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[Several methodologic problems in the control of cell cultures]
Voprosy Virusologii
|May 1, 1976
Summary
This study detected various viruses and mycoplasma in human and animal cell lines. HeLa cell contamination was indicated by specific chromosomes and G-6-PDG enzyme motility.
Area of Science:
- Cell biology
- Virology
- Molecular biology
Background:
- Continuous cell lines are crucial for biological research.
- Potential contamination can compromise experimental results.
- Characterizing cell line contaminants is essential for data integrity.
Purpose of the Study:
- To investigate the presence of contaminants in human and animal cell lines.
- To identify viral agents and mycoplasma within cell cultures.
- To assess potential HeLa cell contamination in human cell lines.
Main Methods:
- Karyological analysis
- Electron microscopy
- Virological assays
- Molecular biological techniques
- Electrophoretic motility of glucose-6-phosphate dehydrogenase (G-6-PDG)
Main Results:
- Mycoplasma contamination was found in all tested cell lines.
- Various oncornaviruses (Types A, B, C), and paramyxoviruses were identified.
- High molecular RNA (64-70 S) associated with reverse transcriptase activity confirmed oncornaviruses.
- HeLa cell marker chromosomes, absence of Y chromosomes, and G-6-PDG Type A motility suggested HeLa contamination.
Conclusions:
- Human and animal cell lines frequently harbor viral and mycoplasma contaminants.
- Oncornaviruses were characterized by high molecular RNA and reverse transcriptase activity.
- Specific markers indicate a high likelihood of HeLa cell contamination in the examined human cell lines.