Introduction

Rocio virus (ROCV) is a member of the genus Flavivirus in the family Flaviviridae. Like other members of the family Flaviviridae, ROCV is an enveloped virus containing positive-sense RNA genome of approximately 11 kb1. The viral RNA encodes a single open reading frame (ORF) that is flanked by untranslated regions at the 5′ and 3′ ends (5′UTR and 3′UTR). The ORF encodes a single polyprotein, which is co- and post-translationally cleaved into 3 structural (C, prM and E) and 7 nonstructural proteins (NS1-NS2A-NS2B-NS3-NS4A-NS4B-NS5)2. Phylogenetic analysis suggests that ROCV is closely related to the members of Japanese encephalitis virus (JEV) serogroup, which also includes West Nile virus (WNV)3. ROCV was isolated from a pool of mosquitoes of the Psorophora ferox species, confirming that it is transmitted by mosquitoes4.

ROCV was responsible for an outbreak of encephalitis which occurred in 1975 in the Ribeira Valley, located at the southern coast of Sao Paulo State, Brazil5. A total of 465 cases of encephalitis with 61 deaths (13% case fatality rate) were reported from that outbreak6. From 1976, one year after the outbreak, ROCV cases subsided, however seroprevalence studies in humans, horses and water buffaloes in different regions of Brazil have suggested that ROCV maintains circulation across the country, indicating the risk of re-emergence of this highly virulent virus7,8,9,10,11.

The clinical manifestations presented by patients during the outbreak included fever, malaise, lassitude, vomit, lethargy, severe headache, dizziness, photophobia, lower-extremity weakness, and severe neurologic disorders. Neuropsychiatric sequelae were observed in 20% of the patients. Permanent sequelae included variable degrees of paralysis and other cerebral and cerebellar dysfunctions6,12. Autopsies of eight fatal cases of encephalitis caused by ROCV virus revealed histopathologic lesions in the brain with interstitial mononuclear infiltration, microglial proliferation and perivascular lymphocytic cuffing13. Recently, evaluation of the inflammatory process caused by ROCV in an animal model has shown a significant increase of pro-inflammatory cytokines such as interferon alpha (IFN-α), interleukine-1 beta (IL1-β) and tumor necrosis factor alpha (TNF-α) in the central nervous system (CNS), as well as the presence of inflammatory cell, neuronal degeneration and apoptosis14. The type I interferons (IFN-α/β) are the major cytokines produced in response to viral infections that are responsible for the activation of a complex signaling cascade, leading to regulation of the expression of several IFN-stimulated genes (ISGs) such as IL1-β and TNF-α, among others, to fight viral infections15,16. The roles of IFN-α/β as antiviral molecules have been widely studied17. The virus’ ability to block or escape the IFN-α/β response may determine viral pathogenicity18. Inhibition of IFN-α/β signaling by nonstructural proteins of flaviviruses such as Dengue virus (DENV), JEV, Tick borne encephalitis virus (TBEV), and WNV and its contribution to virulence has been previously demonstrated19,20,21,22. The American WNVNY99 strain was shown to be more virulent in mice than the Australian Kunjin virus (KUNV), a naturally attenuated subtype of WNV, and this was attributed to the more efficient inhibition of type I IFN response mediated by non-structural proteins, including NS5520,23,24. On the other hand, an attenuated JEV vaccine candidate was shown to have reduced ability to block the IFN-α/β signaling that was caused by a single E138K mutation in the structural E protein25.

Recently, we have described a simple and efficient method for generation of WNV infectious cDNAs, termed circular polymerase extension cloning (CPEC), and used it to produce chimeric viruses between attenuated Australian and virulent American WNV strains in order to identify viral genetic determinants of virulence26,27,28. In the current study, we employed the CPEC method to generate infectious cDNA of ROCV and reciprocal prM-E chimeric viruses between ROCV and Australian strain of WNV. We employed these chimeric viruses to show that ROCV prM-E proteins are the major contributors to the virulence of ROCV and identified unexpected role of ROCV prM-E proteins in inhibition of IFN-α/β signaling.

