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Drug-resistance gene film chip for detecting mycobacterium tuberculosis

A technology of Mycobacterium tuberculosis and membrane chip, which is applied in the direction of nucleotide library, microbe-based method, microbial measurement/testing, etc., can solve the problems of slow growth of Mycobacterium tuberculosis, inability to meet clinical detection, and high requirements for culture conditions

Inactive Publication Date: 2012-04-11
GUANGXI MEDICAL UNIVERSITY
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  • Description
  • Claims
  • Application Information

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Problems solved by technology

The detection results of this method are reliable, but the biggest disadvantage is that the culture conditions are high and the growth of Mycobacterium tuberculosis is slow, which often takes 6 to 8 weeks; at the same time, the detection rate of sputum culture is low, only about 30%. The recovery rate is only about 30%, which cannot meet the needs of clinical testing

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  • Drug-resistance gene film chip for detecting mycobacterium tuberculosis
  • Drug-resistance gene film chip for detecting mycobacterium tuberculosis
  • Drug-resistance gene film chip for detecting mycobacterium tuberculosis

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Embodiment Construction

[0088] The technical solutions of the present invention will be further described below through specific embodiments.

[0089] 1. The membrane chip used for detection is 2cm wide and 6.5cm long.

[0090] 2. Equipment required for testing: PCR instrument, shaking table, hybridization furnace, constant temperature water bath.

[0091] 3. Required reagents:

[0092] 20×SSC solution: NaCl 175.3g, sodium citrate 88.2g, dissolve in 900ml water to adjust pH to 7.0, add water to make up to 1L, and sterilize at high temperature and autoclave.

[0093] 10% SDS: dissolve 100g of electrophoresis-grade SDS in 900ml of water, heat to 68°C to help dissolve, add a few drops of concentrated hydrochloric acid, adjust the pH to 7.2, and add water to make up to 1L.

[0094] Solution A (2×SSC, 0.1% SDS, pH 7.4) was sterilized by high temperature and high pressure.

[0095] Solution B (0.5×SSC, 0.1% SDS, pH 7.4) was sterilized by high temperature and high pressure.

[0096] Solution C (0.1M sod...

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Abstract

The invention relates to a drug-resistance gene film chip for detecting mycobacterium tuberculosis which is prepared by designing 54 probe spotting on a nylon film by aiming at the mutant sites of mycobacterium tuberculosis rpoB, katG, embB, inhA, ahpC, gyrA, rrs, rpsL and pncA gene; 12 pairs of specific primers with biotin-labeled at 5' end are utilized; a sample DNA is subjected to triple PCR and amplified to form a large amount of gene fragment products with biotin; the amplified products and the probes on the film chip carry out specific hybridization; and then film washing, enzyme-linking and color reaction are carried out, thus preparing the chip. The gene film chip and the detection method thereof can detect the common gene mutations of the mycobacterium tuberculosis on the drug resistance of drugs such as isoniazid, rifampicin, streptomycin, ethambutol, pyrazinamide, quinolone and the like at one step, and are applicable to extracorporeal detection sputum sample, clinical isolation strains and mycobacterium tuberculosis multi-drug resistant gene in the organization sample.

Description

technical field [0001] The invention relates to a gene membrane chip and a detection method thereof, in particular to a genotype membrane chip for detecting multidrug resistance of Mycobacterium tuberculosis. It can be applied to in vitro detection of MDR gene of Mycobacterium tuberculosis in sputum samples, clinical isolates and tissue samples. Background technique [0002] At present, the research on the molecular mechanism of drug resistance of Mycobacterium tuberculosis mainly focuses on the target sites of various anti-tuberculosis drugs and the mutations of related genes. The types of Mycobacterium tuberculosis gene mutations that have been found are mainly point mutations, which are essentially the insertion, deletion or substitution of one or several nucleotides within a gene, resulting in the translation of the wrong nucleotide code into the wrong amino acid sequence. , leading to resistance of Mycobacterium tuberculosis to anti-TB drugs. The main drug-resistant a...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): C12Q1/68C40B40/06C12R1/32
Inventor 何敏韦世录何晓
Owner GUANGXI MEDICAL UNIVERSITY
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