WO1992001045A1

WO1992001045A1 - Equine herpesvirus-4 tk- vaccine

Info

Publication number: WO1992001045A1
Application number: PCT/GB1991/001100
Authority: WO
Inventors: David Edward Onions; Lesley Nicolson
Original assignee: The University Court Of The University Of Glasgow; Equine Virology Research Foundation
Priority date: 1990-07-06
Filing date: 1991-07-05
Publication date: 1992-01-23
Also published as: HU217213B; EP0538299A1; HUT67778A; JPH05508538A; ZA915231B; HU9300010D0; GB9014951D0; CA2086740A1; NZ238834A; AU8212891A

Abstract

The present invention is concerned with an attenuated EHV-4 vaccine. The attenuation can be achieved by a deletion and/or insertion in the thymidine kinase gene of EHV-4. The invention also relates to a vector vaccine comprising an EHV-4 mutant having a foreign gene inserted into the EHV-4 genome.

Description

Equine herpesvirus-4 TK^~ vaccine

The present invention is concerned with an Equine herpesvirus-4 mutant (EHV-4) , a- recombinant DNA molecule comprising EHV-4 DNA, host cell containing said reccmbinant DNA molecule, process for the preparation of said EHV-4 mutant, cell culture infected with the EHV-4 mutant., a vaccine derived from the EHV-4 mutant as well as a process for the preparation of such a vaccine.

Equine herpesvirus-4 (EKV-4) is, like the related Equine herpesvirus-1, an alphaherpesvirus responsible for significant economic losses within the equine industry. EHV-4 is primarily associated with respiratory disease though ΞHV-4 induced abortions are occasionally reported.

The genome of EHV-4 has beer, characterized as a double-snranded linear DNA molecule consisting of two ccvalen iy linked segments (L, 109 kbp; S, 35 kbp) the latter being flanked by inverted repeats.

Ccnrrol by vaccination of EHV-4 infection has been a long-sought goal.

Current: vaccines comprise chemically inactivated virus vaccines and modified live-virus vaccines. However, inactivated vaccines generally induce only a low level of immunity, requiring additional immunizations, disadvantageously require adjuvants and are expensive to produce. Further, some infectious virus particles may survive the inactivation process and causes disease after administration to the animal.

In general, attenuated live virus vaccines are preferred because they evoke a more long-lasring immune response (often both humoral and cellular) and are easier to produce.

Up to now only live attenuated, EHV-4 vaccines are available which are based on live EHV-4 viruses attenuated by serial passages of virulent strains in tissue culture. However, because of this treatment uncontrolled mutations are introduced into the viral genome, resulting in a population of virus particles heterogeneous in their virulence and immunizing properties. In addition it is well known that such traditional attenuated live virus vaccines can revert to virulence resulting in disease of the inoculated animals and the possible spread of the pathogen to other animals. Furthermore, with the existing live attenuated EHV-4 vaccines a positive serological test is obtained for EHV- 4 infection. Thus, with the existing EHV-4 vaccines, it is not possible to determine by a (serological) test, e.g. an Elisa, whether a specific animal is a (latent) carrier of the virulent virus or is vaccinated.

It is an object of the present invention to provide an EHV-4 mutant which can be used for the preparation of a vaccine against EHV-4 infection, the mutant viruses being attenuated in a controlled way in a manner which excludes the reversion to virulence and which still elicit a strong immune response in host animals.

According to the present invention such a mutant EHV-4 is characterized in that it does not produce a functional thymidine kinase (TK~) as a result of a deletion and/or insertion in the gene encoding thymidine kinase.

The development of techniques for controlled manipulation of genetic material has allowed the possibility of obtaining attenuated virus vaccines which avoid the disadvantages of the classic attenuated virus vaccines.

However, up to now no information was available with respect to the exact localisation on the EHV-4 genome of a region involved with the virulence of EHV-4 making the production of an genetic engineered attenuated EHV-4 impossible.

The gene encoding thymidine kinase was mapped within the BamHI C fragment of the EHV-4 genome and was further localised to an about 2 kbp EcoRV/XhoI fragment thereof, with a map position of approximately 0,48 (fig.l). The nucleic acid sequence of the TK gene was determined and is shown in SEQ ID NO: 1 from which restriction enzyme cleavage sites to be used for the genetic manipulation of the gene can be d -rived.

