State Key Laboratory for Agro-Biotechnology and Department of Plant Pathology, China Agricultural University, Beijing, 100193, China.
Cereal Crops Institute, Henan Academy of Agricultural Science, Zhengzhou, 450002, China.
New Phytol. 2017 Aug;215(3):1156-1172. doi: 10.1111/nph.14645. Epub 2017 Jun 19.
Sugarcane mosaic virus (SCMV) is the most important cause of maize dwarf mosaic disease. To identify maize genes responsive to SCMV infection and that may be involved in pathogenesis, a comparative proteomic analysis was performed using the first and second systemically infected leaves (termed 1 SL and 2 SL, respectively). Seventy-one differentially expressed proteins were identified in 1 SL and 2 SL upon SCMV infection. Among them, eight proteins showed the same changing patterns in both 1 SL and 2 SL. Functional annotations of regulated proteins and measurement of photosynthetic activity revealed that photosynthesis was more inhibited and defensive gene expression more pronounced in 1 SL than in 2 SL. Knockdown of regulated proteins in both 1 SL and 2 SL by a brome mosaic virus-based gene silencing vector in maize indicated that protein disulfide isomerase-like and phosphoglycerate kinase were required for optimal SCMV replication. By contrast, knockdown of polyamine oxidase (ZmPAO) significantly increased SCMV accumulation, implying that ZmPAO activity might contribute to resistance or tolerance. The results suggest that combining comparative proteomic analyses of different tissues and virus-induced gene silencing is an efficient way to identify host proteins supporting virus replication or enhancing resistance to virus infection.
甘蔗花叶病毒(SCMV)是引起玉米矮花叶病的最重要原因。为了鉴定对 SCMV 感染有反应并可能参与发病机制的玉米基因,使用第一和第二系统感染的叶片(分别称为 1 SL 和 2 SL)进行了比较蛋白质组学分析。在 SCMV 感染后,在 1 SL 和 2 SL 中鉴定出了 71 种差异表达的蛋白质。其中,有 8 种蛋白质在 1 SL 和 2 SL 中表现出相同的变化模式。受调控蛋白的功能注释和光合作用活性的测量表明,在 1 SL 中光合作用受到的抑制比在 2 SL 中更严重,防御基因的表达更为明显。通过基于大麦黄花叶病毒的基因沉默载体在玉米中敲低 1 SL 和 2 SL 中的调控蛋白表明,蛋白二硫键异构酶样和磷酸甘油酸激酶对于 SCMV 的最佳复制是必需的。相比之下,敲低多胺氧化酶(ZmPAO)显著增加了 SCMV 的积累,这意味着 ZmPAO 活性可能有助于抗性或耐受性。结果表明,结合不同组织的比较蛋白质组学分析和病毒诱导的基因沉默是鉴定支持病毒复制或增强病毒感染抗性的宿主蛋白的有效方法。