Multiplication of Legionella pneumophila in HeLa cells in the presence of cytoskeleton and metabolic inhibitors

Microbiol Immunol. 1998;42(4):271-9. doi: 10.1111/j.1348-0421.1998.tb02283.x.

Abstract

A study has been carried out on the action of cytoskeleton and metabolic inhibitors on intracellular multiplication in HeLa cells of a virulent strain of Legionella pneumophila serogroup 6. The effects of the substances were separately tested on both penetration and intracellular multiplication of L. pneumophila. Only cytochalasin A and 2-deoxy-D-glucose (2dG) affected bacterial internalisation, whereas intracellular multiplication was inhibited by cytochalasins A, B, C, D and J (D being the most active) and by 2dG with a dose-response effect. The action of 2dG was counteracted by 50 mM glucose. Experiments carried out with cytochalasin D and a rhodamine-phalloidin conjugate showed the involvement of cytoskeletal elements in intracellular multiplication of Legionella; compounds acting on microtubules had no effect.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 2,4-Dinitrophenol / pharmacology
  • Antimetabolites / pharmacology*
  • Cytochalasin D / pharmacology
  • Cytochalasins / pharmacology*
  • Cytoskeleton / physiology*
  • Deoxyglucose / pharmacology*
  • Dose-Response Relationship, Drug
  • HeLa Cells
  • Humans
  • Legionella pneumophila / drug effects
  • Legionella pneumophila / growth & development*
  • Legionella pneumophila / pathogenicity
  • Microscopy, Electron
  • Microscopy, Fluorescence
  • Vincristine / pharmacology
  • Virulence

Substances

  • Antimetabolites
  • Cytochalasins
  • Cytochalasin D
  • Vincristine
  • Deoxyglucose
  • 2,4-Dinitrophenol