<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Chen H</submitter><funding>Research Project of Jinan Microecological Biomedicine Shandong Laboratory</funding><funding>Shandong Provincial Laboratory Project</funding><funding>the Fundamental Research Funds for the Central Universities</funding><pagination>24</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10918965</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>23(1)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Klebsiella variicola is considered a newly emerging human pathogen. Clinical isolates of carbapenemase and broad-spectrum β-lactamase-producing K. variicola remain relatively uncommon. A strain of K. variicola 4253 was isolated from a clinical sample, and was identified to carry the bla&lt;sub>IMP-4&lt;/sub> and bla&lt;sub>SFO-1&lt;/sub> genes. This study aims to discern its antibiotic resistance phenotype and genomic characteristics.&lt;h4>Methods&lt;/h4>Species identification was conducted using MALDI-TOF/MS. PCR identification confirmed the presence of the bla&lt;sub>IMP-4&lt;/sub> and bla&lt;sub>SFO-1&lt;/sub> genes. Antibiotic resistance phenotype and genomic characteristics were detected by antimicrobial susceptibility testing and whole-genome sequencing. Plasmid characterization was carried out through S1-PFGE, conjugation experiments, Southern blot, and comparative genomic analysis.&lt;h4>Results&lt;/h4>K. variicola 4253 belonged to ST347, and demonstrated resistance to broad-spectrum β-lactamase drugs and tigecycline while being insensitive to imipenem and meropenem. The bla&lt;sub>IMP-4&lt;/sub> and bla&lt;sub>SFO-1&lt;/sub> genes harbored on the plasmid p4253-imp. The replicon type of p4253-imp was identified as IncHI5B, representing a multidrug-resistant plasmid capable of horizontal transfer and mediating the dissemination of drug resistance. The bla&lt;sub>IMP-4&lt;/sub> gene was located on the In809-like integrative element (Intl1-bla&lt;sub>IMP-4&lt;/sub>-aacA4-catB3), which circulates in Acinetobacter and Enterobacteriaceae.&lt;h4>Conclusions&lt;/h4>This study reports the presence of a strain of K. variicola, which is insensitive to tigecycline, carrying a plasmid harboring bla&lt;sub>IMP-4&lt;/sub> and bla&lt;sub>SFO-1&lt;/sub>. It is highly likely that the strain acquired this plasmid through horizontal transfer. The bla&lt;sub>IMP-4&lt;/sub> array (Intl1-bla&lt;sub>IMP-4&lt;/sub>-aacA4-catB3) is also mobile in Acinetobacter and Enterobacteriaceae. So it is essential to enhance clinical awareness and conduct epidemiological surveillance on multidrug-resistant K. variicola, conjugative plasmids carrying bla&lt;sub>IMP-4&lt;/sub>, and the In809 integrative element.</pubmed_abstract><journal>Annals of clinical microbiology and antimicrobials</journal><pubmed_title>Coexistence of bla&lt;sub>IMP-4&lt;/sub> and bla&lt;sub>SFO-1&lt;/sub> in an IncHI5B plasmid harbored by tigecycline-non-susceptible Klebsiella variicola strain.</pubmed_title><pmcid>PMC10918965</pmcid><funding_grant_id>SYS202202</funding_grant_id><funding_grant_id>2022ZFJH003</funding_grant_id><funding_grant_id>JNL-2022001A</funding_grant_id><pubmed_authors>Shen J</pubmed_authors><pubmed_authors>Zheng B</pubmed_authors><pubmed_authors>Liu R</pubmed_authors><pubmed_authors>Chen H</pubmed_authors><pubmed_authors>Xu H</pubmed_authors><pubmed_authors>Li L</pubmed_authors></additional><is_claimable>false</is_claimable><name>Coexistence of bla&lt;sub>IMP-4&lt;/sub> and bla&lt;sub>SFO-1&lt;/sub> in an IncHI5B plasmid harbored by tigecycline-non-susceptible Klebsiella variicola strain.</name><description>&lt;h4>Background&lt;/h4>Klebsiella variicola is considered a newly emerging human pathogen. Clinical isolates of carbapenemase and broad-spectrum β-lactamase-producing K. variicola remain relatively uncommon. A strain of K. variicola 4253 was isolated from a clinical sample, and was identified to carry the bla&lt;sub>IMP-4&lt;/sub> and bla&lt;sub>SFO-1&lt;/sub> genes. This study aims to discern its antibiotic resistance phenotype and genomic characteristics.&lt;h4>Methods&lt;/h4>Species identification was conducted using MALDI-TOF/MS. PCR identification confirmed the presence of the bla&lt;sub>IMP-4&lt;/sub> and bla&lt;sub>SFO-1&lt;/sub> genes. Antibiotic resistance phenotype and genomic characteristics were detected by antimicrobial susceptibility testing and whole-genome sequencing. Plasmid characterization was carried out through S1-PFGE, conjugation experiments, Southern blot, and comparative genomic analysis.&lt;h4>Results&lt;/h4>K. variicola 4253 belonged to ST347, and demonstrated resistance to broad-spectrum β-lactamase drugs and tigecycline while being insensitive to imipenem and meropenem. The bla&lt;sub>IMP-4&lt;/sub> and bla&lt;sub>SFO-1&lt;/sub> genes harbored on the plasmid p4253-imp. The replicon type of p4253-imp was identified as IncHI5B, representing a multidrug-resistant plasmid capable of horizontal transfer and mediating the dissemination of drug resistance. The bla&lt;sub>IMP-4&lt;/sub> gene was located on the In809-like integrative element (Intl1-bla&lt;sub>IMP-4&lt;/sub>-aacA4-catB3), which circulates in Acinetobacter and Enterobacteriaceae.&lt;h4>Conclusions&lt;/h4>This study reports the presence of a strain of K. variicola, which is insensitive to tigecycline, carrying a plasmid harboring bla&lt;sub>IMP-4&lt;/sub> and bla&lt;sub>SFO-1&lt;/sub>. It is highly likely that the strain acquired this plasmid through horizontal transfer. The bla&lt;sub>IMP-4&lt;/sub> array (Intl1-bla&lt;sub>IMP-4&lt;/sub>-aacA4-catB3) is also mobile in Acinetobacter and Enterobacteriaceae. So it is essential to enhance clinical awareness and conduct epidemiological surveillance on multidrug-resistant K. variicola, conjugative plasmids carrying bla&lt;sub>IMP-4&lt;/sub>, and the In809 integrative element.</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Mar</publication><modification>2026-06-22T03:11:34.634Z</modification><creation>2025-04-04T12:35:26.785Z</creation></dates><accession>S-EPMC10918965</accession><cross_references><pubmed>38448920</pubmed><doi>10.1186/s12941-024-00680-9</doi></cross_references></HashMap>