Inactivation of viruses by delipidation

Abstract

The present invention relates to vaccines containing enveloped viruses whose envelopes have been depleted of lipids using methyl -cyclodextrin (MBCD). Delipidation of enveloped viruses in a two-step process abolishes the infectivity of those viruses, which allows delipidated viruses to be used safely in vaccines. Use of MBCD to deplete lipids such as cholesterol, in contrast to other methods, results in viruses with less than 20% of the cholesterol of an untreated virus but such delipidated viruses retain at least 85% of the protein content of an untreated virus. Delipidation by MBCD also preserves the immunogenicity of the viral proteins. The present invention of using MBCD treatment in a two-step process to delipidate enveloped virus represents a new alternative for generation of inactivated viruses which are incorporated into effective vaccines.

Claims

1. A method of preparing an inactivated enveloped virus comprising: mixing a solution comprising an enveloped virus with a first methyl -cyclodextrin (MBCD) solution to obtain a first mixture; incubating the first mixture for a first time period; mixing the enveloped virus from the first mixture with a second MBCD solution to obtain a second mixture; and incubating said second mixture for a second time period.

2. The method of claim 1 wherein a concentration of MBCD in the first mixture is at least 5 mM to about 100 mM.

3. The method of claim 1 wherein a concentration of MBCD in the first mixture is about 20 mM to about 40 mM.

4. The method of claim 1 wherein a concentration of MBCD in the second mixture is about 10 mM to about 100 mM.

5. The method of claim 1 wherein a concentration of MBCD in the second mixture is about 30 mM to about 50 mM.

6. The method of claim 1 wherein the first time period is about 15 minutes to about 24 hours.

7. The method of claim 1 wherein the first time period is about 4 hours to about 24 hours.

8. The method of claim 1 wherein the second time period is about 4 hours to about 48 hours.

9. The method of claim 1 wherein the second time period is about 24 hours, about 36 hours, or about 48 hours.

10. The method of claim 1 wherein a temperature of at least one of the first time period and the second time period is about 20 C. to about 25 C.

11. The method of claim 10 wherein the temperature is about 22 C. to about 24 C.

12. The method of claim 1 wherein the enveloped virus is isolated from the first mixture prior to the step of obtaining the second mixture.

13. The method of claim 1 wherein the enveloped virus is Porcine Reproductive and Respiratory Syndrome (PRRS) virus.

14. The method of claim 1 wherein at least one of the first time period and the second time period further comprises stirring of the first mixture and/or the second mixture.

15. A method of making a vaccine comprising: mixing a solution comprising an enveloped virus with a first methyl -cyclodextrin (MBCD) solution containing a concentration of MBCD of at least 5 mM to about 100 mM to obtain a first mixture; incubating the first mixture for a first time period of about 15 minutes to about 24 hours; mixing the enveloped virus from the first mixture with a second MBCD solution containing a concentration of MBCD of at least 10 mM to about 100 mM to obtain a second mixture; incubating said second mixture for a second time period of about 4 hours to about 48 hours; isolating the enveloped virus; and combining the isolated enveloped virus with at least one of: an adjuvant, a stabilizer, a preservative, and a blending diluent; wherein a temperature of at least one of the first time period and the second time period is about 20 C. to about 25 C.

16. The method of claim 15 wherein the enveloped virus is Porcine Reproductive and Respiratory Syndrome (PRRS) virus.

Description

EXAMPLE 1

(1) The human influenza virus H1N1 A/WSN/33 strain is delipidated using the procedures below. In the examples below, delipidation of the influenza virus (IFV) impairs infectivity. Because the delipidation method of the present invention preserves viral envelope proteins, animals inoculated with the delipidated IFV are expected to develop immunogenic responses that protect them from infection of a pathogenic dose of the virulent virus.

(2) Reagents:

(3) The human influenza virus H1N1 A/WSN/33 strain and its host cell line MDCK are available from Wuxi AppTec (Shanghai, China). Other reagents include MEM (Invitrogen, Carlsbad, Calif.); EMEM (Sigma-Aldrich, St. Louis, Mo.); ULTRAMDCK Serum-Free Medium (Lonza, Inc., Allendale, N.J.); fetal bovine serum (FBS; Invitrogen); 0.25% Trypsin-EDTA (ethylenediaminetetraacetic acid; Invitrogen); methyl--cyclodextrin (MBCD, Sigma-Aldrich); AMPLEX Red Cholesterol Assay Kit (Invitrogen); PIERCE BCA Protein Assay Kit (Rockford, Ill.); and MTT (Sigma-Aldrich).

(4) Propagation of H1N1 A/WSN/33 Influenza Virus in MDCK Cell Line:

(5) Cells are seeded with IFV according to the following procedure. Medium is removed from MDCK cells grown in T-75 flasks, the MDCK cell monolayers are rinsed with 5 mL of PBS at room temperature, and the cells are detached with 1.5 mL of trypsin/EDTA at 37 C. Cells are resuspended in 10 mL MEM containing 10% FBS and pelleted by centrifugation at 800 rpm for 5 minutes at 4 C. Cells are resuspended in MEM containing 10% FBS, and the cell density is adjusted to 2.510.sup.5 cell/mL. Fifteen mL of the MDCK cell suspension are seeded into each T-75 flask, and flasks are placed at 37 C. with 5% CO.sub.2 and incubated overnight.

