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. 2016 May 12;6:26077. doi: 10.1038/srep26077

Table 1. Distribution of MIC values of SET-M33L in the collection of clinical bacterial isolates, including distribution with respect to resistance phenotypes.

Species and resistance phenotypes (no. isolates)a,b MIC
[μM] 0.18 0.35 0.7 1.4 2.8 5.6 11.2 >11.2
[μg/mL] 1 2 4 8 16 32 64 >64
Pseudomonas aeruginosa (76)   0 1 8 64 2 0 1 0
MDR (32)   0 0 2 29 1 0 0 0
 MDR, MBL (11)   0 0 0 11 0 0 0 0
non-MDR (44)   0 1 6 35 1 0 1 0
Klebsiella pneumoniae (73)   0 0 22 33 11 3 3 1
MDR (31)   0 0 12 10 5 1 2 1
 MDR, CP, CR (6)   0 0 0 0 2 1 2 1
 MDR, CP (10)   0 0 6 2 2 0 0 0
 MDR, ESBL, CR (1)   0 0 0 0 1 0 0 0
 MDR, ESBL (12)   0 0 4 8 0 0 0 0
non-MDR (42)   0 0 10 23 6 2 1 0
 Non-MDR, ESBL (2)   0 0 0 2 0 0 0 0
  MIC50 [μM] [μg/mL]   MIC90 [μM] [μg/mL]    
Pseudomonas aeruginosa (no. 76)   1.4 8     1.4 8    
Klebsiella pneumoniae (no. 73)   1.4 8     2.8 16    

aStrains were identified according to the presence of relevant resistance phenotypes and genotypes as follows: MDR, multidrug resistant (according to the definition of Magiorakos et al.39); CP, carbapenemase-producing; CR, colistin-resistant; ESBL, extended spectrum β-lactamase-producing; MBL, metallo-β-lactamase-producing.

bBacterial strains belonging to the successful epidemic P. aeruginosa Sequence Type 621, producing the IMP-13 MBL, and K. pneumoniae Sequence Type 512, producing a KPC-type carbapenemase, were included.