Department of Pathology and Genomic Medicine, Houston Methodist Hospital, 6565 Fannin Street, Houston, TX 77030, USA.
Int J Mol Sci. 2020 May 27;21(11):3784. doi: 10.3390/ijms21113784.
Mycoplasma contamination of cell line cultures is a common, yet often undetected problem in research laboratories. Many of the existing techniques to detect mycoplasma contamination of cultured cells are time-consuming, expensive, and have significant drawbacks. Here, we describe a mycoplasma detection system that is useful for detecting multiple species of mycoplasma in infected cell lines. The system contains three dye-labeled detection aptamers that can specifically bind to mycoplasma-infected cells and a dye-labeled control aptamer that minimally binds to cells. With this system, mycoplasma-contaminated cells can be detected within 30 min by using a flow cytometer, fluorescence microscope, or microplate reader. Further, this system may be used to detect mycoplasma-contaminated culture medium. This study presents an novel mycoplasma detection model that is simple, rapid, inexpensive, and sensitive.
支原体污染细胞系培养是一个常见的,但往往未被发现的问题在研究实验室。许多现有的技术来检测支原体污染的培养细胞是费时,昂贵的,并有显著的缺点。在这里,我们描述了一个支原体检测系统,可用于检测多种支原体在感染的细胞系。该系统包含三个染料标记的检测适体,可以特异性地结合支原体感染的细胞和一个染料标记的对照适体,最小结合到细胞。用这个系统,支原体污染的细胞可以在 30 分钟内通过使用流式细胞仪,荧光显微镜,或微孔板读数仪检测到。此外,该系统可用于检测支原体污染的培养基。本研究提出了一种新型的支原体检测模型,该模型简单、快速、廉价、灵敏。