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使用非放射性BACTEC MGIT 960系统检测结核分枝杆菌对吡嗪酰胺的敏感性。

Testing of susceptibility of Mycobacterium tuberculosis to pyrazinamide with the nonradiometric BACTEC MGIT 960 system.

作者信息

Pfyffer Gaby E, Palicova Frantiska, Rüsch-Gerdes Sabine

机构信息

Swiss National Center for Mycobacteria, Department of Medical Microbiology, University of Zurich, Gloriastrasse 30, 8028 Zurich, Switzerland.

出版信息

J Clin Microbiol. 2002 May;40(5):1670-4. doi: 10.1128/JCM.40.5.1670-1674.2002.

Abstract

The reliability of the novel BACTEC MGIT 960 pyrazinamide (PZA) kit (Becton Dickinson Microbiology Systems, Sparks, Md.) was assessed for testing of susceptibility of Mycobacterium tuberculosis to PZA. Results generated by the BACTEC MGIT 960 system (Becton Dickinson) were compared with those obtained with the BACTEC 460TB system. Extensive proficiency testing (phase I) and reproducibility testing (phase II) as well as susceptibility testing of blinded strains of M. tuberculosis from the Centers for Disease Control and Prevention (phase III) were performed prior to testing 58 strains isolated from clinical specimens (phase IV). After resolution of discrepant results obtained by the two BACTEC methods by two other laboratories which acted as independent arbiters (phase V), overall agreement of the BACTEC MGIT 960 system with the BACTEC 460TB system for PZA testing of phase IV strains was 96.6%. Between the two systems there was no statistically significant difference in time until results were obtained, i.e., 6.8 days (BACTEC MGIT 960) versus 5.4 days (BACTEC 460TB), the latter not counting the time required for a subculture with a growth index of 200, however. The new BACTEC MGIT PZA susceptibility testing procedure works equally well for inocula prepared from liquid (MGIT) and solid (Löwenstein-Jensen) cultures. PZA MGIT medium in plastic tubes yielded results equivalent to medium dispensed in glass tubes.

摘要

对新型BACTEC MGIT 960吡嗪酰胺(PZA)试剂盒(Becton Dickinson微生物系统公司,马里兰州斯帕克斯)检测结核分枝杆菌对PZA敏感性的可靠性进行了评估。将BACTEC MGIT 960系统(Becton Dickinson公司)产生的结果与BACTEC 460TB系统获得的结果进行比较。在对从临床标本中分离出的58株菌株进行检测(第四阶段)之前,进行了广泛的能力验证检测(第一阶段)、重复性检测(第二阶段)以及对来自疾病控制和预防中心的结核分枝杆菌盲法菌株的敏感性检测(第三阶段)。由另外两个充当独立仲裁者的实验室解决了两种BACTEC方法获得的不一致结果(第五阶段)后,BACTEC MGIT 960系统与BACTEC 460TB系统对第四阶段菌株PZA检测的总体一致性为96.6%。在两种系统之间,获得结果所需的时间没有统计学上的显著差异,即BACTEC MGIT 960为6.8天,而BACTEC 460TB为5.4天,但后者不包括生长指数为200时传代培养所需的时间。新的BACTEC MGIT PZA敏感性检测程序对于从液体(MGIT)和固体(罗-琴)培养物制备的接种物同样有效。塑料试管中的PZA MGIT培养基产生的结果与玻璃试管中分配的培养基相当。

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