Literature DB >> 33331814

ICTV Virus Taxonomy Profile: Pospiviroidae.

Francesco Di Serio1, Robert A Owens2, Shi-Fang Li3, Jaroslav Matoušek4, Vicente Pallás5, John W Randles6, Teruo Sano7, Jacobus Th J Verhoeven8, Georgios Vidalakis9, Ricardo Flores5.   

Abstract

Members of the family Pospiviroidae have single-stranded circular RNA genomes that adopt a rod-like or a quasi-rod-like conformation. These genomes contain a central conserved region that is involved in replication in the nucleus through an asymmetric RNA-RNA rolling-circle mechanism. Members of the family Pospiviroidae lack the hammerhead ribozymes that are typical of viroids classified in the family Avsunviroidae. The family Pospiviroidae includes the genera Apscaviroid, Cocadviroid, Coleviroid, Hostuviroid and Pospiviroid, with >25 species. This is a summary of the ICTV Report on the family Pospiviroidae, which is available at ictv.global/report/pospiviroidae.

Entities:  

Keywords:  ICTV Report; Pospiviroidae; taxonomy

Mesh:

Substances:

Year:  2021        PMID: 33331814      PMCID: PMC8116940          DOI: 10.1099/jgv.0.001543

Source DB:  PubMed          Journal:  J Gen Virol        ISSN: 0022-1317            Impact factor:   3.891


Genome

Members of the family Pospiviroidae have circular single-stranded RNA genomes of a few hundred nucleotides. They may assume rod-like or quasi-rod-like conformations containing a central conserved region (CCR) and a terminal conserved hairpin (TCH) or a terminal conserved region (TCR) (Table 1, Fig. 1) [1-3]. The G+C content is >50 %. The genome of viroids does not encode any proteins.
Table 1.

Characteristics of members of the family Pospiviroidae

Example:

potato spindle tuber viroid (V01465), species Potato spindle tuber viroid, genus Pospiviroid

Genome

Single-stranded circular RNA of 246–375 nt that adopts a rod-like or quasi-rod-like conformation of minimum free energy and contains typical conserved motifs

Replication

Mediated by nuclear DNA-dependent RNA polymerase II, with oligomeric RNAs of (+) polarity cleaved by a type III RNase and circularized by DNA ligase 1

Translation

Absent

Host range

Plants (dicotyledons and some monocotyledons)

Taxonomy

Several genera including >25 species

Fig. 1.

Rod-like structure models for viroids, The positions of the central conserved region (CCR), the terminal conserved region (TCR) and the terminal conserved hairpin (TCH) are indicated by shading. The sequence-specific TCH and TCR elements have never been found together in the same viroid.

Rod-like structure models for viroids, The positions of the central conserved region (CCR), the terminal conserved region (TCR) and the terminal conserved hairpin (TCH) are indicated by shading. The sequence-specific TCH and TCR elements have never been found together in the same viroid. Characteristics of members of the family Pospiviroidae Example: potato spindle tuber viroid (V01465), species Potato spindle tuber viroid, genus Pospiviroid Genome Single-stranded circular RNA of 246–375 nt that adopts a rod-like or quasi-rod-like conformation of minimum free energy and contains typical conserved motifs Replication Mediated by nuclear DNA-dependent RNA polymerase II, with oligomeric RNAs of (+) polarity cleaved by a type III RNase and circularized by DNA ligase 1 Translation Absent Host range Plants (dicotyledons and some monocotyledons) Taxonomy Several genera including >25 species

Replication

Replication is nuclear and mediated by DNA-dependent RNA polymerase II, which is redirected to use RNA templates through an asymmetric RNA–RNA rolling-circle mechanism. Circular RNA molecules of (+) polarity (by convention the most abundant strand in vivo) are repeatedly transcribed into oligomeric complementary (−) RNAs. Such intermediates serve as templates for generating oligomeric (+) RNAs that are cleaved by a host enzyme of the RNase III class. The termini of the resulting linear monomers are ligated by the host DNA ligase 1 to generate the mature circular viroid RNA [4]. In contrast to members of the family Avsunviroidae, the (−) oligomeric RNAs of members of the family Pospiviroidae are not cleaved and do not generate the corresponding circular forms.

Taxonomy

Current taxonomy: ictv.global/taxonomy. Demarcation of genera is based upon the type of CCR and the presence of a TCH or TCR (Fig. 1), as well as phylogenetic clustering in trees based upon whole-genome sequences (Fig. 2). Species demarcation criteria include there being <90 % sequence identity and distinct biological properties with respect to other members of the genus [5]. Members of the genus Pospiviroid, such as potato spindle tuber viroid, share the same CCR and have a TCR. Most infect herbaceous hosts, mainly solanaceous species. Hostuviroids, such as hop stunt viroid, share the same CCR and have a TCH, except for members of the species Dahlia latent viroid, which have a TCR instead of the TCH. Hop stunt viroid has a wide natural host range, while dahlia latent viroid is restricted to Dahlia spp. Cocadviroids, such as coconut cadang-cadang viroid, share the same CCR and have a TCH. Some members infect monocotyledons, while others can only infect dicotyledons. Apscaviroids, such as apple scar skin viroid, share the same CCR and have a TCR. Apscaviroids mainly infect woody plants. Coleviroids, such as Coleus blumei viroid 1, share the same CCR and have a TCR or a TCH. The natural host range of coleviroids is restricted to species in the genus Coleus.
Fig. 2.

