Human stem cell-derived hepatocyte-like cells support Zika virus replication and provide a relevant model to assess the efficacy of potential antivirals

Zika virus (ZIKV) infection during pregnancy has been extensively linked to microcephaly in newborns. High levels of ZIKV RNA were, however, also detected in mice and non-human primates in organs other than the brain, such as the liver. As ZIKV is a flavivirus closely related to the dengue and yellow fever virus, which are known to cause hepatitis, we here examined whether human hepatocytes are susceptible to ZIKV infection. We demonstrated that both human pluripotent stem cell (hPSC)-derived hepatocyte-like cells (HLCs) and the Huh7 hepatoma cell line support the complete ZIKV replication cycle. Of three antiviral molecules that inhibit ZIKV infection in Vero cells, only 7-deaza-2’-C-methyladenosine (7DMA) inhibited ZIKV replication in hPSC-HLCs, while all drugs inhibited ZIKV infection in Huh7 cells. ZIKV-infected hPSC-HLCs but not Huh7 cells mounted an innate immune and NFκβ response, which may explain the more extensive cytopathic effect observed in Huh7 cells. In conclusion, ZIKV productively infects human hepatocytes in vitro. However, significant differences in the innate immune response against ZIKV and antiviral drug sensitivity were observed when comparing hPSC-HLCs and hepatoma cells, highlighting the need to assess ZIKV infection as well as antiviral activity not only in hepatoma cells, but also in more physiologically relevant systems.


Introduction
Zika virus (ZIKV) is a mosquito-borne flavivirus mostly transmitted by Aedes mosquitos.Cases of sexual transmission and transmission via blood transfusion have, however, also been described [1][2][3][4].Most ZIKV-infected patients are asymptomatic or present with mild clinical symptoms such as rash, conjunctivitis and arthralgia [5,6].A major public health concern is, however, the link between ZIKV infection and abnormalities during fetal development, and more specifically brain development.The virus has been detected in the amniotic fluid of pregnant women and in the brain tissue of fetuses with microcephaly [7,8].Furthermore, the African ZIKV MR766 strain was reported to infect human induced pluripotent stem cell (hiPSC)derived cortical neuroprogenitors (NPCs), causing increased NPC apoptosis, as well as hiPSCderived cortical and motor neurons [9][10][11][12].Additionally, several newborns with microcephaly were also diagnosed with Guillain-Barre ´syndrome and eye defects [13,14].It was hypothesized that the eye defects are due to endogenous hypervitaminosis as a result of ZIKV-induced hepatitis and liver damage [15].
Recently, others and we reported on mouse models to study ZIKV infection.In these mice, high viral loads were not only detected in the brain and spinal cord but also in the kidney, spleen, liver and testes [16][17][18].The dynamics of ZIKV infection, replication and shedding have also been studied in pregnant ZIKV-infected rhesus and cynomolgus macaques [19][20][21].ZIKV RNA was detected in the fetal brain and liver, in the placenta and in the maternal brain, eyes, liver and spleen upon delivery [22].Furthermore, elevated alanine aminotransferase (ALT) and aspartate aminotransferase (AST) levels were detected in the blood of ZIKVinfected macaques, indicating liver damage [21].Of note, a case report published in 1954 described the occurrence of liver damage and jaundice in two patients with elevated ZIKV antibodies [23].Interestingly, the association between ZIKV infection and liver injury was also demonstrated in a more recent case report in 2017.Both, ALT and AST levels were significantly increased and blood coagulation parameters were remarkably altered [24].However, to the best of our knowledge, there are no reports of any experimental demonstration of ZIKV replication in human hepatocytes.
Both dengue virus (DENV) and yellow fever virus (YFV), which together with ZIKV belong to the family of the Flaviviridae, are known to infect human hepatocytes [25][26][27].Unfortunately, research into the permissiveness of human hepatocytes for ZIKV is complicated by the fact that the availability of primary human hepatocytes (PHHs) is limited and that they rapidly dedifferentiate in culture, losing their hepatocyte characteristics [28,29].Others and we previously demonstrated that human pluripotent stem cell (hPSC)-derived hepatocyte-like cells (HLCs) support the complete replication cycle of hepatotropic viruses, including hepatitis E virus (HEV) [30], hepatitis B virus (HBV) [31][32][33], hepatitis C virus (HCV) [34][35][36][37] and DENV [38].Given the fact that ZIKV can infect hepatocytes in mice and non-human primates, and the fact that other Flaviviridae are known to infect human hepatocytes, we here explored whether hPSC-HLCs are susceptible to ZIKV infection and, hence, could be used as a model to test antiviral approaches for ZIKV.We demonstrate that hPSC-HLCs as well as hepatoma cell line Huh7 support the complete ZIKV life cycle, including entry, replication and production of infectious virions.Interestingly, we also observed a significant difference, both in the innate immune response mounted against ZIKV in the two models, and in drug sensitivity of ZIKV replication.