(6) When the MDCK cells are more than 90% confluent, MEM is removed from the T75 flasks, 5 mL EMEM maintenance media containing 1% FBS and 1 g/mL trypsin is added, and the cells are infected with influenza virus at a Multiplicity of Infection (MOI) of 0.01. Flasks are incubated for 60-90 minutes at 37 C. with 5% CO.sub.2 and gently shaken every 15 minutes. Ten mL EMEM maintenance media containing 1% FBS and 1 g/mL trypsin are added to each flask, and the flasks are incubated for 48 hours at 37 C. and 5% CO.sub.2. When approximately 80% of the cytopathic effect (CPE) of the virus is achieved (generally after about 48 hours), the culture supernatants are harvested to obtain IFV.

(7) Purification and Titration of H1N1 A/WSN/33 IFV:

(8) IFV is purified according to the following procedure. The collected culture supernatant is centrifuged at 3,000 rpm for 20 minutes to remove cell debris, and the supernatant is collected. The supernatant is centrifuged at 38,000 rpm for 60 minutes to pellet the IFV. The IFV pellets are resuspended in an appropriate volume of physiologically buffered saline (PBS) to give a final titer of >1.010.sup.9 plaque-forming units/mL (PFU/mL). Aliquots of 100 L of this concentrated IFV stock solution are stored at 80 C.

(9) The IFV are titrated for in vitro infectivity using the following procedure. Using the cell culture and transfer procedures above, MDCK cells are suspended in MEM containing 10% FBS at a final density of 2.510.sup.5 cell/mL. Two mL of the MDCK cell suspension are added to each well of a 6-well plate, and the plates are incubated overnight at 37 C. with 5% CO.sub.2. Viral stocks are thawed in a 37 C. water bath, followed by centrifugation at 500g for 10 minutes at 4 C. A 1/10 dilution series of the stock solution is prepared and stored at 4 C. until use, using ULTRAMDCK Serum Free Medium and 2.5 g/mL trypsin as the dilution buffer.

(10) When the cells are at least 90% confluent, the medium is removed, and 0.5 mL dilution buffer and 0.5 mL of the virus dilution are added into each well. For the negative control, 1.0 mL dilution buffer is used. The plates are gently shaken immediately after each dilution is added. Plates are incubated for 60-90 minutes at 37 C. in 5% CO.sub.2 and rocked every 15 minutes. Each well of each 6-well plate is then overlaid with 3 mL of a 1:4 mixture of 2.5% low melting point agarose in PBS solution and dilution buffer at 37 C. The plates are incubated at room temperature for 15 minutes to allow the overlay mixture to solidify; then the plates are incubated at 37 C. with 5% CO.sub.2 for 3 days.

(11) Plaques are visualized using the following procedure. After the plaques are fully developed (3 days post-infection), 1 mL 4% paraformaldehyde is added, and the plates are incubated at room temperature for 1 hour. Solubilized agarose is discarded, and 0.1 mL of 0.5% crystal violet is added to each well. The number of plaques is counted after 15 minutes of incubation and converted to a titer based on the dilution factors.

(12) Delipidation:

(13) The delipidation process for the purified IFV is run in two parallel reactions: a solvent treatment comprising contacting the IFV with MBCD and a mock treatment, where the IFV are treated in the same manner, but without exposure to MBCD. The same titer of IFV is used in both the mock and solvent treatments. The IFV in the mock treatment can be titered to provide an indirect measure of the amount of delipidated IFV remaining after the solvent treatment.

(14) Solvent and mock treatments are conducted according to the following procedure. Aliquots (100 L) of the IFV stock prepared above (>1.010.sup.9 PFU/mL) are diluted into 900 L PBS in Eppendorf tubes to achieve a final titer of 1.0-5.010.sup.8 PFU/mL. MBCD in PBS is added to a final concentration of 50 mM for the solvent treatment, or an equal volume of PBS is added to the mock treatment. Eppendorf tubes are then capped and sealed with parafilm. All the samples are secured in an SHZ-82 constant-temperature orbital air-bath shaker (Changzhou Guohua Appliance Co., China) preheated to 37 C. The solvent- and mock-treated samples are spun at an orbital rotation speed of 220 rpm at 37 C. for either 30 minutes or 45 minutes. The samples are spun in a micro-centrifuge for 1 minute, and the supernatants containing IFV are transferred to ultracentrifuge tubes. Tubes are centrifuged at 200,000g (OPTIMA L-100XP; Beckman Coulter, Inc., Indianapolis Ind.) for 30 minutes to pellet the IFV, and the supernatants are discarded. The IFV pellets are resuspended in 1/10 of original volume added to each Eppendorf tube above and stored at 80 C. until further analyses.

(15) Characterization of Delipidated IFV:

(16) The protein content of the delipidated and mock-treated IFV is determined using a BCA assay (PIERCE BCA Protein Assay Kit) according to the manufacturer's instructions. The cholesterol content is determined using a cholesterol assay (AMPLEX Red Cholesterol Assay Kit, Life Technologies, Grand Island, N.Y.) performed according to manufacturer's instruction. In vitro infectivity is measured using the same titration procedures as set forth above.

(17) Hemagglutination (HA) activity is determined as follows. Freshly isolated chicken blood is washed three times with PBS, and the red blood cells (RBC) are resuspended in PBS at a concentration of 1%. Virus dilutions (50 L) are made in PBS and mixed with 50 L of the RBC suspension. The mixture is added to individual wells in a 96-well plate and the RBC are allowed to settle for 45 minutes. The wells are judged to be HA negative (i.e. no agglutination of RBC) if a dot or pellet of RBC is present, and a well is judged to be positive if a smooth suspension of RBC is present.

