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      A DNA vaccine encoding the viral hemorrhagic septicemia virus genotype IVb glycoprotein confers protection in muskellunge ( Esox masquinongy), rainbow trout ( Oncorhynchus mykiss), brown trout ( Salmo trutta), and lake trout ( Salvelinus namaycush)

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          Abstract

          Background

          The viral hemorrhagic septicemia virus (VHSV) is one of the most serious fish pathogens. In 2003, a novel sublineage (genotype IVb) of this deadly virus emerged in the Great Lakes basin causing serious fish kills. We have previously demonstrated that a DNA plasmid (pcDNA), containing a cytomegalovirus (CMV) promoter and the viral hemorrhagic septicemia virus (VHSV) genotype IVb glycoprotein (G) gene insert (designated pVHSivb-G) confers moderate protection in muskellunge ( Esox masquinongy), a highly susceptible species upon challenge. In order to achieve optimal protection, we investigated a number of factors including the incubation time [i.e. the number of degree days (° days)] before challenge, and viral challenge dose and route. Additionally, we tested if pVHSivb-G provides protection against VHSV-IVb to less susceptible salmonids such as rainbow trout ( Oncorhynchus mykiss), brown trout ( Salmo trutta) and lake trout ( Salvelinus namaycush).

          Results

          An increase in the period lapsed between vaccination and challenge to 1880° days resulted in 95% relative percent protection (RPS) in muskellunge following a single administration of the pVHSivb-G plasmid and viral challenge. An RPS of 100% for muskellunge was achieved with a longer incubation period (2400° days) and in conjunction with a booster dose of the plasmid. The pVHSivb-G vaccine also elicited significant protection in all three salmonid species, reaching 100% RPS in lake trout following an incubation period of 1001° days prior to viral challenge. Vaccination with pVHSivb-G was also associated with the development of significant levels of circulating VHSV-binding antibodies in muskellunge as measured by indirect ELISA, which reached peak levels 6–7 weeks post-vaccination. Viral shedding in vaccinated survivors was minimal and of transient nature.

          Conclusions

          The study shows that the pVHSivb-G plasmid can elicit a protective response against the wild virus strain in a range of species important in recreational and commercial Great Lakes fisheries.

          Electronic supplementary material

          The online version of this article (doi:10.1186/s12985-016-0662-8) contains supplementary material, which is available to authorized users.

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            Potency testing of fish vaccines

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              Evolution of the fish rhabdovirus viral haemorrhagic septicaemia virus.

              Viral haemorrhagic septicaemia (VHS) caused by the rhabdovirus VHSV is economically the most important viral disease in European rainbow trout farming. Until 1989, this virus was mainly isolated from freshwater salmonids but in the last decade, it has also been isolated from an increasing number of free-living marine fish species. To study the genetic evolution of VHSV, the entire G gene from 74 isolates was analysed. VHSV from wild marine species caught in the Baltic Sea, Skagerrak, Kattegat, North Sea, and English Channel and European freshwater isolates, appeared to share a recent common ancestor. Based on the estimated nucleotide substitution rate, the ancestor of the European fresh water isolates was dated some 50 years ago. This finding fits with the initial reports in the 1950s on clinical observations of VHS in Danish freshwater rainbow trout farms. The study also indicates that European marine VHSV and the North American marine line separated approx. 500 years ago. The codon substitution rate among the freshwater VHSV isolates was found to be 2.5 times faster than among marine isolates. The data support the hypothesis of the marine environment being the original reservoir of VHSV and that the change in host range (to include rainbow trout) may have occurred several times. Virus from the marine environment will therefore continue to represent a threat to the trout aquaculture industry.
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                Author and article information

                Contributors
                standi13@msu.edu
                millarde@msu.edu
                brenden@msu.edu
                +1-517-884-2019 , faisal@cvm.msu.edu
                Journal
                Virol J
                Virol. J
                Virology Journal
                BioMed Central (London )
                1743-422X
                2 December 2016
                2 December 2016
                2016
                : 13
                : 203
                Affiliations
                [1 ]Department of Pathobiology and Diagnostic Investigation, College of Veterinary Medicine, Michigan State University, East Lansing, MI 48824 USA
                [2 ]Department of Fisheries and Wildlife, College of Agriculture and Natural Resources, Michigan State University, East Lansing, MI 48824 USA
                Article
                662
                10.1186/s12985-016-0662-8
                5134280
                27912771
                9036a001-e60f-4903-b721-7438bf690f15
                © The Author(s). 2016

                Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License ( http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

                History
                : 6 May 2016
                : 29 November 2016
                Funding
                Funded by: FundRef http://dx.doi.org/10.13039/100001145, Great Lakes Fishery Trust;
                Award ID: 2012.1257
                Award Recipient :
                Categories
                Research
                Custom metadata
                © The Author(s) 2016

                Microbiology & Virology
                dna vaccine,viral hemorrhagic septicemia virus,fish
                Microbiology & Virology
                dna vaccine, viral hemorrhagic septicemia virus, fish

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