The TK gene consists of 1056 nucleotides encoding a 352 amino acid enzyme of predicted molecular weight of 38.300 D. The efficiency of the expression of TK is regulated by the presence of expression control sequences. For example promoter sequences are involved in the binding of RNA poly erase to the DNA template and control the site and onset of the mRNA. Such sequences are often found within a 100 bp region before the transcription initiation site. Downstream transcriptional control signals are inter alia, the transcription termination codon and a polyadenylation signal. The TATA box positioned at base pair 21-25 is the putative promoter TATA box of the EHV-4 TK gene. A potential RNA polymerase initiation site is located 22 bp downstream of the TATA box. A poly A signal is positioned 42 bp downstream of the termination codon (SEQ ID NO: 1) .

It will be understood that for the DNA sequence of the EHV-4 TK gene natural variations can exist between individual EHV-4 viruses. These variations may result in a change of one or more nucleotides in the TK gene which, however still encodes a functional TK. Moreover, the potential exists to use genetic engineering technology to bring about above-mentioned variations resulting in a DNA sequence related to the sequence shown in SEQ ID NO: 1. It is clear that EHV-4 mutants comprising a deletion and/or insertion in such a related nucleic acid sequence are also included within the scope of the invention.

The EHV-4 deletion mutants of the present invention comprise a TK gene from which a DNA fragment has been deleted so that no functional TK enzyme is produced upon replication of the virus, e.g. as result of a change of the tertiary structure of the altered TK protein or as a result of a shift of the reading frame.

In addition the deletion in the genome of the EHV-4 mutant may comprise the complete TK gene.

EHV-4 mutants according to the invention can also be obtained by inserting a nucleic acid sequence into the TK coding region thereby preventing the expression of a functional TK enzyme. Such a nucleic acid sequence can inter alia be an oligonucleotide, for example of about 10-60 bp, preferably also containing one or more translational stop codons, or a gene encoding a polypeptide. Said nucleic acid sequence can be derived from any source, e.g. synthetic, viral, prokaryotic or eukaryotic.

In another embodiment of the present invention the EHV-4 deletion mutants can contain above-mentioned nucleic acid sequence in place of the deleted EHV-4 DNA.

It is another object of the present invention to provide a mutant EHV-4 which can be used not only for the preparation of a vaccine against EHV-4 infection but also against other equine infectious diseases. Such a vector vaccine based on a safe live attenuated EHV-4 mutant offers the possibility to immunize against other pathogens by the expression of antigens of said pathogens within infected cells of the immunized host and can be obtained by inserting a heterologous nucleic acid sequence encoding a polypeptide heterologous to EHV-4 in an insertion-region of the EHV-4 genome. However, the prerequisite for a useful EHV-4 vector is that the heterologous nucleic acid sequence is incorporated in a permissive position or -region of the geno ic EHV-4 sequence, i.e. a position or region which can be used for the incorporation of a heterologous sequence v:ithout disrupting essential functions of EHV-4 such as those necessary for infection or replication. Such a region is called an insertion-region. Prior to the present invention no insertion-region in the EHV-4 genome has been described.

According to the present invention EHV-4 mutants are provided which can be used as a viral vector, characterized in that said mutants do not produce a functional TK as a result of an insertion of a heterologous nucleic acid sequence encoding a polypeptide m the gene encoding TK.

EHV-4 insertion mutants as described above having a heterologous nucleic acid sequence inserted in place of deleted TK DNA are also within the scope of the present invention.

The term "EHV-4 insertion mutants" comprises inter alia infective viruses which have been genetically modified by the incorporation into the virus genome of a heterologous nucleic acid sequence, i.e. a gene which codes for a protein or part thereof said gene being different of a gene naturally present in EHV-4.

On infection of a cell by said EHV-4 insertion mutant it expresses the heterologous gene in the form of a heterologous polypeptide.

The term "polypeptide" refers to a molecular chain of a ino acids with a biological activity, does not refer to a specific length of the product and if required can be modified in vivo or in vitro, for example by glycosylation, amidation, carboxylation or phosphorylation thus inter alia peptides, oligopeptides and proteins are included within the definition of polypeptide.

The heterologous nucleic acid sequence to be incorporated into the EHV-4 genome according to the present invention can be derived from any source, e.g. viral, prokaryotic, eukaryotic or synthetic. Said nucleic acid sequence can be derived from a pathogen, preferably an equine pathogen, which after insertion into the EHV-4 genome can be applied to induce immunity against disease. Preferably, nucleic acid sequences derived from EHV-1, equine influenza virus, -rotavirus, -infectious anemia virus, arteritis virus, -encephalitis virus, Borna disease virus of horses, Berue virus of horses, E.coli or Streptococcus equi are contemplated of for incorporation into the insertion-region of the EHV-4 genome.

