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本文引用的文献

1
Detection of Mycobacterium tuberculosis in respiratory specimens by strand displacement amplification of DNA.通过DNA链置换扩增检测呼吸道标本中的结核分枝杆菌。
J Clin Microbiol. 1996 Apr;34(4):860-5. doi: 10.1128/jcm.34.4.860-865.1996.
2
Diagnostic performance of amplified Mycobacterium tuberculosis direct test with cerebrospinal fluid, other nonrespiratory, and respiratory specimens.结核分枝杆菌直接扩增检测对脑脊液、其他非呼吸道标本及呼吸道标本的诊断性能。
J Clin Microbiol. 1996 Apr;34(4):834-41. doi: 10.1128/jcm.34.4.834-841.1996.
3
Diagnosis of mycobacterial infections by nucleic acid amplification: 18-month prospective study.通过核酸扩增诊断分枝杆菌感染:18个月的前瞻性研究。
J Clin Microbiol. 1996 Feb;34(2):304-12. doi: 10.1128/jcm.34.2.304-312.1996.
4
Utility of PCR in diagnosing pulmonary tuberculosis.聚合酶链反应在诊断肺结核中的应用。
J Clin Microbiol. 1996 Jun;34(6):1407-11. doi: 10.1128/jcm.34.6.1407-1411.1996.
5
Detection and identification of Mycobacterium tuberculosis directly from sputum sediments by Amplicor PCR.通过Amplicor聚合酶链反应直接从痰液沉淀物中检测和鉴定结核分枝杆菌。
J Clin Microbiol. 1995 Oct;33(10):2686-91. doi: 10.1128/jcm.33.10.2686-2691.1995.
6
Improved recovery of mycobacteria from respiratory secretions of patients with cystic fibrosis.提高从囊性纤维化患者呼吸道分泌物中分离分枝杆菌的回收率。
J Clin Microbiol. 1993 Apr;31(4):861-4. doi: 10.1128/jcm.31.4.861-864.1993.
7
Large-scale use of polymerase chain reaction for detection of Mycobacterium tuberculosis in a routine mycobacteriology laboratory.在常规分枝杆菌学实验室中大规模使用聚合酶链反应检测结核分枝杆菌。
J Clin Microbiol. 1993 Aug;31(8):2049-56. doi: 10.1128/jcm.31.8.2049-2056.1993.
8
Direct detection of Mycobacterium tuberculosis in respiratory specimens in a clinical laboratory by polymerase chain reaction.在临床实验室中通过聚合酶链反应直接检测呼吸道标本中的结核分枝杆菌。
J Clin Microbiol. 1993 Jul;31(7):1688-94. doi: 10.1128/jcm.31.7.1688-1694.1993.
9
Detection of Mycobacterium tuberculosis in clinical specimens by polymerase chain reaction and Gen-Probe Amplified Mycobacterium Tuberculosis Direct Test.通过聚合酶链反应和基因探针扩增结核分枝杆菌直接试验检测临床标本中的结核分枝杆菌。
J Clin Microbiol. 1993 Dec;31(12):3270-4. doi: 10.1128/jcm.31.12.3270-3274.1993.
10
Chemiluminescent detection of strand displacement amplified DNA from species comprising the Mycobacterium tuberculosis complex.结核分枝杆菌复合群中各物种链置换扩增DNA的化学发光检测
Mol Cell Probes. 1993 Oct;7(5):395-404. doi: 10.1006/mcpr.1993.1058.

通过多重链置换扩增法确认分枝杆菌生长指示管(MGIT)中结核分枝杆菌和其他分枝杆菌的存在。

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

作者信息

Badak F Z, Kiska D L, O'Connell M, Nycz C M, Hartley C, Setterquist S, Hopfer R L

机构信息

Becton Dickinson Research Center, Research Triangle Park, North Carolina, USA.

出版信息

J Clin Microbiol. 1997 May;35(5):1239-43. doi: 10.1128/jcm.35.5.1239-1243.1997.

DOI:10.1128/jcm.35.5.1239-1243.1997
PMID:9114414
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC232736/
Abstract

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.

摘要

多重链置换扩增(mSDA)能够同时扩增三个不同的DNA序列。这些序列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以及一个内部对照。mSDA用于检测在分枝杆菌生长指示管(MGIT)系统中培养的154份临床标本(72份阳性、76份阴性和6份检测失败)中这些靶序列的存在。处理和培养了多种标本类型。一旦这些培养物经MGIT荧光判定为阳性或在培养8周后判定为阴性,就对MGIT培养物的等分试样进行mSDA分析。采用化学发光微孔测定法检测扩增产物。该程序相对简单,完成时间不到6小时。与MGIT培养相比,mSDA检测抗酸杆菌的灵敏度为96.4%。当考虑所有临床标准时,灵敏度和特异性分别为97.2%和96.1%。mSDA被证明是一种快速有效的方法,可用于确认阳性MGIT培养物中结核分枝杆菌和其他分枝杆菌的存在。