Background
Originally discovered in Uganda in 1947, Zika virus (ZIKV) has recently emerged in the Americas to spread rapidly in Central and South American countries and has caused widespread outbreaks in Brazil [
1‐
4]. While mosquito-borne transmission is the most common, other routes of transmission, including sexual transmission, have been reported [
5,
6]. Studies of virus pathogenesis in endothelial cells and skin cells have been described [
7,
8]. However, kinetics of peripheral dissemination has not been completely elucidated. Numerous studies show that the ZIKV is able to gain access to immune privilege sites like the testes and eyes [
9,
10]. In addition, both clinical and animal model data show transplacental transmission of ZIKV has long term consequences for the fetus including microcephaly and other neurological defects [
11,
12]. This ability of ZIKV to gain access to immune privilege sites points to the ability of the virus cross the permeability barrier to gain access to the tissue space and seems an important factor in the dissemination of the virus in the host.
Polarized cells differentially distribute lipids and proteins in the plasma membrane creating a distinct apical and basolateral surface [
13,
14]. Tight junctions form a fence like barrier separating these apical and basolateral surfaces and render the cell monolayer selectively permeable to solutes and fluid [
15,
16]. This requires specific targeting of ion channels, transporters and other accessory proteins to the two cell membranes [
13]. This has important consequences during virus infection and dissemination. In order to establish infection, viruses have to invade the monolayer of epithelial cells [
17‐
19]. Both the entry and the release of viruses may be polarized, and can take place selectively at either the apical or the basolateral membrane [
20,
21]. Thus, receptors and other necessary entry factors may be differentially distributed at different membranes or even be inaccessible at one surface during infection. This lack of access can thus cause changes in cell susceptibility. Similarly, in addition to the normal sorting machinery, reports suggest that polarized epithelial cells have specific endosomal compartments that participate in specific apical of basolateral targeting [
22,
23]. Viruses exploit this sorting pathway during infection which facilitate their delivery at a specific membrane for assembly and release [
24]. This results into specific entry and egress kinetics in viruses with infection and budding being more efficient at one surface or another, and thus affecting virus dissemination in the host as a whole.
Caco-2 cells serve as an excellent model to study the permeability barrier since they readily form tight junctions when grown on a semipermeable barrier [
25,
26]. Polarized Caco-2 cells have been used to investigate pathogenesis of a number of flaviviruses including, Japanese Encephalitis Virus (JEV) and Tick-borne encephalitis virus (TBEV)(−[
27,
28]. In this study, we present evidence that infection of ZIKV occurs with greater efficiency on apical surface. Unlike other flaviviruses like TBEV or JEV, replication occurs without significant changes in paracellular permeability. Despite this, ZIKV is released vectorially through the basolateral route, indicating it’s an active transport across the epithelial barrier and not passive leakage. Thus, translocation may be one of the ways ZIKV crosses the tight junction barrier during dissemination in the host.
Methods
Cells and virus
Caco-2 cells (ATCC) were maintained in minimal essential medium (MEM; Invitrogen) supplemented with 2% or 10% fetal bovine serum (Invitrogen). Zika virus PR (Puerto Rico; GenBank KX087101.3; passage 3 and 4) was used for all the experiments and titers were determined with plaque assay performed on Vero-E6 cells.
Transepithelial electrical resistance (TEER) measurements
4 × 10
4 Caco-2 cells were seeded onto 6.5 mm diameter, 1 μm pore size polycarbonate membrane trans-wells (Costar) and media was replaced at 2 d intervals. Establishment of confluence was determined by measuring transepithelial electrical resistance (TEER) over the monolayer, using a Millicell-ERS volt-ohmmeter (Millipore, Billerica, MA).The electrodes of the epithelial volt-ohmmeter were first rinsed with 70% ethanol, followed by incubation in MEM without FBS supplementation for 10 mins at RT. All TEER measurements were made in a cell culture hood. Since temperature is known to affect resistance, measurements were made within 5 mins of removal of Transwells from the incubator [
28]. Values were obtained by subtraction of a background value (i.e., TEER of filters without cell growth) and by multiplication by the area of the filter.
