阅读说明：本技术 Hsp70抑制剂广谱抗黄病毒活性的应用 (Use of HSP70 inhibitors for broad spectrum anti-flavivirus activity ) 是由 钟武 曹瑞源 杨晶晶 李薇 李松 于 2021-01-15 设计创作，主要内容包括：本发明涉及HSP70抑制剂广谱抗黄病毒活性的应用,具体提供了式I所示化合物在制备药物中的用途,所述药物用于治疗或预防黄病毒科病毒的病毒性传染病。该化合物具有广谱的抗黄病毒活性,在3种不同细胞系中对4种黄病毒,包括寨卡病毒,登革病毒,乙脑病毒和黄热病毒均表现出良好的病变保护效应,具有良好的成药性。(The invention relates to application of an HSP70 inhibitor in broad-spectrum anti-flavivirus activity, and particularly provides application of a compound shown in a formula I in preparing a medicament for treating or preventing viral infectious diseases of flaviviridae viruses. The compound has broad-spectrum anti-flavivirus activity, shows good pathological change protection effect on 4 flaviviruses including Zika virus, dengue virus, Japanese encephalitis virus and yellow fever virus in 3 different cell lines, and has good druggability.)

1. The use of a compound of formula I for the preparation of a medicament for the treatment or prevention of viral infections of Flaviviridae,

2. the use of claim 1, wherein the medicament is for treating or preventing a non-immunodeficient mammalian flaviviridae viral infection;

preferably, the non-immunodeficient mammal is a non-IFN receptor deficient mammal;

preferably, the non-immunodeficient mammal is a non-RIG-I deficient mammal;

preferably, the mammal is a human or a mouse.

3. The use of claim 1, wherein the flaviviridae virus is selected from at least one of Zika virus, dengue virus, Japanese encephalitis virus, yellow fever virus, flavivirus, enterovirus, rhinovirus, herpes virus.

4. Use of a compound of formula I for anti-flavivirus activity or for enhancing or increasing cell viability or cell survival of cells infected with a virus of the Flaviviridae family, for non-therapeutic purposes,

5. use of a compound of formula I in the preparation of an agent for anti-flavivirus activity or for enhancing or increasing the cell viability or cell survival of a cell infected with a flavivirus family virus,

6. the use of claim 4 or 5, wherein the cell is selected from at least one of Vero, hamster kidney cell (BHK), human hepatoma cell (Huh7), human hepatoma cell (Huh 7.5);

preferably, the cell is a non-IFN receptor deficient cell;

preferably, the cell is a non-RIG-I deficient cell;

7. the use of claim 4 or 5, wherein the flaviviridae virus is selected from at least one of Zika virus, dengue virus, encephalitis B virus, yellow fever virus, flavivirus, enterovirus, rhinovirus, herpes virus.

8. The use of claim 4 or 5, wherein the anti-flavivirus activity, or enhancing or increasing the cell viability or cell survival of a cell infected with a flavivirus is achieved by at least one of:

A. reducing the cellular CPE level of a virus of the Flaviviridae family (preferably Zika virus, dengue virus, Japanese encephalitis virus, and yellow fever virus);

B. reducing the level of viral nucleic acid load and the number of viral particles in cells infected with a flaviviridae virus;

C. reducing production of flaviviridae (preferably Zika virus) E protein and NS1 protein;

D. inhibiting RNA replication of a virus of the flaviviridae family (preferably zika virus);

E. the antiviral effect is exerted in the later stage of virus adsorption;

regulating lipid metabolism and natural immunity of cells to play an antiviral role;

F. upregulation of the IFN expression of a flaviviridae virus (preferably Zika virus) exerts an antiviral effect.

Technical Field

The invention relates to the field of biological medicine, in particular to application of broad-spectrum anti-flavivirus activity of an HSP70 inhibitor.

Background

At present, an increasing number of viral infections are known as a major threat to public health. Among them, the multiple prevalence of flaviviridae viruses over the last decades has made it the focus of research by scientists in various countries. The pandemic of Zika virus occurring in the Asia-Pacific region between 2015-2017 caused thousands of cases of microcephaly and Guillain-Barre syndrome; the number of dengue virus infections exceeds 3.9 million annually, resulting in an economic loss of about $ 21 million; japanese encephalitis B has about 6.79 ten thousand new infected persons each year, the death rate is up to 20-30%, and 30-50% of survivors bear sequelae caused by nerve damage caused by virus infection. Yellow fever virus causes considerable mortality in south america and in regions of sub-saharan africa. Under this severe background, there is still no approved antiviral drug in clinic, and thus the development of small molecule drugs with good anti-flavivirus activity is imminent.

