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  1. KRISHI Publication and Data Inventory Repository
  2. Animal Science A4
  3. ICAR-National Institute of Veterinary Epidemiology and Disease Informatics E3
  4. AS-NIVEDI-Publication
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Please use this identifier to cite or link to this item: http://krishi.icar.gov.in/jspui/handle/123456789/71550
Title: Avidin-Biotin recombinant antigen capture ELISA for the detection of peste des petits ruminants virus in the clinical specimens of sheep and goats
Other Titles: Not Available
Authors: Balamurugan V
Varghese B
Sowjanya Kumari S
Vinod Kumar K
Muthuchelvan D
Nagalingam M
Roy P
ICAR Data Use Licennce: http://krishi.icar.gov.in/PDF/ICAR_Data_Use_Licence.pdf
Author's Affiliated institute: National Institute of Veterinary Epidemiology and Disease Informatics
Division of Virology, ICAR-Indian Veterinary Research Institute, Campus Mukteswar, Nainital, 263 138, Uttarakhand, India.
Published/ Complete Date: 2021-02-18
Project Code: Not Available
Keywords: PPR
Recombinant protein
Nucleocapsid
Polyclonal antibodies
Avidin-Biotin
Antigen capture ELISA
Diagnosis
Surveillance
Publisher: Elsevier Publishing
Citation: Balamurugan V, Varghese B, Sowjanya Kumari S, Vinod Kumar K, Muthuchelvan D, Nagalingam M, Roy P. Avidin-Biotin recombinant antigen capture ELISA for the detection of peste des petits ruminants virus in the clinical specimens of sheep and goats. J Virol Methods. 2021 May;291:114103. doi: 10.1016/j.jviromet.2021.114103. Epub 2021 Feb 18. PMID: 33610651.
Series/Report no.: Not Available;
Abstract/Description: This study describes the development of Avidin-Biotin recombinant Antigen Capture ELISA (ABrAC ELISA) for the detection of the peste des petits ruminants virus (PPRV) antigens in the clinical specimens of sheep and goats. The assay uses the truncated recombinant PPRV N-terminal immunogenic region of nucleoprotein (rPPRV-NPN) as a reference positive antigen and its polyclonal antibodies as capture/detective antibodies and the rabbit PPRV polyclonal antibodies as coating antibodies. The cut-off value was determined as double times the mean reactivity of blank control based on the reactivity of the PPR confirmed negative and positive control panel samples. On assessing the specificity with the related differential diagnosis of the disease-causing viruses and bacteria, the assay showed specific detective reactivity to PPRV. Further, on evaluation using clinical specimens (n-274) of sheep and goats, the assay showed that the relative diagnostic sensitivity of 86.49 % (95 % confidence interval (CI): 71.23–95.46 %) and diagnostic specificity of 96.20 % (95 % CI: 92.91–98.25 %) against PPRV nucleoprotein-specific monoclonal antibody-based sandwich-ELISA (PPR s-ELISA) kit, with an accuracy of 94.89 % (95 % CI: 91.58–97.18 %) and Cohen's Kappa value of 0.791 + 0.055 SE (95 % CI: 0.68−0.90) with substantial agreements. The ABrAC-ELISA is an alternative method of an immunoassay for the rapid, sensitive, and specific detection of the PPRV antigens m the clinical specimens of sheep and goats for surveillance or diagnosis of PPR. This study also shows that the rPPRV-NPN and its specific polyclonal antibodies could be the sustainable source of safe diagnostic reagents without the need to handle the infectious virus during the eradication and post-eradication phases in endemic countries like India or PPR non-endemic countries
Description: Not Available
ISSN: 0166-0934
Type(s) of content: Research Paper
Sponsors: Not Available
Language: English
Name of Journal: Journal of Virological Methods
Journal Type: Peer reviewer journal
NAAS Rating: 7.79
Impact Factor: 2.014
Volume No.: 291
Page Number: 1-7
Name of the Division/Regional Station: Not Available
Source, DOI or any other URL: 10.1016/j.jviromet.2021.114103
URI: http://krishi.icar.gov.in/jspui/handle/123456789/71550
Appears in Collections:AS-NIVEDI-Publication

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