(18) Two batches of delipidated and mock-treated IFV samples are prepared according the procedure described above. The IFV stock used for the tests has a titer of 2.210.sup.10 PFU/mL. In the first batch (preparation A), the delipidation time is 30 minutes; in the second batch (preparation B), the delipidation time is 45 minutes. After ultracentrifugation, the delipidated and the mock-treated samples are characterized.

(19) In vitro infectivity shows that the PFU of the delipidated samples are about 1/7,000 of those of the corresponding mock samples. The infectivity results are shown in TABLE 1, below. Despite the difference in titers, the protein contents of the various samples are within 10% of each other. The protein content of the delipidated IFV from preparation A is 97% of the mock sample; and the protein content of the delipidated IFV from preparation B is 93% of the mock sample (see TABLE 1). It is also observed that after the treatment approximately 20% of starting material is recovered, as determined by the protein content. The percentage recovery based on protein content is comparable with the measured titers of the starting material (2.210.sup.9 PFU/mL) and the mock-treated samples (4.010.sup.8 PFU/mL, which is 18% of the starting titer). After the delipidation, less than 2% of cholesterol remains, compared to the mock treatment (see TABLE 1).

(20) TABLE-US-00001 TABLE 1 In vitro Protein Cholesterol infectivity content content Treatment (PFU/mL) (mg/mL) (g/mL) Preparation A Mock 4 10.sup.8 1.49 16.4 (30 minutes) Delipidated 6 10.sup.4 1.44 (97%) .sup.b 0.25 (1.5%) .sup.b (1/6667) .sup.a Preparation B Mock 2 10.sup.8 1.39 15.9 (45 minutes) Delipidated 3 10.sup.4 1.29 (93%) .sup.b 0.1 (0.6%) .sup.b (1/6667) .sup.a Notes: .sup.a fraction of infectivity, compared to the mock treatment; .sup.b percentage compared to the mock treatment.

(21) The mock treatment indicates that physical treatment (shaking and centrifugation) results in a loss of titer and protein. Delipidation by MBCD preferentially removes cholesterol, but not protein, from IFV. Further, IFV treated with MBCD has less in vitro infectivity, but infectivity was not completely abolished.

(22) Comparison of IFV Delipidation with Dilsopropyl Ether and MBCD:

(23) In addition to MBCD, another lipid solvent, diisopropyl ether (DIPE) is used to delipidate IFV. IFV samples of the same starting material are treated with different concentrations of DIPE or with 50 mM MBCD. Aliquots of the same quantity of IFV are treated with 2%, 4%, 8%, or 12% DIPE or 50 mM MBCD for 37 C. for 30 minutes. After a brief centrifugation at 2,000g for 3 minutes, visible solvent is removed, and the aqueous materials are left to dry in a fume hood for 20 minutes. The samples are then centrifuged at 200,000g for 30 minutes to recover virus particles. The in vitro infectivity, HA activities, protein content, and cholesterol content of the IFV are shown in TABLE 2.

(24) DIPE treatment at concentration up to 12% is not as effective in removing cholesterol as 50 mM MBCD under the same conditions. While 12% DIPE removes about 80% of cholesterol from IFV, 50 mM MBCD removes more than 98%. The IFV infectivities of these two treatments are reduced 32- and 2250-fold, respectively, compared to the mock-treatment, as determined by comparing the PFU/mL. The removal of cholesterol by both solvents is relatively specific, because protein content is reduced by less than 20% in the various treatments. Within the ability to quantify haemagglutination (HA) activity, 50 mM MBCD affects HA activity by the same degree as 2%-8% DIPE.

(25) TABLE-US-00002 TABLE 2 HA Protein Cholesterol Treatment PFU/mL units (mg/mL) (g/mL) Mock 9.0 10.sup.8 64 0.39 8.26 2% DIPE 1.2 10.sup.8 32 0.39 (100%) .sup.a 6.61 (80.0%) .sup.a 4% DIPE 1.4 10.sup.8 32 0.32 (82%) .sup.a 4.88 (59.1%) .sup.a 8% DIPE 9.0 10.sup.7 32 0.36 (92%) .sup.a 3.47 (42.0%) .sup.a 12% DIPE 2.8 10.sup.7 16 0.33 (85%) .sup.a 1.81 (21.9%) .sup.a 50 mM MBCD 4.0 10.sup.5 32 0.33 (85%) .sup.a 0.14 (1.7%) .sup.a Note: .sup.a percentage compared to the mock treatment.

(26) Treatment with Solvents for 45 Minutes:

(27) The treatments above are repeated, except that the MBCD treatment duration is extended from 30 to 45 minutes. The results are shown below in TABLE 3.

(28) TABLE-US-00003 TABLE 3 HA Protein Cholesterol Treatment PFU/mL units (mg/mL) (g/mL) Mock .sup.a 1.2 10.sup.7 32 0.42 6.16 10% DIPE .sup.a 1.0 10.sup.5 16 0.21 (50%) .sup.c 1.32 (21.4%) .sup.c 50 mM 1.0 10.sup.3 32 0.39 (94%) .sup.c 0.15 (2.5%) .sup.c MBCD.sup.b Note: .sup.a end-over-end rotation at 37 C. for 30 minutes. .sup.bend-over-end rotation at 37 C. for 45 minutes. .sup.c percentage compared to the mock treatment.

(29) As with a 30 minute treatment, a 45 minute treatment with 50 mM MBCD removes about 97% of cholesterol for IFV and renders the virus over 10,000-fold less infectious in vitro, compared to the mock treatment. In contrast, 10% DIPE (30 minute treatment) is less effective in removing cholesterol (about 80%) and results in about a 120-fold decrease in infectivity in vitro. The HA activity is not measurably affected by MBCD, while it was measurably reduced by 10% DIPE. The protein content is reduced to 50% after 10% DIPE treatment, compared to a 6% reduction by 50 mM MBCD.

