Source:http://linkedlifedata.com/resource/pubmed/id/20045026
Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
5
|
pubmed:dateCreated |
2010-2-17
|
pubmed:abstractText |
Interferons (IFNs) and their receptors exist in all classes of vertebrates, where they represent early elements in innate and adaptive immunity. Both types I and II IFNs have been discovered in fish and type I IFN has recently been classified into two groups based on their primary protein sequences and biological activities. Thus, although groups I and II zebrafish IFN show powerful antiviral activities, only group I (IFNphi1) is able to protect the fish against bacterial infection. In addition, group II IFNs (IFNphi2 and IFNphi3) induce a rapid and transient expression of antiviral genes, while group I IFN exerts a slow but more powerful induction of several antiviral and pro-inflammatory genes. To gain further insight into the IFN system of fish, we have developed a waterborne infection model of zebrafish larvae with the spring viremia of carp virus (SVCV). Larvae were challenged 3 days post-fertilization by immersion, which considerably reduces the manipulation of fish and represents a more natural route of infection. Using this infection model, we unexpectedly found an inability on the part of zebrafish larvae to mount a protecting antiviral response to waterborne SVCV. Nevertheless, zebrafish larvae showed a functional antiviral system since ectopic expression of the cDNA of both groups I and II IFN was able to protect them against SVCV via the induction of IFN-stimulated genes (ISGs). Interestingly, group II IFNs also induced group I IFN, suggesting crosstalk between these two kinds of antiviral IFN. These results further confirm the antiviral activities of type I IFN in the zebrafish and provide the first viral infection model for zebrafish larvae using a natural route of infection. This model, in combination with the powerful gene overexpression and morpholino-mediated knockdown techniques, will help to illuminate the IFN system of teleost fish.
|
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical | |
pubmed:status |
MEDLINE
|
pubmed:month |
May
|
pubmed:issn |
1879-0089
|
pubmed:author | |
pubmed:copyrightInfo |
Copyright (c) 2009 Elsevier Ltd. All rights reserved.
|
pubmed:issnType |
Electronic
|
pubmed:volume |
34
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
546-52
|
pubmed:meshHeading |
pubmed-meshheading:20045026-Animals,
pubmed-meshheading:20045026-Cloning, Molecular,
pubmed-meshheading:20045026-Cytokines,
pubmed-meshheading:20045026-Fish Proteins,
pubmed-meshheading:20045026-Gene Expression Regulation,
pubmed-meshheading:20045026-Immunity, Innate,
pubmed-meshheading:20045026-Interferon Type I,
pubmed-meshheading:20045026-Interferon-gamma,
pubmed-meshheading:20045026-Larva,
pubmed-meshheading:20045026-Rhabdoviridae,
pubmed-meshheading:20045026-Rhabdoviridae Infections,
pubmed-meshheading:20045026-Transgenes,
pubmed-meshheading:20045026-Virulence,
pubmed-meshheading:20045026-Zebrafish
|
pubmed:year |
2010
|
pubmed:articleTitle |
Zebrafish larvae are unable to mount a protective antiviral response against waterborne infection by spring viremia of carp virus.
|
pubmed:affiliation |
Department of Cell Biology and Histology, Faculty of Biology, University of Murcia, Murcia, Spain.
|
pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
|