Viroid quasispecies revealed by deep sequencing
Jazyk angličtina Země Spojené státy americké Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
28027000
PubMed Central
PMC5367258
DOI
10.1080/15476286.2016.1272745
Knihovny.cz E-zdroje
- Klíčová slova
- Error rate, Pospiviroid, error threshold, quasispecies, sequence network mapping, sequencing error, viroid-specific small RNA,
- MeSH
- genom virový * MeSH
- mutace MeSH
- reassortantní viry genetika MeSH
- replikace viru MeSH
- RNA virová genetika MeSH
- viroidy genetika MeSH
- vysoce účinné nukleotidové sekvenování * MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- RNA virová MeSH
Viroids are non-coding single-stranded circular RNA molecules that replicate autonomously in infected host plants causing mild to lethal symptoms. Their genomes contain about 250-400 nucleotides, depending on viroid species. Members of the family Pospiviroidae, like the Potato spindle tuber viroid (PSTVd), replicate via an asymmetric rolling-circle mechanism using the host DNA-dependent RNA-Polymerase II in the nucleus, while members of Avsunviroidae are replicated in a symmetric rolling-circle mechanism probably by the nuclear-encoded polymerase in chloroplasts. Viroids induce the production of viroid-specific small RNAs (vsRNA) that can direct (post-)transcriptional gene silencing against host transcripts or genomic sequences. Here, we used deep-sequencing to analyze vsRNAs from plants infected with different PSTVd variants to elucidate the PSTVd quasipecies evolved during infection. We recovered several novel as well as previously known PSTVd variants that were obviously competent in replication and identified common strand-specific mutations. The calculated mean error rate per nucleotide position was less than [Formula: see text], quite comparable to the value of [Formula: see text] reported for a member of Avsunviroidae. The resulting error threshold allows the synthesis of longer-than-unit-length replication intermediates as required by the asymmetric rolling-circle mechanism of members of Pospiviroidae.
Zobrazit více v PubMed
Navarro B, Gisel A, Rodio M, Delgado S, Flores R, Di Serio F. Viroids: How to infect a host and cause disease without encoding proteins. Biochimie 2012; 94:1474-80; PMID:22738729; http://dx.doi.org/10.1016/j.biochi.2012.02.020 PubMed DOI
Palukaitis P. What has been happening with viroids? Virus Genes 2014; 49:175-184; PMID:25164861; http://dx.doi.org/10.1007/s11262-014-1110-8 PubMed DOI
Gago-Zachert S. Viroids, infectious long non-coding RNAs with autonomous replication. Virus Res 2015; 212:12-24; PMID:26319312 PubMed
Flores R, Grubb D, Elleuch A, MÁ Nohales, Delgado S, Gago S. Rolling-circle replication of viroids, viroid-like satellite RNAs and hepatitis delta virus: variations on a theme. RNA Biol 2011; 8:200-206; PMID:21358283; http://dx.doi.org/10.4161/rna.8.2.14238 PubMed DOI
Gago S, Elena SF, Flores R, Sanjuán R. Extremely high mutation rate of a hammerhead viroid. Science 2009; 323:1308; PMID:19265013; http://dx.doi.org/10.1126/science.1169202 PubMed DOI
Eigen M. Selforganization of matter and the evolution of biological macromolecules. Naturwissenschaften 1971; 58:465-523; PMID:4942363; http://dx.doi.org/10.1007/BF00623322 PubMed DOI
Domingo E. Quasispecies theory in virology. J Virology 2002; 76:463-65; http://dx.doi.org/10.1128/JVI.76.1.463-465.2002 PubMed DOI PMC
Bull J, Meyers L, Lachmann M. Quasispecies made simple. PLoS Comput Biol 2005; 1:e61; PMID:16322763; http://dx.doi.org/10.1371/journal.pcbi.0010061 PubMed DOI PMC
Flores R, Serra P, Minoia S, Di Serio F, Navarro B. Viroids: from genotype to phenotype just relying on RNA sequence and structural motifs. Front Microbiol 2012; 3:217; PMID:22719735; http://dx.doi.org/10.3389/fmicb.2012.00217. PubMed DOI PMC
