AI Article Synopsis

  • Bud necrosis (BN) significantly reduces the yield of Vitis vinifera L., and double pruning management is used in Brazilian vineyards to mitigate these losses by optimizing plant cycles during winter and summer.
  • RNA-seq analysis of healthy versus necrotic grape tissues reveals that genes associated with cell death are more active in necrotic tissues, potentially due to the influence of endophytic microorganisms.
  • The study suggests that harsh conditions and low carbohydrate levels in buds may trigger a shift in endophytic fungi like Alternaria alternata from a biotrophic (nutrient-gain) to a necrotrophic (harmful) mode, contributing to the onset of BN.

Article Abstract

Bud necrosis (BN) is a common disorder that affects Vitis vinifera L. and reduces its potential yield. To minimize the losses caused by BN, the double pruning management was applied in Brazilian Southeast vineyards. In this management strategy plants are pruned at the winter to promote a vegetative cycle and then, at summer, to promote the reproductive cycle at optimal environmental conditions. To investigate the relationship of BN and the double pruning management RNA-seq libraries were sequenced from healthy and necrotic tissues at four different stages of the year. The comparison of differentially expressed genes in necrotic and non-necrotic tissues showed an enhanced expression of genes related to cell death possibly induced by endophytic microorganisms in the necrotic tissues. The de novo assembly, characterization and quantification of transcripts within the RNA-seq libraries showed that genes from the endophytic fungus Alternaria alternata, responsible for the production of toxic compounds were highly expressed under BN. Here we propose a model in which unfavorable conditions and reduced carbohydrate levels in buds can promote the switch from a biotrophic lifestyle to a necrotrophic lifestyle in the endophytic fungi, which seems to be involved in the development of BN.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7290027PMC
http://dx.doi.org/10.1038/s41598-020-66500-0DOI Listing

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