Quantifying rapid bacterial evolution and transmission within the mouse intestine

Due to limitations on high-resolution strain tracking, selection dynamics during gut microbiota colonization and transmission between hosts remain mostly mysterious. Here, we introduced hundreds of barcoded Escherichia coli strains into germ-free mice and quantified strain-level dynamics and metagenomic changes. Mutations in genes involved in motility and metabolite utilization are reproducibly selected within days. Even with rapid selection, coprophagy enforced similar barcode distributions across co-housed mice. Wholegenome sequencing of hundreds of isolates revealed linked alleles that demonstrate between-host transmission. A population-genetics model predicts substantial fitness advantages for certain mutants and that migration accounted for similar to 10% of the resident microbiota each day. Treatment with ciprofloxacin suggests interplay between selection and transmission. While initial colonization was mostly uniform, in two mice a bottleneck reduced diversity and selected for ciprofloxacin resistance in the absence of drug. These findings highlight the interplay between environmental transmission and rapid, deterministic selection during evolution of the intestinal microbiota.

Automated summary

By introducing barcoded Escherichia coli strains into germ-free mice, it was found that mutations in genes involved in motility and metabolite utilization are reproducibly selected within days, and coprophagy enforces similar barcode distributions across co-housed mice. Whole-genome sequencing of isolates revealed linked alleles that demonstrate between-host transmission, and a population-genetics model predicts substantial fitness advantages for certain mutants. Treatment with ciprofloxacin suggests an interplay between selection and transmission, with migration accounting for approximately 10% of the resident microbiota each day.