Rainbow trout surviving infections of viral haemorrhagic septicemia virus (VHSV) show lasting antibodies to recombinant G protein fragments

Rainbow trout antibodies (Abs) binding to recombinant fragments (frgs) derived from the protein G of the viral haemorrhagic septicemia virus (VHSV)-07.71 strain, could be detected by ELISA (frg-ELISA) in sera from trout surviving laboratory-controlled infections. Abs were detected not only by using sera from trout infected with the homologous VHSV isolate but also with the VHSV-DK-201433 heterologous isolate, which had 13 amino acid changes. Sera from healthy trout and/or from trout surviving infectious haematopoietic necrosis virus (IHNV) infection, were used to calculate cut-off absorbances to differentiate negative from positive sera. Specific anti-VHSV Abs could then be detected by using any of the following frgs frg11 (56-110), frg15 (65-250), frg16 (252-450) or G21-465. While high correlations were found among the ELISA values obtained with the different frgs, no correlations between any frg-ELISA and complement-dependent 50% plaque neutralization test (PNT) titres could be demonstrated. Between 4 and 10 weeks after VHSV infection, more trout sera were detected as positives by using heterologous frg-ELISA rather than homologous PNT. Furthermore, the percentage of positive sera detected by frg11-ELISA increased with time after infection to reach 100%, while those detected by complement-dependent PNT decreased to 29.4%, thus confirming that the lack of neutralizing Abs does not mean the lack of any anti-VHSV Abs in survivor trout sera. Preliminary results with sera from field samples suggest that further refinements of the frg-ELISA could allow detection of anti-VHSV trout Abs in natural outbreaks caused by different heterologous VHSV isolates. The homologous frg-ELISA method could be useful to follow G immunization attempts during vaccine development and/or to best understand the fish Ab response during VHSV infections. The viral frgs approach might also be used with other fish species and/or viruses. © 2011 Elsevier Ltd.

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Main Authors: Encinas, Paloma, Gómez Casado, Eduardo, Fregeneda Grandes, J. M., Olesen, N. J., Lorenzen, N., Estepa, Amparo, Coll Morales, Julio
Other Authors: Encinas, Paloma [0000-0001-9596-8070]
Format: artículo biblioteca
Language:English
Published: Elsevier 2011
Subjects:Trout antibodies, Viral haemorrhagic septicemia, VHSV, G protein, Fragments,
Online Access:http://hdl.handle.net/10261/294047
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spelling dig-inia-es-10261-2940472024-10-24T13:01:17Z Rainbow trout surviving infections of viral haemorrhagic septicemia virus (VHSV) show lasting antibodies to recombinant G protein fragments Encinas, Paloma Gómez Casado, Eduardo Fregeneda Grandes, J. M. Olesen, N. J. Lorenzen, N. Estepa, Amparo Coll Morales, Julio Encinas, Paloma [0000-0001-9596-8070] Consejo Superior de Investigaciones Científicas [https://ror.org/02gfc7t72] Trout antibodies Viral haemorrhagic septicemia VHSV G protein Fragments Rainbow trout antibodies (Abs) binding to recombinant fragments (frgs) derived from the protein G of the viral haemorrhagic septicemia virus (VHSV)-07.71 strain, could be detected by ELISA (frg-ELISA) in sera from trout surviving laboratory-controlled infections. Abs were detected not only by using sera from trout infected with the homologous VHSV isolate but also with the VHSV-DK-201433 heterologous isolate, which had 13 amino acid changes. Sera from healthy trout and/or from trout surviving infectious haematopoietic necrosis virus (IHNV) infection, were used to calculate cut-off absorbances to differentiate negative from positive sera. Specific anti-VHSV Abs could then be detected by using any of the following frgs frg11 (56-110), frg15 (65-250), frg16 (252-450) or G21-465. While high correlations were found among the ELISA values obtained with the different frgs, no correlations between any frg-ELISA and complement-dependent 50% plaque neutralization test (PNT) titres could be demonstrated. Between 4 and 10 weeks after VHSV infection, more trout sera were detected as positives by using heterologous frg-ELISA rather than homologous PNT. Furthermore, the percentage of positive sera detected by frg11-ELISA increased with time after infection to reach 100%, while those detected by complement-dependent PNT decreased to 29.4%, thus confirming that the lack of neutralizing Abs does not mean the lack of any anti-VHSV Abs in survivor trout sera. Preliminary results with sera from field samples suggest that further refinements of the frg-ELISA could allow detection of anti-VHSV trout Abs in natural outbreaks caused by different heterologous VHSV isolates. The homologous frg-ELISA method could be useful to follow G immunization attempts during vaccine development and/or to best understand the fish Ab response during VHSV infections. The viral frgs approach might also be used with other fish species and/or viruses. © 2011 Elsevier Ltd. 2023-02-20T10:34:45Z 2023-02-20T10:34:45Z 2011 artículo http://purl.org/coar/resource_type/c_6501 Fish and Shellfish Immunology 30: 929-935 (2011) 1050-4648 http://hdl.handle.net/10261/294047 10.1016/j.fsi.2011.01.021 en Departamento de Biotecnología Sí none Elsevier
institution INIA ES
collection DSpace
country España
countrycode ES
component Bibliográfico
access En linea
databasecode dig-inia-es
tag biblioteca
region Europa del Sur
libraryname Biblioteca del INIA España
language English
topic Trout antibodies
Viral haemorrhagic septicemia
VHSV
G protein
Fragments
Trout antibodies
Viral haemorrhagic septicemia
VHSV
G protein
Fragments
spellingShingle Trout antibodies
Viral haemorrhagic septicemia
VHSV
G protein
Fragments
Trout antibodies
Viral haemorrhagic septicemia
VHSV
G protein
Fragments
Encinas, Paloma
Gómez Casado, Eduardo
Fregeneda Grandes, J. M.
