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Table 1.

DNA sequences of oligonucleotides used in polymerase chain reactions to detect carbapenemase and outer-membrane proteins of A. baumannii isolates.

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Table 2.

Minimum inhibitory concentration of antibiotics and resistance mechanisms of 20 A. baumannii isolates.

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Table 2 Expand

Table 3.

Determination of minimum inhibitory concentration by microdilution, resistance genes, and molecular profile of six A. baumannii isolates.

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Table 4.

Results of the three different methods (FICI, 2-well, and time-kill assay) used to evaluate in vitro synergism of antibiotic combinations against 20 A. baumannii isolates.

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Table 5.

In vitro synergistic effect, according to two different methods (FICI and 2-well) of antimicrobial combinations against 20 isolates of multi-drug resistant Acinetobacter baumannii.

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Fig 1.

Time-kill curve of isolates using drugs alone and in combination at 1 x MIC and 0.5 x MIC, respectively, against an A. baumannii isolate.

(A) Isolate 23 –Colistin (16 and 8 mg/L)/Vancomycin (64 and 32mg/L), (B) Isolate 28—Colistin (8 and 4 mg/L)/Rifampicin (4 and 2mg/L), (C) Isolate 1—Imipenem (256 and 128mg/L)/Tigecycline (1 and 0.5mg/L), (D) Isolate 5—Fosfomycin (128 and 64mg/L)/Amikacin (64 and 32mg/L).

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Table 6.

Clinical, demographic, and vancomycin time-kill synergism data of 18 patients colonized and infected by multidrug-resistant Acinetobacter baumannii.

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Table 6 Expand