Application of a new real-time polymerase chain reaction assay for surveillance studies of lymphocystis disease virus in farmed gilthead seabream
© Valverde et al. 2016
Received: 6 July 2015
Accepted: 30 March 2016
Published: 6 April 2016
Lymphocystis disease (LCD) is the main viral infection reported to affect cultured gilthead seabream (Sparus aurata) in Europe. The existence of subclinical Lymphocystis disease virus (LCDV) infection in this fish species has been recognised by using polymerase chain reaction (PCR)-based methods. Nevertheless, these methods do not provide quantitative results that can be useful in epidemiological and pathological studies. Moreover, carrier fish have been involved in viral transmission, therefore the use of specific and sensitive diagnostic methods to detect LCDV will be relevant for LCD prevention.
We have developed a real-time PCR (qPCR) assay to detect and quantify LCDV. The assay was evaluated for viral diagnosis in surveillance studies in gilthead seabream farms, and also to identify viral reservoirs in a hatchery. The prevalence of LCDV infection in the asymptomatic gilthead seabream populations tested varied from 30 to 100 %, including data from one farm without previous records of LCD. Estimated viral load in caudal fin of subclinically infected fish was two to five orders of magnitude lower than in diseased fish. The qPCR assay allowed the detection of carrier fish in broodstock from a farm with a history of clinical LCD in juvenile fish. In addition, the quantitative detection of LCDV was achieved in all samples collected in the hatchery, including fertilized eggs, larvae and fingerlings, and also rotifer cultures and artemia metanauplii and cysts used for larval rearing.
The qPCR assay developed in this study has proved to be a rapid, sensitive, and reliable method for LCDV diagnosis, which could be valuable to identify LCDV reservoirs or to study viral replication in gilthead seabream.
KeywordsLymphocystis disease virus Virus surveillance Farmed gilthead seabream Real-time PCR
Lymphocystis disease (LCD) affects a wide variety of wild and cultured fish species with an extensive geographical distribution . In Southern Atlantic and Mediterranean aquaculture, this disease is the main viral infection reported to affect cultured gilthead seabream (Sparus aurata) [2–4]. The typical sign of lymphocystis disease is the presence of small pearl-like nodules on the skin and fins of affected fish, that may occur singly or more generally grouped in raspberry-like clusters of tumorous appearance [5, 6]. Although this disease is rarely fatal, fish showing these symptoms appear unsightly and cannot be commercialized, causing important economic losses . Moreover, in fish farms, LCD outbreaks may favour secondary bacterial infections, cannibalism and/or parasitic infestations, factors that may increase mortality rates [4, 8–10].
The etiological agent of LCD is the Lymphocystis disease virus (LCDV), a member of the genus Lymphocystivirus, family Iridoviridae. On the basis of the major capsid protein (MCP) gene sequence, nine genotypes of Lymphocystivirus have been proposed [11–15]. All LCDV isolates from gilthead seabream and Senegalese sole (Solea senegalensis) sequenced so far are included in genotype VII [10, 14, 16].
The only adequate measure for LCD prevention in the aquaculture systems is the use of general prophylactic practices, such as good husbandry practices, reduced stocking density and the virological control of fish to be introduced in the farm facilities in order to detect carrier fish . These animals may pose a risk for the introduction of LCDV in fish farms, as direct contact between fish specimens is considered the main route of LCDV spreading . More recently, asymptomatic carrier breeders have also been involved in LCDV transmission to fish larvae . The detection of subclinical viral infections in carrier fish requires the use of sensitive diagnostic methods . In this context, polymerase chain reaction (PCR)-based methods have proved to be adequate for LCDV detection in apparently healthy fish [10, 16, 19–21]. The PCR-hybridization assay developed by Cano et al.  not only allowed the detection of LCDV in carrier gilthead seabream, but also in rotifer and artemia used as live food for larval stages, which makes it a valuable tool for the detection of other potential LCDV foci in fish farms [17, 22]. Nevertheless, this assay is relatively time-consuming, not readily applied to screening large sample numbers, and does not provide quantitative results, that can be useful in epidemiological and pathological studies of LCDV.
Real-time PCR (qPCR) has been used for the detection and quantification of numerous viral fish pathogens, including LCDV in yellow perch (Perca flavescens) , and has been proved to be useful to overcome the disadvantages of conventional PCR above mentioned [23–25]. Recently, a qPCR assay has been developed and applied for the detection and quantification of LCDV in a low number of samples of diseased and recovered gilthead seabream. Nevertheless, the use of the assay for LCDV monitoring in different stages of the fish production cycle was not investigated .