Results

Construction of the full-length infectious cDNA of ROCV by CPEC

To generate infectious cDNA of ROCV, viral RNA was purified from the supernatant of C6/36 cell culture infected with ROCV (SPH 34675 strain) and used to generate 7 cDNA fragments spanning the complete viral genome by RT-PCR (Fig. 1a). Equimolar amounts of the 7 RT-PCR fragments and a flavi-UTR-linker fragment containing CMV promoter, conserved first and last 22 nucleotides of viral sequence and hepatitis delta virus ribozyme26, were used in CPEC reaction (Fig. 1a, Supplementary Table S1). The circular DNA product obtained in the CPEC reaction was transfected into HEK293T cells, which were incubated for five days before collecting virus-containing culture fluid (passage 0, p0). Recovered virus was then passaged once in HEK293T cells (p1) and compared with wt ROCV isolate. Both viruses produced plaques of similar size and morphology in BHK cells (Fig. 1b), and replicated with similar efficiencies in mouse embryonic fibroblasts (MEF) (Fig. 1c). These results demonstrate that ROCV was successfully recovered using CPEC, and the CPEC-generated ROCV is indistinguishable from the parental virus. The recovered ROCV and both chimeric viruses (all passage 1 stock) were sequenced using Illumina Nextera XT. Sequencing results showed a number of changes from previously published ROCV sequence that were present in the recovered ROCV and also in the corresponding ROCV regions in respective chimeric viruses (denoted in green in Supplementary Table S2). These are likely to be either mistakes in the previous sequence of ROCV deposited to GenBank3 or changes accumulated during passaging of the ROCV isolate used in this study. We have previously shown that CPEC methodology allows recovery of a virus that accurately represents the original virus population27; thus deep sequencing of the ROCV isolate used for CPEC recovery was deemed unnecessary. The only other differences identified by sequencing were mixed population of Ala and Ser residues at position 111 in the C gene and a mixed population of T and C nucleotides in Ala residue at position 66 in the NS2A gene (not causing amino acid change) in the ROCV/WNV-prME chimeric virus compared to the recovered ROCV (denoted in red in Supplementary Table S2). A mixed population of Asn and Ser residues at position 89 in the E gene was also identified in both the recovered ROCV and WNV/ROCV-prME chimeric virus with Ser being more prominent in both viruses (denoted in blue in Supplementary Table S2).

Figure 1: Generation by CPEC and characterization of ROCV.
figure 1

(a) The strategy for constructing the full-length infectious cDNA of ROCV by CPEC reaction. (b) Plaque morphology of parental and CPEC-generated ROCV (passage 1) in BHK-21 cells. (c) Replication efficiencies of parental and CPEC-generated ROCV in mouse embryonic fibroblasts (MEF). Cells were infected at MOI = 0.1 with parental or CPEC-generated ROCV, culture supernatant were collected at 0, 24, 48 and 72 hours post-infection, and viral titers were determined by plaque assay on BHK-21 cells. The dashed line represents the LOD of the assay.

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ROCV prM-E proteins confer advantage in replication in mammalian cells

We have shown previously that American WNVNY99 strain was more virulent than the Australian WNVNSW2011 strain in mice and mapped the nonstructural proteins of WNVNY99 strain as major contributors to increased virulence through their ability to more efficiently inhibit IFN-α/β response26,29. To analyze the potential role of ROCV proteins in virulence, we constructed two reciprocal chimeric viruses between ROCV and WNVNSW2011 using CPEC. WNVNSW2011 was chosen for generating chimeric viruses as it also belongs to the JEV serogroup of encephalitis flaviviruses and is less virulent in adult mice. The first chimeric virus, ROCV/WNV-prME, contains prM-E genes of WNVNSW2011 on the backbone of ROCV. The second chimeric virus, WNV/ROCV-prME, contains prM-E genes of ROCV on the backbone of WNVNSW2011 (Fig. 2a). Plaque assays of collected culture fluids from CPEC-transfected HEK293 cells on BHK cells showed that both chimeric viruses were successfully generated (Fig. 2b). Sequencing of the C-prM and E-NS1 junctions confirmed the correct sequences in generated chimeric viruses (data not shown). Interestingly, WNV/ROCV-prME chimeric virus produced larger plaques than parental WNVNSW2011, and even than the parental ROCV in BHK cells (Fig. 2b). In contrast, ROCV/WNV-prME chimeric virus produced plaques smaller than parental ROCV, and similar to those produced by WNVNSW2011 (Fig. 2b). Replicative efficiencies of chimeric and parental viruses were then compared in IFN-α/β response-competent (WT) or IFN-α/β response–deficient (IFNAR−/−) mouse embryonic fibroblasts (MEF). In WT MEF cells, ROCV/WNV-prME chimeric virus replicated less efficiently than parental ROCV, while WNV/ROCV-prME chimeric virus replicated more efficiently than parental WNVNSW2011 (Fig. 2c), suggesting that the ROCV prME proteins would be involved in inhibition of the IFN-α/β response. This was further supported by the similar replication efficiencies of ROCV and ROCV/WNV-prME chimeric virus in IFNAR−/− MEF (Fig. 2d). However, WNV/ROCV-prME chimeric virus replicated significantly more efficiently than all other viruses in IFNAR−/− MEF (Fig. 2d), indicating that prME of ROCV may also enhance virus replication independently of the inhibition of IFN-α/β response (Fig. 2d). Importantly, unlike the results in WT MEF, ROCV/WNV-prME chimeric virus reached similar to the parental ROCV titres at 48 h and 72 h after infection in IFNAR−/− MEF (Fig. 2d) indicating that chimerization did not avertedly affect replication of this chimeric virus in the absence of functional IFN-α/β response.

