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基于聚合酶链反应的支原体优化检测方法

Optimized PCR-based detection of mycoplasma.

作者信息

Dobrovolny Paige L, Bess Dan

机构信息

Product Management, Sigma-Aldrich.

出版信息

J Vis Exp. 2011 Jun 20(52):3057. doi: 10.3791/3057.

Abstract

The maintenance of contamination-free cell lines is essential to cell-based research. Among the biggest contaminant concerns are mycoplasma contamination. Although mycoplasma do not usually kill contaminated cells, they are difficult to detect and can cause a variety of effects on cultured cells, including altered metabolism, slowed proliferation and chromosomal aberrations. In short, mycoplasma contamination compromises the value of those cell lines in providing accurate data for life science research. The sources of mycoplasma contamination in the laboratory are very challenging to completely control. As certain mycoplasma species are found on human skin, they can be introduced through poor aseptic technique. Additionally, they can come from contaminated supplements such as fetal bovine serum, and most importantly from other contaminated cell cultures. Once mycoplasma contaminates a culture, it can quickly spread to contaminate other areas of the lab. Strict adherence to good laboratory practices such as good aseptic technique are key, and routine testing for mycoplasma is highly recommended for successful control of mycoplasma contamination. PCR-based detection of mycoplasma has become a very popular method for routine cell line maintenance. PCR-based detection methods are highly sensitive and can provide rapid results, which allows researchers to respond quickly to isolate and eliminate contamination once it is detected in comparison to the time required using microbiological techniques. The LookOut Mycoplasma PCR Detection Kit is highly sensitive, with a detection limit of only 2 genomes per μl. Taking advantage of the highly specific JumpStart Taq DNA Polymerase and a proprietary primer design, false positives are greatly reduced. The convenient 8-tube format, strips pre-coated with dNTPs, and associated primers helps increase the throughput to meet the needs of customers with larger collections of cell lines. Given the extreme sensitivity of the kit, great care must be taken to prevent inadvertent contamination of samples and reagents. The step-by-step protocol we demonstrate highlights the precautions and practices required for reliable mycoplasma detection. We also show and discuss typical results and their interpretation. Our goal is to ensure the success of researchers using the LookOut Mycoplasma PCR Detection Kit.

摘要

维持无污染物的细胞系对于基于细胞的研究至关重要。最大的污染物问题之一是支原体污染。虽然支原体通常不会杀死被污染的细胞,但它们很难检测到,并且会对培养的细胞产生多种影响,包括代谢改变、增殖减慢和染色体畸变。简而言之,支原体污染损害了这些细胞系在为生命科学研究提供准确数据方面的价值。实验室中支原体污染的来源极难完全控制。由于在人类皮肤上发现了某些支原体物种,它们可能通过不良的无菌技术引入。此外,它们可能来自受污染的补充剂,如胎牛血清,最重要的是来自其他受污染的细胞培养物。一旦支原体污染了一种培养物,它可以迅速传播以污染实验室的其他区域。严格遵守良好的实验室规范,如良好的无菌技术是关键,强烈建议对支原体进行常规检测以成功控制支原体污染。基于PCR的支原体检测已成为细胞系常规维护中非常流行的方法。基于PCR的检测方法高度灵敏,可以快速得出结果,与使用微生物技术所需的时间相比,这使得研究人员一旦检测到污染就能迅速做出反应,分离并消除污染。LookOut支原体PCR检测试剂盒高度灵敏,检测限仅为每微升2个基因组。利用高度特异性的JumpStart Taq DNA聚合酶和专有的引物设计,大大减少了假阳性。方便的8管形式、预涂有dNTPs的条带和相关引物有助于提高通量,以满足拥有大量细胞系的客户的需求。鉴于该试剂盒的极高灵敏度,必须格外小心以防止样品和试剂的意外污染。我们展示的分步方案突出了可靠的支原体检测所需的预防措施和操作。我们还展示并讨论了典型结果及其解释。我们的目标是确保使用LookOut支原体PCR检测试剂盒的研究人员取得成功。

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