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Method Article

Arbovirus Infections As Screening Tools for the Identification of Viral Immunomodulators and Host Antiviral Factors

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DOI:

10.3791/58244

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September 13th, 2018

 ,  , 
1Department of Microbiology, University of Texas Southwestern Medical Center

In This Article

Summary

Here, we present the protocols to identify 1) virus-encoded immunomodulators that promote arbovirus replication and 2) eukaryotic host factors that restrict arbovirus replication. These fluorescence- and luminescence-based methods allow researchers to rapidly obtain quantitative readouts of arbovirus replication in simplistic assays with low signal-to-noise ratios.

Abstract

RNA interference- and genome editing-based screening platforms have been widely used to identify host cell factors that restrict virus replication. However, these screens are typically conducted in cells that are naturally permissive to the viral pathogen under study. Therefore, the robust replication of viruses in control conditions may limit the dynamic range of these screens. Furthermore, these screens may be unable to easily identify cellular defense pathways that restrict virus replication if the virus is well-adapted to the host and capable of countering antiviral defenses. In this article, we describe a new paradigm for exploring virus-host interactions through the use of screens that center on naturally abortive infections by arboviruses such as vesicular stomatitis virus (VSV). Despite the ability of VSV to replicate in a wide range of dipteran insect and mammalian hosts, VSV undergoes a post-entry, abortive infection in a variety of cell lines derived from lepidopteran insects, such as the gypsy moth (Lymantria dispar). However, these abortive VSV infections can be "rescued" when host cell antiviral defenses are compromised. We describe how VSV strains encoding convenient reporter genes and restrictive L. dispar cell lines can be paired to set-up screens to identify host factors involved in arbovirus restriction. Furthermore, we also show the utility of these screening tools in the identification of virally encoded factors that rescue VSV replication during coinfection or through ectopic expression, including those encoded by mammalian viruses. The natural restriction of VSV replication in L. dispar cells provides a high signal-to-noise ratio when screening for the conditions that promote VSV rescue, thus enabling the use of simplistic luminescence- and fluorescence-based assays to monitor the changes in VSV replication. These methodologies are valuable for understanding the interplay between host antiviral responses and viral immune evasion factors.

Introduction

The ability of a virus to productively replicate in a particular host is in part governed by the availability of host cell factors that support viral entry and replication1. The virus-host range can also be dictated by the capacity of a virus to counter cellular antiviral defenses that would otherwise impede viral replication2,3. It is the outcome of these complex virus-host interactions that ultimately decide whether a virus will be able to complete its life cycle in a particular host. Given the potentially pathogenic consequences for the host if viral replication ensues, it is critical to develop experimental strategies to further our understanding of the key virus-host interactions that may tip the balance between abortive and productive infections. Elucidating the molecular features of virus-host interplay will be instrumental in the development of new and alternative antiviral therapeutic strategies.

With the advent of RNA interference (RNAi)4,5 and genome-editing tools (e.g., CRISPR-Cas9, Zinc finger nucleases, TALENs)6,7, it has become experimentally feasible to alter the expression of cellular factors on genome-wide scales and explore the impact of these alterations on virus replication. Indeed, numerous RNAi and genome-editing-based screens have been conducted in invertebrate and vertebrate host cell types that have unveiled new facets of virus-host interactions8,9,10,11,12. These screens typically employ viruses encoding reporters, such as firefly luciferase (LUC) or fluorescent proteins (e.g., GFP, DsRed), that provide convenient means of quantitatively assessing viral gene expression as a readout for viral replication9,12. This strategy allows researchers to identify host factors that either promote or antagonize viral replication as evidenced by increases or decreases, respectively, in viral reporter signals9,12. However, in the vast majority of cases, these screens have been conducted using viruses that are well-adapted to the host cell type in which they are being studied. While this strategy can be important for understanding coevolutionary relationships between viral pathogens and their natural hosts, it does pose fundamental concerns regarding their use in uncovering host antiviral factors. In these cases, an enhancement in virus reporter signal upon RNAi knockdown is being looked for, or the inactivation of a cellular factor that normally impedes viral replication. First, if a virus is already able to robustly replicate in the host cell being examined under control conditions, the dynamic range of the screen (i.e., the ability to distinguish between background and enhanced viral reporter signals) may be limited. Second, this issue is further compounded by the situations in which the virus is well-adapted to the host cell and effective at countering host defense pathways that are being targeted in the screen.

