key: cord-1009203-kihn83ny
authors: Armesto, Maria; Casais, Rosa; Cavanagh, Dave; Britton, Paul
title: Transient Dominant Selection for the Modification and Generation of Recombinant Infectious Bronchitis Coronaviruses
date: 2007-11-28
journal: SARS- and Other Coronaviruses
DOI: 10.1007/978-1-59745-181-9_19
sha: e80062e30cc1372df72091af45112a8047258c8d
doc_id: 1009203
cord_uid: kihn83ny

We have developed a reverse genetics system for the avian coronavirus infectious bronchitis virus (IBV) in which a full-length cDNA corresponding to the IBV genome is inserted into the vaccinia virus genome under the control of a T7 promoter sequence. Vaccinia virus as a vector for the full-length IBV cDNA has the advantage that modifications can be introduced into the IBV cDNA using homologous recombination, a method frequently used to insert and delete sequences from the vaccinia virus genome. Here we describe the use of transient dominant selection as a method for introducing modifications into the IBV cDNA. We have used it successfully for the substitution of specific nucleotides, deletion of genomic regions, and the exchange of complete genes. Infectious recombinant IBVs are generated in situ following the transfection of vaccinia virus DNA containing the modified IBV cDNA into cells infected with a recombinant fowlpox virus expressing T7 DNA-dependent RNA polymerase.

The avian coronavirus, infectious bronchitis virus (IBV), is a highly infectious pathogen of domestic fowl and like other coronaviruses is an enveloped virus that replicates in the cell cytoplasm and contains a single-stranded, positive-sense RNA genome of 28 kb for IBV. Molecular analysis of the role of individual genes in pathogenesis of RNA viruses has been advanced by the availability of full-length cDNAs, for the generation of infectious RNA transcripts that can replicate and result in infectious viruses. The assembly of full-length coronavirus cDNAs was hampered owing to regions from the replicase gene being unstable in bacteria. We therefore devised a reverse genetics strategy for IBV involving insertion of the full-length cDNA, under the control of a T7 RNA promoter, into the vaccinia virus genome. This is followed by the in situ recovery of infectious IBV in cells transfected with the vaccinia virus DNA and infected with a recombinant fowlpox virus expressing T7 RNA polymerase (1).

An advantage of using vaccinia virus, in addition to the stability of the IBV cDNA, is the ability to generate modified IBV cDNAs by homologous recombination for the subsequent rescue of recombinant IBVs (rIBVs). We use the vaccinia virus-based transient dominant selection (TDS) recombination method (2) for modifying the IBV cDNA sequence within the vaccinia virus genome (3-5).

The method relies on a three-step procedure. In the first step, the modified IBV cDNA is inserted into a plasmid containing a selective marker under the control of a vaccinia virus promoter. In our case we use a plasmid, pGPTNEB193 [ Fig. 1; (6) ], which contains a dominant selective marker gene, Escherichia coli guanine phosphoribosyltransferase (Ecogpt; (7) ), under the control of the vaccinia virus P 7.5 K early/late promoter. In the second step, the complete plasmid sequence, containing a region of the IBV cDNA to be modified, is integrated into the IBV sequence in the vaccinia virus genome (Fig. 2) . This occurs as a result of a single crossover event involving homologous recombination between the IBV cDNA in the plasmid and the IBV cDNA sequence in the vaccinia virus genome. Recombinant vaccinia viruses (rVV) expressing the Ecogpt gene are selected for resistance against mycophenolic acid (MPA) in the presence of xanthine and hypoxanthine. In the third step, the MPA-resistant rVVs are grown in the absence of MPA selection, resulting in loss of the Ecogpt gene owing to a single homologous recombination event between duplicated sequences, present in the vaccinia virus genome resulting from integration of the plasmid sequence (Fig. 3) . During the third step two recombination events can occur, each of them with equal frequency. One event will result in the generation of the original (unmodified) IBV sequence and the other in the generation of an IBV cDNA containing the desired modification.

