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Clinical and Diagnostic Laboratory Immunology, July 2000, p. 645-651, Vol. 7, No. 4
INGENASA, 28037 Madrid,1 and Centro Nacional de
Biotecnologia (CSIC-UAM), 28049 Madrid,2 Spain
Received 31 January 2000/Returned for modification 4 April
2000/Accepted 5 May 2000
The routine technique for detecting antibodies specific to
infectious bursal disease virus (IBDV) is a serological evaluation by
enzyme-linked immunosorbent assay (ELISA) with preparations of whole
virions as the antigens. To avoid using complete virus in the standard
technique, we have developed two new antigens through the expression of
the VPX and VP3 genes in insect cells. VPX and especially VP3 were
expressed at high levels in insect cells and simple to purify. The
immunogenicity of both proteins was similar to that of the native
virus. VPX was able to elicit neutralizing antibodies but VP3 was not.
Purified VPX and VP3 were tested in an indirect ELISA with more than
300 chicken sera. There was an excellent correlation between the
results of the ELISA using VPX and those of the two commercial kits.
VP3 did not perform as well as VPX, and the linear correlation was
significantly lower. A comparison with the standard reference
technique, seroneutralization, showed that the indirect ELISA was more
sensitive. Therefore, VPX-based ELISA is a good alternative to
conventional ELISAs that use whole virions.
1071-412X/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.
Antigenic Properties and Diagnostic Potential of
Baculovirus-Expressed Infectious Bursal Disease Virus Proteins VPX
and VP3
*
Corresponding author. Mailing address: INGENASA, Hnos
Garcia Noblejas 41, 4, 28037 Madrid, Spain. Phone: 34 91 3680501. Fax: 34 91 4087598. E-mail: icasal{at}ingenasa.es.
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