Amplification primer for detecting echinococcosis through ddPCR and construction method and application of amplification primer
An amplification primer and a construction method technology, applied in the field of hydatid disease diagnosis, can solve the problems of inability to realize early diagnosis, shorten the judgment period of drug treatment effect period, etc., and achieve the enhancement of clinical application effect, good detection effect, and avoidance of false positives. Effect
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Embodiment 1
[0067] Such as figure 1 A method for constructing an amplification primer for ddPCR detection of echinococcosis shown specifically comprises the following steps:
[0068] (A) screening the common gene segment of Echinococcus granulosus and Echinococcus multilocularis, and designing multiple first primers based on the common gene segment;
[0069] (B) using the first primer to amplify the plasma cfDNA sample of the first patient group, using the first primer capable of amplifying the plasma cfDNA sample of the first patient group as the second primer;
[0070] (C) Using the ddPCR reaction system including the second primer to detect the plasma cfDNA samples of the second patient group, and screening out the second primer with a positive detection rate greater than the preset value as the amplification primer for the ddPCR detection of echinococcosis.
[0071] In some embodiments, the preset value is 90%. In one or more embodiments, the constructed target primers must obtain po...
Embodiment 2
[0084] On the basis of Example 1, adopt this construction method to screen amplification primers, comprising the following steps:
[0085] Based on the genome-wide data of Echinococcus granulosus, Echinococcus multilocularis, and other tapeworms that are susceptible to human beings and have known whole-genome data, BLAST comparison and mummer comparison were performed to exclude human genomes, non-granular or multilocular The pollution effect of the Echinococcus genome, screening out the common gene fragments of Echinococcus granulosus and Echinococcus multilocularis;
[0086] Based on these common gene fragments, a multiplex PCR chip containing 462 pairs of primers was constructed, through which the DNA extracts from lesion tissues of patients with cystic echinococcosis and alveolar echinococcosis were detected, and the detection coverage respectively reached 89.29% and 90.15%;
[0087] The chip was used to detect circulating free DNA samples in the plasma of 41 patients wit...
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