Chinese hospital, was a recently discovered KPC enzyme. To compare the characteristics of KP...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2014
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4216079/ https://www.ncbi.nlm.nih.gov/pubmed/25360633 http://dx.doi.org/10.1371/journal.pone.0111491 |
_version_ | 1782342206847188992 |
---|---|
author | Wang, Dongguo Chen, Jiayu Yang, Linjun Mou, Yonghua Yang, Yijun |
author_facet | Wang, Dongguo Chen, Jiayu Yang, Linjun Mou, Yonghua Yang, Yijun |
author_sort | Wang, Dongguo |
collection | PubMed |
description | Sixteen different variants (KPC-2 to KPC-17) in the KPC family have been reported, and most current studies are focusing on KPC-2 and KPC-3. The KPC-15 variant, which isolated from Klebsiella pneumoniae in a Chinese hospital, was a recently discovered KPC enzyme. To compare the characteristics of KPC-15 and KPC-2, the variants were determined by susceptibility testing, PCR amplification and sequencing, and study of kinetic parameters. The strain harboring the KPC-15 showed resistance to 18 conventional antimicrobial agents, especially to cabapenem antibiotics, and the strain involving the KPC-2 also indicated resistance to cabapenem antibiotics, but both strains were susceptible to polymyxin B and colistin. The conjugation experiments showed that the changes of MIC values to the antibiotics were due to the transferred plasmids. The differences of amino acids were characterised at sites of 119 leucine and 146 lysine with KPC-15 and KPC-2. The minimum evolution tree indicated the KPC alleles evolution, and showed that the KPC-15 appeared to be homogenous with KPC-4 closely. Steady-state kinetic parameters showed the catalytic efficiency of KPC-15 was higher than that of KPC-2 for all tested antibiotics in this study. The catalytic efficiency of KPC-15 caused resistance to β-lactam antibiotics was higher than that of KPC-2. Meanwhile, an evolutionary transformation changed KPC from an efficient carbapenemase to its variants (KPC-15) with better ceftazidimase catalytic efficiency, and the old antibiotics polymyxin B and colistin might play a role in the therapy for multi-resistant strains. |
format | Online Article Text |
id | pubmed-4216079 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-42160792014-11-05 Phenotypic and Enzymatic Comparative Analysis of the KPC Variants, KPC-2 and Its Recently Discovered Variant KPC-15 Wang, Dongguo Chen, Jiayu Yang, Linjun Mou, Yonghua Yang, Yijun PLoS One Research Article Sixteen different variants (KPC-2 to KPC-17) in the KPC family have been reported, and most current studies are focusing on KPC-2 and KPC-3. The KPC-15 variant, which isolated from Klebsiella pneumoniae in a Chinese hospital, was a recently discovered KPC enzyme. To compare the characteristics of KPC-15 and KPC-2, the variants were determined by susceptibility testing, PCR amplification and sequencing, and study of kinetic parameters. The strain harboring the KPC-15 showed resistance to 18 conventional antimicrobial agents, especially to cabapenem antibiotics, and the strain involving the KPC-2 also indicated resistance to cabapenem antibiotics, but both strains were susceptible to polymyxin B and colistin. The conjugation experiments showed that the changes of MIC values to the antibiotics were due to the transferred plasmids. The differences of amino acids were characterised at sites of 119 leucine and 146 lysine with KPC-15 and KPC-2. The minimum evolution tree indicated the KPC alleles evolution, and showed that the KPC-15 appeared to be homogenous with KPC-4 closely. Steady-state kinetic parameters showed the catalytic efficiency of KPC-15 was higher than that of KPC-2 for all tested antibiotics in this study. The catalytic efficiency of KPC-15 caused resistance to β-lactam antibiotics was higher than that of KPC-2. Meanwhile, an evolutionary transformation changed KPC from an efficient carbapenemase to its variants (KPC-15) with better ceftazidimase catalytic efficiency, and the old antibiotics polymyxin B and colistin might play a role in the therapy for multi-resistant strains. Public Library of Science 2014-10-31 /pmc/articles/PMC4216079/ /pubmed/25360633 http://dx.doi.org/10.1371/journal.pone.0111491 Text en © 2014 Wang et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Wang, Dongguo Chen, Jiayu Yang, Linjun Mou, Yonghua Yang, Yijun Phenotypic and Enzymatic Comparative Analysis of the KPC Variants, KPC-2 and Its Recently Discovered Variant KPC-15 |
title | Phenotypic and Enzymatic Comparative Analysis of the KPC Variants, KPC-2 and Its Recently Discovered Variant KPC-15 |
title_full | Phenotypic and Enzymatic Comparative Analysis of the KPC Variants, KPC-2 and Its Recently Discovered Variant KPC-15 |
title_fullStr | Phenotypic and Enzymatic Comparative Analysis of the KPC Variants, KPC-2 and Its Recently Discovered Variant KPC-15 |
title_full_unstemmed | Phenotypic and Enzymatic Comparative Analysis of the KPC Variants, KPC-2 and Its Recently Discovered Variant KPC-15 |
title_short | Phenotypic and Enzymatic Comparative Analysis of the KPC Variants, KPC-2 and Its Recently Discovered Variant KPC-15 |
title_sort | phenotypic and enzymatic comparative analysis of the kpc variants, kpc-2 and its recently discovered variant kpc-15 |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4216079/ https://www.ncbi.nlm.nih.gov/pubmed/25360633 http://dx.doi.org/10.1371/journal.pone.0111491 |
work_keys_str_mv | AT wangdongguo phenotypicandenzymaticcomparativeanalysisofthekpcvariantskpc2anditsrecentlydiscoveredvariantkpc15 AT chenjiayu phenotypicandenzymaticcomparativeanalysisofthekpcvariantskpc2anditsrecentlydiscoveredvariantkpc15 AT yanglinjun phenotypicandenzymaticcomparativeanalysisofthekpcvariantskpc2anditsrecentlydiscoveredvariantkpc15 AT mouyonghua phenotypicandenzymaticcomparativeanalysisofthekpcvariantskpc2anditsrecentlydiscoveredvariantkpc15 AT yangyijun phenotypicandenzymaticcomparativeanalysisofthekpcvariantskpc2anditsrecentlydiscoveredvariantkpc15 |