Development of a new real-time PCR for the detection of pilchard orthomyxovirus (POMV) in apparently healthy fish

Pilchard orthomyxovirus (POMV) is a virus of concern to the Atlantic salmon aquaculture industry in Tasmania. First isolated from wild pilchards in southern Australia in 1998, the virus is now a recognised pathogen of farmed Atlantic salmon (Salmo salar) in Tasmania. While the current real-time PCR...

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Published in:Aquaculture
Main Authors: Samsing, Francisca, Tengesdal, Hedda Kjølleberg, Nylund, Are, Rigby, Megan, Wiltshire, Kathryn H., Morrison, Richard N., Godwin, Scott, Giles, Carla, Wilson, Teresa, Mohr, Peter G., Hoad, John, Wynne, James W.
Format: Article in Journal/Newspaper
Language:English
Published: Elsevier 2022
Subjects:
Online Access:https://hdl.handle.net/11250/3037627
https://doi.org/10.1016/j.aquaculture.2021.737404
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author Samsing, Francisca
Tengesdal, Hedda Kjølleberg
Nylund, Are
Rigby, Megan
Wiltshire, Kathryn H.
Morrison, Richard N.
Godwin, Scott
Giles, Carla
Wilson, Teresa
Mohr, Peter G.
Hoad, John
Wynne, James W.
author_facet Samsing, Francisca
Tengesdal, Hedda Kjølleberg
Nylund, Are
Rigby, Megan
Wiltshire, Kathryn H.
Morrison, Richard N.
Godwin, Scott
Giles, Carla
Wilson, Teresa
Mohr, Peter G.
Hoad, John
Wynne, James W.
author_sort Samsing, Francisca
collection University of Bergen: Bergen Open Research Archive (BORA-UiB)
container_start_page 737404
container_title Aquaculture
container_volume 547
description Pilchard orthomyxovirus (POMV) is a virus of concern to the Atlantic salmon aquaculture industry in Tasmania. First isolated from wild pilchards in southern Australia in 1998, the virus is now a recognised pathogen of farmed Atlantic salmon (Salmo salar) in Tasmania. While the current real-time PCR for POMV targets segment 5 of the viral genome, recent viral gene expression data suggests that other segments of the POMV genome presented higher transcription levels and thus may be better candidates for the early detection of the virus. This study aimed to design and begin validating a more sensitive reverse transcriptase real-time PCR (RT-qPCR) assay to detect POMV. Primers and probes were developed targeting two independent viral genes derived from segments 7 and 8, which presented higher transcription levels than segment 5 in both cell culture and infected fish. These were compared with the current POMV RT-qPCR. The POMV segment 8 assay had a higher analytical sensitivity than segment 7, detecting at least 1 plasmid copy μl−1, and was 10-fold more sensitive than both POMV segment 7 and 5 assays when analysing nucleic acid from a positive field sample. Both new assays also had high analytical specificity, detecting the 11 POMV isolates tested (inclusivity testing) and not amplifying nucleic acids from other viruses, including ISAV, a related orthomyxovirus. In the latent class model analysis, the diagnostic sensitivity of the segment 8 and 7 assays were higher than segment 5 in 93% and 92% of simulations, respectively. Seven samples (18.4%), all from subclinical fish infected with POMV, returned a positive result only with the segment 8 assay. Both new assays showed reproducible results when applied to aliquots of the same samples tested in three different laboratories. The new POMV segment 8 assay shows promising results as a surveillance tool for detecting POMV in fish without any symptoms. publishedVersion
format Article in Journal/Newspaper
genre Atlantic salmon
Salmo salar
genre_facet Atlantic salmon
Salmo salar
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institution Open Polar
language English
op_collection_id ftunivbergen
op_doi https://doi.org/10.1016/j.aquaculture.2021.737404
op_relation urn:issn:0044-8486
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https://doi.org/10.1016/j.aquaculture.2021.737404
cristin:2021890
Aquaculture. 2022, 547, 737404.
