Aquafin CRC - Atlantic Salmon Aquaculture Subprogram: development of an AGD vaccine: phase II

Project number: 2004-217
Project Status:
Completed
Budget expenditure: $500,823.00
Principal Investigator: Chris Prideaux
Organisation: CSIRO Australian Animal Health Laboratory
Project start/end date: 30 Mar 2005 - 21 May 2008
Contact:
FRDC

Need

Health is one of the major issues associated with intensive culture industries, including aquaculture. Unhealthy stock relates to unhealthy industry – higher production costs, reduced viability, poor market and public image. Outbreaks of infectious salmon anaemia (ISA) in Scotland resulted in some salmon companies going into receivership. The use of medication increases production costs and negatively impacts on the market.
In Australia, salmon aquaculture is relatively disease free, which provides a possible marketing advantage. However, Amoebic Gill Disease costs are 9.4% of the gross value of production; a significant production cost for farming Atlantic salmon in Tasmania. The disease outbreaks seem to intensify as the industry develops and now are prevalent not only during summer months but also in winter. Outputs of the CRC Health Program such as improved treatment of AGD infected fish, AGD risk forecasting ability and vaccine production against AGD will increase the profitability and competitiveness of the Australian salmon industry.
AGD is severely limiting further expansion of the industry because it ties up resources that could be directed elsewhere, and it limits farming sites due to reliance on freshwater for bathing. Current treatment of AGD while environmentally friendly is not viable in the long-term and alternatives are required. Other treatments may be more reliant on antibiotics or chemicals, a risk to the image of the industry. Although vaccine development can be seen as a high-risk research target the potential rewards justify the risk

Objectives

1. To identify potential protective antigens from N. pemaquidensis using a combined DNA/protein approach.
2. To identify and characterize attachment molecules involved in the infection process of Atlantic Salmon by N. pemaquidensis..
3. To demonstrate protection of Atlantic salmon against clinical AGD via cDNA and/or recombinant protein vaccination.

Final report

ISBN: 978-1-921424-41-0
Author: Chris Prideaux
Final Report • 2009-03-20 • 1.05 MB
2004-217-DLD.pdf

Summary

Amoebic gill disease (AGD) is considered to be the most significant health problem for farmed Atlantic salmon in Tasmania, costing the industry an estimated $15-20 million pa. It is caused by the presence of Neoparamoeba spp. on the gills and if untreated can lead to death. Although some control of the disease is achieved by freshwater bathing, this procedure is not considered a viable, long-term solution. It is not fully efficacious – more than one treatment is usually required; it is very labour-intensive; it requires large volumes of freshwater, and is stressful to the fish, which further impacts on their health and growth. Furthermore, recent experience indicates an increase in the required frequency for freshwater bathing in an attempt to control the disease.

Vaccine development is part of a multifaceted approach to develop short-, medium- and long-term solutions to the control of AGD; development of a sub-unit vaccine being the long-term approach of the overall research strategy. The essential objective is to develop a set of strategies and tools to provide the salmon industry with a substantial reduction to the economic impact of AGD in an economically and environmentally sustainable way.

The most significant outcome of this project is the commencement in July 2007 of sea trials for the experimental DNA vaccine made up of six antigens shown to provide a relative increase in protection of approximately 40 percent in laboratory based amoebic gill disease (AGD) trials.

Keywords: Atlantic salmon, Neoparamoeba, DNA vaccine, recombinant protein, response

Related research

Industry
Industry
Industry

Aquafin CRC - Atlantic Salmon Aquaculture Subprogram: molecular assessment of resistance to AGD in Atlantic salmon

Project number: 2004-218
Project Status:
Completed
Budget expenditure: $106,048.00
Principal Investigator: Nick G. Elliott
Organisation: CSIRO Oceans and Atmosphere Hobart
Project start/end date: 29 Jun 2004 - 31 Aug 2008
Contact:
FRDC

Need

Management costs (ca. 10% GVP) associated with AGD are severely limiting further expansion and sustainability of the Tasmanian Atlantic salmon industry. A holistic approach that combines alternative treatments, better management procedures, the use of a vaccine and selection of stock that are more resistant to infection would greatly reduce the impact of AGD. With the exception of selection the other areas are all active components of the Aquafin CRC Health Program. A more resistant stock along with even a partially effective treatment and vaccine would be of major benefit to the long-term sustainability of the industry.

An international consultant recommended to the industry and State Government in March 2003 that a selective breeding program should be established as soon as practical. A business plan for such a program has been developed and is under consideration by the industry. A major trait for inclusion in the program was resistance to AGD. Research in relation to understanding AGD resistance for use in selective breeding was ranked second to oral treatments in an industry survey of AGD priorities in June 2003.

Selection for resistance to external parasites in breeding programs is relatively novel and AGD is an issue specific to the Tasmanian industry, therefore unlike most other production traits in a breeding program reliance on overseas research and experience is impossible. With recent advances in molecular technologies it is now possible to investigate and understand variation to disease at the genetic level. Such knowledge on AGD will allow both improved understanding of the phenotypic variation (that will benefit other research areas) and identification of specific genetic markers that would allow faster genetic gains in resistance to be made in a selection program than would be possible via standard phenotypic selection alone.

Objectives

1. To define the molecular events underlying the progression of clinical AGD within Atlantic salmon
2. To undertake a molecular assessment of the inherent genetic resistance to AGD in Atlantic salmon
3. To identify molecular markers associated with AGD resistance for application in a selective breeding program

Final report

ISBN: 9781921424670
Author: Nicholas Elliott
Final Report • 2009-03-23
2004-218-DLD.pdf

Summary

The outcome of this project is the development, at the request of industry, of a proposal to enhance the genetic gains in the industry selective breeding program for AGD resistance through marker assisted selection. The confidence to proceed with such a proposal is brought about by the extensive knowledge and understanding gained on the molecular basis of AGD resistance through this project.

The project completed the first comparison of genetic variation at a coding gene between the domesticated Australian Atlantic salmon and their ancestral Canadian population; results were also compared to that published for European populations.

In contrast to previously reported variation at non-coding microsatellite loci, a high level of variation at the major histocompatibility (MH) genes was observed within the domesticated Australian population, and observed sequence diversity exceeded that reported for other cultured Atlantic salmon populations.

The project also completed the first study to examine resistance to AGD at a molecular level. The association between MH polymorphism and severity of AGD infection was examined in 30 full-sibling families by acute challenge.

Keywords: Atlantic salmon, Salmo salar, amoebic gill disease, AGD, Neoparamoeba, resistance, gene expression, DNA microarray.