Figure 2: Construction and characterization of ROCV/WNV chimeric viruses.
figure 2

(a) Schematic representation of ROCV/WNVNSW2011 chimeric viruses. (b) Plaque morphology of parental (ROCV and WNV) and chimeric (ROCV/WNV-prME and WNV/ROCV-prME) viruses in BHK-21 cells (upper) and comparison of plaque size areas (lower). Plaque areas (mm2) for 25–40 randomly selected plaques were measured using ImageJ software (National Institutes of Health, USA) and plotted as mean ± SD. (c) Growth kinetics of parental and chimeric viruses in IFN-competent mouse embryonic fibroblasts (WT MEF) and (d) IFNAR−/− MEF cells infected at MOI = 0.1. Viral titers were determined by plaque assay on BHK-21 cells at the indicated time points. The dashed lines represent the LOD of the assay. Parametric one-way ANOVA test was used to compare within groups. *P-value ≤ 0.05, ****P-value ≤ 0.0001.

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ROCV prM-E proteins inhibit JAK/STAT signaling

To further investigate downstream mechanisms of inhibition of the IFN-α/β response by ROCV prM-E proteins, we used IRF3−/− × IRF7−/− MEF cells, which lack the ability to produce IFN-α/β in response to infection, but maintain the ability to respond to exogenous IFN-α/β. IRF3−/− × IRF7−/− MEF were infected with the parental and chimeric viruses at MOI = 0.1 for 48 h and then treated with 10,000 IU of mouse IFN-β for 30 min. Cells were collected and analyzed by flow cytometry by first gating to a single cell population, and then to infected cells. The intensity of pSTAT1 staining was then analyzed for the population of infected cells (Fig. 3a). The phosphorylation of STAT1 was inhibited in cells infected with ROCV and WNV/ROCV-prME, but not in cells infected with WNVNSW2011 or ROCV/WNV-prME (Fig. 3a). Results from two independent experiments demonstrated that ROCV- and WNV/ROCV-prME-infected cells consistently showed reduced pSTAT1 expression in response to IFN-β treatment compared to WNVNSW2011 -infected cells (Fig. 3b). The results show that ROCV prM-E proteins are likely to be responsible for the inhibition of JAK-STAT signaling.

Figure 3: pSTAT1 analysis in IRF3−/− × IRF7−/− MEF cells infected with parental and chimeric viruses and treated with mouse IFN-β.
figure 3

(a) IRF3−/− × IRF7−/− MEF cells were infected with parental or chimeric viruses at MOI = 0.1, and treated with 10,000 IU of mouse IFN-β at 48 h.p.i. Cells were gated to the single-cell infected population, and cell counts were plotted to fluorescence intensity of pSTAT1. (b) Relative expression of pSTAT1 normalized to ROCV. Data represent the mean of two independent experiments; each performed in duplicate. Parametric one-way ANOVA test was used to compare within groups. *P-value ≤ 0.05.