Infectious rIBVs are generated from the rVV DNA transfected into primary chick kidney (CK) cells previously infected with a recombinant fowlpox virus expressing T7 RNA polymerase [rFPV-T7; (8)]. In addition, a plasmid, pCi-Nuc (1, 9) , expressing the IBV nucleoprotein (N), under the control of both the cytomegalovirus (CMV) RNA polymerase II promoter and the T7 RNA promoter, is co-transfected into the CK cells. Expression of T7 RNA polymerase in the presence of the IBV N protein and the rVV DNA, containing the Fig. 1 . Schematic diagram of the recombination vector for insertion of genes into a vaccinia virus genome using TDS. Plasmid pGPTNEB193 contains the Ecogpt selection gene under the control of the vaccinia virus early/late P 7.5 k promoter, a multiple cloning region for the insertion of the sequence to be incorporated into the vaccinia virus genome and the bla gene (not shown) for ampicillin selection of the plasmid in E. coli. For modification of the IBV genome, a sequence corresponding to the region being modified, plus flanking regions of 500 to 800 nucleotides, for recombination purposes is inserted into the multiple cloning sites using an appropriate restriction endonuclease. The plasmid is purified from E. coli and transfected into Vero cells previously infected with a recombinant vaccinia virus containing a full-length cDNA copy of the IBV genome.

full-length IBV cDNA under the control of a T7 promoter, results in the generation of infectious IBV RNA, which in turn results in the production of infectious rIBVs (Fig. 4) .

The overall procedure can be divided into two parts, modification of the IBV cDNA by TDS in recombinant vaccinia viruses and the recovery of infectious rIBV. The generation of the Ecogpt plasmids, based on pGPTNEB193, containing the modified IBV cDNA, is by standard Escherichia coli cloning methods (10,11) and is not described here. General methods for growing vaccinia virus and for using the TDS method for modifying the vaccinia virus genome have been published (12,13). . The diagram shows a potential first single-step recombination event between the modified IBV sequence within pGPTNEB193 and the IBV cDNA within vNotI-IBV FL . In order to guarantee a single-step recombination event any potential recombinant vaccinia viruses are selected in the presence of MPA; only vaccinia viruses expressing the Ecogpt gene are selected. The main IBV genes are indicated: the replicase, spike (S), membrane (M), and nucleocapsid (N) genes. The IBV gene 3 and 5 gene clusters that express three and two gene products, respectively, are also indicated. In the example shown a modified region of the S gene is being introduced into the IBV genome. fetal calf serum (Autogen Bioclear), 0.3% tryptose phosphate broth (TPB; BDH), 500 U/ml nystatin (Sigma) and 100 U/ml penicillin and streptomycin (Sigma). (I) the original sequence of the input vaccinia virus IBV cDNA sequence, in this case shown as a recombination event between the two copies of the 3 -end of the replicase gene, which results in loss of the modified S gene sequence along with Ecogpt gene; or (II) retention of the modified S gene sequence and loss of the original S gene sequence and Ecogpt gene as a result of a potential recombination event between the two copies of the 5 -end of the S gene sequence. This event results in a modified S gene sequence within the IBV cDNA in a recombinant vaccinia virus. 4 . A schematic representation of the recovery process for obtaining rIBV from DNA isolated from a recombinant vaccinia virus containing a full-length IBV cDNA under the control of a T7 promoter: (A) In addition to the vaccinia virus DNA containing the full-length IBV cDNA under the control of a T7 promoter, a plasmid, pCI-Nuc, expressing the IBV nucleoprotein, required for successful rescue of IBV, is transfected into CK cells previously infected with a recombinant fowlpox virus, FPV-T7, expressing T7 RNA polymerase. The T7 RNA polymerase results in the synthesis of an infectious RNA from the vaccinia virus DNA that consequently leads to the generation of infectious IBV being released from the cell. (B) Any recovered rIBV present in the media of P 0 CK cells is used to infect P 1 CK cells. The medium is filtered though a 0.22-m filter to remove any FPV-T7 virus. IBV-induced CPE is normally observed in the P 1 CK cells following a successful recovery experiment. Any rIBV is passaged a further two times, P 2 and P 3 , in CK cells. Total RNA is extracted from the P 1 to P 3 CK cells and the IBV-derived RNA analyzed by RT-PCR for the presence of the required modification. 

Two or three of the plaque purified gpt + rVVs are used for generation of new rVVs in the absence of MPA selection medium to generate viruses with a gptphenotype. 1 . Vero cell monolayers in six-well plates. 2. PBSa. 3. 1X E-MEM 4. 1X E-MEM containing 1% low-melting agarose (see Note 7). 5. 1X E-MEM containing 1% low-melting agarose and 0.01% neutral red (see Note 7). 6. Ecogpt selection medium containing 1% low-melting agarose (see Note 7).

