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Detection of Mycoplasma in cell cultures
Abstract
Mycoplasma is a prokaryotic organism that is a frequent and occult contaminant of cell cultures. This organism can modify many aspects of cell physiology, rendering experiments that are conducted with contaminated cells worthless. Because of their small size, Mycoplasmas can pass through filters used to prevent bacterial and fungal contamination and potentially spread to all the cultures in a laboratory. It is essential that all new cell cultures entering a laboratory and all cell banks are tested for the presence of Mycoplasma. It is recommended that two techniques be used, selected from a PCR-based method, indirect staining and an agar and broth culture. This protocol describes these three tests for detecting Mycoplasma, which take from 1 d to 3-4 weeks, and such tests should be an obligatory component of quality control in every tissue culture laboratory.
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“Contamination with mycoplasma was ruled out by PCR testing according to standard protocols37.”
From Common germline variants of the human APOE gene modulate melanoma progression and survival (2020) · cites this paper as [37]
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Treating Cells as Reagents to Design Reproducible Assays
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Kalita, A., Das, M., Das, B., & Baro, M. R. (2022) · Beni-Suef University Journal of Basic and Applied Sciences · doi:10.1186/s43088-022-00214-2 · Cited by 23
“The cells were tested for any kind of Mycoplasma contamination before the experiments following the PCR-based method [34, 35].”
Canlı, S. D., Seza, E. G., Sheraj, I., Gömceli, İ., Turhan, N., Carberry, S., Prehn, J. H. M., Gure, A. O., & Banerjee, S. (2020) · Carcinogenesis · doi:10.1093/carcin/bgaa072 · Cited by 23
Metabolomics reveals mycoplasma contamination interferes with the metabolism of PANC-1 cells
Yu, T., Wang, Y., Zhang, H., Johnson, C. H., Jiang, Y., Li, X., Wu, Z., Liu, T., Krausz, K. W., Yu, A., et al. (2016) · Analytical and Bioanalytical Chemistry · doi:10.1007/s00216-016-9525-9 · Cited by 18
“Contamination of cell cultures with mycoplasma presents a challenging issue in terms of detectability and prevention since no overt changes are observed in media pH, turbidity, and direct microscopic visualization [3, 4, 7].”
BackgroundBi, W., Yang, M.-Y., Xing, P., & Huang, T. (2022) · Bioengineered · doi:10.1080/21655979.2022.2083855 · Cited by 17
“Monthly mycoplasma tests to ensure cells purity [25].”
RetractedThe Role of miR-375-3p and miR-200b-3p in Gastrointestinal Stromal Tumors
Gyvytė, U., Lukoševičius, R., Inčiūraitė, R., Streleckienė, G., Gudoitytė, G., Bekampytė, J., Valentini, S., Šaltenienė, V., Ruzgys, P., Šatkauskas, S., et al. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21145151 · Cited by 18
“Cell lines were tested for mycoplasma contamination using specific primers [43].”
MethodRapid Detection of Mycoplasma-Infected Cells by an ssDNA Aptamer Probe.
Liu, Y.-T., Jiang, W.-Q., Yang, S., Hu, J., Lu, H.-B., Han, W., Wen, J.-G., Zeng, Z.-H., Qi, J., Xu, L., et al. (2019) · ACS Sensors · doi:10.1021/acssensors.9b00582 · Cited by 17
Mitoribosomal synthetic lethality overcomes multidrug resistance in MYC-driven neuroblastoma
Borankova, K., Krchniaková, M., Leck, L. Y. W., Kubistova, A., Neradil, J., Jansson, P. J., Hogarty, M. D., & Skoda, J. (2023) · Cell Death and Disease · doi:10.1038/s41419-023-06278-x · Cited by 16
“Subsequently, cell con fl uency was determined every 4 h using live cell imaging system Incucyte ® SX1 (Sartorius, Göttingen, Germany) and plotted relative to initial values.”
