Early steps in reovirus infection are associated with dramatic changes in supramolecular structure and protein conformation: analysis of virions and subviral particles by cryoelectron microscopy and image reconstruction

Three structural forms of type 1 Lang reovirus (virions, intermediate subviral particles [ISVPs], and cores) have been examined by cryoelectron microscopy (cryoEM) and image reconstruction at 27 to 32-A resolution. Analysis of the three-dimensional maps and known biochemical composition allows determination of capsid protein location, globular shape, stoichiometry, quaternary organization, and interactions with adjacent capsid proteins. Comparisons of the virion, ISVP and core structures and examination of difference maps reveal dramatic changes in supra-molecular structure and protein conformation that are related to the early steps of reovirus infection. The intact virion (approximately 850-A diam) is designed for environmental stability in which the dsRNA genome is protected not only by tight sigma 3-mu 1, lambda 2-sigma 3, and lambda 2-mu 1 interactions in the outer capsid but also by a densely packed core shell formed primarily by lambda 1 and sigma 2. The segmented genome appears to be packed in a liquid crystalline fashion at radii < 240 A. Depending on viral growth conditions, virions undergo cleavage by enteric or endosomal/lysosomal proteases, to generate the activated ISVP (approximately 800-A diam). This transition involves the release of an outer capsid layer spanning radii from 360 to 427 A that is formed by 60 tetrameric and 60 hexameric clusters of ellipsoidal subunits of sigma 3. The vertex- associated cell attachment protein, sigma 1, also undergoes a striking change from a poorly visualized, more compact form, to an extended, flexible fiber. This conformational change may maximize interactions of sigma 1 with cell surface receptors. Transcription of viral mRNAs is mediated by the core particle (approximately 600-A diam), generated from the ISVP after penetration and uncoating. The transition from ISVP to core involves release of the 12 sigma 1 fibers and the remaining outer capsid layer formed by 200 trimers of rod-shaped mu 1 subunits that span radii from 306 to 395 A. In the virion and ISVP, flower- shaped pentamers of the lambda 2 protein are centered at the vertices. In the ISVP-to-core transition, domains of the lambda 2 subunits rotate and swing upward and outward to form a turret-like structure extending from radii 305 to 400 A, with a diameter of 184 A, and a central channel 84 A wide. This novel conformational change allows the potential diffusion of substrates for transcription and exit of newly synthesized mRNA segments.(ABSTRACT TRUNCATED AT 400 WORDS)

[1]  W. Joklik,et al.  Protein σ1 is the reovirus cell attachment protein , 1981 .

[2]  M. Nibert,et al.  Mechanisms of viral pathogenesis. Distinct forms of reoviruses and their roles during replication in cells and host. , 1991, The Journal of clinical investigation.

[3]  S. Fuller,et al.  The T=4 envelope of sindbis virus is organized by interactions with a complementary T=3 capsid , 1987, Cell.

[4]  W. Joklik Studies on the effect of chymotrypsin on reovirions. , 1972, Virology.

[5]  W. Joklik The Reovirus Particle , 1983 .

[6]  T. Dermody,et al.  Structure of the Reovirus Cell-Attachment Protein : a Model for the Domain Organization of orlt , 2022 .

[7]  M. Nibert,et al.  Structure of the reovirus cell-attachment protein: a model for the domain organization of sigma 1 , 1990, Journal of virology.

[8]  T S Baker,et al.  Reconstruction of the three-dimensional structure of simian virus 40 and visualization of the chromatin core. , 1988, Proceedings of the National Academy of Sciences of the United States of America.

[9]  K. Tyler,et al.  Molecular basis of viral neurotropism , 1985, Neurology.

[10]  H. Zweerink,et al.  Studies on the structure of reovirus cores: Selective removal of polypeptide λ2 , 1976 .

[11]  R. Bassel-Duby,et al.  A sigma 1 region important for hemagglutination by serotype 3 reovirus strains , 1990, Journal of virology.

[12]  A. Bellamy,et al.  Biophysical studies of reovirus type 3. , 1974, Virology.

[13]  H. Weiner,et al.  Molecular basis of reovirus virulence: role of the S1 gene. , 1977, Proceedings of the National Academy of Sciences of the United States of America.