Small stocks of the plaque-derived rVVs have to be produced for extraction of DNA for screening purposes. The vaccinia DNA is used as a template for PCR and sequence analysis to check for the presence of the modified sequence and confirmation that the Ecogpt gene has been lost. 

Vaccinia virus DNA for a recovery of IBV requires partial purification of the rVV through a sucrose cushion. and sonicate for 2 min using a cup form sonicator (Heat Systems Ultrasonic Inc., Model W-375), continuous pulse at 70% duty cycle, seven-output control. This will be the stock virus for selection of a rVV containing the intended modification. The virus can be stored at -20 • or -70 • C.

Isolation of gpt + rVVs is by plaque assay on Vero cells. (assay each dilution in duplicate). 5. Incubate for 1-2 h at 37 • C, 5% CO 2 . 6. Remove the inoculum and add 3 ml of the Ecogpt selection medium in 1% lowmelting agarose overlay (see Note 7). 7. Incubate for 4 days at 37 • C, 5% CO 2 and stain the cells by adding 2 ml of 1X E-MEM containing 1% agarose and 0.01% neutral red. 8. Incubate the cells at 37 • C, 5% CO 2 for 6 h and pick ten-well isolated plaques for each recombinant by taking a plug of agarose directly above the plaque. Place the plug of agarose in 400 l of 1X E-MEM. 9. Perform two further rounds of plaque purification for each selected recombinant vaccinia virus (two or three of the picked plaques from step 8) in the presence of selection medium, as described in steps 1-8, using a dilution of 10 -1 for each virus.

1. Take the MPA resistant plaque-purified rVVs and freeze-thaw the virus three times (37 • C/dry ice) and sonicate for 2 min using a cup form sonicator (Heat Systems Ultrasonic Inc., Model W-375), continuous pulse at 70% duty cycle, seven-output control (see Notes 1-4).

PBSa. 3. Prepare 10 -1 and 10 -2 dilutions of the gpt + plaque-purified recombinant vaccinia viruses in 1X E-MEM 4. Remove the PBSa from the Vero cells and add 500 l of the diluted gpt + plaquepurified recombinant vaccinia viruses to each well (assay each dilution in duplicate). 5. Incubate the infected Vero cells for 1-2 h at 37 • C, 5% CO 2 . 6. Remove the inoculum and add 3 ml of overlay containing 1X E-MEM and 1% agarose. 7. Incubate the infected Vero cells for 4 days at 37 • C, 5% CO 2 and stain the cells by adding 2 ml of 1X E-MEM containing 1% agarose and 0.01% neutral red. At the end of the day or the following morning, choose approximately ten isolated plaques for each recombinant and resuspend in 400 l of 1X E-MEM. 8. Plaque purify each recombinant vaccinia virus three times in the absence of selection medium following the same procedure in Section 3.3, as described for plaque purification in presence of selection medium. However, dilutions of 10 -1 , 10 -2 , and 10 -3 are required. Dilution 10 -1 is plated in the presence of Ecogpt selection medium, to identify the presence of any MPA-resistant rVVs. Dilutions 10 -2 and 10 -3 are carried out in the absence of selection medium. Once there is no evidence of MPA-resistant rVVs in the MPA selection controls, it can be assumed that the Ecogpt gene has been lost and the recombinant vaccinia viruses can be screened for the presence of the required modifications and the presence/absence of the Ecogpt gene confirmed. 9. Select several plaques and place the plug of agarose in 400 l of 1X EMEM. 10 . Take 700 l of the resuspended cells as virus stocks and store at -20 • C. 11. To the remaining 100 l of the resuspended cells add 100 l 2X proteinase K buffer and 2 l of the 10 mg/ml proteinase K stock to give a final concentration of 0.1 mg/ml. Gently mix to prevent shearing of the vaccinia virus DNA and incubate at 50 • C for 2 h (see Note 5). 12. Add 200 l of phenol-chloroform to the proteinase K-treated samples and mix by inverting the tube five to ten times and centrifuge at 13,000 rpm (16,000 × g) for 5 min. 13. Take the upper phase (aqueous phase) and repeat step 12 twice more. 14. Add 200 l of chloroform to the upper phase from the final step of 13. Mix well and centrifuge at 13,000 rpm (16,000 × g) for 5 min. 15. Take the upper phase and precipitate the vaccinia virus DNA by adding 2.5 volumes of absolute ethanol; the precipitated DNA should be visible. Centrifuge the precipitated DNA at 13,000 (16,000 × g) for 20 min. Discard the supernatant and wash the pelleted DNA with 400 l 70% ethanol. 16. Centrifuge at 13,000 rpm (16,000 × g) for 10 min, carefully discard the supernatant and remove the last drops of 70% ethanol using a capillary tip. 17. Resuspend the DNA in 30 l of water, briefly heat the DNA at 50 • C (with the lid of the Eppendorf tube opened) to remove any remaining ethanol, and store at 4 • C. 18. At this stage the rVV DNA from step 17 is analyzed by PCR and/or sequence analysis for the presence/absence of the Ecogpt gene and for the modifications within the IBV cDNA sequence. The rVVs that have lost the Ecogpt gene and contain the desired IBV modifications are used to produce larger stocks of virus, as described in Section 3.1 (but using smaller amounts) for further analysis and for the preparation of larger stocks of vaccinia virus DNA for recovery of rIBV.