Lai, M., Iacono, E., Spezia, P. G., Lottini, G., Rocca, V. L., Quaranta, P., Pistello, M., & Freer, G. (2021) · Journal of Virological Methods · doi:10.1016/j.jviromet.2021.114327 · Cited by 16
Sensitive Assay for Mycoplasma Detection in Mammalian Cell Culture
Degeling, M. H., Maguire, C. A., Bovenberg, M. S. S., & Tannous, B. A. (2012) · Analytical Chemistry · doi:10.1021/ac2033112 · Cited by 19
Chronic chromosome instability induced by Plk1 results in immune suppression in breast cancer
Kandala, S., Ramos, M., von Voithenberg, L. V., Diaz-Jimenez, A., Chocarro, S., Keding, J., Brors, B., Imbusch, C. D., & Sotillo, R. (2023) · Cell Reports · doi:10.1016/j.celrep.2023.113266 · Cited by 25
Becker, K. N., Pettee, K. M., Sugrue, A., Reinard, K. A., Schroeder, J. L., & Eisenmann, K. M. (2022) · Cells · doi:10.3390/cells11091559 · Cited by 17
“All cell lines were routinely screened for mycoplasma, as described [41].”
MethodCRTC1/MAML2 directs a PGC-1α-IGF-1 circuit that confers vulnerability to PPARγ inhibition
Musicant, A. M., Parag‐Sharma, K., Gong, W., Sengupta, M., Chatterjee, A., Henry, E. C., Tsai, Y., Hayward, M. C., Sheth, S. H., Betancourt, R., et al. (2021) · Cell Reports · doi:10.1016/j.celrep.2021.108768 · Cited by 19
“All cell lines were confirmed mycoplasma-free by PCR as previously described (Young et al., 2010) and using mycoplasma detection primers (see Table S6).”
PD-L1 promotes oncolytic virus infection via a metabolic shift that inhibits the type I IFN pathway
Hodgins, J. J., Abou‐Hamad, J., O’Dwyer, C., Hagerman, A., Yakubovich, E., de Souza, C. T., Marotel, M., Buchler, A., Fadel, S., Park, M. M., et al. (2024) · The Journal of Experimental Medicine · doi:10.1084/jem.20221721 · Cited by 19
Concurrent inhibition of ALK and SRC kinases disrupts the ALK lung tumor cell proteome
Diaz-Jimenez, A., Ramos, M., Helm, B., Chocarro, S., Frey, D. L., Agrawal, S., Somogyi, K., Klingmüller, U., Lu, J., & Sotillo, R. (2024) · Drug Resistance Updates · doi:10.1016/j.drup.2024.101081 · Cited by 14
Zając, Z., Kulisz, J., Woźniak, A., Bartosik, K., Foucault-Simonin, A., Moutailler, S., & Cabezas-Cruz, A. (2023) · Pathogens · doi:10.3390/pathogens12091186 · Cited by 14
“In the real-time PCR reaction, we applied primers identical to those used in a previously published paper [25,26].”
InfluentialByun, J., Lee, S. H., Moon, E. J., Park, M.-H., Jang, H., Weitzel, D. H., Kim, H.-H., Basnet, N., Kwon, D.-Y., Lee, C.-T., et al. (2023) · British Journal of Cancer · doi:10.1038/s41416-023-02148-7 · Cited by 14
“All cell lines were routinely tested for mycoplasma contamination using a PCR-based method [13].”
MethodTSC2 regulates tumor susceptibility to TRAIL‐mediated T‐cell killing by orchestrating mTOR signaling
Lin, C., Traets, J. J. H., Vredevoogd, D. W., Visser, N. L., & Peeper, D. S. (2023) · The EMBO Journal · doi:10.15252/embj.2022111614 · Cited by 19
Rodríguez-Barbosa, J.-I., Azuma, M., Zelinskyy, G., Pérez‐Simón, J. A., & del Rio, M. (2020) · Cancer Immunology Immunotherapy · doi:10.1007/s00262-020-02520-z · Cited by 18
Kazemiha, V. M., Amanzadeh, A., Memarnejadian, A., Azari, S., Shokrgozar, M., Mahdian, R., & Bonakdar, S. (2014) · Cytotechnology (Dordrecht) · doi:10.1007/s10616-013-9640-9 · Cited by 14
“This explains the advantageous of the PCR over the classical methods especially in the case of low level contaminations (right before invasion of infection or after eradication of agents) (Young et al. 2010).”