The objective of this study was to establish the applicability of a new qPCR assay for LCDV diagnosis in surveillance studies. In addition, this assay has been evaluated using samples from a gilthead seabream hatchery, in order to demonstrate its utility to detect several sources of LCDV in the fish farm.
Fish farms owners accepted to participate in the study, and specialized personnel in each farm facility carried out the sampling procedures described below. Fish used in this study have been treated in compliance with the Spanish legislation (Law 32/2007, and RD 53/2013).
Sample collection and DNA extraction
Juvenile gilthead seabream specimens were sampled at four aquaculture farms. In two of these farms (farms A and B), a total of 11 diseased and 25 asymptomatic (i.e., without signs of lymphocystis disease) fish were collected during an outbreak of LCD, whereas in the other two (farms C and D), only asymptomatic fish were observed, and 24 of them were collected. Juvenile fish were euthanized by anaesthetic overdose (MS-222) (Sigma-Aldrich, St. Louis, MO, USA) before sampling. Samples of caudal fin (approximately 1 cm2 in size) were aseptically cut off, frozen immediately at -20 °C in dry ice and sent to the lab. In addition, 9 gilthead seabream samples were collected at the hatchery in another farm suffering LCD outbreaks over several years (farm E). Samples consisted of fertilized eggs (one sample of 100 mg), larvae (4 pools of 10–15 animals), and fingerlings (up to 2 g of weight) (4 pools of 5–10 animals). No LCD clinical signs were observed in any of the sampled fingerlings. Larvae and fingerlings were also euthanized by anaesthetic overdose. One sample of each rotifers (100 mg), commercial artemia cysts (100 mg), decapsulated artemia cysts (100 mg) and artemia metanauplii (100 mg) used as live food for larvae were also collected. These samples were washed with sterile seawater, gently dried and fresh frozen for shipment to the lab. In this farm, 50 broodstock were also analysed. These animals neither showed symptoms of LCD nor had LCD history, as stated by the farm records. For sampling purposes, these specimens were anaesthetized with MS-222 in seawater at a final concentration of 30 mg/ml. For each specimen, samples of caudal fin and blood were obtained. Blood samples were collected from the branchial arches using S-Monovette 4.5 ml LH (Sarstedt, Nümbrecht, Germany), chilled to 4 °C and sent to the lab for analysis within 24 h, whereas samples of caudal fin were obtained and stored as described above.
Samples were homogenized in Leibovitz’s L-15 medium (Gibco, Life Technologies, Carlsbad, CA, USA) (10 % w/v) as described previously , except samples of eggs, rotifers and artemia, which were ground in liquid nitrogen. Total DNA was extracted from 200 μl of tissue homogenates or 50 mg of tissue powder using the QIAamp DNA Minikit (Qiagen, Valencia, CA, USA) according to the manufacturer’s instructions. Finally, DNA was extracted from 200 μl of heparinised blood using the ReliaPrep Blood gDNA Miniprep System (Promega, Madison, WI, USA). In all cases, DNA was eluted in a final volume of 100 μl and stored at -20 °C until use as template for PCR-hybridization and qPCR. Prior to PCR assays, purified DNA was quantified spectrophotometrically using a NanoDrop 1000 spectrophotometer (Thermo Scientific, West Palm Beach, FL, USA), and DNA was diluted to achieve a final concentration of 20 ng/μl.
LCDV genome was detected using the PCR-hybridization assay described by Cano et al. . Briefly, a 270-bp fragment of the MCP gene of LCDV was amplified by PCR. PCR products were denatured and blotted onto a Hybond-N nylon membrane (GE Healthcare, Waukesha, WI, USA), and hybridization was carried out using an LCDV-specific DIG-labelled probe and the chemiluminescent substrate CSPD (Roche Applied Science, Mannhein, Germany).