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ROCV prM-E proteins provide major contribution to virulence in mice

To investigate if the inhibition of JAK-STAT signaling by ROCV prM-E and enhanced replication of WNV/ROCV-prME chimeric virus in MEF also result in increased virulence in vivo, we infected groups of ten, 6-week-old C57BL6 female mice with 2.6 × 104 pfu of parental or chimeric viruses via the intraperitoneal route. Mice were monitored for 21 days for signs of encephalitis, at which point the animals were immediately sacrificed. Infection with WNVNSW2011 or ROCV/WNV-prME viruses resulted in 10% and 20% mortality, respectively (Fig. 4). In contrast, infection with ROCV resulted in 100% mortality, while infection with WNV/ROCV-prME chimeric virus resulted in 90% mortality (Fig. 4). Statistical significance was observed for ROCV v.s. ROCV/WNV-prME (p ≤ 0.0001) and for WNVNSW2011 v.s. WNV/ROCV-prME (p ≤ 0.001). The results clearly demonstrate that ROCV prM-E proteins provide major contribution to the virus virulence in adult immunocompetent mice.

Figure 4: Survival of 6-week-old C57BL6 female mice after infection with parental and chimeric viruses.
figure 4

Six-week-old C57BL6 mice in groups of 10 were infected with 2.6 × 104 pfu of the indicated viruses via the intraperitoneal route and monitored for signs of encephalitis for 21 days post-infection.

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Discussion

We have successfully generated infectious cDNA of ROCV and of chimeric viruses between ROCV and WNV using CPEC method. We have used this method previously for construction of infectious cDNAs of WNV and of chimeric viruses between Australian and American strains of WNV to identify genetic determinants involved on virulence26,27. The chimeric ROCV/WNV viruses generated in this study contained prM-E genes swapped between WNV and ROCV with the remaining genomic sequences left intact. ROCV prM-E differ from WNVNSW2011 prM-E by 248 from a total of 668 amino acids (62.8% homology). Previous studies with chimeric flaviviruses demonstrated that prM-E genes can be successfully exchanged, even between distantly related flaviviruses30,31,32,33,34; thus the successful recovery of ROCV/WNVNSW2011 chimeric viruses despite substantial amino acid differences was not entirely unexpected. We showed that chimeric ROCV containing WNV prM-E genes in comparison with the parental ROCV exhibited significantly reduced replication in IFN-α/β response-competent cells, decreased efficiency in inhibition of JAK-STAT signaling and lower virulence in mice. In agreement with these findings, the reciprocal chimeric WNV containing ROCV prM-E genes in comparison with the parental WNVNSW011 virus showed the exactly opposite characteristics, i.e. enhanced replication in IFN-α/β response-competent cells, increased efficiency in inhibition of JAK-STAT signaling, and higher virulence in mice. Deep sequencing of the recovered viruses identified a number of the same changes from the previously published sequence in all recovered viruses, which we believe to be either mistakes in the original published sequence or changes accumulated during passaging of the ROCV isolate used in this study. Two other identified potential changes, both reflecting mixed virus populations, one at residue 111 in the C gene (mixture of Ala and Ser) and one in NS2A gene (synonymous change at Ala 66 residue) in ROCV/WNV-prME chimeric virus are unlikely to cause profound changes in the virus properties. A mixed population was also identified at residue 89 in the E gene of both, ROCV and WNV/ROCV-prME chimeric virus, likely to produce similar effect on properties of both viruses.

Viruses have evolved many mechanisms to evade the IFN system, blocking at almost every step of the signaling pathway17. Several studies, including ours, showed that non-structural proteins of flaviviruses such as DENV, JEV, TBEV, and WNV were responsible for the inhibition of IFN signaling19,20,24,35,36. Therefore, our findings that ROCV prM-E proteins exhibited strong IFN antagonistic activity was rather unexpected. Interestingly, E protein of JEV was also shown to be involved in inhibition of IFN-α/β response, with a E138K mutation identified in the attenuated strain of JEV shown to result in decreased efficiency in inhibiting IFN-α/β signaling and reduced virulence in mice25. The authors suggested that inefficient binding of virions to glycosaminoglycans on cell membrane, viral entry, and/or delayed virus replication exhibited by E138K mutant virus were likely contributing factors to the increased sensitivity to IFN; indicating that a direct interactions of E protein with intracellular cytoplasmic signaling factors were unlikely. In a separate study by Arjona et al.37, cells treated ectopically with recombinant WNV E protein were shown to have reduced signaling and production of cytokines associated with the dsRNA sensing pathways, mainly inhibition of RIP1 polyubiquitination. The inhibitory effect was dependent on glycosylation, a feature present in both, WNVNSW2011 and ROCV, E proteins. Thus, how membrane-sequestered prM and/or E proteins could interact with intracellular cytoplasmic signaling factors remains undetermined. Further studies with ectopically expressed ROCV prM-E proteins are required to determine whether their IFN antagonistic activity is independent of virus replication and to elucidate the exact mechanisms involved.

