Structure of avian orthoreovirus virion by electron cryomicroscopy and image reconstruction

Xing Zhang, Jinghua Tang, Stephen B. Walker, David O'Hara, Max L. Nibert, Roy Duncan, Timothy S. Baker

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65 Citas (Scopus)

Resumen

Among members of the genus Orthoreovirus, family Reoviridae, a group of non-enveloped viruses with genomes comprising ten segments of double-stranded RNA, only the "non-fusogenic" mammalian orthoreoviruses (MRVs) have been studied to date by electron cryomicroscopy and three-dimensional image reconstruction. In addition to MRVs, this genus comprises other species that induce syncytium formation in cultured cells, a property shared with members of the related genus Aquareovirus. To augment studies of these " fusogenic" orthoreoviruses, we used electron cryomicroscopy and image reconstruction to analyze the virions of a fusogenic avian orthoreovirus (ARV). The structure of the ARV virion, determined from data at an effective resolution of 14.6 Å, showed strong similarities to that of MRVs. Of particular note, the ARV virion has its pentameric λ-class core turret protein in a closed conformation as in MRVs, not in a more open conformation as reported for aquareovirus. Similarly, the ARV virion contains 150 copies of its monomeric σ-class core-nodule protein as in MRVs, not 120 copies as reported for aquareovirus. On the other hand, unlike that of MRVs, the ARV virion lacks "hub-and-spokes" complexes within the solvent channels at sites of local sixfold symmetry in the incomplete T = 13l outer capsid. In MRVs, these complexes are formed by C-terminal sequences in the trimeric μ-class outer-capsid protein, sequences that are genetically missing from the homologous protein of ARVs. The channel structures and C-terminal sequences of the homologous outer-capsid protein are also genetically missing from aquareoviruses. Overall, the results place ARVs between MRVs and aquareoviruses with respect to the highlighted features.

Idioma originalEnglish
Páginas (desde-hasta)25-35
Número de páginas11
PublicaciónVirology
Volumen343
N.º1
DOI
EstadoPublished - dic. 5 2005

Nota bibliográfica

Funding Information:
R.D. expresses his sincere thanks to Jingyun Shou for laboratory support and technical assistance. We also thank Kevin Coombs for reviewing a draft of the manuscript and for sharing unpublished ARV sequence data for Table 1 and Fig. 4 . This work was supported in part by research grants from the National Institutes of Health, USA, to T.S.B. (R37 GM33050) and M.L.N. (R01 AI46440 and R01 AI47904); by research grants from the Canadian Institutes of Health Research and the Natural Sciences and Engineering Research Council, Canada, to R.D.; by shared equipment grant BIR 9112921 from the National Science Foundation, USA, to T.S.B. for purchase of the CM200 FEG microscope; and by a Purdue University reinvestment grant for support of structural biology. S.B.W. was also supported by predoctoral fellowships from the Purdue Research Foundation and from research training grant T32 GM08296 from the National Institutes of Health, USA, to the Biophysics Degree Program at Purdue University. D.O. was also supported by a predoctoral fellowship from the Natural Sciences and Engineering Research Council, Canada. R.D. is the recipient of a Canadian Institutes of Health Research-Regional Partnership Program Investigator Award.

ASJC Scopus Subject Areas

  • Virology

PubMed: MeSH publication types

  • Journal Article
  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

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