Mutation supply and the repeatability of selection for antibiotic resistance

• Published in: Physical biology 2017-08, Vol.14 (5), p.055005-055005
• Main Authors: van Dijk, Thomas, Hwang, Sungmin, Krug, Joachim, de Visser, J Arjan G M, Zwart, Mark P
• Format: Article
• Language: English
• Subjects: Anti-Bacterial Agents - pharmacology; antibiotic resistance; bacteria; beta-Lactamases - genetics; beta-Lactamases - metabolism; Dose-Response Relationship, Drug; Drug Resistance, Microbial; Escherichia coli - drug effects; Escherichia coli - genetics; Escherichia coli - metabolism; Escherichia coli Proteins - genetics; Escherichia coli Proteins - metabolism; Evolution; Mutation Rate; predictability and repeatability of evolution; Selection, Genetic; TEM-1 Beta-lactamase
• ISSN: 1478-3975; 1478-3967; 1478-3975
• DOI: 10.1088/1478-3975/aa7f36

Whether evolution can be predicted is a key question in evolutionary biology. Here we set out to better understand the repeatability of evolution, which is a necessary condition for predictability. We explored experimentally the effect of mutation supply and the strength of selective pressure on the repeatability of selection from standing genetic variation. Different sizes of mutant libraries of antibiotic resistance gene TEM-1 β-lactamase in Escherichia coli, generated by error-prone PCR, were subjected to different antibiotic concentrations. We determined whether populations went extinct or survived, and sequenced the TEM gene of the surviving populations. The distribution of mutations per allele in our mutant libraries followed a Poisson distribution. Extinction patterns could be explained by a simple stochastic model that assumed the sampling of beneficial mutations was key for survival. In most surviving populations, alleles containing at least one known large-effect beneficial mutation were present. These genotype data also support a model which only invokes sampling effects to describe the occurrence of alleles containing large-effect driver mutations. Hence, evolution is largely predictable given cursory knowledge of mutational fitness effects, the mutation rate and population size. There were no clear trends in the repeatability of selected mutants when we considered all mutations present. However, when only known large-effect mutations were considered, the outcome of selection is less repeatable for large libraries, in contrast to expectations. We show experimentally that alleles carrying multiple mutations selected from large libraries confer higher resistance levels relative to alleles with only a known large-effect mutation, suggesting that the scarcity of high-resistance alleles carrying multiple mutations may contribute to the decrease in repeatability at large library sizes.