Olesen, N. J.
Lorenzen, N.
Estepa, Amparo
Coll Morales, Julio
Rainbow trout surviving infections of viral haemorrhagic septicemia virus (VHSV) show lasting antibodies to recombinant G protein fragments
description Rainbow trout antibodies (Abs) binding to recombinant fragments (frgs) derived from the protein G of the viral haemorrhagic septicemia virus (VHSV)-07.71 strain, could be detected by ELISA (frg-ELISA) in sera from trout surviving laboratory-controlled infections. Abs were detected not only by using sera from trout infected with the homologous VHSV isolate but also with the VHSV-DK-201433 heterologous isolate, which had 13 amino acid changes. Sera from healthy trout and/or from trout surviving infectious haematopoietic necrosis virus (IHNV) infection, were used to calculate cut-off absorbances to differentiate negative from positive sera. Specific anti-VHSV Abs could then be detected by using any of the following frgs frg11 (56-110), frg15 (65-250), frg16 (252-450) or G21-465. While high correlations were found among the ELISA values obtained with the different frgs, no correlations between any frg-ELISA and complement-dependent 50% plaque neutralization test (PNT) titres could be demonstrated. Between 4 and 10 weeks after VHSV infection, more trout sera were detected as positives by using heterologous frg-ELISA rather than homologous PNT. Furthermore, the percentage of positive sera detected by frg11-ELISA increased with time after infection to reach 100%, while those detected by complement-dependent PNT decreased to 29.4%, thus confirming that the lack of neutralizing Abs does not mean the lack of any anti-VHSV Abs in survivor trout sera. Preliminary results with sera from field samples suggest that further refinements of the frg-ELISA could allow detection of anti-VHSV trout Abs in natural outbreaks caused by different heterologous VHSV isolates. The homologous frg-ELISA method could be useful to follow G immunization attempts during vaccine development and/or to best understand the fish Ab response during VHSV infections. The viral frgs approach might also be used with other fish species and/or viruses. © 2011 Elsevier Ltd.
author2 Encinas, Paloma [0000-0001-9596-8070]
author_facet Encinas, Paloma [0000-0001-9596-8070]
Encinas, Paloma
Gómez Casado, Eduardo
Fregeneda Grandes, J. M.
Olesen, N. J.
Lorenzen, N.
Estepa, Amparo
Coll Morales, Julio
format artículo
topic_facet Trout antibodies
Viral haemorrhagic septicemia
VHSV
G protein
Fragments
author Encinas, Paloma
Gómez Casado, Eduardo
Fregeneda Grandes, J. M.
Olesen, N. J.
Lorenzen, N.
Estepa, Amparo
Coll Morales, Julio
author_sort Encinas, Paloma
title Rainbow trout surviving infections of viral haemorrhagic septicemia virus (VHSV) show lasting antibodies to recombinant G protein fragments
title_short Rainbow trout surviving infections of viral haemorrhagic septicemia virus (VHSV) show lasting antibodies to recombinant G protein fragments
title_full Rainbow trout surviving infections of viral haemorrhagic septicemia virus (VHSV) show lasting antibodies to recombinant G protein fragments
title_fullStr Rainbow trout surviving infections of viral haemorrhagic septicemia virus (VHSV) show lasting antibodies to recombinant G protein fragments
title_full_unstemmed Rainbow trout surviving infections of viral haemorrhagic septicemia virus (VHSV) show lasting antibodies to recombinant G protein fragments
title_sort rainbow trout surviving infections of viral haemorrhagic septicemia virus (vhsv) show lasting antibodies to recombinant g protein fragments
publisher Elsevier
publishDate 2011
url http://hdl.handle.net/10261/294047
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