Related Experiment Video
Updated: Apr 12, 2026

Using Click Chemistry to Measure the Effect of Viral Infection on Host-Cell RNA Synthesis
Published on: August 9, 2013
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.
Abstract:
Viroporins are a family of low-molecular-weight hydrophobic transmembrane proteins that are encoded by various animal viruses. Viroporins form transmembrane pores in host cells via oligomerization, thereby destroying cellular homeostasis and inducing cytopathy for virus replication and virion release. Among the Picornaviridae family of viruses, the 2B protein encoded by enteroviruses is well understood, whereas the viroporin activity of the 2B protein encoded by the foot-and-mouth disease virus (FMDV) has not yet been described. An analysis of the FMDV 2B protein domains by computer-aided programs conducted in this study revealed that this protein may contain two transmembrane regions. Further biochemical, biophysical and functional studies revealed that the protein possesses a number of features typical of a viroporin when it is overexpressed in bacterial and mammalian cells as well as in FMDV-infected cells. The protein was found to be mainly localized in the endoplasmic reticulum (ER), with both the N- and C-terminal domains stretched into the cytosol. It exhibited cytotoxicity in Escherichia coli, which attenuated 2B protein expression. The release of virions from cells infected with FMDV was inhibited by amantadine, a viroporin inhibitor. The 2B protein monomers interacted with each other to form both intracellular and extracellular oligomers. The Ca(2+) concentration in the cells increased, and the integrity of the cytoplasmic membrane was disrupted in cells that expressed the 2B protein. Moreover, the 2B protein induced intense autophagy in host cells. All of the results of this study demonstrate that the FMDV 2B protein has properties that are also found in other viroporins and may be involved in the infection mechanism of FMDV.
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.
More Related Videos
09:13Using Reverse Genetics to Manipulate the NSs Gene of the Rift Valley Fever Virus MP-12 Strain to Improve Vaccine Safety and Efficacy
Published on: November 1, 2011
18:10Isolation of Fidelity Variants of RNA Viruses and Characterization of Virus Mutation Frequency
Published on: June 16, 2011
Related Concept Videos
Leaky Scanning
Inhibitors of Viral Protein Synthesis
Subviral Agents
Retroviruses
Viruses with RNA Genomes