Literature DB >> 17657600

Complete nucleotide sequence of Nootka lupine vein-clearing virus.

Nancy L Robertson1, Fabien Côté, Christine Paré, Eric Leblanc, Michel G Bergeron, Denis Leclerc.   

Abstract

The complete genome sequence of Nootka lupine vein-clearing virus (NLVCV) was determined to be 4,172 nucleotides in length containing four open reading frames (ORFs) with a similar genetic organization of virus species in the genus Carmovirus, family Tombusviridae. The order and gene product size, starting from the 5'-proximal ORF consisted of: (1) polymerase/replicase gene, ORF1 (p27) and ORF1RT (readthrough) (p87), (2) movement proteins ORF2 (p7) and ORF3 (p9), and, (3) the 3'-proximal coat protein ORF4, (p37). The genomic 5'- and 3'-proximal termini contained a short (59 nt) and a relatively longer 405 nt untranslated region, respectively. The longer replicase gene product contained the GDD motif common to RNA-dependent RNA polymerases. Phylogenetically, NLVCV formed a subgroup with the following four carmoviruses when separately comparing the amino acids of the coat protein or replicase protein: Angelonia flower break virus (AnFBV), Carnation mottle virus (CarMV), Pelargonium flower break virus (PFBV), and Saguaro cactus virus (SgCV). Whole genome nucleotide analysis (percent identities) among the carmoviruses with NLVCV suggested a similar pattern. The species demarcation criteria in the genus Carmovirus for the amino acid sequence identity of the polymerase (<52%) and coat (<41%) protein genes restricted NLVCV as a distinct species, and instead, placed it as a tentative strain of CarMV, PFBV, or SgCV when both the polymerase and CP were used as the determining factors. In contrast, the species criteria that included different host ranges with no overlap and lack of serology relatedness between NLVCV and the carmoviruses, suggested that NLVCV was a distinct species. The relatively low cutoff percentages allowed for the polymerase and CP genes to dictate the inclusion/exclusion of a distinct carmovirus species should be reevaluated. Therefore, at this time we have concluded that NLVCV should be classified as a tentative new species in the genus Carmovirus, family Tombusviridae.

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Year:  2007        PMID: 17657600     DOI: 10.1007/s11262-007-0139-3

Source DB:  PubMed          Journal:  Virus Genes        ISSN: 0920-8569            Impact factor:   2.332


  29 in total

1.  Mutation analysis of cis-elements in the 3'- and 5'-untranslated regions of satellite tobacco necrosis virus strain C RNA.

Authors:  D H Bringloe; C W Pleij; R H Coutts
Journal:  Virology       Date:  1999-11-10       Impact factor: 3.616

2.  A comprehensive open reading frame phylogenetic analysis of isometric positive strand ssRNA plant viruses.

Authors:  G W Stuart; P K Moffett; R F Bozarth
Journal:  Arch Virol       Date:  2006-01-03       Impact factor: 2.574

3.  Analysis of sequences and predicted structures required for viral satellite RNA accumulation by in vivo genetic selection.

Authors:  C D Carpenter; A E Simon
Journal:  Nucleic Acids Res       Date:  1998-05-15       Impact factor: 16.971

4.  The coat protein of turnip crinkle virus suppresses posttranscriptional gene silencing at an early initiation step.

Authors:  Feng Qu; Tao Ren; T Jack Morris
Journal:  J Virol       Date:  2003-01       Impact factor: 5.103

Review 5.  Evolution and taxonomy of positive-strand RNA viruses: implications of comparative analysis of amino acid sequences.

Authors:  E V Koonin; V V Dolja
Journal:  Crit Rev Biochem Mol Biol       Date:  1993       Impact factor: 8.250

6.  Characterization and in vitro translation analysis of pelargonium flower break virus.

Authors:  J Díez; J F Marcos; V Pallás
Journal:  Arch Virol       Date:  1999       Impact factor: 2.574

7.  Use of highly conserved motifs in plant virus RNA polymerases as the tags for specific detection of carmovirus-related RNA-dependent RNA polymerase genes.

Authors:  E V Ryabov; R M Leiser; S K Zavriev
Journal:  Virology       Date:  1995-02-20       Impact factor: 3.616

8.  Complete nucleotide sequence and genome organization of Pelargonium flower break virus.

Authors:  P Rico; C Hernández
Journal:  Arch Virol       Date:  2003-11-13       Impact factor: 2.574

9.  3'-Terminal RNA secondary structures are important for accumulation of tomato bushy stunt virus DI RNAs.

Authors:  Marc R Fabian; Hong Na; Debashish Ray; K Andrew White
Journal:  Virology       Date:  2003-09-01       Impact factor: 3.616

10.  Primary structural comparison of RNA-dependent polymerases from plant, animal and bacterial viruses.

Authors:  G Kamer; P Argos
Journal:  Nucleic Acids Res       Date:  1984-09-25       Impact factor: 16.971

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  1 in total

1.  Metagenomic-Based Screening and Molecular Characterization of Cowpea-Infecting Viruses in Burkina Faso.

Authors:  Essowè Palanga; Denis Filloux; Darren P Martin; Emmanuel Fernandez; Daniel Gargani; Romain Ferdinand; Jean Zabré; Zakaria Bouda; James Bouma Neya; Mahamadou Sawadogo; Oumar Traore; Michel Peterschmitt; Philippe Roumagnac
Journal:  PLoS One       Date:  2016-10-20       Impact factor: 3.240

  1 in total

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