TABLE 1.
Isolate type | No. of isolates | CBDE colistin MIC (μg/ml) without EDTA (no.) | CBDE with 1 mM EDTA |
|
---|---|---|---|---|
No. (%) of isolates with a reduction of colistin MIC | MIC (μg/ml) doubling dilution reduction (no.) | |||
mcr-producing isolatesc | 12 | 2 (2) | 2 (100) | ≥1 |
4 (7) | 7 (100) | ≥2 | ||
>4 (3) | 3 (100) | ≥2 (2) | ||
≥3 (1) | ||||
CREd | 73 | ≤1 (55) | NA | NAe |
2 (2) | 3 (16.7) | ≥1 (1)a | ||
4 (1) | ≥2 (1)b | |||
>4 (15) | ≥3 (1)b |
One E. cloacae isolate tested as 2 μg/ml by the CBDE method and as ≤1 μg/ml by the EDTA-CBDE method, resulting in a ≥1 doubling dilution difference.
Two K. pneumoniae isolates tested as >4 μg/ml and 4 μg/ml by the CBDE method and as ≤1 μg/ml by the EDTA-CBDE method, resulting in ≥2 and ≥3 doubling dilution differences, respectively.
The 12 MCR-producing isolates included 7 Escherichia coli isolates (6 mcr-1 and 1 mcr-2), 2 Salmonella enterica serovar Typhimurium isolates (mcr-3 and mcr-4), 1 Salmonella enterica serovar Enteritidis isolate (mcr-1), and 1 Salmonella enterica serovar Oslo isolate (mcr-3) (see Table S1 in the supplemental material).
The clinical carbapenem-resistant Enterobacteriales (CRE) included 39 Klebsiella pneumoniae isolates, 16 Enterobacter cloacae complex isolates, 8 E. coli isolates, 4 Citrobacter freundii isolates, 3 Serratia marcescens isolates, 1 Klebsiella (formerly Enterobacter) aerogenes isolate, 1 Klebsiella oxytoca isolate, and 1 Proteus mirabilis isolate. The CRE were previously characterized for carbapenemase production and included 35 carbapenemase-producing CRE (29 KPC, 3 NDM, 2 KPC and NDM, and 1 NDM and OXA-48) (see Table S1).
NA, not applicable.