Microbiology
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


Microbiology 144 (1998), 3447-3454; DOI  10.1099/00221287-144-12-3447
This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via CrossRef
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Salman, M.
Right arrow Articles by Rottem, S.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Salman, M.
Right arrow Articles by Rottem, S.
Agricola
Right arrow Articles by Salman, M.
Right arrow Articles by Rottem, S.

Mycoplasma penetrans infection of Molt-3 lymphocytes induces changes in the lipid composition of host cells

Michael Salman, Zipi Borovsky and Shlomo Rottem

Department of Membrane and Ultrastructure Research, The Hebrew University-Hadassah Medical School, POB 12272, Jerusalem 91010, Israel

ABSTRACT

Summary: The AIDS-associated Mycoplasma penetrans is capable of inducing its own uptake by non-phagocytic cells. The ability of M. penetrans to both adhere to and invade Molt-3 lymphocytes was markedly increased in the presence of polyethylene glycol 8000 (PEG). The effect of PEG was more pronounced in the more alkaline pH range, where the binding kinetics were much faster and almost unaffected by temperature (4-37 °C). Incubation of [14C]oleic-acid-labelled Molt-3 cells with viable M. penetrans resulted in a substantial release of radioactive fatty acids, whereas treating the host cells with heat-inactivated mycoplasmas, isolated M. penetrans membrane preparations, or M. penetrans growth medium, had no effect. Total lipid analysis of Molt-3 lymphocytes infected by M. penetrans revealed an augmented level of the neutral lipid fraction that was associated with a decrease in the relative amounts of polar lipids, mainly a decrease in the amount of phosphatidylserine and diphosphatidylglycerol. Analysis of the neutral lipid fraction in the infected Molt-3 cells revealed a fivefold increase in the relative amount of diacylglycerol and a marked increase in the free fatty acid (FFA) fraction. The profile of the FFAs released was dominated by a relatively high concentration of the polyunsaturated fatty acid docosahexaenoic acid. The release of lipid intermediates suggests that the degradation of Molt-3 cell phospholipids induced by M. penetrans may initiate a signal transmission cascade in the host cell.

Author for correspondence: Shlomo Rottem. Tel: +972 2 675 8148. Fax: +972 2 678 4010. e-mail: rottem@cc.huji.ac.il


Keywords: mollicutes, Mycoplasma penetrans, phospholipase, membrane lipids, diacylglycerol




This article has been cited by other articles:


Home page
Hum ReprodHome page
F. J. Diaz-Garcia, A. P. Herrera-Mendoza, S. Giono-Cerezo, and F. M. Guerra-Infante
Mycoplasma hominis attaches to and locates intracellularly in human spermatozoa
Hum. Reprod., June 1, 2006; 21(6): 1591 - 1598.
[Abstract] [Full Text] [PDF]


Home page
Physiol. Rev.Home page
S. Rottem
Interaction of Mycoplasmas With Host Cells
Physiol Rev, April 1, 2003; 83(2): 417 - 432.
[Abstract] [Full Text] [PDF]


Home page
Nucleic Acids ResHome page
P. de Diesbach, F. N'Kuli, M. Delmee, and P. J. Courtoy
Infection by Mycoplasma hyorhinis strongly enhances uptake of antisense oligonucleotides: a reassessment of receptor-mediated endocytosis in the HepG2 cell line
Nucleic Acids Res., February 1, 2003; 31(3): 886 - 892.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
INT J SYST EVOL MICROBIOL MICROBIOLOGY J GEN VIROL
J MED MICROBIOL ALL SGM JOURNALS
Copyright © 1998 Society for General Microbiology.