(30) The two sets of experiments presented herein demonstrate that 50 mM MBCD selectively removes cholesterol and renders the delipidated IFV less infectious while maintaining most of the proteins. However, neither of these treatments was able to completely abolish infectivity and thus completely inactivate the virus, so further optimization of the procedure is required to completely inactivate influenza viruses. The further optimization could include, without limitation, increasing time of MBCD treatment and treating the virus a second time period with MBCD.

EXAMPLE 2

(31) Treatment of PRRSV with MBCD selectively removes cholesterol, decreases viral infectivity, and maintains most of the viral protein content.

(32) Reagents:

(33) The PRRSV virus strain used in this example is RESP (Jiangsu Academy of Agriculture Sciences, China). The host cell used is Marc-145 (Wuxi AppTec, Shanghai, China). Other reagents used are the same as in Example 1, above, except for DMEM (Invitrogen), which is used when culturing Marc-145 cells.

(34) Propagation of PRRSV in Marc-145 Cells:

(35) Cells are seeded with PRRSV according to the following procedure. Medium is removed from Marc-145 cells grown in T-75 flasks, the Marc-145 cell monolayers are rinsed with 5 mL of PBS at room temperature, and the cells are detached with 1.5 mL of trypsin/EDTA at 37 C. Cells are resuspended in 10 mL DMEM medium containing 10% FBS and pelleted by centrifugation at 800 rpm for 5 minutes at 4 C. Cells are resuspended in DMEM medium containing 10% FBS, and the cell density is adjusted to 2.510.sup.5 cell/mL. Fifteen mL of the Marc-145 cell suspension are seeded into each T75 flask, and flasks are placed at 37 C. with 5% CO.sub.2 and incubated overnight.

(36) When the Marc-145 cells are more than 90% confluent, DMEM is removed from the T-75 flasks, 5 mL EMEM maintenance media containing 2% FBS is added, and the cells are infected with PRRSV at a MOI of 0.1. Flasks are incubated for 60-90 minutes at 37 C. with 5% CO.sub.2 and gently shaken every 15 minutes. Ten mL EMEM maintenance media containing 2% FBS are added to each flask, and the flasks are incubated for 96 hours at 37 C. and 5% CO.sub.2. When 80% of CPE is achieved (generally 96 hours), the culture supernatants are harvested to obtain PRRSV.

(37) Purification of PRRSV:

(38) PRRSV is purified according to the following procedure. The collected culture supernatant is centrifuged at 3,000 rpm for 20 minutes to remove cell debris, and the supernatant is collected. The supernatant is centrifuged at 100,000g for 60 minutes to pellet the PRRSV. The PRRSV pellets are resuspended in an appropriate volume of physiologically buffered saline (PBS) to a titer of about 110.sup.9 PFU/mL. Aliquots of 100 L concentrated PRRSV are stored at 80 C.

(39) The PRRSV are titrated for in vitro infectivity using the following procedure. Using the cell culture and transfer procedures above, Marc-145 cells are suspended in DMEM containing 10% FBS at a final density of 1.510.sup.5 cell/mL. Two mL of the Marc-145 cell suspension are added to each well of a 6-well plate, and the plates are incubated overnight at 37 C. with 5% CO.sub.2. Virus samples are thawed in a 37 C. water bath, followed by centrifugation at 500g for 10 minutes at 4 C. A 1/10 dilution series of viruses is prepared and stored at 4 C. until use, using EMEM as the dilution buffer.

(40) When the Marc-145 cells are at least 90% confluent, the medium is removed, and 0.5 mL dilution buffer and 0.5 mL of the virus dilution are added into each well. For the negative control, 1.0 mL dilution buffer is used. The plates are gently shaken immediately after each dilution is added. Plates are incubated for 60-90 minutes at 37 C. in 5% CO.sub.2 and rocked every 15 minutes. Each well of each 6-well plate is then overlaid with 3 mL of a 1:4 mixture of 2.5% low melting point agarose in PBS solution and dilution buffer at 37 C. The plates are incubated at room temperature for 15 minutes to allow the overlay mixture to solidify, and then the plates are incubated at 37 C. with 5% CO.sub.2 for 96 hours.

(41) Plaques are visualized using the following procedure. After the plaques are fully developed (96 hours post-infection), 1 mL 4% paraformaldehyde is added, and the plates are incubated at room temperature for 1 hour. Solubilized agarose is discarded, and 0.5 mL of 0.5% crystal violet is added to each well. The number of plaques is counted after 15 minutes of incubation with the crystal violet and converted to a titer based on the dilution factors.

(42) In Vitro Propagation of PRRSV:

(43) A PRRSV titer greater than 110.sup.7 PFU/mL is preferred for the protein and cholesterol assay. The propagation of PRRSV-RESP strain in Marc-145 cells yields a concentrated virus sample having a titer >110.sup.8 PFU/mL.

