ICTV Virus Taxonomy Profile: Arteriviridae 2021

1Virions are pleomorphic but roughly spherical (diameter 50 to 74 nm). Nucleocapsid protein dimers form a roughly spherical capsid of about 30 nm in diameter lacking icosahedral symmetry. The capsid is surrounded by a lipid envelope derived from the infected cell. Small surface projections, consisting of the major viral envelope protein glycoprotein 5 and the associated membrane protein, cover the virion surface. The virion surface also contains complexes of the minor structural proteins (short spikes) (Table 1, Fig. 1).

2The genome is a single molecule of positive-sense RNA ranging from 12.7 to 15.7 kb (Fig. 2) with a 5′-type I cap and a 3′-terminal poly(A) tract that is infectious when transfected into permissive cells. Most arterivirus genomes have 10–11, mostly overlapping, functional ORFs, but viruses in the subfamily Simarterivirinae have genomes with 15 ORFs, due to a tandem duplication in the minor structural gene region.

3After virion attachment, endocytosis and membrane fusion, the genome is released into the cytoplasm. The largest (overlapping) ORFs, 1a and 1b are translated to produce the pp1a polyprotein, and after frameshifting, pp1ab. Polyproteins are autoproteolytically cleaved by several viral PL proteases and a 3 CL protease into 13 to 17 mature nonstructural proteins that induce double-membrane vesicles and form the associated viral RNA replication/transcription complexes. These include the NiRAN, RdRp and HEL1 enzymes, which catalyse viral RNA synthesis. Full-length negative-sense RNA is the template for genome replication. Subgenomic negative-sense RNAs are produced by a discontinuous transcription mechanism and function as the templates for subgenomic mRNAs encoding the structural proteins. The various subgenomic mRNAs contain different lengths of 3′-sequence as well as the 5′-leader sequence. Nucleocapsid dimers and a nascent genome RNA associate to form roughly spherical capsids in the cytoplasm, which then bud into the lumen of the endoplasmic reticular membrane at regions with inserted viral envelope proteins. Virions are transported through the secretory pathway and released by endocytosis. Arterivirus infections in non-human mammals are often persistent and can be asymptomatic or produce overt disease.

4Current taxonomy: www.ictv.global/taxonomy. Since the ninth report, arterivirus taxonomy has advanced several times. The current classification is based on DEmARC analysis of the 3CLpro, NiRAN, RdRp, ZBD and HEL1 protein sequences that are also conserved in other nidoviruses. Local minima in the clustering cost distribution of pairwise distances were used to delimit four ranks and demarcate monophyletic taxa. The family Arteriviridae belongs to the suborder Arnidovirineae of the order Nidovirales that also includes the families Coronaviridae, Tobaniviridae, Mesoniviridae and Roniviridae and nine others. Nidoviruses share a similar genome functional organization and expression strategy, and each family forms a monophyletic cluster. Compared to members of other families in the order, arterivirus genomes are the smallest, and are unique in virion size, structure and composition.

5Full ICTV Report on the family Arteriviridae: www.ictv.global/report/arteriviridae.