Mycoplasma Eradication Review
Mycoplasma contamination in cell cultures
Mycoplasma contamination of cultured cells is a major problem in both basic research and industrial production. 50% or more of cell lines may be contaminated by mycoplasma.
Mycoplasma infection can affect virtually any function and activity of eukaryotic cells leading to experimental artifacts and unreliable results.
It is usually recommended that an infected cell culture be immediately autoclaved to prevent the infection from spreading and to use only mycoplasma-free cultures. However, some cell lines are irreplaceable and require an effective eradication treatment.
Antibiotics active against Mycoplasma
The use of specific antibiotics can efficiently eliminate mycoplasma contaminations. Antibiotics commonly used in cell culture are inactive on mycoplasma (e.g. penicillins and streptomycin).
Three classes of antibiotics have been shown to kill mycoplasma at relatively low concentrations: tetracyclines, macrolides and quinolones. Tetracyclines and macrolides block the protein synthesis by interfering with ribosome translation, while quinolones inhibit the replication of bacterial DNA.
Commercially available anti-mycoplasma agents for cell culture
Several antibiotics are commercially available for the removal of mycoplasma: BM-Cyclin (Roche) contains a macrolide and a tetracycline, Ciprobay (Bayer, available only with a prescription) and MRA (ICN) are both quinolones. Plasmocin™ (InvivoGen) is the only antimycoplasma reagent that combines a macrolide and a quinolone.
Unlike BM-Cyclin that requires the sequential and cyclic use of two antibiotics, Plasmocin™ is ready-to-use and can be added to the culture medium directly.
Furthermore, both components in Plasmocin™ act on separate targets blocking protein synthesis and DNA replication, whereas the two antibiotics in BM-Cyclin are both inhibitors of protein synthesis. Therefore, Plasmocin™ is more effective in removing mycoplasma and prevents the appearance of resistant strains.
In contrast to other anti-mycoplasma compounds, Plasmocin™ is active on both free mycoplasma as well as intracellular forms. This advantage is conferred by one component of Plasmocin™ which is actively transported into mammalian cells. It ensures that following treatment with Plasmocin™ a cell culture is not reinfected by mycoplasma released from intracellular compartments of infected cells.
To date, no consistent and permanent alterations that affect the eukaryotic cells during and after the treatment have been detected [1].
Comparison of the most common anti-mycoplasma agents
| Product | Supplier | Treatment | Ease of use | Efficacy | Cytotoxicity | Resistance |
|---|---|---|---|---|---|---|
| BM-Cyclin | Roche | 3 weeks | - | +++ | + | +/- |
| Ciprobay | Bayer | 12 to 20 days | + | ++ | +/- | + |
| MRA | ICN | 1 to 2 weeks | + | ++ | +/- | + |
| Plasmocin | InvivoGen | 2 weeks | + | ++++ | +/- | - |
1. Uphoff CC, Drexler HG., 2005. Eradication of mycoplasma contaminations. Methods Mol Biol. 290:25-34.
2. Somasundaram C. et al., 1992. Use of ciprofloxacin and BM-Cyclin in mycoplasma decontamination. In vitro Cell Dev Biol. 28A(11-12):708-10.
3. Drexler HG. et al., 1994. Treatment of mycoplasma contamination in a large panel of cell cultures. In vitro Cell Dev Biol Anim. 30A(5):344-7

