Neutralization assays for differential henipavirus serology using Bio-Plex Protein Array Systems

被引:104
作者
Bossart, Katharine N.
McEachern, Jennifer A.
Hickey, Andrew C.
Choudhry, Vidita
Dimitrov, Dimiter S.
Eaton, Bryan T.
Wang, Lin-Fa
机构
[1] CSIRO, Livestock Ind, Australian Anim Hlth Lab, Geelong, Vic 3220, Australia
[2] Uniformed Serv Univ Hlth Sci, Dept Microbiol & Immunol, Bethesda, MD 20814 USA
[3] CCR, Prot Interact Grp, CCRNP, Frederick, MD 21702 USA
关键词
Hendra; Nipah; envelope; receptor; multiplexed neutralization;
D O I
10.1016/j.jviromet.2007.01.003
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Hendra virus (HeV) and Nipah virus (NiV) are related emerging paramyxoviruses classified in the genus Henipavirus. Both cause fatal disease in animals and humans and are classified as biosafety level 4 pathogens. Here we detail two new multiplexed microsphere assays, one for antibody detection and differentiation and another designed as a surrogate for virus neutralization. Both assays utilize recombinant soluble attachment glycoproteins (sG) whereas the latter incorporates the cellular receptor, recombinant ephrin-B2. Spectrally distinct sG(HeV)- and sG(NiV)-coupled microspheres preferentially bound antibodies from HeV- and NiV-seropositive animals, demonstrating a simple procedure to differentiate antibodies to these closely related viruses. Soluble ephrin-B2 bound sG-coupled microspheres in a dose-dependent fashion. Specificity of binding was further evaluated with henipavirus G-specific sera and MAbs. Sera from henipavirus-seropositive animals differentially blocked ephrin-B2 binding, suggesting that detection and differentiation of HeV and NiV neutralizing antibodies can be done simultaneously in the absence of live virus. (c) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:29 / 40
页数:12
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