Currently, the validated drug targets with broad-spectrum anti-flavivirus activity are quite limited, and HSP70 has attracted the attention of the inventors as a newly discovered drug target with good potential. HSP70 is a series of highly conserved proteins involved in cellular responses to changes in temperature and nutritional environment, pathogen invasion, and oxidative stress. HSP70 in the plasma coat has been reported to be involved in various stages of DENV infection, including viral entry, RNA replication, and virion biosynthesis. The co-localization research of HSP70 and ZIKV protein shows that HSP70 is involved in ZIKV infection and plays an important role. In addition, HSP70 is also capable of interacting with domain III of JEV envelope proteins and its interactions, and playing a role in the entry, replication and protein synthesis of the virus; participate in YFV replication and NS3/4A cutting; binding to the NS5A protein of HCV is involved in viral RNA replication and assembly of viral particles.

In addition, the HSP70 protein has a plurality of domains with drug binding function on the surface, so that a plurality of small molecule compounds with different structures have HSP70 inhibitory activity, and the method is very beneficial to the discovery of small molecule drugs with HSP70 inhibitory activity. Currently reported HSP70 inhibitors include: ATP analogues, benzothiazines and flavonoids acting on NBD domain, Glastrin derivatives binding to C-terminal EEVD sequence, and Phenylethanesulfonamide binding to SBD. In this context, the inventors have selected various HSP70 inhibitors with different mechanisms of action for the evaluation of anti-flavivirus activity and hoped that small molecule compounds with broad-spectrum anti-flavivirus activity could be selected for pharmaceutical studies.

Disclosure of Invention

The present application is based on the discovery and recognition by the inventors of the following facts and problems:

after a large number of experimental screens, the inventor discovers that the HSP70 inhibitor compound Apoptozole (a compound shown in a formula I) has broad-spectrum anti-flavivirus activity, shows good pathological change protection effect on 4 flaviviruses including Zika virus, dengue virus, Japanese encephalitis virus and yellow fever virus in 3 different cell lines, and has good druggability.

To this end, in a first aspect of the invention, the invention provides the use of a compound of formula I (Apoptozole) for the preparation of a medicament for the treatment or prophylaxis of viral infections of viruses of the Flaviviridae family,

in some embodiments, the medicament is for treating or preventing a non-immunodeficient mammalian flaviviridae viral infection.

In some embodiments, the non-immunodeficient mammal is a non-IFN receptor deficient mammal.

In some embodiments, the non-immunodeficient mammal is a non-RIG-I deficient mammal.

In some embodiments, the mammal is a human or a mouse.

In some embodiments, the flaviviridae family virus is selected from at least one of zika virus, dengue virus, encephalitis b virus, yellow fever virus, flavivirus, enterovirus, rhinovirus, herpes virus.

In a second aspect of the invention, there is provided the use of a compound of formula I (Apoptozole) for anti-flavivirus activity, or for enhancing or increasing the cell viability or cell survival of cells infected with a virus of the Flaviviridae family, for non-therapeutic purposes, such as in scientific research,

in a third aspect of the invention, the invention provides the use of a compound of formula I (Apoptozole) in the manufacture of an agent for anti-flavivirus activity, or for enhancing or increasing the cell viability or cell survival of a cell infected with a virus of the Flaviviridae family,

in some embodiments, the cell is selected from at least one of Vero cells, hamster kidney cells (BHK), human hepatoma cells (Huh7), human hepatoma cells (Huh 7.5).

In some embodiments, the cell is a non-IFN receptor deficient cell.

In some embodiments, the cell is a non-RIG-I deficient cell.

In some embodiments, the flaviviridae family virus is selected from at least one of zika virus, dengue virus, encephalitis b virus, yellow fever virus, flavivirus, enterovirus, rhinovirus, herpes virus.

In some embodiments, the anti-flavivirus activity, or enhancing or increasing the cell viability or cell survival of a cell infected with a flavivirus is achieved by at least one of:

A. reducing the cellular CPE level of a virus of the Flaviviridae family (preferably Zika virus, dengue virus, Japanese encephalitis virus, and yellow fever virus);

B. reducing the level of viral nucleic acid load and the number of viral particles in cells infected with a flaviviridae virus;

C. reducing production of flaviviridae (preferably Zika virus) E protein and NS1 protein;

D. inhibiting RNA replication of a virus of the flaviviridae family (preferably zika virus);

E. the antiviral effect is exerted in the later stage of virus adsorption;

regulating lipid metabolism and natural immunity of cells to play an antiviral role;

