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Mycoplasma fermentans (Incognitus Strain) Cells Are Able to Fuse with T Lymphocytes

Characteristics of the fusion of Mycoplasma fermentans (incognitus strain) with cultured lymphocytes were investigated. The rate and extent of fusion were monitored continuously in an assay that measured lipid mixing on the basis of dequenching of a fluorescent probe, octadecylrhodamine (R18), incor...

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Bibliographic Details
Published in:Clinical infectious diseases 1993-08, Vol.17 (Supplement-1), p.S305-S308
Main Authors: Dimitrov, D. S., Franzoso, G., Salman, M., Blumenthal, R., Tarshis, M., Barile, M. F., Rottem, S.
Format: Article
Language:English
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Summary:Characteristics of the fusion of Mycoplasma fermentans (incognitus strain) with cultured lymphocytes were investigated. The rate and extent of fusion were monitored continuously in an assay that measured lipid mixing on the basis of dequenching of a fluorescent probe, octadecylrhodamine (R18), incorporated into mycoplasmas. Fusion of M. fermentans was detected with CD4+ (Molt-3) cells, CD4− (12E1) cells, and primary peripheral-blood lymphocytes. The level of fusion was relatively low (8%–12%). Detection of a similarly low level of fusion by fluorescence microscopy suggested the involvement of a specific lymphocyte subpopulation. After a short lag period, fusion at 37°C proceeded exponentially for ∼30 minutes and was virtually complete at 60 minutes. Throughout the process, lymphocytes remained intact. Fusion was stimulated by CaCl2 but not by MgCl2; its inhibition by antisera to M. fermentans and by pretreatment of M. fermentans with proteolytic enzymes implied that the mycoplasmas possessed a proteinase-sensitive receptor involved in fusion. Mycoplasmas were rendered nonfusogenic by treatment with the uncoupler CCCP (carbonyl cyanide m-chlorophenylhydrazone; 5 µM) but were unaffected by treatment with chlorpromazine (10 µM) or DCCD (dicyclohexylcarbodiimide; 50 µM); these findings suggested that a proton gradient across the cell membrane is required for fusion.
ISSN:1058-4838
1537-6591
DOI:10.1093/clinids/17.Supplement_1.S305