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Nova · Professor Researcher · re-ranking top 20…
Christa Olson

Christa Olson

· Department Chair

University of Wisconsin-Madison · Arts & Humanities

Active 2006–2024

h-index6
Citations112
Papers3911 last 5y
Funding
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Research topics

  • Biology
  • Medicine
  • Zoology
  • Ecology
  • Evolutionary biology
  • Dermatology
  • Surgery
  • Intensive care medicine
  • Pediatrics
  • Genetics

Selected publications

  • LONG-TERM PROPHYLACTIC TREATMENT PREFERENCES OF PATIENTS WITH HEREDITARY ANGIOEDEMA

    Annals of Allergy Asthma & Immunology · 2024 · 1 citations

    • Medicine
    • Dermatology
    • Intensive care medicine
  • Physiological and evolutionary contexts of a new symbiotic species from the nitrogen-recycling gut community of turtle ants

    The ISME Journal · 2023 · 10 citations

    • Biology
    • Ecology
    • Evolutionary biology

    While genome sequencing has expanded our knowledge of symbiosis, role assignment within multi-species microbiomes remains challenging due to genomic redundancy and the uncertainties of in vivo impacts. We address such questions, here, for a specialized nitrogen (N) recycling microbiome of turtle ants, describing a new genus and species of gut symbiont-Ischyrobacter davidsoniae (Betaproteobacteria: Burkholderiales: Alcaligenaceae)-and its in vivo physiological context. A re-analysis of amplicon sequencing data, with precisely assigned Ischyrobacter reads, revealed a seemingly ubiquitous distribution across the turtle ant genus Cephalotes, suggesting ≥50 million years since domestication. Through new genome sequencing, we also show that divergent I. davidsoniae lineages are conserved in their uricolytic and urea-generating capacities. With phylogenetically refined definitions of Ischyrobacter and separately domesticated Burkholderiales symbionts, our FISH microscopy revealed a distinct niche for I. davidsoniae, with dense populations at the anterior ileum. Being positioned at the site of host N-waste delivery, in vivo metatranscriptomics and metabolomics further implicate I. davidsoniae within a symbiont-autonomous N-recycling pathway. While encoding much of this pathway, I. davidsoniae expressed only a subset of the requisite steps in mature adult workers, including the penultimate step deriving urea from allantoate. The remaining steps were expressed by other specialized gut symbionts. Collectively, this assemblage converts inosine, made from midgut symbionts, into urea and ammonia in the hindgut. With urea supporting host amino acid budgets and cuticle synthesis, and with the ancient nature of other active N-recyclers discovered here, I. davidsoniae emerges as a central player in a conserved and impactful, multipartite symbiosis.

Frequent coauthors

  • L. E. Baumgartener

    14 shared
  • Daniel Segrè

    Boston University

    9 shared
  • Misao Onuma

    Hokkaido University

    8 shared
  • Janice M. Miller

    Dana-Farber Cancer Institute

    8 shared
  • Ikuo Takashima

    Hokkaido University

    8 shared
  • Yi Hu

    Drexel University

    6 shared
  • D M Driscoll

    5 shared
  • Steven M. Entine

    University of Wisconsin–Madison

    4 shared

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