Senecavirus

VIRION

Non-enveloped, spherical, about 30 nm in diameter, T=pseudo3 icosahedral capsid surrounding the naked RNA genome. The capsid consists of a densely-packed icosahedral arrangement of 60 protomers, each consisting of 4 polypeptides, VP1, VP2, VP3 and VP4. VP4 is located on the internal side of the capsid.

GENOME

Monopartite, linear, ssRNA(+) genome of 7.3 kb, polyadenylated, composed of a single ORF encoding a polyprotein. Viral genomic RNA has a viral protein (VPg) at its 5’ end instead of a methylated nucleotide cap structure. The 5’ end contains an internal ribosome entry site probably of type IV. The P1 region encodes the structural polypeptides. The P2 and P3 regions encode the nonstructural proteins associated with replication. Probably encodes a unique protease 3C.

GENE EXPRESSION

The virion RNA is infectious and serves as both the genome and viral messenger RNA. The IRES allows direct translation of the polyprotein that is subsequently processed into the functional products.
Ribosomal skipping is used at the junction of the 2A and downstream sequence.

REPLICATION

CYTOPLASMIC

  1. Attachement of the virus to host receptors mediates endocytosis of the virus into the host cell.
  2. The capsid undergoes a conformational change and releases VP4 that opens a pore in the host endosomal membrane. The viral genomic RNA penetrates into the host cell cytoplasm.
  3. VPg is removed from the viral RNA, which is then translated into a processed polyprotein.
  4. Replication occurs in viral factories made of membrane vesicles derived from the ER. A dsRNA genome is synthesized from the genomic ssRNA(+).
  5. The dsRNA genome is transcribed/replicated thereby providing viral mRNAs/new ssRNA(+) genomes.
  6. New genomic RNA is believed to be packaged into preassembled procapsids.
  7. Cell lysis and virus release.