Prevention and treatment of sub-clinical PCVD
The present invention relates to the use of an immunogenic composition comprising a porcine circovirus type 2 (PCV2) antigen for the prevention and treatment of sub-clinical PCV2 infection in animals, preferably in pigs.
1. A method for the prophylaxis and treatment of a sub-clinical PCV2 infection in an pig or a group of pigs, comprising the step of once administering an immunogenic composition comprising a PCV2 ORF2 protein to a pig or group of pigs in need of such administration wherein the sub-clinical PCV2 infection is characterized by individual infected pigs that are infected with PCV2 but are clinically asymptomatic and that have at or below 10 6 viral copies of PCV2 per ml of serum for at least 6 weeks in the absence of one or more clinical symptoms of PCVD.
2. The method according to claim 1 , wherein the sub-clinical PCV2 infection is characterized by a maximum of 20% of pigs within a group of pigs with viral titers above 10 6 genomic copies per ml serum.
3. The method according to claim 1 , wherein the sub-clinical PCV2 infection is characterized by no morbidity or a low morbidity rate of less than 25% of the PCV2 positive pigs within a group of pigs.
4. The method according to claim 1 , wherein the sub-clinical PCV2 infection is further characterized by low mortality rate of less than 20% of the PCV2 positive pigs within a group of pigs.
5. The method according to claim 1 , wherein said PCV2 ORF2 protein comprises a polypeptide selected from the group consisting of:
i. a polypeptide comprising the sequence of SEQ ID NO. 5, SEQ ID NO. 6, or SEQ ID NO. 11;
ii. a polypeptide having at least 80% sequence homology with the polypeptide of i;
iii. a polypeptide that is encoded by a DNA comprising the sequence of SEQ ID NO. 3 or SEQ ID NO. 4; or
iv. a polypeptide that is encoded by a polynucleotide having at least 80% sequence homology with the polynucleotide of iii.
6. The method according to claim 1 , wherein said PCV-2 ORF2 protein is a recombinant baculovirus expressed ORF-2 protein of PCV2.
7. The method according to claim 1 , wherein said PCV2 ORF2 protein is included in Ingelvac® CircoFLEX™.
8. A method of reducing an impact of PCV2 sub-clinical infection, wherein the sub-clinical PCV2 infection is characterized by individual infected pigs that are infected with PCV2 but are clinically asymptomatic and that have at or below 10 6 viral copies of PCV2 per ml of serum for at least 6 weeks in the absence of one or more clinical symptoms of PCVD, said impact being selected from the group consisting of reduction of viral load, reduction of the proportion of PCV2 positive animals with 10 6 genomic copies, duration of viremia, and combinations thereof, said method comprising the step of once administering an immunogenic composition comprising a PCV2 ORF2 protein to a pig in need of such administration.
9. The method according to claim 8 , wherein said PCV2 ORF2 protein comprises a polypeptide selected from the group consisting of:
i. a polypeptide comprising the sequence of SEQ ID NO. 5, SEQ ID NO. 6, or SEQ ID NO. 11;
ii. a polypeptide having at least 80% sequence homology with the polypeptide of i;
iii. a polypeptide that is encoded by a DNA comprising the sequence of SEQ ID NO. 3 or SEQ ID NO. 4; or
iv. a polypeptide that is encoded by a polynucleotide having at least 80% sequence homology with the polynucleotide of iii.
10. The method according to claim 8 , wherein said PCV-2 ORF2 protein is a recombinant baculovirus expressed ORF-2 of PCV2.
11. The method according to claim 8 , wherein said PCV2 ORF2 protein is included in Ingelvac® CircoFLEX™.
12. The method of claim 8 , wherein the step of administering an immunogenic composition comprises a single dose of 0.2 μg to about 400 μg/dose PCV2 ORF2 protein.
13. A method for the reduction of the number of pigs with viral load above 10 6 genomic copies per ml serum in at least 80% of the animals in a group of pigs (herds) sub-clinically infected with PCV2, wherein the sub-clinical PCV2 infection is characterized by individual infected pigs that are infected with PCV2 but are clinically asymptomatic and that have at or below 10 6 viral copies of PCV2 per ml of serum for at least 6 weeks in the absence of one or more clinical symptoms of PCVD, comprising the step of once administering an immunogenic composition comprising 0.2 μg to about 400 μg/dose PCV2 ORF2 protein or an immunogenic composition comprising a PCV2 antigen to a group of pigs in need of such administration.
14. The method according to claim 13 , wherein said PCV2 ORF2 protein comprises a polypeptide selected from the group consisting of:
an ORF2 protein comprising a polypeptide selected from the group consisting of:
i. a polypeptide comprising the sequence of SEQ ID NO. 5, SEQ ID NO. 6, or SEQ ID NO. 11;
ii. a polypeptide having at least 80% sequence homology with the polypeptide of i;
iii. a polypeptide that is encoded by a DNA comprising the sequence of SEQ ID NO. 3 or SEQ ID NO. 4; or
iv. a polypeptide that is encoded by a polynucleotide having at least 80% sequence homology with the polynucleotide of iii.
15. The method according to claim 13 , wherein said PCV-2 ORF2 protein is a recombinant baculovirus expressed ORF-2 of PCV2.
16. The method according to claim 13 , wherein the PCV2 ORF2 protein is included in Ingelvac® CircoFLEX™.
17. The method of claim 13 , said immunogenic composition further comprising a polymer of acrylic or methacrylic acid.