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作 者:杨华卫[1] 杨树德[1] 庄玉辉[2] 李国利[2] 李邦印[2]
机构地区:[1]北京医院卫生部临床检验中心,北京100730 [2]解放军309医院结核病研究室,北京100091
出 处:《微生物学报》2000年第2期143-149,共7页Acta Microbiologica Sinica
基 金:国家自然科学基金!资助项目 ( 396 70 6 96 )
摘 要:为改进结核杆菌DNA探针的特异性与实用性,研制了以生物素标记的两种对结核分支杆菌特异的DNA探针:一个5’端标记的20bp的寡核苷酸探针和一个采用PCR方法合成的188bp长链探针。两种探针分别与结核分支杆菌的全染色体DNA,以及基因组上IS6110序列的一段317bp的PCR扩增产物进行斑点杂交,以碱性磷酸酶(AP)催化的染色反应检测,测试了两个探针的敏感性和特异性。系统地比较研究了两种探针杂交检测条件:探针的浓度选择,杂交温度与洗膜温度的选择,以及杂交与洗膜温度对检测的敏感性与特异性的影响。寡核苷酸探针和188bp探针杂交检测纯化结核分支杆菌基因组DNA的敏感性分别为100ng与6ng,杂交检测PCR产物的敏感性分别是400pg与50pg。两探针的最佳杂交浓度均为40~160ng/ml,最佳杂交温度分别是42℃与68℃,最佳洗膜温度分别是60℃与60~68℃之间。两种探针均仅与结核分支杆菌及BCG有杂交信号,而与其它受试分支杆菌及非分支杆菌杂交结果都呈阴性。它们的特异性都很强,但188bp探针的敏感性约是寡核苷酸探针的7~16倍,而且188bp探针检测本底较低。Two different biotinylated DNA probes which are highly specific to \%M.tuberculosis\%(MT) were made and studied. One probe is a 20bp oligonucleotide labeled with biotin at 5'end, the other is a long DNA probe produced by PCR amplification procedure allowed for the incorporation of biotin labeled UTP. The two probes were hybridized with MT genome DNA and a 317bp PCR product amplified from IS6110 sequence of MT, and then detected by alkaline phosphatase conjugates through colorimetric reaction. The detection sensitivity and specificity of the two probes were comparatively studied. The hybridization condition including concentration of probe, temperature of hybridization and washing filter thereafter were also investigated preliminary. The detection limit of the oligonucleotide probe and the 188bp PCR probe were 100ng and 6ng of DNA respectively in detection of M.T genome, and 400pg and 50pg of DNA respectively in detection of PCR products of MT. The two probes can be only hybridized to MT and BCG, but not with other 24 mycobacterium or non-mycobacterium tested. The optimal hybridization temperature and washing filter temperature of oligonucleotide were 42℃ and 60℃ respectively; and that of 188bp probe, 68℃ and 60℃~68℃. Generally the specificity of two probes were all high, but the sensitivity of 188bp DNA probe was 7~16 times that of the oligonucleotide probe. The higher sensitivity, lower hybridization background and faster revelation of the 188bp DNA probe made it a better choice in detection of MT.
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