Cell cultures
The human embryonic stem cell (hESC) line H9 and the hiPSC line were purchased from WiCell Research Institute (Madison, US) and Sigma-Aldrich (Saint Louis, MO), respectively.Both hPSC lines were maintained on human matrigel (BD Biosciences, San Jose, CA) coated plates in E8 Flex medium (Gibco) in a humidified 5% CO 2 incubator at 37˚C.hPSCs were differentiated towards HLCs following a previously published 20-day differentiation protocol with minor adjustments [30,39]: namely, dimethyl sulfoxide (DMSO) at a concentration of 0.6% was added from day 0 until day 12 and increased to 2% from day 12 of differentiation onwards until the end of the hepatocyte differentiation.The human hepatoma cell lines Huh7 (kindly provided by Ralf Bartenschlager, University of Heidelberg, Germany) and Huh7.5 (ATCC, Virginia, US) were maintained in Dulbecco's modified Eagle's medium (DMEM) (Gibco) supplemented with 10% fetal bovine serum (FBS) (Gibco), 1% non-essential amino acids (NEAA) (Gibco) and 1% penicillin-streptomycin in a humidified 5% CO 2 incubator at 37˚C.

Virus
Infections were performed using the ZIKV strain MR766 (Rhesus/1947/Uganda) (obtained from the European Virus Archive (EVA)) and the PRVABC59 clinical isolate (obtained from the World Reference Center for Emerging Viruses and Arboviruses (WRCEVA), through the University of Texas Medical Branch (UTMB) at Galveston, USA).Viral stocks were generated as previously described [16].

Virus inoculation
On day 16 of hepatocyte differentiation, hPSC-HLCs were inoculated with either 0.02% or 2% ZIKV MR766 stock (viral titer: 1x10 3 PFU/mL) or 0.0125% ZIKV PRVABC59 stock (viral titer: 1.6x10 5 PFU/mL) in hepatocyte differentiation medium and incubated for 6h at 37˚C in a 5% CO 2 humidified incubator.Following incubation, cells were washed extensively with PBS and fresh hepatocyte differentiation medium was added.Half of the hepatocyte medium was replaced every other day and supernatant was collected 2, 4 and 6 days post infection (d pi).Cells were lysed with 350μL RLT buffer at 4 and 6d pi (Qiagen, Hilden).Infection of Huh7 cells and Huh7.5, a derivative clone, were performed similarly.Mock infection was performed as a negative control.

RNA isolation and RT-qPCR
Viral RNA was extracted from 150μL supernatant using the Nucleospin RNA virus kit (Macherey-Nagel, Du ¨ren) following the manufacturer's protocol.Intracellular RNA was isolated by means of the RNeasy Mini kit (Qiagen).RT-qPCR was performed to analyze viral RNA levels as previously described [16].Viral RNA levels in the lysates were normalized for total RNA content, which was measured by spectrometry (Nanodrop ND-1000, Thermo Fischer Scientific).For gene expression analysis, cDNA synthesis was performed using the Superscript III First-Strand synthesis kit (Invitrogen).Following cDNA synthesis, qPCR was performed with the Platinum SYBR green qPCR supermix-UDG kit (Invitrogen) using the ViiA7 Real-Time PCR instrument (Thermo Fischer Scientific, Waltham, US).

Albumin ELISA
Enzyme-linked immunosorbent assay (ELISA) for albumin was performed following the manufacturer's protocol (Bethyl, Montgomery, TX).At day 20 of HLC differentiation, supernatant was collected and incubated with a primary albumin antibody for 60 min at room temperature.Afterwards an HRP-detection antibody was added for 60 min at room temperature followed by an incubation with TMB-peroxidase solution for 15 min in the dark.The reaction was stopped by the addition of a 0.18M H2SO4 solution.The absorbance was measured at a wave length of 450nm.