Semancik J, Szychowski J, Rakowski A, Symons R. Isolates of citrus exocortis viroid recovered by host and tissue selection. J Gen Virol 1993; 74:2427-36; PMID:8245858; http://dx.doi.org/10.1099/0022-1317-74-11-2427 PubMed DOI
Matoušek J, Orctová L, Ptáček J, Patzak J, Dědič P, Steger G, Riesner D. Experimental transmission of pospiviroid populations to weed species characteristic of potato and hop fields. J Virol 2007; 81:11891-99; PMID:17715233; http://dx.doi.org/2199454810.1128/JVI.01165-07 PubMed DOI PMC
Elena S, Gómez G, Daròs J. Evolutionary constraints to viroid evolution. Viruses 2009; 1:241-254; PMID:21994548; http://dx.doi.org/10.3390/v1020241 PubMed DOI PMC
Matoušek J, Stehlík J, Procházková J, Orctová L, Wullenweber J, Füssy Z, Kováčik J, Duraisamy GS, Ziegler A, Schubert J, et al.. Biological and molecular analysis of the pathogenic variant C3 of potato spindle tuber viroid (PSTVd) evolved during adaptation to chamomile (Matricaria chamomilla). Biol Chem 2012; 393:605-615; PMID:22944665; http://dx.doi.org/1137615810.1515/hsz-2011-0286 PubMed DOI
Papaefthimiou I, Hamilton A, Denti M, Baulcombe D, Tsagris M, Tabler M. Replicating potato spindle tuber viroid RNA is accompanied by short RNA fragments that are characteristic of post-transcriptional gene silencing. Nucleic Acids Res 2001; 29:2395-2400; PMID:11376158; http://dx.doi.org/10.1093/nar/29.11.2395 PubMed DOI PMC
Hammann C, Steger G. Viroid-specific small RNA in plant disease. RNA Biol 2012; 9:809-819; PMID:22617880; http://dx.doi.org/10.4161/rna.19810 PubMed DOI
Navarro B, Gisel A, Rodio ME, Delgado S, Flores R, Di Serio F. Small RNAs containing the pathogenic determinant of a chloroplast-replicating viroid guide the degradation of a host mRNA as predicted by RNA silencing. Plant J 2012; 70:991-1003; PMID:22332758; http://dx.doi.org/10.1111/j.1365-313X.2012.04940.x PubMed DOI
Avina-Padilla K, Martinez de la Vega O, Rivera-Bustamante R, Martinez-Soriano J, Owens R, Hammond R, Vielle-Calzada J. In silico prediction and validation of potential gene targets for pospiviroid-derived small RNAs during tomato infection. Gene 2015; 564:197-205; PMID:25862922; http://dx.doi.org/10.1016/j.gene.2015.03.076 PubMed DOI
Adkar-Purushothama C, Brosseau C, Giguère T, Sano T, Moffett P, Perreault J. Small RNA derived from the virulence modulating region of the Potato spindle tuber viroid silences callose synthase genes of tomato plants. Plant Cell 2015; 27:2178-94; PMID:26290537; http://dx.doi.org/10.1105/tpc.15.00523 PubMed DOI PMC
Adkar-Purushothama CR, Perreault JP, Sano T. Analysis of small RNA production patterns among the 2 potato spindle tuber viroid variants in tomato plants. Genom Data 2015; 25:65-66; http://dx.doi.org/10.1016/j.gdata.2015.08.008 PubMed DOI PMC
Li R, Gao S, Hernandez A, Wechter W, Fei Z, Ling K. Deep sequencing of small RNAs in tomato for virus and viroid identification and strain differentiation. PLoS ONE 2012; 7:e37127; PMID:22623984; http://dx.doi.org/10.1371/journal.pone.0037127 PubMed DOI PMC
Zhang Z, Qi S, Tang N, Zhang X, Chen S, Zhu P, Ma L, Cheng J, Xu Y, Lu M, et al.. Discovery of replicating circular RNAs by RNA-seq and computational algorithms. PLoS Pathog 2014; 10:e1004553; PMID:25503469; http://dx.doi.org/10.1371/journal.ppat.1004553 PubMed DOI PMC
Seguin J, Rajeswaran R, Malpica-LÃ3pez N, Martin R, Kasschau K, Dolja V, Otten P, Farinelli L, Pooggin M. De novo reconstruction of consensus master genomes of plant RNA and DNA viruses from siRNAs. PLoS ONE 2014; 9:e88513; PMID:24523907; http://dx.doi.org/10.1371/journal.pone.0088513 PubMed DOI PMC
