Atlantic salmon post-smolts adapted for a longer time to seawater develop an effective humoral and cellular immune response against Salmonid alphavirus

Salmonid alphavirus (SAV) causes pancreas disease (PD) in Atlantic salmon (Salmo salar L.) and disease outbreaks are mainly detected after seawater transfer. The influence of the smoltification process on the immune responses, specifically the adaptive response of Atlantic salmon after SAV infection...

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Published in:Fish & Shellfish Immunology
Main Authors: Nuñez-Ortiz, Noelia, Moore, Lindsey, Jarungsriapisit, Jiraporn, Nilsen, Tom Ole, Stefansson, Sigurd Olav, Morton, Hugh Craig, Taranger, Geir Lasse, Secombes, Christopher J., Patel, Sonal
Format: Article in Journal/Newspaper
Language:English
Published: 2018
Subjects:
Online Access:http://hdl.handle.net/11250/2581477
https://doi.org/10.1016/j.fsi.2018.08.059
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spelling ftimr:oai:imr.brage.unit.no:11250/2581477 2023-05-15T15:30:25+02:00 Atlantic salmon post-smolts adapted for a longer time to seawater develop an effective humoral and cellular immune response against Salmonid alphavirus Nuñez-Ortiz, Noelia Moore, Lindsey Jarungsriapisit, Jiraporn Nilsen, Tom Ole Stefansson, Sigurd Olav Morton, Hugh Craig Taranger, Geir Lasse Secombes, Christopher J. Patel, Sonal 2018 application/pdf http://hdl.handle.net/11250/2581477 https://doi.org/10.1016/j.fsi.2018.08.059 eng eng Norges forskningsråd: 224885 Fish and Shellfish Immunology. 2018, 82 579-590. urn:issn:1050-4648 http://hdl.handle.net/11250/2581477 https://doi.org/10.1016/j.fsi.2018.08.059 cristin:1612518 579-590 82 Fish and Shellfish Immunology Journal article Peer reviewed 2018 ftimr https://doi.org/10.1016/j.fsi.2018.08.059 2021-09-23T20:15:53Z Salmonid alphavirus (SAV) causes pancreas disease (PD) in Atlantic salmon (Salmo salar L.) and disease outbreaks are mainly detected after seawater transfer. The influence of the smoltification process on the immune responses, specifically the adaptive response of Atlantic salmon after SAV infection, is not fully understood. In this study, Atlantic salmon post-smolts were infected by either bath immersion (BI) or intramuscular injection (IM) with SAV subtype 3, 2 weeks (Phase A) or 9 weeks (Phase B) after seawater transfer. The transcript levels of genes related to cellular, humoral and inflammatory responses were evaluated on head kidney samples collected at 3, 7, 14, 21, and 28 days post-infection (dpi). Corresponding negative control groups (CT) were established accordingly. Significant differences were found between both phases and between the IM and BI groups. The anti-inflammatory cytokine IL-10 was up-regulated in Phase A at a higher level than in Phase B. High mRNA levels of the genes RIG-1, SOCS1 and STAT1 were observed in all groups except the BI-B group (BI-Phase B). Moreover, the IM-B group showed a higher regulation of genes related to cellular responses, such as CD40, MHCII, and IL-15, that indicated the activation of a strong cell-mediated immune response. CD40 mRNA levels were elevated one week earlier in the BI-B group than in the BI-A group (BI-Phase A). A significant up-regulation of IgM and IgT genes was seen in both IM groups, but the presence of neutralizing antibodies to SAV was detected only in Phase B fish at 21 and 28 dpi. In addition, we found differences in the basal levels of some of the analysed genes between non-infected control groups of both phases. Findings suggest that Atlantic salmon post-smolts adapted for a longer time to seawater before they come into contact with SAV, developed a stronger humoral and cell-mediated immune response during a SAV infection. submittedVersion Article in Journal/Newspaper Atlantic salmon Salmo salar Institute for Marine Research: Brage IMR Sav’ ENVELOPE(156.400,156.400,68.817,68.817) Fish & Shellfish Immunology 82 579 590
institution Open Polar
collection Institute for Marine Research: Brage IMR
op_collection_id ftimr
language English
