Uphoff Cord C, Drexler Hans G
DSMZ-German Collection of Microorganisms and Cell Cultures, Braunschweig, Germany.
Methods Mol Biol. 2005;290:13-23. doi: 10.1385/1-59259-838-2:013.
Mycoplasma contamination of cell lines is one of the major problems in cell culture technology. The specific, sensitive, and reliable detection of mycoplasma contamination is an important part of mycoplasma control and should be an established method in every cell culture laboratory. New cell lines as well as cell lines in continuous culture must be tested in regular intervals. The polymerase chain reaction (PCR) methodology offers a fast and sensitive technique to monitor all cultures in a laboratory. The technique can also be used to determine the contaminating mycoplasma species. The described assay can be performed within 3 h, including sample preparation, DNA extraction, performing the PCR reaction, and analysis of the PCR products. Special precautions necessary to avoid false-negative results resulting from inhibitors of the Taq polymerase present in the crude samples and the interpretation of the results are also described.
细胞系的支原体污染是细胞培养技术中的主要问题之一。支原体污染的特异性、灵敏性和可靠检测是支原体控制的重要组成部分,应成为每个细胞培养实验室的既定方法。新细胞系以及连续培养的细胞系必须定期进行检测。聚合酶链反应(PCR)方法提供了一种快速且灵敏的技术,可用于监测实验室中的所有培养物。该技术还可用于确定污染的支原体种类。所描述的检测方法可在3小时内完成,包括样品制备、DNA提取、进行PCR反应以及分析PCR产物。文中还介绍了为避免粗样品中存在的Taq聚合酶抑制剂导致假阴性结果而需采取的特殊预防措施以及结果的解读。