Tsibris AMN, Korber B, Arnaout R, Russ C, Lo CC, Leitner T, Gaschen B, Theiler J, Paredes R, Su Z, et al.. Quantitative deep sequencing reveals dynamic HIV-1 escape and large population shifts during CCR5 antagonist therapy in vivo. PLoS One 2009; 4:1-12; PMID:19479085; http://dx.doi.org/2299603110.1371/journal.pone.0005683 PubMed DOI PMC
Rozera G, Abbate I, Ciccozzi M, Presti AL, Bruselles A, Vlassi C, D'Offizi G, Narciso P, Giombini E, Bartolini B, et al.. Ultra-deep sequencing reveals hidden HIV-1 minority lineages and shifts of viral population between the main cellular reservoirs of the infection after therapy interruption. J Med Virol 2012; 84:839-844; PMID:22996031; http://dx.doi.org/10.1002/jmv.23292 PubMed DOI
Timm C, Akpinar F, Yin J. Quantitative characterization of defective virus emergence by deep sequencing. J Virol 2013; 88:2623-32; PMID:24352442; http://dx.doi.org/10.1128/JVI.02675-13 PubMed DOI PMC
Astrovskaya I, Tork B, Mangul S, Westbrooks K, Mandoiu I, Balfe P, Zelikovsky A. Inferring viral quasispecies spectra from 454 pyrosequencing reads. BMC Bioinformatics 2011; 12:S1; PMID:21989211; http://dx.doi.org/10.1186/1471-2105-12-S6-S1 PubMed DOI PMC
Andino R, Domingo E. Viral quasispecies. Virology 2015; 479-480:46-51; PMID:25824477; http://dx.doi.org/10.1016/j.virol.2015.03.022 PubMed DOI PMC
Biebricher C, Eigen M. The error threshold. Virus Res 2005; 107:117-127; PMID:15649558; http://dx.doi.org/10.1016/j.virusres.2004.11.002 PubMed DOI
Rocheleau L, Pelchat M. The Subviral RNA Database: a toolbox for viroids, the hepatitis delta virus and satellite RNAs research. BMC Microbiol 2006; 6:24; PMID:16519798; http://dx.doi.org/10.1186/1471-2180-6-24 PubMed DOI PMC
Gozmanova M, Denti M, Minkov I, Tsagris M, Tabler M. Characterization of the RNA motif responsible for the specific interaction of potato spindle tuber viroid RNA (PSTVd) and the tomato protein Virp1. Nucleic Acids Res 2003; 31:5534-43; PMID:14500815; http://dx.doi.org/10.1093/nar/gkg777 PubMed DOI PMC
Kalantidis K, Denti M, Tzortzakaki S, Marinou E, Tabler M, Tsagris M. Virp1 is a host protein with a major role in Potato spindle tuber viroid infection in Nicotiana plants. J Virol 2007; 81:12872-80; PMID:17898061; http://dx.doi.org/10.1128/JVI.00974-07 PubMed DOI PMC
Zhong X, Leontis N, Qian S, Itaya A, Qi Y, Boris-Lawrie K, Ding B. Tertiary structural and functional analyses of a viroid RNA motif by isostericity matrix and mutagenesis reveal its essential role in replication. J Virol 2006; 80:8566-81; PMID:16912306; http://dx.doi.org/10.1128/JVI.00837-06 PubMed DOI PMC
Lynch M. Evolution of the mutation rate. Trends Genet 2010; 26:345-352; PMID:20594608; http://dx.doi.org/10.1016/j.tig.2010.05.003 PubMed DOI PMC
Carey L. RNA polymerase errors cause splicing defects and can be regulated by differential expression of RNA polymerase subunits. Elife 2015; 4:e09945; PMID:26652005; http://dx.doi.org/10.7554/eLife.09945 PubMed DOI PMC
Glouzon J, Bolduc F, Wang S, Najmanovich R, Perreault J. Deep-sequencing of the peach latent mosaic viroid reveals new aspects of population heterogeneity. PLoS ONE 2014; 9:e87297; PMID:24498066; http://dx.doi.org/10.1371/journal.pone.0087297 PubMed DOI PMC
Tsushima D, Tsushima T, Sano T. Molecular dissection of a dahlia isolate of potato spindle tuber viroid inciting a mild symptoms in tomato. Virus Res 2015; 214:11-18; PMID:26732488; http://dx.doi.org/10.1016/j.virusres.2015.12.018 PubMed DOI
Podstolski W, Góra-Sochacka A, Zagórski W. Co-inoculation with 2 non-infectious cDNA copies of potato spindle tuber viroid (PSTVd) leads to the appearance of novel fully infectious variants. Acta Biochim Pol 2005; 52:87-98; PMID:15827608 PubMed
Qi Y, Ding B. Differential subnuclear localization of RNA strands of opposite polarity derived from an autonomously replicating viroid. Plant Cell 2003; 15:2566-77; PMID:14555700; http://dx.doi.org/10.1105/tpc.016576 PubMed DOI PMC
