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一种抗传染性鲑鱼贫血病毒单克隆抗体的特性与应用

Characterization and applications of a monoclonal antibody against infectious salmon anaemia virus.

作者信息

Falk K, Namork E, Dannevig B H

机构信息

National Veterinary Institute, Oslo, Norway.

出版信息

Dis Aquat Organ. 1998 Oct 8;34(2):77-85. doi: 10.3354/dao034077.

Abstract

The preparation of the first monoclonal antibody (MAb) against the orthomyxovirus-like infectious salmon anaemia (ISA) virus is described. Characterization of the MAb included isotyping, enzyme-linked immunosorbent assay (ELISA), immunofluorescent staining of virus infected cell cultures (SHK-1 cells), immunoelectron microscopy (IEM) of negatively stained virus preparations, virus neutralization assay and haemagglutination inhibition assay. The MAb reacted with ISA virus preparations both with immunofluorescent staining and in ELISA. No reactions were observed in cell cultures infected with other viruses infecting salmonids including infectious pancreatic necrosis (IPN) virus, viral haemorrhagic septicaemia (VHS) virus and infectious haematopoietic necrosis (IHN) virus. The MAb was also shown to neutralize ISA virus infection in cell cultures and to inhibit the haemagglutination reaction. IEM demonstrated binding to the surface of negatively stained ISA virions. Thus, it is concluded that the MAb binds to the haemagglutinin on the virion surface. Furthermore, using immunofluorescent staining of virus infected cell cultures, reactivity against all the 13 ISA virus strains currently available was demonstrated. Using the MAb, a simple, rapid direct immunofluorescent assay for ISA virus detection and titration in 96-well tissue culture plates was developed. Infectivity titrations by this method correlated well with titration by cytopathic effects. The reliability of the assay was demonstrated by close agreement in virus infectivity titres among different assays for the same virus that were performed on the same day and on different days. A method for detection of viral antigen in cryosections from ISA diseased fish is also reported that may prove useful for the diagnosis and control of ISA.

摘要

本文描述了针对正黏液病毒样传染性鲑鱼贫血症(ISA)病毒的第一种单克隆抗体(MAb)的制备方法。该单克隆抗体的特性鉴定包括:确定其免疫球蛋白类型、酶联免疫吸附测定(ELISA)、对病毒感染的细胞培养物(SHK - 1细胞)进行免疫荧光染色、对经负染色的病毒制剂进行免疫电子显微镜检查(IEM)、病毒中和试验以及血凝抑制试验。该单克隆抗体通过免疫荧光染色和ELISA与ISA病毒制剂发生反应。在用包括传染性胰腺坏死(IPN)病毒、病毒性出血性败血症(VHS)病毒和传染性造血坏死(IHN)病毒等其他感染鲑鱼的病毒感染的细胞培养物中未观察到反应。该单克隆抗体还显示出在细胞培养物中可中和ISA病毒感染并抑制血凝反应。免疫电子显微镜检查表明其与经负染色的ISA病毒粒子表面结合。因此,可以得出结论,该单克隆抗体与病毒粒子表面的血凝素结合。此外,通过对病毒感染的细胞培养物进行免疫荧光染色,证明该单克隆抗体对目前可用的所有13种ISA病毒株均有反应。利用该单克隆抗体,开发了一种在96孔组织培养板中用于检测和滴定ISA病毒的简单、快速的直接免疫荧光测定法。通过这种方法进行的感染性滴定与通过细胞病变效应进行的滴定相关性良好。同一天和不同天对同一病毒进行的不同测定之间的病毒感染性滴度密切一致,证明了该测定法的可靠性。还报道了一种检测ISA患病鱼冷冻切片中病毒抗原的方法,该方法可能对ISA的诊断和控制有用。

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