EP3172319B1 - Coronavirus - Google Patents

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EP3172319B1
EP3172319B1 EP15750093.5A EP15750093A EP3172319B1 EP 3172319 B1 EP3172319 B1 EP 3172319B1 EP 15750093 A EP15750093 A EP 15750093A EP 3172319 B1 EP3172319 B1 EP 3172319B1
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coronavirus
seq
virus
replicase gene
protein
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EP3172319A1 (de
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Erica Bickerton
Sarah KEEP
Paul Britton
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Pirbright Institute
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Pirbright Institute
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    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K39/00—Medicinal preparations containing antigens or antibodies
    • A61K39/12—Viral antigens
    • A61K39/215—Coronaviridae, e.g. avian infectious bronchitis virus
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    • C07—ORGANIC CHEMISTRY
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    • C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • C07K14/005—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from viruses
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
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    • C12N9/00—Enzymes; Proenzymes; Compositions thereof; Processes for preparing, activating, inhibiting, separating or purifying enzymes
    • C12N9/10—Transferases (2.)
    • C12N9/12—Transferases (2.) transferring phosphorus containing groups, e.g. kinases (2.7)
    • C12N9/1241—Nucleotidyltransferases (2.7.7)
    • C12N9/127—RNA-directed RNA polymerase (2.7.7.48), i.e. RNA replicase
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    • C12Y207/00—Transferases transferring phosphorus-containing groups (2.7)
    • C12Y207/07—Nucleotidyltransferases (2.7.7)
    • C12Y207/07048—RNA-directed RNA polymerase (2.7.7.48), i.e. RNA replicase
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K39/00—Medicinal preparations containing antigens or antibodies
    • A61K2039/51—Medicinal preparations containing antigens or antibodies comprising whole cells, viruses or DNA/RNA
    • A61K2039/525—Virus
    • A61K2039/5254—Virus avirulent or attenuated
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K39/00—Medicinal preparations containing antigens or antibodies
    • A61K2039/54—Medicinal preparations containing antigens or antibodies characterised by the route of administration
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K39/00—Medicinal preparations containing antigens or antibodies
    • A61K2039/70—Multivalent vaccine
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    • C12N2770/00011—Details
    • C12N2770/20011—Coronaviridae
    • C12N2770/20021—Viruses as such, e.g. new isolates, mutants or their genomic sequences
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    • C12N2770/00011—Details
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    • C12N2770/20051—Methods of production or purification of viral material
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    • C12N2770/20061—Methods of inactivation or attenuation
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    • C12N2770/00011—Details
    • C12N2770/20011—Coronaviridae
    • C12N2770/20071—Demonstrated in vivo effect

Definitions

  • a plasmid comprising a replicase gene as defined in the claims is provided.
  • a method for making the coronavirus as defined in the claims which comprises the following steps:
  • the recombining virus may be a vaccinia virus.
  • a cell capable of producing a coronavirus according to the first aspect is provided.
  • the present invention also provides a method for producing a vaccine as defined in the claims which comprises the step of infecting a cell as defined in the claims with a coronavirus as defined in the claims.
  • the present invention provides a coronavirus comprising a variant replicase gene which, when expressed in the coronavirus, causes the virus to have reduced pathogenicity compared to a corresponding coronavirus which comprises the wild-type replicase gene.
  • Gammacoronavirus is a genus of animal virus belonging to the family Coronaviridae.
  • Coronaviruses are enveloped viruses with a positive-sense single-stranded RNA genome and a helical symmetry.
  • Coronaviruses primarily infect the upper respiratory or gastrointestinal tract of mammals and birds. Five to six different currently known strains of coronaviruses infect humans. The most publicized human coronavirus, SARS-CoV which causes severe acute respiratory syndrome (SARS), has a unique pathogenesis because it causes both upper and lower respiratory tract infections and can also cause gastroenteritis. Middle East respiratory syndrome coronavirus (MERS-CoV) also causes a lower respiratory tract infection in humans. Coronaviruses are believed to cause a significant percentage of all common colds in human adults.
