- Research Article
- Open Access
Target organs for lymphocystis disease virus replication in gilthead seabream (Sparus aurata)
© The Author(s) 2017
- Received: 1 February 2017
- Accepted: 20 March 2017
- Published: 11 April 2017
The lymphocystis disease (LCD), the main viral pathology described in cultured gilthead seabream (Sparus aurata), is a self-limiting condition characterized by the appearance of hypertrophied fibroblasts (named lymphocysts) in the connective tissue of fish, primarily in the skin and fins. The causative agent of the disease is the Lymphocystis disease virus (LCDV), a member of the Iridoviridae family. In the present study, LCDV genome and transcripts were detected by real-time PCR in caudal fin, as well as in several internal organs, such as intestine, liver, spleen, kidney and brain, from asymptomatic, diseased and recovered gilthead seabream juveniles. These results indicate that the LCDV has a broad range tissue tropism, and can establish a systemic infection, even in subclinically infected fish. As showed by in situ hybridization, the permissive cells for LCDV infection seem to be fibroblasts, hepatocytes and cells of the mononuclear phagocyte system. Histopathological alterations associated with LCD were observed in all the organs analysed, including necrotic changes in liver and kidney, inflammatory response in the intestine submucosa or brain haemorrhage, although lymphocysts were only detected in the dermis of the caudal fin. Nevertheless, these histological changes were reverted in recovered animals.
- Viral Gene Expression
- Major Capsid Protein
- Mononuclear Phagocyte System
- Diseased Fish
- Gilthead Seabream
Lymphocystis disease (LCD) is the viral infection most frequently reported in gilthead seabream (Sparus aurata) farms in the South Atlantic and Mediterranean areas . The aetiological agent of this disease is the Lymphocystis disease virus (LCDV), a member of the Iridoviridae family .
LCD is a self-limiting disease characterized by the hypertrophy of fibroblastic cells in the connective tissue of fish . These hypertrophied cells, named lymphocysts or lymphocystis cells, are usually observed on the skin and fins, although they have also been described in several internal organs (such as the stomach, spleen, liver, kidney and heart) [4–8]. In gilthead seabream, lesions associated with LCD have only been observed in the skin and fins of affected fish, and usually disappear after 20–45 days depending on water temperature [9–11].
Data on LCDV pathogenesis are very scarce and generally limited to histopathological studies of skin lesions [9, 12, 13]. However, several studies have shown that viral antigens can be detected in a number of organs of infected fish, not only in lymphocystis lesions [13–15]. In gilthead seabream, DNA–DNA hybridization and immunohistochemistry were used to detect LCDV in diseased and recovered juveniles . Viral genomes and antigens were detected in the different organs analysed, including the caudal fin, gills, intestine, liver, spleen and kidney, suggesting that LCDV establishes a systemic and persistent infection in this fish species. In addition, LCDV is frequently detected by PCR-based methods in apparently healthy seabream [14, 16, 17], which indicates that they may be subclinically infected. However, further studies are necessary to confirm these results and to establish if these infections are productive.
Thus, the objective of the present study was to determine the target organs and cells that support LCDV replication in gilthead seabream juveniles, both lymphocystis (LC)-diseased and subclinically infected. In addition, a histopathological study of LCD was also conducted.
Gilthead seabream specimens were obtained from two fish farms located in southwestern Spain. In the first farm, fish without signs of LCD (6–10 g in weight) were collected, and constituted the group named “asymptomatic”. This farm had no record of any LCD outbreaks in over 15 years. In the second farm, diseased individuals (6–10 g) showing typical external signs of LCD were collected, and 2 months after the disease signs had disappeared, another group of fish from the same population (15–20 g) was sampled. These fish constituted the “diseased” and the “recovered” groups, respectively. Fish used in this study were treated according to the Spanish directive (RD 53/2013, BOE no. 34), and were euthanized by anaesthetic overdose (MS-222, Sigma-Aldrich, St. Louis, MO, USA).
