The evolutionary genomics of adaptation to stress in wild rhizobium bacteria

• Published in: Proceedings of the National Academy of Sciences - PNAS Vol. 121; no. 13; p. e2311127121
• Main Authors: Kehlet-Delgado, Hanna, Montoya, Angeliqua P, Jensen, Kyson T, Wendlandt, Camille E, Dexheimer, Christopher, Roberts, Miles, Torres Martínez, Lorena, Friesen, Maren L, Griffitts, Joel S, Porter, Stephanie S
• Format: Journal Article
• Language: English
• Published: United States National Academy of Sciences 26.03.2024
• Subjects: Adaptation; Alleles; Bacteria; Biological Sciences; Discordance; Evolution; Evolutionary genetics; Gene transfer; Genetics; Genomes; Genomic islands; Genomics; Grasslands; Heavy metals; Horizontal transfer; Humans; Metals, Heavy - toxicity; Microbiota; Microorganisms; Natural selection; Nickel; Rhizobium - genetics; Serpentine; Serpentine soils; Soil; Soil bacteria; Soil chemistry; Soil conditions; Soil microorganisms; Soil stresses; Soils; Substitutes; Symbionts; population genomics; adaptation; serpentine soil; rhizobia; mobile genetic element
• ISSN: 0027-8424; 1091-6490
• DOI: 10.1073/pnas.2311127121

Microbiota comprise the bulk of life's diversity, yet we know little about how populations of microbes accumulate adaptive diversity across natural landscapes. Adaptation to stressful soil conditions in plants provides seminal examples of adaptation in response to natural selection via allelic substitution. For microbes symbiotic with plants however, horizontal gene transfer allows for adaptation via gene gain and loss, which could generate fundamentally different evolutionary dynamics. We use comparative genomics and genetics to elucidate the evolutionary mechanisms of adaptation to physiologically stressful serpentine soils in rhizobial bacteria in western North American grasslands. In vitro experiments demonstrate that the presence of a locus of major effect, the operon, is necessary and sufficient to confer adaptation to nickel, a heavy metal enriched to toxic levels in serpentine soil, and a major axis of environmental soil chemistry variation. We find discordance between inferred evolutionary histories of the core genome and genes, which often reside in putative genomic islands. This suggests that the evolutionary history of this adaptive variant is marked by frequent losses, and/or gains via horizontal acquisition across divergent rhizobium clades. However, different alleles confer distinct levels of nickel resistance, suggesting allelic substitution could also play a role in rhizobium adaptation to serpentine soil. These results illustrate that the interplay between evolution via gene gain and loss and evolution via allelic substitution may underlie adaptation in wild soil microbiota. Both processes are important to consider for understanding adaptive diversity in microbes and improving stress-adapted microbial inocula for human use.