Three-Dimensional Structure of Theiler Virus

• Published in: Proceedings of the National Academy of Sciences - PNAS 1992-03, Vol.89 (6), p.2061-2065
• Main Authors: Grant, Robert A., Filman, David J., Fujinami, Robert S., Icenogle, Joseph P., Hogle, James M.
• Format: Article
• Language: English
• Subjects: Animals; Biological and medical sciences; Capsid - ultrastructure; Capsid proteins; Cell Line; Cellular biology; Demyelinating diseases; Electrical phases; Electron density; Fundamental and applied biological sciences. Psychology; Maus Elberfeld virus - ultrastructure; Medical research; Mengovirus; Microbiology; Models, Molecular; Models, Structural; Morphology, structure, chemical composition, physicochemical properties; Nervous system; Pathogenesis; Picornaviridae; Picornaviridae - ultrastructure; Protein Conformation; Viral morphology; Virions; Virology; Viruses; X-Ray Diffraction - methods
• ISSN: 0027-8424; 1091-6490
• DOI: 10.1073/pnas.89.6.2061

Theiler murine encephalomyelitis virus strains are categorized into two groups, a neurovirulent group that rapidly kills the host, and a demyelinating group that causes a generally nonlethal infection of motor neurons followed by a persistent infection of the white matter with demyelinating lesions similar to those found in multiple sclerosis. The three-dimensional structure of the DA strain, a member of the demyelinating group, has been determined at 2.8 Å resolution. As in other picornaviruses, the icosahedral capsid is formed by the packing of wedge-shaped eight-stranded antiparallel β barrels. The surface of Theiler virus has large star-shaped plateaus at the fivefold axes and broad depressions spanning the twofold axes. Several unusual structural features are clustered near one edge of the depression. These include two finger-like loops projecting from the surface (one formed by residues 78-85 of VP1, and the other formed by residues 56-65 of VP3) and a third loop containing three cysteines (residues 87, 89, and 91 of VP3), which appear to be covalently modified. Most of the sequence differences between the demyelinating and neurovirulent groups that could play a role in determining pathogenesis map to the surface of the star-shaped plateau. The distribution of these sequence differences on the surface of the virion is consistent with models in which the differences in the pathogenesis of the two groups of Theiler viruses are the result of differences in immunological or receptor-mediated recognition processes.