An Optimized Method for the Production Using PEI, Titration and Neutralization of SARS-CoV Spike Luciferase Pseudotypes

Materials and Reagents

1. MultiGuard Barrier pipette tips 1-20 and 1-200 μl (Sorenson BioScience, catalog number: 30550T )
   
2. Nunc^TM Cell-Culture Treated Multidishes (6-well) (Thermo Fisher Scientific, Thermo Scientific^TM, catalog number: 140675 )
   
3. Microcentrifuge tube Safe-Lock write-on graduated with lid latch 1.5 ml
   
4. Sterile syringes (10 ml), Generic
   
5. Millex-HA 0.45 µm filters (Merck, catalog number: SLHAM33SS )
   
6. 96-well white plate (Thermo Fisher Scientific, Thermo Scientific^TM, catalog number: 136101 )
   
7. HEK 293T/17 cells (ATCC, catalog number: CRL-11268 )
   
8. Huh7 cells (Cell Signaling Technology, catalog number: 300156 )
   
9. Plasmids
   1. Glycoprotein expression plasmid: pCAGGS-SARS-CoV spike
      
   2. Lentiviral vector expressing firefly luciferase: pCSFLW
      
   3. Second-generation lentiviral packaging construct plasmid: p8.91 (expresses gag, pol and rev)
   Note: Information on the plasmids above can be found in Temperton et al. (2005) and Carnell et al. (2015). Plasmids available from Viral Pseudotype Unit, University of Kent. n.temperton@kent.ac.uk
   
10. Dulbecco’s modified Eagle medium (DMEM) with GlutaMAX (Thermo Fisher Scientific, catalog number: 31966021 ) supplemented with 10% foetal bovine serum (FBS) (Pan-Biotech, catalog number: P40-37500 ) and 1% penicillin/streptomycin (P/S) (Pan Biotech, catalog number: P06-07100 )
    
11. Gibco Reduced Serum media Opti-MEM^® (Thermo Fisher Scientific, catalog number: 31985047 )
    
12. Branched Polyethyleneimine (PEI) solution at concentration of 1 mg/ml (Sigma-Aldrich, catalog number: 408727 ).
    Note: PEI is dissolved in dH₂O to a concentration of 1 mg/ml and the pH is adjusted to 7 using diluted (1:3) concentrated HCl.
    
13. Phosphate-buffered saline (PBS)
    
14. Trypsin-EDTA (0.05%), phenol red (Thermo Fisher Scientific, Gibco^TM, catalog number: 25300054 )
    
15. Positive control antibody (monoclonal/polyclonal or post-infection serum) that can neutralize the SARS pseudotype
    
16. Bright Glo^TM luciferase assay system (Promega, catalog number: E2650 )
    

Equipment

1. Class II biosafety cabinet (Thermo Fisher Scientific, Thermo Scientific^TM, model: MSC-Advantage^TM )
   
2. Water bath or incubator
   
3. Pipettes (Gilson, model: PIPETMAN^® Classic, P2 , P20 , P200 and P1000 )
   
4. Optional: BIO-RAD TC20^TM Automated Cell Counter (Bio-Rad Laboratories, catalog number: 1450102EDU )
   
5. Plate centrifuge (ELMI, model: SkyLine CM-6MT )
   
6. Glomax 96 luminometer (Promega, model: GloMax^® 96 )
   Note: This product has been discontinued.
   

Procedure

1. Transfection steps
   Note: All steps should be carried out in a class II biosafety cabinet to avoid contamination. Timeline: Transfection–24 h.
   1. 293T/17 cells should be subcultured into 6-well plates at a ratio that will deliver 70-90% confluence at the time of transfection. Typically seeding 4 x 10⁵ cells per well will achieve this level of confluency. Example is shown in Figure 2.
      
      
      Figure 2. Example of the confluency expected prior to transfection of HEK293T/17 cells
      
      
   Timeline: Day of transfection.
   2. DMEM/10% FBS/1% P/S and Opti-MEM^® should be pre-warmed to 37 °C using a water bath or an incubator.
      