BackgroundDowdell, A. S., Cartwright, I. M., Kitzenberg, D., Kostelecky, R. E., Mahjoob, O., Saeedi, B. J., Welch, N., Glover, L. E., & Colgan, S. P. (2022) · Cell Reports · doi:10.1016/j.celrep.2022.111409 · Cited by 14
“All cell lines used were tested for mycoplasma at least once a month using established protocols (Young et al., 2010).”
MethodRendošová, M., Gyepes, R., Maruščáková, I. C., Mudroňová, D., Sabolová, D., Kello, M., Vilková, M., Almáši, M., Huntošová, V., Zemek, O., et al. (2020) · Dalton Transactions · doi:10.1039/d0dt03332d · Cited by 20
15‐LOX‐1 has diverse roles in the resensitization of resistant cancer cell lines to doxorubicin
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Salling, H. K., & Bang-Christensen, S. R. (2016) · Biologicals · doi:10.1016/j.biologicals.2016.03.003 · Cited by 12
Longmate, W. M., Norton, E., Duarte, G. A., Wu, L., DiPersio, M. R., Lamar, J. M., & DiPersio, C. M. (2024) · Matrix Biology · doi:10.1016/j.matbio.2024.02.003 · Cited by 14
Rideau, F., Villa, A., Belzanne, P., Verdier, E., Hosy, E., & Arfi, Y. (2022) · bioRxiv · doi:10.1128/spectrum.00645-22 · Cited by 12
“As mycoplasmas are frequent contaminants of these cultures (79), mycoplasmologists might be barred from accessing these facilities with live cells.”
BackgroundDeogharkar, A., Singh, S. V., Bharambe, H. S., Paul, R., Moiyadi, A. V., Goel, A. H., Shetty, P. M., Epari, S., Gupta, T., Jalali, R., et al. (2021) · Human Molecular Genetics · doi:10.1093/hmg/ddab134 · Cited by 12
Metadata
- Authors
- Young, L., Sung, J., Stacey, G., & Masters, J. R.
- Affiliations
- University College London (GB)
- Corresponding author
- Masters, John R
- ORCID
- Stacey, Glyn
- Venue
- Nature Protocols
- Published
- 2010-04-22
- Volume
- 5
- Issue
- 5
- Pages
- 929-934
- ISSN
- 1750-2799 (ISSN-L)
- 1754-2189
- OpenAlex
- W2092105616
- Cited by
- 437
- References
- 11
- Citations by year
- 2026: 23 · 2025: 44 · 2024: 43 · 2023: 53 · 2022: 32 · 2021: 41 · 2020: 36 · 2019: 40 · 2018: 35 · 2017: 19 · 2016: 12 · 2015: 17 · 2014: 14 · 2013: 9 · 2012: 10
- FWCI
- 8.25
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature Protocols (publishedVersion)
- PubMed (publishedVersion)
- UCL Discovery (University College London) (submittedVersion)
- Topics
- Life Sciences › Immunology and Microbiology › Microbiology › Microbial infections and disease research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Viral Infectious Diseases and Gene Expression in Insects
- Health Sciences › Medicine › Microbiology (medical) › Bacterial Identification and Susceptibility Testing
- Keywords
- mycoplasma detection, cell culture contamination, PCR detection, laboratory quality control, tissue culture
- MeSH terms
- Bacteriological Techniques, DNA, Bacterial, Electrophoresis, Agar Gel, Mycoplasma, Sensitivity and Specificity, Staining and Labeling, Time Factors, Polymerase Chain Reaction
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