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The Journal of General Virology logoLink to The Journal of General Virology
. 2022 May 5;103(5):001738. doi: 10.1099/jgv.0.001738

ICTV Virus Taxonomy Profile: Potyviridae 2022

Alice K Inoue-Nagata 1,*, Ramon Jordan 2, Jan Kreuze 3, Fan Li 4, Juan José López-Moya 5, Kristiina Mäkinen 6, Kazusato Ohshima 7, Stephen J Wylie 8; ICTV Report Consortium
PMCID: PMC12642016  PMID: 35506996

Abstract

The family Potyviridae includes plant viruses with single-stranded, positive-sense RNA genomes of 8–11 kb and flexuous filamentous particles 650–950 nm long and 11–20 nm wide. Genera in the family are distinguished by the host range, genomic features and phylogeny of the member viruses. Most genomes are monopartite, but those of members of the genus Bymovirus are bipartite. Some members cause serious disease epidemics in cultivated plants. This is a summary of the International Committee on Taxonomy of Viruses (ICTV) Report on the family Potyviridae, which is available at ictv.global/report/potyviridae.

Keywords: ICTV Profile, taxonomy, Potyviridae

Virion

The flexuous, filamentous particles are typically 650–950 nm long and 11–20 nm wide, with helical symmetry and a pitch of about 3.4–3.5 nm (Fig. 1, Table 1), but members of the genus Bymovirus are bipartite with particles of two modal lengths of 250–300 nm and 500–600 nm. Virions contain a core capsid protein (CP) of 28.5–47 kDa [1]; the tip of the particle may contain the virus-encoded proteins genome-linked protein (VPg), helper-component protease (HC-Pro), cylindrical inclusion (CI) and the host factor elF4E. There are serological relationships among many members.

Fig. 1. (Left) Cryo-electron microscopy reconstruction of a section of a virion of turnip mosaic virus (TuMV). Depicted are the ssRNA (red), and the central globular domain (pale yellow), N-terminal arm (blue) and C-terminal region (grey) of the capsid protein. In the upper section some of the densities are cut-away. (Right) Cryo-electron micrograph of TuMV virions where the periodic organization of the helical filaments is apparent. Bar, ~500 nm. Images are courtesy of R. Cuesta and M. Valle, CIC bioGUNE, Spain, based on [7].

Fig. 1.

Table 1. Characteristics of members of the family Potyviridae.

Example potato virus Y-O (U09509), species Potato virus Y, genus Potyvirus
Virion Non-enveloped, flexuous and filamentous particles, 650–950 nm long and 11–20 nm in diameter with a core capsid protein
Genome 8.2–11.5 kb of positive-sense, single-stranded, usually monopartite RNA (bipartite in the genus Bymovirus)
Replication Cytoplasmic, initiated in virus replication complexes on 6K2-induced membranous vesicles at endoplasmic reticulum exit sites
Translation Directly from genomic RNA
Host range Plants; transmission by arthropods, plasmodiophorids (Bymovirus), seeds or pollen
Taxonomy Realm Riboviria, kingdom Orthornavirae, phylum Pisuviricota, class Stelpaviricetes, order Patatavirales: >10 genera including >230 species

Genome

The positive-sense ssRNA genome ranges from 8.2 kb (members of the species Artichoke latent virus, genus Macluravirus, and species Bellflower veinal mottle virus, genus Bevemovirus) to 11.5 kb (species Celery latent virus, genus Celavirus), with a VPg covalently linked to the 5′-end, and a polyadenylated 3′-terminus (Fig. 2). The genome of the celavirus celery latent virus is not polyadenylated. Most genomes are monopartite, but those of members of the genus Bymovirus are bipartite. The major large ORF of monopartite genomes encodes a polyprotein that is cleaved into functional proteins at semi-conserved sites by two or three viral proteases [2]. Bipartite Bymovirus genomes encode two polyproteins that are cleaved by two proteases. A second small ORF, PIPO, is generated by a polymerase slippage mechanism and is expressed as the trans-frame protein P3N-PIPO [3]. Another additional small ORF, PISPO, is generated through a transcriptional slippage mechanism among sweet potato-subgroup potyviruses and leads to the production of a trans-frame protein P1N-PISPO. Some viruses lack one or both of the P1 and HC-Pro N-terminal coding regions, and may be replaced by genus-specific or species-specific regions.

Fig. 2. Schematic diagram of the genome organization of potato virus Y. VPg, virus protein genome-linked (indicated by an ellipse at the 5′-terminus); P1, protein 1 protease; HC-Pro, helper component protease; P3, protein 3; PIPO, pretty interesting Potyviridae ORF; 6K1, 6 kDa peptide 1; CI, cylindrical inclusion; 6K2, 6 kDa peptide 2; NIa-Pro, nuclear inclusion a-protease; NIb, nuclear inclusion b, RNA-directed RNA polymerase; CP, capsid protein. Arrowheads indicate cleavage sites of P1 (blue), HC-Pro (red) and NIa-Pro (black).

Fig. 2.

Replication

Genomic RNA serves as a template for both translation and replication (reviewed by [4]). The genomic RNA replicates via the production of a full-length negative-sense RNA, which takes place in the cytoplasmic viral replication complex (VRC). The VRC is formed by virus proteins, such as NIb, 6K2, VPg, NIa-Pro, HC-Pro, CI, and possibly P3 and 6K1, and host factors. The viral genome is transported cell-to-cell through the plasmodesmata, probably in the form of particles, involving the coordinated action of CP, CI, P3, 6K2 and P3N-PIPO [5].

Taxonomy

Current taxonomy: ictv.global/taxonomy. Members of different genera in the family are distinguished by host range, vector, genomic features and phylogeny, with species demarcation typically based upon sequence identity of the large ORF (or, if necessary, the CP-coding region) being <76 % (nt) and <82 % (aa) [6]. Thresholds for other coding regions are usually 58 % (P1 coding region) or 74–78 % (other regions). Members of the family Potyviridae are transmitted by aphids, eriophyid mites, whiteflies and plasmodiophorids, but the vector is not known for members of five genera. New species or genera in the family will be considered after analyses based on complete genome sequences and additional data about biological characteristics.

Resources

Full ICTV Report on the family Potyviridae: ictv.global/report/potyviridae.

Acknowledgements

Members of the ICTV Report Consortium are Stuart G. Siddell, Elliot J. Lefkowitz, Sead Sabanadzovic, Peter Simmonds, F. Murilo Zerbini, Donald B. Smith, and Luisa Rubino.

Abbreviations

CI

cylindrical inclusion

CP

capsid protein

HC-Pro

helper-component protease

VPg

virus protein genome-linked

VRC

viral replication complex

Footnotes

Funding: Production of this summary, the online chapter and associated resources was funded by a grant from the Wellcome Trust (WT108418AIA).

Contributor Information

Alice K. Inoue-Nagata, Email: alice.nagata@embrapa.br.

Ramon Jordan, Email: ramon.jordan@usda.gov.

Jan Kreuze, Email: j.kreuze@cgiar.org.

Fan Li, Email: fanli@ynau.edu.cn.

Juan José López-Moya, Email: juanjose.lopez@cragenomica.es.

Kristiina Mäkinen, Email: kristiina.makinen@helsinki.fi.

Kazusato Ohshima, Email: ohshimak@cc.saga-u.ac.jp.

Stephen J. Wylie, Email: s.wylie@murdoch.edu.au.

ICTV Report Consortium, Email: donald.smith.ictv@gmail.com.

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