Detection kits for the detection and differentiation of a variety of common large and medium-sized tapeworms with dogs as their ultimate hosts
A detection kit and terminal host technology, applied in biochemical equipment and methods, microbial determination/inspection, etc., can solve the problems of pollution of the surrounding environment, cumbersome detection process, waste of materials, etc., and achieve sensitive, fast and accurate detection response. Etiological identification and high specificity of test results
Patent Information
- Authority / Receiving Office
- CN · China
- Patent Type
- Patents(China)
- Current Assignee / Owner
- Publication Date
- 2020-04-03
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Abstract
Description
technical field
[0001] The invention relates to the technical field of parasite differentiation and detection, in particular to a detection kit for detecting and distinguishing a variety of common large and medium-sized tapeworms with dogs as their final hosts. Background technique
[0002] There are many types and large numbers of tapeworms parasitic on livestock and poultry, belonging to the class Cestoidea of the phylum Platyhelminthes, of which only tapeworms of the order Cyclophyllidea and Pseudophyllidea are infectious to livestock and poultry and humans . The distribution of tapeworms is extremely wide, and adults and metacestode larvae - tapeworm larvae can cause serious harm to humans and animals, and cause serious public health problems. Adults parasitize vertebrates, larvae mainly parasitize vertebrates, and can also parasitize invertebrates. For example, there are many kinds of cestodes in the round leaf order with dogs as their final hosts. Taenia multiceps ...
Examples
Embodiment 1
[0029] In this embodiment, dog feces were selected for detection of four kinds of tapeworm infection including Taenia alveosum. Take an appropriate amount of dog feces (2-5g), float the eggs and body fragments in the dog feces by saturated salt water flotation method, collect by centrifugation, and use the fecal DNA extraction kit to extract the whole genome DNA, and measure the concentration of the extracted DNA for later use. Prepare a compound PCR reaction solution in a PCR reaction tube, using a 50 μL reaction system, including 5 μL of 10×PCR Buffer, MgCl 2 (25mmol / μL) 5μL, upstream primer F1 for specific detection of Taenia vesicularis: 5'-AGT TCC ATA TTA TTT ACA GTT TTG TTA TTA C-3'(Th NO.1) 1μL (50μmol / mL) And downstream primer R1: 5'-TAA CAT AAT ACT TGA AGA CAC CCC CA-3'(ThNO.2) 1 μL (50 μmol / mL), upstream primer F2 for specific detection of Taenia polycephalum: 5'-GTT GTT GAT GTG GCT TAA GTTTTT GTG T-3'(Tm NO.1) 1μL (50μmol / mL) and downstream primer R2: 5'-TCT ATA AA...