Cloning a fragment of MCP gene
Lymphocystis disease virus isolate SA9 was used as source of LCDV DNA . A fragment of the viral MCP gene was amplified by PCR using the primers LCDVs-F and LCDVs-R described by Kitamura et al. . PCR was performed in a 50-μl reaction volume containing 10 μl of 5X Colorless GoTaq Flexi Buffer (Promega), 3 mM MgCl2 (Promega), 5 μl of 0.2 mM dNTP (Roche), 1.25 U of GoTaq DNA polymerase (Promega), and 2 μl of each primer at 15 pmol/μl. DNA was amplified by the use of one denaturation step at 95 °C for 5 min, followed by 35 cycles of denaturation (95 °C for 1 min), annealing (50 °C for 30 s), and extension (72 °C for 1 min), and a final extension step at 72 °C for 10 min. PCR products were run in 2 % agarose gels, purified using the HighPure PCR Product Purification kit (Roche), and cloned into the pCR4-TOPO vector (TOPO TA cloning kit) (Invitrogen, Life Technologies, Carlsbad, CA, USA) for subsequent transformation in Escherichia coli (One Shot competent cells, Invitrogen) following manufacturer’s instructions. Recombinant plasmid DNA was purified from E. coli cells with a commercial kit (High Pure Plasmid Isolation kit, Roche), and insert size was verified by PCR and sequencing, using the M13 primers provided in the cloning kit. The cloned MCP gene fragment was 609 bp in length, corresponding with nucleotide positions 99 to 707 of the LCDV SA9 MCP gene (GenBank accession no. GU320728).
Real-time PCR assay
Primers for qPCR (RT-LCDV-F: 5′-ACGTTTCTCGAGGCGGAGAT-3′, and RT-LCDV-R: 5′-CGGACGTTTGCTTGACCAA -3′) were designed to target the MCP gene of LCDV genotype VII, using Primer Express Software v3.0 (Applied Biosystems, Life Technologies, Carlsbad, CA, USA). This primer set generates a 150-bp amplicon within the 609-bp cloned fragment of MCP gene (nucleotide positions 173 to 322 of the LCDV SA9 MCP gene).
Real-time PCR reactions were carried out in 96-well plates (Applied Biosystems), in a final volume of 50 μl containing 25 μl of 2x Power SYBR Green PCR Master Mix (Applied Biosystems), 3 μl of each primer at 15 pmol/μl, and 10 μl of DNA. PCR amplifications were performed in a 7500 Real-Time PCR System (Applied Biosystems). The thermal profile was: 50 °C for 2 min; 95 °C for 10 min, and 40 cycles at 95 °C for 15 s and 60 °C for 1 min. Finally, dissociation curve analysis was carried out automatically in order to allow detection of non-specific amplification products.
Standard curve for LCDV quantification
To quantify the amount of viral DNA in different samples, a standard curve was generated using the recombinant plasmid described above. The concentration of the purified plasmid was determined by spectrophotometry as described above, and the plasmid stock was diluted to serve as template for qPCR (10-fold serial dilutions ranging from 106 to 102 copies, and then two-fold dilutions from 50 to 25 copies, and from 16 copies to 1 copy).
The sensitivity of the qPCR assay was also determined in terms of infective viral particles. LCDV SA9 stock was titrated in SAF-1 cells, using the 50 % cell culture infectious dose (TCID50) endpoint dilution assay as described previously . An aliquot of 1 ml of the viral stock with a titre adjusted to 1 x 106 TCID50/ml was subjected to a 10-fold serial dilution in Leibovitz’s L-15 medium. The DNA of each dilution was extracted as previously specified, and used for qPCR. The amount of infective virus analysed per reaction was 1 x 105 to 1 x 100 TCID50.
Milli-Q water and DNA from one LCDV-negative gilthead seabream sample  were included within each qPCR run as no-template and negative controls, respectively. In each 96-well, plasmid dilutions for the standard curve were run along with the samples and controls, using three technical replicates. The number of copies of LCDV DNA in each well was calculated from its cycle threshold (Ct) value by interpolation in the standard curve (Ct versus log copy number), using the SDS Software v1.3 (Applied Biosystem). The amplification efficiency (E) was calculated from standard curves using the formula E = (10-1/S - 1) x 100 (S being the slope of the linear fit). Viral loads in samples were calculated as the mean of the three replicates, and expressed as viral DNA copies per milligram of tissue (per μl in blood samples).
Assay repeatability and reproducibility
To evaluate the precision of the qPCR, the intra- and inter-assay variability was determined using the recombinant plasmid. To assess intra-assay variation, four plasmid DNA dilution series (from 105 to 2 copies per reaction) were prepared and tested simultaneously in the same plate. Four separate PCR runs were carried out to assess inter-assay variation, using also seven dilutions of plasmid DNA. The mean, standard deviation (SD) and coefficient of variation (CV) were calculated independently for each DNA dilution.
