- Research article
- Open Access
First detection, isolation and molecular characterization of infectious salmon anaemia virus associated with clinical disease in farmed Atlantic salmon (Salmo salar) in Chile
© Godoy et al; licensee BioMed Central Ltd. 2008
- Received: 19 March 2008
- Accepted: 04 August 2008
- Published: 04 August 2008
Infectious salmon anaemia (ISA) is a viral disease of marine-farmed Atlantic salmon (Salmo salar) caused by ISA virus (ISAV), which belongs to the genus Isavirus, family Orthomyxoviridae. The virus is considered to be carried by marine wild fish and for over 25 years has caused major disease outbreaks in marine-farmed Atlantic salmon in the Northern hemisphere. In the Southern hemisphere, ISAV was first detected in Chile in 1999 in marine-farmed Coho salmon (Oncorhynchus kisutch). In contrast to the classical presentation of ISA in Atlantic salmon, the presence of ISAV in Chile until now has only been associated with a clinical condition called Icterus Syndrome in Coho salmon and virus isolation has not always been possible. During the winter of 2007, unexplained mortalities were registered in market-size Atlantic salmon in a grow-out site located in Chiloé in Region X of Chile. We report here the diagnostic findings of the first significant clinical outbreak of ISA in marine-farmed Atlantic salmon in Chile and the first characterization of the ISAV isolated from the affected fish.
In mid-June 2007, an Atlantic salmon marine farm site located in central Chiloé Island in Region X of Chile registered a sudden increase in mortality following recovery from an outbreak of Pisciricketsiosis, which rose to a cumulative mortality of 13.6% by harvest time. Based on the clinical signs and lesions in the affected fish, and laboratory tests performed on the fish tissues, a confirmatory diagnosis of ISA was made; the first time ISA in its classical presentation and for the first time affecting farmed Atlantic salmon in Chile. Rapid sequencing of the virus-specific RT-PCR products amplified from the fish tissues identified the virus to belong to the European genotype (Genotype I) of the highly polymorphic region (HPR) group HPR 7b, but with an 11-amino acid insert in the fusion glycoprotein, and ability to cause cytopathic effects (CPE) in CHSE-214 cell line, characteristics which make it distinct from common European Genotype ISAV isolates from Europe and North America.
In conclusion, the present work constitutes the first report of a case of ISA in farmed Atlantic salmon in Chile. The clinical signs and lesions are consistent with the classical descriptions of the disease in marine-farmed Atlantic salmon in the Northern hemisphere. The outbreak was caused by ISAV of European genotype (or Genotype I) of HPR 7b but distinct from common European Genotype ISAV isolates.
- Atlantic Salmon
- Avian Influenza Virus
- Infectious Salmon Anaemia Virus
- Epithelioma Papulosum Cyprini
- Farm Atlantic Salmon
Infectious salmon anaemia (ISA) is a viral disease of marine-farmed Atlantic salmon (Salmo salar) caused by ISA virus (ISAV), which belongs to the genus Isavirus, family Orthomyxoviridae . In the Northern hemisphere, the first registered outbreak of ISA was in 1984 in Atlantic salmon "parr", on the southwestern coast of Norway . Subsequently the disease was reported in Canada in 1996 , in Scotland in 1998 , in Faeroe Islands in 1999 , and in Maine, USA, in 2000 . The clinical disease in farmed Atlantic salmon is characterized by variable mortality ranging from 0 to 50% with ascites, exophthalmia, petechiation of the visceral adipose tissue, haemorrhagic liver necrosis, renal interstitial haemorrhage and tubular nephrosis, filamental sinus congestion of the gills, splenic congestion with concomitant erythrophagocytosis, and congestion of the lamina propria of the stomach and foregut [2, 7–10]. ISAV remains an emerging fish pathogen that continues to cause severe economic losses to the salmon-farming industry in an increasing number of countries, although the disease can be successfully eradicated as was managed by Scotland in the late 1990s . In the Southern hemisphere, ISAV was first detected in Chile in 1999 in marine-farmed Coho salmon (Oncorhynchus kisutch) and was shown to be of the North American genotype . In contrast to the classical presentation of ISA in Atlantic salmon, the presence of ISAV in Chile up until now has only been associated with a clinical condition called Icterus Syndrome in Coho salmon and virus isolation has not always been possible . Between 2001 and 2003, ISAV of the North American genotype was found in apparently normal Atlantic salmon in Lake Llanquihue (Oscar Gárate, personal communication), which is not in the same zone as where the present disease outbreak occurred. It is not known why the North American variant of ISAV has not caused typical ISA outbreaks as those known to occur in Eastern Canada and Maine, USA, and yet the virus has become widespread in the Atlantic salmon industry in Chile.
