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Development, Characterisation and Application of Monoclonal Antibodies for the Detection and Quantification of Infectious Salmon Anaemia Virus in Plasma Samples Using Luminex Bead Array Technology.
Hoare, R; Thompson, K D; Herath, T; Collet, B; Bron, J E; Adams, A.
Afiliación
  • Hoare R; Institute of Aquaculture, School of Natural Sciences, University of Stirling, Stirling, FK9 4LA, United Kingdom.
  • Thompson KD; Institute of Aquaculture, School of Natural Sciences, University of Stirling, Stirling, FK9 4LA, United Kingdom.
  • Herath T; Moredun Research Institute, Pentlands Science Park, Penicuik EH26 0PZ, United Kingdom.
  • Collet B; Department of Animal Production, Welfare and Veterinary Sciences, Harper Adams University, Newport, Shropshire TF10 8NB, United Kingdom.
  • Bron JE; Marine Scotland, Marine Laboratory, 375 Victoria Road, Aberdeen AB11 9PA, United Kingdom.
  • Adams A; Institute of Aquaculture, School of Natural Sciences, University of Stirling, Stirling, FK9 4LA, United Kingdom.
PLoS One ; 11(7): e0159155, 2016.
Article en En | MEDLINE | ID: mdl-27434377
Infectious salmon anaemia virus (ISAV) is an orthomyxovirus that has had a significant economic impact on Atlantic salmon farming in Europe, North America and Chile. Monoclonal antibodies (mAbs) were developed against Segment 3 (encoding the viral nucleoprotein, NP) of the virus. Six of the mAbs were shown to be specific to ISAV and recognised all isolates from Scotland, Norway and Canada. They reacted with ISAV in enzyme-linked immunosorbent assay (ELISA), indirect fluorescent antibody technique (IFAT) and western blotting. They were also used to develop a novel detection method based on Luminex (Bio-Plex) bead-based flow cytometric technology for the detection of ISAV in the plasma of Atlantic salmon (Salmo salar L.) smolts experimentally infected with ISAV. Fish were challenged by intraperitoneal (i.p.) injection of virus at 50% Tissue Culture Infective Dose (TCID50) = 2.8 x106 per animal. Virus present in plasma of infected fish, collected at 0, 4, 8, 12, 16, 21 and 28 days post infection using a non-lethal sampling method (n = 12 at each time point), was quantified using the optimised Bio-Plex assay. The results obtained with this assay were compared with absolute quantification of the virus by RT-qPCR using SYBR Green I and TaqMan chemistries. The Bio-Plex assay developed using the NP mAbs appears to be a rapid, sensitive method for detecting and quantifying ISAV in small volumes of fish plasma and has the potential to be multiplexed for the detection of other fish pathogens (e.g. during co-infections). To our knowledge this is the first report of the use of Luminex (Bio-Plex) technology for the detection of a fish pathogen.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Infecciones por Orthomyxoviridae / Isavirus / Anticuerpos Monoclonales Tipo de estudio: Diagnostic_studies Límite: Animals País/Región como asunto: America do norte / America do sul / Chile / Europa Idioma: En Revista: PLoS One Asunto de la revista: CIENCIA / MEDICINA Año: 2016 Tipo del documento: Article País de afiliación: Reino Unido Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Infecciones por Orthomyxoviridae / Isavirus / Anticuerpos Monoclonales Tipo de estudio: Diagnostic_studies Límite: Animals País/Región como asunto: America do norte / America do sul / Chile / Europa Idioma: En Revista: PLoS One Asunto de la revista: CIENCIA / MEDICINA Año: 2016 Tipo del documento: Article País de afiliación: Reino Unido Pais de publicación: Estados Unidos