Furthermore, nucleic acid sequences encoding polypeptides for pharmaceutical or diagnostic application, in particular immune modulators such as lymphokines, interferons or cytokines, may be incorporated into said insertion-region.

An essential requirement for the expression of the heterologous nucleic acid sequence in a EHV-4 mutant is an adequate promoter operably linked to the heterologous nucleic acid sequence. It is obvious to those skilled in the art that the choice of a promoter extends to any eukaryotic, prokaryotic or viral promoter capable of directing gene transcription in cells infected by the EHV-4 mutant, such as the SV-40 promoter (Science 222. 524-527, 1983) or, e.g., the metallothionein promoter (Nature 296, 39-42, 1982) or a heat shock promoter (Voellmy et al., Proc. Natl. Acad. Sci. USA 82., 4949-53, 1985) or the human cytomegalovirus IE promoter or promoters present in EHV-4, e.g. the TK promoter.

Well-known procedures for inserting DNA sequences into a cloning vector and in vivo homologous recombination can be used to introduce a deletion and/or an insertion into the EHV-4 genome (Maniatis, T. et al. (1982) in "Molecular cloning", Cold Spring Harbor Laboratory; European Patent Application 74.808; Roizman, 3. and Jenkins, F.J. (1985), Science 229, 1208; Higuchi, R. et al. (1988), Nucleic Acids Res. 15, 7351). 3riefly, this can be accomplished by constructing a recombinant DNA molecule for recombination with EHV-4 DNA. Such a recombinant DNA molecule may be derived from any suitable plasmid, cosmid, virus or phage, plasmids being most preferred, and contains EHV-4 DNA possibly having a nucleic acid sequence inserted therein if desired operably linked to a promoter. Examples of suitable cloning vectors are plasmid vectors such as pBR322, the various pUC and Bluescript plasmids, bacteriophages, e.g. λ gt-WES-λ B, charon 28 and the M13mp phages or viral vectors such as SV40, Bovine papillomavirus, Polyoma and Adeno viruses. Vectors to be used in the present invention are further outlined in the art, e.g. Rodriguez, R.L. and D.T. Denhardt, edit., Vectors: A survey of molecular cloning vectors and their uses, Butterworthε, 1988.

First, an EHV-4 DNA fragment comprising the insertion region, i.e. the TK gene, is inserted into the cloning vector according to recDNA techniques. Said DNA fragment may comprise part of the TK gene or substantially the complete TK gene, and if desired flanking sequences thereof.

Second, if an EHV-4 TK deletion mutant is to be obtained at least part of TK gene is deleted from the recombinant DNA molecule obtained from the first step. This can be achieved for example by appropriate exonuclease III digestion or restriction enzyme treatment of the recombinant DNA molecule from the first step. In the case an EHV-4 insertion mutant is to be obtained the nucleic acid sequence is inserted into the TK gene present in the recombinant DNA molecule of the first step or in place of the TK DNA deleted from said recombinant DNA molecule. The EHV-4 DNA sequences which flank the deleted TK D?^TA or the inserted nucleic acid sequence should be of appropriate length as to allow homologous recombination with the viral EHV-4 genome to occur.

If desired, a construct can be made which contains two or more different inserted (heterologous) nucleic acid sequences derived from e.g. the same or different pathogens said sequences being flanked by insertion- region sequences of EHV-4 defined herein. Such a recombinant DNA molecule can be employed to produce an EHV-4 mutant which expresses two or more different antigenic polypeptides to provide a ultivalent vaccine.

