The complete open reading frame (ORF) of the turbot nk-lysin (nkl) gene was obtained from a previous 454-pyrosequencing of turbot tissues (35) and confirmed by sequencing using specific primers (Table S1 in Supplementary Material). A local blast against the turbot genome (36) was conducted to identify other potential nkl genes and to determine the number of exons/introns constituting the turbot nkl.

The presence of signal peptide was analyzed with the SignalP 3.0¹ server (37) and the presence of specific domains with SMART 4.0² (38). The three-dimensional (3D) structure of turbot Nkl was predicted using I-TASSER server (39) selecting the model with the best C-score and viewed by PyMOL.³ An alignment between several Nkls/granulysins protein sequences from fish, birds, and mammals was conducted using the ClustalW server (40). A phylogenetic tree was drawn using Mega 6.0 software (41) and selecting the model of protein evolution that best fits a given alignment according to the ProtTest 2.4⁴ server (42). Sequence similarity and identity scores were calculated with the software MatGAT (43) using the BLOSUM62 matrix. The GenBank accession numbers of the sequences used in this section are listed in Table S2 in Supplementary Material.

Juvenile and adult turbot (average weight 2.5 and 125 g, respectively) were obtained from a commercial fish farm (Insuiña S.L., Galicia, Spain). Prior to experiments, fish were acclimatized to the laboratory conditions for 2 weeks. When necessary, fish were euthanized via MS-222 overdose (500 mg/L). All the experimental procedures were reviewed and approved by the CSIC National Committee on Bioethics under approval number ES360570202001/16/FUN01/PAT.05/tipoE/BNG.

Viral hemorrhagic septicemia virus (strain UK-860/94) was propagated in the Epithelioma Papulosum Cyprini (EPC) cell line (ATCC, CRL-2872) at 14°C in MEM (Gibco) supplemented with 2% FBS (Gibco), and 100 µg/mL Primocin (InvivoGen). The virus stock was titrated into 96-well plates according to established protocols (44, 45). VHSV aliquots were stored at −80°C until use.

The expression plasmid pMCV1.4-nkl was synthesized by ShineGene Molecular Biotech, Inc. (Shanghai, China) using the pMCV1.4 plasmid (Ready-Vector, Madrid, Spain) and the nucleotide sequences encoding the turbot Nkl mature peptide. The plasmid was cloned by transforming One Shot TOP10F’ competent cells (Invitrogen) and purified using the PureLink™ HiPure Plasmid Midiprep Kit (Invitrogen).

Human HEK-293 cells (ATCC CRL-1573) were grown in Eagle’s Minimum Essential Medium (Gibco) supplemented with 100 µg/mL primocin (InvivoGen), 1× non-essential amino acids (Gibco), 1-mM sodium pyruvate (Gibco), and 10% FBS. The cells were incubated in a 5% CO₂ atmosphere at 37°C.

Recombinant Nkl was produced by transfection of 6 µg of the plasmid pMCV1.4-nkl into HEK-293 cells at 70–80% confluence (T-25 flask) using the XtremeGENE HP DNA Transfection Reagent (Roche) according to the manufacturer’s instructions. The same process was conducted with the corresponding empty plasmid pMCV1.4. Forty-eight hours after transfection, the supernatants were collected, filtered by 0.22 µm, and stored at −80°C until further use.

Emini surface accessibility scale (45), Kolaskar and Tongaonkar antigenicity scale (46), and Bepipred Linear Epitope Prediction (47) methods were used to predict the best Nkl antigen binding regions of antibodies. Based on this information, two peptides were chosen (RSLEINIDDQEQVC and CLFYPKQEESQTE). To obtain the anti-Nkl polyclonal antibody (New England Peptide, Gardner, MA, USA), rabbits were co-immunized with both synthetic peptides. Blood was collected before injection (pre-immune serum) and 30 days after the immunization (polyclonal antibody).