7. The partially purified vaccinia virus particles form a pellet under the sucrose cushion. After centrifugation carefully remove the top layer (usually pink) and the sucrose layer with a pipette. Wipe the sides of the tube carefully with a tissue to remove any sucrose solution. 8. Resuspend each pellet using 5 ml of TE buffer and store at -70 • C.

1. Defrost the partially purified vaccinia virus from step 3.6.8 at 37 • C and add 5 ml of prewarmed 2X proteinase K buffer and 100 l of 10 mg/ml proteinase K. Incubate at 50 • C for 2 h (see Notes 1-4). In order to visualize the DNA pellet 2 l of pellet paint (Novagen) per sample can be added before the 3 M sodium acetate, mix, add the ethanol, mix again, and incubate for 2 min at room temperature before centrifugation. 6. Discard the supernatant and wash the DNA using 10 ml of 70% ethanol. Leave on ice for 5 min and centrifuge at 1200 × g, 4 • C for 30 min. Discard the supernatant and remove the last drops of ethanol using a capillary tip. Dry the inside of the tube using a tissue to remove any ethanol. 7. Resuspend the vaccinia DNA in 300 l of water and briefly heat at 50 • C to remove any remaining ethanol. Gently flick the tube until the DNA dissolves. Note: more water may have to be added, depending on the viscosity of the DNA solution. 8. Leave the tubes at 4 • C overnight. If the pellet has not totally dissolved, add more water. 9. Keep the vaccinia virus DNA at 4 • C. DO NOT FREEZE (see Note 6). 10 . Digest 1 g of the DNA with a suitable restriction enzyme in a 20-l volume to check the quality of the DNA by pulse field agarose gel electrophoresis. agarose gel is suitable for separating DNA ranging between 20 and 300 kb. 3. Place the required amount of agarose in 100 ml of 0.5X TBE, microwave until the agarose is dissolved, and cool to approximately 50 • -60 • C. 4. Clean the gel frame and comb with MQ water followed by ethanol. Place the gel frame on a level surface, assemble the comb, and pour the cooled agarose into the gel frame. Remove any bubbles using a pipette tip, allow the agarose to set (approx. 30-40 min), and store in the fridge until required. 5. Place the remaining 0.5X TBE buffer into the CHEF-DR R II PFGE electrophoresis tank and switch the cooling unit on. Leave the buffer circulating to cool. 6. Add the sample loading dye to the digested vaccinia virus DNA samples (Section 3.7, step 10) and incubate at 65 • C for 10 min. 7. Place the agarose gel in the electrophoresis chamber; load the samples using tips with cut ends (widened bore) and appropriate DNA markers (see Note 5). 8. The DNA samples are analyzed by PFGE at 14 • C in gels run with a 0.1-1.0 sec switch time for 16 h at 6 V/cm at an angle of 120 • or with a switch time of 3.0-30.0 sec for 16 h at 6 V/cm, depending on the concentration of agarose used. Table 1 summarizes the standard conditions for 0.8% and 1.0% agarose gels for PFGE. 9. Following PFGE place the agarose gel in a sealable container with 400 ml of 0.1 g/ml ethidium bromide and gently shake for 30 min at room temperature. 10. Wash the ethidium-stained agarose gel in 400 ml of MQ water by gently shaking for 30 min. 11. Visualize DNA bands using a suitable UV system for analyzing agarose gels.

An example of recombinant vaccinia virus DNA digested with the restriction enzyme SalI and analyzed by PFGE is shown in Fig. 5 . 