F. upregulation of the IFN expression of a flaviviridae virus (preferably Zika virus) exerts an antiviral effect.

Advantageous effects

After long-term research, the inventor of the invention finds some new action characteristics of Apoptozole in cells:

first, Apoptozole can reduce the cellular CPE levels of Zika virus, dengue virus, Japanese encephalitis virus and yellow fever virus at micromolar concentrations in an in vitro antiviral assay; this protective effect was reduced in RIG-I deficient huh7.5 cells;

secondly, Apoptozole can reduce the virus nucleic acid load level in cells and the number of infectious virus particles secreted in supernatant after different Zika virus isolates infect different cell lines under micromolar concentration, and simultaneously, Apoptozole has a reduced inhibiting effect on the formation of virus RNA and infectious virus particles in RIG-I deficient Huh7.5 cells;

third, Apoptozole reduced the production of Zika virus E protein and NS1 protein at micromolar concentrations, and this effect was also reduced in RIG-I deficient Huh7.5 cells, suggesting that Apoptozole antiviral effect is associated with innate immunity;

fourthly, Apoptozole shows in time series experiments that the antiviral effect is mainly exerted in the later stage of virus adsorption, and is different from the prior literature reports, thereby suggesting a new mechanism of the HSP70 inhibitor for resisting flavivirus;

fifth, transcriptome analysis showed that Apoptozole acts primarily by regulating lipid metabolism and innate immunity of Huh7 cells, consistent with earlier experimental conclusions;

sixth, Apoptozole can provide about 60% protection at a concentration of 1mg/kg in 1-day-old ICR mice infected with Zika virus, and reduce viremia caused by Zika virus infection by up-regulating IFN expression at a concentration of 10 mg/kg.

Seventh, Apoptozole was not significantly protected against Zika virus infection in immunodeficient mice, thereby further demonstrating that Apoptozole may exert antiviral effects by modulating innate immunity.

Drawings

Figure 1 shows that HSP70 inhibitors exhibit broad spectrum anti-flavivirus activity in different cell lines. Apoptozole showed a dose-dependent protective effect against 4 flavivirus infections in different cell lines (BHK, Vero, Huh7) and significantly reduced Cytopathic effects (CPE) caused by viral infections.

In FIG. 1, A, B and C are the protective effects of Apoptozole on BHK, Vero and Huh7 infected by Zika virus SMGC-1 strain; the inhibiting effects of Apoptozole on 4 different flaviviruses including Zika virus (ZIKV-SMGC-1), Japanese encephalitis B virus (JEV-SA14), yellow fever virus (YFV-17D) and dengue virus (DENV-NGC) in 3 different cell lines are sequentially shown in the steps of D, E and F (D is BHK cells, E is Vero cells and F is Huh7 cells); g, H, I in turn are the toxicity of Apoptozole to BHK, Vero and Huh7 cells at the working concentration.

FIG. 2 shows that Apoptozole inhibits replication of Zika virus RNA and formation of infectious viral particles. Apoptozole showed significant inhibitory effects on viral RNA replication and infectious viral particle production in Vero, BHK, A549, Huh7 and Huh7.5 cells for two different Zika virus isolates, strains SMGC-1 and MR766, and showed dose-dependence. Also, Apoptozole was found to have reduced antiviral effects in RIG-1 inactivating mutant Huh7.5 cells.

In FIG. 2, A-E are the inhibitory effects of Apoptozole on RNA synthesis of Zika virus SMGC-1 strain and MR766 strain in Vero, BHK, A549, Huh7 and Huh7.5 cell lines in this order; F-J is the inhibition effect of Apoptozole on infectious virus particles of the Zika virus SMGC-1 strain and the MR766 strain in Vero, BHK, A549, Huh7 and Huh7.5 cell lines in sequence; K-O is in turn the toxicity of Apoptozole on Vero, BHK, A549, Huh7 and Huh7.5 cells at the working concentration.

FIG. 3 shows that Apoptozole inhibits the production of Zika virus E protein and NS1 protein. Apoptozole was effective in inhibiting the production of envelope protein (E-protein, IFA) and non-structural protein 1(NS1, WB) of Zika virus in different cell lines (A549, Huh7, Huh 7.5).

In FIG. 3, DAPI is the nuclear channel labeled by nuclear dye in IF imaging, and MERGE is the co-localization (combination) picture of the nuclear channel and the fluorescence signal of the target protein. In the figure, A, C and E are the inhibiting effect of Apoptozole on the Zika virus E protein in A549, Huh7 and Huh7.5 cell lines in sequence, and B, D and F are the corresponding quantitative analysis results in sequence; g is the inhibitory effect of Apoptozole on Zika virus NS1 protein production in Vero, Huh7 and Huh7.5 cell lines, and H-J is the corresponding quantitative data.

