Biliverdin preparation and application thereof in prevention and treatment of porcine reproductive and respiratory syndrome, and detection method
A technology for respiratory syndrome and biliverdin, which is applied in the field of biomedicine to achieve obvious effects, convenient use, and easy transportation
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Embodiment 1
[0033] The preparation of embodiment 1 biliverdin
[0034] Dissolve biliverdin (purchased from Sigma, USA) in 0.1 mol / L NaOH, adjust the pH value to 7.4 with 1 mol / L HCL, then dilute with PBS, filter and sterilize with a 0.2 μM filter membrane, and separate Wrap it with tinfoil and store at -80°C for later use.
Embodiment 2
[0035] Example 2 Biliverdin Treatment of Marc-145 Cells Infected by PRRSV
[0036] Marc-145 cells at 1×10 5 The density of cells / ml was cultured in a six-well cell culture plate containing DMEM medium (containing penicillin 100 U / ml, streptomycin 50 μg / ml, 10% fetal bovine serum), 37 ° C, 5% CO 2 Culture in a humid incubator until 70%-80% confluent, discard the medium. Insert 0.1 MOI of PRRSV into each well, incubate at 37°C for 1 h, discard unadsorbed virus liquid, and wash 3 times with 1 ml PBS / well. Add 2ml of culture medium containing different concentrations (10 μM, 20 μM, 50 μM, 100 μM, 150 μM) of biliverdin diluted in Example 1 to each well, place at 37° C., 5% CO 2 cultured in a humidified incubator. 48h after virus infection, the cell supernatant and cells were collected respectively.
Embodiment 3
[0037] Example 3 qPCR detection of PRRSV ORF7 mRNA expression after treatment with different concentrations of biliverdin
[0038] After the cells treated in Example 2 were digested with trypsin, they were collected in a 1.5 ml centrifuge tube, centrifuged at 500 g at 4° C. for 10 min, and the supernatant was discarded. 1ml TRIzol (purchased from Invitrogen) was added to each tube, and total RNA was extracted according to the instructions. RNA was reverse-transcribed into cDNA using PrimeScript RT reagent Kit Perfect Real Time kit (purchased from TAKARA).
[0039] Finally, the SYBR GREEN kit (purchased from Roche Company) and the above reverse-transcribed cDNA template and the designed upstream and downstream primers of the PRRSV ORF7 gene were used to perform real-time fluorescent quantitative PCR detection on the StepOnePlus Real-Time PCRSystem of Applied Biosystems.
[0040] The reaction conditions were as follows: denaturation at 95°C for 10 min; 40 cycles of reaction at ...
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