Samples of the caudal fin, intestine, liver, spleen, kidney and brain of nine individuals from each experimental group were aseptically collected and individually processed for subsequent homogenization and nucleic acid extraction. In addition, the same organs were collected from three fish in each group for in situ hybridization (ISH) and histological examination. Fish samples were fixed in 4% paraformaldehyde (Sigma-Aldrich) in DEPC-treated PBS (pH 7.2) for 24 h at 4 °C, and embedded in paraffin using standard histological procedures. Fixed caudal fin samples were decalcified with a solution containing 10% EDTA (Sigma-Aldrich) and 4% paraformaldehyde in DEPC-treated water at pH 7.0 for 10–15 days at 4 °C. Tissue sections (5–7 µm) were mounted on TESPA (3-triethoxysilylpropylamine, Sigma-Aldrich)-treated slides.
DNA and RNA extraction and cDNA synthesis
Total DNA and RNA were extracted using the E.Z.N.A. Tissue DNA Kit and the E.Z.N.A. Total RNA Kit I (Omega Bio-tek Inc., Norcross, GA, USA), respectively, following the manufacturer’s instructions. Total RNA was treated with RNase-free DNase I (Roche Applied Science, Mannhein, Germany) for 30 min at 37 °C. RNA purity and quantity was determined using NanoDrop 1000 (Thermo Scientific, West Palm Beach, FL, USA). After DNase treatment, total RNA was used in the qPCR reaction in order to control for the absence of viral genomic DNA. First-strand DNA synthesis was carried out with 1 µg of total RNA and random hexamer primers using the Transcriptor First Strand cDNA Synthesis Kit (Roche). DNA and cDNA were stored at −20 °C until used as template for qPCR.
LCDV DNA quantification and gene expression
The qPCR protocol described by Valverde et al.  was used to quantify the amount of viral DNA in the samples. The number of copies of LCDV DNA was calculated by interpolation in a standard curve, and viral loads expressed as viral DNA copies per milligram of tissue.
Relative quantification of major capsid protein (MCP) gene expression was carried out by RT-qPCR, following the protocol mentioned above but using 20-µL final volume reactions and 2 µL of cDNA (at a 1/30 dilution). Normalized relative MCP expression levels were calculated for each sample applying the formula: F = log10 [(E + 1)40−Ct/N] , where E is the amplification efficiency of the qPCR, Ct (threshold cycle) corresponds to the PCR cycle number, N is the maximal number of viral DNA copies/mg of tissue detected minus the number of viral DNA copies/mg of tissue determined by absolute qPCR for the sample, and Ct of 40 arbitrarily corresponds to “no Ct” by qPCR.
Results obtained for viral DNA quantification and relative gene expression were analysed statistically using a Mann–Whitney U test followed by a Holm–Bonferroni correction for multiple comparisons.
RNA in situ hybridization and histopathology
Digoxigenin (DIG)-labelled RNA probes were synthesized by in vitro transcription with the DIG RNA Labelling Kit (Roche) using a 150-bp fragment of the viral MCP gene (nucleotide positions 173–322 of the LCDV SA9 MCP gene, GenBank accession no. GU320728) cloned into the pCRII Dual Promoter vector (Invitrogen, Life Technologies, Carlsbad, CA, USA) as the template. The RNA probes were produced from 1 µg of linearized plasmid using T7 (antisense) or SP6 (sense) polymerases.
Deparaffinised and rehydrated tissue sections were permeabilized for 30 min with 10 µg/mL proteinase K in a buffer containing Tris–HCl 0.05 M pH 7.6 (40%, v/v) and CaCl2 1 M (4%, v/v) in DEPC-treated water at 37 °C. Sections were pre-hybridized with formamide (50%, v/v), 20× SSC (25%, v/v), torula yeast RNA (50 mg/mL), heparin sodium salt (5 mg/mL), Denhardt’s solution (2%, v/v), CHAPS (2%, w/v) and Tween 20 (0.5%, v/v) in DEPC-treated water for 3 h in a 2× SSC saturated atmosphere at 55 °C. Sense and antisense probes were denatured at 85 °C for 5 min, and hybridization was performed overnight at 60 °C. After hybridization, sections were washed as previously described  and treated with 1% blocking reagent (Roche) in maleic acid buffer (0.1 M maleic acid, 0.15 M NaCl, pH 7.5) for 1 h at room temperature. Then, the slides were incubated with anti-digoxigenin-AP (Roche) overnight at 4 °C, and the hybridization signals were detected using NBT/BCIP (Roche) according to the manufacturer’s instructions. All reagents were supplied by Sigma-Aldrich unless otherwise stated. Finally, sections were dehydrated and mounted in Eukitt® quick-hardening mounting medium (Sigma-Aldrich).
