Use of Crystal Violet to Improve Visual Cytopathic Effect-based Reading for Viral Titration using TCID50 Assays

Podsumowanie

This protocol shows an accurate and objective approach to visualize viral titrations using crystal violet, by comparing it with optical microscopy and immunocytochemical staining.

Streszczenie

Viral titration is a key assay for virology research. The detection of cytopathic effect (CPE) via TCID50 assays and plaque-forming units (PFU) assays are the two main methods to calculate the titer of a virus stock and are often based on microscopy detection or cell staining for visualization. In the case of TCID50 assay, objective visualization is commonly based on immunocytochemical (ICC) staining of intracellular virus to calculate titers combined with visual CPE detection via microscopy. However, ICC staining is costly and time consuming. In this study, we compared visual CPE observation via microscopy, ICC staining and crystal violet staining to determine the titers of two CPE-forming viruses, Influenza A virus (IAV) of swine origin and Porcine Reproductive and Respiratory Syndrome virus (PRRSV). We show that both crystal violet and ICC staining are more accurate than visual CPE detection, presenting nearly identical levels of precision on both IAV and PRRSV. For this reason, here we present crystal violet staining as a faster and more affordable way to determine viral titrations on a TCID50 assay for CPE-forming viruses titrated in cell lines.

Wprowadzenie

Viral titration via TCID50 assay is a commonly used technique in infectious disease research¹. Although variations on the math behind this method have been proposed over time^1,2,3,4, the currently applied methods of infection detection rely on visual confirmation through the presence of cytopathic effect (CPE) using microscopy⁵. To confirm CPE visualization more objectively on TCID50 assays, immunocytochemical (ICC) intracellular staining targeting the proteins of the virus is one of the most-commonly used methods⁶ as different viruses can produce varying forms of CPE. In our case, the cell morphological changes are similar when infected with both Influenza A virus (IAV) and Porcine Reproductive and Respiratory Syndrome Virus (PRRSV), where infected cells round up and detach from the plate. In the case of PRRSV, it causes a CPE known as "total destruction", where all cells end up detaching from the well. IAV on the other hand, can present both total destruction and an additional CPE known as "subtotal destruction" where a small number of cells do not detach after infection⁷. However, this technique is time consuming to perform and requires the use of relatively costly reagents. It is important to note that ICC does not label CPE, but rather the number of cells successfully infected by the virus. This implies that the cells that were successfully infected by the end of the incubation will be seen as positive even if the infection has not caused CPE yet, and thus, a higher percentage of ICC positive cells compared to CPE is expected. For that reason, in this study we describe a complementary method of visual detection of CPE in a TCID50 assay based on crystal violet, a chemical with a positive charge that attaches to cell membranes and is used to stain adherent cells. Crystal violet is often utilized in virology research to measure plaque-forming units, among others⁸.

In this study, we compare the sensitivity of non-stained microscopy CPE detection with crystal violet staining and immunocytochemical staining based on viral protein recognition, which is known to be more objective due to its high sensitivity. This study shows that both crystal violet and immunocytochemical staining are more accurate than visual microscopy-based CPE detection and can be used to objectively identify infected wells in a TCID50 titration. Given their ability to reach nearly identical level of accuracy on the cytopathic viruses tested in cell lines, crystal violet is presented as a faster and more affordable way to determine viral titrations on a TCID50 assay. The proposed method using crystal violet staining takes a total time of 40 min to perform, with 15 min for paraformaldehyde (PFA) incubation, 5 min for crystal violet incubation and a maximum of 15 min for material preparation, buffer washes, and drying. The immunocytochemistry protocol applied for comparison takes an average time of 4 h 30 min and was performed as previously described^9,10. The method proposed aims to help visualize a completed viral titration. Infection and incubation times can be performed with different layout depending on the virus. Here we tested two RNA viruses with cytopathic effect on cell lines.

Protokół

1. Titration protocol

NOTE: Use a cytopathic virus infecting adherent cells. For this demonstration, Influenza A Virus (IAV) of swine origin (A/California/07/2009/(H1N1)) and Porcine Reproductive and Respiratory Syndrome Virus (PRRSV) Type 2, strain NC 1-7-4 were used.

1. Titrate these viruses in 96 well plates for 7 days in a biosafety cabinet located in a Biosafety Level 2 (BSL-2) laboratory.
   1. To perform these titrations, seed 96 well plates with the required cell line. For PRRSV, use MA-104 cell line and for IAV use MDCK cell line. For the cell culture, use DMEM medium supplemented with 10% FBS, L-Glutamine and Penicillin-Streptomycin and grow the cells to confluency.
   2. Before infection, wash the cells using 200 µL of PBS.
   3. Dilute the virus stocks using 10 fold dilutions series by mixing 900 µL of media and 100 µL of virus. Make sure to properly vortex the tube to ensure proper mixing of the medium and virus and to avoid dilution errors.
   4. Mark the layout of the plate on the lid. Wash the wells with 1x phosphate saline buffer (PBS). Add 50 µL of the inoculum in the corresponding wells following previously described titration methods^2,3.
   5. Incubate at 37 °C in a 5% CO₂ incubator for 7 days.