(44) Delipidation of PRRSV:

(45) Solvent and mock treatments are conducted according to the following procedure. One hundred L aliquots of the concentrated PRRSV stock at about 110.sup.9 PFU/mL are diluted into 900 L PBS in Eppendorf tubes to achieve a final titer of 1.0-5.010.sup.8 PFU/mL. MBCD in PBS is added to the desired concentration for the solvent treatment, or an equal volume of PBS is added for the mock treatment. Eppendorf tubes are then capped and sealed with parafilm. All the samples are secured in an SHZ-82 constant-temperature orbital air-bath shaker (Changzhou Guohua Appliance Co., China) preheated to 37 C. The solvent- and mock-treated samples are spun at an orbital rotation speed of 220 rpm at 37 C. for the desired time. The respective samples are spun in a micro-centrifuge for 1 minute, and the supernatants containing IFV are transferred to ultracentrifuge tubes. Tubes are centrifuged at 100,000g (OPTIMA L-100XP centrifuge; Beckman Coulter, Inc., Indianapolis Ind.) for 30 minutes to pellet the PRRSV, and the supernatants are discarded. The PRRSV pellets are resuspended in 200 L PBS and stored at 80 C. until further analyses.

(46) Characterization of Delipidated PRRSV:

(47) The protein content of the delipidated and mock-treated PRRSV is determined using a BCA assay (PIERCE BCA Protein Assay Kit) according to the manufacturer's instructions. The cholesterol content also is determined using a cholesterol assay (Amplex Red Cholesterol Assay Kit, Life Technologies, Grand Island, N.Y.) performed according to manufacturer's instruction. In vitro infectivity is measured using the same procedures as set forth above.

(48) Concentration Dependence of MBCD:

(49) In the first delipidation experiment, PRRSV is delipidated with 5, 10, 20, 30, and 50 mM MBCD for 60 minutes at 37 C. After ultracentrifugation, the mock-treated and delipidated samples are tested for in vitro infectivity in the Marc-145 cells, and protein and cholesterol contents are determined, using the procedures set forth above. The infectivity, protein content, and cholesterol content of the delipidated PRRSV are shown in TABLE 4.

(50) TABLE-US-00004 TABLE 4 In Vitro Protein Cholesterol Infectivity Content Content Treatment (PFU/mL) (mg/mL) (g/mL) Mock 1.6 10.sup.7 4.46 11.64 5 mM MBCD 1.4 10.sup.7 3.94 (88%) .sup.a 9.82 (84%) .sup.a 10 mM MBCD 7.0 10.sup.6 4.00 (89%) .sup.a 4.66 (40%) .sup.a 20 mM MBCD 2.8 10.sup.6 4.05 (90%) .sup.a 4.46 (38%) .sup.a 30 mM MBCD 1.2 10.sup.5 4.36 (97%) .sup.a 4.00 (34%) .sup.a 50 mM MBCD 4.2 10.sup.4 4.40 (98%) .sup.a 3.29 (28%) .sup.a Note: .sup.a percentage compared to the mock treatment.

(51) The titer of the starting PRRSV-RESP stock is 1.010.sup.8 PFU/mL, of which 0.1 mL is mixed with 0.9 mL PBS, together with appropriate amount of MBCD. After orbital shaking at 220 RPM for 60 min at 37 C., the virus samples are pelleted by ultracentrifugation and suspended in a final volume of 0.2 mL of PBS. The titer of the mock-treated sample is 1.610.sup.7 PFU/mL (TABLE 4), suggesting that more than 30% of viral activity is recovered after the mock treatment. MBCD treatment reduces the infectivity and cholesterol content in a largely concentration-dependent manner, while the 88%-98% of the total protein content is recovered at all MBCD concentrations (see TABLE 4). After treatment with 50 mM MBCD, the delipidated PRRSV retains about 28% of starting amount of cholesterol compared to the mock sample, and the PRRSV infectivity is reduced by about 380-fold, but again is not completely abolished.

(52) Blind Passage Assay of a Dellpidated PRRSV Sample:

(53) The titer of one of the delipidated PRRSV samples (100 mM MBCD for 90 minutes) is under the limit of detection. This raises the question whether there are any infectious virus particles in the sample. To address the question of whether such infectious virus particles are present, a new sample is delipidated with 100 mM MBCD for 90 minutes and is subjected to the blind passage assay described below. While a control PRRSV-RESP sample has a titer of 1.610.sup.6 PFU/mL, no plaques are detected by the blind passage assay from the PRRSV sample delipidated with 100 mM MBCD for 90 minutes. Delipidation with 100 mM MBCD for 90 minutes likely inactivates PRRSV-RESP completely.

(54) The blind passage assay is conducted according to the following procedure. One hundred L of the delipidated PRRSV sample is transferred to each well of a 6-well plate containing the Marc-145 cells, prepared by the procedure above. The plates are incubated for 4 days at 37 C. in 5% CO.sub.2. Three consecutive freeze-thaw cycles are preformed to lyse the cells, and the supernatants containing PRRSV are harvested and centrifuged at 800 rpm for 5 min at 4 C. Four hundred L of the supernatant are transferred to a flask of Marc-145 cells. The flasks are incubated for 4 days at 37 C. and 5% CO.sub.2. The freeze-thaw cycles are repeated, and the supernatants are again harvested, centrifuged, and transferred to a flask of Marc-145 cells as before. The freeze-thaw cycles are repeated once more, the supernatants are again harvested and centrifuged, and the supernatants containing the PRRSV are frozen at 80 C. until further use. The PRRSV titer of the final, harvested samples is determined using Marc-145 cells as above.

EXAMPLE 3

(55) The objective of this study was to determine the time dependency for the inactivation of PRRSV strain ND 99-14 through a delipidation method that utilizes methyl cyclodextrin (MBCD). MBCD was purchased in powder form from CTD, Inc. (Alachua, Fla.). A 300 mM stock solution was prepared by adding 1000 mL of water to 280 g of MBCD to generate the stock solution.

