Viroporin Activity of the Foot-and-Mouth Disease Virus Non-Structural 2B Protein

Da Ao1, Hui-Chen Guo2, Shi-Qi Sun2

  • 1State Key Laboratory of Veterinary Etiological Biology and OIE/National Foot and Mouth Disease Reference Laboratory, Lanzhou Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Lanzhou, Gansu, China; College of Veterinary Medicine, Sichuan Agricultural University, Ya'an, Sichuan, China.

Plos One
|May 7, 2015
PubMed

Insights

The foot-and-mouth disease virus (FMDV) 2B protein acts as a viroporin, forming pores in host cells. This pore formation disrupts cell function and is crucial for FMDV infection and replication.

Area of Science:

  • Virology
  • Molecular Biology
  • Cell Biology

Background:

  • Viroporins are viral proteins forming pores in host cells, crucial for viral replication.
  • The 2B protein of enteroviruses is a known viroporin, but its role in foot-and-mouth disease virus (FMDV) is uncharacterized.

Purpose of the Study:

  • To investigate the viroporin activity and cellular functions of the FMDV 2B protein.
  • To determine the role of FMDV 2B protein in the viral infection mechanism.

Main Methods:

  • Bioinformatic analysis of FMDV 2B protein domains.
  • Biochemical, biophysical, and functional studies in bacterial and mammalian cells.
  • Confocal microscopy for protein localization.
  • Inhibition assays using amantadine.

Main Results:

  • FMDV 2B protein possesses two predicted transmembrane regions and exhibits viroporin-like features upon overexpression.
  • The protein localizes to the endoplasmic reticulum, induces cytotoxicity in E. coli, and increases intracellular Ca(2+) levels.
  • FMDV virion release is inhibited by amantadine, and 2B protein forms oligomers, disrupts membrane integrity, and induces autophagy.

Conclusions:

  • The FMDV 2B protein functions as a viroporin, sharing characteristics with other known viroporins.
  • The pore-forming activity of FMDV 2B protein likely contributes to cytopathy and is involved in the FMDV infection cycle.

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