  • CoV canine coronavirus
  • MHV mouse hepatitis virus
  • Coronaviruses are divided into four groups, as shown below:
  • the variant replicase gene of the coronavirus of the present invention may be derived from an alphacoronavirus such as TGEV; a betacoronavirus such as MHV; or a gammacoronavirus such as IBV.
  • the term "derived from” means that the replicase gene comprises substantially the same nucleotide sequence as the wild-type replicase gene of the relevant coronavirus.
  • the variant replicase gene of the present invention may have up to 80%, 85%, 90%, 95%, 98% or 99% identity with the wild type replicase sequence.
  • the variant coronavirus replicase gene encodes a protein comprising a mutation in one or more of non-structural protein (nsp)-10, nsp-14, nsp-15 or nsp-16 when compared to the wild-type sequence of the non-structural protein.
  • the IBV strain Beaudette was derived following at least 150 passages in chick embryos. IBV Beaudette is no longer pathogenic for hatched chickens but rapidly kills embryos.
  • the virus isolated from the Dutch cases was identified by the Dutch Research Institute at Deventer as a new strain that they called D388.
  • a live attenuated QX-like IBV vaccine strain has now been developed.
  • IBV is an enveloped virus that replicates in the cell cytoplasm and contains an non-segmented, single-stranded, positive sense RNA genome. IBV has a 27.6 kb RNA genome and like all coronaviruses contains the four structural proteins; spike glycoprotein (S), small membrane protein (E), integral membrane protein (M) and nucleocapsid protein (N) which interacts with the genomic RNA.
  • S spike glycoprotein
  • E small membrane protein
  • M integral membrane protein
  • N nucleocapsid protein
  • the genome is organised in the following manner: 5'UTR - polymerase (replicase) gene - structural protein genes (S-E-M-N) - UTR 3'; where the UTR are untranslated regions (each ⁇ 500 nucleotides in IBV).
  • the lipid envelope contains three membrane proteins: S, M and E.
  • the IBV S protein is a type I glycoprotein which oligomerizes in the endoplasmic reticulum and is assembled into homotrimer inserted in the virion membrane via the transmembrane domain and is associated through non-covalent interactions with the M protein. Following incorporation into coronavirus particles, the S protein is responsible for binding to the target cell receptor and fusion of the viral and cellular membranes.
  • the S glycoprotein consists of four domains: a signal sequence that is cleaved during synthesis; the ectodomain, which is present on the outside of the virion particle; the transmembrane region responsible for anchoring the S protein into the lipid bilayer of the virion particle; and the cytoplasmic tail.
  • coronaviruses also encode a set of accessory protein genes of unknown function that are not required for replication in vitro, but may play a role in pathogenesis.
  • IBV encodes two accessory genes, genes 3 and 5, which both express two accessory proteins 3a, 3b and 5a, 5b, respectively.
  • the variant replicase gene of the coronavirus of the present invention may be derived from an IBV.
  • the IBV may be IBV Beaudette, H120, H52, IB QX, D388 or M41.
  • the IBV may be IBV M41.
  • M41 is a prototypic Massachusetts serotype that was isolated in the USA in 1941. It is an isolate used in many labs throughout the world as a pathogenic lab stain and can be obtained from ATCC (VR-21TM). Attenuated variants are also used by several vaccine producers as IBV vaccines against Massachusetts serotypes causing problems in the field. The present inventors chose to use this strain as they had worked for many years on this virus, and because the sequence of the complete virus genome is available.
  • the M41 isolate, M41-CK used by the present inventors was adapted to grow in primary chick kidney (CK) cells and was therefore deemed amenable for recovery as an infectious virus from a cDNA of the complete genome. It is representative of a pathogenic IBV and therefore can be analysed for mutations that cause either loss or reduction in pathogenicity.
  • the genome sequence of IBV M41-CK is provided as SEQ ID NO: 1.
  • 'replicase protein' is used herein to refer to the pp1 a and pp1ab polyproteins or individual nsp subunits.
  • 'replicase gene' is used herein to refer to a nucleic acid sequence which encodes for replicase proteins.