(56) Virus Delipidation:

(57) Inactivation kinetics experiments were conducted using PRRSV strain ND99-14, described in application U.S. Ser. No. 62/296,658, filed Feb. 18, 2016. In general the method involves the addition of MBCD at a final concentration of 40 mM and a total of 72 hours of incubation time at room temperature with constant mixing. Addition of MBCD occurs in 2 steps, 20 mM to start the inactivation process, an additional 20 mM of MBCD is added 24 hour later and incubated an additional 48 hours at room temperature with constant mixing. Room temperature is between about 20 C. and about 25 C., and optimally between about 22 C. and about 24 C.

(58) A 300 mM stock of MBCD solution was initially added to the virus to a final concentration of 20 mM by adding 567 mL of MBCD solution to 8.5 L of virus stock. The virus was incubated for 24 hours at room temperature with mixing at 50 rpm. 30 mL of virus was collected at 0 hours, 15 minutes, 4, 8, 12, 16, 20 and 24 hours post MBCD addition. Aliquots for each time point were stored at 4 C. and 70 C. until further use.

(59) After the 24 hour sample was collected, virus was transferred to a new container. An additional 20 mM of MBCD was added (650 mL MBCD added to 9.75 L of virus stock) to arrive at a final concentration of 40 mM. The virus was incubated an additional 48 hours at room temperature. 30 mL of virus was collected at 30, 36, 42, 48, 60, 72, 84 and 96 hours following the first MBCD addition. Aliquots for each time point were stored at 4 C. and 70 C. until further use.

(60) Virus Measurement:

(61) Ten-fold serial dilutions (10.sup.1-10.sup.9) of mock inactivated and inactivated virus were added to MARC145 cells cultured on 96 well plates. The plates were incubated at 37 C. and 5% CO.sub.2 for 96 hours to allow live virus to infect cells. Virus replication was determined by observation of cytopathic effect (CPE) due to virus infection of the MARC145 cells. Each well containing a virus dilution was scored either positive or negative with regards to CPE and the resulting numbers of positive or negatice wells for each dilution were used to determine the TCID.sub.50/mL using the Reed-Muench TCID.sub.50 calculation. The mock inactivated virus was treated to the same media and temperature conditions as the inactivated virus without the addition of the inactivation agent.

(62) Three consecutive blind passages of mock inactivated and inactivated virus as well as a media only control were performed using MARC145 cells cultured on T-225 flasks. The inactivated and control samples were added to a 2 day culture of MARC145 cells and incubated for 7 days at 37 C. and 5% CO.sub.2 (3 mL of sample into 27 mL of media). The flasks were visually inspected for the presence of CPE. Each flask was scored either positive (+) or negative () with regards to CPE and recorded. The supernatants from the flasks were harvested and added to a new set of T-225 flasks containing 2 day cultures of MARC-145 cells and incubated for 7 days at 37 C. and 5% CO.sub.2. The above process was repeated twice to obtain CPE observations for 3 consecutive virus passages.

(63) PRRS virus titers were determined for all time points collected during the 96 hour incubation period using samples stored at 2 different temperatures as shown. 0 indicates the titer was undetectable or undetermined by the PRRS Live VirusTCID.sub.50 determination assay. The results presented in Table 5 demonstrated that 40 mM added in a 2 step process was able to inactivate PRRS virus with a titer of at least 8 log.sub.10 TCID.sub.50/mL. Higher titers demonstrated incomplete inactivation with 20 mM MBCD, but virus was undetectable after the second addition of MBCD to bring up the concentration to 40 mM. The results also showed that time was less of a contributing factor for inactivation. Longer incubation times at a given concentration of MBCD did not increase the level of inactivation. A 20 mM concentration of MBCD reduced live virus by approximately 2.5 logs after 15 minutes of incubation and the level of live virus detected remained constant for 24 hours. A second addition of 20 mM MBCD at 24 hours of incubation inactivated the virus to undetectable levels by the next time point sample collected (30 hours). Differences in viability were also observed in the presence of 40 mM MBCD at different storage temperatures. Time point samples with detectable live virus had at least 100 fold less virus when stored at 70 C. versus 4 C.

(64) TABLE-US-00005 TABLE 5 Samples stored Samples stored Hour at 4 C. at 70 C. 0.25 5.8.sup.a 3.3 4 5.8 nd 8 5.9 2.8 12 5.6 3.2 16 5.6 3.2 20 5.6 3.4 24 5.6 3.6 30 0 0 36 0 0 42 0 0 48 0 0 56 0 0 64 0 0 72 0 0 84 0 0 96 0 0 .sup.aLog.sub.10 TCID.sub.50/mL

EXAMPLE 4

(65) The objective of this study was to evaluate the safety and efficacy of experimental inactivated PRRSV vaccines in a vaccination-challenge study. Vaccines were evaluated on their ability to reduce lung lesions and viremia levels. Vaccine characteristics of interest included storage temperature, number of doses (1 vs 2) and adjuvant addition. The study was conducted in BSL-2 facilities at Veterinary Resources, Inc., Cambridge, Iowa. Laboratory assays were conducted at the Iowa State University Veterinary Diagnostic Laboratory, Ames, Iowa and South Dakota State University Veterinary Diagnostic Laboratory, Brookings, S. Dak. Sixty (60) clinically healthy, weaned pigs about 3 weeks of age that were seronegative to PRRSV were enrolled in the study. Pigs were ranked by decreasing body weight and 10 blocks of 6 animals each were formed. Pigs were randomly assigned to one of six treatment groups (10 pigs per group). Treatment groups included a non-vaccinated control group (T01) and five groups vaccinated with experimental inactivated PRRSV vaccines. The vaccines were inactivated by means of delipidation using methyl-beta-cyclodextrin (MBCD). Groups T02 and T03 vaccines contained no adjuvant and were stored at either 2-8 C. (T02) or 20 C. (T03). Groups T04 and T05 vaccines contained MONTANIDE Gel 01 adjuvant (Seppic) and were administered either once (T04) or twice (705). Group T06 vaccine contained MONTANIDE IMS 1313 VG N PR adjuvant (Seppic) and was given twice.