Immunofluorescence microscopy
Caco-2 cells were seeded on polycarbonate transwell inserts (Corning; 6.5 mm; 3.0 μM pore size) and infected with 3 plaque forming unit (pfu)/ cell ZIKV. After infection, cells were fixed with 10% PBS buffered formalin and processed for immunofluorescence as described with some modifications (
http://www.zonapse.net/protocols/id6.html). Briefly, Culture inserts were fixed in 10% buffered formalin overnight followed by washing with PBS. Cells were equilibriated with IMF buffer (20 mM HEPES, pH 7.5, 0.1% Triton-X-100, 150 mM sodium chloride, 5 mM EDTA and 0.02% sodium azide as a preservative) for 5 min at room temperature (RT) followed by overnight incubation with anti-E-cadherin or mouse polyclonal sera against ZIKV at 4 °C. Following which the cells were incubated with Alexa flour-conjugated secondary antibodies for 1 h at RT. The cells were then incubated with Hoechst 33258 in PBS at 10 μg/ml for 1 h at RT to stain the nuclei. Membranes were then cut out using a scalpel blade, mounted on glass slides with Prolong anti-fade reagent (Invitrogen) and covered with cover-slips and left to dry overnight in dark at 4 °C. The cells were visualized using an Eclipse Ti confocal microscope (Nikon) and NIS Elements Imaging Software.
RNA extraction and RT PCR
Trizol was added to cell monolayer (1 ml/ well) samples in the appropriate amount and allowed to homogenize from 10 min at room temperature (RT). RNA was extracted as per the manufacturer’s protocol and quantified using Verso-1 step (Verso SYBR Green one-step qRT-PCR kit) using specific primers (Additional file
1: Table S1).
SDS-PAGE and western blotting
Infected cells were harvested in RIPA lysis buffer supplemented with LDS buffer (Invitrogen) and boiled in reducing sample buffer for 10 min at 80 °C. The samples were then subjected to reducing Novex 4–12% Bis-Tris gel electrophoresis Separated proteins were electroblotted to PVDF membranes by using the NOVEX Xcell Blot II module and probed with Zika virus M protein antibody (GeneTex) or GAPDH antibody (ThermoFisher) or Axl (Cell Signaling Technology).
Entry assay
4 × 104 Caco-2 cells were seeded onto 6.5 mm diameter, 1 mm pore size polycarbonate membrane trans-wells (Costar) and fresh medium was added at 2 d intervals. At Day 6 post-seeding, the cells were verified to have around 100 Ω resistance before being used for infection. 50 μl of ZIKV suspension at a concentration of 3 pfu/ cell was added either apically or basolaterally, and incubated for 1 h at 37 °C, and washed three times with PBS, followed by addition of 2% fetal bovine serum medium and incubation at 37 °C. Cells were harvested in Trizol reagent and RIPA buffer for RNA and protein analysis respectively at appropriate lysis buffer at indicated time points, and ZIKV M was detected by sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) and qRT-PCR.
Egress assay
Polarized Caco-2 cells (Day 6 post seeding) were infected with ZIKV-PR (3 pfu/ cell) either apically or basolaterally, and incubated for 1 h at 37 °C, and washed three times with PBS, followed by addition of 2% fetal bovine serum medium and incubation at 37 °C. Following 48 h incubation, the supernatants from the top and bottom were harvested and the volume was equalized by adding appropriate amount of MEM supplemented with 2% FBS. The supernatants were then used as inoculum to infect Vero cells. For this purpose, 6 well plates were seeded at a density of 0.3 × 10
6 per well. The ZIKV supernatant was added onto the cells and incubated for 1 h at 37 °C, followed by removal of inoculum and addition of 2% fetal bovine serum medium and incubated at 37 °C. At 48 h post infection, the cells were harvested in RIPA buffer for protein analysis. Alternatively, the supernatants were spiked with equal concentration of MS-2 phage for normalization and harvested in Trizol LS for qPCR analysis as previously described [
29].