The anti-Nkl polyclonal antibody was validated by western blot (WB). For this, 15 µL of the supernatants from HEK-293 cells transfected with pMCV1.4-nkl or pMCV1.4 were mixed with 1× NuPAGE LDS Sample Buffer (Invitrogen) and resolved in a 4–20% Mini-PROTEAN TGX™ gel (Bio-Rad) (with and without 2-Mercaptoethanol and heat treatment 5 min at 95°C), and transferred to a nitrocellulose membrane (Bio-Rad). The membrane was blocked for 2 h with 3% (w/v) bovine serum albumin (BSA) in TBST buffer (20-mM Tris, 0.5-M NaCl, 0.1% Tween 20) and incubated for 2 h with the rabbit anti-Nkl polyclonal antibody (dilution 1:500 in 1% BSA-TBST buffer) at room temperature (RT). After three 10-min washes with TBST, membrane was incubated with a goat anti-rabbit-HRP antibody (Sigma) (dilution 1:10,000) for 1 h at RT, washed again, and revealed by chemiluminescence detection with Luminata™ Forte Western HRP Substrate (Millipore), and visualized with the ChemiDoc XRS + system (Bio-Rad).

To examine the constitutive expression of nkl, 11 different tissues (peritoneal exudate cells – PEC–, blood, head kidney, trunk kidney, spleen, gill, liver, intestine, heart, brain and muscle) were obtained from three adult healthy fish. PECs were obtained as previously described (48).

The modulation of nkl was also analyzed after an in vivo VHSV infection. A total of 50 juvenile turbot were divided into two groups. The first group (n = 25) was intraperitoneally (i.p.) injected with 50 µL of a VHSV suspension containing 2 × 10⁶ TCID₅₀/mL. The second group was injected with the same volume of culture medium. The head kidney and spleen were removed from five turbot at 1, 2, 3, and 7 days post-infection (dpi), constituting five biological replicates for each tissue and sampling point. These samples were processed for the analysis of nkl expression.

nkl expression was analyzed in the head kidney samples from four turbot families showing different mortality rates after VHSV infection. Two VHSV-resistant (1 and 4) and two-susceptible families (2 and 3) were previously described by Diaz-Rosales et al. (49). Five animals of each family were analyzed before (naïve) and 24 h after the VHSV challenge conducted by Díaz-Rosales et al. (49). The expression of nkl was analyzed by quantitative polymerase chain reaction (qPCR).

Additionally, the correlation between the constitutive expression level of nkl gene in blood before a viral infection and the resistance to a VHSV challenge was determined. Approximately 20 µL of blood were extracted from the caudal vein of juvenile turbot using a heparinized syringe and cells were processed for the analysis of nkl expression. One week after the blood extraction, the turbot were i.p. injected with 100 µL of a VHSV suspension (3 × 10⁷ TCID₅₀/mL). Mortality was recorded for 15 days and the size and weight of each turbot were also registered. The correlation between nkl mRNA levels in blood before the infection, the day of death, size and weight was determined using the Spearman’s rho correlation test.

The expression of nkl and the replication of VHSV in blood and in purified erythrocytes were analyzed by qPCR. Blood was taken from the caudal vein of three adult turbot using a heparinized syringe. Erythrocytes were purified in a Percoll (GE Healthcare) 51% gradient by centrifuging at 400× g for 30 min at 4°C without brake. Total blood cells and purified erythrocytes were adjusted to 10⁸ cells/mL in MEM (Gibco) supplemented with 2% FBS (Gibco) and 100 µg/mL Primocin (InvivoGen). Cells (250 µL) were distributed onto 24-well plates. A proportion of these cells were infected with VHSV (10⁴ TCID₅₀/mL) and the remaining wells were maintained as controls. Cells were incubated at 15°C and collected 2, 3, 5, and 7 dpi for the quantification of nkl transcripts and VHSV glycoprotein gene by qPCR.

For qPCR analysis, erythrocytes were purified, seeded, infected with VHSV, and maintained as mentioned above. A proportion of the erythrocytes were incubated with CQ (25 µM; Sigma-C6628) or rapamycin (RAP) (5 µM; Sigma-R0395). Cell samples were taken 1, 2, and 3 dpi for the quantification of nkl, becn1 and atg5 transcripts and VHSV glycoprotein gene.

For confocal microscopy analysis, total blood cells were incubated with CQ (25 µM) or RAP (5 µM) for 3 days. Cells were fixed and immunostained as described below.