Due to the above concerns regarding traditional virus-host interaction screening methods, we developed a new paradigm for studying virus-host interactions that exploit naturally abortive arbovirus infections in lepidopteran insect cells. This strategy derives from an observation that the well-studied human arbovirus, VSV, undergoes an abortive infection in cells derived from the gypsy moth (L. dispar)13. VSV is naturally transmitted by dipteran insects (i.e., sand flies) to mammalian hosts, and has been shown experimentally to infect a wide range of invertebrate and vertebrate hosts both in cell culture and in vivo14. The 11-kb negative-sense single-stranded RNA genome of VSV encodes five subgenomic mRNAs that are each translated into the proteins that make up the enveloped virion. However, VSV reverse genetic systems have allowed for the creation of replication-competent strains encoding LUC or fluorescent proteins, in addition to the five natural VSV gene products15,16,17. Because these reporter proteins are not incorporated into the VSV virion, they provide a convenient readout for VSV gene expression that occurs post-entry. Using VSV strains encoding GFP or LUC, we have previously shown that VSV gene expression is severely restricted upon the entry of LD652 cells and that VSV titers do not increase by 72 hours post-infection (hpi). In contrast, the coinfection of LD652 cells with VSV and the mammalian poxvirus, vaccinia virus (VACV), leads to logarithmic increases in both VSV gene expression and titers by this time point. VACV undergoes early gene expression, DNA replication, and late gene expression in LD652 cell infections, but the VACV replication cycle is ultimately abortive due to incomplete virion morphogenesis18. The large ~192-kb DNA genome of VACV encodes > 200 proteins, many of which display immunomodulatory properties that promote viral replication through the suppression of host immune responses19. Therefore, we hypothesized that the "rescue" of VSV replication in LD652 cells by VACV coinfection was likely mediated by VACV immunomodulators that inhibited L. dispar responses normally restricting VSV replication. In support of this, the treatment of LD652 cells with the host RNA polymerase II inhibitor actinomycin D also rescues VSV replication in LD652 cells, indicating that the transcription-dependent host responses block VSV replication post-entry13.

The above observations suggest that the naturally restrictive nature of LD652 cells to VSV infection may provide a relatively low background when screening for the conditions that enhance VSV-encoded reporter signals (i.e., those that inhibit host antiviral defenses). Here, we provide the methods for using fluorescence or LUC-based assays to screen for conditions that relieve VSV restriction in lepidopteran cells. First, we show how these assays can be used to identify virally encoded immunomodulatory factors that break VSV restriction during either coinfection experiments or through ectopic expression of candidate viral factors. As an example, we illustrate how we used these screening techniques to identify poxvirus-encoded A51R proteins as a new family of immunomodulatory factors that rescue VSV replication in the absence of other poxvirus factors13. Second, we illustrate how RNAi screening in restrictive VSV-LD652 cell infections can be used to directly identify eukaryotic host factors involved in arbovirus restriction13.

