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Updated: Aug 20, 2026

Generation and Assembly of Virus-Specific Nucleocapsids of the Respiratory Syncytial Virus
Published on: July 27, 2021
The structure of foot-and-mouth disease virus
E E Fry1, D I Stuart, D J Rowlands
1Division of Structural Biology, Wellcome Trust Centre for Human Genetics, Roosevelt Drive, Oxford, OX3 7BN, UK.
Abstract:
Structural studies of foot-and-mouth disease virus (FMDV) have largely focused on the mature viral particle, providing atomic resolution images of the spherical protein capsid for a number of sero- and sub-types, structures of the highly immunogenic surface loop, Fab and GAG receptor complexes. Additionally, structures are available for a few non-structural proteins. The chapter reviews our current structural knowledge and its impact on our understanding of the virus life cycle proceeding from the mature virus through immune evasion/inactivation, cell-receptor binding and replication and alludes to future structural targets.
Insights
Structural studies reveal foot-and-mouth disease virus (FMDV) capsid and key proteins. This knowledge aids understanding of FMDV
Area of Science:
- Virology
- Structural Biology
- Immunology
Background:
- Foot-and-mouth disease virus (FMDV) structural studies have primarily examined the mature viral particle.
- Atomic resolution images of the FMDV protein capsid are available for multiple sero- and sub-types.
- Structures of immunogenic surface loops and receptor complexes are also documented.
Purpose of the Study:
- To review current structural knowledge of FMDV.
- To assess the impact of structural data on understanding the FMDV life cycle.
- To identify future structural targets for FMDV research.
Main Methods:
- Review of existing structural data from various studies.
- Analysis of atomic resolution images of viral components.
- Integration of structural findings with knowledge of FMDV life cycle processes.
Main Results:
- Comprehensive structural information exists for the FMDV capsid and surface loops.
- Structural data illuminates interactions with host cell receptors (GAG).
- Structures of some non-structural proteins provide insights into viral replication.
Conclusions:
- Current structural knowledge provides a foundation for understanding FMDV infection.
- Structural insights are crucial for comprehending immune evasion and inactivation mechanisms.
- Further structural studies are needed to target key viral components and processes.
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