In this study, highly carbapenem-resistantPseudomonas aeruginosa(h-CRPA) 18102011 (the MIC value of IP for h-CRPA is 4,096 μg/mL) was isolated from the bile of an intensive care unit (ICU) burn patient in China. The genome’s molecular characteristics were analyzed to assess the genetic environment ofblaKPC-2andblaVIM-2. ANI comparisons were used for precise species-level identification, while serotyping, multi-locus sequence typing, and the identification of acquired resistance genes, and virulence genes were also carried out. The h-CRPA 18102011 strain carryingblaKPC-2andblaVIM-2was identified as strain ST2374 and the O4 serotype. Virulence genes (plcH,exoST) and resistance genes (aph(3’)-IIb,aac(6’)-Ib-cr,ant(2’’)-Ia,blaOXA-396,blaPAO,blaKPC-2,blaVIM-2,blaPER-1,sul1,catB7,qnrVC6,fosA) were both identified in the genome. In addition, the IncpRBL16type mega-plasmid pP2011-1 carryingblaVIM-2and the IncP6 type plasmid pP2011-2 carryingblaKPC-2were identified in the strain. The genetic environment ofblaVIM-2andblaKPC-2was specifically evaluated to assess their origins.blaVIM-2was located in the region of In2075 that was inserted into plasmid pP2011-1, this plasmid contained 3 novel recombination sites, as well as the typical recombination site 2 (umuC) observed for IncpRBL16type plasmids. However, the core module Tn3-ISKpn27-blaKPC-ΔISKpn6was identified as theblaKPC-2platform in plasmid pP2011-2. Conjugation experiments revealed that the plasmids pP2011-1 and pP2011-2 of the h-CRPA 18102011 strain could be transferred into Escherichia coli with a conjugation transfer efficiency of 10-6.