(66) Pigs were fed standard commercial medicated (CTC/DENAGARD) starter diets (NRC, 2012) ad libitum via top-load feeders. Pigs had access to clean drinking water ad libitum via nipple waterers. All study pigs were treated with EXCEDE 10 days post-vaccination (DPV). In addition, all pigs were treated with a single dose of VITAL E-500 and another treatment of EXCEDE 21 DPV. All medications were administered according to label directions.

(67) Vaccines

(68) PRRSV strain SD 11-21 (passage level 84) was used as the antigen in the current study. SD11-21 is a field strain that was adapted for growth in cell culture through 84 passages through the MARC-145 cell line as well as three rounds of plaque purification and sucrose gradient centrifugation, as described in application U.S. Ser. No. 62/296,658, filed Feb. 18, 2016. Passage 85 (p85) was produced in a 5 L BioBLU single use bioreactor (Eppendorf, Hamburg, Germany) seeded with MARC-145 attached to HILLEX II microcarriers (Pall Corporation, Port Washington, N.Y.) in OPTI-MEM media (Life Technologies, Grand Island, N.Y.) supplemented with 2% Fetal Bovine Serum (Sigma, St. Louis, Mo.) and 50 ug/mL of Gentamycin (Life Technologies, Grand Island, N.Y.). The titer of the harvested p85 virus stock was 7.3 log.sub.10TCID.sub.50 as determined by the virus titration assay described in Example 3.

(69) In a 1 L bottle, 19.7 mL of the 300 mM MBCD (Sigma, St. Louis, Mo.) stock solution was added to 300 mL of the SD 11-21 virus stock. The mixture was incubated at room temperature with constant mixing at 50 rpm for 24 hours. Following the 24 hour incubation an additional 9.8 mL of MBCD stock solution was added and the mixture incubated at room temperature with constant mixing at 50 rpm for an additional 24 hours. The final concentration of MBCD was 30 mM with a total of 48 hours of room temperature incubation. A mock inactivated virus stock was also prepared adding an equivalent amount of water in place of MBCD, incubation times and mixing were identical to the inactivated virus. The mock inactivated virus was used as a control for virus measurement assays. After treatment, the mock inactivated virus was present at 6.5 log.sub.10TCID.sub.50/mL, whereas no live virus was detected in MBCD-inactivated virus solution.

(70) The virus stocks were stored at 4 C. until further use.

(71) Vaccines were formulated to include a stabilizer and a preservative. OPTI-MEM I Reduced Serum Medium was used as the blending diluent. Adjuvants included commercial formulations of MONTANIDE Gel 01 (Seppic) and MONTANIDE 1313 VG N PR (Seppic). The control product was a commercial preparation (Corning Cellgro, Mediatech Inc. of phosphate buffered saline (PBS). Vaccines without adjuvant contained delipated virus, 25% Stabililzer B, 25 g/ml gentamycin as a preservative, and blending diluent. Vaccines with adjuvant contained 20% of the indicated adjuvant. Stabilizer B contained 2.5% D-mannitol (Sigma), 1.2% gelatin type A (Fisher, Pittsburgh, Pa.), 1% NZ amine casein hydrosylate (Sigma), 5% sucrose (Sigma), and 6.2% trehalose (Fisher) in ultra-pure water (Life Technologies) at pH 7.0-7.2.

(72) Vaccination and Challenge

(73) Each of the 60 pigs enrolled in the study were vaccinated on Day 35 pre-challenge. Pigs in T01-T05 were injected with their assigned treatment as a 1.0 mL intramuscular dose in the right side of the neck. Pigs in T06 were injected with 1.5 mL. Pigs in T01-T03 and T05 and T06 were vaccinated again 14 days later (21 days pre-challenge) in the same manner. On 0 DPC, the challenge material was prepared by thawing the frozen aliquots of strain NADC-20 immediately prior to challenge. Titer was determined to be 1.2610.sup.5.0 TCID.sub.50/ml after dilution in Minimum Essential Medium Eagle with Earle's salts and L-glutamine (MEM) from Mediatech, Inc. Each pig was physically restrained for the challenge with the head oriented upwards. A 3 mL non-luer lock syringe was used to deliver a 2 mL dose intranasally, with approximately 1 mL per nostril.

(74) Results

(75) At 14 DPC, animals were humanely euthanized per site procedures. Lungs were excised and scored by the Study Investigator who was blinded to treatment. Each of the seven pulmonary lobes was examined both visually and by palpation for gross characteristic lesions attributed to PRRSV. The amount of lesion/consolidation in each pulmonary lobe was scored as an actual value between 0 and 100% of the lobe. The score for each lobe was entered into a weighted formula to calculate the percentage of lung with lesions. Percentage of total lung with lesions was calculated according to the following formula: Percentage of total lung with lesions={(0.10left apical)+(0.10left cardiac)+(0.25left diaphragmatic)+(0.10right apical)+(0.10right cardiac)+(0.25right diaphragmatic)+(0.10intermediate)}.

