Infectious salmon anaemia virus infection of Atlantic salmon gill epithelial cells
© Weli et al.; licensee BioMed Central Ltd. 2013
Received: 22 August 2012
Accepted: 5 December 2012
Published: 2 January 2013
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© Weli et al.; licensee BioMed Central Ltd. 2013
Received: 22 August 2012
Accepted: 5 December 2012
Published: 2 January 2013
Infectious salmon anaemia virus (ISAV), a member of the Orthomyxoviridae family, infects and causes disease in farmed Atlantic salmon (Salmo salar L.). Previous studies have shown Atlantic salmon endothelial cells to be the primary targets of ISAV infection. However, it is not known if cells other than endothelial cells play a role in ISAV tropism. To further assess cell tropism, we examined ISAV infection of Atlantic salmon gill epithelial cells in vivo and in vitro. We demonstrated the susceptibility of epithelial cells to ISAV infection. On comparison of primary gill epithelial cell cultures with ISAV permissive fish cell cultures, we found the virus yield in primary gill epithelial cells to be comparable with that of salmon head kidney (SHK)-1 cells, but lower than TO or Atlantic salmon kidney (ASK)-II cells. Light and transmission electron microscopy (TEM) revealed that the primary gill cells possessed characteristics consistent with epithelial cells. Virus histochemistry showed that gill epithelial cells expressed 4-O-acetylated sialic acid which is recognized as the ISAV receptor. To the best of our knowledge, this is the first demonstration of ISAV infection in Atlantic salmon primary gill epithelial cells. This study thus broadens our understanding of cell tropism and transmission of ISAV in Atlantic salmon.
Infectious salmon anaemia (ISA) in Atlantic salmon (Salmo salar L.) is a World Organisation for Animal Health (OIE) notifiable disease. Clinical ISA is characterized by circulatory disturbances including anaemia, gill pallor, ascites, intestinal congestion, liver and spleen enlargement and petechial haemorrhage of the skin and visceral organs . The disease was first recognized in Norway in 1984, but has been subsequently identified, with high associated mortalities, in farmed Atlantic salmon in Europe, and North- and South America [2–7].
ISA is caused by the infectious Salmon Anaemia Virus (ISAV), the only member of the genus Isavirus in the family Orthomyxoviridae. The virus has been characterized morphologically [8–11], bio-physiochemically [9, 12–15] and genomically [16–23]. However, the pathogenesis of ISAV is not clear and in particular, the site/s of entry into Atlantic salmon remains unknown. In cell culture, ISAV replication has been demonstrated only in SHK-1, ASK-II, TO and Atlantic salmon (AS) cells, although replication of some Canadian ISAV isolates has also been demonstrated in Chinook salmon embryo (CHSE)-214 cells [24–27]. With the exception of AS and CHSE-214, all these cell-cultures are derived from Atlantic salmon adherent head kidney macrophages and mitogen-stimulated peripheral blood leucocytes [24, 25, 27], and will not, therefore, reveal the virus entry-site into the Atlantic salmon.
The gills, comprising the vasculature and surrounding epithelia [28, 29], provide a key interface between the fish and the environment, acting as site for gas exchange, body fluid regulation and waste excretion . As they filter large amounts of water they offer a suitable target for invading infectious agents. While RT-PCR detection of ISAV on whole gill preparations has suggested the gills as an entry-site for ISAV infection , in vivo studies have only reported ISAV infection within endothelial cells and leucocytes [11, 32, 33]. We showed previously that gill and hind-gut mucosal epithelial cells express the ISAV 4-O-acetylated sialic acid receptor on the cell surface , indicating the potential for ISAV-infection of epithelial cells. High prevalences of ISAV positive gills by RT-PCR, have been documented, both for low pathogenic ISAV-HPR0 cases in the Faroe Islands , and in high pathogenic ISA outbreaks in Norway . However, analysis of whole gill samples, comprising different cell types, does not allow identification of the specific cell type infected with the virus, or prove the gill to be the entry-site for infection.
If the gill does represent an entry site for ISAV, the virus must penetrate the protective mucosal epithelial barrier. Possible mechanisms include transcytosis, infection of tissue macrophages orchestrated by antigen sampling cells (i.e. dendritic cells) or by direct infection of the epithelial cells . Interestingly, mammalian and avian orthomyxoviruses use upper and lower respiratory epithelial cells (analogous to gill epithelial cells) for replication [37, 38].
Different approaches have been used to study viral cell tropism. Some studies have used immunohistochemistry  or in situ hybridization during natural or experimental infection. Others have used ex-vivo organ cultures [40, 41] or specialized, immortalized cell lines. The study of viral disease in Atlantic salmon is made difficult by the limited availability of specific cell cultures. Thus, in such cases, utilisation of primary cell cultures closely representing the in vivo situation can be rewarding [42, 43].