Infectious recombinant IBVs are generated in situ by co-transfection of vaccinia virus DNA, containing the modified IBV cDNA and pCi-Nuc into CK cells previously infected with a recombinant fowlpox virus expressing T7 DNAdependent RNA polymerase. This protocol covers the procedure for infecting primary avian chicken embryo fibroblasts (CEF) cells with a recombinant fowlpox virus (rFPV/T7) expressing the bacteriophage T7 RNA polymerase under the direction of the vaccinia virus P 7.5 early-late promoter (8). Preparation of a 200-ml stock of rFPV/T7 uses ten T75 flasks containing confluent monolayers of CEF cells. 1 . Remove the culture growth medium from the cells and infect with 2 ml of rFPV/T7 at an MOI of 0.1, previously diluted in CEF maintenance medium. 2. Incubate the infected cells for 2 h at 37 • C 5% CO 2 ; then without removing the inoculum add 20 ml of CEF maintenance medium.

To check for the presence of any recovered rIBVs, the medium from the P 0 CK cells (Section 3.11, step 7) is passaged three times, P 1 to P 3 , on CK cells (Fig. 4B) , checking for any IBV-associated CPE. Total RNA is extracted from the P 1 to P 3 CK cells and analyzed for the presence of IBV RNA by specific RT-PCR reactions (see Note 8). For passage 1 (P 1 ):

10X TBE buffer: 1 M Tris, 0.9 M boric acid pH 8, and 10 mM EDTA

Agarose (Biorad, pulsed field certified ultrapure DNA-grade agarose)

DNA markers (e.g., 8-48 kb markers, Biorad)

MQ water

CHEF-DR R II pulse field gel electrophoresis (PFGE) apparatus (Biorad)

6X sample loading buffer: 62.5% glycerol, 62.5 mM Tris-HCl pH 8, 125 mM EDTA and 0.06% bromophenol blue (BDH)

Preparation of rFP-T7 Stock Virus 1. CEF growth medium: 1X 199 Medium with Earle's Salts, 0.3% TPB, 8% new born calf serum (NBCS), 0.225% sodium bicarbonate

U/ml penicillin, 100 U/ml streptomycin and 500 U/ml nystatin

CEF maintenance medium: as above but containing 2% NBCS. 3. CEF cells

T75 (75-cm 2 ) flasks

A Beckman CS-15R centrifuge or an equivalent centrifuge

Take the plaque-purified rVVs and freeze-thaw three times (37 • C/dry ice) and sonicate for 2 min using a cup form sonicator (Heat Systems Ultrasonic Inc., Model W-375), continuous pulse at 70% duty cycle, seven-output control

Wash the Vero cells with PBSa

Dilute 150 l of the sonicated rVVs in 350 l of 1X BES medium

Remove the virus inoculum and add 2.5 ml of 1X BES medium

Incubate the infected Vero cells at 37 • C, 5% CO 2 until the cells show signs of vaccinia virus-induced CPE in about 70-80% of the Vero cell monolayer

Scrape the Vero cells into the medium and centrifuge for 1 min at 13,000 rpm (16,000 × g)

large batches of vaccinia virus as described in Section 3.1. Ten T150 flasks are normally sufficient (see Notes 1-4)

Freeze-thaw the 2-ml aliquots, from Section 3.1, step 9, three times (37 • C/dry ice) and sonicate for 2 min using a cup form sonicator (Heat Systems Ultrasonic Inc., Model W-375), continuous pulse at 70% duty cycle

Place the aliquots on ice and then pool identical aliquots in 50-ml Falcon tubes and centrifuge (Beckman CS-15R) at 750 × g for 10 min at 4 • C to remove the cell nuclei

Add TE buffer to the supernatants to give a final volume of 13 ml

Add 16 ml of the 30% sucrose solution into a Beckman ultra-clear (25 × 89 mm) ultracentrifuge tube and carefully layer 13 ml of the cell lysate from step 4 onto the sucrose cushion

Centrifuge the samples using a Sorvall OTD65B ultracentrifuge with a superspin 630 rotor at 14,000 rpm (36,000 × g) at 4 • C for 60 min

Tap the flasks to detach the cells from the plastic and disperse the cells into the medium by pipetting them up and down

Freeze-thaw the cells, as described in Section 3.1, step 1, and centrifuge at 750 × g, 4 • C for 5 min to remove the cell debris. Store the supernatant containing the virus stock at -80 o C until required

Determine the titer of the virus stock using CEF cells

Infection CK Cells with rFPV-T7

Seed CK cells in 13 × 60-mm dishes to give a 50% confluent monolayers on the day after seeding. Normally, for each recovery we prepare twelve dishes, ten replicates for the recovery experiment and two controls, rFPV-T7-infected and mock-infected CK cells

