Abstract
Portogloboviridae is a family of viruses with circular, double-stranded DNA genomes of about 20 kbp. Their icosahedral virions have a diameter of 87 nm, and consist of an outer protein shell, an inner lipid layer and a nucleoprotein core wound up into a spherical coil. Portogloboviruses infect hyperthermophilic archaea of the genus Saccharolobus, order Sulfolobales and are presumably nonlytic. Portogloboviruses encode mini-CRISPR arrays which they use to compete against other co-infecting viruses. This is a summary of the International Committee on Taxonomy of Viruses (ICTV) Report on the family Portogloboviridae, which is available at ictv.global/report/portogloboviridae.
Keywords: ICTV, taxonomy, Portogloboviridae
Virion
Virions are icosahedral, with a diameter of about 87 nm from vertex to vertex and 83 nm from facet to facet (Table 1, Fig. 1a) and consist of three structural units: (a) the outer icosahedral protein shell, (b) the subcapsomer proteins and lipid membrane and (c) a circular nucleoprotein wrapped into a spherical core (Fig. 1b) [1, 2]. The outer shell carries capsid proteins VP4 and VP10, both displaying a single jelly-roll fold. VP10 and VP4 form pentameric and hexameric capsomers, respectively, which assemble into a T=43 icosahedral shell. The fivefold vertices of the capsid are decorated with the vertex complexes extending above the capsid surface and potentially involved in receptor binding [2]. The internal membrane of the virus also displays an icosahedral shape, presumably due to the presence of an intricate array of subcapsomer proteins that span the space between the membrane and the external icosahedral capsid [2, 3]. Lipids are selectively acquired from the pool of host lipids, with the lipid compositions in the viral and host membranes being quantitatively very different [2]. The nucleoprotein filament, formed by multiple copies of the nucleocapsid protein VP1 and circular dsDNA, is condensed into a globular core with a characteristic appearance of concentric rings, seen in the axial view, and striations, seen in the side view (Fig. 1a) [1, 2]. The viral dsDNA is stored in the capsid in the A-form (11.0 bp/turn) [2], as previously observed for filamentous archaeal viruses of the realm Adnaviria [3, 4].
Table 1.
Characteristics of members of the family Portogloboviridae
|
Example: |
Sulfolobus polyhedral virus 1 (KY780159), species Sulfolobus alphaportoglobovirus 1, genus Alphaportoglobovirus |
|---|---|
|
Virion |
Icosahedral virion, 87 nm in diameter, consisting of an outer protein shell, an inner lipid layer and a spherical nucleoprotein core |
|
Genome |
Circular, double-stranded DNA genome of about 20 kbp |
|
Replication |
Viral replication occurs without observable cell lysis |
|
Translation |
Not characterized |
|
Host range |
Hyperthermophilic archaea of the genus Saccharolobus, order Sulfolobales |
|
Taxonomy |
One genus, two species |
Fig. 1.
Electron micrograph of Sulfolobus polyhedral virus 1 virions. (a) Sample embedded in vitreous ice. Open arrowhead - projection in axial view, filled arrowhead - projection in side view. Scale bars, 100 nm [from [1], copyright American Society for Microbiology]. (b) Overall cryo-EM density map of Sulfolobus polyhedral virus 1, rendered to display the outer capsid (left half) and a central slice showing the interior of the virus (right half). The virus is coloured by radius. The red rectangle, triangle and pentagon denote the twofold, threefold and fivefold axes of symmetry, respectively. The grey numbered hexagons outline the hexameric VP4 capsomers from one asymmetric unit of the icosahedral capsid [2].
Genome
The circular dsDNA genome of Sulfolobus polyhedral virus 1 is 20 222 bp long and contains 45 open reading frames (ORFs) [1, 5]. ORFs are generally short (median 103 codons) and are tightly arranged, occupying 89.1 % of the genome (Fig. 2). Sequence analyses allow the assignment of putative functions to nine ORFs, of which seven encode putative DNA-binding proteins and the other two encode the glycosyltransferase and the methyltransferase (Fig. 2) [1].
