Antiviral drug combination for livestock
An anti-virus and composition technology, applied in the direction of anti-viral agents, using vectors to introduce foreign genetic material, antibodies, etc., can solve the problems of anti-viral application restrictions and few methods
Patent Information
- Authority / Receiving Office
- CN · China
- Current Assignee / Owner
- Publication Date
- 2009-12-30
- Estimated Expiration
- Not applicable · inactive patent
Abstract
Description
Technical field
[0001] The invention relates to an antiviral agent, in particular to an antiviral agent for poultry and livestock.
Background technique
[0002] IFN-α is a cytokine with strong antiviral activity. It has been widely used in the treatment of human viral diseases and has become an essential therapy. For example, in the treatment of hepatitis C, IFN-α plays an irreplaceable role. Since the antiviral effect of IFN-α is indirect and works by inducing other antiviral mechanisms in the body, one of its important characteristics is that it has no virus specificity, that is to say, IFN-α has anti-virus activity; However, another important feature of the antiviral effect of IFN-α is species specificity, that is to say, IFN-α from a certain species is only effective against viruses infected by that species, but not against viruses infected by other species . For example, human IFN-α is only effective for human virus infection, but not for other species including ...
Examples
Embodiment 1
[0045] 1. Preparation of antiviral protein from cyanobacteria
[0046] (1) extract total RNA from cyanobacteria, amplify the gene fragment of cyanobacteria antiviral protein by RT-PCR, the amino acid sequence of cyanobacteria antiviral protein is:
[0047] LGKFSQTCYNSAIQGSVLTSTCERTNGGYNTSSIDLNSVIENVDGSLKWQPSNFIETCRNTQLAGSSELAAECKTRAQQFVSTKINLDDHIANIDGTLKYE.
[0048] The nucleotide sequence of the cyanobacteria antiviral protein is:
[0049] cttggtaaattctcccagacctgctacaactccgctatccagggttccgttctgacctccacctgcgaacgtaccaacggtggttacaacacctcctccatcgacctgaactccgttatcgaaaacgttgacggttccctgaaatggcagccgtccaacttcatcgaaacctgccgtaacacccagctggctggttcctccgaactggctgctgaatgcaaaacccgtgctcagcagttcgtttccaccaaaatcaacctggacgaccacatcgctaacatcgacggtaccctgaaatacgaataa
[0050] (2) After sequencing to confirm that the sequence is correct, clone the above nucleotide sequence into the pET26b(+) vector and express it in E.coli BL21 competent cells;
[0051] (3) The engineered bacteria were induced to expr...