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Real Time RT-PCR Assays for Detection and Typing of African Horse Sickness Virus

Although African horse sickness (AHS) can cause up to 95% mortality in horses, naïve animals can be protected by vaccination against the homologous AHSV serotype. Genome segment 2 (Seg-2) encodes outer capsid protein VP2, the most variable of the AHSV proteins. VP2 is also a primary target for AHSV...

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Autores principales: Bachanek-Bankowska, Katarzyna, Maan, Sushila, Castillo-Olivares, Javier, Manning, Nicola M., Maan, Narender Singh, Potgieter, Abraham C., Di Nardo, Antonello, Sutton, Geoff, Batten, Carrie, Mertens, Peter P. C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3983086/
https://www.ncbi.nlm.nih.gov/pubmed/24721971
http://dx.doi.org/10.1371/journal.pone.0093758
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author Bachanek-Bankowska, Katarzyna
Maan, Sushila
Castillo-Olivares, Javier
Manning, Nicola M.
Maan, Narender Singh
Potgieter, Abraham C.
Di Nardo, Antonello
Sutton, Geoff
Batten, Carrie
Mertens, Peter P. C.
author_facet Bachanek-Bankowska, Katarzyna
Maan, Sushila
Castillo-Olivares, Javier
Manning, Nicola M.
Maan, Narender Singh
Potgieter, Abraham C.
Di Nardo, Antonello
Sutton, Geoff
Batten, Carrie
Mertens, Peter P. C.
author_sort Bachanek-Bankowska, Katarzyna
collection PubMed
description Although African horse sickness (AHS) can cause up to 95% mortality in horses, naïve animals can be protected by vaccination against the homologous AHSV serotype. Genome segment 2 (Seg-2) encodes outer capsid protein VP2, the most variable of the AHSV proteins. VP2 is also a primary target for AHSV specific neutralising antibodies, and consequently determines the identity of the nine AHSV serotypes. In contrast VP1 (the viral polymerase) and VP3 (the sub-core shell protein), encoded by Seg-1 and Seg-3 respectively, are highly conserved, representing virus species/orbivirus-serogroup-specific antigens. We report development and evaluation of real-time RT-PCR assays targeting AHSV Seg-1 or Seg-3, that can detect any AHSV type (virus species/serogroup-specific assays), as well as type-specific assays targeting Seg-2 of the nine AHSV serotypes. These assays were evaluated using isolates of different AHSV serotypes and other closely related orbiviruses, from the ‘Orbivirus Reference Collection’ (ORC) at The Pirbright Institute. The assays were shown to be AHSV virus-species-specific, or type-specific (as designed) and can be used for rapid, sensitive and reliable detection and identification (typing) of AHSV RNA in infected blood, tissue samples, homogenised Culicoides, or tissue culture supernatant. None of the assays amplified cDNAs from closely related heterologous orbiviruses, or from uninfected host animals or cell cultures.
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spelling pubmed-39830862014-04-15 Real Time RT-PCR Assays for Detection and Typing of African Horse Sickness Virus Bachanek-Bankowska, Katarzyna Maan, Sushila Castillo-Olivares, Javier Manning, Nicola M. Maan, Narender Singh Potgieter, Abraham C. Di Nardo, Antonello Sutton, Geoff Batten, Carrie Mertens, Peter P. C. PLoS One Research Article Although African horse sickness (AHS) can cause up to 95% mortality in horses, naïve animals can be protected by vaccination against the homologous AHSV serotype. Genome segment 2 (Seg-2) encodes outer capsid protein VP2, the most variable of the AHSV proteins. VP2 is also a primary target for AHSV specific neutralising antibodies, and consequently determines the identity of the nine AHSV serotypes. In contrast VP1 (the viral polymerase) and VP3 (the sub-core shell protein), encoded by Seg-1 and Seg-3 respectively, are highly conserved, representing virus species/orbivirus-serogroup-specific antigens. We report development and evaluation of real-time RT-PCR assays targeting AHSV Seg-1 or Seg-3, that can detect any AHSV type (virus species/serogroup-specific assays), as well as type-specific assays targeting Seg-2 of the nine AHSV serotypes. These assays were evaluated using isolates of different AHSV serotypes and other closely related orbiviruses, from the ‘Orbivirus Reference Collection’ (ORC) at The Pirbright Institute. The assays were shown to be AHSV virus-species-specific, or type-specific (as designed) and can be used for rapid, sensitive and reliable detection and identification (typing) of AHSV RNA in infected blood, tissue samples, homogenised Culicoides, or tissue culture supernatant. None of the assays amplified cDNAs from closely related heterologous orbiviruses, or from uninfected host animals or cell cultures. Public Library of Science 2014-04-10 /pmc/articles/PMC3983086/ /pubmed/24721971 http://dx.doi.org/10.1371/journal.pone.0093758 Text en © 2014 Bachanek-Bankowska et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Bachanek-Bankowska, Katarzyna
Maan, Sushila
Castillo-Olivares, Javier
Manning, Nicola M.
Maan, Narender Singh
Potgieter, Abraham C.
Di Nardo, Antonello
Sutton, Geoff
Batten, Carrie
Mertens, Peter P. C.
Real Time RT-PCR Assays for Detection and Typing of African Horse Sickness Virus
title Real Time RT-PCR Assays for Detection and Typing of African Horse Sickness Virus
title_full Real Time RT-PCR Assays for Detection and Typing of African Horse Sickness Virus
title_fullStr Real Time RT-PCR Assays for Detection and Typing of African Horse Sickness Virus
title_full_unstemmed Real Time RT-PCR Assays for Detection and Typing of African Horse Sickness Virus
title_short Real Time RT-PCR Assays for Detection and Typing of African Horse Sickness Virus
title_sort real time rt-pcr assays for detection and typing of african horse sickness virus
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3983086/
https://www.ncbi.nlm.nih.gov/pubmed/24721971
http://dx.doi.org/10.1371/journal.pone.0093758
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