Characterization of a foxtail mosaic virus vector for gene silencing and analysis of innate immune responses in Sorghum bicolor.
Melissa BredowMartha Ibore NatukundaBliss M BeerninkAline Sartor ChicowskiMaria G Salas-FernandezSteven A WhithamPublished in: Molecular plant pathology (2022)
Sorghum is vulnerable to many biotic and abiotic stresses, which cause considerable yield losses globally. Efforts to genetically characterize beneficial sorghum traits, including disease resistance, plant architecture, and tolerance to abiotic stresses, are ongoing. One challenge faced by sorghum researchers is its recalcitrance to transformation, which has slowed gene validation efforts and utilization for cultivar development. Here, we characterize the use of a foxtail mosaic virus (FoMV) vector for virus-induced gene silencing (VIGS) by targeting two previously tested marker genes: phytoene desaturase (PDS) and ubiquitin (Ub). We additionally demonstrate VIGS of a subgroup of receptor-like cytoplasmic kinases (RLCKs) and report the role of these genes as positive regulators of early defence signalling. Silencing of subgroup 8 RLCKs also resulted in higher susceptibility to the bacterial pathogens Pseudomonas syringae pv. syringae (B728a) and Xanthomonas vasicola pv. holcicola, demonstrating the role of these genes in host defence against bacterial pathogens. Together, this work highlights the utility of FoMV-induced gene silencing in the characterization of genes mediating defence responses in sorghum. Moreover, FoMV was able to systemically infect six diverse sorghum genotypes with high efficiency at optimal temperatures for sorghum growth and therefore could be extrapolated to study additional traits of economic importance.
Keyphrases
- genome wide
- genome wide identification
- immune response
- transcription factor
- high efficiency
- genome wide analysis
- dna methylation
- high glucose
- bioinformatics analysis
- randomized controlled trial
- clinical trial
- copy number
- quality improvement
- small molecule
- gene expression
- endothelial cells
- escherichia coli
- open label
- cystic fibrosis
- study protocol
- arabidopsis thaliana
- multidrug resistant
- binding protein