Thereafter, cells, for example rabbit cells, TK⁺ or TK^" phenotype, or equine cells, e.g. equine dermal cells, can be transfected with EHV-4 DNA in the presence of the recombinant DNA molecule containing the deletion and/or insertion of (heterologous) nucleic acid sequence flanked by appropriate EHV-4 sequences whereby recombination occurs between the corresponding regions in the recombinant DNA molecule and the EHV-4 genome. Recombination can also be brought about by transfecting EHV-4 genomic DNA containing host cells with a DNA containing the (heterologous) nucleic acid sequence flanked by appropriate flanking insertion-region sequences without vector DNA sequences. Recombinant viral progeny is thereafter produced in cell culture and can be selected for example genotypically or phenotypically, e.g. by hybridization, detecting enzyme activity encoded by a gene co-integrated along with the (heterologous) nucleic acid sequence, screening for EHV-4 mutants which do not produce functional TK (Roiz an, B. and Jenkins, F.J. (1985), ibid)) or detecting the antigenic heterologous polypeptide expressed by the EHV-4 mutant immunologically. The selected EHV-4 mutant can be cultured on a large scale in cell culture whereafter EHV- 4 mutant containing material or heterologous polypefcides expressed by said EHV-4 can be collected therefrom. Alternatively, mutant EHV-4 could be generated by cotransfection of several cosmids, containing between them the entire EHV-4 genome, where an insertion and/or deletion has been engineered into the cosmid possessing EHV-4 TK DNA.

According to the present invention a live attenuated EHV-4 mutant which does not produce a functional TK, and if desired expresses one or more different heterologous polypeptides of specific pathogens can be used to vaccinate horses, susceptible to EHV-4 and these pathogens.

Vaccination with such a live vaccine is preferably followed by replication of the EHV-4 mutant within the inoculated host, expressing in vivo EHV-4 polypeptides, and if desired heterologous polypeptides. An immune response will subsequently be elicited against EHV-4 and the heterologous polypeptides. An animal vaccinated with such an EHV-4 mutant will be immune for a certain period to subsequent infection of EHV-4 and above-mentioned pathogen(s) .

An EHV-4 mutant according to the invention optionally containing and expressing one or more different heterologous polypeptides can serve as a monovalent or multivalent vaccine.

An EHV-4 mutant according to the invention can also be used to prepare an inactivated vaccine.

For administration to animals, the EHV-4 mutant according to the presentation can be given inter alia by aerosol, spray, drinking water, orally, intrader ally, subcutaneously or intramuscularly. Ingredients such as skimmed milk or glycerol can be used to stabilise the virus. It is preferred to vaccinate horses by intranasal administration. A dose of 10³ to 10⁸ TCID₅₀ of the EHV-4 mutant per horse is recommended in general

It is a further object of the present invention to produce subunit vaccines, pharmaceutical and diagnostic preparations comprising a heterologous polypeptide expressed by an EHV-4 mutant according to the invention. This can be achieved by culturing cells infected with said EHV-4 mutant under conditions that promote expression of the heterologous polypeptide. The heterologous polypeptide may then be purified with conventional techniques to a certain extent depending on its intended use and processed further into a preparation with immunizing therapeutic or diagnostic activity.

The above described active immunization against specific • pathogen- will be applied as a protective treatment in healthy animals. It goes without saying that animals already infected with a specific pathogen can be treated with antiserum comprising antibodies evoked by an EHV-4 mutant according to the invention. Antiserum directed against an EHV-4 mutant according to the invention can be prepared by immunizing animals with an effective amount of said EHV-4 mutant in order to elicit an appropriate immune response. Thereafter the animals are bled and antiserum can be prepared.

Example 1

Isolation and characterization cf EHV-4 insertion region.

1. Culturing of EHV-4 virus

Roller bottles of slightly sub-confluent onolayers of equine dermal cells (NBL-6) grown in Earle's Minimum Essential Medium (Flow) supplemented with 0,2% sodium bicarbonate, 1% non-essential amino acids, 1% gluta ine, 100 units/ml penicillin, 100 mg/ml streptomycin and 10% foetal calf serum were infected with virus of the EHV-4 strain 1942 at a .o.i. of 0,003 and allowed to adsorb for 60 min at 37 °C. They were incubated at 31 °C until extensive c.p.e. was evident and the majority of cells had detached from the bottle surface (2-6 days) . The infected cell medium was centrifuged at 5.000 r.p.m. for

5 min to pellet the cells, and the supernatant was centrifuged at 12.000 r.p.m. for 2 hours in a Sorvall GSA

6 X 200 ml rotor. The pellet was resuspended in 5 ml PBS, sonicated and centrifuged at 11.000 r.p.m. in a Sorvall ΞS34 rotor for 5 min to spin down cellular debris. Virus was then pelleted by centrifugation at 18.000 r.p.m. in a Sorvall SS34 rotor for 1 hour. Ratios of virus particles to plaque-forming units were approximately 1.000 to 5.000.

