Project description:In this study, we used transcriptomic and hormonomic approaches to examine drought-induced changes in barley roots and leaves and its rhizosphere. By studying hormonal responses, alternative splicing events in barley, and changes in the rhizosphere microbiome, we aimed to provide a comprehensive view of barley drought-adaptive mechanisms and potential plant-microbe interactions under drought stress. This approach improved our understanding of barley adaptive strategies and highlighted the importance of considering plant-microbe interactions in the context of climate change.
Project description:Pseudomonas fluorescens SBW25 cultures were inoculated into the rhizospheres of barley seedlings of the Chevallier and Tipple varieties growing in axenic cultures. Bacterial cells were collected from the rhizosphere one and five days after inculation and RNA extracted from them. Culture used for inoculation (but not exposed to the rhizospheres) were used as control. The aim of the experiment was to determine the changes in gene expression of P. fluorescens SBW25 upon exposure to barley rhizosphere and also to determine if the rhizospehres of the two varieties of Barley had different effects on gene expression of P. fluorescens SBW25.
Project description:Structure and functions of the bacterial root microbiota in wild and domesticated barley and signatures of positive selection in the rhizosphere metagenome
Project description:Waterlogging is a major abiotic stress causing oxygen depletion and carbon dioxide accumulation in the rhizosphere. Barley is more susceptible to waterlogging stress than other cereals. To gain a better understanding of the effect of waterlogging stress in barley, we carried out a genome-wide gene expression analysis in roots of Yerong and Deder2 barley genotypes under waterlogging and control (well-watered) conditions by RNA-Sequencing, using Illumina HiSeq™ 4000 platform.
Project description:Ustilago hordei is a basidiomycete fungus that infects barley and oats. It has a narrow host range and can infect only germinating seedlings. Symptoms do not occur until heading of the mature plants when the fungus has proliferated in meristematic tissue and replaces kernels with masses of black teliospores. Incompatibility is due to the presence of an avirulence effector product, UhAVR1, expressed in the fungus upon infection and secreted into the host, which is subsequently recognized by the barley plant resistance gene product RUH1 in cultivar Hannchen, leading to plant cell death, fungal growth arrest, and no disease. We have identified UhAvr1, and the transcriptome response of the barley plant to strains with and deleted for this gene was assessed using the 22K Affymetrix barley array. Incompatibility and cell death is apparent at 48 hrs after inoculation, so the transcriptome was assessed at this time point. For comparison, the transcriptome of barley cultivar Odessa, which lacks resistance gene Ruh1, during a compatible interaction was also assessed.