Removal of PCR Inhibitors in Real-time PCR for Mycobacterium tuberculosis

H. Yun, H. Kim, Young Kyung Lee, H. Kang, Jae Seok Kim, W. Song, K. Lee
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Abstract

Background: The inhibition rates for nucleic acid tests of Mycobacterium tuberculosis have been reported to range from less than 1% to more than 10%. Specimen dilution, boiling, addition of bovine serum albumin (BSA), and a silica membrane can be used to override amplification inhibitors in nucleic acid tests of M. tuberculosis. The inhibition rate for real-time PCR of M. tuberculosis (COBAS TaqMan MTB test; Roche Diagnostics, Manheim, Germany) and effective strategies to override PCR inhibitors were investigated in this study. Methods: The inhibition rate for COBAS TaqMan MTB test was investigated in 980 clinical specimens. The effectiveness of PCR inhibitor removal by repeated run, dilution, boiling, addition of BSA, and use of silica membrane were evaluated in the inhibited specimens. Results: Inhibitory substances were present in 4.1% of specimens (40/980). Among 40 inhibited specimens, inhibitory substances were removed in 12 (30%), 30 (75%), 27 (67.5%), 25 (62.5%) and 12 (30%) specimens with repeated run, dilution, addition of RBS, boiling and use of silica membrane, respectively. Conclusion: The overall inhibition rate for the COBAS TaqMan MTB test was 4.1%. Dilution, boiling and addition of BSA were shown to be more effective than repeated run and use of silica membrane for removal of PCR inhibitors. A combination of two methods might be useful and should be studied in the future. (Korean J Clin Microbiol 2011;14:97-102)
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结核分枝杆菌实时荧光定量PCR中PCR抑制剂的去除
背景:据报道,结核分枝杆菌核酸检测的抑制率从小于1%到大于10%不等。标本稀释、煮沸、加入牛血清白蛋白(BSA)和二氧化硅膜可用于在结核分枝杆菌核酸检测中覆盖扩增抑制剂。实时PCR检测结核分枝杆菌(COBAS) TaqMan MTB的抑制率罗氏诊断,曼海姆,德国)和有效的策略,以覆盖PCR抑制剂在本研究中进行了研究。方法:对980例临床标本进行COBAS TaqMan MTB试验,考察其抑菌率。通过反复运行、稀释、煮沸、添加牛血清白蛋白和使用二氧化硅膜去除PCR抑制剂的效果在抑制的标本中进行评估。结果:4.1%(40/980)标本中存在抑菌物质。在40份被抑制的样品中,分别通过反复运行、稀释、添加RBS、煮沸和使用二氧化硅膜去除12份(30%)、30份(75%)、27份(67.5%)、25份(62.5%)和12份(30%)样品中的抑制物质。结论:COBAS对TaqMan MTB试验的总抑制率为4.1%。稀释、煮沸和添加牛血清白蛋白比重复运行和使用二氧化硅膜去除PCR抑制剂更有效。两种方法的结合可能是有用的,应该在未来进行研究。(韩国临床微生物学杂志2011;14:97-102)
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