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Protocol

1. General Lymantria dispar (LD652) Cell and Virus Culture

  1. LD652 cell culturing and plating
    1. To culture L. dispar-derived LD652 cells, maintain a monolayer of cells in a growth medium (Table of Materials) incubated at 27 °C under normal atmosphere. Maintain the cells in 10 cm tissue-culture-treated dishes and passage the cells upon reaching 80% confluency.
    2. To plate, dislodge adherent LD652 cells from the plate by pipetting the media repeatedly onto the monolayer (these cells do not require trypsinization to dislodge), and dilute the sample in growth media to an approximate density of 1 x 105 cells/mL. Pipette 1 mL of diluted culture/well of a 24-well plate. Seed a minimum of three replicate wells/treatment type for each time point (a maximum of eight treatments/plate).
    3. Allow the cells to settle for a minimum of 1 h.
  2. Vaccinia virus preparation
    1. To prepare the stocks of VACV, amplify the virus in HeLa cells20 or African Green Monkey kidney cells (BSC-1 or BSC-40 cells)20,21,22.
      NOTE: VACV strain Western Reserve (VACV-WR) works well in the assays described here.
    2. Titrate the VACV strain via plaque assay on BSC-1 or BSC-40 cells20,22.
      NOTE: All indicated VACV multiplicity of infection (MOI) described here for LD652 cell infections are based on titers obtained from BSC-40 plaque assays.
  3. Vesicular stomatitis virus preparation
    1. To prepare VSV stocks, amplify the virus in BHK cells23.
    2. Titrate VSV by plaque assay on BSC-40 or BHK cell monolayers13,23.
      NOTE: All VSV MOIs described here for LD652 cell infections are based on titers obtained from BSC-40 plaque assays.

2. Fluorescence-based VSV Rescue Assay Using Co-infection and Live-cell Imaging

  1. Seeding and infection of LD652 cells
    1. Plate 40,000 LD652 cells/well of an 8-well chamber.
    2. For fluorescence-based live-cell imaging, use VSV strains encoding fluorescent proteins. The experiments presented here use VSV-DsRed17, a recombinant VSV strain that expresses free DsRed protein that is not fused to any other VSV protein.
      NOTE: VSV infection of LD652 cells is not cytopathic by 96 hpi and, thus, the cell death is not a confounding factor when evaluating VSV replication within this time frame.
    3. Prepare VSV-DsRed and VACV-FL-GFP in a serum-free media (SFM; Table of Materials) at an MOI of 1 and 25, respectively.
      NOTE: VACV-FL-GFP is a recombinant VACV strain that expresses a fusion between LUC and GFP24. Using an MOI of 25 or greater for VACV strains ensures that all LD652 cells are infected13. If using a different coinfecting virus, the MOI will have to be determined empirically by the user. Each infection treatment should be set up in duplicate wells and include mock-infected treatments in which only SFM is added to the cells.
    4. Incubate the cells in 0.2 mL of inoculum for 2 h at 27 °C.
    5. Wash the cells with 0.5 mL/well of growth media.
    6. Incubate the cells in 25 μM of cell viability dye (Table of Materials) in growth media for 45 min at 27 °C.
    7. Aspirate the media and wash the wells 1x with 0.5 mL/well to remove excess dye.
    8. Maintain the cells in 0.3 mL/well of the growth media.
  2. Live cell image capturing
    1. Turn on a confocal microscope 30 min in advance and load an 8-well chamber dish.
      NOTE: LD652 cells can be imaged at room temperatures ranging from 20–25 °C, but for optimal conditions, the temperature of the room should be adjusted to 27 °C.
    2. Set up the appropriate excitation/emission settings for each fluorescent marker protein to be imaged, as well as the phase contrast image settings.
    3. Adjust the laser intensity for each channel.
      NOTE: This may require running a pilot experiment to determine the range of fluorescent signal intensities observed throughout the time course to be used in the final experiment.
    4. Using the 10X objective, capture the phase contrast and fluorescence images of each well every 1–5 h for the duration of the infection up to a desired time point (e.g., 48–72 hpi).
      NOTE: It is important to capture multiple fields of view in each well to accurately estimate the infection rates throughout the culture.
  3. Image analysis
    1. Use image analysis software for automated image analysis of appropriate fluorescent channels (e.g., 405 nm, 488 nm, 568 nm).
    2. To calculate the percentage of cells that are infected, divide the total number of fluorescent cells indicating VSV infection (e.g., DsRed-positive cells for VSV-DsRed infections) by the total number of viable cells labeled by cell viability dye for each field of view across all treatments.

