Related Experiment Video
Updated: Aug 17, 2026

Immunofluorescent Labeling of Plant Virus and Insect Vector Proteins in Hemipteran Guts
Published on: May 14, 2021
Identification and characterization of a prawn white spot syndrome virus gene that encodes an envelope protein VP31
1Key Laboratory of Marine Biogenetic Resources, Third Institute of Oceanography, Xiamen, P.R. China.
Abstract:
Based on a combination of SDS-PAGE and mass spectrometry, a protein with an apparent molecular mass of 31 kDa (termed as VP31) was identified from purified shrimp white spot syndrome virus (WSSV) envelope fraction. The resulting amino acid (aa) sequence matched an open reading frame (WSV340) of the WSSV genome. This ORF contained 783 nucleotides (nt), encoding 261 aa. A fragment of WSV340 was expressed in Escherichia coli as a glutathione S-transferase (GST) fusion protein with a 6His-tag, and then specific antibody was raised. Western blot analysis and the immunoelectron microscope method (IEM) confirmed that VP31 was present exclusively in the viral envelope fraction. The neutralization experiment suggested that VP31 might play an important role in WSSV infectivity.
Insights
Researchers identified a 31 kDa protein (VP31) in the white spot syndrome virus (WSSV) envelope. This VP31 protein is exclusively found in the viral envelope and may be crucial for WSSV infectivity.
Area of Science:
- Virology
- Molecular Biology
- Proteomics
Background:
- Shrimp white spot syndrome virus (WSSV) is a significant pathogen in aquaculture.
- Understanding the structural and functional components of WSSV is crucial for disease control.
Purpose of the Study:
- To identify and characterize viral envelope proteins of WSSV.
- To investigate the potential role of identified proteins in WSSV infectivity.
Main Methods:
- Sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) and mass spectrometry were used for protein identification.
- The identified protein's sequence was analyzed against the WSSV genome.
- Recombinant protein expression in Escherichia coli and antibody generation were performed.
- Western blot analysis and immunoelectron microscopy (IEM) were employed for protein localization.
- Neutralization experiments were conducted to assess the protein's function.
Main Results:
- A protein with an apparent molecular mass of 31 kDa, designated VP31, was identified in the purified WSSV envelope fraction.
- The amino acid sequence of VP31 matched an open reading frame (WSV340) in the WSSV genome, encoding 261 amino acids.
- Western blot and IEM confirmed that VP31 is exclusively localized to the WSSV envelope.
- Neutralization experiments indicated a potential role for VP31 in WSSV infectivity.
Conclusions:
- VP31 is a WSSV envelope protein with a potential role in viral infectivity.
- Further studies on VP31 could lead to novel strategies for WSSV control in shrimp aquaculture.
Related Concept Videos
Leaky Scanning
Subviral Agents