The modulation of the nkl gene and the protein abundance and distribution of Nkl under vaccination and/or infection conditions were evaluated by qPCR and flow cytometry. Twelve adult turbot were intramuscularly (i.m.) injected with 50 µL of a DNA vaccine (2 µg/fish) encoding the G glycoprotein from VHSV (pMCV1.4-G₈₆₀) (50), whereas the other 12 fish were injected with the same amount of the empty plasmid (pMCV1.4). One month after vaccination, 6 fish from each group were i.p. injected with 50 µL of VHSV (2 × 10⁶ TCID₅₀/mL) and the remaining six fish were injected with cell culture medium. The head kidney, spleen, and blood were taken at 48 h post-infection (hpi). Cell suspensions from the head kidney and spleen were prepared by passing the tissue through a 40-µm nylon mesh in phosphate-buffered saline (PBS). Blood was collected from the caudal vein using a heparinized syringe and diluted in PBS. All the samples were divided into two groups to be analyzed at the same time by qPCR and flow cytometry.

Total RNA from the different tissue samples was extracted using the Maxwell^® 16 LEV simplyRNA Tissue kit (Promega) with the automated Maxwell^® 16 Instrument in accordance with instructions provided by the manufacturer. The cDNA synthesis was performed with the SuperScript II Reverse Transcriptase (Invitrogen) using 0.5 µg of RNA and following the manufacturer indications, except for the blood cell samples, in which case the cDNA synthesis was conducted with SuperScript III Reverse transcriptase (Invitrogen) using 0.1 µg of RNA.

Gene expression profiles were determined using real-time qPCR. Specific qPCR primers were designed using the Primer3 program (51) and their amplification efficiency was calculated using seven, fivefold serial dilutions of cDNA from unstimulated turbot with the threshold cycle (CT) slope method (52). The identity of the amplicon was confirmed by sequencing. Individual qPCR reactions were conducted in 25-µL reaction volume using 12.5 µL of SYBR GREEN PCR Master Mix (Applied Biosystems), 10.5 µL of ultrapure water (Sigma-Aldrich), 0.5 µL of each specific primer (10 µM), and 1 µL of fivefold diluted cDNA template in MicroAmp optical 96-well reaction plates (Applied Biosystems). All reactions were performed using technical triplicates in a 7300 Real-Time PCR System thermocycler (Applied Biosystems) with an initial denaturation (95°C, 10 min) followed by 40 cycles of a denaturation step (95°C, 15 s) and one hybridization–elongation step (60°C, 1 min). No-template controls were also included on each plate to detect possible contamination or primer dimers formed during the reaction. An analysis of melting curves was performed for each reaction. Relative expression of each gene was normalized using the eukaryotic translation elongation factor 1 alpha (ef1a) as reference gene, which was constitutively expressed and not affected by the experimental treatments, and was calculated using the Pfaffl method (52). Primer sequences used for the quantification of nkl, becn1, atg5, and VHSV glycoprotein transcripts are listed in Table S1 in Supplementary Material.

The head kidney, spleen, total blood cells, and purified erythrocytes samples were obtained as previously described from adult turbots. Cells were fixed with 2% paraformaldehyde during 15 min at 4°C. After washing, the cells were blocked by incubating for 1 h in PBS with 0.1% saponin (Sigma) and 2% of BSA (Sigma). Then, cells were incubated overnight at 4°C with the preimmune serum or with the rabbit anti-Nkl polyclonal antibody in staining buffer (PBS with 0.1% saponin and 0.1% BSA) (dilution 1:250). Cells were then washed and incubated with the secondary antibody Alexa Fluor^® 488 goat anti-rabbit IgG (Molecular Probes-Life Technologies; 1:1,000) for 1 h at RT. Samples were washed and resuspended in PBS. The expression of Nkl was analyzed using a FACSCalibur flow cytometer (BD Biosciences) in dot plots of relative size (forward-light-scatter, FSC) and complexity (side-light-scatter, SSC) in linear and logarithmic scale. FL1-H histograms were used to compare the fluorescence levels emitted by samples labeled with the anti-Nkl antibody and the preimmune serum. The percentage of positive fluorescent events and the intensity of fluorescence (median) were registered.

