Venkataraman Sangita, Selvarajan Ramasamy, Subramanian Sundaram S, Handanahalli Savithri S
Department of Biotechnology, Anna University, Guindy, Chennai, 600025 India.
ICAR National Research Centre for Banana, Thayanur Post, Tiruchirapalli, 620102 India.
3 Biotech. 2022 Jul;12(7):144. doi: 10.1007/s13205-022-03204-4. Epub 2022 Jun 7.
Banana is the major staple food crop for approximately 400 million people. Bunchy top disease of banana is one of the most devastating diseases caused by banana bunchy top virus (BBTV), which results in stunting of plants, bunchy appearance of leaves and a significant loss of yield. While many isolates of BBTV from various regions of India have been characterized by different groups, no structural study exists for this important virus. To bridge this gap, the pET28a clone of the coat protein (CP) gene from BBTV isolate of Hill banana grown in lower Pulney Hills (Virupakshi) of Tamilnadu was expressed in BL21 (DE3) pLysS. Purification of the CP was achieved by Ni-NTA affinity chromatography. In vitro capsid assembly studied using sucrose density gradient centrifugation suggested that the CP did not assemble as a virus-like particle (VLP), but remained as smaller oligomers. Studies using dynamic light scattering (DLS) indicate that the purified protein is poly-dispersed, represented majorly as pentamers. Homology modeling studies provided useful insights into the probable fold of the CP suggesting that it is a β-sandwich, similar to that seen in the majority of plant viruses. In silico capsid reconstruction aided the understanding of the quaternary organization of subunits in the capsid and their molecular interactions. The location of the aphid-binding EAG motif was identified on the surface loops close to the pentameric axis indicating its role in vector-mediated transmission. Comparison with the CP and capsid structure of geminiviruses provided useful insights into the mode of nucleic acid binding and the role of genome during capsid assembly.
The online version contains supplementary material available at 10.1007/s13205-022-03204-4.
香蕉是约4亿人的主要主食作物。香蕉束顶病是由香蕉束顶病毒(BBTV)引起的最具毁灭性的病害之一,会导致植株矮化、叶片呈束状,并造成显著的产量损失。虽然印度不同地区的许多BBTV分离株已被不同研究团队进行了特征分析,但对于这种重要病毒尚无结构研究。为填补这一空白,从泰米尔纳德邦下普尔内山(维鲁帕克希)种植的山地香蕉的BBTV分离株中获取的外壳蛋白(CP)基因的pET28a克隆在BL21(DE3)pLysS中表达。通过镍-氮三乙酸亲和层析法实现了CP的纯化。使用蔗糖密度梯度离心法进行的体外衣壳组装研究表明,CP并未组装成病毒样颗粒(VLP),而是以较小的寡聚体形式存在。使用动态光散射(DLS)的研究表明,纯化后的蛋白具有多分散性,主要以五聚体形式存在。同源建模研究为CP可能的折叠方式提供了有用的见解,表明它是一种β-三明治结构,类似于大多数植物病毒中的结构。计算机辅助衣壳重建有助于理解衣壳中亚基的四级结构及其分子相互作用。在靠近五聚体轴的表面环上鉴定出了蚜虫结合EAG基序的位置,表明其在载体介导的传播中的作用。与双生病毒的CP和衣壳结构进行比较,为核酸结合模式和衣壳组装过程中基因组的作用提供了有用的见解。
在线版本包含可在10.1007/s13205-022-03204-4获取的补充材料。