Background
Porcine epidemic diarrhea virus (PEDV), which belongs to the Alphacoronavirus genus of the Coronaviridae family, is an etiological agent of porcine epidemic diarrhea (PED) and causes an enteric disease that affects all ages of swine [
1,
2]. The clinical presentations and complications of infection are characterized by acute vomiting, dehydration, watery diarrhea, and high mortality in sucking piglets [
3] and are indistinguishable from those of infection by either transmissible gastroenteritis virus (TGEV) or porcine enteric alphacoronavirus (PEAV) [
4,
5].
First detected in the UK in 1971, PEDV resulted in mass epidemics within Europe in the 1970s and 1980s [
6]. Before 2013, PED was prevalent in Asia and Europe [
1]. After spring 2013, however, PED outbreaks reached North America, which was due to variant PEDV strains that researchers revealed might derive from Chinese variants [
7,
8]. In spite of widespread immunization with the currently marketed vaccine, PED still persists in swine raising countries and resulted in devastating damage to the pork producers [
9].
PEDV is an enveloped single-strand RNA coronavirus with a 28 kb genome, which includes 4 open reading frames encoding spike (S), envelope (E), membrane (M), nucleocapsid (N), as well as 3 open reading frames encoding replicase 1a, 1b and ORF3 [
10]. As known for other coronaviruses, the three PEDV S glycoproteins form a club-shaped functional S trimer, which is localized on the surface of the virion and mediates essential biological functions, such as membrane fusion and receptor binding. The S protein is also responsible for the induction of nAbs and protective immunity, making it an appropriate candidate for developing an effective vaccine and diagnostic reagents [
1,
11,
12]. In addition, variation in the S gene leads to antigenic diversity, and thus the S protein is useful in evaluating genetic diversity [
13].
Little has been known about the components of the immune system that are effective in the protection of a pig against PEDV infection. The quantity of nAbs generated by vaccination correlates with the degree of protection against many diseases [
14]. Considering the significance of nAbs in providing protection, understanding the mechanism of neutralization is necessary for development of a vaccine that elicits strong nAbs. The fragment antigen-binding (Fab) domain binds to specific pathogen targets, which prevents microbial interactions with host cell receptors and thus blocks infection [
15,
16]. The protection of nAbs results from blocking interaction of free virus particles with target cell receptors. Additionally, for other nAbs, infection can be blocked through inhibiting critical intracellular processes, for example rotavirus transcription [
17], nuclear translocation of human papilloma virus DNA [
18], adenoviral uncoating [
19], or measles virus assembly [
20]. Several studies demonstrated that spike mAb can neutralize PEDV [
21‐
26]. These studies mainly focused on locating the neutralizing domains of PEDV S protein, however, the mechanisms by which spike nAb neutralize the virus have not been defined completely. To fill this knowledge gap, we generated four mAbs that exhibited potent neutralizing activity against PEDV in vitro. Notably, 2B11 and 2G8 were found to block PEDV entry into Vero cell.
Methods
Cells, viruses and reagents
The Vero E6 cell line was cultured and maintained at 37 °C in DMEM containing 10% FBS and antibiotics (100 U/mL of penicillin and 100 μg/mL of streptomycin) (Solarbio, Beijing, China). Sf9 insect cell line was maintained as suspension in serum-free SF900II medium at 27 °C in spinner flasks at a speed of 90 to 100 rpm. PEDV-GDS01 (KM089829.1) and PEDV-GDS03 (AB857235.1) were propagated in Vero cells with 10 μg/mL trypsin. PEDV strain used in this study indicated GDS01 strain unless otherwise noted.
Preparation and purification of PEDV virus antigen
PEDV was propagated and purified as in previously described [
27]. Briefly, Vero cells were washed twice with phosphate buffered saline (PBS) to remove residual DMEM, followed by 1 h incubation with PEDV at 37 °C and wash with PBS. Next, the cells were infected by the virus via addition of DMEM containing 10 μg/mL of trypsin. The cells were harvested at 36 h after infection, when all cells showed characteristic cytopathogenic effect. Three cycles of freeze-thaws were done to release the intracellular virus particles, and a 30-min centrifugation at 10000 g was performed to pellet cellular debris. After clarification, the supernatant was enriched 100 times by the ultracentrifugation at 30000 g and then purified by sucrose density gradient centrifugation using sucrose solutions at: 20%(
w/w), 40% (w/w) and 60% (w/w), respectively. The purified products were analyzed by SDS-PAGE and western blot.
