Comparison of Atlantic salmon individuals with different outcomes of cardiomyopathy syndrome (CMS)

<p>Abstract</p> <p>Background</p> <p>Cardiomyopathy syndrome (CMS) is a severe disease of Atlantic salmon (<it>Salmo salar</it> L.) associated with significant economic losses in the aquaculture industry. CMS is diagnosed with a severe inflammation and degra...

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Main Authors: Timmerhaus Gerrit, Krasnov Aleksei, Takle Harald, Afanasyev Sergey, Nilsen Pål, Rode Marit, Jørgensen Sven
Format: Article
Language:English
Published: BMC 2012-05-01
Series:BMC Genomics
Online Access:http://www.biomedcentral.com/1471-2164/13/205
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spelling doaj-7564fd9d91874668938e26bd3155d2fb2020-11-25T00:19:12ZengBMCBMC Genomics1471-21642012-05-0113120510.1186/1471-2164-13-205Comparison of Atlantic salmon individuals with different outcomes of cardiomyopathy syndrome (CMS)Timmerhaus GerritKrasnov AlekseiTakle HaraldAfanasyev SergeyNilsen PålRode MaritJørgensen Sven<p>Abstract</p> <p>Background</p> <p>Cardiomyopathy syndrome (CMS) is a severe disease of Atlantic salmon (<it>Salmo salar</it> L.) associated with significant economic losses in the aquaculture industry. CMS is diagnosed with a severe inflammation and degradation of myocardial tissue caused by a double-stranded RNA virus named piscine myocarditis virus (PMCV), with structural similarities to the <it>Totiviridae</it> family. In the present study we characterized individual host responses and genomic determinants of different disease outcomes.</p> <p>Results</p> <p>From time course studies of experimentally infected Atlantic salmon post-smolts, fish exhibited different outcomes of infection and disease. High responder (HR) fish were characterized with sustained and increased viral load and pathology in heart tissue. Low responder (LR) fish showed declining viral load from 6–10 weeks post infection (wpi) and absence of pathology. Global gene expression (SIQ2.0 oligonucleotide microarray) in HR and LR hearts during infection was compared, in order to characterize differences in the host response and to identify genes with expression patterns that could explain or predict the different outcomes of disease. Virus-responsive genes involved in early antiviral and innate immune responses were upregulated equally in LR and HR at the first stage (2–4 wpi), reflecting the initial increase in virus replication. Repression of heart muscle development was identified by gene ontology enrichment analyses, indicating the early onset of pathology. By six weeks both responder groups had comparable viral load, while increased pathology was observed in HR fish. This was reflected by induced expression of genes implicated in apoptosis and cell death mechanisms, presumably related to lymphocyte regulation and survival. In contrast, LR fish showed earlier activation of NK cell-mediated cytotoxicity and NOD-like receptor signaling pathways. At the late stage of infection, increased pathology and viral load in HR was accompanied by a broad activation of genes involved in adaptive immunity and particularly T cell responses, probably reflecting the increased infiltration and homing of virus-specific T cells to the infected heart. This was in sharp contrast to LR fish, where recovery and reduced viral load was associated with a significantly reduced transcription of adaptive immunity genes and activation of genes involved in energy metabolism.</p> <p>Conclusions</p> <p>In contrast to LR, a stronger and sustained expression of genes involved in adaptive immune responses in heart tissue of HR at the late stage of disease probably reflected the increased lymphocyte infiltration and pathological outcome. In addition to controlled adaptive immunity and activation of genes involved in cardiac energy metabolism in LR at the late stage, recovery of this group could also be related to an earlier activation of NOD-like receptor signaling and NK cell-mediated cytotoxicity pathways.</p> http://www.biomedcentral.com/1471-2164/13/205
collection DOAJ
language English
format Article
sources DOAJ
author Timmerhaus Gerrit
Krasnov Aleksei
Takle Harald
Afanasyev Sergey
Nilsen Pål
Rode Marit
