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Emergence of OXA-484-Producing Klebsiella variicola in China

PURPOSE: The frequent and inappropriate use of antibiotics has caused a dramatic rise in the number, species, and degree of multi-drug resistant bacteria, making them more prevalent and difficult to treat. In this context, the aim of the present study was to characterize the OXA-484-producing strain...

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Autores principales: Ge, Haoyu, Qiao, Jie, Xu, Hao, Liu, Ruishan, Zhao, Junhui, Chen, Ruyan, Li, Chenyu, Chen, Mantao, Guo, Xiaobing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10065429/
https://www.ncbi.nlm.nih.gov/pubmed/37008750
http://dx.doi.org/10.2147/IDR.S404551
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author Ge, Haoyu
Qiao, Jie
Xu, Hao
Liu, Ruishan
Zhao, Junhui
Chen, Ruyan
Li, Chenyu
Chen, Mantao
Guo, Xiaobing
author_facet Ge, Haoyu
Qiao, Jie
Xu, Hao
Liu, Ruishan
Zhao, Junhui
Chen, Ruyan
Li, Chenyu
Chen, Mantao
Guo, Xiaobing
author_sort Ge, Haoyu
collection PubMed
description PURPOSE: The frequent and inappropriate use of antibiotics has caused a dramatic rise in the number, species, and degree of multi-drug resistant bacteria, making them more prevalent and difficult to treat. In this context, the aim of the present study was to characterize the OXA-484-producing strains isolated from a perianal swab of a patient by using whole-genome analysis. PATIENTS AND METHODS: In this study, carbapenemase-producing Klebsiella variicola was identified by matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF MS), average nucleotide identity (ANI) and PCR. S1 nuclease pulsed-field gel electrophoresis (S1-PFGE) and Southern blotting were utilized to characterize the plasmid profiles of K. variicola 4717. In particular, WGS was performed to obtain genomic information on this clinical isolate, and assemble all the plasmids of the bla(OXA-484)-harboring strain. RESULTS: The antimicrobial susceptibility pattern of K. variicola 4717 revealed that it was resistant to a range of antibiotics, including aztreonam, imipenem, meropenem, ceftriaxone, cefotaxime, ceftazidime, levofloxacin, ciprofloxacin, piperacillin-tazobactam, methylene-sulfamer oxazole, amoxicillin-clavulanic acid, cefepime, and tigecycline. Its susceptibility to chloromycin was intermediate, while it was still susceptible to amikacin, gentamicin, fosfomycin, and polymyxin B. The presence of two companion plasmids, p4717_1 and p4717_2, together with a plasmid carrying the bla(OXA-484) gene was observed. An in-depth investigation of p4717-OXA-484 uncovered that it is an IncX3-type plasmid and shares a similar segment encoded by IS26. Given the similar genetic background, it was conceivable that bla(OXA-484) could have developed from bla(OXA-181) through a series of mutations. CONCLUSION: Herein, we described the first genome sequence of K. variicola strain harbouring the class D β-actamase bla(OXA-484) in an Inc-X3-type plasmid. Our work also uncovered the genetic characterization of K. variicola 4717 and the importance of initiating antimicrobial detection promptly.
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spelling pubmed-100654292023-04-01 Emergence of OXA-484-Producing Klebsiella variicola in China Ge, Haoyu Qiao, Jie Xu, Hao Liu, Ruishan Zhao, Junhui Chen, Ruyan Li, Chenyu Chen, Mantao Guo, Xiaobing Infect Drug Resist Original Research PURPOSE: The frequent and inappropriate use of antibiotics has caused a dramatic rise in the number, species, and degree of multi-drug resistant bacteria, making them more prevalent and difficult to treat. In this context, the aim of the present study was to characterize the OXA-484-producing strains isolated from a perianal swab of a patient by using whole-genome analysis. PATIENTS AND METHODS: In this study, carbapenemase-producing Klebsiella variicola was identified by matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF MS), average nucleotide identity (ANI) and PCR. S1 nuclease pulsed-field gel electrophoresis (S1-PFGE) and Southern blotting were utilized to characterize the plasmid profiles of K. variicola 4717. In particular, WGS was performed to obtain genomic information on this clinical isolate, and assemble all the plasmids of the bla(OXA-484)-harboring strain. RESULTS: The antimicrobial susceptibility pattern of K. variicola 4717 revealed that it was resistant to a range of antibiotics, including aztreonam, imipenem, meropenem, ceftriaxone, cefotaxime, ceftazidime, levofloxacin, ciprofloxacin, piperacillin-tazobactam, methylene-sulfamer oxazole, amoxicillin-clavulanic acid, cefepime, and tigecycline. Its susceptibility to chloromycin was intermediate, while it was still susceptible to amikacin, gentamicin, fosfomycin, and polymyxin B. The presence of two companion plasmids, p4717_1 and p4717_2, together with a plasmid carrying the bla(OXA-484) gene was observed. An in-depth investigation of p4717-OXA-484 uncovered that it is an IncX3-type plasmid and shares a similar segment encoded by IS26. Given the similar genetic background, it was conceivable that bla(OXA-484) could have developed from bla(OXA-181) through a series of mutations. CONCLUSION: Herein, we described the first genome sequence of K. variicola strain harbouring the class D β-actamase bla(OXA-484) in an Inc-X3-type plasmid. Our work also uncovered the genetic characterization of K. variicola 4717 and the importance of initiating antimicrobial detection promptly. Dove 2023-03-27 /pmc/articles/PMC10065429/ /pubmed/37008750 http://dx.doi.org/10.2147/IDR.S404551 Text en © 2023 Ge 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
Ge, Haoyu
Qiao, Jie
Xu, Hao
Liu, Ruishan
Zhao, Junhui
Chen, Ruyan
Li, Chenyu
Chen, Mantao
Guo, Xiaobing
Emergence of OXA-484-Producing Klebsiella variicola in China
title Emergence of OXA-484-Producing Klebsiella variicola in China
title_full Emergence of OXA-484-Producing Klebsiella variicola in China
title_fullStr Emergence of OXA-484-Producing Klebsiella variicola in China
title_full_unstemmed Emergence of OXA-484-Producing Klebsiella variicola in China
title_short Emergence of OXA-484-Producing Klebsiella variicola in China
title_sort emergence of oxa-484-producing klebsiella variicola in china
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10065429/
https://www.ncbi.nlm.nih.gov/pubmed/37008750
http://dx.doi.org/10.2147/IDR.S404551
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