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Development of an avian avulavirus 1 (AAvV-1) L-gene real-time RT-PCR assay using minor groove binding probes for application as a routine diagnostic tool.
Sutton, David A; Allen, David P; Fuller, Chad M; Mayers, Jo; Mollett, Benjamin C; Londt, Brandon Z; Reid, Scott M; Mansfield, Karen L; Brown, Ian H.
Afiliación
  • Sutton DA; Qiagen, Skelton House, Lloyd St N, Manchester M15 6SH, United Kingdom.
  • Allen DP; Animal and Plant Health Agency (APHA), Woodham Lane, Addlestone, Surrey, KT15 3NB, United Kingdom.
  • Fuller CM; Okanagan National Alliance, 3535 Old Okanagan Highway, Westbank, BC, V4T 3L7, Canada.
  • Mayers J; Animal and Plant Health Agency (APHA), Woodham Lane, Addlestone, Surrey, KT15 3NB, United Kingdom. Electronic address: jo.mayers@apha.gov.uk.
  • Mollett BC; Animal and Plant Health Agency (APHA), Woodham Lane, Addlestone, Surrey, KT15 3NB, United Kingdom.
  • Londt BZ; hVivo, Queen Mary BioEnterprises Innovation Centre, 42 New Road, London, E1 2AX, United Kingdom.
  • Reid SM; Animal and Plant Health Agency (APHA), Woodham Lane, Addlestone, Surrey, KT15 3NB, United Kingdom.
  • Mansfield KL; Animal and Plant Health Agency (APHA), Woodham Lane, Addlestone, Surrey, KT15 3NB, United Kingdom.
  • Brown IH; Animal and Plant Health Agency (APHA), Woodham Lane, Addlestone, Surrey, KT15 3NB, United Kingdom.
J Virol Methods ; 265: 9-14, 2019 03.
Article en En | MEDLINE | ID: mdl-30579921
Newcastle disease is a devastating disease of poultry caused by Newcastle disease virus (NDV), a virulent form of avian avulavirus 1 (AAvV-1). A rapid, sensitive and specific means for the detection of NDV is fundamental for the control of this notifiable transboundary virus. Although several real-time RT-PCR assays exist for the detection of AAvV-1, diagnostic sensitivity and specificities can be sub-optimal. In this study, we describe a modification to an existing AAvV-1 l-gene RT-PCR screening assay, where the original probe set was replaced with minor groove binding (MGB) probes, to create the MGB l-gene assay. The diagnostic sensitivity and specificity of this assay was evaluated against a broad panel of both Class I and Class II AAvV-1 viruses of diverse and representative lineages/genotypes in both clinical samples and amplified viruses, and compared with a number of previously published real-time RT-PCR screening assays for AAvV-1. The MGB l-gene assay outperformed all other assays in this assessment, with enhanced sensitivity and specificity, detecting isolates from a broad range of virus lineages/genotypes (including contemporaneously-circulating strains). The assay has also proved its value for screening original clinical samples for the presence of AAvV-1, thus providing an improved screening assay for routine detection of this notifiable disease agent.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Enfermedades de las Aves / Avulavirus / Cartilla de ADN / Reacción en Cadena de la Polimerasa de Transcriptasa Inversa / Infecciones por Avulavirus / Reacción en Cadena en Tiempo Real de la Polimerasa Tipo de estudio: Diagnostic_studies / Evaluation_studies Límite: Animals Idioma: En Revista: J Virol Methods Año: 2019 Tipo del documento: Article País de afiliación: Reino Unido

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Enfermedades de las Aves / Avulavirus / Cartilla de ADN / Reacción en Cadena de la Polimerasa de Transcriptasa Inversa / Infecciones por Avulavirus / Reacción en Cadena en Tiempo Real de la Polimerasa Tipo de estudio: Diagnostic_studies / Evaluation_studies Límite: Animals Idioma: En Revista: J Virol Methods Año: 2019 Tipo del documento: Article País de afiliación: Reino Unido