首页 | 本学科首页   官方微博 | 高级检索  
     


Development of an internally controlled PCR assay for broad range detection of bacteria in platelet concentrates
Authors:Rood I G H  Koppelman M H G M  Pettersson A  Savelkoul P H M
Affiliation:aSanquin, Diagnostic Services Division, Amsterdam, Plesmanlaan 125, 1066 CX, Amsterdam, The Netherlands;bDepartment of Medical Microbiology and Infection Control, VU University Medical Center, De Boelelaan 1117 Amsterdam, 1081 HV, Amsterdam, The Netherlands
Abstract:
A real-time PCR assay based on the 16S rRNA gene was optimized for the detection of a broad range of bacteria in plasma and platelet concentrates (PC). A lambda phage internal control was constructed and implemented in the assay, which made it suitable for diagnostic use. Spiking studies in plasma and PCs were performed to determine the analytical sensitivity of the assay. Thirty three colony forming units (CFU)/ml of E. coli and 72 CFU/ml of Staphylococcus epidermidis could be detected in plasma, and 97 CFU/ml of S. epidermidis in PCs. The assay detected all bacteria relevant for bacterial contamination of PCs. The short turn around time of the assay made it suitable for testing PCs for bacterial contamination prior to transfusion.
Keywords:16S rRNA real-time PCR assay   Lambda phage IC   Bacterial contamination   Platelet concentrates
本文献已被 ScienceDirect PubMed 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号