Salmon gill poxvirus
The present document is directed to a new poxvirus infecting salmon. The present document further discloses the genomic sequence of this double-stranded DNA virus and the use of this sequence information for detection, diagnosis and/or vaccine development for the virus.
1. An isolated nucleic acid molecule consisting of 18 to 100 contiguous nucleotides of a nucleic acid sequence according to SEQ ID NO:1-9, or a nucleic acid sequence complementary to said nucleic acid sequence, wherein said nucleic acid molecule is a nucleic acid probe comprising a label selected from the group consisting of a radioactive label, a fluorescent label, a chemiluminescent label, an enzyme substrate, and an enzyme molecule.
2. The nucleic acid fragment according to claim 1 , wherein said nucleic acid molecule is a nucleic acid probe, the nucleic acid sequence of which probe is as defined in any one of SEQ ID NO:4-7.
3. The nucleic acid molecule according to claim 1 , wherein said nucleic acid molecule is a primer, wherein said primer is as defined in any one o SEQ ID NO: 8-9.
4. A method for detecting a Piscine poxvirus in a tissue sample isolated from fish, said method comprising:
a) contacting said sample with a nucleic acid primer and/or probe, wherein said nucleic acid primer and/or probe specifically binds to a nucleic acid consisting of 18 to 100 consecutive nucleic acid bases of a nucleic acid sequence according to any one of SEQ ID NO:1-9, or a sequence complementary thereto, wherein said nucleic acid primer and/or probe comprises a label selected from the group consisting of a radioactive label, a fluorescent label, a chemiluminescent label, an enzyme substrate, and an enzyme molecule; and
b) detecting the formation of a complex between said nucleic acid and said probe or primer, wherein the presence of said complex indicates the presence of a Piscine poxvirus specific nucleic acid in said sample.
5. The method of claim 4 , wherein said method comprises a polymerase chain reaction method.
6. The method of claim 4 , wherein said method comprises in situ hybridization.
7. The method of claim 4 , wherein the presence of said Piscine poxvirus specific nucleic acid in said sample is indicative of Piscine poxvirus infection in said sample.
8. The method of claim 4 , wherein said label is a fluorophore in combination with a minor groove binding non-fluorescence quencher (MGBNFG).
9. The nucleic acid molecule of claim 1 , wherein said label is a fluorophore in combination with a MGBNFG.
10. A composition comprising a first isolated nucleic acid molecule consisting of 18 to 100 contiguous nucleotides of a nucleic acid sequence according to SEQ ID NO:1-9 or a nucleic acid sequence complementary to said nucleic acid sequence, wherein said nucleic acid molecule is a nucleic acid probe comprising a label selected from the group consisting of a radioactive label, a fluorescent label, a chemiluminescent label, an enzyme substrate, and an enzyme molecule; and a second isolated nucleic acid comprising a primer consisting of 18 to 100 contiguous nucleotides of a nucleic acid sequence according to SEQ ID NO:1-9, or a sequence complementary thereto.
11. The method of claim 4 , wherein said primer is as defined in any one of SEQ ID NO:8-9.
12. The nucleic acid molecule according to claim 1 , wherein said nucleic acid molecule consists of 18 to 100 contiguous nucleotides of a nucleic acid sequence according to SEQ ID NOs:2-3.
13. The method according to claim 4 , wherein said nucleic acid primer and/or probe specifically binds to a nucleic acid consisting of 18 to 100 contiguous nucleotides of a nucleic acid sequence according to SEQ ID NOs:2-3.
14. The composition of claim 10 , wherein said nucleic acid molecule consists of 18 to 100 contiguous nucleotides of a nucleic acid sequence according to SEQ ID NOs:2-3.