Molecular inversion probe for detecting hepatitis B virus yvdd drug resistance mutation and its application
A technology of molecular inversion probe and hepatitis B virus, which is applied in the direction of microbe-based methods, recombinant DNA technology, microbiological measurement/testing, etc., can solve the problems of complicated DNA sequencing operations, difficult standardization and judgment of results, and poor repeatability. Achieve the effect of low cost, high specificity and simple operation
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Embodiment 1
[0052] 1. Design of Molecular Inversion Probe:
[0053] Aiming at the base sequences on both sides of the hepatitis B virus YVDD drug resistance site, a molecular inversion probe is designed, which consists of 6 parts: 2 complementary sequences of the target gene (gene complementary sequence A and gene complementary sequence B, respectively, as shown in SEQ ID NO:1, and SEQ ID NO:2), 1 UNG enzyme recognition site ("-TTUUUTT-"), 2 primer recognition sequences (respectively shown in SEQ ID NO:3 and SEQ ID NO: 4) and an unrelated sequence (shown in SEQ ID NO: 5) as the middle connecting sequence. There are 21 bases at the 5' end of the probe, and 19 bases at the 3' end to specifically recognize the base sequences on both sides of the YVDD drug resistance site. The secondary structure of the molecular inversion probe was analyzed using DNAMAN version6 software (Lynnon Biosoft, USA), and the irrelevant sequence in the middle was designed according to the principle of obtaining the...
Embodiment 2
[0080] Embodiment 2 Determination of Molecular Inversion Probe Detection Sensitivity
[0081] 1. The hepatitis B virus DNA was serially diluted to a concentration of 100nM, 10nM, 1nM, and 100pM.
[0082] 2. Apply the reaction system and optimized reaction conditions obtained in Example 1 to the determination of the detection sensitivity of the molecular inversion probe. That is, the molecular inversion probe was used to detect hepatitis B virus DNA at concentrations of 100 nM, 10 nM, 1 nM, and 100 pM, and the detection sensitivity was clarified.
[0083] The doubling dilution experiment of hepatitis B virus DNA shows that: the minimum template concentration that the molecular inversion probe can detect is 100pM (see Figure 6 ).
Embodiment 3
[0084] Example 3 Detection of hepatitis B virus YVDD drug-resistant site clinical isolates
[0085] 1. Isolate hepatitis B virus DNA from the plasma of clinical hepatitis B patients, and use sequencing methods to analyze the YVDD drug resistance sites of clinical isolates of hepatitis B virus, and clarify the wild type of hepatitis B virus YVDD drug resistance sites. strains and mutants.
[0086] 2. Apply the reaction system and optimized reaction conditions obtained in Example 1 to the analysis of the molecular inversion probe to the YVDD drug resistance site of the clinical isolate of hepatitis B virus. By comparing the results of molecular inversion probes and sequencing methods on the analysis of YVDD drug resistance loci in clinical isolates of hepatitis B virus, the accuracy of molecular inversion probes in the detection of clinical isolates was clarified.
[0087] The experiment of molecular inversion probe used in the detection of clinical isolates shows that the mole...
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