Re-infection assay
hESC-HLCs were inoculated with supernatant derived from ZIKV-infected hESC-HLCs (1:10 dilution), which was harvested at 6d pi.After incubation for 6h at 37˚C in a 5% CO 2 humidified incubator, the inoculum was removed and cells were washed extensively with PBS.Supernatant was collected 2d pi and 4d pi.On 4d pi, cells were lysed with 350μl RLT buffer (Qiagen).Viral RNA was quantified by RT-qPCR.
Plaque assay.4x10 5 Baby Hamster Kidney (BHK) cells were seeded in a 12-well plate in 10% growth medium (DMEM with 10% FBS).Viral dilutions of supernatant harvested at 6d pi (1:10-1:50-1:250-1:1250) were prepared using 2% BHK medium (MEM REGA3 + 2% fetal calf serum).The cells were incubated for 2 hours with the virus dilutions in a humidified 5% CO 2 incubator at 37˚C.The virus dilutions were removed and a 0.8% carboxymethyl cellulose (CMC; Sigma Aldrich) overlay was added to the wells.After 1 week, the BHK cells were fixed and the samples were incubated for 5 min in 1% Crystal Violet (Sigma Aldrich), after which the cells were thoroughly washed with water and dried.

Stem cell-derived hepatocyte-like cells and Huh7 cells are susceptible to ZIKV infection
To study the susceptibility of human hepatocytes to ZIKV infection, hESCs and hiPSCs were differentiated towards HLCs, that homogenously express different hepatocyte markers such as AFP, ALB, HNF4α and NTCP and secrete ALB (S1A-S1C Fig) [39].On day 16 of hepatocyte differentiation, hPSC-progeny were infected with the African ZIKV MR766 strain (with an MOI of 8x10 -5 (further described as high MR766 inoculum) or an MOI of 8x10 -7 (further described as low MR766 inoculum)).We also infected the Huh7 hepatoma cells as a control.ZIKV RNA levels were quantified by RT-qPCR in culture supernatant on day 2, 4 and 6d pi and in cellular lysates on 4 and 6d pi.Infection efficiency upon infection with the high MR766 inoculum was comparable between ZIKV-infected hPSCs-HLCs and Huh7 cells, with 10 8 −10 9 viral RNA copies/mL in the supernatant and 10 8 −10 9 viral RNA copies/μg in cellular lysates at 2d pi (Fig 1A).Infection levels seen in hPSC-HLCs appeared to be higher compared to previously published ZIKV infection levels found in hPSC-motor and cortical neuron progeny [12], suggesting a higher replication potential of ZIKV in the stem cellderived hepatocytes compared to the stem cell-derived neurons.ZIKV infection of hPSC-HLCs and Huh7 cells was confirmed on 4d pi by immunofluorescence staining for ZIKV NS3 and the liver-enriched transcription factor HNF4α, demonstrating 6.4 ± 1.0% and 7.1 ± 2.0% ZIKV-infected hPSC-HLCs and Huh7 cells, respectively (Fig 1B).Additionally, we infected hPSC-HLCs and Huh7 cells with a 100-fold lower MR766 ZIKV inoculum (i.e.low MR766 inoculum), since extremely high levels of RNA copies in the supernatant and lysates were observed as early as 2d pi.RNA copies in the supernatant and lysates of hPSC-HLCs and Huh7 were measured at 2, 4 and 6d pi.Replication efficiency at 2d pi in hPSCs-HLCs was approximately 10 6 viral RNA copies/mL or viral RNA copies/μg in the supernatant or cellular lysates, respectively.The replication efficiency increased to approximately 10 8 viral RNA copies/mL or /μg at 4d pi, which was similar to the replication efficiency when using the high MR766 inoculum (S1D Fig) .By contrast, the low MR766 inoculum was not sufficient to infected Huh7 cells, suggesting that hPSC-HLCs are more susceptible to ZIKV infection than Huh7 cells.
Next, we tested whether the recent clinical strain PRVABC59 from the Asian lineage [7,40,41], which is linked to an increased risk of microcephaly in newborns in Brazil, also caused a productive infection in hPSC-HLCs.Replication of the Asian ZIKV strain (MOI of 8x10 -5 ) in hPSC-HLCs was confirmed by measuring ZIKV RNA levels in culture supernatant and cellular lysates, and by immunofluorescence staining for ZIKV NS3 (Fig 1C and 1D).Strain PRVABC59 replicated at an efficiency of 10E 11 -10E 12 viral RNA copies/mL or viral RNA copies/μg in the supernatant or cellular lysates, respectively, indicating that the Asian ZIKV strain appeared to be more infectious than the African ZIKV strain (Fig 1A).However, immunofluorescence staining for ZIKV NS3 antigen showed that the infection rate between MR766 ZIKV-infected hPSCs-HLCs and PRVABC59 ZIKV-infected hPSC-HLCs was comparable: 6.4 ± 1.0% and 5.0 ± 2.4% of the HLCs were ZIKV NS3 positive, respectively (Fig 1B and  1D).