  • Nsp-15 associated NendoU (nidoviral endoribonuclease, specific for U) RNase activity has been reported for a number of coronaviruses, including SARS-CoV, MHV and IBV. The activities were consistently reported to be significantly enhanced by Mn 2+ ions and there was little activity in the presence of Mg 2+ and Ca 2+ . NendoU cleaves at the 3' side of uridylate residues in both single-stranded and double-stranded RNA. The biologically relevant substrate(s) of coronavirus NendoUs remains to be identified.
  • Nsp-16 has been predicted to mediate ribose-2'-O-methyltransferase (2'-O-MTase) activity and reverse-genetics experiments have shown that the 2'-O-MTase domain is essential for viral RNA synthesis in HCoV-229E and SARS-CoV.
  • the enzyme may be involved in the production of the cap 1 structures of coronavirus RNAs and it may also cooperate with NendoU and ExoN in other RNA processing pathways. 2'-O-MTase might also methylate specific RNAs to protect them from NendoU-mediated cleavage.
  • genomic and protein sequences for nsp-10, -14, -15 and -16 are provided as SEQ ID NO: 2-5 and 6-9, respectively.
  • the live, attenuated coronavirus of the present invention comprises a variant replicase gene as defined in the claims which causes the virus to have reduced pathogenicity compared to a coronavirus expressing the corresponding wild-type gene.
  • pathogenicity is used herein according to its normal meaning to refer to the potential of the virus to cause disease in a subject. Typically the pathogenicity of a coronavirus is determined by assaying disease associated symptoms, for example sneezing, snicking and reduction in tracheal ciliary activity.
  • reduced pathogenicity is used to describe that the level of pathogenicity of a coronavirus is decreased, lessened or diminished compared to a corresponding, wild-type coronavirus.
  • pathogenicity of a coronavirus may be assessed utilising methods well-known in the art. Typically, pathogenicity is assessed by assaying clinical symptoms in a subject challenged with the virus, for example a chicken.
  • the chicken may be challenged at 8-24 days old by nasal or ocular inoculation.
  • Clinical symptoms, associated with IBV infection may be assessed 3-10 days post-infection.
  • Clinical symptoms commonly assessed to determine the pathogenicity of a coronavirus, for example an IBV include gasping, coughing, sneezing, snicking, depression, ruffled feathers and loss of tracheal ciliary activity.
  • the variant replicase of the present invention when expressed in a coronavirus, may cause a reduced level of clinical symptoms compared to a coronavirus expressing a wild-type replicase.
  • a coronavirus expressing the variant replicase may cause a number of snicks per bird per minute which is less than 90%, less than 80%, less than 70%, less than 60%, less than 50%, less than 40%, less than 30%, less than 20% or less than 10% of the number of snicks caused by a virus expressing the wild type replicase.
  • a coronavirus expressing a variant replicase according to the present invention may cause wheezing in less than 70%, less than 60%, less than 50%, less than 40%, less than 30%, less than 20% or less than 10% of the number of birds in a flock infected with the a virus expressing the wild type replicase.
  • a coronavirus expressing a variant replicase according to the present invention may result in tracheal ciliary activity which is at least 60%, at least 70%, at least 80%, at least 90% or at least 95% of the level of tracheal ciliary activity in uninfected birds.
  • the variant replicase of the present invention when expressed in a coronavirus, may cause the virus to replicate at non-pathogenic levels in ovo.
  • a viral particle must be sufficiently efficient at replicating and propagating to ensure that it is not neutralized by the maternally-derived antibodies against the virus.
  • Maternally-derived antibodies are a finite pool of effective antibodies, which decrease as the chicken ages, and neutralization of the virus in this manner does not equate to the establishment of long-term immunity for the embryo/chick.
  • the embryo and hatched chicken In order to develop long-term immunity against the virus, the embryo and hatched chicken must develop an appropriate protective immune response which is distinct to the effect of the maternally-derived antibodies.
  • the virus must also not replicate and propagate at a level which causes it to be pathogenic to the embryo.
  • Reduced pathogenicity in terms of the embryo may mean that the coronavirus causes less reduction in hatchability compared to a corresponding, wild-type control coronavirus.
  • the term "without being pathogenic to the embryo” in the context of the present invention may mean "without causing reduced hatchability" when compared to a control coronavirus.
  • a suitable variant replicase may be identified using methods which are known in the art. For example comparative challenge experiments following in ovo vaccination of embryos with or without maternally-derived antibodies may be performed (i.e. wherein the layer has or has not been vaccinated against IBV).