In summary, we have demonstrated that ROCV prM-E proteins are major contributors to virus virulence in mice and are involved in inhibition of IFN-α/β signaling in infected cells.

Methods

Cells lines

Baby hamster kidneys 21 (BHK-21) cells, human embryonic kidney 293 (HEK293T) cells, mouse embryonic fibroblast (MEF) cells, interferon alpha/beta receptor deficient (IFNAR−/−) MEF cells, and interferon response factors 3 and 7 deficient (IRF3−/− × IRF7−/−) MEF cells were maintained in Dulbecco’s Modified Eagle Medium (DMEM) supplemented with 4–10% of fetal bovine serum (FBS) (Gibco, USA) at 37 °C with 5% of CO2. Aedes albopictus (C6/36) cells were maintained in Roswell Park Memorial Institute (RPMI) 1640 medium, supplemented with 10% FBS (Gibco, USA) at 28 °C. DMEM and RPMI were supplemented with penicillin (100 U/mL) and streptomycin (100 μg/mL).

Viruses

Rocio virus (SPH 34675 strain) and West Nile virus (NSW2011 strain) were maintained in C6/36 cell cultures. The virus titres were determined using plaque assay on BHK cells and expressed as plaque forming units per mL (pfu/mL). The limit of detection (LOD) of this method was 50 PFU/mL. Briefly, 2.5 × 105 cells per well were grown in 6-well plates and infected with ten-fold serial dilutions of the viruses for 1 h at 37 °C; subsequently, 2 mL of 0.375% Low-Melting Point (LMP) agarose in DMEM medium supplemented with 2% FBS were added. Three days post-infection cells were fixed with 4% formaldehyde for 2 hours at room temperature. The LMP agarose medium was removed and the cells were stained with 0.2% crystal violet solution to reveal the plaques.

Viral RNA purification

The viral RNA was purified from supernatant of infected C6/36 cells using the NucleoSpin RNA Virus kit (MACHEREY-NAGEL, Germany), following the manufacturer’s recommendations.

Generation of parental and chimeric viruses by CPEC method

The recombinant viruses were generated using CPEC protocol adapted from Setoh et al. (2015)24. Briefly, RT-PCR fragments spanning the complete viral genome and the flavi-UTR-linker fragment were used to assemble the full-length cDNA. Flavi-UTR-linker fragment contains CMV promoter, conserved first and last 22 nucleotides of viral sequence and hepatitis delta virus ribozyme23. Each cDNA fragment contained overlapping ends (21–24 bp) to the adjacent fragments at the 5′and 3′ ends. Fragments of the 5′UTR and 3′UTR regions contained overlapping ends with a flavi-UTR-linker, which allow the generation a circular DNA product and the transcription of the viral RNA in mammalian cells. Primers used to amplify the overlapping cDNA fragments of ROCV, WNV and chimeric viruses are described in the Supplementary Table S1. The DNA bands were purified from the agarose gel using a Wizard SV Gel and PCR Clean-Up System (Promega, USA), following the manufacturer’s recommendations. CPEC reaction was performed with the Q5-Hot Start High Fidelity DNA Polymerase (New England Biolab, UK), using equimolar amounts of all viral genomic fragments and the flavi-UTR-linker fragment. The amplification cycle consisted of an initial denaturation step at 98 °C for 3 minutes, followed by 20 cycles of amplification at 98 °C for 15 seconds, 60 °C for 30 second, and 72 °C for 7 minutes; and a final incubation at 72 °C for 15 minutes. The CPEC reaction product containing the full-length cDNA of the viruses was directly transfected into HEK293T cells (5 × 105 cells per well), using the Lipofectamine LTX reagent (Invitrogen, USA), following the manufacturer’s recommendation. Five days after transfection (passage 0), an aliquot of the supernatant was further passed (passage 1) in HEK293T and/or C6/36 cells. The virus from passage 0 and 1 were titrated by the plaque assay in BHK-21 cells and then stored at −80 °C until use.