Differences in the activity of ZIKV antivirals in HLCs and Huh7 cells
We next tested if ZIKV infection in hPSC-HLCs could be inhibited by specific antiviral compounds.We previously demonstrated that ZIKV replication in Vero cells is inhibited by three viral RNA-dependent RNA polymerase inhibitors, i.e. 7-deaza-2'-C-methyladenosine (7DMA), 2'-C-methylcytidine (2'CMC), and 6-fluoro-3-hydroxy-2-pyrazinecarboxamide (Favipiravir; T705).Moreover, 7DMA was also shown to delay ZIKV-induced mortality in mice and inhibited ZIKV-induced cytopathic effect in hiPSC-derived cortical and motor neurons [12,16].7DMA and 2'CMC were initially developed as polymerase inhibitors against the hepatitis C virus [42,43].T-705 is a broad-spectrum inhibitor with antiviral activity against many RNA viruses including flaviviruses [44].Treatment of ZIKV MR766-infected hPSC-HLCs and Huh7 cells with 7DMA resulted in a concentration-dependent reduction of viral replication (as assessed by quantifying viral RNA levels in the culture supernatant and in the cellular lysates).However, viral replication was not completely inhibited as the virus continued to replicate to some extent over time, both in hPSC-HLCs infected with a high and a low inoculum (Fig 2A and 2B and S2C Fig).Despite the fact that 2'CMC and T705 inhibited ZIKV replication in Huh7 cells, both antivirals failed to inhibit replication in ZIKV MR766-infected The inhibitory effect of 7DMA on ZIKV replication was further confirmed in hESC-HLCs, infected with the PRVABC59 strain.Although, the PRVABC59 strain seemed initially to be inhibited more efficiently by 7DMA treatment than the MR766 strain, 7DMA was also unable to fully inhibit the replication of the PRVABC59 strain.Thus, although endowed with an antiviral effect, 7DMA is not considered a potent inhibitor since it only delays ZIKV replication.

ZIKV-infected hPSC-HLCs produce infectious virions
To determine if ZIKV-infected hPSC-HLCs support the production of infectious ZIKV virions, supernatant from HLCs, infected with a high and low titer inoculum of MR766, was collected on 6d pi and used to re-infect hPSC-HLCs.ZIKV RNA was present at 2 and 4d pi in the supernatant and at 4d pi in the cellular lysates of secondary infected hPSC-HLC cultures (Fig 3).This demonstrates that ZIKV-infected hPSC-HLCs were able to produce new virions that were infectious as was additionally confirmed by plaque assays (S3 Fig) .At 2d pi, the supernatant of 7DMA-treated primary infected cultures contained less virus particles, since lower ZIKV RNA levels were detected in the medium of secondary infected hPSC-HLCs cultures than in the medium of secondary cultures infected supernatant from untreated, infected cells.However, this effect had disappeared on 4d pi in the case of a secondary infection with supernatant from HLCs infected with a high MR766 inoculum.This initial drop in ZIKV RNA levels might also partially be explained by a carry-over effect of 7DMA from the primary cultures.In secondary infections with supernatant from HLCs infected with a low MR766 inoculum, treatment of the primary cultures with 7DMA resulted in a larger drop in the viral RNA load in the cellular lysates (Fig 3B ) and, thus, a larger inhibition of virion formation in the secondary infected cultures.

