A total of 18 Enterobacteriaceae (17 from gulls and 1 from a clinical sample) collected from Australia, carrying IncA/C plasmids with the IMP-encoding In809-like integrons, were studied. Seven plasmids, being representatives of different origins, plasmid sizes, replicon combinations, and resistance genes, were completely sequenced. Plasmid pEc158, identified in a clinical Escherichia coli ST752 isolate, showed extensive similarity to type 2 IncA/C 2 plasmids. pEc158 carried none of the bla CMY-2 -like region or ARI-B and ARI-A regions, while it contained a hybrid transposon structure. The six remaining plasmids, which were of wildlife origin, were highly similar to each other and probably were fusion derivatives of type 1 and type 2 A/C 2 plasmids. The latter plasmids contained an ARI-B region and hybrid transposon structures. In all plasmids, hybrid transposon structures containing In809-like integrons were inserted 3,434 bp downstream of the rhs2 start codon. In all cases, the one outermost 38-bp inverted repeat (IR) of the transposon was associated with the Tn1696 tnp module, while the other outermost 38-bp IR of the transposon was associated with either a Tn6317-like module or a Tn21 mer module. However, the internal structure of the transposon and the resistance genes were different in each plasmid. These findings indicated that, for the specific periods of time and settings, different IncA/C 2 plasmid types carrying In809-like elements circulated among isolates of wildlife and clinical origins. Additionally, they provided the basis for speculations regarding the reshuffling of IncA/C 2 plasmids with In809-like integrons and confirmed the rapid evolution of IncA/C 2 plasmid lineages.KEYWORDS IMP, metallo--lactamases, PMLST, Klebsiella pneumoniae, Escherichia coli, Citrobacter freundii P lasmids of the IncA/C group are big molecules with a broad host range. These plasmids are commonly identified among agricultural and clinical bacterial isolates in the United States, Europe, and elsewhere. Among resistance genes, the IncA/C plasmids have often been found to disseminate bla CMY-2 -like cephalosporinase genes (1). However, recent reports describing the epidemic emergence of bla NDM metallo--lactamase (ML) genes in Enterobacteriaceae, associated with IncA/C 2 plasmids (2), revived interest in this plasmid group. Additionally, other studies have reported the emergence of IncA/C 2 plasmids carrying the bla IMP and bla VIM ML genes from clinical