In the present study we examined ISAV infection of gill epithelial cells following emersion (bath) challenge and by infection of primary gill epithelial cell cultures. We demonstrated the susceptibility of Atlantic salmon gill epithelial cells to ISAV both in vivo and in vitro. When compared with ISAV- permissive fish cell lines, primary epithelial cells showed virus yields comparable to SHK-1 cells.
Previous studies have demonstrated ISAV receptor expression on gill mucosal epithelial cells  and high prevalences of ISAV positive gills by RT-PCR [31, 34], suggesting ISAV infection of gill cells. However, such infections have not been confirmed at the cellular level. In the present study, we performed in vivo immersion challenge experiments to investigate ISAV infection and cell tropism in Atlantic salmon gills and in vitro experiments utilising primary gill epithelial cells.
To confirm that the isolated primary gill cells were of epithelial origin, immunocytochemical staining with an epithelial-specific cytokeratin marker was performed. Cells consistently stained positive for cytokeratin, and showed little contamination with other cell types (Figure 2b), indicating that the cultured gill epithelial cells were largely monomorphic. Using transmission electron microscopy (TEM), we assessed 7-day-old cultures for epithelial characteristics. We found tight junctions, nuclei and cytoplasmic organelles including endoplasmic reticulum (Figure 2c-f), all features consistent with epithelial cells. We were however, unable to localize desmosomes. A possible explanation for this may lie in our sample preparation, as some studies indicate that a freeze fracture technique is required to characterize complete regions of tight membrane-to-membrane contact .
Differential permissiveness of Atlantic salmon primary gill epithelial cells, ASK-II, SHK-1, and TO cells to ISAV infection
†ISA virus titres (TCID50/mL)
Atlantic salmon primary gill epithelial cells
1.0 x 105
1.0 x 107
4.0 x 105
1.0 x 106
In summary, this study constitutes the first documentation of ISAV infection of gill epithelial cells, in vivo and in vitro, and provides evidence of the gill as a potential port of entry for ISAV. The Atlantic salmon primary gill epithelial cells described here were used to study ISAV cell tropism and infection. The cells are not a new cell line, and not optimal for maximum yield of pathogenic ISAV strains. Also, attempts to passage the cells were unsuccessful. However, they are of interest for two reasons. Firstly, they possess epithelial characteristics and express ISAV 4-O-acetylated sialic acids receptors critical for ISAV infection. Secondly, they provide further evidence that Atlantic salmon gill epithelial cells could be a target for ISAV. They may also provide a system for working with so far uncultivable gill-infecting agents, e.g., low pathogenic ISAV HPRO strains, and also other suspected gill-pathogenic agents such as pox virus .
Primary cultures of gill epithelial cells from juvenile Atlantic salmon (5-10 g) were isolated as previously described , with some modifications. Briefly, fish were euthanized by anaesthetic overdose in ethyl 3-aminobenzoate methanesulfonate salt (Sigma-Aldrich), gill arches excised, washed in phosphate buffer saline (PBS) without Ca2 + and Mg2 + containing 200 μg/mL Penicillin/Streptomycin (Invitrogen), 400 μg/mL gentamicin sulfate (Lonza), and 2.5 μg/mL Amphotericin B (Lonza). Cultures were prepared from filaments utilising three cycles of enzymatic digestion with trypsin-EDTA (Lonza), and cell washing in PBS supplemented with 2% foetal bovine serum (FBS). Cells were re-suspended in L-15 medium supplemented with FBS (20%), Penicillin/Streptomycin (100 μg/mL), ß-mercaptoethanol (1 mM), nonessential amino acid (0.1 mM), L-glutamine (2 mM) and seeded on 24 well plates at 15°C. To monitor growth characteristics, cells were observed daily by light microscopy and assessed for viability by trypan-blue exclusion , morphology and susceptibility to ISAV infection.
The highly pathogenic Norwegian ISAV strain Glesvaer/2/90  was propagated in ASK-II cells  in Leibovitz L-15 medium (L-15) supplemented with 10% FBS, glutamine (4 mM), and gentamicin (50 μg/ml) at 20°C. The virus was used for in vivo (fish immersion experiments), for in vitro infection of the primary gill epithelial cells, and for preparation of ISAV antigen for virus histochemistry as previously described . Unless otherwise stated, primary gill epithelial cells with the fluid overlay removed were inoculated with virus at a multiplicity of infection of 0.1 in L-15 with 2% FBS. Infectivity titrations were done by end point titration in 96-well culture plates as previously described .
