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. 2017 Jul 25;6:e25100. doi: 10.7554/eLife.25100

Figure 5. Chromosomal neighborhood influences the fitness cost of amplifications.

(A) Chromosomal location of reporter cassette in strains BΔIS5I and E (IS distances not drawn to scale). (B) Example fluorescence trajectories. Left: low-cost amplifications expand in correlation with the increase in tetracycline concentration over 10 days. Middle: Cost-limited amplifications fail to expand at higher tetracycline concentrations resulting in extinction. Right: Amplifications can escape extinction in combination with other mutations increasing tetA-yfp expression, resulting in higher final YFP/CFP. RFU = relative fluorescence units (see Materials and methods), r.c. = relative concentration as multiples of MIC. (C) Final YFP/CFP ratios of rescued amplifications in strains expected to have a higher (strain BΔIS5I) or lower (strain E) cost of amplifications compared to strain B. n = initial number of replicate populations used for analysis. Crosses = populations rescued by amplifications without additional mutations. Other symbols = secondary mutations (see legend). p-values: permutation tests in comparison with strain B. (D) Final YFP/CFP ratios of rescued amplifications in strains A-D. n = 285 includes replicate evolution experiments to increase statistical power. Symbols and p-values as in (C).

DOI: http://dx.doi.org/10.7554/eLife.25100.023

Figure 5—source data 1. Source data for Figure 5C and D.
Mutations identified in combination with amplifications and respective final YFP/CFP ratios (points indicated by symbols other than crosses in Figure 5CD).
DOI: 10.7554/eLife.25100.024

Figure 5.

Figure 5—figure supplement 1. Rescued populations of strains BΔIS5I and E by mutation type.

Figure 5—figure supplement 1.

Number of rescued populations out of 95 replicates, shown by mutation type. Colored dots = later mutations occurring on top of earlier mutations.