2. Cytopathic effect (CPE) assessment via microscopy

1. After the 7-day incubation, wash all wells with 200 µL of 1x PBS twice.
2. Assess all wells of the plate under a light microscope to visually detect CPE. In the case of both PRRSV and IAV, their CPE consists of cell death and subsequent detachment from the plate, leading to monolayer disruption. However, other viruses may present different types of CPE.

3. Staining protocol

NOTE: Cytopathic effect (CPE) was assessed via crystal violet staining.

1. After the 7-day incubation, wash all the wells using 200 µL of 1x PBS twice.
2. Fix the cells by adding 50 µL/well of 4% paraformaldehyde (PFA) in 1x PBS and incubate for 15 min at room temperature (RT).
3. After incubation, wash the cells twice with 200 µL of 1x PBS. Then, add 50 µL/well of crystal violet diluted to 4% in water and incubate for 5 min at RT.
   NOTE: Crystal violet chemical stains the cells that remain attached to the plate at the time of fixation, leaving the sections of the well where the cells detached as unstained.
4. Finally, aspirate crystal violet from the wells and optionally leave the plates to air dry for 2-5 min at RT or wash the plate with 200 µL of water to remove excess stain prior to visualization.
5. Use previously described methods to mathematically calculate the titer. Here, Karber formula and Muench formula were applied for PRRSV and IAV, respectively^2,3. Details of these equations are presented in the representative result section.

4. Immunocytochemical (ICC) labeling

NOTE: Immunocytochemistry labeling for both viruses was performed following previously described methods^9,10,11.

1. After the 7-day incubation of the titration, fix the cells using PFA as described in step 3.2.
2. Wash the plates with a solution composed by 100 mL of 1 M Tris hydrochloride, 1 g of Saponin, and 8.5 g of NaCl in 900 mL of H₂O. Then, complete two additional washes with a mixture of 1x PBS and 5% Fetal Bovine Serum (FBS) and incubate with that Tris-Saponin-NaCl solution at Room temperature (RT) for 20 min.
3. Incubate all the wells with the primary antibody for 2 h at RT.
   NOTE: The volume of primary antibodies for each virus was 100 µL and was prepared using a 1:300 dilution of 2% FBS in 1x PBS.
4. Wash the cells twice with the Tris, Saponin, and NaCl solution prepared in step 4.2.
5. Incubate all the wells with the secondary antibody for 1 h at RT.
   NOTE: The volume of secondary antibody was 100 µL and was prepared using a 1:250 dilution of 2% FBS in 1x PBS.
6. Wash the cells with the Tris, Saponin, and NaCl dilution as described in step 4.2.
7. Aspirate the previous dilution and incubate the plates with 200 µL/well of aminoethyl carbazole (AEC) solution at a final dilution of 1:50 in water following the manufacturer's directions for 30 min at RT.
8. After incubation, discard the AEC solution and add 100 µL/well of 1x PBS for imaging via microscopy.
9. Mathematically derive the titer as described in step 3.5.

Wyniki

The equations used for mathematically calculating the titer were previously described^2,3.

Briefly, for PRRSV, we apply the Karber method:

Titer (TCID50) = 10 ^{T + 1.3} where:

In this formula d = negative log of the last dilution with complete positive virus response: five posi...

Dyskusje

Viral titrations are routinely used in virology research, with PFU detection and TCID50 assays most commonly used^1,2,3,4. Both methods rely on the detection of CPE in infected cells, and even though they can be visually assessed via microscopy, a staining is usually applied to obtain a more objective result or to even reduce incubation times. In the case of TCID50, one of the most comm...

Materiały

Name	Company	Catalog Number	Comments
96-well cell culture plates	Genesee	25-221	Clear, flat bottom
AEC solution	Thermo Fisher	1122
Crystal violet	Thermo Fisher	C581-25; C581-100
DMEM	Corning	10-017-CV
Fetal bovine serum	BioWest	S1480
Paraformaldehide	Thermo Fisher	J19943
Primary Influenza Antibody	Bioss	BS-0344R
Primary PRRSV Antibody	Bioss	BS-10043R
Saponin	Thermo Scientific	AAA1882014
Secondaty antibody	Invitrogen	31460
Tris Hydrochloride	Thermo Scientific	AM9856