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Biology subjects

Courtney, C.

Publications and source records attributed to Courtney, C..

4 recordsLinked to original sources

Larval antibiosis to cabbage stem flea beetle (Psylliodes chrysocephala) is absent within oilseed rape (Brassica napus)

BACKGROUNDInsect pests present a global threat to crops, with plant resistance representing a key breeding goal. The cabbage stem flea beetle (Psylliodes chrysocephala; CSFB) is a key pest of oilseed rape (Brassica napus; OSR) within Europe; however, CSFB resistance is yet to be found within B. napus. To address this, we examine CSFB larval development over time, explore antibiosis across a genetically diverse B. napus panel, and test whether larvae can develop within model Brassicaceae species (Brassica rapa and Arabidopsis thaliana). RESULTSCSFB larvae completed development from four-weeks post-infestation, undergoing a 20-fold size increase, with larval recovery after two weeks allowing semi-high throughput resistance phenotyping. Applying this method to 98 Brassicaceae genotypes (97 B. napus and a single Sinapis alba), we found weak evidence for genotype effects on larval survival. However, phenotype validation with resistant and susceptible B. napus genotypes showed no differences in larval survival or adult emergence. Larval antibiosis was consistently observed in S. alba. Finally, we showed that model B. rapa and A. thaliana genotypes represent suitable hosts for CSFB, with larvae increasing 8-10x in size after two weeks. CONCLUSIONCSFB larval antibiosis appears absent within B. napus, possibly due to bottlenecks experienced during domestication. However, larval antibiosis is present within S. alba, and future work should study the basis of this resistance. Further, CSFB larval screening in Brassicaceae model species presents an opportunity to explore CSFB resistance genetics, informing breeding progress for insect resistance in B. napus.

plant biology↗

Developing future resilience from signatures of adaptation across the sorghum pangenome

While the green revolution adapted a handful of crops to homogenous and high-input industrialized agriculture, much of the global population still relies on local food production from low-input smallholder farms that grow highly variable crop cultivars. The high diversity of the grain and bioenergy crop sorghum 1-4, and many other crops that were not homogenized during the green revolution 5, not only provides the raw materials for breeders to make substantial gains in cultivar improvement, but also constrains breeding efforts due to highly specialized locally adapted plant phenotypes 6. Here, we construct a 33-member pangenome and identify trait-associated variants in 1,988 cultivars and landraces. We then apply these resources to explore the complex interplay between historical contingency, ongoing adaptation, and the potential for future gains through climate-aware genome-enabled breeding. Specifically, our analyses conclusively demonstrate that multiple nested, deeply diverged, and previously uncharacterized structural variants in the domestication gene SHATTERING1 distinguish the previously established multicentric origin of sorghum. We then apply landscape genomics tests to reveal how gene flow, adaptation, and secondary contact created the complex genetic mosaic in current global breeding networks. Further analysis of climate-gene associations highlights candidate loci underlying adaptation, including the biosynthetic gene cluster for the cyanogenic glucoside dhurrin. Combined, the pangenome-informed variants developed here will enable both trait discovery and subsequent marker assays to accelerate breeding and provide a framework for similar applications in other diverse and non-model crops.

genomics↗

DeltaBreed: A BrAPI-centric breeding data information system

DeltaBreed is a unified breeding data management system designed by Breeding Insight (BI, Cornell University) to serve the wide diversity of USDA-ARS specialty crop and animal breeding programs. DeltaBreed has a RESTful microservice architecture that utilizes the BrAPI Java Test Server as its primary database. The system is interoperable with many BrAPI-compliant applications (BrApps), including Field Book, and is continually aligned with the most recent BrAPI specifications. Here, we describe the features of DeltaBreed and provide several interoperability test cases to illustrate successes and challenges encountered during development. We also discuss future expansion and enhancement plans for DeltaBreed, as well as outline possible solutions to known limitations.

bioinformatics↗

Single-Cell Analysis Reveals Regional Reprogramming during Adaptation to Massive Small Bowel Resection in Mice

Background & AimsThe small intestine (SI) displays regionality in nutrient and immunological function. Following SI tissue loss (as occurs in short gut syndrome, or SGS), remaining SI must compensate, or adapt; the capacity of SI epithelium to reprogram its regional identity has not been described. Here, we apply single-cell resolution analyses to characterize molecular changes underpinning adaptation to SGS.\n\nMethodsSingle-cell RNA-sequencing was performed on epithelial cells isolated from distal SI of mice following 50% proximal small bowel resection (SBR) vs. sham surgery. Single-cell profiles were clustered based on transcriptional similarity, reconstructing differentiation events from intestinal stem cells (ISCs) through to mature enterocytes. An unsupervised computational approach to score cell identity was used to quantify changes in regional (proximal vs distal) SI identity, validated using immunofluorescence, immunohistochemistry, qPCR, western blotting, and RNA-FISH.\n\nResultsUniform Manifold Approximation and Projection-based clustering and visualization revealed differentiation trajectories from ISCs to mature enterocytes in sham and SBR. Cell identity scoring demonstrated segregation of enterocytes by regional SI identity: SBR enterocytes assumed more mature proximal identities. This was associated with significant upregulation of lipid metabolism and oxidative stress gene expression, which was validated via orthogonal analyses. Observed upstream transcriptional changes suggest retinoid metabolism and proximal transcription factor Creb3l3 drive proximalization of cell identity in response to SBR.\n\nConclusionsAdaptation to proximal SBR involves regional reprogramming of ileal enterocytes toward a proximal identity. Interventions bolstering the endogenous reprogramming capacity of SI enterocytes--conceivably by engaging the retinoid metabolism pathway--merit further investigation, as they may increase enteral feeding tolerance, and obviate intestinal failure, in SGS.\n\n\n\nO_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=83 SRC=\"FIGDIR/small/615054v1_ufig1.gif\" ALT=\"Figure 1\">\nView larger version (26K):\norg.highwire.dtl.DTLVardef@156d1b4org.highwire.dtl.DTLVardef@e1a3fcorg.highwire.dtl.DTLVardef@1d519bforg.highwire.dtl.DTLVardef@18d4e9d_HPS_FORMAT_FIGEXP M_FIG C_FIG SynopsisHere, single-cell RNA sequencing reveals interactions between the retinoid metabolism pathway and regional reprogramming of distal small intestinal epithelium to a proximal identity following proximal small bowel resection. This provides novel insight into physiological adaptation to short gut syndrome.

genomics↗