Jørgensen Sven
spellingShingle Timmerhaus Gerrit
Krasnov Aleksei
Takle Harald
Afanasyev Sergey
Nilsen Pål
Rode Marit
Jørgensen Sven
Comparison of Atlantic salmon individuals with different outcomes of cardiomyopathy syndrome (CMS)
BMC Genomics
author_facet Timmerhaus Gerrit
Krasnov Aleksei
Takle Harald
Afanasyev Sergey
Nilsen Pål
Rode Marit
Jørgensen Sven
author_sort Timmerhaus Gerrit
title Comparison of Atlantic salmon individuals with different outcomes of cardiomyopathy syndrome (CMS)
title_short Comparison of Atlantic salmon individuals with different outcomes of cardiomyopathy syndrome (CMS)
title_full Comparison of Atlantic salmon individuals with different outcomes of cardiomyopathy syndrome (CMS)
title_fullStr Comparison of Atlantic salmon individuals with different outcomes of cardiomyopathy syndrome (CMS)
title_full_unstemmed Comparison of Atlantic salmon individuals with different outcomes of cardiomyopathy syndrome (CMS)
title_sort comparison of atlantic salmon individuals with different outcomes of cardiomyopathy syndrome (cms)
publisher BMC
series BMC Genomics
issn 1471-2164
publishDate 2012-05-01
description <p>Abstract</p> <p>Background</p> <p>Cardiomyopathy syndrome (CMS) is a severe disease of Atlantic salmon (<it>Salmo salar</it> L.) associated with significant economic losses in the aquaculture industry. CMS is diagnosed with a severe inflammation and degradation of myocardial tissue caused by a double-stranded RNA virus named piscine myocarditis virus (PMCV), with structural similarities to the <it>Totiviridae</it> family. In the present study we characterized individual host responses and genomic determinants of different disease outcomes.</p> <p>Results</p> <p>From time course studies of experimentally infected Atlantic salmon post-smolts, fish exhibited different outcomes of infection and disease. High responder (HR) fish were characterized with sustained and increased viral load and pathology in heart tissue. Low responder (LR) fish showed declining viral load from 6–10 weeks post infection (wpi) and absence of pathology. Global gene expression (SIQ2.0 oligonucleotide microarray) in HR and LR hearts during infection was compared, in order to characterize differences in the host response and to identify genes with expression patterns that could explain or predict the different outcomes of disease. Virus-responsive genes involved in early antiviral and innate immune responses were upregulated equally in LR and HR at the first stage (2–4 wpi), reflecting the initial increase in virus replication. Repression of heart muscle development was identified by gene ontology enrichment analyses, indicating the early onset of pathology. By six weeks both responder groups had comparable viral load, while increased pathology was observed in HR fish. This was reflected by induced expression of genes implicated in apoptosis and cell death mechanisms, presumably related to lymphocyte regulation and survival. In contrast, LR fish showed earlier activation of NK cell-mediated cytotoxicity and NOD-like receptor signaling pathways. At the late stage of infection, increased pathology and viral load in HR was accompanied by a broad activation of genes involved in adaptive immunity and particularly T cell responses, probably reflecting the increased infiltration and homing of virus-specific T cells to the infected heart. This was in sharp contrast to LR fish, where recovery and reduced viral load was associated with a significantly reduced transcription of adaptive immunity genes and activation of genes involved in energy metabolism.</p> <p>Conclusions</p> <p>In contrast to LR, a stronger and sustained expression of genes involved in adaptive immune responses in heart tissue of HR at the late stage of disease probably reflected the increased lymphocyte infiltration and pathological outcome. In addition to controlled adaptive immunity and activation of genes involved in cardiac energy metabolism in LR at the late stage, recovery of this group could also be related to an earlier activation of NOD-like receptor signaling and NK cell-mediated cytotoxicity pathways.</p>
url http://www.biomedcentral.com/1471-2164/13/205
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