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A comprehensive survey of secondary metabolites encoded in bacteria identifies large differences in biosynthetic diversity among genera and pinpoints those that can be targeted for novel chemistries provisionally suitable as antimicrobials.
Large-scale gut microbiome analysis of a widely use mouse model of inflammatory bowel disease reveals that the gut microbiome is a driver of variability across genetically identical mice, in particular two species that are associated with variable treatment endpoints.
Phylogeography and phylogenomic analyses of E. coli isolates collected from humans and domesticated and wild animals across 99 households in Nairobi reveal strong intra-household, and lower but detectable inter-household and inter-host, strain-sharing patterns.