
Christa Olson
· Department ChairUniversity of Wisconsin-Madison · Arts & Humanities
Active 2006–2024
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
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
- 14 shared
L. E. Baumgartener
- 9 shared
Daniel Segrè
Boston University
- 8 shared
Misao Onuma
Hokkaido University
- 8 shared
Janice M. Miller
Dana-Farber Cancer Institute
- 8 shared
Ikuo Takashima
Hokkaido University
- 6 shared
Yi Hu
Drexel University
- 5 shared
D M Driscoll
- 4 shared
Steven M. Entine
University of Wisconsin–Madison
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