Parallel, Continuous Monitoring and Quantification of Programmed Cell Death in Plant Tissue.
Alexander Silva Pinto CollinsHasan KurtCian DugganYasin CoturPhilip CoatsworthAtharv NaikMatti KaistiTolga Osman BozkurtFirat GüderPublished in: Advanced science (Weinheim, Baden-Wurttemberg, Germany) (2024)
Accurate quantification of hypersensitive response (HR) programmed cell death is imperative for understanding plant defense mechanisms and developing disease-resistant crop varieties. Here, a phenotyping platform for rapid, continuous-time, and quantitative assessment of HR is demonstrated: Parallel Automated Spectroscopy Tool for Electrolyte Leakage (PASTEL). Compared to traditional HR assays, PASTEL significantly improves temporal resolution and has high sensitivity, facilitating detection of microscopic levels of cell death. Validation is performed by transiently expressing the effector protein AVRblb2 in transgenic Nicotiana benthamiana (expressing the corresponding resistance protein Rpi-blb2) to reliably induce HR. Detection of cell death is achieved at microscopic intensities, where leaf tissue appears healthy to the naked eye one week after infiltration. PASTEL produces large amounts of frequency domain impedance data captured continuously. This data is used to develop supervised machine-learning (ML) models for classification of HR. Input data (inclusive of the entire tested concentration range) is classified as HR-positive or negative with 84.1% mean accuracy (F1 score = 0.75) at 1 h and with 87.8% mean accuracy (F1 score = 0.81) at 22 h. With PASTEL and the ML models produced in this work, it is possible to phenotype disease resistance in plants in hours instead of days to weeks.
Keyphrases
- machine learning
- cell death
- big data
- high throughput
- electronic health record
- loop mediated isothermal amplification
- deep learning
- artificial intelligence
- high resolution
- single molecule
- immune response
- cell cycle arrest
- magnetic resonance imaging
- randomized controlled trial
- cell proliferation
- label free
- binding protein
- solid state
- pi k akt
- gestational age
- signaling pathway
- dual energy
- innate immune