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Antigen capture ELISA system for henipaviruses using polyclonal antibodies obtained by DNA immunization
Authors:Yoshihiro Kaku  Akira Noguchi  Glenn A Marsh  Jennifer A Barr  Akiko Okutani  Kozue Hotta  Boldbaatar Bazartseren  Christopher C Broder  Akio Yamada  Satoshi Inoue  Lin-Fa Wang
Institution:Department of Veterinary Science, National Institute of Infectious Diseases, 1-23-1, Toyama, Shinjuku, Tokyo 162-8640, Japan. ykaku@nih.go.jp
Abstract:A novel antigen-capture sandwich ELISA system targeting the glycoproteins of the henipaviruses Nipah virus (NiV) and Hendra virus (HeV) was developed. Utilizing purified polyclonal antibodies derived from NiV glycoprotein-encoding DNA-immunized rabbits, we established a system that can detect the native antigenic structures of the henipavirus surface glycoproteins using simplified and inexpensive methods. The lowest detection limit against live viruses was achieved for NiV Bangladesh strain, 2.5 × 10(4) TCID(50). Considering the recent emergence of genetic variants of henipaviruses and the resultant problems that arise for PCR-based detection, this system could serve as an alternative rapid diagnostic and detection assay.
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