   3. Prepare two labelled sterile 1.5 ml microcentrifuge tubes (tube 1 and tube 2) for each well of a 6-well plate which will be used for transfections.
      
   4. Add the following plasmid constructs for transfection to tube 1:
      pCAGGS-SARS-CoV spike: 450 ng
      p8.91-lentiviral vector: 500 ng
      pCSFLW: 750 ng
      
   5. Add 100 µl Opti-MEM^® to the plasmid DNA mix (tube 1).
      
   6. Add 100 µl Opti-MEM^® and 17.5 µl of 1 mg/ml PEI to tube 2.
      
   7. Incubation step: Mix both tubes by gently flicking and incubate for 5 min at room temperature (RT).
      
   8. After incubation, pipette the Opti-MEM^®/PEI solution from tube 2 into the Opti-MEM^®/DNA solution in tube 1.
      
   9. Incubation step: Incubate the tube at RT for 20 min whilst gently flicking the tube to mix every 3-4 min.
      
   10. Whilst the transfection mix is incubating, the culture media on the 293T/17 cells should be removed and 2 ml of fresh DMEM/10% FBS/1% P/S added per well. It is imperative at this point to add culture media slowly to one side of the well to avoid detaching the adherent cell monolayer.
       
   11. After 20 min incubation, pipette the DNA/Opti-MEM^®/PEI solution onto the 293T/17 cells by adding dropwise throughout the total surface area of the well. Swirl the 6-well plate(s) gently to ensure an even dispersal of reagent mix.
       
   12. Incubation step: Incubate the plate at 37 °C, 5% CO₂ overnight (o/n). In our hands incubation times of between 12-16 h result in equivalent final PV production RLU titres.
       
   Timeline: 12-16 h post transfection.
   13. Post o/n incubation the culture media on the cells should be carefully removed and 2 ml fresh DMEM/10% FBS/1% P/S added. Again, add media slowly to one side of the well to avoid cell detachment.
       
   14. Incubate the 6-well plates at 37 °C 5% CO₂ o/n for 32-36 h.
       
   Timeline: 44-52 h post transfection.
   15. Supernatant containing the viral pseudotype particles are harvested using a 2.5 ml sterile syringe and subsequently filtered into Falcon or microcentrifuge tubes via a syringe driven Millex HA-0.45 µm filter.
       
   16. Store all filtered supernatants at -80 °C until downstream use. It is recommended that supernatant is stored as aliquots to avoid multiple freeze-thaw cycles that may impact viral RLU titres.
       Note: Supernatant may be stored at 4 °C for up to one week with no detectable loss of RLU titre.
       
   17. Optional step: Additional culture media may be added to cells to allow a second harvest 18-24 h later by adding further DMEM/10% FBS/1% P/S. In this case, extreme care must be taken in initial PV collection (step A15) to avoid damage to the cell monolayer. We have observed that cells in poor health after first harvest result in significantly lower PV production RLU titres upon second harvest.
       
   Note: A control pseudotype virus can be created by following the steps outlined above but omitting the pCAGGS-SARS-CoV spike construct. This produces particles that do not express a viral surface glycoprotein (Delta Env control, Figure 3).
   
   

2. Titration steps (Figure 3)
   Note: Titration consists of transduction of reporter (in this case firefly luciferase) into target cells mediated by the viral glycoprotein expressed on the viral pseudotype (SARS-CoV spike). Controls for titration are provided via the inclusion of ‘cell only’ and ‘Delta Env’ columns. Control for transduction can be provided via a PV bearing the Vesicular stomatitis virus G protein (VSV-G) which utilizes a ubiquitous receptor which results in high RLU titres in all cell lines tested.
   
   
   Figure 3. 96-well plate set-up for pseudotype titration. Serial dilution step showing addition of 100 µl of pseudotype virus supernatant to each well of row A and dilution of 50 µl taken from this well to row B. This process is continued to end of plate (row H) at which point the final 50 µl is discarded. Delta Env control is indicated in red (column 11) and cell only control is indicated in green (column 12). One set of pipette tips can be used per dilution series (plate).
   