The infection experiment was performed at the Norwegian Veterinary Institute in freshwater tanks at 8°C. A total of 31 Atlantic salmon presmolts (20 g) confirmed free of ISAV, infectious pancreatic necrosis (IPNV), proliferative kidney disease (PKD) and Salmonid alpha virus (SAV) by RT-PCR analysis were used. Fish were challenged by immersion (bath) for 3 hours with 104 TCID50 per ml. Un-infected control fish were kept in a separate tank. Three - five fish were sampled at 8 h, 24 h, 48 h, 8 days and 20 days post infection (p.i.), and gill tissues collected in buffered 4% formaldehyde. Fish were anesthetized with methane tricaine sulphonate (MS222, Sigma, 0.1 mg/mL) before handling.
Fish sampling for preparation of primary gill epithelial cells and experimental infection were preformed according to internationally recognized ethical guidelines. The experiments were approved by The Norwegian Animal Research Authority (NARA); identification number 2697.
Immunohistochemistry was performed as previously described  on gill samples from in vivo immersion experiments and tissues samples from the Faroe Islands. Briefly, formalin-fixed paraffin-embedded tissue sections were de-waxed and subjected to microwave oven treatment. Rabbit antibody to recombinant ISAV NP  and Vectastain ABC-AC kit (Vectastain anti rabbit Ig ABC-AP kit, AK 5001, Vector Laboratories, Inc.) were used for detection, employing Fast Red (1 mg/ml) and Naphtol AS-MX phosphate (0.2 mg/ml) with 1 mM Levamisole in 0.1 M TBS (pH8.2) as substrate.
Immunocytochemistry was performed to demonstrate purity of the primary gill epithelial cultures as previously described . Briefly, cultures were washed in PBS and fixed in 4% formaldehyde in PBS for 10 min. Non-specific binding was blocked by incubation in 5% FBS in PBS for 20 min. Labelling was performed by overnight incubation at 4°C with mouse monoclonal anti-cytokeratin (AE1/AE3) (Invitrogen) diluted 1:50 in PBS with 2% FBS, followed by 30 min incubation with HRP-labelled secondary antibody (Envision® K4007; DAKO). 3,3’-diaminobenzidine (DAB) was used as a substrate.
Immunofluorescent antibody test (IFAT) was used for ISAV detection in infected primary gill epithelial cells as previously described , with some modifications. Briefly, 7 day old primary gill cultures were inoculated with ISAV at a multiplicity of infection (MOI) of 0.1 in Leibovitz's L-15 medium with 2% FBS and allowed to adsorb for 2 h at 15°C. The inoculum was removed and fresh L-15 medium supplemented with FBS (10%), Penicillin/Streptomycin (100 μg/mL), ß-mercaptoethanol (1 mM), nonessential amino acid (0.1 mM), L-glutamine (2 mM) added and incubated for 4 days. Cultures were washed in PBS, fixed in 80% acetone for 10 min, and IFAT was performed with anti ISAV haemagglutinin esterase (HE) monoclonal antibody  and FITC-labelled goat anti-mouse Ig (Southern Biotech).
Transmission electron microscopy (TEM) was performed on 7-day-old primary gill epithelial cells as previously described . Briefly, cultures were washed in PBS, fixed in 2.5% glutaraldehyde in 0.5 M cacodylate buffer postfixed in 2% OsO4 in 0.1 m cacodylate buffer pH7.2 for 2 h, dehydrated in ascending concentrations of ethanol and embedded in LX 112 Resin (Ladd Research Industries). Ultra-thin sections were mounted on uncoated copper grids, stained with uranyl acetate and lead citrate using standard methodology before examination.
For detection of the ISAV 4-O-acetylated sialic acid receptor, virus histochemistry was performed on primary gill cultures as previously described . Briefly, cultures were washed in PBS, fixed in 4% formaldehyde in PBS for 10 min. Labelling was performed by incubating with each of the following for 1 h: ISAV antigen (100 HAU mL-1), anti ISAV HE monoclonal antibody  and HRP-labelled secondary antibody (Envision® K4007; DAKO). DAB was used as a substrate. Cultures were counterstained with Mayer’s haematoxylin. To document binding specificity, control cells were de-O-acetylated by mild alkaline saponification using 0.1 M sodium hydroxide for 30 min .
To further characterize ISAV infection of the primary gill epithelial cells, comparisons of ISAV replication in primary gill epithelial cells were made with ASK-II, SHK-1 and TO cells. Cultures of primary gill epithelial cells, ASK-II, SHK-1 and TO cells were inoculated with ISAV as previously described, and incubated for 4 days. Supernatants were collected four days p.i., and infectivity titrations performed on ASK-II cells by end point titration in 96-well culture plates as previously described . The 50% tissue culture infective dose (TCID50) was estimated by the method of Kärber .
The work was supported by Norwegian Research Council (grant no. 186907), The Atlantic innovation Fund, Canada Inc and Novartis Animal Health.
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