Dengue chimeric viruses
The invention relates to Dengue chimeric viruses which are less prone to accumulate point mutations and genetic variations. In these Dengue chimeric viruses, the NS5 gene, which encodes polymerase, has been replaced by the corresponding NS5 sequence of a Yellow Fever virus.
1. An isolated, attenuated chimeric Dengue virus comprising the 5′-noncoding region (NCR), structural sequences capsid (C), premembrane/membrane (prM/M), and envelope (E), and non structural sequences NS1, NS2A, NS2B, NS3, NS4A, and NS4B of one Dengue strain; the non structural sequence NS5 of a Yellow fever virus; and either the 3′-NCR sequence of said Dengue strain or the 3′-NCR sequence of said Yellow Fever virus.
2. The isolated chimeric Dengue virus of claim 1 , wherein the 3′ NCR sequence of the Dengue virus has been replaced by the 3′NCR sequence of the same Yellow Fever virus.
3. The isolated chimeric Dengue virus according to claim 1 , wherein said Dengue virus is selected from the group consisting of Dengue serotype 1, Dengue serotype 2, Dengue serotype 3, and Dengue serotype 4 viruses.
4. The isolated chimeric Dengue virus according to claim 1 , wherein said Dengue virus is a live attenuated Dengue virus.
5. The isolated chimeric Dengue virus according to claim 1 , wherein said one Dengue strain is LAV1 (SEQ ID No.9).
6. The isolated chimeric Dengue virus according to claim 1 , wherein said Yellow Fever virus is the vaccinal strain YF17D (SEQ ID No.7).
7. An immunogenic composition comprising a chimeric Dengue virus according to claim 1 or 2 in a pharmaceutically acceptable carrier.
8. The immunogenic composition according to claim 7 , which is a monovalent composition.
9. The immunogenic composition according to claim 7 , which is a multivalent composition.