» Articles » PMID: 16503362

Nidovirales: Evolving the Largest RNA Virus Genome

Overview
Journal Virus Res
Specialty Microbiology
Date 2006 Mar 1
PMID 16503362
Citations 522
Authors
Affiliations
Soon will be listed here.
Abstract

This review focuses on the monophyletic group of animal RNA viruses united in the order Nidovirales. The order includes the distantly related coronaviruses, toroviruses, and roniviruses, which possess the largest known RNA genomes (from 26 to 32kb) and will therefore be called "large" nidoviruses in this review. They are compared with their arterivirus cousins, which also belong to the Nidovirales despite having a much smaller genome (13-16kb). Common and unique features that have been identified for either large or all nidoviruses are outlined. These include the nidovirus genetic plan and genome diversity, the composition of the replicase machinery and virus particles, virus-specific accessory genes, the mechanisms of RNA and protein synthesis, and the origin and evolution of nidoviruses with small and large genomes. Nidoviruses employ single-stranded, polycistronic RNA genomes of positive polarity that direct the synthesis of the subunits of the replicative complex, including the RNA-dependent RNA polymerase and helicase. Replicase gene expression is under the principal control of a ribosomal frameshifting signal and a chymotrypsin-like protease, which is assisted by one or more papain-like proteases. A nested set of subgenomic RNAs is synthesized to express the 3'-proximal ORFs that encode most conserved structural proteins and, in some large nidoviruses, also diverse accessory proteins that may promote virus adaptation to specific hosts. The replicase machinery includes a set of RNA-processing enzymes some of which are unique for either all or large nidoviruses. The acquisition of these enzymes may have improved the low fidelity of RNA replication to allow genome expansion and give rise to the ancestors of small and, subsequently, large nidoviruses.

Citing Articles

Molecular basis of host recognition of human coronavirus 229E.

Tsai Y, Chien Y, Hsu M, Khoo K, Hsu S Nat Commun. 2025; 16(1):2045.

PMID: 40016196 PMC: 11868633. DOI: 10.1038/s41467-025-57359-8.


Structural and Phylogenetic Analysis on the Proofreading Activity of SARS-CoV-2.

Ghosh S, Biswas S, Mohanty R, Misra N, Suar M, Kushwaha G Curr Microbiol. 2025; 82(4):149.

PMID: 39992393 DOI: 10.1007/s00284-025-04130-3.


Diverse effects of coronavirus-defective viral genomes on the synthesis of IFNβ and ISG15 mRNAs and coronavirus replication.

Hsu H, Chang L, Yang C, Lin C, Teng Y, Hsu P Virol J. 2025; 22(1):37.

PMID: 39953551 PMC: 11827481. DOI: 10.1186/s12985-025-02654-5.


Biological Significance and Therapeutic Promise of Programmed Ribosomal Frameshifting.

Ramamonjiharisoa M, Liu S Int J Mol Sci. 2025; 26(3).

PMID: 39941062 PMC: 11818727. DOI: 10.3390/ijms26031294.


Giant RNA genomes: Roles of host, translation elongation, genome architecture, and proteome in nidoviruses.

Neuman B, Smart A, Gilmer O, Smyth R, Vaas J, Boker N Proc Natl Acad Sci U S A. 2025; 122(7):e2413675122.

PMID: 39928875 PMC: 11848433. DOI: 10.1073/pnas.2413675122.


References
1.
Almazan F, Galan C, Enjuanes L . The nucleoprotein is required for efficient coronavirus genome replication. J Virol. 2004; 78(22):12683-8. PMC: 525053. DOI: 10.1128/JVI.78.22.12683-12688.2004. View

2.
Yount B, Roberts R, Sims A, Deming D, Frieman M, Sparks J . Severe acute respiratory syndrome coronavirus group-specific open reading frames encode nonessential functions for replication in cell cultures and mice. J Virol. 2005; 79(23):14909-22. PMC: 1287583. DOI: 10.1128/JVI.79.23.14909-14922.2005. View

3.
Sawicki S, Sawicki D, Younker D, Meyer Y, Thiel V, Stokes H . Functional and genetic analysis of coronavirus replicase-transcriptase proteins. PLoS Pathog. 2005; 1(4):e39. PMC: 1298938. DOI: 10.1371/journal.ppat.0010039. View

4.
Snijder E, Horzinek M, Spaan W . The coronaviruslike superfamily. Adv Exp Med Biol. 1993; 342:235-44. DOI: 10.1007/978-1-4615-2996-5_37. View

5.
de Groot R, Luytjes W, Horzinek M, van der Zeijst B, Spaan W, Lenstra J . Evidence for a coiled-coil structure in the spike proteins of coronaviruses. J Mol Biol. 1987; 196(4):963-6. PMC: 7131189. DOI: 10.1016/0022-2836(87)90422-0. View