Development and purification of PEDV monoclonal antibodies
Standard procedures were used to generate hybridoma cells that secrete PEDV-specific antibodies [
28] with some modifications. Briefly, female BALB/c mice (6 weeks) were immunized with the purified PEDV inactivated by β-propiolactone in complete Freund’s adjuvant (Sigma, St. Louis, MO, USA). The mouse was immunized with the purified PEDV containing of 10 μg spike protein determined through SDS-PAGE and gray scanning. Two booster immunizations were administered at 2-week intervals with PEDV in incomplete Freund’s adjuvant (Sigma, St. Louis, MO, USA). Next, the mice were sacrificed following a 3-day booster inoculation by intraperitoneal injection. PEG1450 [50% (
v/v)] (Sigma, St. Louis, MO, USA) was used for fusion of spleen cells from immunized mice with sp2/0 myeloma cells, and hybridoma cells was cultured in 96-well plates at 37 °C in HAT (Sigma, St. Louis, MO, USA) screening culture medium. Positive hybridoma clones were picked by indirect immunofluorescence assay (IFA), followed by cloning via limiting dilution for at least three rounds. Polyclonal antibodies against PEDV were taken as positive control and normal mouse serum was taken as a negative control. Mouse Monoclonal Antibody Isotyping Reagents (Sigma, St. Louis, MO, USA) were used for the identification of the subtype of mAbs secreted by the final hybridoma clones. Ascites fluid was collected from primed BALB/c mice with paraffin oil and purified using Protein G Sepharose™ 4 Fast Flow (GE Healthcare, Pittsburgh, USA) according to the manufacturer’s instructions. Purified mAb was quantified by BCA kit (Thermo fisher, USA).
Indirect immunofluorescence assay (IFA)
The supernatant of hybridoma cell cultures was screened for the presence of PEDV-specific mAbs by IFA. For this, primary Vero cells were grown to 100% confluency in 96 well plates and infected with GDS01 for 36 h at a multiplicity of infection (MOI) of 0.1. After fixation with 4% paraformaldehyde, the monolayers were permeabilized with 0.5% triton X-100, followed by a 1 h incubation with the supernatants of the hybridoma cell at 37 °C. Then, unbound antibodies were removed by washing with PBS and specific mAbs were detected with Cy3-conjugated Affinipure Goat Anti-Mouse IgG (H + L) (Proteintech, Rosemont, USA).
Identification of the target protein of monoclonal antibody
In order to determine the conformational epitopes bound by the mAbs, the main structural proteins of PEDV, including SP (the S1 and partly S2 gene fragment, 1-954aa), N, M, and ORF3, were expressed by Bac-to-Bac expression system (Invitrogen Carlsbad, CA) following the manufacturer’s instructions. The sf9 cells were infected with recombinant baculovirus (MOI = 5), followed by fixation, permeabilization and incubation with supernatants of the hybridoma cells 3 days later, reactivity of the mAbs with recombinant proteins was measure with an IFA.
In order to determine the linear epitopes bound by the mAbs, truncated SP and full length of N genes were also cloned into pET-32a, the details of 7 truncated SP proteins refer to previous study [
29]. The recombinant DNA was then used to transform BL21 cells for the following protein expression. Referring to the manufacturer’s instructions, Ni-Chelating Sepharose Fast Flow (GE, USA) was used for the purification of proteins by affinity chromatography. Purified protein was quantified by BCA kit (Thermo fisher, USA). The reaction of mAbs with truncated SP and N protein was evaluated by ELISA. Briefly, 96-well plates (Griener, Germany) were coated with the purified protein (100 ng) at 4 °C overnight, and then blocked with 5% milk for 1 h. After washing three times with PBS, 100 μL supernatant was added and the sample was incubated at 37 °C for 1 h. Subsequently, the plates were washed with PBS and incubated with HRP-conjugated goat anti-mouse IgG (Proteintech, USA) at 37 °C for 1 h. The absorbance was measured at 450 nm. All samples were repeated three times and the sample was considered positive when the relation OD sample/OD negative control was higher than 2.1.