Cells were adjusted to 10⁶ cells/mL and distributed onto 24-well plates with 12-mm glass coverslips and incubated at 15°C for 2 h before the fixation. Cells were fixed with 2% paraformaldehyde for 15 min at 4°C. After washing, the cells were blocked by incubating for 1 h in PBS with 0.1% saponin (Sigma) and 2% of BSA (Sigma). Then, cells were incubated overnight at 4°C with the corresponding primary antibody in staining buffer (PBS with 0.1% saponin and 0.1% BSA). Cells were then washed and incubated with the secondary antibody for 1 h at RT. Nkl was stained using the rabbit anti-Nkl polyclonal antibody (1:250) and the secondary antibody Alexa Fluor^® 488 goat anti-rabbit IgG or Alexa Fluor^® 546 goat anti-rabbit IgG (Molecular Probes-Life Technologies) (1:1,000), depending on the experiment. Autophagy activity was analyzed using a rabbit anti-LC3A/B polyclonal antibody (Cell Signaling; 4108S) (1:200), or a mouse anti-LC3B monoclonal antibody (Nanotools; 0231-100/LC3-5F10) (1:20) for co-localization assays. The Alexa Fluor^® 546 goat anti-rabbit IgG and Alexa Fluor^® 488 goat anti-mouse IgG (1:1,000) were used as secondary antibodies, respectively. The immune detection of VHSV in blood samples was performed using the mouse anti-N VHSV monoclonal antibody 3E7 (1:1,000) (53) and the secondary antibody Alexa Fluor^® 635 goat anti-mouse IgG (Molecular Probes-Life Technologies) (1:1,000). All samples were stained with a DAPI solution (Molecular Probes-Life Technologies) for nuclear localization and mounted using ProLong Antifade Reagents (Life Technologies). LysoSensor blue DND-167 reagent (Molecular Probes-Life Technologies) was used to stain the acidic lysosomal vesicles in live cells. Confocal images were captured using a TSC SPE confocal microscope (Leica) using the LAS AF software (Leica). The 3D reconstructions were performed using the Image Surfer⁵ software.

Blood samples were fixed overnight with 2% glutaraldehyde in 0.1-M cacodylate buffer at pH 7.4. Then, samples were washed and incubated with 1% tannic acid in 0.1-M cacodylate buffer at 4°C for 1 h and washed again. The cells were centrifuged at 1,000× g for 5 min and included in 1% agarose blocks, which were sectioned in 1 mm³ pieces and washed with 0.1-M cacodylate buffer. The sections were incubated for 1 h with 1% osmium tetroxide at 4°C and washed and dehydrated in increasing concentrations of ethanol. After the dehydration, samples were embedded in Epon resin and 65–85 nm sections were prepared using the ultramicrotome and mounted on metal grids. Ultrathin sections were stained with 50% uranyl acetate in methanol and lead citrate prior to observation with the JEOL JEM-1010 transmission electron microscope (Electron Microscopy Unit of CACTI, University of Vigo, Spain).

Both qPCR expression results and flow-cytometry fluorescence data were represented graphically as the mean/median + the standard deviation of the biological replicates. To determine significant differences, data were analyzed with the computer software package SPSS v.19.0 using the Student’s t-test or ANOVA as appropriate. For the correlation analysis, Spearman’s Rho correlation coefficient was calculated. Differences were considered statistically significant at p < 0.05.

The complete coding region of the turbot nkl gene was deposited in GenBank under Acc. No. KU705506. The characteristic saposin B (SapB) domain of the saposin-like proteins (SAPLIP) family was identified (Figure 1A). The 3D structure was constructed with a moderate confidence value using Nkl from pig as a template (TM score = 0.582) (Figure 1B). On the other hand, the gene structure (exon/intron organization) was conserved among teleost fish (Figure 1C) and compared with other vertebrates.

A multiple alignment of several Nkls/granulysin amino-acid sequences from fish, birds, and mammals revealed six cysteine residues that were well conserved among the different species (Figure S1A in Supplementary Material). A phylogenetic tree showed two main clusters, one of them containing teleost Nkl and the other one containing avian and mammalian sequences (Figure S1B in Supplementary Material). As expected, an identity/similarity matrix (Table S3 in Supplementary Material) revealed that turbot Nkl shares the highest scores with the other flatfish species, but when it was compared with sequences from birds and mammals, the identity ranked between 16 and 20% and the similarity between 36 and 45%.

The constitutive expression of the nkl gene was determined in different tissues from healthy turbot. nkl transcription was detected in all the tested tissues but the highest expression levels were detected in immune tissues (peritoneal exudate cells –PEC–followed by the spleen and head kidney) (Figure 2A). When turbot were infected with VHSV, the nkl gene was overexpressed in the two main immune organs in fish, head kidney (Figure 2B) and spleen (Figure 2C), suggesting an antiviral response.

