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Partitioning the Effects of Soil Legacy and Pathogen Exposure Determining Soil Suppressiveness via Induced Systemic Resistance.

Na ZhangChengzhi ZhuZongzhuan ShenChengyuan TaoYannan OuRong LiXuhui DengQirong ShenFrancisco Dini-Andreote
Published in: Plants (Basel, Switzerland) (2022)
Beneficial host-associated bacteria can assist plant protection against pathogens. In particular, specific microbes are able to induce plant systemic resistance. However, it remains largely elusive which specific microbial taxa and functions trigger plant immune responses associated with disease suppression. Here, we experimentally studied this by setting up two independent microcosm experiments that differed in the time at which plants were exposed to the pathogen and the soil legacy (i.e., soils with historically suppressive or conducive). Overall, we found soil legacy effects to have a major influence on disease suppression irrespective of the time prior to pathogen exposure. Rhizosphere bacterial communities of tomato plants were significantly different between the two soils, with potential beneficial strains occurring at higher relative abundances in the suppressive soil. Root transcriptome analysis revealed the soil legacy to induce differences in gene expression, most importantly, genes involved in the pathway of phenylpropanoid biosynthesis. Last, we found genes in the phenylpropanoid biosynthesis pathway to correlate with specific microbial taxa, including Gp6 , Actinomarinicola , Niastella , Phaeodactylibacter , Longimicrobium , Bythopirellula , Brevundimonas , Ferruginivarius , Kushneria , Methylomarinovum , Pseudolabrys , Sphingobium , Sphingomonas , and Alterococcus . Taken together, our study points to the potential regulation of plant systemic resistance by specific microbial taxa, and the importance of soil legacy on disease incidence and eliciting plant-defense mechanisms.
Keyphrases
  • plant growth
  • gene expression
  • microbial community
  • immune response
  • cell wall
  • heavy metals
  • candida albicans
  • single cell
  • risk assessment
  • multidrug resistant
  • toll like receptor
  • gram negative