[14]  A. Bellamy,et al.  Biophysical studies of reovirus type 3. IV. Low-angle x-ray diffraction studies. , 1981, Virology.

[15]  S. Morozov A possible relationship of reovirus putative RNA polymerase to polymerases of positive-strand RNA viruses. , 1989, Nucleic acids research.

[16]  M. Yeager,et al.  Three-dimensional structure of rhesus rotavirus by cryoelectron microscopy and image reconstruction , 1990, The Journal of cell biology.

[17]  R. Milligan,et al.  Molecular structure determination of crystalline specimens in frozen aqueous solutions. , 1984, Ultramicroscopy.

[18]  R. Glaeser,et al.  Preparation of frozen-hydrated specimens for high resolution electron microscopy. , 1984, Ultramicroscopy.

[19]  M. Unser,et al.  Magnification mismatches between micrographs: corrective procedures and implications for structural analysis. , 1992, Ultramicroscopy.

[20]  T S Baker,et al.  Magnification calibration and the determination of spherical virus diameters using cryo-microscopy. , 1989, Ultramicroscopy.

[21]  A. Kohn,et al.  Mechanisms of Viral Pathogenesis , 1984, Developments in Molecular Virology.

[22]  M. Cyrklaff,et al.  The three‐dimensional structure of reovirus obtained by cryo‐electron microscopy. , 1991, The EMBO journal.

[23]  B. L. Trus,et al.  Liquid-crystalline, phage-like packing of encapsidated DNA in herpes simplex virus , 1991, Cell.

[24]  A. Shatkin,et al.  Translational effects and sequence comparisons of the three serotypes of the reovirus S4 gene. , 1992, Virology.

[25]  J. Lepault,et al.  Three-dimensional structure of unstained, frozen-hydrated extended tails of bacteriophage T4. , 1985, Journal of molecular biology.

[26]  M. Nibert,et al.  A carboxy-terminal fragment of protein mu 1/mu 1C is present in infectious subvirion particles of mammalian reoviruses and is proposed to have a role in penetration , 1992, Journal of virology.

[27]  P. C. Lee,et al.  The N-terminal quarter of reovirus cell attachment protein sigma 1 possesses intrinsic virion-anchoring function. , 1990, Virology.

[28]  R. Smith,et al.  Polypeptide components of virions, top component and cores of reovirus type 3. , 1969, Virology.

[29]  W. Joklik,et al.  Reovirus-coded polypeptides in infected cells: isolation of two native monomeric polypeptides with affinity for single-stranded and double-stranded RNA, respectively. , 1976, Virology.

[30]  K. Tyler,et al.  Monoclonal antibodies to reovirus reveal structure/function relationships between capsid proteins and genetics of susceptibility to antibody action , 1991, Journal of virology.

[31]  K A Taylor,et al.  Electron microscopy of frozen hydrated biological specimens. , 1976, Journal of ultrastructure research.

[32]  B L Trus,et al.  Molecular structure of the cell-attachment protein of reovirus: correlation of computer-processed electron micrographs with sequence-based predictions , 1990, Journal of virology.

[33]  M. Nibert,et al.  Sigma 1 protein of mammalian reoviruses extends from the surfaces of viral particles , 1988, Journal of virology.

[34]  D. Spriggs,et al.  Evidence for functional domains on the reovirus type 3 hemagglutinin. , 1982, Virology.

[35]  T. Baker,et al.  Structures of bovine and human papillomaviruses. Analysis by cryoelectron microscopy and three-dimensional image reconstruction. , 1991, Biophysical journal.

[36]  D. Pickup,et al.  High-level synthesis of biologically active reovirus protein sigma 1 in a mammalian expression vector system. , 1988, Virology.

[37]  A. C. Steven,et al.  A procedure for evaluation of significant structural differences between related arrays of protein molecules , 1978 .

[38]  R. Crowther,et al.  Procedures for three-dimensional reconstruction of spherical viruses by Fourier synthesis from electron micrographs. , 1971, Philosophical transactions of the Royal Society of London. Series B, Biological sciences.

[39]  William H. Press,et al.  Numerical recipes : the art of scientific computing : FORTRAN version , 1989 .