2. Preparation of EHV-4 DNA

The pelleted virus was resuspended in 10 ml NTE

(NaCl/Tris/EDTA) and briefly sonicated. Contaminating cellular DNA was degraded by adding DNase at 10 μg/ml and incubating at

37 °C for 1 hour. SDS was added to a final concentration of 2%, and the preparation was extracted approximately 3 times with NTE equilibrated phenol until a clear interphase was obtained.

A chloroform extraction was followed by ethanol precipitation of the DNA as described above. The DNA was pelleted, washed with 70% ethanol, resuspended in 10 ml of 100 mM NaCl and 10 μg/ml RNase and left overnight at room temperature. Further purification was achieved by treatment with 1 mg/ml proteinase K for 2 hours at 31 °C. The DNA was extracted once with phenol:chloroform (1:1 vol/vol) , once with chloroform, ethanol precipitated, drained well and resuspended in 0.1 X SSC.

3. Cloninσ of EHV-4 DNA

EHV-4 BamHI DNA fragments were ligated into the vector pUC9, a plasmid which includes the ampicillin-resistance gene from pBR322 and the polylinker region from M13mp9 (Vieira, J. and Messing, J. (1982), Gene 19_, 259). 5 μg of EHV-4 DNA and 5 μg pUC9 DNA were separately digested with BamHI.

Complete digestion was verified by gel electrophoresis of aliquots of the reactions and then the DNA was extracted twice with an equal volume of phenol:chloroform (1:1) and ethanol-precipitated. Ligation was performed essentially by the method of Tanaka and Weisblum (J. Bact. 121. 354, 1975). Approximately 0.1 μg of BamHI digested pUC9 and 1 μg of BamHI-digested EHV-4 DNA were mixed in 50 mM Tris- HC1 pH 7,5, 3 mM MgCl₂, 10 mM dithiothreitol, 1 mM ATP in a final volume of 40 μl. 2 units of T4 DNA ligase (0,5 μl) were then added. The reaction was incubated at 4 °C for 16 hours.

Calcium-shocked E.coli DHI cells (Hanahan, D. (1983) , J. Mol. Biol. 166, 557) were transformed with the recombinant plasmids essentially described by Cohen et al. (Proc. Natl. Acad. Sci., USA 69., 2110, 1972). Additional clones were derived by restriction digestion of recombinant plasmid pUC9 containing BamHI C fragment (fig. lb) , followed by recovering of the specific E ^tT-4 restriction fragments and sub-cloning thereof within the multi-cloning site of the Bluescript M13⁺ plasmid vector (Stratagen ; Maniatis, T. et al. ibid) . 20 μg of each construct was transfected into monolayer BHK TK^" cells by a modification of the technique of Graham and van der Eb (Virology 52., 456, 1973; CellPhect Transfection Kit, according to manufactures instructions) TK^"1" colonies were selected in HAT supplemented medium (Hypoxanthine lθ~⁴ M, A inopterin 4 x 10~⁵ M, thymidine

1,6 X 10^"5 M) .

TK transforming activity was thus localised to a 2 kbp EcoRV/XhoI fragment (RX2) , cloned in construct pBSRX2, with a map position of approximately 0,48 (fig. lb).

The nucleotide sequence of both. trands of fragment RX2 was determined by using single stranded plasmid DNA as template and Bluescript-derived custom-made oligonucleotides as primers in a Sanger dideoxy sequencing strategy (Sanger et al., Proc. Natl. Acad. Sci: Z _L,5463,1977) (fig.lc). The exact localisation, nucleic acid sequence and corresponding amino acid sequence of the TK gene is shown in the SEQ ID NO: 1.

Example 2

Preparation cf TK-deleted plasmids.

Restriction mapping and sequence analysis of DNA spanning the EHV-4 TK gene indicated that unique Smal and BstXI sites exist within fragment RS3 (fig 1,2) and unique Smal and BstEII sites exist within RX2, all of which map within the TK coding region. A 0,73kbp deletion within the TK gene was achieved by cloning RS3 into pUC 8 (at the Smal and Sail sites within the multicloning site) and digesting the contruct with Smal and BstXI. The vector fragment plus EHV-4 DNA flanking the deletion was isolated and the overhang generated by BstXI filled in using T4 pol. The linear plasmid was then self ligated to produce a plasmid containing RS3 fragment deleted from the Smal-BstXI site (fig. 2b) . A 0,52kbp deletion within the TK gene was achieved by cloning EHV-4 RX2 into a Bluescript vector (at the Smal and Xhol sites within the multicloning site) and deleting from the Smal-BstEII sites within the TK gene by restriction digestion with these enzymes. The larger vector fragment was separated from the 0,52 kbp EHV-4 fragment, the overhang filled in and the plasmid religated. The resultant plasmid possesses the 5' and 3¹ coding regions of the EHV-4 TK gene but is deleted from the Smal-BstEII sites (figure 2c) .

