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Distribution of salmonid diseases in New Zealand Trout and salmon (salmonids) are Northern Hemisphere species. Introductions to this country began in 1867, when brozun trout eggs were imported by a sportfish group, the Acclimatisation Society,from Scottish stock being reared in Tasmania. Further introductions of various species of salmonids from Europeanand North American countriescontinued until the 1960s"'. Commercial farming of salmon be- gan in New Zealand in fresh water in the mid 1970s and in sea-cages some 6 years later. Intensive screening of salmonids for disease followed this commercial development. There are three sport fish hatcheries in the North Island, at Tongariro,Ngongotaha and Napier (Figure l),which specialise in rearing rainbow trout for restocking angling waters. The South Island has one sport fish hatchery at Wanaka and 23 salmon farms rearing Quinnat (Oncorhynchus tshauiytscha) and sockeye (0.nerka) salmon. The salmon farms are spread throughout the South Island and in Stewart Island. Information on salmonid diseases in New Zealand has been collected during investigations of disease episodes on fish farms and on-site inspection, and laboratory testing for export certification. Export testing has been directed at the detection of Myxobolus cerebralis, the protozoan agent of whirling disease, and viral haemorrhagic septicaemia (VHS).However, the tissue culture cell lines used are susceptible to a number of fish viruses and a birnavirus, infectious pancreatic necrosis virus (IPNV),has been isolated from healthy sea-run adult Quinnat salmon during export te~ting@)(~)(~). In 1977 MAF established a specialist fish disease diagnostic section at the Central Animal Health Laboratory (CAHL), Continued next page Figure 1: Locations offish hatcheries and isolations of disease organisrrzs Surveillance 23(4) 1996 23 Wallaceville, Upper Hutt. Export testing of salmon farms for the certification of salmon meat commenced there in 1985. All 'lots' (year, classes and species) on about 20 South Island salmon properties have been tested annually for whirling disease and viruses. On average, 60-120 salmon from each property were tested for Myxobolus cerebralis and 120-180salmon were tested for viruses. During 9 years of export testing, diagnostic examinations and surveys, 12,920salmonids have been tested at CAHL for M . cerebralis and 23,183 salmonids have been sampled for viral tissue culture examination. For the same period, 1,809 salmonid were examined for bacterial diseases. Pathogenic organisms identified by CAHL in salmonids over the period 1977 to 1995 include the following: Virus: infectious pancreatic necrosis virus (IPNV) Bacteria: Flexibacfer sp. Hafnia alvei Strepfococciis sp. Vibrio ordalii Yersinia ruckeri Protozoa: Chilodonella sp. Ichthyophtkirus multifilis Myxobolus cerebralis Paramoeba sp. The locations in which disease agents were isolated are shown in Figure 1. Four disease agents in the above list are of particular interest. M. cerebralis was first detected in New Zealand at a trout hatchery near Dunedin in 1972'". A survey carried out at that time, and following detection of whirling disease in Canterb~ry'~"'',identified the organism in 1980 in rainbow trout farmed near Christchurch. Since thenM. cerebralis has been found at a further six locations, in fish that were sampled for research or export certification, but that showed no signs of whirling disease. M. cerebralis has never been detected in the North Island. V . ordalii was first identified in 1984 during disease investigation on a salmon 24 Surveillance 23(4) 1996 farm near Owaka in Otago(xl.In the early years of sea-cage rearing of salmon in New Zealand, vibriosis outbreaks were common in the warm summer months. Fish in their first year in seawater were most often affected, and oral antibiotic medication and vaccination were used to limit mortalities. However, since 19S9 vibriosis outbreaks have been rare arid antibiotic medication and vaccination are no longer necessary. Y. ruckeri was first isolated in 1989 from dying fingerling salmon on a Canterbury salmon farm. A survey was carried out to determine the distribution of this agent and to test for the exotic fish pathogen Aeronzonas salmonicida. Salmonids and native fish were sampled at aquaculture and wild locations in both Islands. Y . ruckeri was detected at two sites already known to be positive. A. saltnonicida was not i~olated'~'. IPN virus was first isolated in 1985 duringroutine testing for export purposes of healthy sea-run Quinnat salmod2,. It has since been isolated seven times from this class of stock, but there have been no isolations from other age classes on these or other salmonproperties. Clinical signs of the disease, which are seen with other strains of this virus group, have never been observed in New Zealand. The short list of diseases illustrates New Zealand's relative absence of serious fish diseases compared with almost all other countries that farm salmonids"0'. Three factors have played major parts in this favourable health status. Firstly, salmonids were introduced as eggs, which are the safest life stage at which to translocate fish from the point of view of disease transmission'"'. These introductions occurred when fish farming was in its infancy and when the movement of salmonids, within and between countries, had been minimal. Secondly, New Zealand is an island nation comparatively isolated from the rest of world. Thirdly, for the last 20 years New Zealand has had in place border controls to prevent the introduction of exotic fish diseases with imports of salmonids and their unsterilised products. References ( I ) Scott D. The migratory trout (Sulmo trurtu L.) in New Zealand. 1. The introduction of stocks. Transactions of the Royal Society of New Zealand, Zoology 4(17), 209-227, 1964. (2) Tisdall DJ, Phipps JC. Isolation and characterisation of a marine birnavirus from returning Quinnat salmon (Oncorhynchus r.shawyrschu) in the South Island of New Zealand. New Zealand Veterinary Journal 35, 217-218, 1987. (3) ChiefVeterinary0fficer.AnnualReport 1992. Surveillance 20(3), 7, 1993. (4) Chiefveterinary Officer. AnnualReport 1993. Surveillance 21(3), 8, 1994. (5) Hewitt GC, Little RW. Whirling disease in New Zealand trout caused by Myxosornu cerehrulis (Hofer, 1903) (Protozoa: Myxosporida). New Zealand Journal of Marine and Freshwater Research 6(1 & 2), 1-10, 1972. (6) Hewitt GC. Survey of New Zealand trout hatcheries for whirling disease caused by Mvxosomci cerebralis. New Zealand Journal of Marine and Freshwater Research 6(4), 463-468, 1972. (7) Boustead N. Whirling disease survey results. Freshwater Catch, Summer, 9-1 1, 1982. (8) Wards BJ, Patel HH, Anderson CD, de Lisle G. Characterisation by restriction endonuclease analysih and plasmid profiling of Vibrio ordalii strains from salmon (Oncorhynchus tshawy/scha and Oncorhynchus nerku) with vibriosis in New Zealand. New Zealand Journal of Marine and Freshwater Research 25, 345-350, I99 I . (9) AndersonC,KnowlesG,deLisleG.Asurvey for Yersiniu ruckeri and A e r o m o n u s salmonicidu in farmed and wild fish. Surveillance 2 I (3), 39-40, 1994. ( I 0) Anderson C. Important diseases of salmonid fish and the risk they pose to New Zealand. Surveillance 17(2), 17-18, 1990. ( 1 1 ) Turner GE. Codes of practice and manual of procedures for consideration of introductions and transfers of marine and freshwater organisms. European Inland Fisheries Advisory Commission, Food and Agriculture Organisation of the United Nations, Occasional paper 23, 1-44, 1988. Colin Anderson MAF Quality Management Central Animal Health Laboratory Email: andersoncm wallacevil1e.mqm.govt.nz