   
   1. In a 96-well white plate add 50 µl of DMEM/10% FBS/1% P/S to the entire column of ‘cell only’ control (see Figure 3 column 12).
      
   2. Add 50 µl of DMEM/10% FBS/1% P/S from row B to H that are to contain PV or Delta-Env control virus.
      
   3. Add 100 µl of SARS pseudotype virus supernatant to each well of row A (excluding control columns) and add 100 µl of Delta-Env to column 11 (see Figure 3).
      
   4. Remove 50 µl from row A virus-containing wells and perform two-fold serial dilutions down all the wells beneath it.
      
   5. With each dilution step use a pipette to mix 8 times by pipetting up and down and taking care not to produce air bubbles.
      
   6. After completing serial dilution the final 50 µl from the final well of each column should be discarded.
      Note: At this point each well should contain 50 µl of mixed DMEM and PV supernatant.
      
   7. Prepare a plate of susceptible target cells (Huh-7 for SARS PV), preferentially subcultured 1:4 48 h before:
      1. Remove culture media from plate.
         
      2. Wash the plate twice with 2 ml of PBS and discard.
         
      3. Add 2 ml of trypsin to the plate to detach cells.
         
      4. After cells have detached add 6 ml of DMEM/10% FBS/1% P/S to the plate to quench trypsin activity, and resuspend cells gently.
         
      5. Count cells using TC20^TM Automated Cell Counter or haemocytometer and add 1 x 10⁴ cells in a total volume of 50 µl to each well.
         
   8. Centrifuge plate for 1 min at 800 x g (Rcf) if there are visible droplets on the sides of the wells.
      
   9. Incubate the plate for 48 h at 37 °C 5% CO₂.
      
   10. Read plate using Bright Glo^TM luciferase assay system on a Glomax 96 luminometer (or equivalent).
   
   
3. Pseudotype based neutralisation assay (pMN)
   Note: pMN is the Inhibition of PV mediated transduction via an antibody (or inhibitor) directed against the SARS glycoprotein.
   1. In a 96-well white plate add 50 µl of DMEM/10% FBS/1% P/S to rows B to H, columns 1-12.
      
   2. Add known amount of antibody (example 5 µl HN and R sera in Figure 4) into wells of row A, columns 2-10 in a total volume of 100 µl DMEM/10% FBS/1% P/S. Add known amount (e.g., 5 µl) of positive and negative antisera into wells A11 and A12 as controls.
      
      
      Figure 4. Anti-SARS antibodies (post-infection sera HN and R) neutralization of SARS viral pseudotype entry into Huh7 cells. Two repeats are plotted for each serum sample.
      
      
   3. Remove 50 µl from row A wells and perform two-fold serial dilutions down all the wells beneath it.
      
   4. With each dilution step use a pipette to mix 15 times by pipetting up and down and taking care not to produce air bubbles.
      
   5. After completing serial dilution the final 50 µl from the final well of each column should be discarded.
      Note: At this point each well should contain 50 µl of mixed DMEM and serial dilutions of antibody/inhibitor.
      
   6. Centrifuge plate for 1 min at 800 x g (Rcf) to ensure no inhibitor or liquid is located on the walls of the well.
      
   7. Using data obtained from the titration, calculate the amount of DMEM required to dilute your SARS-PV to obtain 1 x 10⁶ RLU in 50 µl, with a total volume of 5 ml. For example with an RLU/ml of 1 x 10⁸, 1 ml of PV should be mixed with 4 ml of DMEM.
      
   8. Mix this diluted PV solution using the multichannel pipette, and aliquot 50 µl into each well on the plate, with the exception of wells A6-A12 (cell only control). A1-A6 will serve as virus only control.
      
