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Fusion plasmid enhanced the endemic extensively drug resistant Klebsiella pneumoniae clone ST147 harbored bla(OXA-48) to acquire the hypervirulence and cause fatal infection

BACKGROUND: Klebsiella Pneumoniae (Kp) sequence type (ST) 147 has emerged globally and spread rapidly, particularly the extensively drug resistant (XDR) isolates. However, the infections caused by this subtype is rare reported in China for now. The clinical, microbiological and genomic characteristi...

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Autores principales: Liu, Chao, Du, Pengcheng, Yang, Ping, Lu, Ming, Shen, Ning
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9927049/
https://www.ncbi.nlm.nih.gov/pubmed/36788555
http://dx.doi.org/10.1186/s12941-022-00551-1
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author Liu, Chao
Du, Pengcheng
Yang, Ping
Lu, Ming
Shen, Ning
author_facet Liu, Chao
Du, Pengcheng
Yang, Ping
Lu, Ming
Shen, Ning
author_sort Liu, Chao
collection PubMed
description BACKGROUND: Klebsiella Pneumoniae (Kp) sequence type (ST) 147 has emerged globally and spread rapidly, particularly the extensively drug resistant (XDR) isolates. However, the infections caused by this subtype is rare reported in China for now. The clinical, microbiological and genomic characteristics are unclear. METHODS: A systemic retrospective study was conducted in a Chinese tertiary hospital. Clinical information of the infection cases was collected, and whole-genome sequencing and phenotypic experiments were performed on the ST147 isolates. The resistance and virulence genes were identified, and the plasmids harboring these genes were further studied. RESULTS: Six ST147 isolates from six patients among 720 available clincial Kp isolates were detected. Notably, two isolates, PEKP4035 and PEKP4265, represented both XDR and hypervirulence by acquiring bla(OXA-48), bla(CTX-M-15) and key virulence genes, iucA + rmpA2, representing no fitness cost and resulting fatal infection. Four of the six ST147 isolates presented with more nucleotide differences, whereas the PEKP4035 and PEKP4265 both isolated from the intensive care unit possessed 20 single nucleotide polymorphisms among one year, indicating the prolonged survive and transmission. Interestingly, the two isolates harbored the same fused plasmid composed of sul2 and iucA + rmpA2, which might be generated by recombination of a plasmid like KpvST101_OXA-48 with the pLVPK plasmid via IS26. Besides, two ~ 70 kb plasmids conferring multiple-drug resistance were also identified among the two isolates, which presented resistance genes including bla(OXA-48), bla(CTX-M-16), strA and strB. Interestingly, we reported that bla(CTX-M-15), a common resistance gene within ST147, has successfully transferred into the chromosome by ISEcp1. CONCLUSIONS: XDR hypervirulent ST147 Kp is emerging, suggesting enhanced surveillance is essential. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12941-022-00551-1.
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spelling pubmed-99270492023-02-15 Fusion plasmid enhanced the endemic extensively drug resistant Klebsiella pneumoniae clone ST147 harbored bla(OXA-48) to acquire the hypervirulence and cause fatal infection Liu, Chao Du, Pengcheng Yang, Ping Lu, Ming Shen, Ning Ann Clin Microbiol Antimicrob Research BACKGROUND: Klebsiella Pneumoniae (Kp) sequence type (ST) 147 has emerged globally and spread rapidly, particularly the extensively drug resistant (XDR) isolates. However, the infections caused by this subtype is rare reported in China for now. The clinical, microbiological and genomic characteristics are unclear. METHODS: A systemic retrospective study was conducted in a Chinese tertiary hospital. Clinical information of the infection cases was collected, and whole-genome sequencing and phenotypic experiments were performed on the ST147 isolates. The resistance and virulence genes were identified, and the plasmids harboring these genes were further studied. RESULTS: Six ST147 isolates from six patients among 720 available clincial Kp isolates were detected. Notably, two isolates, PEKP4035 and PEKP4265, represented both XDR and hypervirulence by acquiring bla(OXA-48), bla(CTX-M-15) and key virulence genes, iucA + rmpA2, representing no fitness cost and resulting fatal infection. Four of the six ST147 isolates presented with more nucleotide differences, whereas the PEKP4035 and PEKP4265 both isolated from the intensive care unit possessed 20 single nucleotide polymorphisms among one year, indicating the prolonged survive and transmission. Interestingly, the two isolates harbored the same fused plasmid composed of sul2 and iucA + rmpA2, which might be generated by recombination of a plasmid like KpvST101_OXA-48 with the pLVPK plasmid via IS26. Besides, two ~ 70 kb plasmids conferring multiple-drug resistance were also identified among the two isolates, which presented resistance genes including bla(OXA-48), bla(CTX-M-16), strA and strB. Interestingly, we reported that bla(CTX-M-15), a common resistance gene within ST147, has successfully transferred into the chromosome by ISEcp1. CONCLUSIONS: XDR hypervirulent ST147 Kp is emerging, suggesting enhanced surveillance is essential. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12941-022-00551-1. BioMed Central 2023-02-14 /pmc/articles/PMC9927049/ /pubmed/36788555 http://dx.doi.org/10.1186/s12941-022-00551-1 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Liu, Chao
Du, Pengcheng
Yang, Ping
Lu, Ming
Shen, Ning
Fusion plasmid enhanced the endemic extensively drug resistant Klebsiella pneumoniae clone ST147 harbored bla(OXA-48) to acquire the hypervirulence and cause fatal infection
title Fusion plasmid enhanced the endemic extensively drug resistant Klebsiella pneumoniae clone ST147 harbored bla(OXA-48) to acquire the hypervirulence and cause fatal infection
title_full Fusion plasmid enhanced the endemic extensively drug resistant Klebsiella pneumoniae clone ST147 harbored bla(OXA-48) to acquire the hypervirulence and cause fatal infection
title_fullStr Fusion plasmid enhanced the endemic extensively drug resistant Klebsiella pneumoniae clone ST147 harbored bla(OXA-48) to acquire the hypervirulence and cause fatal infection
title_full_unstemmed Fusion plasmid enhanced the endemic extensively drug resistant Klebsiella pneumoniae clone ST147 harbored bla(OXA-48) to acquire the hypervirulence and cause fatal infection
title_short Fusion plasmid enhanced the endemic extensively drug resistant Klebsiella pneumoniae clone ST147 harbored bla(OXA-48) to acquire the hypervirulence and cause fatal infection
title_sort fusion plasmid enhanced the endemic extensively drug resistant klebsiella pneumoniae clone st147 harbored bla(oxa-48) to acquire the hypervirulence and cause fatal infection
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9927049/
https://www.ncbi.nlm.nih.gov/pubmed/36788555
http://dx.doi.org/10.1186/s12941-022-00551-1
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