microbial pathogens to pharmacotherapies. Nevertheless, little is known about cell
individuality in antibiotic accumulation. Here, we hypothesise that phenotypic diversification
can be driven by fundamental cell-to-cell differences in drug transport rates. To test this
hypothesis, we employed microfluidics-based single-cell microscopy, libraries of fluorescent
antibiotic probes and mathematical modelling. This approach allowed us to rapidly identify …