Table 2.
Correlations between MIC values, dye staining, and light scattering signals for the ampicillin-treated E. coli strain.
| A | ||||
|---|---|---|---|---|
| AUC | 1 × MIC R2 | |||
| AFH | 0.83 | |||
| TO-PRO®-3 | 0.75 | |||
| Area FSC/SSC | 0.65 | |||
| FSC | 0.18 | |||
| B | ||||
| Time (h) | AFH R2 | TO-PRO®-3 R2 | FSC/SSC area R2 | FSC R2 |
| 1 | 0.75 | 0.66 | 0.51 | 0.39 |
| 2 | 0.85 | 0.72 | 0.66 | 0.25 |
| 3 | 0.85 | 0.81 | 0.68 | 0.25 |
| 4 | 0.8 | 0.76 | 0.54 | 0.25 |
To check if the MICs obtained using the standard microdilution assay corresponds to a threshold values impacting the FC measurements, each experiment was described by 2 variables: X[MIC] and Y[FC]. X[MIC] = 1 if the concentration of ampicillin used in the experiment ([Amp]) was ≥ 1 × MIC and X[MIC] = −1 if [Amp] was < 1 × MIC. Y[FC] corresponds to the FC data collected for each parameter for each experiment. (A) Y[FC] corresponds to the areas under the curves (AUCs) of the FC results relative to the time of incubation. (B) Y[FC] corresponds to the FC values obtained at each hour of incubation. The correlation coefficients (R2) between X[MIC] and Y[FC] for each measured parameter (% of cells stained with AFH or TO-PRO®-3, ratios of FSC and the ratios FSC/SSC areas) were calculated for all experiments. Two-tailed P < 0.0001.