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Uptake and transbilayer distribution of phosphatidylcholines in Mycoplasma gallisepticum and their effect on cell

Israel Journal of Medical Sciences
|September 1, 1984
PubMed

Insights

Mycoplasma gallisepticum cells modified their membranes with specific phosphatidylcholines (PCs). Differences in PC incorporation and distribution altered cell morphology, impacting membrane structure.

Area of Science:

  • Microbiology
  • Cell Biology
  • Biochemistry

Background:

  • Mycoplasma gallisepticum is a significant avian pathogen.
  • Phosphatidylcholine (PC) is a major component of cell membranes.
  • Understanding lipid incorporation in M. gallisepticum is crucial for its pathogenesis.

Purpose of the Study:

  • To investigate the incorporation and transbilayer distribution of different phosphatidylcholines (PCs) in Mycoplasma gallisepticum.
  • To determine the effects of exogenous PCs on M. gallisepticum membrane structure and cell morphology.

Main Methods:

  • Culturing M. gallisepticum in serum-free media supplemented with egg-phosphatidylcholine (Egg-PC), dioleoylphosphatidylcholine (DOPC), or dipalmitoylphosphatidylcholine (DPPC).
  • Utilizing lactoperoxidase-mediated radioiodination to assess transbilayer PC distribution.
  • Microscopic examination of cell morphology.

Main Results:

  • Egg-PC and DOPC were highly incorporated and modified by M. gallisepticum, while DPPC was incorporated less and not modified.
  • PC distribution varied: DOPC-grown cells showed even distribution, DPPC-grown cells had PC in the outer leaflet, and Egg-PC-grown cells had PC in the inner leaflet.
  • Asymmetrical PC distribution in Egg-PC- or DPPC-grown cells led to significant alterations in M. gallisepticum cell morphology.

Conclusions:

  • The type and distribution of phosphatidylcholine significantly influence M. gallisepticum membrane structure and cell morphology.
  • Exogenous PCs can be differentially incorporated and modified, leading to membrane asymmetry.
  • These findings provide insights into the adaptability of M. gallisepticum membranes and potential targets for intervention.

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