Neutralization assay
To determine whether an antibody had neutralization activity, we conducted the virus neutralization test as previously described [
30], with modifications. Briefly, after a 30 min inactivation at 56 °C, the test mAbs (diluted to 80 μg/mL) were filtered using a 0.22-μm membrane, followed by two-fold serial dilution. The PEDV GDS01 strain (titer: 100pfu/0.5 mL) was mixed with diluted mAb of an equal volume. The mixture was then added with trypsin (10 μg/mL), followed by 1 h incubation at 37 °C. Next, Vero cell monolayers in 6-well plates were cultured with the mixture (1 mL). After a 1 h adsorption at 37 °C, the inocula were discarded. Next, the plates were washed three times with PBS. DMEM with trypsin (10 μg/mL) was added to each well and plates were incubated at 37 °C for 48 h. The plaque was colored by the neutral red (0.03%). The Serum-neutralization (SN) titer was determined according to the highest mAb dilution, which led to inhibition of formation of viral plaque completely. Neutralization (%) were calculated using the following formula: 1- sample plaque counts/negative control counts.
To determine whether 2G8 and 2B11 could neutralize the infection of GDS03, an IFA neutralization assay was performed. 80 μg of mAb was incubated with an equal volume of 500 TCID50/mL PEDV for 1 h at 37 °C. Then, the sample-virus mixture was transferred to duplicate wells of a 6-well plate containing confluent Vero E6 cells. The plates were incubated at 37 °C for 1 h and then washed gently with PBS to remove unbound viruses, following with 36 h incubation at 37 °C in a 5% CO2 atmosphere. The PEDV-infected cells were fixed with 4% paraformaldehyde and analysed by IFA. 9G11 was used as a detective antibody.
Analysis of PEDV binding to Vero E6 cells with nAb
Virus infection in the presence or absence of antibody was quantified as previously described, with slight modifications [
22]. Diluted antibodies (2B11/100 μg/mL and 2G8/200μg/mL) were mixed with PEDV (1000pfu/mL) of an equal volume, followed by a 1 h incubation at 37 °C. Next, the mixture of antibody-virus was added to triplicate wells of confluent Vero E6 cell monolayers for a 1 h infectious adsorption at 37 °C. To analyze PEDV and nAb binding at two different time points, PEDV was incubated with Vero E6 cells for one hour at 4 °C, followed by addition of antibodies and a 1 h incubation at 37 °C. Trypsin was added throughout the experiment. The cells were washed twice with PBS, and collected for measuring cell-associated PEDV via viral RNA RT-qPCR. Briefly, the cells from each well were obtained after centrifugation at 10,000 rpm for 10 min. RNA was extracted from cells using a TRIzol reagent (Invitrogen, USA) and cDNA was synthesized with 2 μg of RNA using RT-PCR kit (TaKaRa, China). The specific primers (sense: 5’-GAATTCCCAAGGGCGAAAAT-3′; antisense: 5’-TTTTCGACAAATTCCGCATCT-3′) and probes (5’-FAM-CGTAGCAGGCTTGCTTCGGACCCA-BHQ-3′) were designed to amplify and detect the n gene of PEDV. Real-time PCR assays were carried out in 20 μL reaction mixture containing 10 μL of Thunderbird Probe qPCR Mix, 1 μL of cDNA template, 0.04 μL of 50× Rox reference dye, 0.2 μM of probe, and 0.3 μL of primers. The PCR amplification was performed with an Applied Biosystem 7500 Fast instrument (Life Technologies, USA) under the following conditions: 95 °C for 20 s for initial denaturation followed by 40 cycles of 95 °C for 3 s and 60 °C for 30 s. Ten-fold serial dilutions of standard plasmid pET-19 T-N, ranging from 10
7 to 10
2 copies/μL, were tested in five replicates with real-time RT-PCR to generate the standard curve.
Competitive binding ELISA
Ninety six-well plates (Griener, Frickenhausen, Germany) were firstly coated by PEDV at a density of 106 virions/well at 4 °C overnight, followed by a 1 h block with 4% BSA. After washed with PBS for three times and added with 100 μL diluted mAb (1:100), the sample was incubated for 1 h at 37 °C. Next, the plates were rinsed with PBS and cultured for 1 h with mAb 2G8 which labelled with horseradish peroxidase by EZ-Link Maleimide Activated Horseradish Peroxidase Kit (Thermo scientific, USA). The reacting results were visualized using tramethylbenzidine (TMB), stopped by HCL. All samples were repeated three times. The absorbance was determined using a microplate reader (Bio-Tek) at 450 nm.
