Department of Dermatology, Radboud University Medical Center (Radboudumc), Radboud Institute for Molecular Life Sciences (RIMLS), Nijmegen, The Netherlands.
Exp Dermatol. 2020 Jul;29(7):672-676. doi: 10.1111/exd.14126. Epub 2020 Jun 25.
In biomedical research, cell culture contamination is one of the main culprits of experimental failure. Contamination sources and concomitant remedies are numerous and challenging to manage. We herein describe two cases of uncommon contamination of cell cultures that we encountered, and the successful determination and eradication strategies. The first case describes the infection with human adenovirus C that originated from pharyngeal tonsils used for isolation of primary tonsillar epithelial cells. It is known that viral contamination of in vitro cell cultures can occur symptomless and is therefore difficult to identify. The contamination was pervasive and persistent, as it was widely spread in flow cabinets and apparatus, and has caused a serious delay to our research projects and the inevitable loss of valuable (patient-derived) cell sources. Eradication was successful by formalin gas sterilization of the flow cabinet and elimination of all infected cell lines from our biobank after PCR-guided determination. Secondly, we encountered a spore-forming bacterium, namely Brevibacillus brevis, in our cell culture facility. This bacterium originated from contaminated tap water pipes and spread via regular aseptic culture techniques due to survival of the bacterial spores in 70% ethanol. B brevis overgrew the cultures within a few days after seeding of the primary cells. Chlorine solution effectively killed this spore-forming bacterium. Both cases of contamination were identified using DNA sequencing which enabled the deployment of targeted aseptic techniques for the elimination of the persistent contamination.
在生物医学研究中,细胞培养污染是实验失败的主要原因之一。污染来源众多且难以管理。我们在此描述了我们遇到的两种罕见的细胞培养污染情况,以及成功的确定和根除策略。第一个案例描述了源自用于分离原代扁桃体上皮细胞的咽扁桃体的人腺病毒 C 的感染。众所周知,体外细胞培养物的病毒污染可能无症状发生,因此难以识别。污染是广泛且持久的,因为它在通风柜和仪器中广泛传播,并严重延迟了我们的研究项目,以及不可避免的损失有价值的(患者来源)细胞资源。通过对通风柜进行福尔马林气体灭菌,并在 PCR 指导下从我们的生物库中消除所有受感染的细胞系,成功根除了污染。其次,我们在细胞培养设施中遇到了一种形成孢子的细菌,即短芽孢杆菌。这种细菌源自受污染的自来水管道,并通过常规的无菌培养技术传播,因为细菌孢子在 70%乙醇中存活。短芽孢杆菌在接种原代细胞后几天内就会过度生长。氯溶液可有效杀死这种形成孢子的细菌。这两种污染情况均通过 DNA 测序进行了鉴定,从而能够采用有针对性的无菌技术来消除持续的污染。