Góra-Sochacka A, Kierzek A, Candresse T, Zagórski W. The genetic stability of potato spindle tuber viroid (PSTVd) molecular variants. RNA 1997; 3:68-74; PMID:8990400824157838 PubMed PMC
Góra-Sochacka A, Candresse T, Zagórski W. Genetic variability of potato spindle tuber viroid RNA replicon. Acta Biochim Pol 2001; 48:467-476;PMID: 1173261624157838 PubMed
Matoušek J, Orctová L, Steger G, Škopek J, Moors M, Dědič P, Riesner D. Analysis of thermal stress-mediated PSTVd variation and biolistic inoculation of progeny of viroid “thermomutants” to tomato and Brassica species. Virology 2004; 323:9-23; PMID:15165815; http://dx.doi.org/2415783810.1016/j.virol.2004.02.010 PubMed DOI
Matoušek J, L Orctová, Steger G, Riesner D. Biolistic inoculation of plants with viroid nucleic acids. J Virol Methods 2004; 122:153-164; PMID:15542139; http://dx.doi.org/2415783810.1016/j.jviromet.2004.08.011 PubMed DOI
Matoušek J, Kozlova P, Orctova L, Schmitz A, Pešina K, Bannach O, Diermann N, Steger G, Riesner D. Accumulation of viroid-specific small RNAs and increase in nucleolytic activities linked to viroid-caused pathogenesis. Biol Chem 2007; 388:1-13; PMID:17214544; http://dx.doi.org/2415783810.1515/BC.2007.001 PubMed DOI
Ameta S, Winz ML, Previti C, Jäschke A. Next-generation sequencing reveals how RNA catalysts evolve from random space. Nucleic Acids Res 2013; 42:1303-10; PMID:24157838; http://dx.doi.org/10.1093/nar/gkt949 PubMed DOI PMC
Duran-Vila N, Elena S, Daròs JA, Flores R. Structure and evolution of viroids In: Domingo E, Parrish C, Holland J, eds., Origin and Evolution of Viruses, 43–64. London: Academic Press, 2nd edn., 2008; http://dx.doi.org/10.1016/B978-0-12-374153-0.00002-3 DOI
Tsushima D, Adkar-Purushothama CR, Taneda A, Sano T. Changes in relative expression levels of viroid-specific small RNAs and microRNAs in tomato plants infected with severe and mild symptom-inducing isolates of Potato spindle tuber viroid. J General Plant Pathol 2015; 81:49-62; http://dx.doi.org/10.1007/s10327-014-0566-7 DOI
Feldstein P, Hu Y, Owens R. Precisely full length, circularizable, complementary RNA: an infectious form of potato spindle tuber viroid. Proc Natl Acad Sci USA 1998; 95:6560-6565; PMID:9601006; http://dx.doi.org/10.1073/pnas.95.11.6560 PubMed DOI PMC
Schmieder R, Edwards R. Quality control and preprocessing of metagenomic datasets. Bioinformatics 2011; 27:863-64; PMID:21278185; http://dx.doi.org/10.1093/bioinformatics/btr026 PubMed DOI PMC
Bolger AM, Lohse M, Usadel B. Trimmomatic: a flexible trimmer for Illumina sequence data. Bioinformatics 2014; 30:2114-20; PMID:24695404; http://dx.doi.org/10.1093/bioinformatics/btu170 PubMed DOI PMC
Hoffmann S, Otto C, Kurtz S, Sharma CM, Khaitovich P, Vogel J, Stadler PF, Hackermüller J. Fast mapping of short sequences with mismatches, insertions and deletions using index structures. PLoS Comput Biol 2009; 5:e1000502; PMID:19750212; http://dx.doi.org/10.1371/journal.pcbi.1000502 PubMed DOI PMC
Hoffmann S, Otto C, Doose G, Tanzer A, Langenberger D, Christ S, Kunz M, Holdt L, Teupser D, Hackermüller J, et al.. A multi-split mapping algorithm for circular RNA, splicing, trans-splicing, and fusion detection. Genome Biol 2014; 15:R34; PMID:24512684; http://dx.doi.org/10.1186/gb-2014-15-2-r34 PubMed DOI PMC
Domingo E, Biebricher C, Eigen M, Holland J, eds. Quasispecies and RNA virus evolution: principles and consequences. Austin: Landes Bioscience, 2001.
Li H, Handsaker B, Wysoker A, Fennell T, Ruan J, Homer N, Marth G, Abecasis G, Durbin R. The sequence alignment/map format and SAMtools. Bioinformatics 2009; 25:2078-79; PMID:19505943; http://dx.doi.org/10.1093/bioinformatics/btp352 PubMed DOI PMC