Fluorescein leakage test
Permeability of the monolayer was assessed by measuring leakage of fluorescein dye across the monolayer as previously described [
30,
31]. The cells were infected with ZIKV as described above. At 48 hpi cells were washed twice with HBSS. FITC-dextran was added to the upper chamber of ZIKV-infected polarized Caco-2 cells at 48 hpi and incubated for 2 h at 37 °C. Non-polarized cells were used as a control. Levels in the lower chamber were detected by measuring the absorbance at 530 nm.
Discussion
Though there have been reports in literature about polarized release of ZIKV, to our knowledge, this is the first study that evaluates the ability of ZIKV to infect polarized epithelial cells through different membranes. Our data show that polarized Caco-2 cells are susceptible to ZIKV infection. Caco-2 are preferentially infected from the apical surface and vectorially released from the basolateral route without a change in cellular permeability.
ZIKV is known to use Axl as an entry receptor, in microglia, astrocytes and endothelial cells [
7,
40]. However, there are no reports in literature examining polarized Caco-2 cells. Our efforts to establish polarity were also limited my technical difficulties, as we were unable to find an antibody that was suitable for confocal microscopy. Further studies are thus needed to examine the occurrence of surface selective expression of the protein in polarized cells. However, literature shows that this receptors alone may not be the limiting factor for entry. In the case of adeno-associated virus, endosomal processing, rather than receptor availability can be important [
41]. Another possibility is that factors which stabilize virus adsorption may be asymmetrically present on the two surfaces. For instance, several studies have indicated that flaviviruses make initial contact with the host cell by binding to glycosaminoglycans (GAGs) [
42‐
44]. Interestingly, certain GAGs are known to be differentially distributed in polarized cells [
45].
Our data show that ZIKV buds preferentially through the basolateral surface. This is in agreement with recent studies in both epithelial and endothelial cells, which show basolateral budding [
10,
46]. Though the exact viral factors involved in polarized sorting are unclear, it is likely that the signal comprises of tyrosin-based or dileucine based motif occurring on prM and E, since both are known to play a critical role in virus budding [
13,
47,
48]. The microtubule network may also be involved as in the case of WNV polarized budding [
19]. In contrast to other reports however, our reports show that ZIKV does not cause a disruption in cell permeability. Both cell permeability and cell junction architecture remained unaffected during ZIKV infection. This may be because of the cell system used, as other studies used retinal pigment epithelial (RPE), or endothelial cells while our study uses Caco-2 cells. Further, our time window of measurement was upto 48hpi, which is shorter than other reports which go upto 7 days. Therefore, ZIKV may indeed cause cell barrier disruption in Caco-2 cells, but may need a longer period for infection to induce these changes.
Taken together, we show that ZIKV egress occurs in a directed manner, and is not passive translocation due to tight junction disruption as seen in the case of tick-borne encephalitis virus (TBEV) [
38].
It is thought that the ability of a virus to bud apically or basolaterally from epithelial cells plays an important role in the pathogenicity and invasiveness of the virus [
49]. Therefore, the ability to ZIKV to cross the epithelial barrier without being reliant on cell barrier disruption may provide an advantage during viral dissemination in the host.
Conclusions
Our data show that polarized epithelial cells are susceptible to ZIKV infection. The virus enters preferentially through the apical side and buds selectively through the basolateral membrane. Data from permeability assays and electron microscopy indicate that the virus is actually translocating transcellularly rather than paracellular manner, and ZIKV does not need disruption of TJ proteins to cross the epithelial barrier. This translocation across the epithelial membrane may facilitate delivery of virions to sub-epithelial layer and aid in ZIKV dissemination through the host.
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