Key features of the genetic architecture and evolution of host-microbe interactions revealed by high-resolution genetic mapping of the mucosa-associated gut microbiome in hybrid mice
Max Planck Institute for Evolutionary Biology, Plön, Germany; Section of Evolutionary Medicine, Institute for Experimental Medicine, Kiel University, Kiel, Germany
Hanna Fokt
Max Planck Institute for Evolutionary Biology, Plön, Germany; Section of Evolutionary Medicine, Institute for Experimental Medicine, Kiel University, Kiel, Germany
Institute for Clinical Molecular Biology (IKMB), Kiel University, Kiel, Germany; Institute for Medical Microbiology and Hospital Epidemiology, Hannover Medical School, Hannover, Germany
Cecilia J Chung
Max Planck Institute for Evolutionary Biology, Plön, Germany; Section of Evolutionary Medicine, Institute for Experimental Medicine, Kiel University, Kiel, Germany
Max Planck Institute for Evolutionary Biology, Plön, Germany; Section of Evolutionary Medicine, Institute for Experimental Medicine, Kiel University, Kiel, Germany
Determining the forces that shape diversity in host-associated bacterial communities is critical to understanding the evolution and maintenance of metaorganisms. To gain deeper understanding of the role of host genetics in shaping gut microbial traits, we employed a powerful genetic mapping approach using inbred lines derived from the hybrid zone of two incipient house mouse species. Furthermore, we uniquely performed our analysis on microbial traits measured at the gut mucosal interface, which is in more direct contact with host cells and the immune system. Several mucosa-associated bacterial taxa have high heritability estimates, and interestingly, 16S rRNA transcript-based heritability estimates are positively correlated with cospeciation rate estimates. Genome-wide association mapping identifies 428 loci influencing 120 taxa, with narrow genomic intervals pinpointing promising candidate genes and pathways. Importantly, we identified an enrichment of candidate genes associated with several human diseases, including inflammatory bowel disease, and functional categories including innate immunity and G-protein-coupled receptors. These results highlight key features of the genetic architecture of mammalian host-microbe interactions and how they diverge as new species form.