PD vaccination protects against SPDV subtypes 2 and 3 Kristian Ulven MSD Animal Health Norge AS
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1 PD vaccination protects against SPDV subtypes 2 and 3 Kristian Ulven MSD Animal Health Norge AS
2 The cause of Pancreas disease (PD) can descend from different isolates PD is a disease caused by salmon pancreas disease virus (SPDV = SAV) Affects Atlantic salmon (Salmo salar) and Rainbow trout (Oncorhynchus mykiss) Isolates can be separated by sequencing parts of the E2 proteine (genotyping) Current isolates cannot be speparated by serology There are 6 genetical groups of isolates (subtypes) known as: SAV-1, SAV-2, SAV-3, SAV-4, SAV-5 og SAV-6 SAV-1,-4,-5 og -6 isolates: Endemic in Ireland og Scotland SAV-2 isolates: Endemic in France, Norway (north of Hustadvika) and Shetland SAV-3 isolates: Endemic in Norway (south of Hustadvika) 2
3 There is only one serotype of the PD-virus Genotype (subtype of SAV): separated with use of genetic analyzis Serotype: Separated by antibodies that detect variations on the surface proteins 3
4 PD vaccination is efficacious against all known genotypes A comparative cross-neutralization studies from 2013 of the six recognized SAV genotypes shows that : The six genotypes are the same viral species The humoral immunesystem of the fish will recognize all SAV isolates as the same A vaccine based on one isolate will protect against PD caused by a different isolate, independently of their subtype grouping Cross-neutralization studies with salmonid alphavirus subtype 1 6 strains: results with sera from experimental studies and natural infections. Graham et.al. Journal of Fish Diseases
5 The severity of the disease varies with the genotypes Some differences are found in the dynamic of infection among the six genotypes: SAV 1 & 3 isolates showed synchronic infection of cohabitating fish, in addition to the highest viral load in heart tissue, and most severe histopathological changes SAV 2 & 6 isolates showed asynchronic infection in cohabitating fish, and a slower viral spread, lower viral load and milder histopathological changes Only one isolate per subtype was included in this study, therefore results cannot generalize all potential isolates There is probably variations both between, and inside, the subtype groupings Graham DA, Frost P, McLaughlin K, Rowley HM, Gabestad I, Gordon A, McLoughlin MF (2011) A comparative study of marine salmonid alphavirus subtypes 1 6 using an experimental cohabitation challenge. J Fish Dis 34:
6 The severity of the disease varies with the genotypes Mortality and weight loss i atlantic salmon were studied in a cohbitant challenge trial with three norwegian SAV3 and three norwegian SAV2 isolates: SAV2 isolates showed a tendency of lower prevalens and severity of pathological changes There was difference in virulence between the isolates within each subtype Taksdal T,, Bang Jensen B, Bockerman I, McLoughlin MF, Hjortaas MJ, Ramstad A, Sindre H, (2014) Mortality and weight loss of Atlantic salmon, Salmo salar L., experimentally infected with salmonid alphavirus subtype 2 and subtype 3 isolates from Norway. J Fish
7 PD vaccination reduces disease and severity of PD specific lesions following SAV3 challenge Cohabitant challenge with SAV3 isolat Frekvens (%) Heart lesion score 5wpc 5,0 5,0 90,0 AQUAVAC PD vaccinated PD7 45,0 30,0 25,0 Saline Frekvens (%) Pancreas lesion score 5 w.p.c 15,8 84,2 AQUAVAC PD vaccinated PD7 Histopathology: Significant reduction of PD specific histophatological heart and pancreas lesions 5 weeks post PD challenge. 63,2 10,5 26,3 Saline % of the PD vaccinated group had PD specific lesions in heart, while 75% of the unvaccinatd group had PD specific lesions in heart. 7
8 PD vaccination reduces disease and severity of PD specific lesions following SAV2 challenge Heart lesion score 25dpc Cohabitant challenge with SAV2 isolate Pancreas lesion score 25dpc Frequence % 100,0 90,0 80,0 70,0 60,0 50,0 40,0 30,0 20,0 10,0 0,0 6,7 26,7 13,3 53,3 PD PD vaccinated vaksinert 46,7 20,0 26,7 6,7 Kontroll Histopathology: Significant reduction of PD specific histophatological heart and pancreas lesions 26 days post PD challenge Frequency % 100,0 90,0 80,0 70,0 60,0 50,0 40,0 30,0 20,0 10,0 0,0 6,7 33,3 6,7 53,3 PD PD vaccinated vaksinert 13,3 73,3 13,3 Kontroll ,4% of the PD vaccinated group had PD specific lesions in heart, while 93,3% of the unvaccinatd group had PD specific lesions in heart. 8
9 PD vaccination reduces prevalence of SPDV positive sera after cohabitation challenge PD vaccinated Injection dose (ml) PD challenge Prevalence of SPDV positive sera at 21dpc (Ct below 35) (12 C) % RPP (relative percent protection) Yes 0,1 SAV3 1/35 (2,8%) No 0,1 SAV3 28/35 (80%) 96,4 - PD vaccinated Injection dose (ml) PD challenge Prevalence of SPDV positive sera at 17dpc (Ct below 35) (15 C) % RPP (relative percent protection) Yes 0,1 SAV2 3/25 (12%) No 0,1 SAV2 18/25 (72%) Peak viremia 9 83,3 -
10 Summary The humoral immunesystem of the fish will recognize all SPDV/SAV isolates as the same, independently of their subtype grouping It is shown that a vaccine based on one isolate (e.g SAV1 isolate) will protect against PD caused by a different isolate (e.g SAV2 isolate or SAV3 isolate) by reducing disease and the severity of histophatological lesions in heart and pancreas 10
11 Referances Graham et.al. Cross-neutralization studies with salmonid alphavirus subtype 1 6 strains: results with sera from experimental studies and natural infections. Journal of Fish Diseases 2013 Graham DA, Frost P, McLaughlin K, Rowley HM, Gabestad I, Gordon A, McLoughlin MF (2011) A comparative study of marine salmonid alphavirus subtypes 1 6 using an experimental cohabitation challenge. J Fish Dis 34: Taksdal T,, Bang Jensen B, Bockerman I, McLoughlin MF, Hjortaas MJ, Ramstad A, Sindre H, (2014) Mortality and weight loss of Atlantic salmon, Salmo salar L., experimentally infected with salmonid alphavirus subtype 2 and subtype 3 isolates from Norway. J Fish
12 Thanks to Ingunn Sommerset (MSD AH Norway) Petter Frost (MSD AH Innovation) Chris Gould (MSD AH Global) Dag Knappskog Christian Wallace (VESO Vikan) Marian McLoughlin (Fish Vet Group)
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