Quantification of a cell culture contaminant using 16S rDNA

被引:3
|
作者
Xu, Xuebo [1 ,2 ]
Lai, Yueyang [1 ,2 ]
Zhou, Wenzhao [1 ,2 ]
Wu, Leyang [1 ,2 ]
Hua, Zichun [1 ,2 ,3 ,4 ,5 ]
机构
[1] Nanjing Univ, Sch Life Sci, Nanjing, Jiangsu, Peoples R China
[2] Nanjing Univ, State Key Lab Pharmaceut Biotechnol, Nanjing, Jiangsu, Peoples R China
[3] Nanjing Univ, Changzhou High Tech Res Inst, Changzhou, Peoples R China
[4] Jiangsu TargetPharma Labs Inc, Changzhou, Peoples R China
[5] Nanjing Univ, Shenzhen Res Inst, Shenzhen, Peoples R China
关键词
cell culture contaminant; antibiotics; 16S rDNA sequencing; qPCR quantification; NANOBACTERIA-LIKE PARTICLES; STONES;
D O I
10.1002/bab.1792
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
In this study, we identified a "black dot"-like cell culture contaminant as a species belonging to the genus of Pusillimonas using 16S rDNA sequencing. Among all antibiotics tested, a combinatorial treatment of ampicillin and gentamicin both at 100 mu g/mL was able to eliminate this contaminant. The contaminant was then visualized by fluorescence microscopy using propidium iodide staining and was found inside the cytosol of contaminated A549 cells. To characterize the efficacy of antibiotics for contaminant removal, we devised a quantitative method to determine the average number of 16S rDNA copies associated with a single A549 cell, which is directly proportional to the average number of contaminant per A549 cell. By using primers specific to the 16S rDNA sequence of the contaminant, we were able to estimate contaminants per single contaminated cell using both qPCR-based relative and absolute quantification.
引用
收藏
页码:815 / 822
页数:8
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