Multiplex PCR kit for detecting bacterial meningitis pathogens
A meningitis and bacterial technology, applied in the field of multiple PCR kits, can solve the problems of reducing the throughput and limitation of multiple PCR detection, and achieve the effects of reducing non-specific products, reducing detection costs, and simple operation
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Embodiment 1
[0027] Specificity and Sensitivity Detection of Embodiment 1 Multiplex System
[0028] 1. Specific detection of multiplex system
[0029]A multiplex PCR kit for detecting bacterial meningitis pathogens, including conventional multiplex PCR components, and chimeric primers and public primers for common meningitis-infected bacteria; the sequences of chimeric primers and public primers are shown in Table 1, and conventional multiplex PCR components include Taq polymerase, dNTPs, MgCl 2 , PCR buffer, deionized water; positive control primer pair, which can be used to detect the quality of the DNA template and the amplification efficiency of the reaction system, the specific sequence is: SEQ ID NO.14, 5'-AGCGGGAAATCGTGCGTGA-3'; SEQ ID NO.15, 5'- AGTGAGGACCCTGGATGTGA-3'.
[0030] Table 1 Chimeric primers and public primers for bacterial pathogens of meningitis infection
[0031]
[0032] Specific detection of multiplex system: use multi-primer + single-template PCR method to a...
Embodiment 2
[0035] The detection of embodiment two clinical cerebrospinal fluid samples
[0036] Sixty cerebrospinal fluid (CSF) samples suspected of central nervous system infection were collected, and the genomes of the collected CSF samples were extracted according to the extraction method of Gram-positive bacteria in DNAminiKit (Product No. 51304) of QIAgen Company. The multiplex PCR kit for detecting bacterial meningitis pathogens of the present invention is used to detect the genomic DNA of the extracted specimen. The 25 μL reaction system used in the multiplex PCR includes: 5 μL of 10 μM common primers, 0.05 μM (each) chimeric primer mixture 5 μL, 5 U / μL Taqpolymerase 0.15 μL, 25 mM MgCl 2 2 μL, 0.5 μL of 10 mM dNTP, 2.5 μL of 10× TaqBuffer, 1 μL of DNA template, sterilized ddH 2 O8.85 μL; PCR reaction conditions are: pre-denaturation at 95°C for 5 min; denaturation at 95°C for 30 s, annealing at 63.5°C for 30 s, extension at 72°C for 45 s, a total of 10 cycles; extension at 72°C ...
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