ZIKV induces a host innate immune response in hPSC-HLCs, but not in Huh7 cells
Expression of interferon stimulated genes (ISGs) is triggered upon ZIKV infection in human dermal fibroblasts and epidermal keratinocytes [45].Moreover, the virus was recently demonstrated to target the human innate immune response by phosphorylation of STAT1 and STAT2; two transcriptional activators of ISGs [16,17,[46][47][48].Therefore, transcription levels of a number of ISGs (EIF2AK2, MX1, IFNβ and ISG15) were quantified to examine the host immune response of ZIKV-infected cells (Fig 5A).All ISGs were found to be significantly more upregulated in hPSC-HLCs infected with MR766 strain than in Huh7 cells infected with the same strain.Moreover, in ZIKV-infected hPSC-HLCs, ISG expression was significantly and dose-dependently downregulated upon treatment with 7DMA, but not by 2'CMC or T705 treatment, whereas neither 7DMA, 2'CMC nor T705 affected ISG expression in Huh7 cells infected with the MR766 strain (   The innate immunity response of Huh7.5 cells, a derivative clone of Huh7 cells, was previously shown to be more impaired than that of Huh7 cells when both cells were infected with HCV, making these cells highly permissive for this virus [49].To study the potentially superior permissiveness of Huh7.5 cells for ZIKV, we performed a comparative experiment in which both Huh cells lines were infected with a high inoculum of the ZIKV MR766 strain.ZIKV RNA levels in culture supernatant and cellular lysates were quantified at different days pi.Additionally, transcription levels of the ISGs and NFκB and its target genes were determined to examine the innate immune and NFκB stress response of ZIKV-infected Huh7.5 cells.In contrast to HCV, no significant difference was observed in infection efficiency between ZIKVinfected Huh7 cells and its derivative Huh7.5 clone (S5E Fig) .Upon ZIKV infection, IFNβ expression was slightly more upregulated in Huh7 cells than in the ZIKV-infected Huh7.5 cells.This difference, however, was not significant and did not result the expression of the downstream regulated ISGs: EIF2AK2, MX1 and ISG15.Furthermore, no significant difference was observed in the NFκB stress response, which was not induced in both cell lines (S5F Fig) .These results indicate that both Huh cell lines appear to be equally permissive to ZIKV.

Discussion
The differentiation potential of human pluripotent stem cells is an interesting tool to study the tissue tropism of viruses in vitro.Knowledge about the tissue tropism of ZIKV is, however, very limited.Recent studies demonstrated that hiPSC-derived neuroprogenitors are susceptible to ZIKV [9][10][11][12].When interferon-deficient mice or non-human primates were infected with ZIKV, high viral titers of ZIKV were not only found in the brain but also in the testes, spleen, kidney and liver [16,[18][19][20][21][22]46].Also, signs of hepatitis were observed in ZIKV-infected non-human primates [21].Moreover, ZIKV belongs to the family of Flaviviridae, which also includes dengue virus, yellow fever virus and hepatitis C virus; all known to infect human hepatocytes [26,50].Aside from case reports published in 1954 and in 2017 [23,24], no other cases of liver damage in ZIKV-infected individuals have been reported.Based on the findings in ZIKV infection mouse models and non-human primate models, we set out to study whether human hepatocytes are permissive to productive infection by ZIKV.
We demonstrated that both hPSC-HLCs and Huh7 cells can be productively infected with the prototype African ZIKV MR766 strain, as based on the presence of viral RNA, immunofluorescence staining for ZIKV NS3 and the production of infectious virions.In addition, hPSC-HLCs can be productively infected with the ZIKV PRVABC59 that belongs to the Asian lineage.This lineage contains virus strains responsible for the recent ZIKV infection outbreaks in South and Latin America, which have been linked to an increased risk for microcephaly in newborns [7,41].ZIKV infection levels seen in hPSC-HLCs appeared to be higher compared to previously published ZIKV infection levels found in hPSC-neuron progeny [12].This may suggest a higher replication potential of ZIKV in stem cell-derived hepatocytes compared to stem cell-derived neurons.This higher replication potential together with a less time-consuming differentiation protocol and with the use of hepatocytes for drug metabolisation/toxicity screens, indicates that hPSC-HLCs might be an interesting in vitro tool to screen for anti-ZIKV drugs.
We previously reported that 7DMA treatment delays disease progression in a ZIKV infection mouse model [16].7DMA dose-dependently inhibited viral replication of both the African and the Asian ZIKV strain in hPSC-HLCs and Huh7 cells.However, even at the highest concentration, 7DMA did not completely block ZIKV replication in infected hPSC-HLCs, as the supernatant from the 7DMA-treated cells still contained infectious virions.In contrast, 2'CMC and T705, previously shown to inhibit ZIKV replication in Vero cells [16], inhibited ZIKV replication only in Huh7 cells, not in hPSC-HLCs, indicating a possible difference in the compound processing capacity (i.e.uptake and/or drug metabolisation) between hPSC-HLCs and Huh7 cells (and Vero cells).
ZIKV infection caused CPE in both ZIKV-infected hPSC-HLCs and Huh7 cells.Although the percentage of ZIKV-infected cells was comparable between the hepatoma cell line and hPSC-HLCs, CPE was more pronounced in ZIKV-infected Huh7 cells.This discrepancy could be related to the absence of a functional innate immune response in the hepatoma cell line.
Hamel and colleagues reported that ZIKV infection of human dermal fibroblasts and epidermal keratinocytes triggers the expression of ISGs [45].Furthermore, ZIKV was demonstrated to target the human innate immune response through degradation of STAT1 and STAT2; two transcriptional activators of ISGs [47,48].Likewise, we demonstrate an increased expression of ISGs upon ZIKV infection (both MR766 and PRVABC59) of hPSC-HLCs.In ZIKV MR766-infected Huh7 cells, we failed, however, to detect a host innate immune response.Similar results were seen for the expression of NFκB and target genes in hPSC-HLCs and Huh7 cells infected with the MR766 strain: increased expression for NFκB, CXCL2 and CXCL3 in hPSC-HLCs, whereas no increased expression in Huh7 cells, indicating that major differences exist between the hepatoma cell line Huh7 and hPSC-HLCs.In contrast, upon ZIKV infection, no difference was observed in the innate immunity response and the induction of the NFκB pathway in Huh7 cells and its derivative cell line, Huh7.5, resulting in comparable high ZIKV RNA levels in the supernatant and cellular lysates.This is in contrast to the high permissiveness of Huh7.5 for HCV as a result of a weaker innate immunity response compared to that of the Huh7 cells [49].Finally, we observed that the expression of NFκB and its target genes was not induced in hPSC-HLCs infected with the PRVABC59 strain.The lack of a PRVABC59-mediated induction of NFκB has also been observed by others [51,52] and could explain the increased ZIKV replication and cell death seen in hPSC-HLCs infected with the PRVABC59 strain compared to hPSC-HLCs infected with MR766 ZIKV.Studies that aim to understand the different NFκB response induced by the MR766 and PRVABC59 strains might be of interest to gain insights in how to combat the more virulent PRVABC59 ZIKV strain.

