Attenuated RNA virus and applications thereof
The invention encompasses an attenuated RNA virus and methods of using an attenuated RNA virus. The RNA virus comprises, in part, an ion channel protein comprising a peptide tag.
1. An isolated influenza virus, wherein the virus comprises a M2 protein comprising a peptide tag at the carboxyl terminus, wherein
(a) the in vitro function of the M2 protein comprising the peptide tag is not altered compared to the in vitro function of the native M2 protein,
(b) replication of the virus in vitro is similar to that of a virulent strain of the same virus, and the replication of the virus in a host is reduced relative to that of a virulent strain of the same virus, and
(c) the virulence of the virus in a host is reduced relative to that of a virulent strain of the same virus.
2. The isolated influenza virus of claim 1 , wherein the peptide tag is from about 3 amino acids to about 30 amino acids in length.
3. The isolated influenza virus of claim 1 , wherein the virus is influenza A.
4. The isolated influenza virus of claim 3 , wherein the peptide tag is the myc antibody epitope tag, whose amino acid sequence consists of EQKLISEEDL (SEQ ID NO:1).
5. An immunogenic composition, wherein the composition comprises at least one live attenuated influenza virus, the virus comprising M2 protein comprising a peptide tag at the carboxyl terminus, wherein
(a) the in vitro function of the M2 protein comprising a peptide tag is not altered compared to the in vitro function of the native M2 protein, and
(b) replication of the virus in vitro is similar to that of a virulent strain of the same virus, and the replication of the virus in a host is reduced relative to that of a virulent strain of the same virus, and
(c) the virulence of the virus in a host is reduced relative to that of a virulent strain of the same virus.
6. The immunogenic composition of claim 5 , wherein the peptide tag is from about 3 amino acids to about 30 amino acids in length.
7. The immunogenic composition of claim 5 , wherein the virus is influenza A selected from the group consisting of an H1N1 subtype, an H3N2 subtype, an H5N1 subtype, and a combination thereof.
8. The immunogenic composition of claim 7 , wherein the peptide tag is the myc antibody epitope tag, whose amino acid sequence consists of EQKLISEEDL (SEQ ID NO:1).
9. The immunogenic composition of claim 7 , wherein the composition further comprises an attenuated influenza B virus comprising an M2 protein comprising a peptide tag at the carboxyl terminus.
10. A method for inducing an immune response in a subject against an influenza virus, the method comprising administering to the subject an immunogenic composition comprising at least one live attenuated influenza virus, the virus comprising M2 protein comprising a peptide tag at the carboxyl terminus, wherein
(a) the in vitro function of the M2 protein comprising the peptide tag is not altered compared to the in vitro function of the native M2 protein, and
(b) replication of the virus in vitro is similar to that of a virulent strain of the same virus, and the replication of the virus in a host is reduced relative to that of a virulent strain of the same virus, and
(c) the virulence of the virus in a host is reduced relative to that of a virulent strain of the same virus.
11. The method of claim 10 , wherein the peptide tag is from about 3 amino acids to about 30 amino acids in length.
12. The method of claim 10 , wherein the influenza virus is a type A virus selected from the group consisting of an H1N1 subtype, an H3N2 subtype, an H5N1 subtype, and a combination thereof.
13. The method of claim 12 , wherein the peptide tag is the myc antibody epitope tag, whose amino acid sequence consists of EQKLISEEDL (SEQ ID NO:1).