Abstract
Rice sheath blight,caused by Rhizoctonia solani AG1-IA,is a major disease in rice-growing areas worldwide.Effectors of phytopathogenic fungi play important roles during the infection process of fungal pathogens onto their host plants.However,the molecular mechanisms by which R.solani effectors regulate rice immunity are not well understood.Through prediction,78 candidate effector molecules were identified.Using the tobacco rattle virus-host induced gene silencing(TRV-HIGS)system,45 RNAi constructs of effector genes were infiltrated into Nicotiana benthamiana leaves.The results revealed that eight of these constructs resulted in a significant reduction in necrosis caused by infection with the AG1-IA strain GD-118.Additionally,stable rice transformants carrying the double-stranded RNA construct for one of the effector genes,AGLIP1,were generated to further verify the function of this gene.The suppression of the AGLIP1 gene increased the resistance of both N.benthamiana and rice against GD-118,and also affected the growth rate of GD-118,indicating that AGLIP1 is a key pathogenic factor.Small RNA sequencing showed that the HIGS vectors were processed into siRNAs within the plants and then translocated to the fungi,leading to the silencing of the target genes.As a result,AGLIP1 might be an excellent candidate for HIGS,thereby enhancing crop resistance against the pathogen and contributing to the control of R.solani infection.
基金项目
Henan Province Science and Technology Research Project,China(242102110232)
National Natural Science Foundation of China(31801677)
Major Program of Guangdong Basic and Applied Basic Research,China(2019B030302006)
NETL
NSTL
万方数据