Evaluation of the real-time PCR assay
Specificity of the qPCR was determined by analysis of the dissociation curves generated in each experiment. Standard and positive samples gave a single PCR product with a melting temperature of 77.7 ± 0.5 °C, which correspond with that deduced from the sequence of the expected fragment. The size of amplicons was monitored by agarose gel electrophoresis, and bands were observed at the expected size (150 bp).
Intra- and inter-assay variability of the real-time PCR
Cycle threshold (Ct)c
Cycle threshold (Ct)c
1 x 105
19.92 ± 0.16
18.92 ± 0.54
1 x 104
23.34 ± 0.17
22.27 ± 0.60
1 x 103
26.87 ± 0.18
26.14 ± 0.46
1 x 102
30.22 ± 0.27
29.49 ± 0.71
1.6 x 101
32.15 ± 0.47
32.22 ± 0.87
4 x 100
34.15 ± 0.80
33.37 ± 0.89
2 x 100
35.23 ± 0.99
34.09 ± 1.14
Overall CVc (%)
1.38 ± 0.87
2.63 ± 0.48
A linear relationship between the infective titre of a viral suspension and Ct values was also observed for viral amounts ranging from 1 x 104 to 1 x 100 TCID50 per reaction (r = 0.999) (Fig. 1b), with 1 x 100 TCID50 yielding a mean viral DNA copy number of 1.2 x 102.
Surveillance study of LCDV in gilthead seabream farms
In the present study, individual gilthead seabreams were collected from four farms with different background regarding to LCD. Farm C had no records of LCD, either before or after this study, whereas farm D suffered LCD outbreaks in last years. In farms A and B an outbreak of LCD was going on at the time of sampling, affecting several tanks. In these latter farms, fish from two different cycles of production were sampled, one suffering and other unaffected by LCD.
LCDV detection and estimated viral load determined by real-time PCR in caudal fin from diseased and asymptomatic gilthead seabream juveniles
Mean ± SD
(4 ± 3.99) x 100
1.2 x 105–6.6 x 105
(3.53 ± 2.77) x 105
(1.1 ± 1.89) x 102
2.9 x 104–6.9 x 104
(5 ± 1.75) x 104
(1.6 ± 1.56) x 101
(5.3 ± 5.88) x 101
Estimated viral load determined by real-time PCR in samples from a gilthead seabream hatchery
1.5 x 102
1.9 x 102
Decapsulated artemia cysts
1.2 x 101
1.5 x 102
4.1 x 100
3.4 x 100
2.5 x 100
3.6 x 100
5.1 x 100
Fingerlings (0.3 g)
1.1 x 101
Fingerlings (0.9 g)
1.3 x 100
Fingerlings (1.6 g)
2.2 x 101
Fingerlings (2 g)
9.7 x 100
LCDV detection and estimated viral load determined by real-time PCR in caudal fin and blood from asymptomatic gilthead seabream breeders
Mean ± SD
(2.7 ± 1.40) x 101
(1.3 ± 1.37) x 100
LCD outbreaks are frequently observed in the Mediterranean gilthead seabream aquaculture. Although it is usually described as a self-limiting disease, there are several reports on mortalities up to 45 % in juvenile fish, which may be related to secondary bacterial infections or with particularly large growth of lymphocysts, which severely impaired fish breathing or feeding [4, 10, 28]. As no effective treatments or commercially available vaccines currently exist, LCD prevention in hatcheries must rely on the selection of LCDV-free broodstock, the use of effective decontamination methods to prevent viral transmission from asymptomatic broodstock to larvae, and the supply of virus - freelive food [17, 22, 29]. During the growing period, the selection of non-infected fish is also advisable, as LCDV-positive juveniles may become symptomatic under stress conditions such us transport to on-growing facilities. Moreover, little information is available on a number of epidemiological questions concerning LCDV infections, as the number of virus particles required to induce the disease, the number of genome copies present in asymptomatic and diseased fish, and the kinetics of viral replication.