Nucleotide sequencing of chimeric viruses

In order to avoid DNA contamination from CPEC reaction, the viral RNAs were DNase treated before genomic amplification by RT-PCR. To confirm the correct construction of the chimeric viruses, RT-PCR amplicons containing the C-prM and E-NS1 junctions were sequenced by Sanger sequencing at the Australian Genomics Research Facility (AGRF).

Full genome sequencing of recovered viruses

The full genome of the recovered viruses (all from passage 1) were amplified in three ~5000 bp fragments with ~2000 bp overlap between fragments. The primers used for ROCV/WNV-prME are 1F: AGAAATTCACCTGTGTGAAATTTCACC, 1R: TATTCACGATGGGCGACC, 2F: GCAATCAAAGGAAACCGGG, 2R: GGGCCTCCTTTTGTGTATCC, 3F: ATGAATACTACTACGGTGGGC, 3R: AGATCCTGTGTTTTGCAGCACC. The primers used for WNV/ROCV-prME are 1F: AGCTGACAAACTTAGTAGTGTTTG, 1R: TCCAGTGGGGAAGTCTAAAG, 2F: AGGGTCAGAGAAAGCAACAC, 2R: AGAACACATCCACCCCACTC, 3F: GATGAGTACTGCTATGGAGGG, 3R: AGATCCTGTGTTCTCGCACC. Libraries were prepared using the Nextera XT DNA Sample Preparation Kit (Illumina Inc., San Diego, CA, USA). All libraries were sequenced with an Illumina NextSeq500 platform 2 × with 150 bp High Output v.1 run chemistry. Reads were mapped to their respective genomes using Bowtie 238.

Kinetics of virus replication in MEF cells

The kinetics of virus replication was analyzed in WT MEF and IFNAR−/− MEF cells. Briefly, 2.5 × 105 cells per well were grown in 6-well plates and infected (MOI = 0.1) with the viruses for 1 h at 37 °C; subsequently the monolayer was washed twice with warm DMEM and then 2 mL of DMEM supplemented with 5% FBS were added. The supernatants of the cells were harvested at 0, 24, 48 and 72 hours post infection (p.i). The viral titer was determined by plaque assay on BHK-21 cells. Three independent experiments were performed.

Analysis of inhibition of IFN signaling

IRF3−/− × IRF7−/− MEF cells were grown in 6-well plates and infected with the viruses (MOI = 0.1) for 1 h at 37 °C. Cells were washed twice with PBS and then 2 mL of DMEM supplemented with 5% FBS were added. Forty-eight hours after infection, the media was removed and the cells were washed twice with PBS and then treated with 10,000 IU of mouse IFN-β (R&D systems) for 30 minutes at 37 °C. The cells were then fixed with 4% formaldehyde and permeabilized with ice-cold 100% methanol and resuspended in PBS/T before staining with either mouse monoclonal antibody against WNV E (anti-WNV E - 3.91D) and NS1 (anti-WNV NS1–4G4) protein or a polyclonal antibody against ROCV. Cells were also stained with anti-pSTAT1 monoclonal antibody (Cell Signaling Technologies) and analyzed by flow cytometry.

Virulence in mice

All animal procedures had received prior approval from the University of Queensland Animal Ethics Committee in accordance with the guidelines for animal experimentation as set out by the National Health and Medical Research Council, Australia. Six week-old C57BL6 female mice (purchased from Animal Resources Centre) were infected via the intraperitoneal route with viruses at a dose of 2.6 × 104 pfu. This viral dose was determined in pilot experiments as lethal for ROCV, but non-lethal for WNVNSW2011 in mice of this age. Ten mice per group were infected with each virus. Infected animals were monitored daily for 21 days post-infection, and at the first signs of encephalitis (severe hunching, lethargy, eye closure, severe twitching or hind-leg flaccid paralysis) were immediately culled.

Statistical analysis

The data were analyzed using GraphPad Prism 7.0 software (La Jolla, CA, USA). Parametric one-way ANOVA test was used to compare within groups and Turkey’s Post Hoc multiple range test was used to find the difference between the groups at level p < 0.05. The level of statistical significance was set at 95% (p = 0.05). Survival curves were analyzed using the Log-rank (Mantel-Cox) test.

Additional Information

How to cite this article: Amarilla, A. A. et al. Chimeric viruses between Rocio and West Nile: the role for Rocio prM-E proteins in virulence and inhibition of interferon-a/b signaling. Sci. Rep. 7, 44642; doi: 10.1038/srep44642 (2017).

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