Example 3

Use of Recombinant PCR to Produce TK- Constructs

The two plasmid constructs preferred in Example 2 contain EHV-4 DNA with distinct deletions within the TK gene. The positions of these deletions are dictated by the availability of restriction endonuclease sites within the TK gene which could be utilised in the deletion strategy. Both deletions span the N-terminal coding region of the TK gene. Given that this region is likely to contain the promoter for the adjacent UL24-type gene, incorporation of these DNAs into the EHV genome could possibly result in the altered expression of both the UL24-type gene and of the TK gene. DNAs were therefore constructed with deletions within the C-terminal coding region of the TK gene in order to ultimately produce EHV recombinants affected solely in TK expression. Recombinant polymerase chain reaction (PCR) was utilised to prepare these DNAs since, this technique permits the deletion to be localised anywhere within the gene. As shown in Figures 2 and 3 we synthesised two primer sets (primers 1,2 and 3,4) which were utilised independently to prepare DNA fragments mapping to the left and right of the deletion site (step 1). The external primers (primers 1,4) were then utilised to amplify across the products of the first round PCR reactions (primers 2,3 having complementary annealable end regions) to produce the TK-construct (steps 2,3). Such a strategy has the added advantage that restriction endonuclease sites can be inserted at the termini and at the deletion site by incorporation within the primers. These sites can be utilised to facilitate cloning of the TK- DNA PCR product into a suitable plasmid vector (step 4) and to effect cloning within the deletion site. Primers

The 3' terminal sequences of the following primers were derived from the published sequence information on the TK genes of EHV-1 and EHV-4 (sequences underlined below) . 5 sequences incorporating a 'GC clamp (to enhance the efficiency of cleavage with intra-pri er restriction enzymes) , and 3 restriction enzyme sites. In the case of pr.imers 2 and 3 the 5' regions of the primers are complementary in order to facilitate annealing of denatured first round amplification products at step 2.

LMU (Primer 1)

5'-GCGGATCGATAGATCTGCGGCCGCTGCGTTAGTGGTGTT-3' Clal Bglll Notl

LIL (Primer 2)

5'-GAGCTCGATATCTCTAGAGTAGGGCGTGGTAAAGC-3' Sstl EcoRV Xbal

RIU (Primer 3)

5'-TCTAGAGATATCGAGCTCATATTGGAAGTTCACGC-3' Xbal ECORV Sstl

RML (Primer 4)

5'-CCGGGATCCAGATCTGCGGCCGCTCAGAAGATGTGTACGA-3' BamHI Bglll Notl

The PCR technique is carried out as follows. First primers 1 and 2 are hybridized onto the single stranded EHV genome. Then the second strand is extended along the first strand starting from primer 1 using a DNA polymerase until the primer 2 is encountered, when DNA synthesis stops. Similarly a second DNA oligonucleotide strand is synthesised from primer 3 up to primer 4. The strands are then dehybridised into single DNA strands by heating. If necessary the process can be repeated using further quantities of primer in order to amplify the amount of PCR product. 1 ?

Legends

Figure 1. Strategy for the localisation and sequencing of the EHV-4 thymidine kinase gene.

(a) the TK gene was localised on the BamHI C fragment mapping between 0,43 and 0,53.

(b) subfragments of EHV-4 BamHI C were tested for their capacity to biochemically transfrom BHK TK~ cells to TK⁺ phenotype. TK~ transforming activity was localised to a 2 kbp EcoRV/XhoI fragment, RX2.

(c) subcloning of RX2 and sequencing of overlapping fragments resulted in the exact localisation and nucleotide sequence of the TK gene.

Figure 2.

(a) Restriction enzyme pattern of fragment RS3 containing TK gene.

(b) 0,73 kbp deletion in TK gene (Smal-BstXI) deleted from RS3.

(c) 0,52 kbp deletion in TK gene (Smal-BstEII) deleted from RX2.

