The nipah virus fusion protein is cleaved within the endosomal compartment

J Biol Chem. 2005 Aug 19;280(33):29899-903. doi: 10.1074/jbc.M504598200. Epub 2005 Jun 16.

Abstract

Nipah virus (NiV) is a recently emerged and highly pathogenic paramyxovirus that causes a systemic infection in animals and humans and can infect a wide range of cultured cells. Interestingly, the NiV fusion (F) protein has a single arginine at the cleavage site similar to paramyxoviruses that are activated by exogenous trypsin-like enzymes only present in specific cells and tissues and therefore only cause localized infections. We show here that NiV F activation is not mediated by an exogenous serum protease but by an endogenous ubiquitous cellular protease after endocytosis of the protein. In addition to endocytosis, acidification of the endosome is a prerequisite for F cleavage. These results show that activation of the NiV F protein depends on a type of proteolytic cleavage that is clearly different from what is known for other paramyxoviral and orthomyxoviral fusion proteins. To our knowledge, this is the first example of a viral class I fusion protein whose activation depends on clathrin-mediated constitutive endocytosis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Chlorocebus aethiops
  • Dogs
  • Endocytosis
  • Endosomes / metabolism*
  • HeLa Cells
  • Humans
  • Hydrogen-Ion Concentration
  • Molecular Sequence Data
  • Nipah Virus / chemistry*
  • Vero Cells
  • Viral Fusion Proteins / metabolism

Substances

  • Viral Fusion Proteins