Abstract

Groundnut bud necrosis virus (GBNV), a member of the genus Tospovirus, has an extensive host range and is associated with necrosis disease of chilli (Capsicum annuum L.), which is a major threat to commercial production. Plantgrowthpromoting rhizobacteria (PGPR) have been investigated for their antiviral activity in several crops and for their potential use in viral disease management. However, the microbial mechanisms associated with PGPR in triggered immunity against plant viruses have rarely been studied. To understand the innate immune responses activated by Bacillus spp. against GBNV, we studied microbe-associated molecular pattern (MAMP)triggered immunity (MTI) in chilli using transient expression of the flagellin gene of Bacillus amyloliquefaciens CRN9 from Agrobacterium clones, which also induced the expression of EAS1 gene transcripts coding for epi-aristolochene synthase, which is responsible for the accumulation of capsidiol phytoalexin. In addition, the transcript levels of WRKY33 transcription factor and salicylic acid (SA)-responsive defense genes such as NPR1, PAL, PO and SAR8.2 were increased. Jasmonate (JA)-responsive genes, viz., PDF, and LOX genes, were also upregulated in chilli plants challenged with GBNV. Further analysis revealed significant induction of these genes in chilli plants treated with B. amyloliquefaciens CRN9 and benzothiadiazole (BTH). The transcript levels of defense response genes and pathogenesis-related proteins were significantly higher in plants treated with Bacillus and BTH and remained significantly higher at 72h post-inoculation and compared to the inoculated control. The plants treated with flagellin using the agrodrench method and exogenous treatment with B. amyloliquefaciens and BTH showed resistance to GBNV upon mechanical inoculation and a reduced virus titre which was confirmed by qPCR assays. Thus, transient expression of flagellin, a MAMP molecule from B. amyloliquefaciens CRN9, is able to trigger innate immunity and restrain virus growth in chilli via induced systemic resistance(ISR) activated by both the SA and JA/ET signalling pathways.

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