ISAV belongs to the family Orthomyxoviridae, together with influenza viruses . However, the virus is sufficiently different from influenza viruses to be assigned to its own genus, Isavirus. Members of this genus are enveloped particles of 90–140 nm diameter with surface projections consisting of a combined haemagglutinin-esterase (HE) glycoprotein, which is the receptor binding haemagglutinin with receptor destroying enzyme activity demonstrated to be an acetylesterase [14, 15] encoded on segment 6 , and a separate fusion (F) glycoprotein encoded on segment 5 . The genome consists of eight segments of linear, single-stranded negative sense RNA ranging in length from 1.0 to 2.4 kb with a total molecular size of approximately 14.3 kb . Sequence analysis of several ISAV isolates on the eight segments consistently reveals two genotypes that are designated with respect to their geographic origin, European and North American, hereafter designated Genotypes I and II, respectively. Sequence variation in a 35-amino acid highly polymorphic region (HPR) on the HE glycoprotein stalk has allowed the separation of ISAV isolates into different HPR groups, with the HPR0 group consisting of the non-cultivable, non-pathogenic viruses detectable only by RT-PCR  whereas deletion in the HPR of ≥ 13 amino acids (or if less, with deletion or mutation of the motif at amino acid positions 352FNT354) lead to increased pathogenicity, and ability to replicate in cell culture with production of CPE and consequent virus isolation .
This study reports the diagnostic findings of the first occurrence of ISA in the Southern hemisphere, and the first characterization the ISAV isolated from the affected marine-farmed Atlantic salmon in Chile.
Virus antigen detection
Homogenates of pooled spleen and kidney tissues inoculated on Chinook salmon embryo (CHSE-214), Salmon head kidney (SHK-1) and Epithelioma papulosum cyprini (EPC) cell lines produced CPE between 4 and 7 days post inoculation during primary isolation. The CPE, which was reproduced on subsequent passage on fresh cell line monolayers, was characterized initially by cell vacuolization and rounding and then detachment from the substrate involving the whole cell monolayer. The presence of ISAV in the cell lysates was confirmed using RT-PCR and an indirect immunofluorescent antibody test (IFAT) with anti-ISAV monoclonal antibody P10 (Aquatic Diagnostics Ltd) including appropriate controls. Figure 4B shows positive IFAT of a CHSE-214 cell culture inoculated with a tissue sample from affected fish. Similar fluorescence was seen with EPC cell cultures with CPE (data not shown). Neither CPE nor presence of ISAV was detected by RT-PCR or IFAT in inoculated cultures of Bluegill Fry (BF2) cell line.
Tissue samples shipped in RNA later® (Ambion Inc., Foster City CA) to the Regional Diagnostic Virology Laboratory, AVC, UPEI, Canada, were positive for ISAV by RT-PCR and negative for both IHNV and VHSV by nested RT-PCR.
The nucleotide sequences in this report, which are all of ISAV RNA segment 5, are available through GenBank http://www.ncbi.nlm.nih.gov/Genbank, accession nos. EU130923, EU486160, and EU486161. A partial sequence of ISAV RNA segment 6 was generated by the Norwegian Veterinary Institute from duplicate samples of the same ISA outbreak, and appears in GenBank, accession no. AM941715. Tables 1 [see Additional file 6] and 2 [see Additional file 7] show the percent sequence identities between the new Chile ISAV and selected ISAV isolates from Europe and North America. Comparison of the RNA segment 5 sequences of the Chilean ISAV with ISAV strains of Genotype I (European genotype) showed nucleotide sequence identities ≥ 95.9% whereas with ISAV strains of Genotype II (North American genotype), it was ≤ 74.7% [see Additional file 6]. Comparison of the segment 6 sequence of the Chilean ISAV with ISAV strains of Genotype I showed sequence identities ≥ 95.7% whereas with ISAV strains of Genotype II, it was ≤ 79.4% [see Additional file 7]. Thus the new Chile ISAV involved in this outbreak belongs to Genotype I (the European genotype).
