Iqbal M Javed, Majeed Maryam, Humayun Maheen, Lightfoot David A, Afzal Ahmed J
Department of Plant Sciences, University of California, Davis, California, 95616, USA.
Department of Biology, SBA School of Science and Engineering, Lahore University of Management Sciences, Lahore, 54792, Pakistan.
Appl Biochem Biotechnol. 2016 Dec;180(8):1657-1674. doi: 10.1007/s12010-016-2194-5. Epub 2016 Aug 5.
Sudden death syndrome (SDS) is a complex of two diseases of soybean (Glycine max), caused by the soil borne pathogenic fungus Fusarium virguliforme. The root rot and leaf scorch diseases both result in significant yield losses worldwide. Partial SDS resistance has been demonstrated in multiple soybean cultivars. This study aimed to highlight proteomic changes in soybean roots by identifying proteins which are differentially expressed in near isogenic lines (NILs) contrasting at the Rhg1/Rfs2 locus for partial resistance or susceptibility to SDS. Two-dimensional gel electrophoresis resolved approximately 1000 spots on each gel; 12 spots with a significant (P < 0.05) difference in abundance of 1.5-fold or more were picked, trypsin-digested, and analyzed using quadruple time-of-flight tandem mass spectrometry. Several spots contained more than one protein, so that 18 distinct proteins were identified overall. A functional analysis performed to categorize the proteins depicted that the major pathways altered by fungal infection include disease resistance, stress tolerance, and metabolism. This is the first report which identifies proteins whose abundances are altered in response to fungal infection leading to SDS. The results provide valuable information about SDS resistance in soybean plants, and plant partial resistance responses in general. More importantly, several of the identified proteins could be good candidates for the development of SDS-resistant soybean plants.
猝死综合征(SDS)是大豆(Glycine max)的两种病害的复合体,由土壤传播的致病真菌尖镰孢菌(Fusarium virguliforme)引起。根腐病和叶焦病在全球范围内均导致显著的产量损失。多个大豆品种已表现出对SDS的部分抗性。本研究旨在通过鉴定在Rhg1/Rfs2位点对SDS具有部分抗性或易感性的近等基因系(NIL)中差异表达的蛋白质,来突出大豆根系中的蛋白质组变化。二维凝胶电泳在每张凝胶上分离出约1000个斑点;挑选出12个丰度差异显著(P < 0.05)且差异倍数在1.5倍或以上的斑点,进行胰蛋白酶消化,并使用四极杆飞行时间串联质谱进行分析。几个斑点包含不止一种蛋白质,因此总共鉴定出18种不同的蛋白质。对这些蛋白质进行的功能分析表明,真菌感染改变的主要途径包括抗病性、胁迫耐受性和代谢。这是第一份鉴定出因导致SDS的真菌感染而丰度发生改变的蛋白质的报告。这些结果为大豆植株的SDS抗性以及一般植物的部分抗性反应提供了有价值的信息。更重要的是,几种鉴定出的蛋白质可能是培育抗SDS大豆植株的良好候选对象。