In parallel, tissue sections were stained with haematoxylin-eosin (HE) and haematoxylin-V.O.F.  for histological examination.
Viral load and gene expression
RNA in situ hybridization
Viral transcripts were detected by ISH in all organs from the diseased fish, whereas no signal was observed in the sections from fish belonging to the asymptomatic and recovered groups (results not shown). No labelling was observed in the negative controls using sense probe for ISH.
The pathognomonic signs of LCD include the appearance of small pearl-like nodules on the skin and fins that are usually grouped in clusters, papillomatous in appearance, and can cover the entire body surface of the fish . These nodules consist of LCDV-infected hypertrophied dermal fibroblasts (up to 1 mm in diameter), named lymphocysts or lymphocystis cells [11, 21, 22]. LCDV is considered a dermatropic virus ; however, in some fish species, lymphocysts have also been observed in the mesenteries, peritoneum, and several internal organs, which could indicate that the infection can become systemic under certain conditions [4, 7, 23, 24]. Moreover, using sensitive immunological and molecular diagnostic methods, LCDV has been detected in different organs of fish without internal lesions [10, 13, 15, 16, 25]. These findings suggest a systemic condition for LCD although it has not been shown if viruses detected in different organs proceed from productive infections or are actually the result of an underlying viraemia.
In the present study, lymphocystis cells were exclusively observed in the dermis of the skin and fins of diseased juvenile gilthead seabream. Nevertheless, viral genomes were detected by qPCR in all of the organs analysed. Viral gene expression was also detected in all the samples, with the highest relative expression values recorded in the caudal fin, followed by those in the kidney and brain. Accordingly, the highest viral loads were detected in the fins, and the amount of viral genomes in the kidney and brain were significantly (p < 0.01) higher than in other internal organs analysed. These results support that LCDV establishes a systemic infection in gilthead seabream, similar to infections reported for other iridoviruses, such as ranaviruses and megalocytiviruses [26, 27]. Recent studies carried out in Japanese flounder and turbot have shown that LCDV genome copy numbers increased in all organs analysed during the course of experimental infections, and that the extensive range of viral target tissues is, at least partially, the result of the wide distribution of the LCDV-C receptor [28, 29]. Whether this receptor, a membrane protein of 27.8 kDa first identify in FG cells [30, 31], is present in gilthead seabream cells, and also a receptor for LCDV-Sa attachment, needs to be investigated.
Viral MCP transcripts were detected by ISH in order to identify susceptible cells supporting LCDV productive infection. As expected, LCDV expression was observed on lymphocysts located on the caudal fin but also in some cells in the surrounding connective tissue. Viral transcripts were also detected in hepatocytes, and in cells of the splenic pulp, the kidney interstitium, and the brain granular layer. This distribution of viral mRNA is similar to results of previous work that detected viral genomes and antigens in several organs of juvenile gilthead seabream . In the present study, it was not possible to determine which cell type contained viral transcripts in the intestine. Nevertheless, Cano et al.  detected LCDV-positive cells in the connective tissue of the lamina propia. Furthermore, other authors also described the detection of LCDV genomes and/or antigens in the gill lamella of LC-diseased Japanese flounder, black rockfish, and gilthead seabream [13–15]. Together, these results support a broad range tissue tropism for LCDV, similar to that established for megalocytiviruses, which were described to be mesotheliotropic [32, 33].
On the basis of the results obtained, the permissive cells for LCDV replication seem to be fibroblasts, hepatocytes, and cells of the mononuclear phagocyte system, as previously suggested [14, 34]. The LCDV-C receptor has been detected in the membrane of a small portion of turbot peripheral leucocytes, which could indicate that they are susceptible to LCDV infection, resulting in LCDV spreading to different host tissues via the bloodstream . In the gilthead seabream brain, viral transcripts were detected in cells of the granular layer, which suggests that microglial cells or infiltrating macrophages may be susceptible to LCDV, although neurons cannot be ruled out as a susceptible cell type. Further immunocytochemical studies should be carried out to identify LCDV-infected cells in brain, using, for example, OX-42 or FL.1 antibodies that recognize monocyte-derived cells in fish .
