Department of Molecular Genetics and Microbiology, Duke University, NC, Durham, USA.
Department of Biomedical Engineering, Duke University, NC, Durham, USA.
Mol Syst Biol. 2023 Feb 10;19(2):e11300. doi: 10.15252/msb.202211300. Epub 2022 Dec 27.
Plasmid fitness is directed by two orthogonal processes-vertical transfer through cell division and horizontal transfer through conjugation. When considered individually, improvements in either mode of transfer can promote how well a plasmid spreads and persists. Together, however, the metabolic cost of conjugation could create a tradeoff that constrains plasmid evolution. Here, we present evidence for the presence, consequences, and molecular basis of a conjugation-growth tradeoff across 40 plasmids derived from clinical Escherichia coli pathogens. We discover that most plasmids operate below a conjugation efficiency threshold for major growth effects, indicating strong natural selection for vertical transfer. Below this threshold, E. coli demonstrates a remarkable growth tolerance to over four orders of magnitude change in conjugation efficiency. This tolerance fades as nutrients become scarce and horizontal transfer attracts a greater share of host resources. Our results provide insight into evolutionary constraints directing plasmid fitness and strategies to combat the spread of antibiotic resistance.
质粒适应性由两个正交过程指导-通过细胞分裂的垂直转移和通过接合的水平转移。当单独考虑时,两种转移模式的改进都可以促进质粒的传播和持续存在。然而,接合的代谢成本可能会产生一种权衡,限制质粒的进化。在这里,我们提供了 40 个源自临床大肠杆菌病原体的质粒的接合-生长权衡的存在、后果和分子基础的证据。我们发现,大多数质粒在对接合效率有重大生长影响的阈值以下运作,这表明垂直转移受到强烈的自然选择。在这个阈值以下,大肠杆菌对接合效率变化四个数量级表现出惊人的生长耐受性。当营养物质变得稀缺且水平转移吸引更多的宿主资源时,这种耐受性会消失。我们的结果为指导质粒适应性的进化限制和对抗抗生素耐药性传播的策略提供了深入了解。