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http://krishi.icar.gov.in/jspui/handle/123456789/53142
Title: | Recombinant non-structural polyprotein 3AB-based serodiagnostic strategy for FMD surveillance in bovines irrespective of vaccination |
Other Titles: | Not Available |
Authors: | Jajati K Mohapatra Laxmi K Pandey Aniket Sanyal Bramhadev Pattnaik |
ICAR Data Use Licennce: | http://krishi.icar.gov.in/PDF/ICAR_Data_Use_Licence.pdf |
Author's Affiliated institute: | ICAR:-Project Directorate on Foot and Mouth Disease |
Published/ Complete Date: | 2011-11-01 |
Project Code: | Not Available |
Keywords: | FMD serosurveillance, Recombinant 3AB, Indirect ELISA |
Publisher: | Elsevier |
Citation: | Mohapatra JK, Pandey LK, Sanyal A, Pattnaik B. Recombinant non-structural polyprotein 3AB-based serodiagnostic strategy for FMD surveillance in bovines irrespective of vaccination. J Virol Methods. 2011 Nov;177(2):184-92. doi: 10.1016/j.jviromet.2011.08.006. Epub 2011 Aug 11. PMID: 21864578. |
Series/Report no.: | Not Available; |
Abstract/Description: | In India, the proportion of bovines vaccinated against foot-and-mouth disease (FMD) is increasing since the implementation of the Government supported ‘FMD Control Programme’, and non-structural protein (NSP)-based serological assays for discriminating between antibodies induced by infection or vaccination (DIVA) could be useful. The FMD virus NSP 3AB was expressed in a prokaryotic system and an indirect ELISA (r3AB3 I-ELISA) was developed and validated as a screening assay for detecting virus in vaccinated bovines. The diagnostic sensitivity of the assay was estimated to be 96%, while the diagnostic specificity varied between the naïve and vaccinates as 99.1% and 96.4%, respectively. This assay could detect antibodies to 3AB (3AB-Ab) from 10 to as late as 900 days post-infection in cattle infected experimentally. The “in-house” assay demonstrated higher sensitivity than a commercial 3ABC ELISA kit particularly with samples obtained from the late stages of infection. Transient post-vaccinal 3AB-Ab response could be detected in one of the three commercial vaccines during the six-month vaccination regimen, which emphasizes the fact that for a DIVA-compatible diagnostic strategy to be a realistic option, all vaccines need to be quality checked for the NSP content. |
Description: | Not Available |
ISSN: | Not Available |
Type(s) of content: | Research Paper |
Sponsors: | Not Available |
Language: | English |
Name of Journal: | Journal of Virological Methods |
NAAS Rating: | 7.79 |
Volume No.: | 177 (2) |
Page Number: | 184-192 |
Name of the Division/Regional Station: | Not Available |
Source, DOI or any other URL: | https://www.sciencedirect.com/science/article/abs/pii/S0166093411003247?via%3Dihub |
URI: | http://krishi.icar.gov.in/jspui/handle/123456789/53142 |
Appears in Collections: | AS-PDFMD-Publication |
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