Vaccination against pancreas disease in Atlantic salmon, Salmo salar L., reduces shedding of salmonid alphavirus
© The Author(s) 2016
Received: 18 January 2016
Accepted: 9 June 2016
Published: 5 August 2016
Salmon pancreas disease virus, often referred to as salmonid alphavirus (SAV), causes pancreas disease (PD) in European salmonids. SAV transmits horizontally from fish shedding virus into the water and ocean currents are believed to be a main contributor of viral spread between marine farms. Vaccination against PD is previously shown to reduce mortality and severity of clinical PD. In this study, we demonstrate that vaccination against PD significantly reduces viral shedding from infected individuals. The results suggest that PD vaccination can be an important tool to reduce the infection pressure, a known key risk for PD outbreaks at neighbouring farms.
Introduction, methods and results
This animal trial was approved by the Norwegian Animal Research Authority (FOTS ID 6100) and carried out at The Industrial and Aquatic Laboratory (ILAB) wet lab facilities at the Bergen High Technology Centre, Norway. The fish population (Atlantic salmon Salmobreed strain) had been pretested for infectious pancreatic necrosis virus (IPNV), piscine orthoreovirus, infectious salmon anaemia virus (ISAV) and SAV by means of real-time RT-PCR (hereafter referred to as qRT-PCR) analysis provided by Patogen Analysis AS (Ålesund, Norway), and found negative. A total of 260 Atlantic salmon parr with an average weight of 30 grams were anaesthetised with FINQUEL® Vet. (ScanAqua AS, Årnes, Norway) according to manufacturer’s recommendations. 130 fish were vaccinated with AQUAVAC® PD7 (0.1 mL/fish), a commercial heptavalent vaccine containing 5 inactivated bacterial antigens (Aeromonas salmonicida subsp. salmonicida, Vibrio salmonicida, Vibrio anguillarum serotype O1 and O2a, Moritella viscosa) and 2 inactivated viral antigens (IPNV and SAV) in a mineral oil emulsion. As unvaccinated controls, a total of 130 fish were injected intraperitoneally with sterile saline solution (0.9% NaCl, 0.1 mL/fish). The PD vaccinated and unvaccinated groups were kept in individual 500 L tanks with 12 °C flow through fresh water for 6 weeks post vaccination (~500 degree-days) before 120 fish from each group were challenged intramuscularly with 2.05 log10 TCID50/fish (0.05 mL/fish) of a Norwegian SAV isolate (SAV genotype 3) propagated in Chinook salmon embryo (CHSE-214) cell culture. The fish were, while being challenged, allocated to four 150 L challenge tanks (tank 1 to 4), generating duplicate tanks with 60 fish for both vaccinated and unvaccinated groups. The water flow in the tanks was 300 L per hour.
The remaining 20 fish (10 from the AQUAVAC® PD7 vaccinated group and 10 from the unvaccinated controls) were labelled by maxillae clipping, challenged using the same procedure as above and allocated in one 500 L tank (tank 5) in order to estimate the prevalence of infected individuals in the two groups. These 20 fish were sampled for blood and faeces 10 days post challenge (dpc) which by our experience corresponds to the peak viraemia time point following intramuscular (i.m.) challenge with SAV at 12 °C.
One day post i.m. challenge, 10 untreated, naïve cohabitants were labelled by adipose fin clipping and added to tank 1–4 as “detectors” of infectious SAV shed from the challenged fish already present in the tank. These 40 naïve cohabitants in total were blood sampled at day 24 which, by our experience, corresponds to the peak viraemia time point following cohabitation challenge with SAV at 12 °C.
Water samples from tanks 1–4 were collected 1, 4, 10, 14, 18 and 24 days post challenge using sterile 1 L screw-cap PET bottles (VWR). All samples were vacuum filtered through electropositive Zeta Plus® Virosorb® 1 MDS filters (Cuno Inc., USA) according to a method described in Andersen et al.  with minor modifications. Immediately following sampling and prior to filtration each water sample was spiked with 50 μL (5.2 log10 TCID50) of an ISAV isolate (Bremnes/98) which was used as an exogenous filtration control and for the relative quantification of SAV in the water samples. One litre of filtered and deionized water (Milli-Q®, Millipore Corporation), spiked with the same volume of the ISAV suspension, was also subjected to filtration at all sampling points in order to check for potential cross-contamination between water samples. After filtration, individual filters were soaked in 1.4 mL lysis buffer (RNeasy® 96 Kit, Qiagen) for 10 min on a rocker (320 rpm), and 2 × 350 μL (A and B sample) were collected and frozen at −80 °C for subsequent RNA extraction and qRT-PCR analysis. The water samples were analysed by qRT-PCR in triplicate, using the SAV nsP1  and ISAV segment 8 (S8)  assays for specific detection of SAV and ISAV, respectively. Only samples that were positive in triplicate were used for normalization performed as described elsewhere [7, 18]. During qRT-PCR setup, positive, negative and no template controls (NTC) were included in all runs. Mean Ct values (Cycle threshold) for the nsP1 assay were normalized against mean Ct values for the ISAV S8 assay using the Microsoft® Excel based software Q-Gene with Eq. 2 . Mean normalized expression (MNE) values were transformed into fold change by calibrating against the lowest MNE value obtained from water samples during the experiment for a better visualization of the data. The cross-contamination controls (pre-filtered and deionized Milli-Q® water) were all negative for SAV and positive for ISAV by qRT-PCR analysis at all sampling points.
