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A lentinan-loaded calcium alginate hydrogel with a core-shell structure induces broad-spectrum resistance to plant viruses by activating CML19
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  • Shunyu Xiang,
  • Jing Wang,
  • Xiaoyan Wang,
  • Haoran Peng,
  • Xin Zhu,
  • Jin Huang,
  • Mao Ran,
  • Lisong Ma,
  • xianchao sun
Shunyu Xiang
Southwest University

Corresponding Author:[email protected]

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Jing Wang
Southwest University
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Xiaoyan Wang
College of Plant Protection, Southwest University, Chongqing 400715, China
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Haoran Peng
Southwest University
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Xin Zhu
College of Plant Protection, Southwest University, Chongqing 400715, China
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Jin Huang
Southwest University
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Mao Ran
Chongqing Tobacco Science Research Institute, Chongqing, 400715, China
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Lisong Ma
Agriculture and Agri-Food Canada
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xianchao sun
Southwest University
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Abstract

Control of plant virus diseases largely depends on the induced plant defense achieved by the external application of synthetic chemical inducers with the ability to modify defense-signaling pathways. However, most of the molecular mechanisms underlying these chemical inducers remain unknown. Here, we developed a lentinan-loaded hydrogel with a core-shell structure and discovered how it protects plants from different virus infections. The hydrogel was synthesized by adding a chitosan shell on the surface of the polyanion sodium alginate-Ca2+-lentinan (LNT) hydrogel (SL-gel) to form a CSL-gel. CSL-gels exhibit the capacity to prolong the stable release of lentinan and promote Ca2+ release. Application of CSL-gels on the root of plants induces broad-spectrum resistance against TMV, TRV, PVX and TuMV). RNA-seq analysis identified that the calmodulin-like protein 19 gene (CML19) is upregulated by the sustained release of Ca2+ from the CSL-gel, and silencing and overexpression of CML19 alter the susceptibility and resistance of tobacco to TMV. Our findings provide evidence that this novel and synthetic CSL-gel strongly inhibits the infection of plant viruses by the sustainable release of LNT and Ca2+. This study uncovers a novel mode of action by which CSL-gels trigger CML19 expression through the stable and sustained release of Ca2+.