  • the variant replicase enables the virus to propagate at a level which is too high, the embryo will not hatch or will not be viable following hatching (i.e. the virus is pathogenic to the embryo). A virus which is pathogenic to the embryo may kill the embryo.
  • the variant replicase causes a reduction in viral replication and propagation which is too great, the virus will be neutralised by the maternally-derived antibodies. Subsequent challenge of the chick with IBV will therefore result in the development of clinical symptoms (for example wheezing, snicking, loss of ciliary activity) and the onset of disease in the challenged chick; as it will have failed to develop effective immunity against the virus.
  • clinical symptoms for example wheezing, snicking, loss of ciliary activity
  • 'variant' is synonymous with 'mutant' and refers to a nucleic acid or amino acid sequence which differs in comparison to the corresponding wild-type sequence.
  • a variant/mutant sequence may arise naturally, or may be created artificially (for example by site-directed mutagenesis).
  • the mutant may have at least 70, 80, 90, 95, 98 or 99% sequence identity with the corresponding portion of the wild type sequence.
  • the mutant may have less than 20, 10, 5, 4, 3, 2 or 1 mutation(s) over the corresponding portion of the wild-type sequence.
  • wild type is used to mean a gene or protein having a nucleotide or amino acid sequence which is identical with the native gene or protein respectively (i.e. the viral gene or protein).
  • BLAST and FASTA are available for offline and online searching (see Ausubel et al., 1999 ibid, pages 7-58 to 7-60). However, for some applications, it is preferred to use the GCG Bestfit program.
  • a new tool, called BLAST 2 Sequences is also available for comparing protein and nucleotide sequence (see FEMS Microbiol Lett 1999 174(2): 247-50 ; FEMS Microbiol Lett 1999 177(1): 187-8 and tatiana@ncbi.nlm.nih.gov).
  • the sequence may have one or more deletions, insertions or substitutions of amino acid residues which produce a silent change and result in a functionally equivalent molecule.
  • Deliberate amino acid substitutions may be made on the basis of similarity in polarity, charge, solubility, hydrophobicity, hydrophilicity, and/or the amphipathic nature of the residues as long as the activity is retained.
  • negatively charged amino acids include aspartic acid and glutamic acid; positively charged amino acids include lysine and arginine; and amino acids with uncharged polar head groups having similar hydrophilicity values include leucine, isoleucine, valine, glycine, alanine, asparagine, glutamine, serine, threonine, phenylalanine, and tyrosine.
  • the coronavirus of the present invention comprises a variant replicase gene as defined in the claims which encodes a protein which comprises a mutation compared to SEQ ID NO: 7 which, when expressed in a coronavirus, causes the virus to have reduced pathogenicity compared to a coronavirus expressing the corresponding wild-type replicase.
  • the variant replicase gene of the coronavirus as defined in the claims of the present invention may encode a protein comprising a mutation as defined in the M41 mod sequences presented in Figure 10 .
  • the variant replicase gene of the coronavirus of the present invention may encode a protein which comprises the amino acid mutations:
  • the variant replicase gene of the coronavirus of the present invention may encode a protein which does not comprise a mutation in nsp-2, nsp-3, nsp-6 or nsp-13.
  • Ammayappan et al reports the identification of sequence changes responsible for the attenuation of IBV strain Arkansas DPI.
  • the study identified 17 amino acid changes in a variety of IBV proteins following multiple passages, approx. 100, of the virus in embryonated eggs. It was not investigated whether the attenuated virus (Ark DPI 101) is capable of replicating in the presence of maternally-derived antibodies against the virus in ovo, without being pathogenic to the embryo. Given that this virus was produced by multiple passage in SPF embryonated eggs, similar methodology for classical IBV vaccines, it is likely that this virus is pathogenic for embryos. The virus may also be sensitive to maternally-derived antibodies if the hens were vaccinated with a similar serotype.
  • the variant replicase gene of the coronavirus of the present invention may encode a protein which comprises any combination of one or more amino acid mutations provided in the list above.
  • the variant replicase gene may encode a protein which comprises the amino acid mutation Pro to Leu at position 85 of SEQ ID NO: 6.