The expression of nkl was analyzed in head kidney samples from fish belonging to VHSV-resistant and VHSV-susceptible families, before (naïve) and after VHSV challenge. The resistant families (1 and 4) showed a significantly higher expression of nkl than the susceptible ones (2 and 3) before the viral infection. Interestingly, 24 h after VHSV challenge, a significant increase in nkl transcription was only observed in susceptible families (2 and 3) (Figure 2D).

We used a non-destructive method (blood sampling from caudal vein) to determine the nkl transcription level before infection in 35 turbot and, after VHSV challenge, individual mortality was registered. The correlation between nkl mRNA level in blood cells, turbot size and weight, and the day of death after VHSV infection was analyzed using the Spearman’s rho correlation test. Mortalities started 4 days after infection, reaching 90% cumulative mortality at the end of the experiment (15 days after infection). A significant positive correlation between nkl constitutive transcription in the blood and the day of death was observed (R = 0.438; p = 0.008) (Figure 2E): turbot with higher constitutive expression of nkl survived longer after infection than those with low expression level. Turbot size and weight were also correlated with the day of death, but no relationship between size or weight and the level of nkl transcripts was detected (Table S4 in Supplementary Material). Therefore, the basal transcription of nkl is a size/weight-independent factor, and its level is correlated with the resistance to VHSV infection.

The expression levels of nkl in the head kidney, spleen, and blood were analyzed by qPCR 1 month after the injection of a highly efficient DNA vaccine encoding the VHSV glycoprotein (pMCV1.4-G) (50) or the corresponding control empty plasmid (pMCV1.4) under both healthy and VHSV-infected conditions (48 hpi) (Figure 3). In parallel, flow-cytometry analysis of cell populations from the three different tissues was also conducted (Figure 3). Surprisingly, 1 month after vaccination, there was an increase in the transcription of the nkl gene detected in the head kidney and blood samples (Figures 3C,I), but not in the spleen (Figure 3F). Nevertheless, after a VHSV challenge, the expression of nkl increased only in the head kidney from non-vaccinated individuals but decreased in blood samples from vaccinated fish (Figures 3C,I). To detect the presence of Nkl at the protein level, we designed and used an anti-Nkl polyclonal antibody. After confirming the specificity of the antibody by WB (Figure S2 in Supplementary Material), flow-cytometry analysis was conducted. Differences among vaccinated and non-vaccinated turbot (in the absence of infection) were only observed in the spleen, with an increase in the percentage of Nkl-positive cells but a reduction in the median value of fluorescence per cell (Figures 3D,E). After the VHSV challenge, Nkl increased in the head kidney from non-vaccinated fish but decreased in vaccinated turbot (Figure 3B); however, there were no differences in the number of Nkl-positive cells (Figure 3A). In the blood, the percentage of Nkl-positive cells decreased after infection in both vaccinated and non-vaccinated fish (Figure 3G), but no significant differences in the level of Nkl were detected in these cells (Figure 3H).

Flow cytometry was conducted on head kidney cells and total blood samples (Figures 4A,C). Nkl-positive cells gated in the FL1-H histogram were represented in FSC/SSC density plots (Figures 4B,D). In the head kidney, the positive cells were clustered in a heterogeneous population showing low size and complexity (Figure 4B). In blood samples, the fluorescence histogram revealed the presence of two clear populations (Figure 4C) with different positions in the FSC/SSC density plot (Figure 4D). One population corresponded to cells with the lowest fluorescence level and small size and complexity. Erythrocytes are the most abundant cell type in this population. The other population consisted of cells that had a higher fluorescence, were larger in size, and were essentially the white cell population. A clear significant difference in the fluorescence level was detected among both populations. Fluorescence values for erythrocytes were 168 ± 16.5 and 605 ± 52.4 for leukocytes (Figure 4E).

To visualize the expression of Nkl in these cells, the distribution of the Nkl peptide was analyzed by confocal microscopy of the head kidney and blood cells. In the small spherical cells with a high nucleus/cytoplasm ratio, probably corresponding to CTLs and the hypothetical NK-cells, the cytoplasm was completely stained with the anti-Nkl antibody (Figures 4F,G). Turbot erythrocytes were also positive for Nkl-immunostaining (Figures 4F,G).

