Application of sclareol and sclareolide in resisting filovirus infection
A technology of sclareolide and filovirus, which is applied in the field of medicine and can solve the problems of no antiviral activity
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Embodiment 1
[0046] Example 1. Principle of Screening Model
[0047] Filovirus entry into host cells is the first step in virus infection, and inhibiting virus entry can effectively block virus infection. The glycoprotein (Glycoprotein, GP) on the surface of the filovirus envelope is a key protein in the process of filovirus entry.
[0048] We synthesized the envelope GP gene of Zaire type Ebola virus (EBOV-GP, Gene Accession No.L11365), the envelope GP gene of Sudan type Ebola virus (SUDV-GP, Gene Accession No.FJ968794.1) , Tai Forest type Ebola virus envelope GP gene (TAFV-GP, Gene Accession No.FJ217162.1), Marburg virus envelope GP gene (Marburg-GP, Gene Accession No.NC_001608.3) and Cueva virus Envelope GP gene (Cueva-GP, Gene Accession No. JF828358). Expression of GP protein plasmid and pNL4-3-Luc-R by co-transfection - E. - , Filovirus GP can be obtained as a filovirus recombinant virus HIV / Filovirus-GP that coats the HIV core[Chen Q,Tang K,Zhang X,Chen P,Guo Y.Establishment of p...
Embodiment 2
[0049] Example 2. Inhibition of Sclareol and Sclareolide to Filamentous Recombinant Virus Infection
[0050] In the present invention, Zaire type Ebola virus (EBOV, Gene Accession No.L11365), Sudan type Ebola virus (SUDV, Gene Accession No.FJ968794.1), Tai Forest type Ebola virus ( Anti-filovirus infection of TAFV, Gene Accession No.FJ217162.1), Marburg virus (Gene Accession No.NC_001608.3) and Cueva virus (Gene Accession No.JF828358) to sclareol and sclareolide Action for pharmacological activity evaluation:
[0051] Recombinant virus preparation [Chen Q, Tang K, Zhang X, Chen P, Guo Y. Establishment of pseudovirus infection mouse models for in vivo pharmacodynamics evaluation offilovirus entry inhibitors. Acta Pharm Sin B. 2018; 8(2): 200-208.] : Co-transfected with 2 μg pcDNA3.1 / EBOV-GP plasmid (or 2 μg pcDNA3.1 / SUDV-GP plasmid or 2 μg pcDNA3.1 / TAFV-GP plasmid or 2 μg pcDNA3.1 / Marburg-GP plasmid or 2 μg pcDNA3.1 / Cueva -GP plasmid) and 2 μg pNL4-3-Luc-R - E. - Put the pl...
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