Serum (50 μL/fish) and faeces samples (2 × 2 × 2 mm/fish) were spiked with inactivated Equine Influenza Virus (EIV) prior to RNA extraction, serving as an exogenous RNA extraction control and for relative quantification of SAV RNA eventually present in the samples. These samples were analysed by qRT-PCR using the EI H3 assay targeting EIV , and the nsP1 assay targeting SAV. Normalised expression (NE) values obtained from serum and faeces were fold changed by calibrating against the lowest NE value obtained for each tissue and log2 transformed for a better visualization of the data. RNA from serum, faeces and water samples was extracted using the RNeasy® 96 Kit (Qiagen) according to the manufacturer’s protocol (elution volume was 50 μL/RNA sample). qRT-PCR analyses were performed using Verso™ 1-step Q-RT-PCR Kit low ROX (Thermo Scientific) using 4 μL of RNA sample. Primer and probe concentrations for each of the three assays were: Fwd. primer: 900 nM, Reverse primer: 900 nM, Probe: 260 nM. Reactions were run in an ABI PRISM® 7500 FAST Thermocycler from Applied Biosystems at the following conditions: 50 °C/30 min, 95 °C/15 min, 40 cycles of 95 °C/15 s and 60 °C/60 s. Standard curve was generated for each assay from dilution series of SAV, ISAV and EIV in Phosphate-buffered saline (PBS). Slope, R2 and assay efficiency were calculated for each assay using Q-Gene giving the following values (SAV nsP1/ISAV S8/EI H3): −3.1685/−3.8113/−3.4403 (slope), 0.9964/0.9992/0.9976 (R2) and 2.0683/1.8297/1.9529 (E).
Statistical analysis of the effect of PD vaccination on the viral load in the water samples detected by qRT-PCR was performed using the Pair Wise Fixed Reallocation Randomisation Test implemented in the program REST 2009 , using as input the mean Ct values of triplicate measurements on each sample for SAV nsP1 assay (target gene), the mean Ct values for the ISAV spike obtained with ISAV S8 assay (reference gene) and the PCR efficiencies of these assays.
Statistical analysis of the effect of PD vaccination on the prevalence of PCR positive fish in serum of the naïve cohabitant fish at 24 dpc was performed using a Generalized Linear Mixed Model (GLMM) for a binomial distribution (SAS procedure GLIMMIX), on the prevalence of positive fish in each tank, including tank as random effect to account for the correlation in the data.
Statistical analysis of the effect of PD vaccination on the viral load detected by qRT-PCR in the serum sampled from the naïve fish was performed using the Pair Wise Fixed Reallocation Randomisation Test implemented in REST 2009, using as input the individual Ct values for SAV nsP1 assay (target gene), the individual Ct values for the EIV spike obtained with EI H3 assay (reference gene) and the PCR efficiencies of these assays. The Ct values used for the analysis in REST 2009 were censored, i.e. the negative samples (with undetermined SAV Ct values) were assigned a Ct = 40 (=max number of cycles per PCR run).
Statistical comparison of the prevalence of SAV positive fish in tank 5 (detected by RT-PCR on serum and faeces samples) between vaccinated and unvaccinated groups was performed by the Fisher’s exact test. Relative Risks were used to determine Relative Percentage Protection [RPP = (1−RR) × 100] as a measure of the vaccine’s efficacy.
For all statistical analysis the level of significance (α) was set at 0.05 and tests were two-sided. Statistical calculations were executed using REST 2009 for the Fixed Reallocation Randomisation Test (set to 2000 iterations), SAS V9.3 for GLMM and SAS Enterprise Guide V7.1 for Fisher test (SAS Institute Inc. Cary NC, USA).
