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. Author manuscript; available in PMC: 2016 Jul 8.
Published in final edited form as: J Antibiot (Tokyo). 2015 Dec 16;69(6):415–421. doi: 10.1038/ja.2015.127

Table 1.

MICs for polymyxin B and closantel against the A. baumannii strains examined in this study.

Strain MDRa Polymyxin susceptibilityb MICs (mg/L)
Polymyxin B Closantel Closantel in the presence of 2 mg/L polymyxin Bc
ATCC 19606 No S 0.5 >128 NPd
FADDI-AB009e No S (HR) 0.5 >128 NP
2382 Yes S 0.5 >128 NP
2949e Yes S (HR) 1 >128 NP
FADDI-AB065 No R 128 0.5 0.5
FADDI-AB085 No R 32 0.5 0.5
2384 Yes R 8 >128 1
2949A Yes R 64 >128 2
a

Multidrug resistance (MDR) was defined as non-susceptible to ≥1 treating agent in ≥3 antimicrobial categories.12

b

CLSI breakpoints (S, susceptible; R, resistant): Polymyxin B, S ≤2 mg/L, R ≥4 mg/L; breakpoints are not available for closantel.

c

Closantel MICs in the presence of 2 mg/L of polymyxin B.

d

Not performed (NP) for polymyxin-susceptible isolates.

e

Polymyxin B heteroresistant (HR). Heteroresistance to polymyxin B was defined as the existence, in an isolate for which the polymyxin B MIC was ≤2 mg/L, of subpopulations able to grow in the presence of >2 mg/L polymyxin B.9