A highly sensitive internally-controlled real-time PCR assay for mycoplasma detection in cell cultures

被引:13
|
作者
Sung, Julia [1 ,2 ]
Hawkins, J. Ross [1 ]
机构
[1] Natl Inst Biol Stand & Controls, Div Adv Therapies, Blanche Lane, S Mimms EN6 3QG, Herts, England
[2] Publ Hlth England, PHE Culture Collect, Salisbury SP4 0JG, Wilts, England
关键词
Mycoplasma; qPCR assay; European pharmacopeia; CONTAMINATION;
D O I
10.1016/j.biologicals.2019.12.007
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Mycoplasma contamination of cell lines is a common occurrence and may affect the cell line behaviour in a variety of ways. Contamination with mycoplasma is usually not obvious so cell lines should be frequently tested. Several commercially available kits for mycoplasma detection exist, however the Ph. Eur. culture method which can take several weeks to yield results is still considered to be the 'gold standard' method. There is therefore a need for rapid alternative methods with comparable sensitivity, specificity and species range. Here, we describe an internally-controlled Taqman-based real-time PCR assay for cell culture medium without the need for DNA extraction. The assay can detect less than 10 CFU of the most frequently encountered mycoplasma contaminants in mammalian cell cultures. The validated assay has the potential to be used as a routine test in the production of cell culture-based Biologicals.
引用
收藏
页码:58 / 72
页数:15
相关论文
共 50 条
  • [31] Development of a rotor-gene real-time PCR assay for the detection and quantification of Mycoplasma genitalium
    Mueller, Etienne E.
    Venter, Johanna M. E.
    Magooa, Mahlape P.
    Morrison, Charles
    Lewis, David A.
    Mavedzenge, Sue Napierala
    JOURNAL OF MICROBIOLOGICAL METHODS, 2012, 88 (02) : 311 - 315
  • [32] First LightCycler real-time PCR assay for the quantitative detection of Mycoplasma suis in clinical samples
    Hoelzle, Ludwig E.
    Helbling, Marianne
    Hoelzle, Katharina
    Ritzmann, Mathias
    Heinritzi, Karl
    Wittenbrink, Max M.
    JOURNAL OF MICROBIOLOGICAL METHODS, 2007, 70 (02) : 346 - 354
  • [33] Real-time PCR detection of Mycoplasma pneumoniae in respiratory specimens
    Schmitt, Bryan H.
    Sloan, Lynne M.
    Patel, Robin
    DIAGNOSTIC MICROBIOLOGY AND INFECTIOUS DISEASE, 2013, 77 (03) : 202 - 205
  • [34] A novel and highly sensitive real-time nested RT-PCR assay in a single closed tube for detection of enterovirus
    Shen, Xin-xin
    Qiu, Fang-zhou
    Zhao, Huai-long
    Yang, Meng-jie
    Hong, Liu
    Xu, Song-tao
    Zhou, Shuai-feng
    Li, Gui-xia
    Feng, Zhi-shan
    Ma, Xue-jun
    DIAGNOSTIC MICROBIOLOGY AND INFECTIOUS DISEASE, 2018, 90 (03) : 181 - 185
  • [35] EvaGreen-based real-time PCR assay for sensitive detection of salmonid alphavirus
    Shi, Wen
    Wang, Yuting
    Ren, Xuanyu
    Gao, Shuai
    Hua, Xiaojing
    Guo, Mengting
    Tang, Lijie
    Xu, Yigang
    Ren, Tong
    Li, Yijing
    Liu, Min
    MOLECULAR AND CELLULAR PROBES, 2018, 39 : 7 - 13
  • [36] Development and validation of a real-time reverse transcriptase PCR assay for sensitive detection of SFTSV
    Zeng, Peibin
    Yang, Zhendong
    Bakkour, Sonia
    Wang, Bingjun
    Qing, Shuli
    Wang, Jingxing
    Chen, Limin
    Busch, Michael
    Shan, Hua
    Liu, Jing
    Lee, Tzong-Hae
    JOURNAL OF MEDICAL VIROLOGY, 2017, 89 (07) : 1131 - 1138
  • [37] A real-time quantitative PCR assay for specific and sensitive detection of Phytophthora infestans on tomato
    Chowdappa, P.
    Kumar, B. J. Nirmal
    Madhura, S.
    Bhargavi, B. Reddi
    Sandhya, H.
    INDIAN JOURNAL OF AGRICULTURAL SCIENCES, 2013, 83 (04): : 463 - 466
  • [38] Direct detection of Coccidioides from Arizona soils using CocciENV, a highly sensitive and specific real-time PCR assay
    Bowers, J. R.
    Parise, K. L.
    Kelley, E. J.
    Lemmer, D.
    Schupp, J. M.
    Driebe, E. M.
    Engelthaler, D. M.
    Keim, P.
    Barker, B. M.
    MEDICAL MYCOLOGY, 2019, 57 (02) : 246 - 255
  • [39] Parasitological diagnosis combining an internally controlled real-time PCR assay for the detection of four protozoa in stool samples with a testing algorithm for microscopy
    van Coppenraet, L. E. S. Bruijnesteijn
    Wallinga, J. A.
    Ruijs, G. J. H. M.
    Bruins, M. J.
    Verweij, J. J.
    CLINICAL MICROBIOLOGY AND INFECTION, 2009, 15 (09) : 869 - 874
  • [40] Highly sensitive and accurate real-time PCR assay for hepatitis B viral load quantification
    Curtis, M
    Zhu, Y
    Jackson, M
    ANTIVIRAL RESEARCH, 2004, 62 (02) : A46 - A46