Background
DTMUV is an arthropod-borne flavivirus responsible for the severe decline in egg production in ducks. Since 2010, a newly emerging disease characterized by egg-drop syndrome has occurred in ducks in China. Egg production in sick ducks was seriously decreased within 2 weeks after disease onset. The infected ducks mainly showed clinical symptoms such as depression, loss of appetite, growth retardation, even paralysis or death. The disease has caused serious economic losses to the duck industry. Additionally, DTMUV can exhibit pathogenicity to Kunming mice by intracerebral inoculation [
1‐
5]. DTMUV is similar to other flaviviruses, consisting of an 11-kb positive-sense single-stranded RNA genome composed of one long open-reading frame, encoding three structural proteins (capsid [C]; pre-membrane [prM], which is post-translationally cleaved to produce the pr and M proteins; and envelope [E]) and seven non-structural proteins (NS1, NS2A, NS2B, NS3, NS4A, 2KNS4B and NS5) [
6‐
8]. Flavivirus invasion into cells is a complex process involving many cellular receptors and viral components [
9]. Binding to the cellular surface is the first step for flavivirus entry, which mainly depends on E protein. Moreover, prM and phosphatidylserine (PtdSer) can also recognize some cellular receptors [
10]. The crystal structure revealed that flavivirus E protein structures have the following three distinct domains: the N-terminal central β-barrel-shaped domain I; the elongated finger-like domain II, which mediates the low-pH-driven membrane fusion of the viral membrane with the host endosomal membrane, and the C-terminal immunoglobulin-like domain III, which is required for binding to the cellular receptor [
11‐
14].
Flaviviruses are arboviruses that can be transmitted by mosquitoes, and most mammalian cells are susceptible to flavivirus infection. Flavivirus require two different sets of receptors to enter the cell as previously reported [
15]. The first step in the flavivirus infectious cell entry pathway is concentration of the virus on the cell surface by attachment factors. Then, the virion bind to the greater affinitive entry receptor and begin to enter the cells [
9]. Heparin sulfate proteoglycans (HSPGs) are involved in the adsorption of flaviviruses and comprise a core protein structure and GAGs chains. HSPGs are divided into the following three families according to their core protein structure: glypicans, syndecans and perlecans [
16]. Meanwhile, sulfated GAGs, which include heparin sulfate, chondroitin sulfate and dextran sulfate, are expressed on a number of cell types and are utilized as attachment factor by some flaviviruses [
17‐
19]. Flavivirus binding to GAGs is due to the electrostatic interaction of positively charged residues on the surface of the E glycoprotein with negatively charged sulfate groups. Significantly, heparin sulfate, but not other GAGs components, is confirmed as attachment factors for some flaviviruses, such as Dengue Virus (DENV) [
20], Yellow fever virus (YFV) [
21] and Japanese encephalitis virus (JEV) [
22].
DTMUV is a relatively recent virus and has attracted much attention. DTMUV is spread mainly through birds such as ducks and geese, but recent studies have also found that DTMUV can also infect mice [
23]. To further understand the molecular mechanisms of DTMUV invasion, DEF and BHK21 cells were used for subsequent experiments. We first proved that GAGs were involved in the adsorption of DTMUV by sodium chlorate desulfated GAGs. We then indicated that heparin but not chondroitin sulfate A inhibited the absorption of DTMUV. Furthermore, we verified the results with corresponding GAG-lyases including heparinase I and chondroitinase ABC. Finally, we found that heparin only affected virus adsorption but did not affect its entry. Additionally, we briefly discussed which DTMUV structures are involved in adsorption and we found that E protein was important for the adsorption by treating DTMUV with trypsin.
Methods
Virus, cells and chemical
The DTMUV CQW1 strain was propagated in DEF cells as previously described [
2] and the virus titer was 10
5 TCID
50/0.1 ml. Baby Hamster Kidney (BHK21) cells were provided by our laboratory and maintained in Dulbecco’s modified Eagle’s medium (DMEM) (Sigma, St. Louis, MO, USA) supplemented with 10% fetal bovine serum (FBS) (Gibco, Gaithersburg, MD, USA), penicillin 100 IU/ml and streptomycin 100 μg/ml at 37 °C in a 5% CO
2 incubator. Primary duck embryo fibroblast (DEF) cells were obtained from duck embryo and cultured at 37 °C and 5% CO
2 in DMEM with 10% FBS. Heparin and chondroitin sulfate A were purchase from Solarbio (Beijing, China). Heparinase I, chondroitinase ABC and sodium chlorate were purchased from Sigma (St. Louis, MO, USA). The anti-flavivirus group antigen antibody (MAB10216) was purchased from Merck (New Jersey, USA).
