Primer and detection kit for detecting seven types of chicken eimeria tenella
A technology of Eimeria gallinarum and Eimeria gallinarum, which is applied in the field of primers and detection kits for detecting seven kinds of Eimeria gallinarum, can solve problems such as complexity and inaccurate diagnosis and identification techniques, and achieve results To determine the effect of objective, high sensitivity and strong specificity
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Embodiment 1
[0084] Design of 7 pairs of specific primers: In this study, the ribosomal DNA of Eimeria gallinarum isolates from different endemic areas was analyzed for genetic variation, and it was found that the ribosomal IGS sequence and ITS sequence were different in different Eimeria strains of the same species. The differences between insects are very small, but the differences between different species are very large. The inventor designs 7 kinds of specific primers according to the IGS and ITS specific sequences of 7 kinds of Eimeria as following table 1:
[0085] Table 1 Specific primers for fluorescent quantitative PCR of seven Eimeria species
[0086]
Embodiment 2
[0088] Fluorescent quantitative PCR kit for quantitative detection of 7 species of Eimeria
[0089] The kit includes the stool DNA extract to be detected; the SYBR GREEN I reaction mixture of 400 reactions; the final concentration of 7 kinds of Eimeria specific primers shown in Example 1 of 50 pmol / μL; sterile water. The SYBR GREEN I reaction mixture is a reagent purchased from TaKaRa Company, and the SYBR GREEN I reaction mixture contains TaKaRa Ex Taq HS, dNTP Mixture, Mg 2+ and SYBR ? Green I.
[0090] The fecal DNA extract to be tested includes: 140 mL of ASL Buffer for 50 reactions; 1.4 mL of proteinase K; 33 mL of Buffer AL; 19 mL of Buffer AW1; 13 mL of Buffer AW2; 12 mL of Buffer AE; 96% to 100% alcohol; 100 mL of 10% sodium hypochlorite. Among them, ASL Buffer, proteinase K, Buffer AL, Buffer AW1, Buffer AW2 and Buffer AE are derived from the DNA extraction kit of Tiangen. Of course, the extraction of the DNA of the stool sample to be detected in the present inve...
Embodiment 3
[0116] Kit specificity test described in embodiment 2
[0117] Using 5 μL of Eimeria chicken DNA from 7 species of Eimeria gallinarum that has been verified for DNA validity as a template, the 7 pairs of primers were subjected to specific fluorescent quantitative PCR amplification according to the reaction conditions of the kit, and a blank was set at the same time (the template for the blank control was sterile water). The reaction system was: 8 μL of SYBR GREEN I reaction mixture, 1 μL of each primer, 10 μL of double distilled water, and 5 μL of template DNA.
[0118] Fluorescent quantitative PCR amplification conditions are:
[0119]
[0120] The results show that: seven pairs of primers can specifically amplify seven kinds of Eimeria (see Figure 1-7 ).
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