...
首页> 外文期刊>Journal of Clinical Microbiology >Confirmation of the presence of Mycobacterium tuberculosis and other mycobacteria in mycobacterial growth indicator tubes (MGIT) by multiplex strand displacement amplification.
【24h】

Confirmation of the presence of Mycobacterium tuberculosis and other mycobacteria in mycobacterial growth indicator tubes (MGIT) by multiplex strand displacement amplification.

机译:通过多重链置换扩增确认在分枝杆菌生长指示器管(MGIT)中结核分枝杆菌和其他分枝杆菌的存在。

获取原文
           

摘要

Multiplex strand displacement amplification (mSDA) is capable of amplifying three distinct DNA sequences simultaneously. These include sequences present in most genera of mycobacteria, a sequence specific for Mycobacterium tuberculosis, and an internal control. mSDA was used to detect the presence of these target sequences in 154 (72 positive, 76 negative, and 6 failed) clinical specimens cultured in the mycobacterial growth indicator tube (MGIT) system. A wide variety of specimen types were processed and cultured. Once these cultures were deemed positive by MGIT fluorescence or were deemed negative after 8 weeks of incubation, MGIT culture aliquots were processed for mSDA analyses. A chemiluminescent microwell assay was used to detect the amplified products. The procedure was relatively simple and took less than 6 h to complete. The sensitivity of mSDA for detecting acid-fast bacilli was 96.4% compared to that of MGIT culture. Sensitivity and specificity were 97.2 and 96.1%, respectively, when all clinical criteria were considered. mSDA was shown to be a rapid and effective method for confirming the presence of M. tuberculosis and other mycobacteria in positive MGIT cultures.
机译:多重链置换扩增(mSDA)能够同时扩增三个不同的DNA序列。这些包括大多数分枝杆菌属中存在的序列,结核分枝杆菌特异的序列和内部对照。 mSDA用于检测在分枝杆菌生长指示器管(MGIT)系统中培养的154个临床标本中(72个阳性,76个阴性和6个失败)这些靶序列的存在。各种各样的标本类型都经过处理和培养。将这些培养物通过MGIT荧光确认为阳性或孵育8周后视为阴性后,将MGIT培养液等分试样进行mSDA分析。化学发光微孔测定法用于检测扩增产物。该过程相对简单,不到6小时即可完成。与MGIT培养相比,mSDA对耐酸杆菌的检测灵敏度为96.4%。当考虑所有临床标准时,敏感性和特异性分别为97.2%和96.1%。已证明,mSDA是确认阳性MGIT培养物中结核分枝杆菌和其他分枝杆菌的快速有效方法。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

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