op_rights Navngivelse 4.0 Internasjonal
http://creativecommons.org/licenses/by/4.0/deed.no
Crown Copyright 2021
op_source 737404
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spelling ftunivbergen:oai:bora.uib.no:11250/3037627 2025-01-16T21:03:43+00:00 Development of a new real-time PCR for the detection of pilchard orthomyxovirus (POMV) in apparently healthy fish Samsing, Francisca Tengesdal, Hedda Kjølleberg Nylund, Are Rigby, Megan Wiltshire, Kathryn H. Morrison, Richard N. Godwin, Scott Giles, Carla Wilson, Teresa Mohr, Peter G. Hoad, John Wynne, James W. 2022 application/pdf https://hdl.handle.net/11250/3037627 https://doi.org/10.1016/j.aquaculture.2021.737404 eng eng Elsevier urn:issn:0044-8486 https://hdl.handle.net/11250/3037627 https://doi.org/10.1016/j.aquaculture.2021.737404 cristin:2021890 Aquaculture. 2022, 547, 737404. Navngivelse 4.0 Internasjonal http://creativecommons.org/licenses/by/4.0/deed.no Crown Copyright 2021 737404 Aquaculture 547 Journal article Peer reviewed 2022 ftunivbergen https://doi.org/10.1016/j.aquaculture.2021.737404 2023-03-14T17:43:21Z Pilchard orthomyxovirus (POMV) is a virus of concern to the Atlantic salmon aquaculture industry in Tasmania. First isolated from wild pilchards in southern Australia in 1998, the virus is now a recognised pathogen of farmed Atlantic salmon (Salmo salar) in Tasmania. While the current real-time PCR for POMV targets segment 5 of the viral genome, recent viral gene expression data suggests that other segments of the POMV genome presented higher transcription levels and thus may be better candidates for the early detection of the virus. This study aimed to design and begin validating a more sensitive reverse transcriptase real-time PCR (RT-qPCR) assay to detect POMV. Primers and probes were developed targeting two independent viral genes derived from segments 7 and 8, which presented higher transcription levels than segment 5 in both cell culture and infected fish. These were compared with the current POMV RT-qPCR. The POMV segment 8 assay had a higher analytical sensitivity than segment 7, detecting at least 1 plasmid copy μl−1, and was 10-fold more sensitive than both POMV segment 7 and 5 assays when analysing nucleic acid from a positive field sample. Both new assays also had high analytical specificity, detecting the 11 POMV isolates tested (inclusivity testing) and not amplifying nucleic acids from other viruses, including ISAV, a related orthomyxovirus. In the latent class model analysis, the diagnostic sensitivity of the segment 8 and 7 assays were higher than segment 5 in 93% and 92% of simulations, respectively. Seven samples (18.4%), all from subclinical fish infected with POMV, returned a positive result only with the segment 8 assay. Both new assays showed reproducible results when applied to aliquots of the same samples tested in three different laboratories. The new POMV segment 8 assay shows promising results as a surveillance tool for detecting POMV in fish without any symptoms. publishedVersion Article in Journal/Newspaper Atlantic salmon Salmo salar University of Bergen: Bergen Open Research Archive (BORA-UiB) Aquaculture 547 737404
spellingShingle Samsing, Francisca
Tengesdal, Hedda Kjølleberg
Nylund, Are
Rigby, Megan
Wiltshire, Kathryn H.
Morrison, Richard N.
Godwin, Scott
Giles, Carla
Wilson, Teresa
Mohr, Peter G.
Hoad, John
Wynne, James W.
Development of a new real-time PCR for the detection of pilchard orthomyxovirus (POMV) in apparently healthy fish
title Development of a new real-time PCR for the detection of pilchard orthomyxovirus (POMV) in apparently healthy fish
title_full Development of a new real-time PCR for the detection of pilchard orthomyxovirus (POMV) in apparently healthy fish
title_fullStr Development of a new real-time PCR for the detection of pilchard orthomyxovirus (POMV) in apparently healthy fish
title_full_unstemmed Development of a new real-time PCR for the detection of pilchard orthomyxovirus (POMV) in apparently healthy fish
title_short Development of a new real-time PCR for the detection of pilchard orthomyxovirus (POMV) in apparently healthy fish
title_sort development of a new real-time pcr for the detection of pilchard orthomyxovirus (pomv) in apparently healthy fish
url https://hdl.handle.net/11250/3037627
https://doi.org/10.1016/j.aquaculture.2021.737404