blaCTX-M-1/9/1Hybrid Genes May Have Been Generated fromblaCTX-M-15on an IncI2 Plasmid
ABSTRACTThree hybrid CTX-M β-lactamases, CTX-M-64, CTX-M-123, and CTX-M-132, with N and C termini matching CTX-M-1 group enzymes and centers matching CTX-M-9 group enzymes, have been identified. The hybrid gene sequences suggested recombination betweenblaCTX-M-15andblaCTX-M-14, the two most commonblaCTX-Mvariants worldwide. However,blaCTX-M-64andblaCTX-M-123are found in an ISEcp1-blaCTX-Mtransposition unit with a 45-bp “spacer,” rather than the 48 bp usually associated withblaCTX-M-15, and 112 bp of IncA/C plasmid backbone. This is closer to the context ofblaCTX-M-55, which has one nucleotide difference fromblaCTX-M-15, on IncI2 plasmid pHN1122-1. Here, we characterized an IncI2 plasmid carryingblaCTX-M-15with a 45-bp spacer (pHNY2-1) by complete sequencing and also sequenced IncI2 plasmids carryingblaCTX-M-64(pHNAH46-1) orblaCTX-M-132(pHNLDH19) and an IncI1 plasmid carryingblaCTX-M-123(pHNAH4-1). pHNY2-1 has the same ISEcp1-blaCTX-M-IncA/C insertion as pHN1122-1, pHNAH46-1, and pHNLDH19, and all four plasmid backbones are almost identical. pHNAH4-1 (IncI1 sequence type 108 [ST108]) carries a transposition unit that includes a 2,720-bp fragment of the IncI2 backbone, suggesting ISEcp1-mediated transfer ofblaCTX-M-IncA/C-IncI2 to an IncI1 plasmid. All three hybridblaCTX-Mgenes may have resulted from recombination betweenblaCTX-M-14andblaCTX-M-15with a 45-bp spacer on an IncI2 plasmid. Five additionalEscherichia coliisolates of different sequence types from different provinces, farms, and/or animals hadblaCTX-M-64on a pHNAH46-1-like IncI2 plasmid and 9 hadblaCTX-M-123on a pHNAH4-1-like IncI1 ST108 plasmid. Thus, epidemic IncI plasmids may be responsible for the spread ofblaCTX-M-64andblaCTX-M-123between different animals and different locations in China.