Conclusion
In conclusion, hepatoma cells as well as hPSC-HLCs are highly susceptible to ZIKV infection in vitro.The antiviral effect of three viral polymerase inhibitors and the host immune response upon infection were, however, significantly different between ZIKV-infected Huh7 cells and hPSC-HLCs.As hPSC-HLCs more closely resemble primary human hepatocytes (PHHs) compared to transformed Huh7 cells, our study demonstrates the need for assessing the effect of antiviral drugs, not only in cancerous (e.g.hepatoma cells) and immortalized (e.g.Vero cells) cell lines, but also in more physiologically relevant in vitro systems.Moreover, we provide compelling evidence that, in line with the observed ZIKV infection in the hepatocytes of mice and non-human primates, ZIKV can also infect human hepatocytes.It should hence be further explored whether ZIKV may infect the liver, in particular in the developing fetus.

Fig 1 .
Fig 1. hPSC-HLCs and Huh7 were susceptible to ZIKV infection.(A) Infection of hPSC-HLCs and Huh7 cells using a high ZIKV MR766 inoculum.RT-qPCR analysis was used to quantify the viral RNA levels in the supernatant and cellular lysates (intracellular) (d pi = days post infection) (n = 3).(B) Left: Immunofluorescence staining performed at 4d pi for HNF4α and ZIKV NS3 in hPSC-HLCs and Huh7 cells infected with the MR766 strain.Images are representative of three independent experiments (Scale bar = 50μM).Right: Quantification of the immunofluorescence staining.(C) Infection of hPSC-HLCs with the Asian PRVABC59 strain.RT-qPCR analysis was used to quantify the viral RNA levels in the culture supernatant and cellular lysates (intracellular) (d pi = days post infection) (n = 3).(D) Left: Immunofluorescence staining at d4 pi for HNF4α and ZIKV NS3 in hPSC-HLCs and Huh7 cells infected with the PRVABC59 strain.Images are representative of three independent experiments (Scale bar = 50μM).Right: Quantification of immunofluorescence staining.All data are shown as mean±SEM.https://doi.org/10.1371/journal.pone.0209097.g001