[40]  J. Strong,et al.  Biochemical and biophysical characterization of the reovirus cell attachment protein σ1: Evidence that it is a homotrimer , 1991, Virology.

[41]  J. Dubochet,et al.  Cryo-electron microscopy of vitrified specimens , 1988, Quarterly Reviews of Biophysics.

[42]  N. Unwin,et al.  Contrast transfer for frozen-hydrated specimens: determination from pairs of defocused images. , 1988, Ultramicroscopy.

[43]  P. Roy,et al.  Structure of bluetongue virus particles by cryoelectron microscopy. , 1992, Journal of structural biology.

[44]  H. Zarbl,et al.  Reovirus guanylyltransferase is L2 gene product lambda 2 , 1986, Journal of virology.

[45]  W. Joklik,et al.  Characterization of anti-reovirus immunoglobulins secreted by cloned hybridoma cell lines. , 1981, Virology.

[46]  M. Nibert,et al.  Mammalian reoviruses contain a myristoylated structural protein , 1991, Journal of virology.

[47]  M. Morgan,et al.  Reovirus messenger RNA contains a methylated, blocked 5'-terminal structure: m-7G(5')ppp(5')G-MpCp-. , 1975, Proceedings of the National Academy of Sciences of the United States of America.

[48]  B. Fields,et al.  Growth and survival of reovirus in intestinal tissue: role of the L2 and S1 genes , 1989, Journal of virology.

[49]  W. Grochulski,et al.  Use of radial density plots to calibrate image magnification for frozen-hydrated specimens. , 1993, Ultramicroscopy.

[50]  M. Nibert,et al.  Complete nucleotide sequence of the M2 gene segment of reovirus type 3 dearing and analysis of its protein product μ1 , 1988 .

[51]  A. Klug,et al.  Physical principles in the construction of regular viruses. , 1962, Cold Spring Harbor symposia on quantitative biology.

[52]  M. Nibert,et al.  Intracellular digestion of reovirus particles requires a low pH and is an essential step in the viral infectious cycle , 1987, Journal of virology.

[53]  J. Dubochet,et al.  Cryo-electron microscopy of viruses , 1984, Nature.

[54]  John E. Johnson,et al.  Icosahedral RNA virus structure. , 1989, Annual review of biochemistry.

[55]  D. Long,et al.  New Intermediate Subviral Particles in the In Vitro Uncoating of Reovirus Virions by Chymotrypsin , 1973, Journal of virology.

[56]  A. Bellamy,et al.  Subunit structure of the reovirus spike , 1980, Journal of virology.

[57]  M. Nibert,et al.  Distinct binding sites for zinc and double-stranded RNA in the reovirus outer capsid protein sigma 3 , 1988, Molecular and cellular biology.

[58]  J. Dubochet,et al.  Organization of double‐stranded DNA in bacteriophages: a study by cryo‐electron microscopy of vitrified samples. , 1987, The EMBO journal.

[59]  J. Wiener,et al.  The sequences of the reovirus serotype 1, 2, and 3 L1 genome segments and analysis of the mode of divergence of the reovirus serotypes. , 1989, Virology.

[60]  W. Chiu Electron microscopy of frozen, hydrated biological specimens. , 1986, Annual review of biophysics and biophysical chemistry.

[61]  S. E. Miller,et al.  The interaction of a series of hybridoma IgGs with reovirus particles. Demonstration that the core protein lambda 2 is exposed on the particle surface. , 1981, Virology.

[62]  J. Strong,et al.  Conformational and functional analysis of the C-terminal globular head of the reovirus cell attachment protein. , 1991, Virology.

[63]  R. Hendrix,et al.  Symmetry mismatch and DNA packaging in large bacteriophages. , 1978, Proceedings of the National Academy of Sciences of the United States of America.

[64]  S. Silverstein,et al.  THE PENETRATION OF REOVIRUS RNA AND INITIATION OF ITS GENETIC FUNCTION IN L-STRAIN FIBROBLASTS , 1968, The Journal of cell biology.

[65]  J. Wiener,et al.  Evolution of reovirus genes: a comparison of serotype 1, 2, and 3 M2 genome segments, which encode the major structural capsid protein mu 1C. , 1988, Virology.