3. General Viral Infection Protocol for Luminescence-based VSV Rescue Assays in LD652 Cells

  1. Preparation of inoculum
    1. 30 min prior to the infection, thaw the stocks of VSV-LUC16 (a recombinant VSV strain that expresses free firefly luciferase protein not fused to any other VSV protein). If assaying for VSV-LUC rescue during VACV coinfection, also thaw the VACV-WR virus on ice.
      NOTE: Other viruses (besides VACV-WR) may rescue VSV-LUC during the coinfection, but this will have to be determined empirically by each user.
    2. Prepare the inoculum by diluting VSV-LUC in the presence or absence of VACV-WR into SFM such that an MOI of 10 and 25, respectively, is achieved when adding a total inoculum volume of 0.2 mL/well.
  2. Infection of the cells
    1. Aspirate mature LD652 media carefully to avoid disturbing the monolayer and inoculate with 0.2 mL of virus/well. This time is defined as 0 hpi. Add sterile SFM to additional wells to serve as “mock-infected” negative control treatments.
    2. Incubate the cells in inoculum for 2 h at 27 °C.
    3. At 2 hpi, remove inoculum by aspiration and replace with 1 mL/well LD652 growth media.
    4. Allow the infection to proceed 24–72 hpi.

4. Luciferase Assay

  1. Preparation of cell lysates
    1. Carefully aspirate the supernatant and add 1 mL of Dulbecco's phosphate-buffered saline (DPBS)/well.
    2. Using the plunger of a 1 mL syringe, scrape the cells into DPBS.
    3. Transfer the cells to a microcentrifuge tube, and centrifuge at 400 x g for 20 min at 4 °C.
    4. Meanwhile, prepare 1x dilution of 5x reporter lysis buffer (RLB) in sterile H2O.
    5. Following the centrifugation, aspirate the DPBS without disturbing the cell pellet.
    6. Resuspend each pellet in 150 µL of 1x RLB.
    7. Freeze-thaw the samples 1x using a 5-min incubation in a -80 °C freezer followed by a rapid thaw in a room temperature water bath. Store the lysates at -80 °C until ready to analyze.
  2. Luciferase assay
    1. Thaw the lysates on ice.
    2. Pipette 20 μL of lysate into a well of a solid black or white 96-well microplate.
    3. Add 100 μL of luciferase assay reagent to each well.
    4. Immediately measure the light intensity using a luminometer (appropriate settings for specific luminometers will have to be determined empirically by the user).
  3. Luciferase assay analysis
    1. Normalize LU signals for each treatment to LU readings obtained from control treatments (Representative Results). After at least three independent experiments have been performed, the mean LU obtained from each treatment/control group can be analyzed by appropriate statistical tests.

5. Immunoblot

  1. Use lysates extracted for the LUC assays for SDS-PAGE and subsequent immunoblotting, using appropriate reagents and instrumentation.

6. Titer of VSV from LD652 Cell Cultures

  1. Plate LD652 cells according to step 1.1.
  2. Viral infect the cells according to step 3.
  3. At desired time points, collect the supernatants into sterile microcentrifuge tubes.
  4. Pellet the cells using 1,000 x g for 10 min at 4 °C and transfer the supernatants to new tubes.
  5. Store the supernatants at -80 °C or proceed with titration by plaque assay on BSC-40 cells.
    NOTE: If titrating VSV from LD652 cell cultures that contained VACV, it is advisable to add 100 μg/mL cytosine arabinoside (AraC) to the BSC-40 culture media within 2 hpi, to prevent residual VACV particles from forming plaques on BSC-40 monolayers13. AraC is a viral DNA polymerase inhibitor that blocks VACV DNA replication25 but does not affect VSV replication.

