Mycoplasmas and Oncogenesis: Persistent Infection and Multistage Malignant Transformation

• Published in: Proceedings of the National Academy of Sciences - PNAS 1995-10, Vol.92 (22), p.10197-10201
• Main Authors: Tsai, Shien, Wear, Douglas J., Shih, James Wai-Kuo, Lo, Shyh-Ching
• Format: Article
• Language: English
• Subjects: Acquired immune deficiency syndrome; AIDS; AIDS-Related Opportunistic Infections - microbiology; AIDS/HIV; Animals; Antibiotics; Cell culture techniques; Cell Division; Cell growth; Cell Line; Cell lines; Cell Transformation, Neoplastic; Cells, Cultured; Cellular biology; Chromosome Deletion; Chromosome Mapping; Chromosomes; Clone Cells; Cultured cells; Embryo, Mammalian; Embryonic cells; Humans; Infections; Karyotyping; Medical research; Mice; Mice, Inbred C3H; Mice, Nude; Mycoplasma; Mycoplasma fermentans; Mycoplasma Infections - physiopathology; Mycoplasma penetrans; Translocation, Genetic; Tumors
• ISSN: 0027-8424; 1091-6490
• DOI: 10.1073/pnas.92.22.10197

Oncogenic potential of human mycoplasmas was studied using cultured mouse embryo cells, C3H/10T1/2 (C3H). Mycoplasma fermentans and Mycoplasma penetrans, mycoplasmas found in unusually high frequencies among patients with AIDS, were examined. Instead of acute transformation, a multistage process in promotion and progression of malignant cell transformation with long latency was noted; after 6 passages (1 wk per passage) of persistent infection with M. fermentans, C3H cells exhibited phenotypic changes with malignant characteristics that became progressively more prominent with further prolonged infection. Up to at least the 11th passage, all malignant changes were reversible if mycoplasmas were eradicated by antibiotic treatment. Further persistent infection with the mycoplasmas until 18 passages resulted in an irreversible form of transformation that included the ability to form tumors in animals and high soft agar cloning efficiency. Whereas chromosomal loss and translocational changes in C3H cells infected by either mycoplasma during the reversible stage were not prominent, the onset of the irreversible phase of transformation coincided with such karyotypic alteration. Genetic instability--i.e., prominent chromosomal alteration of permanently transformed cells--was most likely caused by mutation of a gene(s) responsible for fidelity of DNA replication or repair. Once induced, chromosomal alterations continued to accumulate both in cultured cells and in animals without the continued presence of the transforming microbes. Mycoplasma-mediated multistage oncogenesis exhibited here shares many characteristics found in the development of human cancer.