Your browser doesn't support javascript.
loading
The use of an indirect ELISA with protein G-peroxidase conjugate and a blocking ELISA to demonstrate recent bluetongue infection in sheep.
Lunt, R A; Blacksell, S D; Newberry, K M.
Affiliation
  • Lunt RA; CSIRO Australian Animal Health Laboratory, Institute of Animal Production and Processing, Geelong.
J Virol Methods ; 48(1): 53-63, 1994 Jun.
Article in En | MEDLINE | ID: mdl-7962260
ABSTRACT
The humoral immune response of sheep infected with bluetongue virus serotypes 3, 9 and 16 was monitored by plaque inhibition (PI), blocking ELISA (BELISA) and indirect ELISA over a period of 63 days post-infection. Results indicated that testing of a single plasma or serum sample by both a BELISA and an indirect ELISA using a recombinant streptococcal protein G (PrG) peroxidase conjugate enabled an assessment of the proximity of a recent infection based on the failure of PrG to bind ovine IgM class antibodies. When BELISA and indirect ELISA results were expressed as a ratio, values indicative of recent infection (> or = 5) were observed for an average duration of 16.5 days (range 8 to 23 days) following the initial detection of antibody by BELISA. This approach has potential to improve diagnosis of a wide range of virus infections by providing an indicator for the relationship of serological status with a recent infection. However, where reinfection may occur, as with bluetongue virus, alternative methods may be required for definitive diagnosis.
Subject(s)
Search on Google
Collection: 01-internacional Database: MEDLINE Main subject: Enzyme-Linked Immunosorbent Assay / Bluetongue / Bluetongue virus / Antibodies, Viral Limits: Animals Language: En Journal: J Virol Methods Year: 1994 Type: Article
Search on Google
Collection: 01-internacional Database: MEDLINE Main subject: Enzyme-Linked Immunosorbent Assay / Bluetongue / Bluetongue virus / Antibodies, Viral Limits: Animals Language: En Journal: J Virol Methods Year: 1994 Type: Article