Literature DB >> 10328532

Fluorescent and electron-microscopy immunoassays employing polyclonal and monoclonal antibodies for detection of goose parvovirus infection.

M Alexandrov1, R Alexandrova, I Alexandrov, S Zacharieva, S Lasarova, L Doumanova, R Peshev, T Donev.   

Abstract

Polyclonal antibodies (PAbs) raised in geese and eight mice hybridomas secreting monoclonal antibodies (MAbs) against the goose parvovirus (GPV) were prepared. They were used for development of immunofluorescence (IF) and immunoelectron-microscopic (IEM) techniques to demonstrate the GPV infection in infected organs and biological fluids. The GPV antigens were established by immunofluorescence within the nuclei and the cytoplasm of many infected cells of the chorioallantoic membrane of goose and Peckin duck embryos, liver and heart of mortally diseased goslings. By means of IEM it was possible to detect the GPV in native organ homogenate supernatants and allantoic fluids. All techniques used in the study could be successfully applied for rapid diagnosis of the GPV infection. The test systems on the basis of MAbs should, however, be preferred. By means of immunoblotting (IB) using PAbs and MAbs four viral proteins (VP) with MW 88, 77, 65 and 60 kDa were demonstrated. Contrary to the others the VP with MW 65 kDa was the most antigenically reactive though invisible in the SDS-PAGE and Coomassie-blue dye-stained preparations.

Entities:  

Mesh:

Substances:

Year:  1999        PMID: 10328532     DOI: 10.1016/s0166-0934(98)00175-x

Source DB:  PubMed          Journal:  J Virol Methods        ISSN: 0166-0934            Impact factor:   2.014


  4 in total

1.  Development of a fluorescent quantitative real-time polymerase chain reaction assay for the detection of Goose parvovirus in vivo.

Authors:  Jin-Long Yang; An-Chun Cheng; Ming-Shu Wang; Kang-Cheng Pan; Min Li; Yu-Fei Guo; Chuan-Feng Li; De-Kang Zhu; Xiao-Yue Chen
Journal:  Virol J       Date:  2009-09-15       Impact factor: 4.099

2.  Development of a restriction length polymorphism combined with direct PCR technique to differentiate goose and Muscovy duck parvoviruses.

Authors:  Chun-He Wan; Hong-Mei Chen; Qiu-Ling Fu; Shao-Hua Shi; Guang-Hua Fu; Long-Fei Cheng; Cui-Teng Chen; Yu Huang; Kai-Hui Hu
Journal:  J Vet Med Sci       Date:  2016-02-05       Impact factor: 1.267

3.  Development of a duplex SYBR Green I-based quantitative real-time PCR assay for the rapid differentiation of goose and Muscovy duck parvoviruses.

Authors:  Su Lin; Shao Wang; Xiaoxia Cheng; Shifeng Xiao; Xiuqin Chen; Shilong Chen; Shaoying Chen; Fusong Yu
Journal:  Virol J       Date:  2019-01-10       Impact factor: 4.099

4.  Characterization of monoclonal antibodies against waterfowl parvoviruses VP3 protein.

Authors:  Xiuchen Yin; Shumei Zhang; Youlan Gao; Jinzhe Li; Shuyi Tan; Hongyu Liu; Xiaoying Wu; Yuhuan Chen; Ming Liu; Yun Zhang
Journal:  Virol J       Date:  2012-11-23       Impact factor: 4.099

  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.