Phylogenetic tree of viroid sequences. Maximum-likelihood analysis was conducted with megax [6]. Nodes are labelled with bootstrap support (1000 replicates) where this was >70%.

Phylogenetic tree of viroid sequences. Maximum-likelihood analysis was conducted with megax [6]. Nodes are labelled with bootstrap support (1000 replicates) where this was >70%.

Resources

Full ICTV Report on the family Pospiviroidae: ictv.global/report/pospiviroidae.
  6 in total

Review 1.  Viroids: survivors from the RNA world?

Authors:  Ricardo Flores; Selma Gago-Zachert; Pedro Serra; Rafael Sanjuán; Santiago F Elena
Journal:  Annu Rev Microbiol       Date:  2014-06-18       Impact factor: 15.500

2.  Current status of viroid taxonomy.

Authors:  F Di Serio; R Flores; J Th J Verhoeven; S-F Li; V Pallás; J W Randles; T Sano; G Vidalakis; R A Owens
Journal:  Arch Virol       Date:  2014-09-13       Impact factor: 2.574

Review 3.  Structure and Associated Biological Functions of Viroids.

Authors:  Gerhard Steger; Jean-Pierre Perreault
Journal:  Adv Virus Res       Date:  2016-03-02       Impact factor: 9.937

4.  Dissecting the secondary structure of the circular RNA of a nuclear viroid in vivo: A "naked" rod-like conformation similar but not identical to that observed in vitro.

Authors:  Amparo López-Carrasco; Ricardo Flores
Journal:  RNA Biol       Date:  2016-08-30       Impact factor: 4.652

5.  MEGA X: Molecular Evolutionary Genetics Analysis across Computing Platforms.

Authors:  Sudhir Kumar; Glen Stecher; Michael Li; Christina Knyaz; Koichiro Tamura
Journal:  Mol Biol Evol       Date:  2018-06-01       Impact factor: 16.240

6.  Comprehensive secondary structure elucidation of four genera of the family Pospiviroidae.

Authors:  Tamara Giguère; Charith Raj Adkar-Purushothama; Jean-Pierre Perreault
Journal:  PLoS One       Date:  2014-06-04       Impact factor: 3.240

  6 in total
  8 in total

Review 1.  Emerging value of the viroid model in molecular biology and beyond.

Authors:  Junfei Ma; Shachinthaka D Dissanayaka Mudiyanselage; Ying Wang
Journal:  Virus Res       Date:  2022-03-06       Impact factor: 3.303

2.  Degradome Analysis of Tomato and Nicotiana benthamiana Plants Infected with Potato Spindle Tuber Viroid.

Authors:  Beatriz Navarro; Andreas Gisel; Pedro Serra; Michela Chiumenti; Francesco Di Serio; Ricardo Flores
Journal:  Int J Mol Sci       Date:  2021-04-02       Impact factor: 5.923

Review 3.  A scenario for the emergence of protoviroids in the RNA world and for their further evolution into viroids and viroid-like RNAs by modular recombinations and mutations.

Authors:  Ricardo Flores; Beatriz Navarro; Pedro Serra; Francesco Di Serio
Journal:  Virus Evol       Date:  2022-01-15

4.  A remodeled RNA polymerase II complex catalyzing viroid RNA-templated transcription.

Authors:  Shachinthaka D Dissanayaka Mudiyanselage; Junfei Ma; Tibor Pechan; Olga Pechanova; Bin Liu; Ying Wang
Journal:  PLoS Pathog       Date:  2022-09-19       Impact factor: 7.464

5.  A nuclear import pathway exploited by pathogenic noncoding RNAs.

Authors:  Junfei Ma; Shachinthaka D Dissanayaka Mudiyanselage; Woong June Park; Mo Wang; Ryuta Takeda; Bin Liu; Ying Wang
Journal:  Plant Cell       Date:  2022-09-27       Impact factor: 12.085

6.  Reassessing species demarcation criteria in viroid taxonomy by pairwise identity matrices.

Authors:  Michela Chiumenti; Beatriz Navarro; Thierry Candresse; Ricardo Flores; Francesco Di Serio
Journal:  Virus Evol       Date:  2021-01-25

7.  Reassessment of the Columnea latent viroid (CLVd) Taxonomic Classification.

Authors:  Parichate Tangkanchanapas; Annelies Haegeman; Monica Höfte; Kris De Jonghe
Journal:  Microorganisms       Date:  2021-05-21

8.  Symptom Severity, Infection Progression and Plant Responses in Solanum Plants Caused by Three Pospiviroids Vary with the Inoculation Procedure.

Authors:  Francisco Vázquez Prol; Joan Márquez-Molins; Ismael Rodrigo; María Pilar López-Gresa; José María Bellés; Gustavo Gómez; Vicente Pallás; Purificación Lisón
Journal:  Int J Mol Sci       Date:  2021-06-08       Impact factor: 5.923

  8 in total

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