A kind of rt-rpa detection kit for rapid detection of Peste des petits ruminants virus and its application
A technology of RT-RPA and Peste des petits ruminants, which is applied in the field of RT-RPA detection kits for rapid detection of Peste des petits ruminants virus and kits for detection of Peste des petits ruminants virus. The effect of test time, portability, and simple method
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Embodiment 1
[0036] Example 1 Establishment of real-time RT-RPA detection kit and detection method for rapid detection of Peste des petits ruminants virus
[0037] 1. Preparation of Sequences
[0038] Primers and probes were designed for the N region of Peste des petits ruminants virus. At the same time, we compared the N gene homologous sequences of X74443, L39878, EU267274, EU267273, AJ849636, FJ905304, AY560591 and AJ563705 from GenBank to further determine the conserved region of Peste des petits ruminant virus, in order to detect as many small Peste ruminant virus. All primers and probes were synthesized by Sangon Biotech (Shanghai, China).
[0039] 2. Virus strains, cells and clinical samples
[0040] All strains used in this study are preserved by our laboratory: PPRV / Nigeria 75 / 1, ORFV / Vaccine / CHA, ORFV / Gansu / CHA, ORFV / HB / CHA, GPV AV40, SPV Jingtai2011 and foot-and-mouth disease virus (FMDV type A / CHA / 2009; FMDV / O / CHA; FMDV / Asia1 / CHA). The PPRV-positive samples (n=14) and PPRV...
Embodiment 2
[0063] Example 2 Application of PPRV real-time RT-RPA detection kit in field detection
[0064] 1. Sample
[0065] 18 samples were collected from sheep with suspected PPRV infection, and 5 tissue samples were from healthy sheep. Virus genome extraction was the same as in Example 1.
[0066] 2. Detection method
[0067] (1) PPRV real-time RT-PRA method
[0068] The extracted and purified viral RNA was used as a template for amplification, and the reaction system was as follows: 13.75 μL rehydration buffer (rehydration buffer, TwistDx exo Kit, Cambridge, United Kingdom), 1.05 μL upstream primer (10 μM), 1.05 μL downstream primer (10 μM) , 0.3 μL of RPA exo probe (10 μM), 2 μL of viral RNA template, 4.6 μL of ddH 2 O and 1.25 μL of magnesium acetate (magnesium acetate, 280 mM). The sequences of the primers and probes are as follows:
[0069] Upstream primer: 5'-CCAAGGCGGTTACGGCACCGGATACGGCAGCTGAC-3' (shown in SEQ ID NO.1);
[0070] Downstream primer: 5'-ACTGCGTCCAGCCACCCTTT...
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