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...
Published in: | Aquaculture International |
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Main Authors: | , , |
Format: | Article in Journal/Newspaper |
Language: | English |
Published: |
Springer
1994
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Subjects: | |
Online Access: | https://hdl.handle.net/20.500.12792/4642 http://hdl.handle.net/10261/294717 https://doi.org/10.1007/BF00231516 |
_version_ | 1821703169793589248 |
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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 |
record_format | openpolar |
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 |