  • the variant replicase gene encodes a protein which comprises the amino acid mutation Val to Leu at position 393 of SEQ ID NO: 7.
  • the variant replicase gene may encode a protein which comprises the amino acid mutation Leu to Ile at position 183 of SEQ ID NO: 8.
  • the variant replicase gene may encode a protein which comprises the amino acid mutation Val to Ile at position 209 of SEQ ID NO: 9.
  • the variant replicase gene may encode a protein which comprises the amino acid mutations Pro to Leu at position 85 of SEQ ID NO: 6, and Val to Leu at position 393 of SEQ ID NO: 7.
  • the variant replicase gene may further encode a protein which comprises the amino acid mutations Pro to Leu at position 85 of SEQ ID NO: 6 Leu to Ile at position 183 of SEQ ID NO: 8.
  • the variant replicase gene may further encode a protein which comprises the amino acid mutations Pro to Leu at position 85 of SEQ ID NO: 6 and Val to Ile at position 209 of SEQ ID NO: 9.
  • the variant replicase gene may encode a protein which comprises the amino acid mutations Val to Leu at position 393 of SEQ ID NO: 7 and Leu to Ile at position 183 of SEQ ID NO: 8.
  • the variant replicase gene may encode a protein which comprises the amino acid mutations Val to Leu at position 393 of SEQ ID NO: 7 and Val to Ile at position 209 of SEQ ID NO: 9.
  • the variant replicase gene may further encode a protein which comprises the amino acid mutations Leu to Ile at position 183 of SEQ ID NO: 8 and Val to Ile at position 209 of SEQ ID NO: 9.
  • the variant replicase gene may encode a protein which comprises the amino acid mutations Pro to Leu at position 85 of SEQ ID NO: 6, Val to Leu at position 393 of SEQ ID NO: 7 and Leu to Ile at position 183 of SEQ ID NO: 8.
  • the variant replicase gene may further encode a protein which comprises the amino acid mutations Pro to Leu at position 85 of SEQ ID NO: 6 Leu to Ile at position 183 of SEQ ID NO: 8 and Val to Ile at position 209 of SEQ ID NO: 9.
  • the variant replicase gene may encode a protein which comprises the amino acid mutations Pro to Leu at position 85 of SEQ ID NO: 6, Val to Leu at position 393 of SEQ ID NO: 7 and Val to Ile at position 209 of SEQ ID NO: 9.
  • the variant replicase gene may encode a protein which comprises the amino acid mutations Val to Leu at position 393 of SEQ ID NO: 7, Leu to Ile at position 183 of SEQ ID NO: 8 and Val to Ile at position 209 of SEQ ID NO: 9.
  • the variant replicase gene may encode a protein which comprises the amino acid mutations Pro to Leu at position 85 of SEQ ID NO: 6, Val to Leu at position 393 of SEQ ID NO: 7, Leu to Ile at position 183 of SEQ ID NO: 8 and Val to Ile at position 209 of SEQ ID NO: 9.
  • the variant replicase gene may also be defined at the nucleotide level.
  • nucleotide sequence of the variant replicase gene of the coronavirus of the present invention may comprise one or more nucleotide substitutions within the regions selected from the list of: 11884-12318, 16938-18500, 18501-19514 and 19515-20423 of SEQ ID NO:1.
  • nucleotide sequence of the variant replicase gene of the coronavirus of the present invention may comprise one or more nucleotide substitutions selected from the list of:
  • substitution is synonymous with the term mutation and means that the nucleotide at the identified position differs to that of the wild-type nucleotide sequence.
  • the nucleotide sequence may comprise substitution G18114C.
  • Recombinants comprising the plasmid may be selected for e.g. using a resistance marker on the plasmid.
  • the vaccine may be administered to any suitable compartment of the egg, including allantoic fluid, yolk sac, amnion, air cell or embryo. It may be administered below the shell (aircell) membrane and chorioallantoic membrane.
  • the vaccine may be administered together with one or more other vaccines, for example, vaccines for other diseases, such as Newcastle disease virus (NDV).
  • NDV Newcastle disease virus
  • the present disclosure also provides a vaccine composition comprising a vaccine disclosed herein together with one or more other vaccine(s).