The present work constitutes the first report of a case of ISA in farmed Atlantic salmon in Chile. The outbreak was caused by ISAV of Genotype I (the European genotype). The gross and microscopic lesions observed in this outbreak are consistent with the classical ISA described in Norway , Canada , Scotland , Faeroe Islands  and United States . In particular, the liver congestion and necrosis, as well as the renal, splenic and enteric congestion/haemorrhage in this outbreak are morphologically consistent with lesions pathognomonic for ISA. However, where these lesions differed from other presentations of the disease were primarily in the kidney, where in the Canadian situation there is profound interstitial haemorrhage, and in the heart, in the Chilean ISA outbreaks there is hydropericardium and severe myocarditis. Previously, such heart lesions have been shown to be prominent only in experimental infections of rainbow trout with ISAV .
The affected fish group in the Chilean ISA outbreak was recovering from Piscirickettsiosis. This particular group had been treated several times against Rickettsia at the farm site, and on this occasion the antibiotic treatment which was administered by injection effectively prevented mortality due to Piscirickettsiosis. Although the pathologic findings in this outbreak were in the range of what is considered as typical ISA, it cannot be categorically stated what contribution, if any, the Piscirickettsiosis disease contributed to the pathology observed.
The virus responsible for the outbreak caused CPE and was recovered using CHSE-214, SHK-1 and EPC cell lines, and confirmed as ISAV by means of RT-PCR and IFA testing. This is the first report of primary isolation of ISAV using EPC cell line, which is a non-salmonid cell line derived from a skin tumour of carp (Cyprinus carpio L.)  and never before reported to be permissive to ISAV. Most recently, EPC cell line was also reported to be permissive to ISAV of North American genotype . Moreover rapid sequencing of virus-specific RT-PCR products amplified from the fish tissues identified the virus as belonging to the European genotype. Up until now, only some strains of ISAV of the North American genotype [31–33] but not the European genotype  have been known to replicate and cause CPE in the CHSE-214 cell line, a property that is not associated with the antigenic subtype of ISAV nor with the HPR group of the HE gene . Thus, the Chilean ISAV has cell line specificities that are different from those of common European Genotype ISAV isolates from Europe and North America.
Now that we have ISAV isolates of both genotypes from Europe, North America, and South America, we should remove the stigmatizing labeling of ISAV genotypes by geographic reference. We therefore propose to designate the European genotype as Genotype I and the North American genotype as Genotype II. Such designation is consistent with our present knowledge, which is not sufficient to explain the anomalous geographic distribution of the two genotypes of ISAV.
The Chilean ISAV responsible for the ISA outbreak is unique in that it has a 33-nucleotide (or 11-amino acid) insert in the middle of RNA segment 5 which encodes the F glycoprotein. This insert has 100% sequence identity with RNA segment 2 of ISAV of Genotype I, and probably arose through a non-homologous recombination between the F and PB1 genes of the same virus. To date, there have been only 8 other ISAV isolates with inserts in RNA segment 5 [20, 21]. All these isolates are Norwegian ISAV isolates; seven of them were recovered between 1999 and 2002  and one was recovered in 2006 . Seven of these isolates had inserts from different parts of RNA segment 5 while in one isolate, the insert was shown to come from RNA segment 3, which encodes the ISAV nucleoprotein. Therefore, this Chilean ISAV is the first known isolate to have an insert in RNA segment 5 coming from RNA segment 2. Overall, this information indicates that this Chilean ISAV is different from common Genotype I ISAV isolates in Europe. The location of the insert in the Chilean ISAV RNA segment 5 is also unique in that it occurs right in the middle of the 265YP266 motif, which was recently shown to be a marker for reduced virulence . The RNA segment 5 of ISAV belonging to HPR0, a non-pathogenic virus, has 265NQ266 at this site but without a sequence insertion , which would be similar to the Chilean ISAV prior to the non-homologous recombination event between the F and PB1 genes. Such recombination events are well known in avian influenza virus (AIV), involving an insertion in the haemagglutinin (HA) gene of AIV near the cleavage site of the protein and leading to emergence of new virulent strains [35–38]. For example, the avian influenza disease outbreak that occurred in Chile in 2002 was attributed to the non-homologous recombination between the HA and nucleoprotein genes of H7N3 AIV .