DTMUV binding assay
BHK21 or DEF cells were grown into monolayers in 12-well cell culture plates and then incubated with 1000TCID50 DTMUV in the absence or presence of heparin and chondroitin sulfate A at 4 °C for 1 h. The unbound DTMUV was removed by washing cells three times with PBS. Total DTMUV RNA levels were determined by qRT-PCR.
Sodium chlorate treatment
The addition of sodium chlorate can block cellular ATP-sulfurylase and sulfate adenyl transferase activities and reduce the sulfation levels of GAGs as previous described [
20,
21]. BHK21 cells were cultured for 1 week in low-sulfated culture medium RPMI with 10% FBS containing the different concentration of sodium chlorate or 4 mM sodium sulfate as a supplement. For virus binding, the cells were grown into monolayers in 12-well plates that were incubated with 1000TCID
50 DTMUV at 4 °C for 1 h. The unbound DTMUV was removed by washing the cells three times with PBS. Total cellular RNA was extracted from infected cells using Trizol Reagent, and DTMUV viral RNA levels were determined by quantitative real-time PCR (qRT-PCR) with mouse β-actin as the endogenous control.
GAG-lyases treatment
Heparinase I can cleave glycosidic linkages in heparin sulfate on the cellular surface and chondroitinase ABC specifically cleaves glycosidic linkages in chondroitin sulfate A, B and C [
24]. BHK21 or DEF cells were grown into monolayers in 12-well cell culture plates and then incubated for 1 h at 37 °C with 300 μl buffer (20 mM Tris-HCl, pH 7.5, 50 mM NaCl, 4 mM CaCl2, and 0.01% BSA) containing heparinase I or 300 μl buffer (50 mM Trizma HCl, pH 8.0, with 60 mM sodium acetate and 0.02% BSA) containing chondroitinase ABC. The cells were washed with PBS three times and then incubated with 1000TCID
50 DTMUV at 4 °C for 1 h. The unbound DTMUV was removed by washing the cells three times with PBS. Total DTMUV RNA levels were determined by qRT-PCR.
DTMUV RNA levels were determined by qRT-PCR
The cellular total RNA was extracted with the Trizol Reagent according to the manufacturer’s instructions. Then 1 μg of RNA per sample was synthesized into cDNA using a One Step TB Green™ PrimeScript™ RT-PCR Kit II (Takara, Dalian, China). Subsequently, relative mRNA levels were quantified using a SYBR Green qPCR kit (Abm, Richmond, BC, Canada) and a real-time cycler (CFX96 Bio-Rad, Hercules, CA, USA). The primers used for qRT-PCR were as described previously [
25]. The reaction conditions were as follow: 94 °C for 3 min, followed by 40 cycles of 94 °C for 10 s and 63 °C for 1 min.
Fifty percent tissue culture infectious dose (TCID50) assay
Viral titers were determined using an endpoint dilution assay. Briefly, BHK21 cells in 96-well tissue culture plates were infected with serial 10-fold dilutions of DTMUV in eight replicates. The plates were incubated for 144 h at 37 °C. The viral titers were calculated using the Reed–Muench method.
Western blotting
Total cellular proteins were boiled in 6x protein loading buffer before separation by 10% SDS-PAGE electrophoresis. Then, the proteins were transferred onto polyvinylidene fluoride (PVDF) membranes (Millipore, Bedford, MA, USA). The membranes were blocked with 5% skim milk in TBST at 37 °C for 1 h. Subsequently, The membranes were incubated with mouse anti-NS5 polyclonal antibodies provided our lab or anti-β-actin antibody (Ruiying Biological, Suzhou, China) overnight at 4 °C. Then, horseradish peroxidase (HRP)-conjugated goat anti-mouse IgG antibody was used as a secondary antibody. Finally, the proteins were visualized by chemiluminescence using an ECL kit (Bio-Rad).
Cell cytotoxicity assay by cell counting kit-8
DEF and BHK21 cells were seeded into 96-well microtiter plates. After 1 day, 100 μl of spent medium was replaced with an equal volume of fresh medium containing 10% CCK8 (MedChemExpress, New Jersey, USA). Then, the cells were incubated at 37 °C for 2 h. The optical density (OD) at 450 nm was measured with a microplate spectrophotometer and was proportional to the number of viable cells in the wells.
Statistical analysis
The unpaired Student’s t-test (GraphPad Prism software) was used to determine the statistical significance of the differences between the experimental groups. Error bars represented the standard error of the mean. The p value < 0.05 was considered statistically significant, and the degree of significance was indicated as follows: * p < 0.05, ** p < 0.01, and *** p < 0.001.