FIG. 4 shows that Apoptozole exerts an antiviral effect in the post-adsorption stage of the Zika virus-infected cell process. The detection after adding Apoptozole in different stages of infecting Zika virus by different cell lines shows that Apoptozole mainly plays a role in the virus replication stage, and has no obvious inhibiting effect on the adsorption and entry of the virus.

In FIG. 4, DAPI is the nuclear channel labeled by nuclear dye in IF imaging, and MERGE is the co-localization (combination) picture of the nuclear channel and the fluorescence signal of the target protein. In the figure, A is a schematic diagram of the time point of Apoptozole addition, and B, C and D are sequential experiments of Apoptozole in Vero, Huh7 and Huh7.5 cells to inhibit the virus RNA replication; e, F, G are sequential experiments performed by Apoptozole in Vero, Huh7 and Huh7.5 cells in order on the inhibitory effect on viral protein expression. 2 '-CMA (2' -C-Methyladenosine, 2-C-Methyladenosine) is a positive compound that has been reported to act specifically on the viral replication stage.

Figure 5 shows that transcriptome analysis revealed that Apoptozole exerts antiviral effects by modulating lipid metabolism and innate immunity.

In FIG. 5, A and B are the heat map and corresponding quantity of the significant change gene caused by Apoptozole; c is a list of all genes with significant changes; d is the GO (Gene ontology) functional annotation analysis result of all significantly-changed genes; e is the result of functional enrichment analysis of KEGG (Kyoto Encyclopedia of Genes and genomes) for all significantly altered Genes.

Figure 6 shows that Apoptozole protects against zika virus infection in wild type mice by up-regulating natural immunity. Apoptozole demonstrated a dose-dependent protective effect on ICR mice vaccinated with a lethal dose of Zika virus; apoptozole can also reduce viremia in Balb/c mice infected with Zika virus by up-regulating the expression of interferon.

In FIG. 6, A is the protective effect of Apoptozole on Zika virus infection in ICR suckling mouse lethal model, and B is the corresponding body weight change; c is the inhibition of Balb/C mouse viremia by Apoptozole, D, E, F, G is the effect of Apoptozole on the change in IFN expression level.

FIG. 7 shows that Apoptozole lost protective effects against Zika virus infection in immunodeficient mice. Apoptozole failed to exert antiviral effects in the A129 and AG6 mouse lethal model of interferon receptor deficiency.

In FIG. 7, A-C are the survival curve, the body weight change curve and the viremia of A129 mice infected with Zika virus and deficient in type I interferon receptor after Apoptozole administration; D-F are the survival curve, body weight change curve and viremia of mice infected with Zika virus and deficient in type I/II interferon receptor association with AG6 after Apoptozole administration.

Detailed Description

The embodiments of the present invention will be described in detail below, and the embodiments described below by referring to the drawings are exemplary and intended to be used for explaining the present invention, and should not be construed as limiting the present invention.

The main objective of the present invention is to find an anti-flavivirus drug with broad-spectrum anti-flavivirus activity for the treatment of various flavivirus infections. The present inventors have discovered through creative studies that various HSP70 inhibitors can protect flaviviridae-infected cells, of which apoltozole is the most prominent. Apoptozole showed good disease protection in 3 different cell lines against 4 flaviviruses including Zika virus, dengue virus, Japanese encephalitis virus and yellow fever virus.

Example 1 HSP70 inhibitor Apoptozole experiment to reduce CPE in cells infected with Zika Virus

Experimental materials and experimental methods used in the present invention:

(1) cell culture and cell lines

The Vero, BHK and human hepatoma cells (Huh7 and Huh7.5) used in the experimental process are preserved in the room, and the sources and the passage times are clear. The cells were cultured at 37 ℃ in 5% CO₂The humidity of (a) saturates the cell culture chamber. Passage is usually carried out at 1:3-1:6, and liquid change is carried out once every 48h during culture, and passage is carried out by trypsinizing 0.25% EDTA for 2min in about 2-5 days (cell confluent monolayer). The complete culture medium for cell growth is a DMEM high-sugar medium added with 10% FBS and the dual-antibody of streptomycin, and the maintenance culture medium is a DMEM high-sugar medium added with 2% FBS and the dual-antibody of streptomycin.

(2) Cell viability assay

Cell viability using CellTiterLuminescent Cell Viability Assay.