  • a kit comprising a vaccine described herein together with one or more other vaccine(s) for separate, sequential or simultaneous administration.
  • the vaccine or vaccine composition of the invention may be used to treat a human, animal or avian subject.
  • the subject may be a chick, chicken or mouse (such as a laboratory mouse, e.g. transgenic mouse).
  • the composition may optionally comprise a pharmaceutically acceptable carrier, diluent, excipient or adjuvant.
  • a pharmaceutically acceptable carrier diluent, excipient or adjuvant.
  • the choice of pharmaceutical carrier, excipient or diluent can be selected with regard to the intended route of administration and standard pharmaceutical practice.
  • the pharmaceutical compositions may comprise as (or in addition to) the carrier, excipient or diluent, any suitable binder(s), lubricant(s), suspending agent(s), coating agent(s), solubilising agent(s), and other carrier agents that may aid or increase the delivery or immunogenicity of the virus.
  • a M41-CK full-length cDNA was produced by replacement of the Beaudette cDNA in the Vaccinia virus reverse genetics system previously described in WO2011/004146 with synthetic cDNA derived from the M41 consensus sequence.
  • the viruses rescued in Example 1 were used to infect 8-day-old specific pathogen free (SPF) chicks by ocular and nasal inoculation to test them for pathogenicity, as observed by clinical signs on a daily basis 3-7 days post-infection and for ciliary activity days 4 and 6 post-infection. Loss of ciliary activity is a well-established method for determining the pathogenicity of IBV.
  • the two M41-R viruses were found to be apathogenic when compared to M41-CK though they did show some clinical signs in comparison to uninfected control chicks ( Fig. 2 ) and some but inconsistent loss in ciliary activity ( Fig. 3 ).
  • M41-R molecular clones of M41-CK were not pathogenic when compared to the parental virus M41-CK.
  • the Nsp10 mutation was repaired and the mutations in Nsp-14, -15 & -16 were repaired and shown to grow in a similar manner as M41-CK ( Fig 9 ).
  • the inventors thus generated the rIBVs, M41R-nsp10rep and M41 R-nsp14, 15, 16rep, using synthetic cDNAs containing the correct nucleotides utilising the inventor's orevious described (TDS) system (see WO2011/004146 ).
  • the full-length cDNA corresponding to M41R-nsp10rep was used to repair the mutations in Nsps14, 15 & 16 using a synthetic cDNA containing the correct nucleotides utilising the TDS system.
  • the rIBVs were shown to grow in a similar manner as M41-CK ( Fig 9 ) and assessed for pathogenicity as described previously.
  • M41-K in which all four mutations had been repaired
  • the other rIBVs demonstrated varying levels of pathogenicity, apart from M41R-nsp10, 15, 16rep, which was essentially apathogenic.
  • Candidate vaccine viruses were tested in studies in which fertilized chicken eggs were vaccinated in ovo at 18 days embryonation and in which the hatchability of the inoculated eggs was determined. The clinical health of the chickens was investigated and the chickens were challenged at 21 days of age with a virulent IB M41 challenge virus at 10 3.65 EID 50 per dose.
  • IB M41-R was safe in commercial eggs, generated protection against clinical signs and to an extent against ciliostasis.
  • IB M41-R has great potential as vaccine to be administered in ovo.

Claims (14)

  1. Lebendes, abgeschwächtes Coronavirus, umfassend eine Polyproteine codierende Replikase-Genvariante, die eine Mutation in nsp-14 umfasst, wobei die Replikase-Genvariante ein Protein codiert, das eine Aminosäuremutation von Val zu Leu an der Position 393 von SEQ ID NO: 7 entsprechenden Position umfasst.
  2. Coronavirus nach Anspruch 1, ferner umfassend eine Mutation in einer oder mehreren von nsp-10 gemäß SEQ ID NO: 6, nsp-15 gemäß SEQ ID NO: 8 und nsp-16 gemäß SEQ ID NO: 9.