Figure 3. shows the strategy for deletion of a region of the TK gene using a polymerase chain reaction (PCR) technique according to steps 1 to 3 of Example 4; and

Figure 4. shows the strategy for cloning of the TK- DNA PCR product obtained from Example 4 into a suitable plasmid vector (step 4) . Sequence Listing

SEQ ID NO : 1

Sequence type : nucleotide with corresponding protein

Sequence length: 1260 base pairs; 352 amino acids.

Strandness : single. Topology : linear Molecule type : genomic DNA

Original source

Organism : Equine herpesvirus -4..

Immediate experimental source : genomic BamHI library.

Features: from 21 to 25 bp putative TATA signal bp 47 putative polymerase initiation site from 109 to 114 bp poly A signal

Properties : thymidine kinase gene .

CCAAATCTTG AACCATTGCG TTATAGAAGC GGTTGTGGCA CCGTATACCC GCTCTGAGTC 60

TGCTTCTAGC GGTGAGACGC TGTTTACGTT TCATCTCCAC AGGCAGTA ATG GCT GCT 117

Met Al a Al a 3

TGC GTA CCC CCG GGA GAA GCT CCA CGA AGC GCC AGC GGA ACG CCC ACC 165 Cys Val Pro Pro Gly Glu Ala Pro Arg Ser Ala Ser Gly Thr Pro Thr 19

CGG CGG CAA GTA ACA ATA GTT AGA ATT TAC CTC GAT GGA GTT TAT GGC 213 Arg Arg Gin Val_. Thr He Val Arg He Tyr Leu Asp Gly Val Tyr Gly 35

ATC GGT AAG AGC ACG ACG GGA CGA GTT ATG GCA TCG GCT GCT AGC GGA 261 He Gly Lys Ser Thr Thr Gly Arg Val Met Ala Ser Ala Ala Ser Gly 51

GGA AGT CCA ACT CTA TAC TTT CCA GAG CCT ATG GCG TAC TGG CGG ACT 309 Gly Ser Pro Thr Leu Tyr Phe Pro Glu Pro Met Ala Tyr Trp Arg Thr 67

CTT TTT GAA ACG GAC GTA ATT AGT GGT ATT TAC GAC ACC CAA AAC CGG 357 Leu Phe Glu Thr Asp Val He Ser Gly He Tyr Asp Thr Gin Asn Arg 83

AAA CAG CAG GGA AAT TTG GCC GTT GAT GAC GCG GCA TTA ATA ACT GCG 405 Lys Gin Gin Gly Asn Leu Ala Val Asp Asp A a Ala Leu He Thr Ala 99

CAT TAC CAA AGC CGC TTT ACC ACG CCC TAC CTG ATA CTC CAC GAT CAC 453 His Tyr Gin Ser Arg Phe Thr Thr Pro Tyr Leu He Leu His Asp His 115 ACT TGT ACG TTG TTT GGG GGA AAC AGC CTA CAG CGT GGA ACA CAA CCG 501

