Key Laboratory of Hebei Province for Plant Physiology and Molecular Pathology, College of Life Sciences, Agricultural University of Hebei, Baoding, Hebei Province, China.
The People's Government of Baian, Town, Xingtai, China.
Plant Biol (Stuttg). 2018 Mar;20(2):318-326. doi: 10.1111/plb.12663. Epub 2018 Jan 7.
The present study aimed to investigate changes in nitric oxide (NO) level and its relationship with callose deposition during the interaction between soybean and Soybean mosaic virus (SMV). Soybean cv. 'Jidou 7' and SMV strains N3 and SC-8 were used to constitute incompatible and compatible combinations. Intracellular NO was labelled with the NO-specific fluorescence probe DAF-FM DA. Confocal laser scanning microscopy (CLSM) was then used to observe changes in NO production during SMV infection-induced defence responses in soybean. The results showed NO fluorescence increased rapidly at 2-72 h post-inoculation, peaked at 72 h and then decreased in the incompatible combination. However, in the compatible combination, extremely weak NO fluorescence appeared in the early stage (2-24 h) post-inoculation, but was not observed thereafter. Injections of the NO scavenger c-PTIO prior to inoculation postponed the onset of NO production to 48 or 72 h post-inoculation. The same occurred when injections of NR or NOS inhibitors were applied prior to inoculation. The observation of callose fluorescence in the incompatible combination revealed that either the elimination or reduction of NO in the early stage led to a delay in callose formation, enabling the virus to cause systemic infection. Together with our previous findings, this study indicates that viral infection could induce NO production and callose deposition during the incompatible interaction between soybean and SMV. The production of NO involves NR and NOS enzymatic pathways, and NO mediates the process of callose deposition at plasmodesmata.
本研究旨在探讨大豆与大豆花叶病毒(SMV)互作过程中一氧化氮(NO)水平的变化及其与胼胝质沉积的关系。采用大豆品种‘冀豆 7 号’和 SMV 株系 N3 和 SC-8 构建了非亲和和亲和组合。利用 NO 特异性荧光探针 DAF-FM DA 标记细胞内 NO。然后,利用共聚焦激光扫描显微镜(CLSM)观察 SMV 感染诱导大豆防御反应过程中 NO 产生的变化。结果表明,NO 荧光在接种后 2-72 h 迅速增加,在 72 h 时达到峰值,然后在非亲和组合中减少。然而,在亲和组合中,接种后早期(2-24 h)出现极弱的 NO 荧光,但此后未观察到。在接种前注射 NO 清除剂 c-PTIO 会将 NO 产生的起始时间推迟到接种后 48 或 72 h。在接种前应用 NR 或 NOS 抑制剂注射也会发生同样的情况。在非亲和组合中观察到胼胝质荧光,表明早期 NO 的消除或减少会导致胼胝质形成延迟,从而使病毒能够引起系统感染。结合我们之前的发现,本研究表明,病毒感染可能在大豆与 SMV 之间的非亲和互作过程中诱导 NO 产生和胼胝质沉积。NO 的产生涉及 NR 和 NOS 酶途径,NO 介导质膜通道中胼胝质沉积的过程。