The Chilean ISAV described here clearly differs from the 7833-1 isolate (of Genotype II) from coho salmon in Chile  in segment 5 and the partial segment 6 amino acid sequences. Thus the 7833-1 virus, which is now wide spread in the Atlantic salmon industry in Chile, is unlikely to have been the source of this new virus. It is interesting that the alignments on RNA segment 6 showed the Chilean ISAV to belong to HPR7b that has previously been found in Scotland and Norway. However, all ISAV isolates of HPR7b sequenced to date on RNA segment 5 do not have the 11-amino acid insert found in the Chilean ISAV. Comparison of the RNA segment 5 sequence of this Chilean ISAV with the HPR0 virus strain SK779/06  showed a nucleotide sequence identity of 98.3% and amino acid sequence identity of 97.1%. In contrast, ISAV strain 390/98, which is also of HPR7 but from Scotland, when compared to the HPR0 virus showed a nucleotide sequence identity of 98.4% and amino acid sequence identity of 99.1% [see Additional file 6]. This suggests that the Chilean ISAV is distinct from common Genotype I ISAV isolates from Europe and North America. The location of the 11-amino acid insert at a motif in the F glycoprotein which is associated with virus virulence, may account for the elusive nature of this Chilean virus. It is therefore necessary to sequence the whole genome of this virus and clarify the epidemiology of this ISA outbreak so as to establish the origin of this virus, its virulence characteristics and the risk factors associated with its presentation and dissemination, in order to institute adequate strategies for the control and prevention of ISA in the Chilean salmon industry.
In conclusion, the present work constitutes the first report of a case of ISA in farmed Atlantic salmon in Chile. The clinical signs and lesions are consistent with the classical descriptions of the disease in marine-farmed Atlantic salmon in the Northern hemisphere. The outbreak was caused by ISAV of Genotype I of HPR 7b but distinct from common European ISAV isolates from Europe and North America.
Atlantic salmon with mean weight of 3.9 Kg, held in seawater rearing cages, were necropsied and submitted for diagnostic testing. Moribund fish were submitted for laboratory analysis to the Biovac S.A. laboratory in Puerto Montt, Chile, where a full necropsy was conducted and samples were collected for histological evaluation, virus isolation, and immunohistochemistry and molecular biology analysis.
Tissue samples for histological analysis were collected in 10% buffered formalin. They were then processed using standard procedures and the sections were stained with Haematoxylin & Eosin (H&E), in order to describe the significant morphological changes. Tissues from 9 fish were additionally submitted to Aquatic Diagnostic Services at the Atlantic Veterinary College in Prince Edward Island, Canada, for histological evaluation.
Virus antigen detection assays
The presence of virus antigens in the fish tissues utilized three different types of assays: immunohistochemistry, immunochromatography, and antigen ELISA. The immunohistochemistry analyses were carried out on waterproofed tissue sections of 5 μm thickness, using anti-ISAV monoclonal antibody P10 (Aquatic Diagnostics Ltd, Stirling, Scotland) with the immunohistochemistry kit from Vector Laboratories. Immunochromatography utilized tissue homogenates applied to a rapid kit with anti-ISAV monoclonal antibody according to the manufacturer's procedures (Aquatic Diagnostics Ltd). The IHNV ELISA kit (Bio-X Diagnostics) and VHSV ELISA kit (Bio-X Diagnostics) were used to rule out IHNV and VHSV in the tissue samples. The ELISA procedures followed the manufacturer's protocols.
Homogenized pools of spleen and kidney were inoculated on monolayers of CHSE-214, EPC, SHK-1 and BF2 cell lines following standard protocols in the OIE Aquatic Manual .
RT-PCR and nucleic acid sequencing
Total RNA was extracted from the same homogenates of pooled spleen and kidney tissues used for virus isolation, using EZNA® kits (Omega Biotech) or the RNeasy® kit (Qiagen) according to the manufacturer's recommended protocol. For tissues preserved in RNA later® (Ambion Inc), the tissues were first washed three times with phosphate buffered saline (PBS) and then homogenized using a tissue homogenizer (Brinkman, Ontario, Canada) prior to total RNA extraction using the RNeasy® kit (Qiagen).