In this study, we demonstrated that following experimental challenge, PD vaccinated Atlantic salmon shed significantly lower levels of SAV into the water compared to unvaccinated fish. The experimental challenge was done by injection (i.m.) to: (1) avoid possible conflict with waterborne challenge material present in a cohabitation model, (2) have a simultaneous and controlled infection in all test animals, and (3) administer infective virions to muscle/blood stream to avoid possible non-specific protection in the intraperitoneal cavity due to the i.p. vaccination. However, i.m. injection of SAV is probably a severe challenge, as all natural barriers are bypassed and infective virions quickly enter the blood stream to give a rapid systemic infection. SAV challenge by i.m. injection is not the natural route, but its suitability to assess vaccine efficacy has been established . In the water samples collected at six time points between 1 and 24 days post challenge, SAV could, by qRT-PCR, not be detected in either of the two duplicated tanks containing PD vaccinated fish (Figure 2), while all water samples were positive for the ISAV spike confirming valid sample preparation. In the tanks containing unvaccinated fish, SAV was detected in one or both tanks at 10, 14 and 24 days post challenge but not at 1, 4 and 18 dpc. Andersen et al.  showed that in water samples collected from tanks containing SAV i.p. injected fish, SAV was detected at day 4, 6, 8, 10 and 13 but not at any later sampling points. As evident from the current study, peak SAV detection in water is somewhat delayed compared to Andersen et al. . In our experience, this is a difference typically seen for i.m. challenge versus i.p. challenge (unpublished). The observed SAV detection kinetics in water is as expected except for the re-occurrence of SAV in tanks 3 and 4 (unvaccinated fish) at day 24. The re-occurrence of SAV in these tanks is probably due to virus shed from the naïve fish added to the tanks as “detectors”. These untreated, naïve fish have been exposed to infective virions shed from the injected fish, corresponding to a classical cohabitant challenge set-up. The time point, 24 days post i.m. challenge of the donor fish and 23 days after adding the naïve fish, corresponds well with expected peak of viraemia (and peak of shedding) following cohabitation challenge at 12 °C [8, 14]. Although, by qRT-PCR, no SAV was detected in any of the water samples from the two tanks containing PD vaccinated fish, some naïve fish added to the tanks were infected (Figure 3). Relatively low concentrations (undetectable by current qRT-PCR method) of infectious SAV must have been present in these two tanks resulting in SAV being detected at low levels in 20 and 40% of the naïve cohabitants at 24 dpc (Figure 3). In comparison, high quantities of SAV (approx. 212.5 fold increase between naïve fish cohabitating PD vaccinated and unvaccinated fish) was detected in 100 and 80% of the naïve fish added to the two tanks containing unvaccinated, i.m. challenged fish. Considering the vaccine efficacy evident in tanks 1 and 2 following i.m. challenge, it is reasonable to presume that if the cohabitants added to these tanks had been PD vaccinated, they would have been protected against this low infection pressure. The results also indicate that a low concentration of infective SAV in the water (undetectable by current qRT-PCR method) is sufficient to infect naïve fish, even when kept under optimal laboratory rearing conditions (low fish density, optimal O2/water flow etc.).
In the field, SAV infection pressure and infected neighbouring sites are known to be key risk factors for clinical PD [10, 11]. Infectious SAV has been reported to have a half-life of 1 day at 10 °C in seawater , consequently giving the high potential for SAV to spread by passive drift in ocean currents [11, 12]. Adding to this risk is the fact that initial SAV infection happens unnoticed since shedding of SAV from infected animals starts a few weeks after viral exposure [8, 14], while time from infection to clinical disease, the typical indicator for management actions, can be several months . Under field conditions, clinical PD typically emerges in cage after cage within a farm with mortality ongoing up to several months post clinical PD diagnosis . Unlike what is observed in laboratory experiments, individuals within a fish population at a farm will not be infected at the same time. It is therefore likely that a farm population will shed SAV to the water for a longer time period thus adding to the infection pressure within the farm and increasing the probability of transferring SAV to neighbouring sites [10, 11], or beyond by human transport activity.
In conclusion, the present study demonstrates that PD vaccination results in a significant decrease in shedding of SAV to the water if the vaccinated fish become infected. In addition to the PD vaccine efficacy, by means of reduction of disease severity and mortality , this vaccine effect can play a major role in reducing the SAV infection pressure within and between farms.
PS, IS, PF and SV are all employees of MSD Animal Health which funded the study. The commercial vaccine (AQUAVAC® PD7) used in the study is a product by MSD Animal Health. MSD Animal Health holds a supplementary protection certificate in Norway for the use of SAV as an active ingredient in vaccines.
SV designed the study, participated in sampling, interpreted results and revised the manuscript. PS participated in study design, coordinated and carried out vaccination, challenge, samplings, analyses, interpreted results and wrote most of the manuscript. IS participated in study design, sampling, interpretation of results and revised the manuscript. PF participated in interpretation of results, wrote parts of the manuscript and revised the manuscript. All authors read and approved the final manuscript.
The authors would like to thank colleagues Linda Melstveit, Kristian Ulven, Jegatheswaran Thevarajan and Glenn Sundnes, MSD Animal Health, for contributions carrying out the experiment. Kjartan Hodneland, MSD Animal Health, and Linda Andersen, The Industrial and Aquatic Laboratory (ILAB), are acknowledged for input regarding interpretation of the results, and Mathieu Hoeijmakers, MSD Animal Health, is acknowledged for guidance on the statistical analyses performed.
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