7. Variations of Luminescence-based VSV Rescue Assays in LD652 Cells: RNAi and Plasmid Transfection Experiments

  1. Preparation of dsRNA for RNAi-mediated knockdown of viral or host transcripts
    1. Design gene-specific primers tailed at the 5’ end with the T7 promoter sequence (TAATACGACTCACTATAGGG) to target either the coinfecting virus (e.g., VACV) or L. dispar mRNA transcripts of interest. These primers should produce a PCR product of 400–600 bp for effective RNAi-mediated knockdown. See Gammon et al.13 for primer sequences used below to knockdown VACV or L. dispar transcripts by dsRNA-mediated RNAi in LD652 cells.
      NOTE: L. dispar mRNA transcripts can be identified from published L. dispar transcriptome databases26,27,28.
    2. Generate a DNA template via RT-PCR (cDNA synthesis: 1 cycle of 50 °C for 30 min; PCR: 40 cycles of 94 °C for 15 s, 50 °C for 30 s, and 68 °C for 45 s each).
    3. Purify the PCR product using a PCR purification kit.
    4. Using the purified PCR product as a template, in vitro transcribe and purify dsRNA using an in vitro transcription and purification kit.
  2. Transfection of dsRNA or plasmid DNA into LD652 cells
    1. Seed 1 x 105 cells/well of a 24-well plate and let the cells settle for at least 1 h.
    2. For each well to be transfected, dilute 4 μL of transfection reagent into 100 μL of SFM. Incubate for up to 15 min at room temperature. This can be scaled to make a master mix for all transfections to be performed.
    3. Dilute up to 1 μg of dsRNA or total plasmid DNA with 100 μL of SFM for each well to be transfected. Incubate for up to 15 min at room temperature.
      NOTE: We have previously found that a transfection of 1 μg of dsRNA/105 LD652 cells is sufficient for >80% knockdown of either viral or host transcripts13, but dsRNA doses needed for modified experimental set-ups/conditions will have to be determined empirically.
    4. Combine transfection reagent and dsRNA/plasmid DNA dilutions with a 1:1 ratio (e.g., 100 μL of diluted dsRNA is mixed with 100 μL of diluted transfection reagent) and incubate for 20 min at room temperature.
    5. Meanwhile, wash the wells with 1 mL/well of SFM, and then add 500 μL of SFM to each well.
    6. Slowly add the transfection reagent dsRNA (or plasmid DNA) mixture dropwise into each well.
    7. Incubate the transfection reagent with the cells for 5 h.
      1. For RNAi experiments involving the knockdown of transcripts encoded by a coinfecting virus (e.g., VACV), replace the transfection reagent after the 5-h transfection incubation period with virus inoculum containing VSV-LUC (with or without VACV or another coinfecting virus) (step 3). Subsequently, replace the virus inoculum containing VSV-LUC with complete growth media 2 hpi. LUC assays (step 4) can then be performed on extracted lysates at various time points to determine if the knockdown of coinfecting virus transcripts leads to a loss of VSV-LUC rescue.
      2. For RNAi experiments involving RNAi of L. dispar transcripts, replace the transfection mix with complete growth media and allow knockdown to ensue for 24 h prior to infection with VSV-LUC (step 4). LUC assays (step 4) can then be performed on extracted lysates at various time points to determine if the knockdown of L. dispar transcripts promotes VSV-LUC rescue.
      3. For experiments involving transfections of plasmid expression vectors expressing candidate immunomodulators, replace the transfection reagent and allow for protein expression for 24 h prior to the infection with VSV-LUC (step 4). LUC assays (step 4) can then be performed on extracted lysates at various time points to determine if the expression of candidate immunomodulatory proteins promotes VSV-LUC rescue.
        NOTE: The transfection conditions described here using 1 μg/well of plasmid DNA result in transfection efficiencies of 40–60%13.

