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dc.contributor.authorMongue, Andrew J.
dc.contributor.authorMartin, Simon H.
dc.contributor.authorManweiler, Rachel E. V.
dc.contributor.authorScullion, Helena
dc.contributor.authorKoehn, Jordyn L.
dc.contributor.authorde Roode, Jacobus C.
dc.contributor.authorWalters, James R.
dc.date.accessioned2023-07-10T16:32:51Z
dc.date.available2023-07-10T16:32:51Z
dc.date.issued2023-05-24
dc.identifier.citationMongue, A.J., Martin, S.H., Manweiler, R.E.V. et al. Genome sequence of Ophryocystis elektroscirrha, an apicomplexan parasite of monarch butterflies: cryptic diversity and response to host-sequestered plant chemicals. BMC Genomics 24, 278 (2023). https://doi.org/10.1186/s12864-023-09350-0en_US
dc.identifier.urihttps://hdl.handle.net/1808/34565
dc.description.abstractApicomplexa are ancient and diverse organisms which have been poorly characterized by modern genomics. To better understand the evolution and diversity of these single-celled eukaryotes, we sequenced the genome of Ophryocystis elektroscirrha, a parasite of monarch butterflies, Danaus plexippus. We contextualize our newly generated resources within apicomplexan genomics before answering longstanding questions specific to this host-parasite system. To start, the genome is miniscule, totaling only 9 million bases and containing fewer than 3,000 genes, half the gene content of two other sequenced invertebrate-infecting apicomplexans, Porospora gigantea and Gregarina niphandrodes. We found that O. elektroscirrha shares different orthologs with each sequenced relative, suggesting the true set of universally conserved apicomplexan genes is very small indeed. Next, we show that sequencing data from other potential host butterflies can be used to diagnose infection status as well as to study diversity of parasite sequences. We recovered a similarly sized parasite genome from another butterfly, Danaus chrysippus, that was highly diverged from the O. elektroscirrha reference, possibly representing a distinct species. Using these two new genomes, we investigated potential evolutionary response by parasites to toxic phytochemicals their hosts ingest and sequester. Monarch butterflies are well-known to tolerate toxic cardenolides thanks to changes in the sequence of their Type II ATPase sodium pumps. We show that Ophryocystis completely lacks Type II or Type 4 sodium pumps, and related proteins PMCA calcium pumps show extreme sequence divergence compared to other Apicomplexa, demonstrating new avenues of research opened by genome sequencing of non-model Apicomplexa.en_US
dc.publisherBMCen_US
dc.rights© The Author(s) 2023. This article is licensed under a Creative Commons Attribution 4.0 International License.en_US
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/en_US
dc.subjectMonarch butterfly parasiteen_US
dc.subjectOEen_US
dc.subjectProtist genomicsen_US
dc.subjectATPaseen_US
dc.subjectSodium potassium pumpen_US
dc.subjectApicomplexan genomicsen_US
dc.subjectCryptic speciesen_US
dc.titleGenome sequence of Ophryocystis elektroscirrha, an apicomplexan parasite of monarch butterflies: cryptic diversity and response to host-sequestered plant chemicalsen_US
dc.typeArticleen_US
kusw.kuauthorManweiler, Rachel E. V.
kusw.kuauthorKoehn, Jordyn L.
kusw.kuauthorWalters, James R.
kusw.kudepartmentEcology and Evolutionary Biologyen_US
dc.identifier.doi10.1186/s12864-023-09350-0en_US
kusw.oaversionScholarly/refereed, publisher versionen_US
kusw.oapolicyThis item meets KU Open Access policy criteria.en_US
dc.identifier.pmidPMC37226080en_US
dc.rights.accessrightsopenAccessen_US


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© The Author(s) 2023. This article is licensed under a Creative Commons Attribution 4.0 International License.
Except where otherwise noted, this item's license is described as: © The Author(s) 2023. This article is licensed under a Creative Commons Attribution 4.0 International License.