Entry of a heparan sulphate-binding HRV8 variant strictly depends on dynamin but not on clathrin, caveolin, and flotillin

Virology. 2011 Mar 30;412(1):55-67. doi: 10.1016/j.virol.2010.12.042. Epub 2011 Jan 22.


The major group human rhinovirus type 8 can enter cells via heparan sulphate. When internalized into ICAM-1 negative rhabdomyosarcoma (RD) cells, HRV8 accumulated in the cells but caused CPE only after 3 days when used at high MOI. Adaptation by three blind passages alternating between RD and HeLa cells resulted in variant HRV8v with decreased stability at acidic pH allowing for productive infection in the absence of ICAM-1. HRV8v produced CPE at 10 times lower MOI within 1 day. Confocal fluorescence microscopy colocalization and the use of pharmacological and dominant negative inhibitors revealed that viral uptake is clathrin, caveolin, and flotillin independent. However, it is blocked by dynasore, amiloride, and EIPA. Furthermore, HRV8v induced FITC-dextran uptake and colocalized with this fluid phase marker. Except for the complete inhibition by dynasore, the entry pathway of HRV8v via HS is similar to that of HRV14 in RD cells that overexpress ICAM-1.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Caveolins / genetics
  • Caveolins / metabolism
  • Cell Line
  • Clathrin / genetics
  • Clathrin / metabolism
  • Cytopathogenic Effect, Viral
  • Dynamin II / genetics
  • Dynamin II / metabolism*
  • Host-Pathogen Interactions*
  • Humans
  • Intercellular Adhesion Molecule-1 / genetics
  • Intercellular Adhesion Molecule-1 / metabolism*
  • Membrane Proteins / genetics
  • Membrane Proteins / metabolism
  • Rhinovirus / genetics
  • Rhinovirus / physiology*
  • Serial Passage
  • Virus Internalization*


  • Caveolins
  • Clathrin
  • Membrane Proteins
  • flotillins
  • Intercellular Adhesion Molecule-1
  • Dynamin II