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. 2020 Apr 9;9(4):273. doi: 10.3390/pathogens9040273

Table 1.

Features of CMY-2-producing E. coli recovered from non-clinical origins in Portugal.

Origin (Sample) a Year of Collection PhG b ST/CC/PFGE-Type c Genetic Environment of blaCMY-2 Plasmid Replicon Content [Inc Family (Size in kb)] Resistance to Non-β-Lactams f
Associated
with blaCMY-2
Other
HH (33) 2014 B22 ST4953/EC2 ΔISEcp1-blaCMY-2-blc-sugE ND d FII + I1 GEN, NET, TOB, STR, TET, CHL, NAL, CIP, SUL
HH (34) 2014 B22 ST4953/EC2 ΔISEcp1-blaCMY-2-blc-sugE ND d FII GEN, NET, TOB, STR, TET, CHL, NAL, CIP, SUL
HH (97) 2014 A0 ST665/EC3 ISEcp1-blaCMY-2-blc-sugE NT e (75) K + B/O STR, TET, NAL, SUL
UCC (6) 2003 A1 ST48/CC10/EC4 ISEcp1-blaCMY-2-blc-sugE A/C2 (150) - KAN, GEN, TOB, STR, TET, CHL, SUL

a HH, healthy humans; UCC, uncooked chicken carcass; b PhG, E. coli phylogenetic group; c ST, Sequence Type, CC, clonal complex; d ND, not determined due to multiple plug degradations; e NT, non-typeable; f CIP, ciprofloxacin; CHL, chloramphenicol; GEN, gentamicin; KAN, kanamycin; NAL, nalidixic acid; NET, netilmicin; STR, streptomycin; SUL, sulphonamides; TET, tetracycline; TOB, tobramycin.