Mumps virus attacking animal model and establishment method thereof
A mumps virus and animal model technology, which is applied to the mumps virus challenge animal model and the field of its establishment, can solve the problems of inability to form and the mumps virus infection efficiency is not high, and achieves the effect of simple operation
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Embodiment 1
[0070] Example 1: Effect of mouse type on morbidity after mumps virus challenge
[0071] The experimental animals were IFNα / βR- / - gene deletion mice (4-6 weeks old, from Huazhong Agricultural University) and 129 mice (4-6 weeks old, purchased from Beijing Weitong Lihua Company). 6 groups, 4 mice in each group, 6 experimental groups were IFNα / βR- / -gene-deficient mice challenged by tail vein, intramuscular and intranasal injection of F genotype mumps virus strain QS-F virus solution 129 mice were challenged by tail vein, intramuscular and intranasal injection of the virus solution of the F genotype mumps virus strain QS-F, and the challenge dose was 1 × 10 6 CCID 50 / Only. 14D after challenge, the blood, lymph nodes, spleen, liver, heart and kidney of mice with IFNα / βR- / - gene deletion in experimental group and 129 mice were collected for quantitative PCR, and IFNα / βR- / - The viral load of mumps virus in blood, lymph nodes, spleen, liver, heart and kidney of gene deletion mice...
Embodiment 2
[0082] Example 2: Effect of challenge dose on morbidity after mumps virus challenge
[0083] The experimental animals were IFNα / βR- / - gene-deficient mice (4-6 weeks old, from Huazhong Agricultural University). The experimental group consisted of 4 groups, each with 4 mice. The 4 groups were all injected with F genotype through tail vein injection. IFNα / βR- / -gene-deficient mice were challenged with the viral solution of mumps virus strain QS-F, and the challenge dose was 1 × 10 3 CCID 50 / only, 1 × 10 4 CCID 50 / only, 1 × 10 5 CCID 50 / only 1×10 6 CCID 50 / Only. After challenge, 3D, 7D, 14D and 28D were collected from the blood of mice with IFNα / βR- / - gene deletion in the experimental group for real-time quantitative PCR (see Example 1 for real-time quantitative PCR), and the experimental group IFNα / βR- / - The viral load of mumps virus in the blood of gene deletion mice, the detection results are shown in Table 3.
[0084] As can be seen from Table 3, 3D after challe...
Embodiment 3
[0087] Example 3: Mumps virus challenge animal model for evaluation of strain virulence
[0088] The evaluation objects are A genotype mumps virus strain JL, F genotype mumps virus strain QS-F, F genotype mumps virus strain QS-F-SH2 and G genotype mumps virus strain MuV (G genotype mumps virus strain QS-F-SH2). genotype), the experimental animals were IFNα / βR- / - gene-deficient mice (4-6 weeks old, from Huazhong Agricultural University). The experimental group consisted of 4 groups with 4 mice in each group. A genotype mumps virus strain JL, F genotype mumps virus strain QS-F, F genotype mumps virus strain QS-F-SH2 and G genotype mumps virus strain MuV (G genotype) IFNα / βR- / -gene-deficient mice challenged with virus fluid, the challenge dose is 1×10 3 CCID 50 / Only. 14D after the challenge, the blood of mice with IFNα / βR- / - gene deletion in the experimental group was collected for quantitative PCR (see Example 1 for fluorescence quantitative PCR), and the mice with IFNα / βR- / ...
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