author_facet Millard, E V
Faisal, M
Millard, E V
Faisal, M
author Millard, E V
Faisal, M
spellingShingle Millard, E V
Faisal, M
Journal of Fish Diseases
Development of neutralizing antibody responses in muskellunge, Esox masquinongy (Mitchill), experimentally exposed to viral haemorrhagic septicaemia virus (genotype IVb)
Veterinary (miscellaneous)
Aquatic Science
author_sort millard, e v
spelling Millard, E V Faisal, M 0140-7775 1365-2761 Wiley Veterinary (miscellaneous) Aquatic Science http://dx.doi.org/10.1111/j.1365-2761.2011.01318.x <jats:title>Abstract</jats:title><jats:p>A complement‐dependent 50% plaque neutralization test was used to assess the neutralizing antibody response in sera of muskellunge, <jats:italic>Esox masquinongy</jats:italic>, experimentally infected with viral haemorrhagic septicaemia virus (VHSV, genotype IVb) by immersion. Groups of muskellunge were challenged with varying concentrations of VHSV: Group 1 with 10<jats:sup>2</jats:sup> plaque‐forming units (pfu) mL<jats:sup>−1</jats:sup>, Group 2 with 4 × 10<jats:sup>3</jats:sup> pfu mL<jats:sup>−1</jats:sup>, Group 3 with 10<jats:sup>5</jats:sup> pfu mL<jats:sup>−1</jats:sup> and Group 4 with 0 pfu mL<jats:sup>−1</jats:sup>. The fish were held at a temperature of 11 ± 1 °C and were sampled over a 20‐week period. Neutralizing antibodies were not detected in sera of any of the negative control fish throughout the study. Low neutralizing titres were detected in Groups 1–3 by 6 days post‐infection (p.i.). Neutralizing titres of &lt;80 were not detected again until 3, 4 and 7 weeks p.i. for Groups 2, 3 and 1, respectively, with peak titres for those groups occurring 16, 11 and 17 weeks p.i., respectively. VHSV was detected in serum for up to 11 weeks p.i. Results of this study show that survivors can be detected by a serological technique, despite being virus negative. This may benefit the investigation of VHSV IVb distribution in the Great Lakes and the study of host immune responses to this emerging sublineage.</jats:p> Development of neutralizing antibody responses in muskellunge, <i>Esox masquinongy</i> (Mitchill), experimentally exposed to viral haemorrhagic septicaemia virus (genotype IVb) Journal of Fish Diseases
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title Development of neutralizing antibody responses in muskellunge, Esox masquinongy (Mitchill), experimentally exposed to viral haemorrhagic septicaemia virus (genotype IVb)
title_unstemmed Development of neutralizing antibody responses in muskellunge, Esox masquinongy (Mitchill), experimentally exposed to viral haemorrhagic septicaemia virus (genotype IVb)
title_full Development of neutralizing antibody responses in muskellunge, Esox masquinongy (Mitchill), experimentally exposed to viral haemorrhagic septicaemia virus (genotype IVb)
title_fullStr Development of neutralizing antibody responses in muskellunge, Esox masquinongy (Mitchill), experimentally exposed to viral haemorrhagic septicaemia virus (genotype IVb)
title_full_unstemmed Development of neutralizing antibody responses in muskellunge, Esox masquinongy (Mitchill), experimentally exposed to viral haemorrhagic septicaemia virus (genotype IVb)
title_short Development of neutralizing antibody responses in muskellunge, Esox masquinongy (Mitchill), experimentally exposed to viral haemorrhagic septicaemia virus (genotype IVb)
title_sort development of neutralizing antibody responses in muskellunge, <i>esox masquinongy</i> (mitchill), experimentally exposed to viral haemorrhagic septicaemia virus (genotype ivb)
topic Veterinary (miscellaneous)
Aquatic Science
url http://dx.doi.org/10.1111/j.1365-2761.2011.01318.x
publishDate 2012
physical 11-18
description <jats:title>Abstract</jats:title><jats:p>A complement‐dependent 50% plaque neutralization test was used to assess the neutralizing antibody response in sera of muskellunge, <jats:italic>Esox masquinongy</jats:italic>, experimentally infected with viral haemorrhagic septicaemia virus (VHSV, genotype IVb) by immersion. Groups of muskellunge were challenged with varying concentrations of VHSV: Group 1 with 10<jats:sup>2</jats:sup> plaque‐forming units (pfu) mL<jats:sup>−1</jats:sup>, Group 2 with 4 × 10<jats:sup>3</jats:sup> pfu mL<jats:sup>−1</jats:sup>, Group 3 with 10<jats:sup>5</jats:sup> pfu mL<jats:sup>−1</jats:sup> and Group 4 with 0 pfu mL<jats:sup>−1</jats:sup>. The fish were held at a temperature of 11 ± 1 °C and were sampled over a 20‐week period. Neutralizing antibodies were not detected in sera of any of the negative control fish throughout the study. Low neutralizing titres were detected in Groups 1–3 by 6 days post‐infection (p.i.). Neutralizing titres of &lt;80 were not detected again until 3, 4 and 7 weeks p.i. for Groups 2, 3 and 1, respectively, with peak titres for those groups occurring 16, 11 and 17 weeks p.i., respectively. VHSV was detected in serum for up to 11 weeks p.i. Results of this study show that survivors can be detected by a serological technique, despite being virus negative. This may benefit the investigation of VHSV IVb distribution in the Great Lakes and the study of host immune responses to this emerging sublineage.</jats:p>
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author Millard, E V, Faisal, M
