首页> 美国卫生研究院文献>Journal of Clinical Biochemistry and Nutrition >Five-antituberculosis Drug-resistance Genes Detection Using Array System
【2h】

Five-antituberculosis Drug-resistance Genes Detection Using Array System

机译:利用阵列系统检测五种抗结核药物耐药基因

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。
获取外文期刊封面目录资料

摘要

Detection of resistance to drugs for Mycobacterium tuberculosis takes about two months from the sample collection using culture-based methods. To test a rapid method for detection of resistance for five antituberculosis drugs using DNA microarray and to examine its potential for clinical use, we employed a DNA microarray for detection of seven mutations genes related to resistance of five kinds of antituberculous drugs using Mycobacterium tuberculosis DNA isolated from sputum. The results of microarray analysis were compared with the results of a standard culture method of Lowenstein-jensen drug sensitivity testing system. DNA microarray analysis showed a high sensitivity (>90%) for all five drugs. Specificity of rifampicin and ethambutol were nearly 90%, however specificity of isoniazid (60%) and kanamycin (67%) were not enough. The amount of Mycobacterium tuberculosis DNA required for microarray analysis corresponded to at least 1–9 Acid-Fast Bacilli per 10 fields by carbolfuchsin staining. DNA microarray analysis appears to be useful for estimation of drug resistances, nevertheless its limitations. To minimize misunderstanding, it is necessary to confirm the number of bacilli in the sputum, and culture method is needed for comparison when use the PCR-based array system.
机译:使用基于培养的方法,从样本收集开始,大约需要两个月的时间才能检测出结核分枝杆菌对药物的耐药性。为了测试使用DNA微阵列检测五种抗结核药物耐药性的快速方法并检验其临床应用潜力,我们使用DNA微阵列使用分离的结核分枝杆菌DNA来检测与五种抗结核药物耐药性相关的七个突变基因从痰。将微阵列分析的结果与Lowenstein-jensen药物敏感性测试系统的标准培养方法的结果进行比较。 DNA芯片分析显示,对所有五种药物都具有很高的敏感性(> 90%)。利福平和乙胺丁醇的特异性接近90%,但是异烟肼(60%)和卡那霉素(67%)的特异性还不够。微阵列分析所需要的结核分枝杆菌DNA量至少相当于每十个领域通过羧化红素染色产生1–9个酸性快速芽孢杆菌。尽管有局限性,DNA微阵列分析似乎可用于估计耐药性。为了最大程度地减少误解,有必要确认痰中的细菌数量,并且使用基于PCR的阵列系统进行比较时需要培养方法。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号