Thr Cys Thr Leu Phe Gly Gly Asn Ser Leu Gin Arg Gly Thr Gin Pro 131

GAC CTG ACC CTT GTG TTT GAC CGC CAC CCG GTC GCC TCT ACC GTA TGC 549

Asp Leu Thr Leu Val Phe Asp Arg His Pro Val Ala Ser Thr Val Cys 147

TTT CCA GCA GCC CGC TAC CTA CTC GGT GAC ATG TCA ATG TGC GCG CTA 597

Phe Pro Ala Ala Arg Tyr Leu Leu Gly Asp Met Ser Met Cys Ala Leu 163

ATG GCT ATG GTT GCT ACT CTA CCA AGA GAA CCC CAG GGT GGT AAC ATT 645

Met Ala Met Val Ala Thr Leu Pro Arg Glu Pro Gin Gly Gly Asn He 179

GTG GTT ACC ACC CTA AAT GTA GAG GAG CAT ATA CGG AGA CTG CGT ACG 693

Val Val Thr Thr Leu Asn Val Glu Glu His He Arg Arg Leu Arg Thr 195

CGG GCT AGA ATA GGA GAA CAA ATT GAC ATT ACG CTG ATT GCT ACA TTG 741

Arg Ala Arg He Gly Glu Gin He Asp He Thr Leu He Ala Thr Leu 211

CGA AAT GTG TAC TTT ATG CTA GTT AAT ACA TGT CAC TTT TTG CGC TCT 789

Arg Asn Val Tyr Phe Met Leu Val Asn Thr Cys His Phe Leu Arg Ser 227

GGG CGA GTT TGG CGC GAC GGT TGG GGT GAG CTA CCC ACT TCC TGT GGG 837

Gly Arg Val Trp Arg Asp Gly Trp Gly Glu Leu Pro Thr Ser Cys Gly 243

GCT TAT AAG CAT CGC GCC ACA CAG ATG GAC GCC TTC CAA GAG CGC GTT 885

Ala Tyr Lys His Arg Ala Thr Gin Met Asp Ala Phe Gin Glu Arg Val 259

TCA CCG GAG CTG GGC GAC ACT CTG TTT GCC CTG TTT AAA ACT CAA GAA 933

Ser Pro Glu Leu Gly Asp Thr Leu Phe Ala Leu Phe Lys Thr Gin Glu ^' 275

CTG CTA GAC GAT CGC GGT GTA ATA TTG GAA GTT CAC GCT TGG GCG TTG 981

Leu Leu Asp Asp Arg Gly Val He Leu Glu Val His Ala Trp Ala Leu 291

GAC GCG CTT ATG CTA AAA CTG CGT AAC CTG AAT GTT TTC AGT GCC GAT 1029

Asp Ala Leu Met Leu Lys Leu Arg Asn Leu Asn Val Phe Ser Ala Asp 307

TTA AGT GGT ACA CCG CGA CAA TGT GCA GCT GTT GTA GAG TCT TTG CTG 1077

Leu Ser Gly Thr Pro Arg Gin Cys Ala Ala Val Val Glu Ser Leu Leu 323

CCA CTT ATG AGC AGC ACC TTA TCA GAT TTT GAT TCC GCC TCT GCT TTA 1125

Pro Leu Met Ser Ser Thr Leu Ser Asp Phe Asp Ser Ala Ser Ala Leu 339

GAG CGG GCG GCA CGC ACC TTT AAC GCG GAG ATG GGC GTC TGA AGCTATATGT 1177

Glu Arg Ala Ala Arg Thr Phe Asn Ala Glu Met Gly Val 352

AATGTTTGTT GTGCCAATGC CAAAATTGTG AAATAAAGATT CATTTGCCAA TATCCATCAT 1237

AGCGCCTTGT GTGTTTCGTG TGT 1260

Claims

1. An EHV-4 mutant, characterized in that it does not produce a functional thymidine kinase as a result of a deletion and/or insertion in the gene encoding thymidine kinase.

2. An EHV-4 mutant according to claim 1 wherein the ends of the region of deletion or insertion do not correspond to endonucleace restriction sites of the thymidine kinase gene.

3. .An EHV-4 mutant according to claim 2 wherein the deletion or insertion is in the C-terminal coding region of the thymidine kinase gene.

4. An EHV-4 mutant according to any preceding claim, characterized in that at least one heterologous nucleic acid sequence encoding a polypeptide is inserted.

5. An EHV-4 mutant according to claim 4 characterized in that the heterologous nucleic acid sequence is under control of a promoter regulating the expression of said nucleic acid sequence in a cell infected with said EHV-4 mutant.

6. An EHV-4 mutant according to claims 4 or 5 characterized in that the heterologous nucleic acid sequence encodes an antigen of an equine pathogen.

7. An EHV-4 mutant according to claim 6 characterized in that the antigen is an EHV-1, or equine influenza antigen.

8. Recombinant DNA molecule comprising a vector molecule and part of the EHV-4 thymidine kinase gene region.

9. Recombinant DNA molecule according to claim 8 characterized in that it has a deletion and/or insertion in the thymidine kinase gene.

10. Host cell containing a recombinant DNA molecule according to claim 9.

11. Process for the preparation of an EHV-4 mutant according to any of claims 1-7 characterized in that cell culture is co-transfected with EHV-4 DNA and a recombinant DNA molecule according to claim 7.

12. Cell culture infected with an EHV-4 mutant according to any of claims 1-7.

13. Vaccine derived from an EHV-4 mutant according to any of claims 1-7.

14. Vaccine which comprises an EHV-4 mutant according to any of claims 1-7 together with a pharmaceutically acceptable carrier therefor.

15. Process for the preparation of an EHV-4 vaccine, characterized in that EHV-4 containing material is collected from a cell culture according to claim 12 and processed into a preparation with immunizing activity.