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抗汉坦病毒核衣壳蛋白单克隆抗体的鉴定及其在啮齿动物和人组织样本免疫组化中的应用。

Characterization of monoclonal antibodies against hantavirus nucleocapsid protein and their use for immunohistochemistry on rodent and human samples.

机构信息

Institute of Biotechnology, Vilnius University, V. Graičiūno 8, 02241 Vilnius, Lithuania.

出版信息

Arch Virol. 2011 Mar;156(3):443-56. doi: 10.1007/s00705-010-0879-6. Epub 2010 Dec 16.

Abstract

Monoclonal antibodies are important tools for various applications in hantavirus diagnostics. Recently, we generated Puumala virus (PUUV)-reactive monoclonal antibodies (mAbs) by immunisation of mice with chimeric polyomavirus-derived virus-like particles (VLPs) harbouring the 120-amino-acid-long amino-terminal region of the PUUV nucleocapsid (N) protein. Here, we describe the generation of two mAbs by co-immunisation of mice with hexahistidine-tagged full-length N proteins of Sin Nombre virus (SNV) and Andes virus (ANDV), their characterization by different immunoassays and comparison with the previously generated mAbs raised against a segment of PUUV N protein inserted into VLPs. All of the mAbs reacted strongly in ELISA and western blot tests with the antigens used for immunization and cross-reacted to varying extents with N proteins of other hantaviruses. All mAbs raised against a segment of the PUUV N protein presented on chimeric VLPs and both mAbs raised against the full-length AND/SNV N protein reacted with Vero cells infected with different hantaviruses. The reactivity of mAbs with native viral nucleocapsids was also confirmed by their reactivity in immunohistochemistry assays with kidney tissue specimens from experimentally SNV-infected rodents and human heart tissue specimens from hantavirus cardiopulmonary syndrome patients. Therefore, the described mAbs represent useful tools for the immunodetection of hantavirus infection.

摘要

单克隆抗体是汉坦病毒诊断中各种应用的重要工具。最近,我们通过用嵌合多瘤病毒衍生的病毒样颗粒(VLPs)免疫小鼠,生成了对普马拉病毒(PUUV)有反应的单克隆抗体(mAbs),这些 VLPs 携带了长度为 120 个氨基酸的 PUUV 核衣壳(N)蛋白的氨基末端区域。在这里,我们描述了通过用六组氨酸标记的辛诺柏病毒(SNV)和安第斯病毒(ANDV)全长 N 蛋白共同免疫小鼠生成两种 mAbs,并用不同的免疫分析方法对其进行了表征,并与之前用插入 VLPs 的 PUUV N 蛋白片段生成的 mAbs 进行了比较。所有 mAbs 在 ELISA 和 Western blot 试验中与用于免疫的抗原强烈反应,并与其他汉坦病毒的 N 蛋白不同程度地发生交叉反应。所有针对嵌合 VLPs 上的 PUUV N 蛋白片段生成的 mAbs 以及针对全长 AND/SNV N 蛋白生成的两种 mAbs 都与感染不同汉坦病毒的 Vero 细胞反应。mAbs 与天然病毒核衣壳的反应性也通过它们在免疫组织化学试验中与实验性 SNV 感染啮齿动物的肾脏组织标本和汉坦病毒心肺综合征患者的人类心脏组织标本的反应性得到了证实。因此,所描述的 mAbs 代表了用于汉坦病毒感染免疫检测的有用工具。

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