Enzyme-linked immunosorbent assay using a virus type-specific peptide based on a subdomain of envelope protein E-rns for serologic diagnosis of pestivirus infections in swine

Citation
Jpm. Langedijk et al., Enzyme-linked immunosorbent assay using a virus type-specific peptide based on a subdomain of envelope protein E-rns for serologic diagnosis of pestivirus infections in swine, J CLIN MICR, 39(3), 2001, pp. 906-912
Citations number
28
Categorie Soggetti
Clinical Immunolgy & Infectious Disease",Microbiology
Journal title
JOURNAL OF CLINICAL MICROBIOLOGY
ISSN journal
00951137 → ACNP
Volume
39
Issue
3
Year of publication
2001
Pages
906 - 912
Database
ISI
SICI code
0095-1137(200103)39:3<906:EIAUAV>2.0.ZU;2-X
Abstract
Peptides deduced from the C-terminal end (residues 191 to 227) of pestiviru s envelope protein E-rns were used to develop enzyme-linked immunosorbent a ssays (ELISAs) to measure specifically antibodies against different types o f pestiviruses. The choice of the peptide was based on the modular structur e of the E-rns protein, and the peptide was selected for its probable indep endent folding and good exposure,,which would make it a good candidate for an antigenic peptide to be used in a diagnostic test. A solid-phase peptide ELISA which was cross-reactive for several types of pestivirus antibodies and which fan be used for the general detection of pestivirus antibodies wa s developed. To identify type-specific pestivirus antibodies, a liquid-phas e peptide ELISA, with a labeled, specific classical swine fever virus (CSFV ) peptide and an unlabeled bovine viral diarrhea virus peptide to block cro ss-reactivity, was developed. Specificity and sensitivity of the liquid-pha se peptide ELISA for CSFV were 98 anti 100%, respectively. Because the pept ide is a fragment of the E-rns protein, it can be used to differentiate bet ween infected and vaccinated animals when a vaccine based on the E2 protein , which is another pestivirus envelope protein, is used.