P-glycoprotein-overexpressing multidrug-resistant cells are resistant to infection by enveloped viruses that enter via the plasma membrane

FASEB J. 2000 Mar;14(3):511-5. doi: 10.1096/fasebj.14.3.511.

Abstract

The multidrug resistance gene product P-glycoprotein confers drug resistance to tumor cells by acting as a transporter that blocks the entry into the cell of a great variety of drugs and hydrophobic peptides. In this study we find that in drug-resistant cells, the insertion of the influenza virus fusion protein (hemagglutinin-2) into the plasma membrane is blocked and that the fusion of the viral envelope with the plasma membrane of these cells is impaired. Multidrug-resistant cells display significant resistance to infection by envelope viruses that invade cells by fusion with the plasma membrane, but not to infection by pH-dependent viruses that penetrate cells by fusion with endocytic vesicles. These observations suggest that multidrug resistance phenomena may protect cells from infection by a large group of disease-causing viruses that includes human immunodeficiency virus, herpes simplex virus, and some cancer-inducing retroviruses.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • ATP Binding Cassette Transporter, Subfamily B, Member 1 / genetics
  • ATP Binding Cassette Transporter, Subfamily B, Member 1 / physiology*
  • Cell Membrane / physiology
  • Cell Membrane / virology
  • Drug Resistance, Multiple*
  • Endocytosis
  • Hemagglutinin Glycoproteins, Influenza Virus / physiology
  • Humans
  • Hydrogen-Ion Concentration
  • KB Cells
  • Membrane Fusion / physiology*
  • Orthomyxoviridae / physiology*
  • Respirovirus / physiology*
  • Viral Fusion Proteins / physiology*

Substances

  • ATP Binding Cassette Transporter, Subfamily B, Member 1
  • Hemagglutinin Glycoproteins, Influenza Virus
  • Viral Fusion Proteins