US2007178563A1PendingUtilityA1
Mosaic infectious bursal disease virus vaccines
Assignee: ID LELYSTAD INST DIERHOUDERIJPriority: Jul 14, 1999Filed: Mar 12, 2007Published: Aug 2, 2007
Est. expiryJul 14, 2019(expired)· nominal 20-yr term from priority
A61K 39/00C07K 2319/00C12N 2720/10061C12N 7/00C07K 14/005
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Claims
Abstract
The invention relates to Infectious Bursal Disease Virus (“IBDV”) and vaccines therefor. Provided are infectious recombinant Infectious Bursal Disease Virus (“rIBDV”) essentially incapable of growing in a cell that is not derived from a bursa cell, or an infectious rIBDV having retained at least part of the very virulent characteristics of a very virulent Infectious Bursal Disease Virus (“vvIBDV”).
Claims
exact text as granted — not AI-modified1 . An infectious recombinant Infectious Bursal Disease Virus (rIBDV) essentially incapable of growing in a non-bursa cell or cell derived from a non-bursa cell.
2 . An infectious rIBDV having retained at least part of the very virulent characteristics of a very virulent Infectious Bursal Disease Virus (vvIBDV).
3 . The rIBDV of claim 1 , wherein the rIBDV has retained at least part of the very virulent characteristics of a very virulent Infectious Bursal Disease Virus (vvIBDV).
4 . The rIBDV of claim 2 , wherein said rIBDV is essentially incapable of growing in a CEF cell, a VERO cell or a QM5 cell.
5 . The rIBDV of claim 3 , wherein the rIBDV's VP2 protein sequence has no asparagine at amino acid position 279.
6 . The rIBDV of claim 5 , wherein the amino acid sequence of protein VP2 has aspartic acid at amino acid position 279.
7 . The rIBDV of claim 3 , wherein the protein VP2 has no threonine at amino acid position 284.
8 . The rIBDV of claim 7 , wherein the protein VP2 has alanine at amino acid position 284.
9 . The rIBDV of claim 8 , wherein the amino acid sequence of protein VP2 comprises a stretch of amino acids from about position 279 to 289 as found in a vvIBDV isolate such as shown in Table 8.
10 . (canceled)
11 . A method for obtaining an infectious recombinant Infectious Bursal Disease Virus (rIBDV) having retained at least part of the very virulent characteristics of a very virulent Infectious Bursal Disease Virus (vvIBDV), said method comprising:
transfecting at least one first cell with a nucleic acid comprising an IBDV genome at least partly derived from a vvIBDV; incubating said at least one first cell in a culture medium; recovering rIBDV from said at least one transfected first cell or said culture medium; and propagating said recovered rIBDV in at least one second cell permissive for said vvIBDV.
12 - 22 . (canceled)
23 . An infectious mosaic IBDV (mIBDV) comprising an rIBDV wherein at least one genome segment comprises nucleic acid derived from at least two different Birna virus isolates.
24 . The mIBDV of claim 23 , wherein at least one of said isolates is a vvIBDV.
25 . The mIBDV of claim 24 , wherein said mIBDV is unable to be propagated on a vvIBDV non-permissive cell selected from the group consisting of a VERO cell, a QM5 cell, and a CEP cell.
26 . The mIBDV of claim 25 , wherein said mIBDV is able to be propagated on a vvIBDV permissive cell.
27 . The mIBDV of claim 26 , wherein at least one of said isolates is a serotype II IBDV.
28 . The mIBDV of claim 27 , lacking at least one immunodominant epitope specific for a serotype I IBDV.
29 . A vaccine comprising the rIBDV of claim 2 .
30 . The rIBDV of claim 8 , wherein the amino acid sequence of protein VP2 at least comprises a stretch of amino acids from about position 229 to 314.Join the waitlist — get patent alerts
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