The experimental protocol was as follows:

digesting the cells paved at the bottom of the bottle with 0.25% EDTA pancreatin, re-suspending the cells with complete culture medium to prepare single cell suspension, counting the single cell suspension, inoculating a 96-well plate with a density of 10000cells per well, and saturating the cells with 5% CO at 37 ℃ and humidity₂Incubated under conditions for 24 hours. Diluting the ZIKV virus stock solution with a maintenance medium, adding96-well plates to a final concentration of 100TCID 50; meanwhile, the HSP70 inhibitor was diluted in a maintenance medium in multiple ratios into 96-well plates at final concentrations of 10 μ M, 3 μ M, 1 μ M,0.3 μ M, 0.1 μ M, and 0.03 μ M, respectively, and a cell control group and a virus control group were set. After 6 days of treatment, the supernatant was discarded, and CellTiter diluted 2-fold with PBS buffer was added to each wellThe luminecent Cell Viability detection solution is subjected to shake lysis for 5min in the dark, is kept stand for 3min, and finally the fluorescence signal intensity is measured by Molecular Devices M5. The cell viability calculation formula is:

the results of the experiment are shown in figure 1 at A, B, C, G, H, I.

Example 2 HSP70 inhibitor Apoptozole experiments to reduce CPE in cells infected with flavivirus, enterovirus, rhinovirus, herpes virus, Zika virus, dengue virus, Japanese encephalitis virus, yellow fever virus

Experimental materials and experimental methods used in the present invention:

(1) cell cultures and cell lines, viral strains

The Vero, BHK and human hepatoma cells (Huh7 and Huh7.5) used in the experimental process are stored in the laboratory, and the sources and the passage times are clear. The cells were cultured at 37 ℃ in 5% CO₂The humidity of (a) saturates the cell culture chamber. Usually subcultured at 1:3-1:6

During the process, the liquid is changed every 48h, and the cells are digested with 0.25% EDTA pancreatin for 2min for about 2-5 days (cell confluent monolayer) for passage. The complete culture medium for cell growth is a DMEM high-sugar medium added with 10% FBS and the dual-antibody of streptomycin, and the maintenance culture medium is a DMEM high-sugar medium added with 2% FBS and the dual-antibody of streptomycin.

(2) Cell viability assay

Cell viability using CellTiterLuminescent Cell Viability Assay.

The experimental protocol is illustrated by using Vero cells as an example, namely: the Vero cells paved on the bottom of the bottle are digested by 0.25% EDTA pancreatin and then resuspended by using a complete culture medium to prepare single cell suspension, the single cell suspension is inoculated to a 96-well plate with the density of 10000cells per well after counting, and 5% CO saturated in humidity at 37 DEG C₂Incubated under conditions for 24 hours. Diluting ZIKV virus stock solution with a maintenance medium, and adding into a 96-well plate to make the final concentration of 100TCID 50; meanwhile, Apoptozole compound was diluted in a maintenance medium in multiple ratios into 96-well plates at final concentrations of 10. mu.M, 3. mu.M, 1. mu.M, 0.3. mu.M, 0.1. mu.M and 0.03. mu.M, respectively, to set a cell control group and a virus control group. After 6 days of treatment, the supernatant was discarded, and CellTiter diluted 2-fold with PBS buffer was added to each wellThe luminecent Cell Viability detection solution is subjected to shake lysis for 5min in the dark, is kept stand for 3min, and finally the fluorescence signal intensity is measured by Molecular Devices M5. The CPE calculation formula is as follows:

the results of the experiment are shown in figure 1 at D, E, F.

Example 3 Apoptozole experiments to reduce viral RNA replication and viral load in supernatant in Zika Virus-infected cells

Experimental materials and experimental methods used in the present invention:

(1) one-step real-time quantitative RT-PCR experiment and transcriptome analysis

Vero, BHK, A549, Huh7 and Huh7.5 cells at 75cm²Culturing in a culture bottle, inoculating 12-hole plates according to the ratio of 1:3 after the bottom of the culture bottle is fully paved, and culturing overnight by adherence. After the cells are completely attached to the wall, diluting the ZIKV virus to a corresponding concentration by using a 2% cell maintenance culture medium, adding the ZIKV virus to a 6-well plate to enable the virus content in each well to be 100TCID50(MOI is 0.01), respectively diluting Apoptozole and HSP70 series compounds to corresponding concentrations by using a 2% cell maintenance solution, adding the Apoptozole and HSP70 series compounds to corresponding wells to enable the final concentrations of the medicines to be 10 mu M, 3 mu M and 1 mu M respectively, continuing to culture for 72h, collecting supernatant when the cells start to have lesions, centrifuging at 8000rpm for 5min, subpackaging, and storing at-80 ℃ for later use.