Previous studies have demonstrated the applicability of a PCR-based method to detect LCDV in asymptomatic gilthead seabream carriers, independently of its size, as well as in rotifer and artemia cultures [17, 19, 22]. Nevertheless, this method is relatively time-consuming, as an additional step of blot-hybridization of the PCR products is required to detect LCDV-positive samples. Furthermore, this assay is not quantitative and applicable for routine diagnosis.
In the present study a qPCR assay has been developed and applied to detect and quantify LCDV in different samples. The assay was specific for LCDV, as demonstrated by analysis of the melting curves generated from each sample. Its analytical sensitivity, determined as the smallest copy number of the plasmid standard reliably detected, was 2 copies of DNA per reaction. The qPCR assay also showed a wide linear dynamic range, extending to 6 log10 concentrations of plasmid DNA, and infective titres from 104 to 1 TCID50. In addition, the precision of the assay was supported by the high correlation coefficients obtained for the standard curves, and the intra- and inter-assay variation of Ct values.
Using the protocol as described, the qPCR assay allows the detection of the virus at levels as low as 1 copy of viral DNA per mg of fish tissue. This high sensitivity, combined with its wide dynamic range, makes the qPCR assay suitable to detect low viral loads in subclinical LCDV infections, and, at the same time, to quantify variable viral loads in the course of infection. In addition, it could be useful in searching for potential LCDV reservoirs.
The application of the qPCR assay to LCDV surveillance in fish farms has shown that monitoring the infection in individual fish, both diseased and subclinically infected, is possible by sampling caudal fin as reported previously [16, 19]. The prevalence of LCDV infection in the asymptomatic gilthead seabream populations analysed varied from 30 to 100 %, even in one farm with no previous LCD records. In these fish, estimated viral load in caudal fin was two to five orders of magnitude lower than in diseased fish. Thus viral load seems to correlate with disease manifestation. However, if the low viral loads detected in subclinical infections represent a status associated with viral replication remains to be determined. In addition, the qPCR assay developed could be a valuable tool to study the correlation between viral multiplication and the onset of symptoms in experimental LCDV infections.
Palmer et al.  developed a real-time PCR method using fluorogenic primers, specific for LCDV genotype IX sequences, which proved to be reliable in the detection of subclinically infected yellow perch, although its sensitivity was 5 x 102 copies of DNA per mgL-1. LCDV quantification by qPCR has also been carried out in a reduced number of samples from diseased and recovered gilthead seabream . The analytical sensitivity of the former assay was 5.2 copies of DNA per reaction that is more than twice the value reported in the present study. Furthermore, although the authors reported some quantitative data, viral loads were not expressed in terms of viral DNA copies per amount of tissue, which prevents further comparisons [15, 26].
Carrier fish were also identified in the broodstock from a farm with LCD records by analysing caudal fin samples by qPCR. The assay was applied in parallel to blood samples, and although LCDV could be detected, estimated viral load, and also clinical sensitivity, was lower than that obtained in caudal fin analysis. In this farm, the q-PCR assay allowed the quantitative detection of LCDV in all samples collected in the hatchery, including fertilized eggs, larvae and fingerlings, and also rotifer cultures and artemia metanauplii and cysts used for larval rearing. In these samples, as well as in caudal fin samples from asymptomatic juvenile fish, the qPCR assay showed the same clinical sensitivity than the PCR-hybridization protocol described by Cano et al. , but is completed in 130 min, including melting curve generation, which considerably reduces the time required for LCDV diagnosis. In addition, the results of this study support the existence of multiple reservoirs of LCDV in the farm facilities, as previously suggested by Cano et al. [17, 22], and the importance of proper application of effective disinfection treatments, as those recommended by the FAO , to avoid viral transmission through fish eggs or live food.
The qPCR assay developed in this study is a sensitive, specific and reliable method for detection and quantification of LCDV in gilthead seabream. The method is rapid and appropriate for LCDV surveys for which the detection of subclinical LCDV infections in carrier fish is essential. The assay could also be valuable to identify LCDV reservoirs or to study viral replication in fish.
Availability of data
All the data supporting the results are included in the article.
We thank Ms L Cruzado and R Crespillo (Universidad de Málaga) for technical assistance.
This study has been supported by a project from the Spanish Government (Ministerio de Ciencia e Innovación), co-funded by the FEDER, granted to D Castro (AGL2010-17880), and a project from Junta de Andalucía (P12-RNM-2261) granted to JJ Borrego. EJ Valverde was supported by a fellowship from the Spanish Government (Ref. BES-2011-043607).
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