Discussion
Multiple alphacoronaviruses, such as the TGEV, PRCoV, feline coronavirus type II and human coronavirus 229E(HCoV-229E), used aminopeptidase N (APN) as a receptor. But APN is not a universal receptor for the alphacoronaviruses as the human coronavirus NL63(HCoV-NL63) used angiotensin converting enzyme2(ACE2) for its entry [
31,
32]. Presently, it is believed [
33‐
35] that porcine APN acts as a functional PEDV receptor, however, whether or not pAPN is a receptor for PEDV has been debated over the years [
36,
37]. Intriguingly, Vero cell lines used for isolation of PEDV strains don’t express APN that inferred from the Vero cell proteome [
38]. Some data indicated that other receptors may be involved in PEDV entry into these cells, such as sialic acid and Neu5Ac [
9,
39]. Isolation a nAb that inhibit virus attachment to the cell surface could help to identify the PEDV receptor.
In this study, we screened 10 mAbs through hybridoma technology. The main structural proteins of PEDV were expressed using prokaryotic and eukaryotic expression system respectively. Because immunogenic proteins were whole virus particles, the determination of the target protein of mAb is a challenge. Prokaryotic expression system expresses the products without any modification and its products are linear proteins. Baculovirus expression system has the ability to express products with glycosylation, phosphorylation and other processing modification after translation, which are similar to natural proteins. 2B11, 1E3, 2B5, 2G10 and 1A5 recognized the expressed SP protein specifically in sf9 cells but did not bind to the SP protein expressed by BL21 cells. 1D11 recognized the expressed N protein in sf9 cells but didn’t bind to the N protein expressed by BL21 cells. The results indicated that 2B11, 1E3, 2B5, 2G10, 1A5 and 1D11 specifically recognized the conformational epitope instead of the linearized epitope. 9G11 and 3F10 recognized the linearized epitope, and 2G8 and 3D9 had no reactivity with any expressed proteins. It’s possible that 2G8 and 3D9 only recognize the trimer of S protein or S2 protein. Coronavirus neutralization by antibodies is often attributed to antibody occupancy of the S trimers and interfering with viral attachment to target cells or entry. In addition, their neutralizing activity was exhibited in a dose-dependent manner. 2G8 and 2B11 have high efficiency neutralization (IC50 < 10 μg/mL), 3D9 and 1E3 have moderate neutralization (10 μg/mL < IC50 < 100 μg/mL). The observations clearly define the SP domain is most critical for PEDV to interact with its target cells.
Then anti-SP mAb 2B11 and 2G8 with the strongest neutralizing capacity were selected to explore the mechanism of nAbs. As previously reported, PEDV enters Vero cells via an initial endocytic uptake, and subsequently, the virus fuses with the PEDV S and host endosomal membrane [
40]. The virus only attaches cell, but doesn’t have fusion with cell membrane at 4 °C. We found 2G8 and anti-SP mAb 2B11 efficiently bound PEDV, and then inhibited virus entry into cell at 37 °C. But if the experiment was designed into two-time points, virus infected the cells at 4 °C for 1 h, and then the mAb was added at 37 °C for 1 h, the results showed that virus could invade and replicate in cells, and the copies of virus in infected-cells had no difference regardless of the presence of 2G8, anti-SP mAb 2B11 and PEDV-negative serum. However, positive serum didn’t prevent the proliferation of intracellular viruses. This may be due to the lack of mAb in positive serum which neutralized the virus inside the cell or the interaction of mAbs makes some mAbs lose the ability of neutralization intracellular or there may exist other possible mechanisms. These results demonstrated if the viral have attached to the target cells, neutralization of 2G8 and anti-SP mAb 2B11 doesn’t work. It seems that PEDV infected cells apparently lower at 4 °C than 37 °C regardless of any antibodies, indicating that PEDV is more efficiently taken up by cells through endocytosis at 37 °C than at 4 °C. This is consistent with that the virus uptake more efficiently through endocytosis at 37 °C than at 4 °C, which was observed in Herpes simplex virus 1 infection [
41]. The epitope targeted by 2G8 is completely distinct from anti-SP mAb 2B11, there may be at least two mechanisms involved neutralization effects by directly inhibiting binding to an epitope.
Conclusions
Our study showed that 2G8 and anti-SP mAb 2B11 completely neutralize PEDV infection through blocking PEDV attachment to cells. At present, no effective prophylactic measure has been found to prevent the infection of PEDV. If the detail structure of the epitopes recognized by the two nAbs is delineated, it will be helpful for searching the new PEDV receptor and providing a new treatment method against PEDV infection.
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