Discussion
Invading the host cell is the first step in the flavivirus infection cycle, and they can utilize multiple receptors to initiate infection [
17]. Virion is first concentrated on the cell surface by binding to attachment factors, and then they are introduced into the endocytosis pathway by a large number of different types of entry receptors, which are internalized into the cell by clathrin-mediated endocytosis [
10,
26]. Finally, the low-pH environment within endosomes interacts within the E glycoprotein leading to membrane fusion of the viral membrane with the endosomal membrane, subsequently promoting nucleocapsid release into the cell cytosol [
17]. Flaviviruses can infect different animals and spread widely. The identification of the flavivirus receptor will allow us to further explore the mechanism of its cross-host transmission. DTMUV, as a member of flaviviruses, can be transmitted by duck and geese and infect mice by intracranial injection [
4,
23]. However, the mechanism of cross-host transmission has remained obscure.
Several studies have indicated that flaviviruses build initial contacts with the host cell by binding to GAGs, such as heparin sulfate and chondroitin sulfate [
10]. GAGs are long, unbranched, sulfated polysaccharides that are exposed on the cell surfaces of all tissues and are primarily involved in electrostatic interactions with concentrated virion at the cell surface [
27,
28]. To determine the DTMUV attachment factors on BHK21 and DEF cells, we compared the effects of GAGs desulfation (Fig.
1), competitive inhibitors (Fig.
2), and GAG-lyses (Fig.
3) on DTMUV adsorption. These results clearly indicated that heparin sulfate but not chondroitin sulfate was involved in DTMUV adsorption on both BHK21 and DEF cells. Heparin sulfate may be required to concentrate virion at the cell surface. Additionally, heparin sulfate not only initiates the infection by some flaviviruses [
16,
19‐
21] but can also interact with other viruses, such as Sindbis virus [
29], Foot-and-mouth disease virus (FMDV) [
30], Herpes simplex virus (HSV) [
31], Vaccinia virus [
32], Venezuelan equine encephalitis virus (VEEV) [
33], Papillomavirus [
34] and Echovirus [
35]. Additionally, Watterson found that interaction between DENV and heparin sulfate occurred through two lysine residues located in domain III of E protein by site-directed mutagenesis studies [
36]. Meanwhile, studies have indicated that N- and 6-O-sulfation but not 2-O-sulfation are important for HCV infection by silencing of the enzymes involved in the heparin sulfate biosynthesis pathway [
9].
Entry receptors can bind specifically to flaviviruses and direct them to the endocytic pathway after flaviviruses attach to the cell surface [
10]. Recently, it has been shown that dendritic cell-specific ICAM-3 grabbing non-integrin (DC-SIGN) and liver/lymph node-specific ICAM-3 grabbing non-Integrin (L-SIGN) that belong to C-type lectins can bind to several flaviviruses, such as Dengue virus [
37‐
39], West Nile virus [
40] and Japanese encephalitis virus [
41]. Additionally, some investigations have also suggested that the T-cell immunoglobulin and mucin domain (TIM) and TYRO3, AXL and MER (TAM) can enhance flavivirus infection by binding to PtdSer on the virion surface rather than E glycoprotein [
42,
43]. To verify the role of heparin sulfate in DTUMV invasion, we compared the effects of heparin on DTMUV adsorption and entry. The results clearly indicated that heparin only affects DTMUV adsorption and does not affect the process of virus internalization. Meanwhile, Philip Hilgard found that DENV E protein is extremely sensitive to trypsin [
20]; so we treated DTMUV with trypsin and conducted DTMUV adsorption experiments. We found that trypsin could degrade E protein showing that E protein was mainly involved in virus adsorption. Despite intensive research, little is known about the identity of the cell receptors that mediate flavivirus entry and infection. Many molecules have been described as candidate receptors for flavivirus on different cell types, but their exact role in viral entry remains unclear. So far, there have been several investigations focused on determining the DTMUV entry receptor by virus overlay protein binding assay (VOPBA). Glucose-regulated protein 78 (GRP78), a receptor on BHK21 cells, and heat shock protein A9, a receptor on DF-1 cell, bind to DTMUV to allow cellular entry [
44,
45]. However, this is far from enough to thoroughly understand DTMUV invasion mechanism in cells and even in animals, which requires further research.
Conclusion
Heparin sulfate, a component of GAGs exposed on the cell surface, is involved in DTMUV attachment but not entry. Moreover, heparinase I but not chondroitinase ABC can inhibit DTMUV attachment. Thus, our results may provide a molecular explanation for the pathogenesis of DTMUV.
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