description Salmonid alphavirus (SAV) causes pancreas disease (PD) in Atlantic salmon (Salmo salar L.) and disease outbreaks are mainly detected after seawater transfer. The influence of the smoltification process on the immune responses, specifically the adaptive response of Atlantic salmon after SAV infection, is not fully understood. In this study, Atlantic salmon post-smolts were infected by either bath immersion (BI) or intramuscular injection (IM) with SAV subtype 3, 2 weeks (Phase A) or 9 weeks (Phase B) after seawater transfer. The transcript levels of genes related to cellular, humoral and inflammatory responses were evaluated on head kidney samples collected at 3, 7, 14, 21, and 28 days post-infection (dpi). Corresponding negative control groups (CT) were established accordingly. Significant differences were found between both phases and between the IM and BI groups. The anti-inflammatory cytokine IL-10 was up-regulated in Phase A at a higher level than in Phase B. High mRNA levels of the genes RIG-1, SOCS1 and STAT1 were observed in all groups except the BI-B group (BI-Phase B). Moreover, the IM-B group showed a higher regulation of genes related to cellular responses, such as CD40, MHCII, and IL-15, that indicated the activation of a strong cell-mediated immune response. CD40 mRNA levels were elevated one week earlier in the BI-B group than in the BI-A group (BI-Phase A). A significant up-regulation of IgM and IgT genes was seen in both IM groups, but the presence of neutralizing antibodies to SAV was detected only in Phase B fish at 21 and 28 dpi. In addition, we found differences in the basal levels of some of the analysed genes between non-infected control groups of both phases. Findings suggest that Atlantic salmon post-smolts adapted for a longer time to seawater before they come into contact with SAV, developed a stronger humoral and cell-mediated immune response during a SAV infection. submittedVersion
format Article in Journal/Newspaper
author Nuñez-Ortiz, Noelia
Moore, Lindsey
Jarungsriapisit, Jiraporn
Nilsen, Tom Ole
Stefansson, Sigurd Olav
Morton, Hugh Craig
Taranger, Geir Lasse
Secombes, Christopher J.
Patel, Sonal
spellingShingle Nuñez-Ortiz, Noelia
Moore, Lindsey
Jarungsriapisit, Jiraporn
Nilsen, Tom Ole
Stefansson, Sigurd Olav
Morton, Hugh Craig
Taranger, Geir Lasse
Secombes, Christopher J.
Patel, Sonal
Atlantic salmon post-smolts adapted for a longer time to seawater develop an effective humoral and cellular immune response against Salmonid alphavirus
author_facet Nuñez-Ortiz, Noelia
Moore, Lindsey
Jarungsriapisit, Jiraporn
Nilsen, Tom Ole
Stefansson, Sigurd Olav
Morton, Hugh Craig
Taranger, Geir Lasse
Secombes, Christopher J.
Patel, Sonal
author_sort Nuñez-Ortiz, Noelia
title Atlantic salmon post-smolts adapted for a longer time to seawater develop an effective humoral and cellular immune response against Salmonid alphavirus
title_short Atlantic salmon post-smolts adapted for a longer time to seawater develop an effective humoral and cellular immune response against Salmonid alphavirus
title_full Atlantic salmon post-smolts adapted for a longer time to seawater develop an effective humoral and cellular immune response against Salmonid alphavirus
title_fullStr Atlantic salmon post-smolts adapted for a longer time to seawater develop an effective humoral and cellular immune response against Salmonid alphavirus
title_full_unstemmed Atlantic salmon post-smolts adapted for a longer time to seawater develop an effective humoral and cellular immune response against Salmonid alphavirus
title_sort atlantic salmon post-smolts adapted for a longer time to seawater develop an effective humoral and cellular immune response against salmonid alphavirus
publishDate 2018
url http://hdl.handle.net/11250/2581477
https://doi.org/10.1016/j.fsi.2018.08.059
long_lat ENVELOPE(156.400,156.400,68.817,68.817)
geographic Sav’
geographic_facet Sav’
genre Atlantic salmon
Salmo salar
genre_facet Atlantic salmon
Salmo salar
op_source 579-590
82
Fish and Shellfish Immunology
op_relation Norges forskningsråd: 224885
Fish and Shellfish Immunology. 2018, 82 579-590.
urn:issn:1050-4648
http://hdl.handle.net/11250/2581477
https://doi.org/10.1016/j.fsi.2018.08.059
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op_doi https://doi.org/10.1016/j.fsi.2018.08.059
container_title Fish & Shellfish Immunology
container_volume 82
container_start_page 579
op_container_end_page 590
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