LCDV was detected at low levels in all of the organs analysed from asymptomatic and recovered fish. In addition, these organs support viral gene expression, indicating that the fish are subclinically infected by LCDV, and that this infection is also systemic. In asymptomatic fish, the highest relative viral expression value was recorded in the caudal fin, whereas the brain seems to be the main organ that supports viral expression in the recovered fish. As previously suggested by other authors [10, 14], LCDV establishes a systemic and persistent infection in gilthead seabream juveniles, which may extend for at least 2 months after disappearance of clinical signs.
Subclinically infected fish may be essential for LCD epizootiology. Thus, asymptomatic fish have been considered responsible for LCD outbreaks that appear in aquaculture facilities under stressful rearing conditions [36–39]. These conditions might stimulate virus replication and the consequent development of symptoms . Moreover, it is assumed that fish can recover from LCD and develop acquired immunity [24, 41]. Nevertheless, recovered fish are persistently infected and, consequently, may be LCDV-carriers that could transmit the virus to naïve fish.
Histopathological studies carried out in LC-diseased fish have been focused on the description of lymphocystis cells, with few reports dealing with histological observations of internal organs, except when lymphocysts were also present [4, 9, 11, 12]. In the present study, LC-diseased gilthead seabream specimens showed lymphocystis cells only in the dermis of the caudal fin, with histological characteristics resembling those previously described in this fish species . Histological alterations of different severities were also observed in all of the organs analysed, including necrotic changes in the liver and kidney, inflammatory response in the intestine submucosa, and intraventricular haemorrhage. Necrotic changes in the epithelium of the proximal renal tubules were the only histological alterations described so far in gilthead seabream juveniles affected by LCD [14, 42]. Nevertheless, histological damages similar to those observed in the present study in the liver, kidney or intestine, have also been described in LC-diseased snakeskin gourami (Trichogaster pectoralis) and kelp bass (Epinephelus moara) [22, 43]. These histopathological changes can be directly related to viral replication, as in the case of the liver, where hepatocytes are actually infected by LCDV (as demonstrated by ISH in the present study or by observation of viral particles by TEM in kelp bass), while in other cases an indirect relation could be proposed. Thus, epithelial necrosis of renal tubules has been associated with substances produced by infected cells in the interstitial tissue, or, alternatively, with severe alterations in osmoregulation resulting from multiple skin lesions [14, 42]. In addition, an increase in the number of MMC was observed in the liver, spleen, and kidney, which could be associated with a cellular response to viral infection . The proliferation of epithelioid cells around lymphocysts has also been described as an immune response against LCDV [4, 12, 45]. Finally, in recovered fish, most organs and tissues showed normal histological features, indicating that histopathological alterations associated with LCD are reversible.
In conclusion, the results demonstrate that LCDV infection is a systemic condition in gilthead seabream, even for subclinical infections, where several organs seem to be primary or secondary targets for virus replication. LCDV has a broad range tissue tropism. In addition to dermis fibroblast that become lymphocysts after LCDV infection, cells from the liver, spleen, kidney, intestine, and brain could support a productive viral infection. The permissive cells for LCDV replication seem to be fibroblasts, hepatocytes and cells of the mononuclear phagocyte system.
The authors declare that they have no competing interests.
Experimental design and interpretation of data: JJB, DC. Sample processing, molecular analysis and statistics: EJV. ISH and histopathology processing and data interpretation: EJV, JBO-D, MCS. Drafting the manuscript: EJV, JJB, DC. Manuscript revision and edition: JJB, DC. All authors read and approved the final manuscript.
This study has been supported by a project from the Spanish Government (Ministerio de Ciencia e Innovación), co-funded by the FEDER, granted to DC (AGL2010-17880), and a project from Junta de Andalucía granted to JJB (P12-RNM-2261). EJV was supported by a fellowship from the Spanish Government (BES-2011-043607).
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