Primer pair compound and kit for detecting and identifying human tissue echinococcosis pathogens
A primer pair and echinococcosis technology, which is applied in the field of disease diagnosis, can solve the problems of easily generating interference reactions, failing to meet the detection and identification of human echinococcosis pathogens, and poor specificity
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Embodiment 1
[0050] Embodiment 1 specificity experiment
[0051] Design 3 groups of experiments altogether to investigate the technical detection of the present invention and the specificity of identification echinococcosis pathogen, 3 groups of experiments are respectively:
[0052] 1, 3 pairs of mixed primers of the present invention carry out the specificity experiment of amplifying the DNA template of three kinds of purpose Echinococcus respectively;
[0053] 2, 3 pairs of mixed primers of the present invention carry out the specificity experiment that the DNA mixed template of three kinds of purpose echinococcus is amplified;
[0054] 3. The three pairs of mixed primers of the present invention are respectively used for the specificity experiment of amplifying the DNA templates of three kinds of Echinococcus and other 8 kinds of closely related cestodes.
[0055] The specific operation is as described in the aforementioned experimental method, and the electrophoresis results can be f...
Embodiment 2
[0060] Embodiment 2 Sensitivity experiment
[0061] Three kinds of Echinococcus DNA were used as templates, and the final template concentrations were: 0.7ng / μl, 0.35ng / μl, 0.18ng / μl, 0.09ng / μl, 0.04ng / μl, 0.02ng / μl, 0.01ng / μl, 0.005ng / μl, amplified according to the aforementioned experimental method.
[0062] Electrophoresis results such as Figure 4 As shown, the template of lanes 1-8 is Echinococcus granulosus G1-G3, the template of lanes 9-16 is Echinococcus multilocularis, and the template of lanes 17-24 is Echinococcus granulosus G6–G10. The final template concentrations in the reaction system were 0.7ng / μl, 0.35ng / μl, 0.18ng / μl, 0.09ng / μl, 0.04ng / μl, 0.02ng / μl, 0.01ng / μl, 0.005ng / μl. The detection limits of the present invention to the DNA of three kinds of insect species are all higher than 0.005ng / μl, indicating that the present invention has very high sensitivity.
Embodiment 3
[0063] Example 3 Application to detection of human lesion tissue samples
[0064] Selected 10 surgical patients to send liver lesion tissue for detection of Echinococcus infection. The DNA extraction and multiplex PCR amplification of the patient to be tested were carried out according to the aforementioned experimental method.
[0065] The amplified band sizes of Echinococcus granulosus G1-G3 type, Echinococcus multilocularis, and Echinococcus granulosus G6-G10 type are 240bp, 152bp and 441bp respectively, and the electrophoresis results are as follows Figure 5 As shown, wherein: lanes 1-10 are the PCR results of samples; lane 11 is the positive control, that is, the PCR amplification results of mixed DNA templates of 3 species of insects and 3 pairs of mixed primers; lane 12 is the negative control; M is the DNA molecular weight Standard marker II.
[0066] The bands in lanes 1, 3, 7, and 10 are 240bp, so the corresponding patient is positive for Echinococcus granulosus G...
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