Fig. 2.

Genome map of Sulfolobus polyhedral virus 1. Genes encoding virion structural proteins are shown in blue; those encoding predicted membrane proteins are indicated with asterisks.
Replication
Viral replication occurs by chronic infection without an apparent lytic cycle [1]. No information is available on entry or egress. The viruses do not encode identifiable DNA and RNA polymerases or other recognizable genome replication initiation proteins [6] and, as in the case of most other viruses that infect members of the Sulfolobales, apparently depend on the host machinery for genome replication and transcription [7]. Portogloboviruses carry mini-CRISPR arrays containing spacers targeting each other as well as other viruses, exemplifying a mechanism promoting inter-viral conflicts and superinfection exclusion in extreme environments [8].
Taxonomy
Current taxonomy: www.ictv.global/taxonomy. The family Portogloboviridae comprises a single genus, Alphaportoglobovirus, with two species. Portogloboviruses infect members of the hyperthermophilic archaeal genus Saccharolobus, order Sulfolobales.
Resources
Full ICTV Report on the family Portogloboviridae: www.ictv.global/report/portogloboviridae.
Funding information
Production of this summary, the online chapter, and associated resources was funded by a grant from the Wellcome Trust (WT108418AIA).
Acknowledgements
Members of the ICTV Report Consortium are Stuart G. Siddell, Elliot J. Lefkowitz, Sead Sabanadzovic, Peter Simmonds, F. Murilo Zerbini, Donald B. Smith, Richard J. Orton and Mart Krupovic.
Conflicts of interest
The authors declare that there are no conflicts of interest
References
- 1.Liu Y, Ishino S, Ishino Y, Pehau-Arnaudet G, Krupovic M, et al. A novel type of polyhedral viruses infecting hyperthermophilic archaea. J Virol. 2017;91:e00589-17. doi: 10.1128/JVI.00589-17. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 2.Wang F, Liu Y, Su Z, Osinski T, de Oliveira GAP, et al. A packing for A-form DNA in an icosahedral virus. Proc Natl Acad Sci U S A. 2019;116:22591–22597. doi: 10.1073/pnas.1908242116. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 3.Baquero D, Liu Y, Wang F, Egelman E, Prangishvili D, et al. Structure and assembly of archaeal viruses. Adv Virus Res. 2020;108:127–164. doi: 10.1016/bs.aivir.2020.09.004. [DOI] [PubMed] [Google Scholar]
- 4.Wang F, Baquero DP, Beltran LC, Su Z, Osinski T, et al. Structures of filamentous viruses infecting hyperthermophilic archaea explain DNA stabilization in extreme environments. Proc Natl Acad Sci U S A. 2020;117:19643–19652. doi: 10.1073/pnas.2011125117. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 5.Liu Y, Brandt D, Ishino S, Ishino Y, Koonin EV, et al. New archaeal viruses discovered by metagenomic analysis of viral communities in enrichment cultures. Environ Microbiol. 2019;21:2002–2014. doi: 10.1111/1462-2920.14479. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 6.Krupovic M, Cvirkaite-Krupovic V, Iranzo J, Prangishvili D, Koonin EV. Viruses of archaea: structural, functional, environmental and evolutionary genomics. Virus Res. 2018;244:181–193. doi: 10.1016/j.virusres.2017.11.025. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 7.Prangishvili D, Bamford DH, Forterre P, Iranzo J, Koonin EV, et al. The enigmatic archaeal virosphere. Nat Rev Microbiol. 2017;15:724–739. doi: 10.1038/nrmicro.2017.125. [DOI] [PubMed] [Google Scholar]
- 8.Medvedeva S, Liu Y, Koonin EV, Severinov K, Prangishvili D, et al. Virus-borne mini-CRISPR arrays are involved in interviral conflicts. Nat Commun. 2019;10:5204. doi: 10.1038/s41467-019-13205-2. [DOI] [PMC free article] [PubMed] [Google Scholar]