② extraction of RNA

1) Taking cells treated by Apoptozole and HSP70 series compounds with different concentrations and cells of a virus control group, adding 350 mu l of Buffer RLT, and blowing and sucking by using a pipette to uniformly mix so as to fully crack the cells;

2) adding 70% ethanol with the same volume, and mixing;

3) transferring the mixed solution into a 2ml collecting tube without RNA enzyme, and centrifuging at 12000rpm for 15 s;

4) adding 700 mu Buffer RW1,12000rpm, centrifuging for 15s, and discarding the waste liquid;

5) adding 500 mu Buffer RPE, centrifuging at 12000rpm for 15s, and discarding the waste liquid;

6) adding 500 mu Buffer RPE, centrifuging at 12000rpm for 2min, and discarding the waste liquid;

7) replacing a new 2ml collecting tube without RNase, centrifuging at 12000rpm for 1min, and drying the filter column;

8) the new 1.5ml collection tube was replaced, 50. mu.l of RNase-free water was added to each tube, and the tube was centrifuged at 12000rpm for 2min to obtain an eluate containing the corresponding RNA, and the concentration of each RNA was determined by Nano Drop.

③Real-time PCR

1) Preparing a standard substance by using the recombinant ZIKV linearized plasmid: the number of copies of the standard was calculated from the linearized plasmid concentration and molecular weight and was diluted exactly to-1, -2, -3, -4, -5, -6, -7, -8, -9. . . Until the copy number is lower than the detection limit of a fluorescent quantitative PCR instrument. And (4) subpackaging the standard substance with each concentration after the standard substance is prepared, and freezing and storing at-80 ℃ for later use.

2) Using One Step PrimeScript from Takara^TMRT-PCR Kit (Perfect Real Time), the ZIKV RNA load in the samples was detected, and three independent replicates were performed for each sample. The sequences of the primers and probes used in the experimental procedure were as follows:

ZIKV-ASF：GGTCAGCGTCCTCTCTAATAAACG

ZIKV-ASR：GCACCCTAGTGTCCACTTTTTCC

ZIKV Probe：AGCCATGACCGACACCACACCGT

(2) pfu detection

(ii) Vero cells at 75cm²Culturing in a culture bottle, inoculating 12-hole plates according to the ratio of 1:3 after the bottom of the culture bottle is fully paved, and culturing overnight by adherence. After the cells are completely attached to the wall, diluting the ZIKV virus to a corresponding concentration by using a 2% cell maintenance culture medium, adding the ZIKV virus to a 6-well plate to enable the virus content in each well to be 100TCID50(MOI is 0.01), respectively diluting Apoptozole and HSP70 series compounds to corresponding concentrations by using a 2% cell maintenance solution, adding the Apoptozole and HSP70 series compounds to corresponding wells to enable the final concentrations of the medicines to be 10 mu M, 3 mu M and 1 mu M respectively, continuing to culture for 72h, collecting supernatant when the cells start to have lesions, centrifuging at 8000rpm for 5min, subpackaging, and storing at-80 ℃ for later use.

② inoculating Vero cells into a 12-hole plate, wherein the inoculation density is the same as that in the first step. After the cells are completely attached to the wall, the supernatant of each treatment group is taken and diluted to 10 percent by 2 percent cell maintenance solution^-3,10^-4,10^-5mu.L of the suspension was inoculated into a 12-well plate, incubated for 2 hours, the supernatant was discarded, 2% low-melting agarose was mixed with 2 × DMEM medium 1:1, and the mixture was cooled to an appropriate temperature and added to a 12-well plate at 1mL per well. The mixture was left to solidify at room temperature and returned to the incubator for further incubation for 96 hours.

③ adding 1mL of 4 percent formaldehyde into the treated 12-hole plate, fixing for 4 hours, washing with running water to remove the upper culture medium, adding 500 mu L of 1 percent crystal violet staining solution into each hole, fixing for 15 minutes, washing with running water, reversing the hole to be dried on absorbent paper, and counting the pfu number of each hole.

The results of the experiment are shown in FIG. 2.

Example 4 Apoptozole experiments to reduce viral protein Synthesis in cells infected with Zika Virus

Experimental materials and experimental methods used in the present invention:

(1) cell culture and cell lines

The Vero, Huh7 and RIG-I inactivating mutant monoclone (Huh7.5) are preserved in the laboratory, and the source and passage times are clear. The culture conditions and method are the same as above.