   9. Centrifuge plate for 1 min at 800 x g (Rcf) to ensure no virus is left on the walls of the well.
      
   10. Incubate the plates for 1 h at 37 °C 5% CO₂, allowing time for the antibody/inhibitor to bind the SARS glycoprotein.
       
   11. Prepare a plate of susceptible target cells (Huh-7 for SARS PV), preferentially subcultured 1:4 48 h before:
       1. Remove culture media from plate.
          
       2. Wash the plate twice with 2 ml of PBS and discard.
          
       3. Add 2 ml of trypsin to the plate to detach cells.
          
       4. After cells have detached add 6 ml of DMEM/10% FBS/1% P/S to the plate to quench trypsin activity, and resuspend cells gently.
          
       5. Count cells using TC20^TM Automated Cell Counter or haemocytometer and add 1 x 10⁴ cells in a total volume of 50 µl to each well.
          
   12. Incubate the plate for 48 h at 37 °C 5% CO₂.
       
   13. Read plate using Bright Glo^TM luciferase assay system on a Glomax 96 luminometer (or equivalent).
       

Data analysis

1. RLU readings are multiplied to RLU/ml by the dilution factor of each well (20x, 40x, 80x, 160x, 320x, 640x, 1,280x, 2,560x). The mean of all 8 RLU/ml values is used as the final value reported for that column in the titration step. A linear relationship should be observed between RLU values and PV dilution, with values decreasing by 50% after each 1:2 dilution. Care should be taken to check this linear relationship before multiplication, as this inherently can lead to false positives despite lack of PV or working PV (Table 1).
   
   Table 1. Analysis of PV titration data. RLU values are multiplied to give an RLU/ml value (example highlighted in green) giving RLU/ml values for each of the dilution points. The mean/average is then calculated from all 8 dilution points. Care must be taken to observe a linear relationship between dilution factor (X factor) and RLU, or multiplication can lead to inflated RLU/ml values (example highlighted in yellow).
   
   
   
2. Protocol read-out and titration results (Figure 5).
   
   
   Figure 5. Results of pseudotype production RLU titres using optimized transfection protocol. SARS; PV with SARS-CoV Spike on surface, Cell; cell only control, Delta Env; PV with no surface glycoprotein, VSV-G; PV with VSV-G on surface.
   
   
3. The protocol outlined provides a rapid and consistent method for the generation of high-titre viral pseudotype particles expressing the SARS-CoV spike protein suitable for further downstream R&D applications. Efficient knock-down (neutralization) of SARS-CoV pseudotype virus entry using two post-infection sera (HN and R) demonstrates potential utility for vaccine immunogenicity and mAb/antiviral screening. The use of readily available reagents should facilitate increased reproducibility.

Acknowledgments

The authors acknowledge Dr Paul Chan (Faculty of Medicine, The Chinese University of Hong Kong) for the two positive post-infection control sera. This work was funded by the Medway School of Pharmacy, Kent, UK. This protocol was modified and improved from PMID: 15757556 and 26587388.

References

1. Carnell, G. W., Ferrara, F., Grehan, K., Thompson, C. P. and Temperton, N. J. (2015). Pseudotype-based neutralization assays for influenza: a systematic analysis. Front Immunol 6: 161.
   
2. Grehan, K., Ferrara, F. and Temperton, N. (2015). An optimised method for the production of MERS-CoV spike expressing viral pseudotypes. MethodsX 13(2): 379-384.
   
3. Temperton, N. J. (2009). The use of retroviral pseudotypes for the measurement of antibody responses to SARS coronavirus. In Lal, S. K. (Ed.). Molecular biology of the SARS-coronavirus. Springer.
   
4. Temperton, N. J., Chan, P. K., Simmons, G., Zambon, M. C., Tedder, R. S., Takeuchi, Y. and Weiss, R. A. (2005). Longitudinally profiling neutralizing antibody response to SARS coronavirus with pseudotypes. Emerg Infect Dis 11(3): 411-416.
   
5. Temperton, N. J., Wright, E. and Scott, S. D. (2015). Retroviral pseudotypes–from scientific tools to clinical utility. eLS 1-11.