The unexpected presence of Nkl in erythrocytes was analyzed in detail. Confocal images of erythrocytes immunostained with the preimmune serum or the anti-Nkl antibody confirmed the specificity of the polyclonal antibody (Figures 5A,B). Almost all erythrocytes were found to be Nkl-positive and this peptide was mainly expressed in a large, spherical cytoplasmic structure; however, a few small Nkl-positive spots were also observed (Figure 5C). The mRNA expression of nkl in this cell type was lower compared with that of total blood cells (Figure 5D), suggesting that the expression of this gene is much higher in other nkl-expressing cells present in blood (leukocytes). The FL1-H fluorescence profile of purified erythrocytes showed a well-defined peak (Figure 5E) corresponding to a homogeneous cell population (Figure 5F).

To further characterize the structure of the cytoplasmic vesicles, a study using Transmission electron microscopy (TEM) was conducted (Figure 5G). At low magnification, a large, spherical cytoplasmic structure was observed in almost all erythrocytes, although in some cells other smaller vesicles were also found. These structures showed a double-membrane surrounding electron-dense structures, which probably correspond to cellular organelles such as mitochondria, Golgi apparatus, and endoplasmic reticulum. LysoSensor staining revealed the acidic nature of these spherical structures in the cytoplasm of erythrocytes (Figure 5H), and immunostaining with a rabbit polyclonal anti-LC3 antibody showed that autophagy is also occurring in these structures (Figure 5I). These data suggested that these Nkl-containing structures probably correspond to autophagolysosomes.

To fully elucidate whether these Nkl-positive vesicles correspond to the LC3-positive structures, we conducted a co-localization analysis after in vitro stimulations of erythrocytes with the autophagy inhibitor CQ and the autophagy activator RAP. The execution of autophagy involves the participation of numerous proteins; however, during the final steps of autophagy, only microtubule-associated protein light chain-3 (LC3) is known to exist in mature autophagolysosomes (54).

Although the spherical Nkl-positive structures were also labeled with the rabbit polyclonal anti-LC3 A/B antibody (Figure 5I), in the co-localization studies, the mouse monoclonal anti-LC3B antibody resulted in LC3B-positive punctate structures that were dispersed in the cytoplasm of untreated erythrocytes (Figure 6A) whereas Nkl was strongly detected in the autophagolysosomes. Therefore, LC3B and Nkl did not co-localize. Interestingly, the incubation of the erythrocytes with CQ and RAP completely modified this pattern after 24 h. In the CQ-treated cells, LC3B was now confined to the autophagolysosomes, and the Nkl signal disappeared (Figure 6A). This is probably because CQ raises intravesicular pH (55) and the SAPLIP show markedly increased activities at acidic pH (56) because of their pH-dependent conformational properties (57). On the other hand, the autophagy activator RAP also affected the distribution of LC3B. In this case, although numerous LC3B-positive puncta were also observed in the cytoplasm, the higher fluorescent signal was found in the autophagolysosomes where a strong co-localization of LC3B and Nkl was detected (Figure 6A). A detailed 3D reconstruction of the erythrocytes incubated with RAP showed that Nkl seems to surround the LC3B signal in the autophagic structures (Figure 6B).

In vitro infection of total blood cells and erythrocytes revealed another interesting finding. Erythrocytes were found to be positive for VHSV infection using immunofluorescence staining (Figure 7A), although flow cytometry revealed that VHSV-positive erythrocytes were less than 1% after 24 h. VHSV replication was analyzed both in total blood cells and erythrocytes by qPCR detection of the viral glycoprotein (G). Viral replication was higher in erythrocytes compared with total blood cells, and the viral detection increased over time (Figure 7B). Opposed to the VHSV replication, the time-course experiment revealed that, both in total blood cells and erythrocytes, the transcription of nkl decreases in a time-dependent, infection-independent manner (Figures S3A,B in Supplementary Material).

The effect of CQ and RAP during in vitro VHSV infection in erythrocytes was also studied. CQ and RAP modulated the mRNA levels of autophagy-related genes (Figures S3C,D in Supplementary Material) and, interestingly, the substances affected the transcription of nkl in an opposite manner. CQ treatment damped the time-dependent reduction of nkl transcription, whereas RAP significantly reduced the level of nkl transcription after 24 h (Figure 7C).

While there were no significant differences in the detection of the VHSV G gene in those erythrocytes incubated with RAP compared with the control, autophagy blockage with CQ favored viral replication, which is reflected through the higher detection of the VHSV G gene in the cells incubated with this compound (Figure 7D). This result indicates that autophagy is an important antiviral defense mechanism in these cells.