author_facet Millard, E V, Faisal, M, Millard, E V, Faisal, M
author_sort millard, e v
container_issue 1
container_start_page 11
container_title Journal of Fish Diseases
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description <jats:title>Abstract</jats:title><jats:p>A complement‐dependent 50% plaque neutralization test was used to assess the neutralizing antibody response in sera of muskellunge, <jats:italic>Esox masquinongy</jats:italic>, experimentally infected with viral haemorrhagic septicaemia virus (VHSV, genotype IVb) by immersion. Groups of muskellunge were challenged with varying concentrations of VHSV: Group 1 with 10<jats:sup>2</jats:sup> plaque‐forming units (pfu) mL<jats:sup>−1</jats:sup>, Group 2 with 4 × 10<jats:sup>3</jats:sup> pfu mL<jats:sup>−1</jats:sup>, Group 3 with 10<jats:sup>5</jats:sup> pfu mL<jats:sup>−1</jats:sup> and Group 4 with 0 pfu mL<jats:sup>−1</jats:sup>. The fish were held at a temperature of 11 ± 1 °C and were sampled over a 20‐week period. Neutralizing antibodies were not detected in sera of any of the negative control fish throughout the study. Low neutralizing titres were detected in Groups 1–3 by 6 days post‐infection (p.i.). Neutralizing titres of &lt;80 were not detected again until 3, 4 and 7 weeks p.i. for Groups 2, 3 and 1, respectively, with peak titres for those groups occurring 16, 11 and 17 weeks p.i., respectively. VHSV was detected in serum for up to 11 weeks p.i. Results of this study show that survivors can be detected by a serological technique, despite being virus negative. This may benefit the investigation of VHSV IVb distribution in the Great Lakes and the study of host immune responses to this emerging sublineage.</jats:p>
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spelling Millard, E V Faisal, M 0140-7775 1365-2761 Wiley Veterinary (miscellaneous) Aquatic Science http://dx.doi.org/10.1111/j.1365-2761.2011.01318.x <jats:title>Abstract</jats:title><jats:p>A complement‐dependent 50% plaque neutralization test was used to assess the neutralizing antibody response in sera of muskellunge, <jats:italic>Esox masquinongy</jats:italic>, experimentally infected with viral haemorrhagic septicaemia virus (VHSV, genotype IVb) by immersion. Groups of muskellunge were challenged with varying concentrations of VHSV: Group 1 with 10<jats:sup>2</jats:sup> plaque‐forming units (pfu) mL<jats:sup>−1</jats:sup>, Group 2 with 4 × 10<jats:sup>3</jats:sup> pfu mL<jats:sup>−1</jats:sup>, Group 3 with 10<jats:sup>5</jats:sup> pfu mL<jats:sup>−1</jats:sup> and Group 4 with 0 pfu mL<jats:sup>−1</jats:sup>. The fish were held at a temperature of 11 ± 1 °C and were sampled over a 20‐week period. Neutralizing antibodies were not detected in sera of any of the negative control fish throughout the study. Low neutralizing titres were detected in Groups 1–3 by 6 days post‐infection (p.i.). Neutralizing titres of &lt;80 were not detected again until 3, 4 and 7 weeks p.i. for Groups 2, 3 and 1, respectively, with peak titres for those groups occurring 16, 11 and 17 weeks p.i., respectively. VHSV was detected in serum for up to 11 weeks p.i. Results of this study show that survivors can be detected by a serological technique, despite being virus negative. This may benefit the investigation of VHSV IVb distribution in the Great Lakes and the study of host immune responses to this emerging sublineage.</jats:p> Development of neutralizing antibody responses in muskellunge, <i>Esox masquinongy</i> (Mitchill), experimentally exposed to viral haemorrhagic septicaemia virus (genotype IVb) Journal of Fish Diseases
spellingShingle Millard, E V, Faisal, M, Journal of Fish Diseases, Development of neutralizing antibody responses in muskellunge, Esox masquinongy (Mitchill), experimentally exposed to viral haemorrhagic septicaemia virus (genotype IVb), Veterinary (miscellaneous), Aquatic Science
title Development of neutralizing antibody responses in muskellunge, Esox masquinongy (Mitchill), experimentally exposed to viral haemorrhagic septicaemia virus (genotype IVb)
title_full Development of neutralizing antibody responses in muskellunge, Esox masquinongy (Mitchill), experimentally exposed to viral haemorrhagic septicaemia virus (genotype IVb)
title_fullStr Development of neutralizing antibody responses in muskellunge, Esox masquinongy (Mitchill), experimentally exposed to viral haemorrhagic septicaemia virus (genotype IVb)
title_full_unstemmed Development of neutralizing antibody responses in muskellunge, Esox masquinongy (Mitchill), experimentally exposed to viral haemorrhagic septicaemia virus (genotype IVb)
title_short Development of neutralizing antibody responses in muskellunge, Esox masquinongy (Mitchill), experimentally exposed to viral haemorrhagic septicaemia virus (genotype IVb)
title_sort development of neutralizing antibody responses in muskellunge, <i>esox masquinongy</i> (mitchill), experimentally exposed to viral haemorrhagic septicaemia virus (genotype ivb)
title_unstemmed Development of neutralizing antibody responses in muskellunge, Esox masquinongy (Mitchill), experimentally exposed to viral haemorrhagic septicaemia virus (genotype IVb)
topic Veterinary (miscellaneous), Aquatic Science
url http://dx.doi.org/10.1111/j.1365-2761.2011.01318.x