(76) In addition, the percentages of total lung with lesions were transformed using the arcsine square root, prior to further analysis. The transformed data were analyzed by a mixed linear model that included the fixed effect of treatment (the MIXED procedure in SAS) and the random effect of block.

(77) Results of the statistical analysis of the lung lesion scores are summarized in Table 6. The main effect of treatment was statistically significant (P=0.0003). Comparisons with the control group (T01) indicated a significantly lower (P<0.05) percent lung involvement in the Gel 01 adjuvanted groups (T04 and T05). Also, non-adjuvanted vaccine administered twice and stored at 2-8 C. (T02) resulted in significantly lower (P<0.05) lesion scores than a similar group treated with a vaccine stored at 20 C. (T03).

(78) TABLE-US-00006 TABLE 6 Mean Lung Lesion Score - Arcsine Transformed Percent Lung Involvement (main effect of treatment: P = 0.0003) Standard Treatment Group Estintate.sup.1 Error Mean.sup.2 T01 (Placebo) 0.4760 0.1085 20.99 T02 (no adjuvant, 2 doses) 0.2761 0.1105 7.43 T03 (Inactivated PRRS 0.6338 0.1085 35.07 stored at 70 C.) T04 (Gel 01 adjuvant, single dose) 0.1678 0.1085 2.79* T05 (Gel 01 adjuvant, 2 doses) 0.2128 0.1141 4.46* T06 (1313 adjuvant, 2 doses) 0.3418 0.1085 11.24 T02 v T03 P-value = 0.0013 T04 v T05 P-value = 0.6692 T02 v T05 P-value = 0.5594 *T01 versus T04 and T05 significantly different at P < 0.05 .sup.1Untransformed means .sup.2Back transformed means

(79) Blood samples for determination of viremia levels were collected on Days 35 and 21 pre-challenge. Additionally, blood samples for determination of viremia levels were collected at 0, 3, 7, 10 and 14 DPC. Samples were tested for the presence of PRRS viral nucleic acids using qRT-PCR techniques

(80) Serology and viremia data were transformed to log.sub.10 units prior to analyses, given a non-normal distribution. The transformed values were analyzed using a repeated measures mixed model (the MIXED procedure). The statistical model included treatment, time, and treatment by time interaction as fixed effects. Block was included in the model as a random effect. If the treatment by time interaction was significant (P<0.05), the effects of within time treatment were evaluated. If the interaction was not significant, the main effect of treatment was assessed. Least squares means (back-transformed) and standard errors are presented.

(81) The analysis of the viremia levels is summarized in Table 7. Viremia was not observed in any pig prior to PRRSV challenge confirming the vaccine virus was inactivated. Time points prior to challenge were excluded from the statistical analysis. Post-challenge, the treatment by day interaction was not significant (P=0.0974), thus the main effect of treatment was evaluated. The effect of treatment was significant (P=0.0107). Comparisons with the control group (T01) indicated significantly lower (P<0.05) levels in all vaccine groups that were adjuvanted (T04, T05 and T06). None of the pre-planned contrasts were statistically significant.

(82) TABLE-US-00007 TABLE 7 Viremia - Geometric Means of PRRSV Genomic Copies/mL on 3, 7, 10 and 14 DPC (log.sub.10 transformed) (main effect of treatment: P = 0.011; treatment by day interaction: P = 0.097) Standard Geometric Treatment Estimate.sup.1 Error Mean.sup.2 T01 (Placebo) 6.2508 0.1149 1781506 T02 (no adjuvant, 2 doses) 5.9855 0.1211 967187 T03 (Inactivated PRRS stored 6.2907 0.1149 1953141 at 70 C.) T04 (Gel 01 adjuvant, single dose) 5.8753 0.1149 750379* T05 (Gel 01 adjuvant, 2 doses) 5.7720 0.1211 591543* T06 (1313 adjuvant, 2 doses) 5.8878 0.1149 772251* T02 vs T03 P-value = 0.0733 T04 vs T05 P-value = 0.5389 T02 vs T05 P-value = 0.2182 *T01 versus T04, T05, T06, significantly different at P < 0.05 .sup.1Untransformed log10 means .sup.2Back transformed means

CONCLUSIONS

(83) Vaccinating pigs with one or two doses of the MBCD inactivated, Gel 01 adjuvanted vaccine was effective in significantly reducing both lung lesions and viremia levels compared to the control group. Lung lesions were numerically reduced in pigs vaccinated with other MBCD inactivated vaccines (T02 and T06) stored at 2-8 C. Due to variation in lung lesion scores, these differences were not significant at the P<0.05 level. All MBCD vaccines that contained an adjuvant (MONTANIDE Gel 01 or 1313) significantly reduced viremia. In future studies, a larger sample size may be needed when the NADC-20 strain is utilized as the challenge material in order to detect meaningful biological differences in both lung lesions and viremia.

(84) Storage temperature appears to have an impact on vaccine efficacy. Storing the vaccine at 20 C. had a negative effect on vaccine efficacy compared to vaccine stored at 2-8 C.

(85) Adding an additional vaccination 14 days following the first did not further improve vaccine efficacy in pigs vaccinated with the MBCD inactivated vaccine adjuvanted with Gel 01.

(86) The inclusion of the Gel 01 adjuvant to the MBCD inactivated vaccine did not affect vaccine efficacy.

(87) MBCD inactivated vaccines were safe for growing swine as evidenced by no post-vaccination systemic reactions, no injection site lesions and only a transient (1 or 2 days) febrile response in the Seppic MONTANIDE Gel 01 adjuvanted groups following second vaccination.