Covert Infection of a Mouse Mammary Tumor Cell Line with Mycoplasma hyorhinis: Cosedimentation with Mouse Mammary Tumor Virus in Sucrose Density Gradients

Supernatant fluids from cultures of a mouse mammary tumor (MT) cell line were found to produce a specific cell detachment effect when inoculated into HeLa cells. The cell detachment factor (CDF) responsible for this effect was examined. Repeated attempts to cultivate this CDF in bacteriologic, funga...

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Veröffentlicht in:In vitro 1981-11, Vol.17 (11), p.997-1003
Hauptverfasser: Sydiskis, Robert J., Weber, Patricia A., Richard A. Delgiudice
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Sprache:eng
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Zusammenfassung:Supernatant fluids from cultures of a mouse mammary tumor (MT) cell line were found to produce a specific cell detachment effect when inoculated into HeLa cells. The cell detachment factor (CDF) responsible for this effect was examined. Repeated attempts to cultivate this CDF in bacteriologic, fungal, and mycoplasma media were unsuccessful. However, using the DNA fluorochrome staining technique and specific immunofluorescent staining procedures, the CDF was identified positively as a noncultivable strain of Mycoplasma hyorhinis. It was also noted that this CDF could be labeled with$[^{3}H]uridine$in MT cell cultures, concentrated, and banded at a density of$1.18 g/cm^3$when centrifuged to equilibrium in a 20 to 60% sucrose gradient. Using a multiple antibiotic treatment regimen, the MT cells were "cured" of the M. hyorhinis contaminant. Re-infection of these cells with an exogenous strain of M. hyorhinis resulted in the same cell detachment effect, and this strain when labeled with$[^{3}H]uridine$also sedimented at a density of$1.18 g/cm^3$. The salient feature of these studies is that M. hyorhinis sediments at the same density of mouse mammary tumor virus (MMTV) in sucrose density gradients. This was demonstrated by sucrose density gradient analyses of a purified sample of MMTV, assaying for reverse transcriptase activity, and a$[^{3}H]uridine$labeled sample of the M. hyorhinis present in the MT cell cultures.
ISSN:0073-5655
DOI:10.1007/BF02618425