<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>13</volume><submitter>Zhang N</submitter><funding>Beijing Nova Program</funding><funding>National Natural Science Foundation of China</funding><pubmed_abstract>&lt;i>Klebsiella michiganensis&lt;/i> is an increasingly important bacterial pathogen causing nosocomial infections in clinical patients. In this study, we described the molecular and genomic characteristics of a carbapenem-resistant &lt;i>K. michiganensis&lt;/i> strain KM166 cultured from a one-month premature baby's blood sample. KM166 showed lower biofilm forming ability in optical density (OD) than &lt;i>K. pneumoniae&lt;/i> NTUH-K2044 (0.271 ± 0.027 vs. 0.595 ± 0.054, &lt;i>p&lt;/i> = 0.001), and the median lethal dose (0.684 lg CFU/mL) was lower than &lt;i>K. pneumoniae&lt;/i> strain NTUH-K2044 (6.679 lg CFU/mL). A IncFII/IncFIA(HI1)/IncFIB(K) multiple replicon plasmid in KM166 was identified carrying three replicon types. It has low homology to &lt;i>Escherichia coli&lt;/i> pMRY09-581ECO_1 and the highest homology similarity to the INcFIA/INcFII(p14)-type plasmid in &lt;i>K. michiganensis&lt;/i> strain fxq plasmid pB_KPC, suggesting that this multiple replicon plasmid was unlikely to have been transmitted from &lt;i>E. coli&lt;/i> and probably a transfer of &lt;i>repFIB&lt;/i> replicon genes from other &lt;i>K. michiganensis&lt;/i> strains into the INcFIA/INcFII(p14)-type plasmid of KM166 had occurred. Mapping of the gene environment revealed that &lt;i>bla&lt;/i> &lt;sub>KPC-2&lt;/sub> in KM166 plasmid 3 had high identity and same Tn3-tnpR-IS481-&lt;i>bla&lt;/i> &lt;sub>KPC-2&lt;/sub>-klcA_1 genomic context structure with &lt;i>K. pneumoniae&lt;/i> strain JKP55, plasmid pKPC-J5501, and &lt;i>bla&lt;/i> &lt;sub>KPC-2&lt;/sub>-carrying plasmid proved to be autonomously transferred under the help of mobile genetic elements into &lt;i>Escherichia coli&lt;/i> 600 by plasmid conjugation experiment. In conclusion, we have characterized a &lt;i>K. michiganensis&lt;/i> strain carrying multi-replicon IncFII/IncFIA(HI1)/IncFIB(K) plasmid and &lt;i>bla&lt;/i> &lt;sub>KPC-2&lt;/sub>-carrying IncFII(p14)/IncFIA plasmid in this study, which provided insights about the evolutionary diversity of plasmids carried by &lt;i>K. michiganensis&lt;/i>.</pubmed_abstract><journal>Frontiers in microbiology</journal><pagination>1086296</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9845883</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>A clinical KPC-producing &lt;i>Klebsiella michiganensis&lt;/i> strain carrying IncFII/IncFIA (HI1)/IncFIB (K) multiple replicon plasmid.</pubmed_title><pmcid>PMC9845883</pmcid><pubmed_authors>Liu X</pubmed_authors><pubmed_authors>Yang X</pubmed_authors><pubmed_authors>Qi L</pubmed_authors><pubmed_authors>Liu J</pubmed_authors><pubmed_authors>Guo J</pubmed_authors><pubmed_authors>Chen J</pubmed_authors><pubmed_authors>Wang C</pubmed_authors><pubmed_authors>Jin M</pubmed_authors><pubmed_authors>Zhang N</pubmed_authors><pubmed_authors>Chen Y</pubmed_authors><pubmed_authors>Liu F</pubmed_authors><pubmed_authors>Qin S</pubmed_authors></additional><is_claimable>false</is_claimable><name>A clinical KPC-producing &lt;i>Klebsiella michiganensis&lt;/i> strain carrying IncFII/IncFIA (HI1)/IncFIB (K) multiple replicon plasmid.</name><description>&lt;i>Klebsiella michiganensis&lt;/i> is an increasingly important bacterial pathogen causing nosocomial infections in clinical patients. In this study, we described the molecular and genomic characteristics of a carbapenem-resistant &lt;i>K. michiganensis&lt;/i> strain KM166 cultured from a one-month premature baby's blood sample. KM166 showed lower biofilm forming ability in optical density (OD) than &lt;i>K. pneumoniae&lt;/i> NTUH-K2044 (0.271 ± 0.027 vs. 0.595 ± 0.054, &lt;i>p&lt;/i> = 0.001), and the median lethal dose (0.684 lg CFU/mL) was lower than &lt;i>K. pneumoniae&lt;/i> strain NTUH-K2044 (6.679 lg CFU/mL). A IncFII/IncFIA(HI1)/IncFIB(K) multiple replicon plasmid in KM166 was identified carrying three replicon types. It has low homology to &lt;i>Escherichia coli&lt;/i> pMRY09-581ECO_1 and the highest homology similarity to the INcFIA/INcFII(p14)-type plasmid in &lt;i>K. michiganensis&lt;/i> strain fxq plasmid pB_KPC, suggesting that this multiple replicon plasmid was unlikely to have been transmitted from &lt;i>E. coli&lt;/i> and probably a transfer of &lt;i>repFIB&lt;/i> replicon genes from other &lt;i>K. michiganensis&lt;/i> strains into the INcFIA/INcFII(p14)-type plasmid of KM166 had occurred. Mapping of the gene environment revealed that &lt;i>bla&lt;/i> &lt;sub>KPC-2&lt;/sub> in KM166 plasmid 3 had high identity and same Tn3-tnpR-IS481-&lt;i>bla&lt;/i> &lt;sub>KPC-2&lt;/sub>-klcA_1 genomic context structure with &lt;i>K. pneumoniae&lt;/i> strain JKP55, plasmid pKPC-J5501, and &lt;i>bla&lt;/i> &lt;sub>KPC-2&lt;/sub>-carrying plasmid proved to be autonomously transferred under the help of mobile genetic elements into &lt;i>Escherichia coli&lt;/i> 600 by plasmid conjugation experiment. In conclusion, we have characterized a &lt;i>K. michiganensis&lt;/i> strain carrying multi-replicon IncFII/IncFIA(HI1)/IncFIB(K) plasmid and &lt;i>bla&lt;/i> &lt;sub>KPC-2&lt;/sub>-carrying IncFII(p14)/IncFIA plasmid in this study, which provided insights about the evolutionary diversity of plasmids carried by &lt;i>K. michiganensis&lt;/i>.</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022</publication><modification>2026-05-09T03:10:55.384Z</modification><creation>2025-02-19T02:38:41.799Z</creation></dates><accession>S-EPMC9845883</accession><cross_references><pubmed>36687642</pubmed><doi>10.3389/fmicb.2022.1086296</doi></cross_references></HashMap>