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Results

As an example of live-cell imaging applications to monitor VSV rescue upon VACV coinfection, LD652 cells were plated in an 8-well chambered dish and then mock-infected or infected with VSV-DsRed (MOI = 1) in the presence or absence of VACV-FL-GFP (MOI = 25). Because VSV-DsRed expresses DsRed as a free protein and is not fused to structural VSV proteins (Figure 1A), it is only detected after VSV entry and gene expression initiates. All cells were then labeled ...

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Discussion

Here we have described simple fluorescence- and luminescence-based assays to screen for conditions that rescue VSV replication in restrictive lepidopteran cell cultures. The abortive infection of VSV in lepidopteran cells creates an excellent signal-to-noise ratio when assaying for VSV gene expression. For example, the LU signals detected in lysates from single VSV-LUC infections were ~1,000-fold higher than in mock-infected lysates, yet these signals only changed approximately twofold over a 72-h time course. In contras...

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Disclosures

The authors have nothing to disclose.

Acknowledgements

D.G. was supported by funding from the University of Texas Southwestern Medical Center's Endowed Scholars Program. The authors thank Michael Whitt (The University of Tennessee Health Science Center) and Sean Whelan (Harvard Medical School) for the provision of VSV-DsRed and VSV-LUC. The authors also thank Gary Luker (University of Michigan Medical School) for the kind gift of the VACV-FL-GFP strain.

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Materials

List of materials used in this article
NameCompanyCatalog NumberComments
6-well tissue culture platesCELLTREAT229106
24-well tissue culture platesCELLTREAT229124
10 cm tissue culture dishesCorningC430167
Grace’s Insect MediumSigmaG8142
EX-CELL 420Sigma14420C
Fetal Bovine Serum - OptimaAtlanta BiologicalsS12450
Growth medium1:1 mixture of Grace's Insect Medium and EX-Cell 420 Serum-Free Medium also containing 1% antibiotic-antimycotic solution and 10% Fetal bovine serum
Antibiotic-Antimycotic Solution (100×)SigmaA5955
Dulbecco’s Phosphate Buffered Saline (DPBS)SigmaD8662
Serum Free Media (SFM)Thermo Fisher10902096
Cytosine arabinosideSigmaC1768
Transfection reagentThermo Fisher10362100
Corning cellgro DMSO (Dimethyl Sulfoxide)Corning25950CQC
Reporter lysis buffer 5xPromegaE3971
Luciferase Assay ReagentPromegaE1483
96-Well MicroplatesCorning3915
Mouse anti-FLAG antibodyWako014-22383
Rabbit anti-firefly luciferase antibodyAbcamab21176
Mouse anti-actin antibodySigmaA2066
Mouse anti-VSV MN/AN/ADr. John Connor (Boston University)
Mouse anti-VACV I3LN/AN/ADr. David Evans (University of Alberta)
8-well Chambered dishLab-Tek II155409
Cell viability dyeThermo FisherC12881
FLUOstar microplate readerBMG LabtechFLUOstar
Confocal microscopeOlympusFV10i-LIV
Image analysis softwareOlympusv1.18cellSens software
Eppendorf 5702 ventilated centrifugeEppendorf22628102
Odyssey Fc Infrared Imaging SystemLi-COR BiosciencesOdyssey Fc
LD652 cellsN/AN/ADr. Basil Arif (Natural Resources Canada)
BSC-40 cellsATCCCRL-2761
BHK cellsATCCCCL-10
HeLa cellsATCCCCL-2
BSC-1 cellsATCCCCL-26
in vitro transcription and purification kitThermo FisherAM1626
PCR purification kitQiagen28104

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Vesicular Stomatitis VirusLepidopteran Insect CellsLuminescence AssaysFluorescence AssaysRNA Interference ScreeningGenome Editing ScreeningVirus Host Interactions
Arbovirus Infections As Screening Tools for the Identification of Viral Immunomodulators and Host Antiviral Factors
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