Zhang Jing-Yan, Liu Qing-Hui, Huang Jie
Yellow Sea Fisheries Research Institute, Chinese Academy of Fishery Sciences, Qingdao, 266071, P. R. China.
J Biosci. 2014 Jun;39(3):381-8. doi: 10.1007/s12038-014-9418-z.
The recognition and attachment of virus to its host cell surface is a critical step for viral infection. Recent research revealed that beta-integrin was involved in White spot syndrome virus (WSSV) infection. In this study, the interaction of beta-integrin with structure proteins of WSSV and motifs involved in WSSV infection was examined. The results showed that envelope proteins VP26, VP31, VP37, VP90 and nucleocapsid protein VP136 interacted with LvInt. RGD-, YGL- and LDV-related peptide functioned as motifs of WSSV proteins binding with beta-integrin. The beta-integrin ligand of RGDT had better blocking effect compared with that of YGL- and LDV-related peptides. In vivo assay indicated that RGD-, LDV- and YGL-related peptides could partially block WSSV infection. These data collectively indicate that multiple proteins were involved in recognition of beta-integrin. Identification of proteins in WSSV that are associated with beta-integrin will assist development of new agents for effective control of the white spot syndrome.
病毒识别并附着于宿主细胞表面是病毒感染的关键步骤。最近的研究表明,β-整合素参与了白斑综合征病毒(WSSV)的感染。在本研究中,检测了β-整合素与WSSV结构蛋白的相互作用以及参与WSSV感染的基序。结果显示,包膜蛋白VP26、VP31、VP37、VP90和核衣壳蛋白VP136与LvInt相互作用。RGD-、YGL-和LDV相关肽作为WSSV蛋白与β-整合素结合的基序。与YGL-和LDV相关肽相比,RGDT的β-整合素配体具有更好的阻断效果。体内试验表明,RGD-、LDV-和YGL相关肽可部分阻断WSSV感染。这些数据共同表明,多种蛋白参与了β-整合素的识别。鉴定WSSV中与β-整合素相关的蛋白将有助于开发有效控制白斑综合征的新型药物。