The microtubule motor protein KIF13A is involved in intracellular trafficking of the Lassa virus matrix protein Z

Cell Microbiol. 2013 Feb;15(2):315-34. doi: 10.1111/cmi.12095. Epub 2013 Jan 10.

Abstract

The small matrix protein Z of arenaviruses has been identified as the main driving force to promote viral particle production at the plasma membrane. Although multiple functions of Z in the arenaviral life cycle have been uncovered, the mechanism of intracellular transport of Z to the site of virus budding is poorly understood and cellular motor proteins that mediate Z trafficking remain to be identified. In the present study, we report that the Z protein of the Old World arenavirus Lassa virus (LASV) interacts with the kinesin family member 13A (KIF13A), a plus-end-directed microtubule-dependent motor protein. Plasmid-driven overexpression of KIF13A results in relocalization of Z to the cell periphery, while functional blockage of endogenous KIF13A by overexpression of a dominant-negative mutant or KIF13A-specific siRNA causes a perinuclearaccumulation and decreased production of both Z-induced virus-like particles and infectious LASV. The interaction of KIF13A with Z proteins from both Old and New World arenaviruses suggests a conserved intracellular transport mechanism. In contrast, the intracellular distribution of the matrix proteins of prototypic members of the paramyxo- and rhabdovirus family is independent of KIF13A. In summary, our studies identify for the first time a molecular motor protein as a critical mediator for intracellular microtubule-dependent transport of arenavirus matrix proteins.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Carrier Proteins / genetics
  • Carrier Proteins / metabolism*
  • Cell Line
  • Cell Membrane / metabolism
  • Cell Membrane / virology
  • Chlorocebus aethiops
  • Gene Expression
  • Host-Pathogen Interactions
  • Humans
  • Kidney / pathology
  • Kidney / virology
  • Kinesins / antagonists & inhibitors
  • Kinesins / genetics
  • Kinesins / metabolism*
  • Lassa virus / physiology*
  • Liver / pathology
  • Liver / virology
  • Microtubules / metabolism*
  • Microtubules / virology
  • Protein Binding
  • Protein Transport
  • RNA, Small Interfering / genetics
  • RNA-Binding Proteins
  • Vero Cells
  • Viral Matrix Proteins / genetics
  • Viral Matrix Proteins / metabolism*
  • Virus Release / physiology*

Substances

  • Carrier Proteins
  • KIF13A protein, human
  • RNA, Small Interfering
  • RNA-Binding Proteins
  • Viral Matrix Proteins
  • protein Z, Lassa virus
  • Kinesins