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Penicillium Chrysogenum Polypeptide Extract Protects Tobacco Plants from Tobacco Mosaic Virus Infection Through Modulation of ABA Biosynthesis and Callose Priming

Overview
Journal J Exp Bot
Specialty Biology
Date 2021 Mar 9
PMID 33687058
Citations 7
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Abstract

The polypeptide extract of the dry mycelium of Penicillium chrysogenum (PDMP) can protect tobacco plants from tobacco mosaic virus (TMV), although the mechanism underlying PDMP-mediated TMV resistance remains unknown. In our study, we analysed a potential mechanism via RNA sequencing (RNA-seq) and found that the abscisic acid (ABA) biosynthetic pathway and β-1,3-glucanase, a callose-degrading enzyme, might play an important role in PDMP-induced priming of resistance to TMV. To test our hypothesis, we successfully generated a Nicotiana benthamiana ABA biosynthesis mutant and evaluated the role of the ABA pathway in PDMP-induced callose deposition during resistance to TMV infection. Our results suggested that PDMP can induce callose priming to defend against TMV movement. PDMP inhibited TMV movement by increasing callose deposition around plasmodesmata, but this phenomenon did not occur in the ABA biosynthesis mutant; moreover, these effects of PDMP on callose deposition could be rescued by treatment with exogenous ABA. Our results suggested that callose deposition around plasmodesmata in wild-type plants is mainly responsible for the restriction of TMV movement during the PDMP-induced defensive response to TMV infection, and that ABA biosynthesis apparently plays a crucial role in PDMP-induced callose priming for enhancing defence against TMV.

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References
1.
Pieterse C, Leon-Reyes A, van der Ent S, Van Wees S . Networking by small-molecule hormones in plant immunity. Nat Chem Biol. 2009; 5(5):308-16. DOI: 10.1038/nchembio.164. View

2.
Pastor-Fernandez J, Pastor V, Mateu D, Gamir J, Sanchez-Bel P, Flors V . Accumulating evidences of callose priming by indole- 3- carboxylic acid in response to . Plant Signal Behav. 2019; 14(7):1608107. PMC: 6619925. DOI: 10.1080/15592324.2019.1608107. View

3.
Mao Y, Botella J, Liu Y, Zhu J . Gene editing in plants: progress and challenges. Natl Sci Rev. 2021; 6(3):421-437. PMC: 8291443. DOI: 10.1093/nsr/nwz005. View

4.
Garcia-Andrade J, Ramirez V, Flors V, Vera P . Arabidopsis ocp3 mutant reveals a mechanism linking ABA and JA to pathogen-induced callose deposition. Plant J. 2011; 67(5):783-94. DOI: 10.1111/j.1365-313X.2011.04633.x. View

5.
Ding B . Intercellular protein trafficking through plasmodesmata. Plant Mol Biol. 1998; 38(1-2):279-310. View