For the detection of ISAV in tissue homogenates, ISAV-specific primers and conditions described by Devold et al.  and Mjaaland et al.  for RNA segment 8, and the primers described in the OIE Aquatic Manual  for RNA segment 6 were used. Briefly, amplification was performed using 50 μl reaction mixture utilizing EzrTth RT-PCR kit (Applied Biosystems, Montreal, Quebec) as follows: EzrTth DNA polymerase – 1 μl, ISA forward primer-0.4 uM, ISA reverse primer- 0.4 uM, Mn-2.5 mM, dNTPs-200 uM each, 5× PCR buffer-10 μl, ddH2O-19 μl and 5 μl RNA template. The amplification was performed in Perkin Elmer Gene Amp PCR System 2400 using the following conditions: 1 cycle at 53°C for 45 min, one cycle at 94°C for 2 min, 35 cycles at 94°C for 15 s, 60°C for 15 s and 72°C for 15 s and 1 cycle at 72°C for 7 min before holding the reactions at 4°C.
Samples were tested for IHNV and VHSV using nested RT-PCR with primers and conditions described by Batts and Winton  and , respectively, with minor modifications. The RT-PCR was performed using 50 μl reaction mixture utilizing EzrTth RT-PCR kit (Applied Biosystems) as follows: EzrTth DNA Polymerase-2.5 units, forward primer-0.4 uM, reverse primer -0.4 uM, Mn-2.5 mM, dNTPs -200 uM each, 5× PCR buffer-10 μl, ddH2O-19 μl and 5 μl RNA template. For IHNV, the primers consisted of IHNV 1F primer and IHNV 1R primer whereas for VHSV they were VHSV 1F primer and VHSV 1R primer. The amplification was performed in Perkin Elmer Gene Amp PCR System 2400 using the following conditions: 1 cycle at 50°C for 15 min, 1 cycle at 95°C for 2 min, 25 cycles at 95°C for 30 s, 50°C for 30 s and 72°C for 60 s, 1 cycle at 72°C for 1 min and 1 cycle at 72°C for 7 min before soaking at 4°C. The second amplification was done using AmpliTaq Gold (Applied Biosystems) utilizing 50 μl mixture as follows: AmpliTaq Gold Polymerase-2.5 units, IHNV 2F primer – 0.4 uM, IHNV 2R primer-0.4 uM for IHNV or VHSV 2F primer – 0.4 uM, VHSV 2R primer-0.4 uM for VHSV, Mg-2 mM, dNTPs -200 mM each, 10× PCR buffer – 5 μl, ddH2O- 33.5 μl and 2 μl RT-PCR mixture. The following cycling conditions were used: 1 cycle of 95°C for 2 min, 25 cycles at 95°C for 30 s, 50°C for 30 s and 72°C for 60 s and 1 cycle at 72°C for 7 min before holding the reactions at 4°C.
For DNA sequencing of ISAV RT-PCR products, total RNA was extracted from 300 μl of tissue homogenate using Trizol LS® (Invitrogen). The RT-PCR was carried out using the Titan® One Tube RT-PCR (Roche Diagnostic), in a PTC-200 DNA Engine Peltier thermal cycler (MJ Research, Inc.) using oligonucleotide primers and cycling conditions as previously described [19, 44]. The PCR products were then either directly sequenced or they were cloned into the pCRII vector using a TOPO TA cloning kit (Invitrogen) in preparation for nucleotide sequencing. Plasmid DNA for sequencing was prepared as described before . DNA sequencing was performed as previously described  by ACGT Corporation (Toronto, Ontario, Canada). DNA Sequencing was done either directly on RT-PCR products or on plasmid DNA containing the cloned RT-PCR products obtained from reactions using total RNA from tissue samples. Sequence analysis used the BLAST programs , the Sequence Manipulation suite version 2 , and the FASTA program package for personal computers .
Funding for this study was provided by Marine Harvest S.A., Puerto Montt, Chile, Biovac S.A., Puerto Montt, Chile, and OIE Reference Laboratory for ISA, Atlantic Veterinary College, University of Prince Edward Island, Charlottetown, PE, Canada.
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