Remove the medium and wash the cells once with PBSa

Add the virus into a final volume of 1 ml of CK cell maintenance medium per dish

Transfection of Vaccinia Virus DNA into CK Cells During the infection of CK cells with rFPV-T7 prepare the transfection reaction reagents: rVV DNA, pCi-Nuc, and Lipofectin (Invitrogen). The reagents are added as follows: 1. Prepare the two master solutions: (A) 15 ml OPTIMEM add 100 g of rVV DNA and 50 g of pCi-Nuc. (B) 15 ml OPTIMEM

Incubate solutions A and B at room temperature for 30 min

Mix A and B together and incubate for a further 15 min at room temperature

Wash the rFPV-T7 infected CK cells twice with OPTIMEM and carefully add 3 ml of the A + B transfection mixture to ten of the dishes of the rFPV-T7-infected CK cells

Incubate the transfected cells at 37 • C, 5% CO 2 for 16 h

Next morning, remove the transfection medium and add 5 ml of fresh BES medium and incubate at 37 • C, 5% CO 2

harvest the cell supernatant, place in Eppendorf tubes, centrifuge for 3 min at 13,000 rpm (16,000 × g), place it into 5-ml Bijoux tubes

Seed CK cells in T25 flasks to be confluent monolayers on the day required. 2. Remove the growth medium and wash once with PBSa

Add 1 ml of the filtered medium from the P 0 CK cells (Section 3.11, step 7) to the confluent CK cells and incubate at 37 • C, 5% CO 2 for 1 h. Then, without removing the inoculum add 4 ml of BES medium

Check the cells for IBV-associated CPE over the next 2-3 days. When about 50-75% of the CK cells show a CPE, infect new cells with some of the cell medium as described in steps 1 to 3. Repeat for serial passages P 2 and P 3 CK cells. Filtration of the infected cell medium is not required after P 1

After P 3 any recovered virus is used to prepare a large stock for analysis of the virus genotype and phenotype

Vaccinia virus is classified as a category 2 human pathogen and its use is therefore subject to local regulations and rules that have to be followed

Always discard any medium of solution containing vaccinia virus into a 1% solution of Virkon

Flasks of cells infected with vaccinia virus should be kept in large Tupperware boxes, which should be labeled with the word vaccinia and biohazard tape

During centrifugation of vaccinia virus infected cells use sealed buckets for the centrifugation to avoid possible spillage

Vaccinia virus DNA is a very large molecule that is very easy to shear; therefore when working with the DNA be gentle and use wide bore tips, cutting the ends off ordinary pipette tips

Always store vaccinia virus DNA at 4 • C; do not freeze the DNA as this leads to degradation of the DNA

1% low-melting agarose can be substituted with 1% agar

In this case, check for the presence of viral RNA by RT-PCR at each passage, starting at P 1 . by the Department of Environment, Food and Rural Affairs (DEFRA) project codes OD1905, OD0712, and OD0717; European Communities specific RTD program Quality of Life and Management of Living Resources QLK2-CT-1999-00002

Reverse genetics system for the avian coronavirus infectious bronchitis virus

Transient Dominant Selection of Recombinant Vaccinia Viruses

Generation of a recombinant avian coronavirus infectious bronchitis virus using transient dominant selection

Gene 5 of the avian coronavirus infectious bronchitis virus is not essential for replication

Neither the RNA nor the proteins of open reading frames 3a and 3b of the coronavirus infectious bronchitis virus are essential for replication

The 131-amino-acid repeat region of the essential 39-kilodalton core protein of fowlpox virus FP9, equivalent to vaccinia virus A4L protein, is nonessential and highly immunogenic

Selection for animal cells that express the E. coli gene coding for xanthine-guanine phosphoribosyl transferase

Expression of bacteriophage T7 RNA polymerase in avian and mammalian cells by a recombinant fowlpox virus

The coronavirus infectious bronchitis virus nucleoprotein localizes to the nucleolus

Molecular Cloning: A Laboratory Manual, 2 nd Ed

The construction and characterisation of vaccinia virus recombinants expressing foreign genes

Expression of genes by vaccinia virus vectors In: Davison

The authors thank Dr. M. Skinner for providing pGPTNEB193. We also thank many colleagues, both past and present, who have been involved in the development of our IBV reverse genetics system. This work was supported