(2)IFA

A549, Huh7 and Huh7.5 Cells are inoculated in a 96-well bottom transparent blackboard according to 10000 Cells/well and cultured in an adherent way overnight. After the cells are completely attached to the wall, diluting the ZIKV virus to a corresponding concentration by using a 2% cell maintenance medium, inoculating the ZIKV virus into a 96-well plate (MOI ═ 0.5), discarding the solution after incubating for 2 hours, adding Apotozole and HSP70 series compounds diluted in advance by using a 2% cell maintenance solution to make the final concentrations respectively 10 μ M, 3 μ M and 1 μ M, continuing to incubate for 48 hours, discarding the solution, washing with PBS for 2 times, adding 100 μ L of 4% formaldehyde to each well for fixing for 30min, discarding the fixing solution, adding PBS buffer solution, performing antibody incubation labeling, and then imaging.

(3) Western blot protein analysis

Vero, Huh7, Huh7.5 cells at 75cm²Culturing in a culture bottle, inoculating 12-hole plates according to the ratio of 1:3 after the bottom of the culture bottle is fully paved, and culturing overnight by adherence. After the cells were completely attached to the wall, ZIKV virus was diluted to the corresponding concentration with 2% cell maintenance medium, and then added to a 6-well plate so that each well contained 100TCID50(MOI ═ 0.01) in the amount of virus, Apoptozole was diluted to the corresponding concentration with 2% cell maintenance solution, and added to the corresponding well so that the final concentrations of the drug were 10 μ M, 3 μ M, 1 μ M,0.3 μ M, and 0.1 μ M, respectively, and the culture was continued for 72 hours, and the supernatant was collected when the cells began to develop lesions. Adherent cells were lysed thoroughly (80. mu.L/well) with a cell lysate (RIPA lysate: 5 XSDS Loading Buffer) to obtain whole cell proteins, boiled at 100 ℃ for 5min to denature thoroughly, and then electrophoresed with 10% SDS-PAGE at 80V/120V for 2h to separate proteins of different sizes. And (3) rotating the protein and the NC membrane for 100min under the current of 200mA so as to ensure that the protein and the NC membrane are fully rotated.

After the membrane is converted, the membrane is cut into a proper size according to the molecular weight of the target protein. Shaking table sealing with 5% skimmed milk powder diluted with TBST for 1 hour at room temperature, adding primary antibody diluted with blocking solution: anti-ZIKV NS1 protein (Non-structural protein I) of Zika virus and GAPDH were incubated overnight at 4 ℃ in a shaker. Adding a secondary antibody: HRP-labeled goat anti-mouse IgG antibody (1:5000 dilution) was incubated for 1 hour at room temperature with shaking. TBST washing 3 times, each time for 5min, then by hypersensitivity chemiluminescence method for color development photograph. Finally, absorbance was analyzed by BioRadChemiDox (chemiluminescence imager from BioRad). The relative density was determined by the absolute density of ZIKV NS1 protein/GAPDH.

(4) Statistical analysis

Statistical significance calculations were performed using analysis of variance (ANOVA). Data are presented as mean ± standard deviation. p <0.05 indicates statistical differences.

The results of the experiment are shown in FIG. 3.

Example 5 discovery of Apoptozole against Zika Virus action stage

Experimental materials and experimental methods used in the present invention:

(1) cell culture and cell lines

The Vero and hamster kidney cell-21 stable transformation ZIKV replicon cell line (BHK-21Rep) used in the experimental process are preserved in the room, and the source and the passage times are clear. The culture conditions and method are the same as above.

(2) Time series experiment

The time series experiments were carried out according to the reported method (Taguwa, et al, 2015) using Apoptozole at a concentration of 10 μ M, ZIKV infection at MOI ═ 1, 2 ' -C-Methyladenosine (2 ' -C-methylidenosine, abbreviated as 2 ' -CMA) as positive control.

(3) Replicon assay

Replicon activity detection was carried out according to the reported method (Jia-Qi Li, et al, 2018), using Heparin (HP for abbreviation) and 2' -CMA as positive controls. BHK-21Rep cells were inoculated into a 96-well bottom-transparent white plate at 10000 cells/well, with final concentrations of Apotozole of 10. mu.M, 3. mu.M, 1. mu.M, 0.3. mu.M and 0.1. mu.M, and luminescence signals were detected after 48 h.

(4) Statistical analysis

Statistical significance calculations were performed using analysis of variance (ANOVA). Data are presented as mean ± standard deviation. p <0.05 indicates statistical differences.

The results of the experiment are shown in FIG. 4.

Example 6 Apoptozole anti-Zika virus mechanism exploration based on RNA-seq technology

Experimental materials and experimental methods used in the present invention:

(1) cell culture and cell lines

Human hepatoma cells (Huh7) used in the experimental process are stored in the laboratory, and the source and the passage times are clear. The culture conditions and method are the same as above.

