A sandwich ELISA to detect VHSV and IPNV in turbot

The recent demonstration that reared turbot (Scophthalmus maximus L) is a natural host for salmonid rhabdoviruses has made their rapid detection relevant to these fish species. A unique protocol to select and use non-competitive monoclonal antibodies (Mabs) for two high-sensitivity sandwich ELISAs h...

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Published in:Aquaculture International
Main Authors: Vázquez Brañas, M., Coll Morales,, Julio, Estepa, A.
Format: Article in Journal/Newspaper
Language:English
Published: Springer 1994
Subjects:
Online Access:https://hdl.handle.net/20.500.12792/4642
http://hdl.handle.net/10261/294717
https://doi.org/10.1007/BF00231516
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author Vázquez Brañas, M.
Coll Morales,, Julio
Estepa, A.
author_facet Vázquez Brañas, M.
Coll Morales,, Julio
Estepa, A.
author_sort Vázquez Brañas, M.
collection Digital.CSIC (Spanish National Research Council)
container_issue 3
container_title Aquaculture International
container_volume 2
description The recent demonstration that reared turbot (Scophthalmus maximus L) is a natural host for salmonid rhabdoviruses has made their rapid detection relevant to these fish species. A unique protocol to select and use non-competitive monoclonal antibodies (Mabs) for two high-sensitivity sandwich ELISAs has been developed to detect both infectious pancreatic necrosis virus (IPNV) and viral haemorrhagic septicaemia virus (VHSV) in turbot kidney extracts to assess the possibility of using them in field diagnosis. For maximum sensitivity, turbot kidney extracts can be two-fold diluted with high-ionic strength buffers and assayed for the presence of the major viral proteins (VMS rhabdovirus nucleoprotein N/Nx and/or IPN birnavirus protein VP3). The use of control plates coated with irrelevant mouse antibodies (IgG1 and IgG2a) in parallel ELISAs allows for a precise estimation of possible false positives. Turbot kidney extracts with low levels of virus might now be assayed directly without using cell culture, with high precision and in a short time during the acute phase of these viral diseases in reared turbot. © 1994, Chapman & Hall. All rights reserved.
format Article in Journal/Newspaper
genre Scophthalmus maximus
Turbot
genre_facet Scophthalmus maximus
Turbot
id ftcsic:oai:digital.csic.es:10261/294717
institution Open Polar
language English
op_collection_id ftcsic
op_doi https://doi.org/20.500.12792/464210.1007/BF00231516
op_relation Aquaculture International 2: 206-217 (1994)
0967-6120
http://hdl.handle.net/20.500.12792/4642
http://hdl.handle.net/10261/294717
doi:10.1007/BF00231516
1573-143X
op_rights none
publishDate 1994
publisher Springer
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spelling ftcsic:oai:digital.csic.es:10261/294717 2025-01-17T00:41:05+00:00 A sandwich ELISA to detect VHSV and IPNV in turbot Vázquez Brañas, M. Coll Morales,, Julio Estepa, A. 1994 https://hdl.handle.net/20.500.12792/4642 http://hdl.handle.net/10261/294717 https://doi.org/10.1007/BF00231516 en eng Springer Aquaculture International 2: 206-217 (1994) 0967-6120 http://hdl.handle.net/20.500.12792/4642 http://hdl.handle.net/10261/294717 doi:10.1007/BF00231516 1573-143X none Turbot (Scophthalmus maximus) Viral diseases VHSV IPNV Mabs Diagnosis ELISA journal article 1994 ftcsic https://doi.org/20.500.12792/464210.1007/BF00231516 2024-01-16T11:37:21Z The recent demonstration that reared turbot (Scophthalmus maximus L) is a natural host for salmonid rhabdoviruses has made their rapid detection relevant to these fish species. A unique protocol to select and use non-competitive monoclonal antibodies (Mabs) for two high-sensitivity sandwich ELISAs has been developed to detect both infectious pancreatic necrosis virus (IPNV) and viral haemorrhagic septicaemia virus (VHSV) in turbot kidney extracts to assess the possibility of using them in field diagnosis. For maximum sensitivity, turbot kidney extracts can be two-fold diluted with high-ionic strength buffers and assayed for the presence of the major viral proteins (VMS rhabdovirus nucleoprotein N/Nx and/or IPN birnavirus protein VP3). The use of control plates coated with irrelevant mouse antibodies (IgG1 and IgG2a) in parallel ELISAs allows for a precise estimation of possible false positives. Turbot kidney extracts with low levels of virus might now be assayed directly without using cell culture, with high precision and in a short time during the acute phase of these viral diseases in reared turbot. © 1994, Chapman & Hall. All rights reserved. Article in Journal/Newspaper Scophthalmus maximus Turbot Digital.CSIC (Spanish National Research Council) Aquaculture International 2 3
spellingShingle Turbot (Scophthalmus maximus)
Viral diseases
VHSV
IPNV
Mabs
Diagnosis
ELISA
Vázquez Brañas, M.
Coll Morales,, Julio
Estepa, A.
A sandwich ELISA to detect VHSV and IPNV in turbot
title A sandwich ELISA to detect VHSV and IPNV in turbot
title_full A sandwich ELISA to detect VHSV and IPNV in turbot
title_fullStr A sandwich ELISA to detect VHSV and IPNV in turbot
title_full_unstemmed A sandwich ELISA to detect VHSV and IPNV in turbot
title_short A sandwich ELISA to detect VHSV and IPNV in turbot
title_sort sandwich elisa to detect vhsv and ipnv in turbot
topic Turbot (Scophthalmus maximus)
Viral diseases
VHSV
IPNV
Mabs
Diagnosis
ELISA
topic_facet Turbot (Scophthalmus maximus)
Viral diseases
VHSV
IPNV
Mabs
Diagnosis
ELISA
url https://hdl.handle.net/20.500.12792/4642
http://hdl.handle.net/10261/294717
https://doi.org/10.1007/BF00231516