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利用抗VP2蛋白单克隆抗体鉴定新型阿留申水貂病病毒B细胞表位

Identification of a novel Aleutian mink disease virus B-cell epitope using a monoclonal antibody against VP2 protein.

作者信息

Yi Li, Cheng Yuening, Zhang Miao, Cao Zhigang, Tong Mingwei, Cheng Shipeng, Yan Xijun

机构信息

Institute of Special Wild Economic Animal and Plant Science, Chinese Academy of Agricultural Sciences, 4899 Juye Street, Changchun, Jilin Province, PR China.

Institute of Special Wild Economic Animal and Plant Science, Chinese Academy of Agricultural Sciences, 4899 Juye Street, Changchun, Jilin Province, PR China.

出版信息

Virus Res. 2016 Sep 2;223:39-42. doi: 10.1016/j.virusres.2016.06.014. Epub 2016 Jun 25.

Abstract

Aleutian mink disease virus (AMDV) is a parvovirus that causes an immune complex-mediated disease in minks. Capsid protein VP2 is a major structural viral protein and can be used to diagnose AMDV. In this study, a specific monoclonal antibody, 1M13, was produced against the AMDV VP2 protein (amino acids 291-502). A linear VP2-protein epitope was identified by subjecting a series of partially overlapping synthesized peptides to be enzyme-linked immunosorbent assay (ELISA) analysis. The results indicated that (386)HLQQNFSTRYIYD(398) was the minimal linear epitope that could be recognized by mAb 1M13. ELISA assays revealed that mink anti-AMDV sera could also recognize the minimal linear epitope. Sequence alignments demonstrated that the linear epitope is highly conserved among AMDV strains except (386)H and is less conserved among Raccoon dog amdovirus, Gray fox amdovirus, Red fox amdovirus, Bat parvovirus and Mink enteritis parvovirus. Taken together, the generation of this VP2-specific mAb with a defined linear peptide epitope may have potential applications in the development of suitable diagnostic techniques for AMDV.

摘要

阿留申水貂病病毒(AMDV)是一种细小病毒,可在水貂中引起免疫复合物介导的疾病。衣壳蛋白VP2是主要的病毒结构蛋白,可用于诊断AMDV。在本研究中,制备了一种针对AMDV VP2蛋白(氨基酸291 - 502)的特异性单克隆抗体1M13。通过对一系列部分重叠的合成肽进行酶联免疫吸附测定(ELISA)分析,鉴定出一个线性VP2蛋白表位。结果表明,(386)HLQQNFSTRYIYD(398)是单克隆抗体1M13能够识别的最小线性表位。ELISA分析显示,水貂抗AMDV血清也能识别该最小线性表位。序列比对表明,除了(386)H之外,该线性表位在AMDV毒株中高度保守,而在貉细小病毒、灰狐细小病毒、赤狐细小病毒、蝙蝠细小病毒和水貂肠炎细小病毒中保守性较低。综上所述,这种具有明确线性肽表位的VP2特异性单克隆抗体的产生可能在开发适用于AMDV的诊断技术方面具有潜在应用。

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