Читать книгу Principles of Virology - Jane Flint, S. Jane Flint - Страница 287

A distinctive feature of the infectious cycle of double-stranded RNA viruses is the production of mRNAs and genomic RNAs from distinct templates in different viral particles. Because the viral genomes are double stranded, they cannot be translated. Therefore, the first step in infection is the production of mRNAs from each viral RNA segment by the virion-associated RdRP (Fig. 6.24). Reoviral mRNAs carry 5′ cap structures but lack 3′ poly(A) sequences.

Figure 6.23 Arenavirus RNA synthesis. Arenaviruses contain two genomic RNA segments, L (large) and S (small) (top). At early times after infection, only the 3′ region of each of these segments is copied to form mRNA: the N mRNA from the S genomic RNA and the L mRNA from the L genomic RNA. Copying of the remainder of the S and L genomic RNAs may be blocked by a stem-loop structure in the genomic RNAs. After the S and L genomic RNAs are copied into full-length strands, their 3′ regions are copied to produce mRNAs: the glycoprotein precursor (GP) mRNA from S RNA and the Z mRNA (encoding an inhibitor of viral RNA synthesis) from the L RNA. Only RNA synthesis from the S RNA is shown in detail.

Figure 6.24 mRNA synthesis and replication of double-stranded RNA genomes. These processes occur in subviral particles containing the RNA templates and necessary enzymes. During cell entry, the virion passes through the lysosomal compartment, and proteolysis of viral capsid proteins activates the RNA synthetic machinery. Single-stranded (+) viral mRNAs, which are synthesized in parental subviral particles, are extruded into the cytoplasm, where they serve either as mRNAs or as templates for the synthesis of (−) RNA strands. In the latter case, viral mRNAs are first packaged into newly assembled subviral particles in which the synthesis of (−) RNAs to produce double-stranded RNAs occurs. These subviral particles eventually become infectious particles. Only 1 of the 10 to 12 double-stranded RNA segments of the reoviral genome is shown.

In the reovirus core, the λ3 polymerase molecules are attached to the inner shell at each fivefold axis, below an RNA exit pore. Viral mRNAs are synthesized by the polymerase inside the subviral parental core and then extruded into the cytoplasm through this pore. Attachment of the polymerase molecules to the pores ensures that mRNAs are actively threaded out of the particle, without depending upon diffusion, which would be very inefficient. Examination of the structure of an actively transcribing human rotavirus, a member of the Reoviridae, has allowed a three-dimensional visualization of how mRNAs are released from the core particle (Box 6.4). Viral (+) strand RNAs that will serve as templates for (−) strand RNA synthesis are first packaged into newly assembled sub-viral particles (Fig. 6.24). Each (+) strand RNA is then copied just once within this particle to produce double-stranded RNA.

Members of different families of double-stranded RNA viruses carry out RNA synthesis in diverse ways. Replication of the genome of bacteriophage ϕ6 (3 RNA segments) and birnaviruses (2 RNA segments) is semiconservative, whereas that of reoviruses (10 to 12 RNA segments) is conservative: only one of the two strands is copied. During conservative replication, the double-stranded RNA that exits the polymerase must be melted, so that the newly synthesized (+) strand is released and the template (−) strand reanneals with the original (+) strand. In reovirus particles, each double-stranded RNA segment is attached to a polymerase molecule, by interaction of the 5′ cap structure with a cap-binding site on the RdRP. Attachment of the 5′ cap to the polymerase facilitates insertion of the 3′ end of the (−) strand into the template channel. This arrangement allows very efficient reinitiation of RNA synthesis in the crowded core of the particle. The RdRPs of bacteriophage ϕ6 and birnaviruses do not have such a cap-binding site, as would be expected for enzymes that copy both strands of the double-stranded RNA segments. This strategy appears less efficient, but may be sufficient when the genome consists of only two or three double-stranded RNA segments.