(2) RNA extraction

1) Taking 10 mu M Apoptozole treated virus infected cells for 24h, virus control and cell control collecting solution, adding 350 mu l Buffer RLT, and blowing and sucking by using a pipette to uniformly mix the mixture to be fully cracked;

2) adding 70% ethanol with the same volume, and mixing;

3) transferring the mixed solution into a 2ml collecting tube without RNA enzyme, and centrifuging at 12000rpm for 15 s;

4) adding 700 mu Buffer RW1,12000rpm, centrifuging for 15s, and discarding the waste liquid;

5) adding 500 mu Buffer RPE, centrifuging at 12000rpm for 15s, and discarding the waste liquid;

6) adding 500 mu Buffer RPE, centrifuging at 12000rpm for 2min, and discarding the waste liquid;

7) replacing a new 2ml collecting tube without RNase, centrifuging at 12000rpm for 1min, and drying the filter column;

8) the new 1.5ml collection tube was replaced, 50. mu.l of RNase-free water was added to each tube, and the tube was centrifuged at 12000rpm for 2min to obtain an eluate containing the corresponding RNA, and the concentration of each RNA was determined by Nano Drop.

(3)RNA seq

And (3) sending the RNA sample obtained in the step (2) to the Meiji organism for transcriptome sequencing and analysis to obtain an RNA-seq analysis result.

The results of the experiment are shown in FIG. 5.

Example 7 Apoptozole can exert anti-ZIKV Activity by upregulating IFN expression in wild-type mice

Experimental materials and experimental methods used in the present invention:

(1) mouse strain

The ICR suckling mouse of 1 day age and Balb/c mouse of 3-4 weeks age used in the experimental process are SPF grade, purchased by Witongliwa laboratory animal technology Limited company, the source is clear, and the test is qualified.

(2) ICR suckling mouse lethal infection protection

3 litters of 1-day-old ICR suckling mice are inoculated with lethal dose of ZIKV virus in the abdominal cavity, meanwhile, the administration doses of the ZIKV virus to the mother mice are placebo, 0.5mg/kg and 1mg/kg respectively, the administration is continuously carried out for 10 days, the weight and the morbidity and mortality of the suckling mice are recorded, and a weight curve and a survival curve are drawn.

(3) Balb/c mouse viremia and detection of cytokines and chemokines

20 Balb/c mice with the age of 3-4 weeks are randomly divided into two groups, one group is a control group, the other group is a dosing group (10mg/kg), the dosing group is dosed for 3 times respectively by i.p. 12h before and 12h after the challenge, 50 mu l of whole blood is taken 24h after the challenge to extract total RNA for detecting the ZIKV RNA content in the blood, the serum is separated at the same time, and the commercial ELISA kit is utilized for detecting the contents of IFN-alpha, IFN-beta, IFN-gamma and MCP-1 in the serum.

(4) Statistical analysis

And (4) calculating the statistical significance of the survival curve by using the Log-Rank. p <0.05 indicates statistical differences.

The results of the experiment are shown in FIG. 6.

Example 8 Apoptozole failed to exert anti-ZIKV Activity in IFN receptor deficient mice

Experimental materials and experimental methods used in the present invention:

(1) mouse strain

The mice A129 and AG6 used in the experiment process are SPF grade mice with the age of 3-4 weeks and 7-8 weeks, and the mice are stored in the laboratory, have clear sources and are qualified through inspection.

(2) Experiment for lethal infection protection of interferon receptor-deficient mice

Appropriate number of a129 and AG6 mice were randomly divided into 3 groups, and placebo, 0.5mg/kg Apoptozole and 1mg/kg Apoptozole were administered intraperitoneally after lethal challenge for 10 consecutive days, body weight and morbidity and mortality, and body weight curves and survival curves were plotted.

(3) Interferon receptor deficient murine viremia detection

16A 129 mice at 3-4 weeks of age or AG6 mice at 7-8 weeks of age were randomly divided into two groups, one group was a control group and the other group was an administration group (1mg/kg) which was administered i.p. for 2 days, after which 50. mu.l of whole blood was taken to extract total RNA and the ZIKV RNA content in the blood was examined.

(4) Statistical analysis

Calculating the statistical significance of the survival curve by using the Log-Rank; statistical significance of viremia was calculated using analysis of variance (ANOVA), and data were presented as mean ± standard deviation. p <0.05 indicates statistical differences.

The results of the experiment are shown in FIG. 7.

The above-mentioned embodiments are intended to illustrate the objects, technical solutions and advantages of the present invention in further detail, and it should be understood that the above-mentioned embodiments are only exemplary embodiments of the present invention, and are not intended to limit the scope of the present invention, and any modifications, equivalent substitutions, improvements and the like made within the spirit and principle of the present invention should be included in the scope of the present invention.