  3. Coronavirus nach Anspruch 2, wobei die Replikase-Genvariante ein Protein codiert, das eine oder mehrere Aminosäuremutationen ausgewählt aus einer Aminosäuremutation von Pro zu Leu an der Position 85 von SEQ ID NO: 6 entsprechenden Position, einer Aminosäuremutation von Leu zu Ile an der Position 183 von SEQ ID NO: 8 entsprechenden Position und einer Aminosäuremutation von Val zu Ile an der Position 209 von SEQ ID NO: 9 entsprechenden Position umfasst.
  4. Coronavirus nach einem vorhergehenden Anspruch, wobei das Replikase-Gen ein Protein codiert, das die folgenden Aminosäuremutationen umfasst: Pro zu Leu an der Position 85 von SEQ ID NO: 6 entsprechenden Position; Val zu Leu an der Position 393 von SEQ ID NO: 7 entsprechenden Position; Leu zu Ile an der Position 183 von SEQ ID NO: 8 entsprechenden Position; und Val zu Ile an der Position 209 von SEQ ID NO: 9 entsprechenden Position.
  5. Coronavirus nach einem vorhergehenden Anspruch, bei dem es sich um ein IBV (Infectious Bronchitis Virus), vorzugsweise IBV M41 handelt.
  6. Coronavirus nach Anspruch 5, das ein S-Protein umfasst, das wenigstens zum Teil von einem anderen IBV-Serotyp als M41 stammt, vorzugsweise wobei die S1-Untereinheit von einem anderen IBV-Serotyp als M41 stammt oder wobei das S-Protein von einem anderen IBV-Serotyp als M41 stammt.
  7. Replikase-Genvariante gemäß einem der Ansprüche 1 bis 4.
  8. Protein, codiert durch eine Coronavirus-Replikase-Genvariante nach Anspruch 7.
  9. Plasmid, umfassend ein Replikase-Gen nach Anspruch 7.
  10. Verfahren zur Herstellung des Coronavirus nach einem der Ansprüche 1 bis 6, das die folgenden Schritte umfasst:
    (i) Transfizieren eines Plasmids nach Anspruch 9 in eine Wirtszelle;
    (ii) Infizieren der Wirtszelle mit einem rekombinierenden Virus, das das Genom eines Coronavirusstamms mit einem Replikase-Gen umfasst, vorzugsweise wobei es sich bei dem rekombinierenden Virus um ein Vacciniavirus handelt;
    (iii) Stattfindenlassen einer homologen Rekombination zwischen den Replikase-Gensequenzen im Plasmid und den entsprechenden Sequenzen im Genom des rekombinierenden Virus, so dass ein modifiziertes Replikase-Gen erzeugt wird; und
    (iv) Selektionieren auf rekombinierendes Virus, das das modifizierte Replikase-Gen umfasst; gegebenenfalls ferner umfassend den Schritt
    (v) Gewinnen von rekombinantem Coronavirus, das das modifizierte Replikase-Gen umfasst, aus der DNA vom rekombinierenden Virus aus Schritt (iv).
  11. Impfstoff, umfassend ein Coronavirus nach einem der Ansprüche 1 bis 6 und einen pharmazeutisch unbedenklichen Träger.
  12. Impfstoff nach Anspruch 11 zur Verwendung beim Vorbeugen einer Krankheit bei einem Individuum, vorzugsweise wobei es sich bei der Krankheit um infektiöse Bronchitis (IB) handelt, ganz besonders bevorzugt wobei es sich bei der Impfung um eine In-ovo-Impfung handelt.
  13. Impfstoff zur Verwendung nach Anspruch 12, wobei der Impfstoff über Augentropfenverabreichung, intranasale Verabreichung, Trinkwasserverabreichung, Post-hatch-Injektion oder In-ovo-Injektion verabreicht wird.
  14. Verfahren zur Erzeugung eines Impfstoffs nach Anspruch 11, das den Schritt Infizieren einer Wirtszelle mit einem Coronavirus nach einem der Ansprüche 1 bis 6 umfasst.
EP15750093.5A 2014-07-23 2015-07-23 Coronavirus Active EP3172319B1 (de)

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JP2017522907A (ja) 2017-08-17
BR112017001310A2 (pt) 2018-04-17
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US10130701B2 (en) 2018-11-20
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BR112017001310B1 (pt) 2022-06-28
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