Adaptive Evolution Compensated for the Plasmid Fitness Costs Brought by Specific Genetic Conflicts

Abstract

New Delhi metallo-β-lactamase (NDM)-carrying IncX3 plasmids is important in the transmission of carbapenem resistance in Escherichia coli. Fitness costs related to plasmid carriage are expected to limit gene exchange; however, the causes of these fitness costs are poorly understood. Compensatory mutations are believed to ameliorate plasmid fitness costs and enable the plasmid’s wide spread, suggesting that such costs are caused by specific plasmid–host genetic conflicts. By combining conjugation tests and experimental evolution with comparative genetic analysis, we showed here that the fitness costs related to ndm/IncX3 plasmids in E. coli C600 are caused by co-mutations of multiple host chromosomal genes related to sugar metabolism and cell membrane function. Adaptive evolution revealed that mutations in genes associated with oxidative stress, nucleotide and short-chain fatty acid metabolism, and cell membranes ameliorated the costs associated with plasmid carriage. Specific genetic conflicts associated with the ndm/IncX3 plasmid in E. coli C600 involve metabolism and cell-membrane-related genes, which could be ameliorated by compensatory mutations. Collectively, our findings could explain the wide spread of IncX3 plasmids in bacterial genomes, despite their potential cost.

Increase in antioxidant capacity associated with the successful subclone of hypervirulent carbapenem-resistant Klebsiella pneumoniae ST11-KL64

“…Plasmids are regarded as conferring new adaptive capabilities to bacteria while also imposing a fitness cost. Adaptive evolution, driven by mutations linked to oxidative stress, nucleotide synthesis, and metabolism, alleviates the costs associated with plasmid carriage, facilitating widespread dissemination 6 , 7 . Therefore, investigating the adaptive evolution of bacteria following the acquisition of virulent plasmids is essential for comprehending the potential prevalence of hv-CRKP.…”