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Oiler, I. M.

Publications and source records attributed to Oiler, I. M..

2 recordsLinked to original sources

Genomic insights into bacterial isolates dominating honeypot ant crop microbiomes reveal metabolically distinct Fructilactobacillus sp.

Honeypot ants engage in a convergently-evolved phenotype called repletism, where specialized workers expand their crops and gasters to store vast amounts of food internally. They then store that food for months to support colonies during times of food scarcity. This fascinating phenotype is not well-understood and very little is known about the microbial interactions happening within the fructose-rich replete crop. Previous research using amplicon sequencing showed that Fructilactobacillus makes up nearly 100% of the crop microbiomes of Myrmecocystus mexicanus repletes. This striking result and successful isolation of those strains led to the present investigation into the phylogenetic diversity of these strains and any clues to the nature of the symbiotic relationship between them and the ant host. We find that the isolates from these repletes represented two evolutionary lineages, both most closely related to F. fructivorans. One of those lineages was also found to be phylogenetically and metabolically distinct from all other Fructilactobacillus reference genomes used in this study. This discovery in a genus of bacteria that are highly relevant for fermented human foods and will also lay the groundwork for future understanding of the convergent evolutionary mechanisms of repletism in ants. 3. Impact statementThese analyses add to the literature by identifying a new microbe within a genus that is relevant to food systems. In addition, the host phenotype is convergently evolved and likely microbe-mediated (or at least highly exposed). Understanding this system allows for the testing of ideas of coevolutionary hypotheses with natural replicates. We expect interest to come from food safety and probiotics researchers, evolutionary biologists that think about the impacts of microbes, microbial ecologists interested in novel systems, and those interested in bacteria that may display unique metabolic possibilities. This output allows for the clear future examination of this system with many clear hypotheses. Our analysis allows for the creation of a new and unique model system of host-microbe symbiosis. 4. Data summaryNew genomes assembled in this work can be found under BioProject ID PRJNA1449409. https://www.ncbi.nlm.nih.gov/bioproject/?term=PRJNA1449409. Reference bacterial genomes were obtained from NCBI at the following accession numbers: SAMN20557570, SAMN28081009, SAMN28081010, SAMN02597458, SAMN43111088, SAMN28081011, SAMN28535231, SAMN04505734, SAMN28081013, SAMN33452149, SAMN37926504, SAMN02849426, SAMN02470196, SAMN02369432, SAMN02797779, SAMN02797782, SAMN02797768, SAMN09762388, SAMN12785275, SAMEA117660288. The honeypot ant genome was obtained from SAMN37666067. Raw proteomics files will be uploaded to ProteomeXchange with a unique identifier upon manuscript acceptance.

genomics↗

Shell-bound archives: uncovering nematode encapsulations in the Galapagos' largest radiation

How macroevolution interacts with ecological networks remains a major question in eco-evolutionary science. We investigate this interplay in the Naesiotus snail radiation of the Galapagos Islands, which encapsulates parasitic nematodes within the shell--a recently discovered gastropod defense. Using a natural history collection, we examined dry shells from 47 species across 12 islands, quantified encapsulations, and sequenced nematode DNA to reconstruct a host-parasite network. Encapsulations were widespread and revealed high nematode diversity, including in snail hosts presumed extinct. Nematode diversity was shaped by habitat, while encapsulation load was better explained by host species identity, suggesting species-specific defenses. Neither trait showed phylogenetic signal, and shell brightness was unrelated to nematode interactions. Similarly, host diversification rate did not predict network position, suggesting that macroevolution may leave a weak or obscured imprint on this host-parasite network. This snail-nematode system in islands readily enables integration of ecological networks, phylogeny, functional traits, and biogeography.

ecology↗