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      Molecular characterization of closteroviruses infecting Cordyline fruticosa L. in Hawaii

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          Abstract

          In Hawaii, common green ti plants ( Cordyline fruticosa L.) have been shown to harbor Cordyline virus 1 (CoV-1) which, along with Little cherry virus 1 (LChV-1), and Grapevine leafroll-associated virus 7 (GLRaV-7), form a distinct clade within the family Closteroviridae. Preliminary work has indicated that, aside from CoV-1, three additional closteroviruses may infect common green ti plants in Hawaii. In this study, pyrosequencing was used to characterize the genomes of closteroviruses infecting a single common green ti plant. The sequence data confirmed the presence of CoV-1 as well as three additional closteroviruses. Although all four viruses had the same general genome organization, the sequence divergence between the RNA-dependent RNA polymerase, heat shock protein 70 homolog, and coat protein ranged from 22 to 61%, indicating these represent four distinct closterovirus species. The names CoV-2, CoV-3, and CoV-4 are proposed for the three new viruses. Phylogenetic analyses placed CoV-2, CoV-3, and CoV-4 in the same clade as CoV-1, LChV-1, and GLRaV-7.

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          GENETIC DIVERSITY AND EVOLUTION OF CLOSTEROVIRUSES.

          A Karasev (1999)
          The family Closteroviridae comprises more than 30 plant viruses with flexuous, filamentous virions and includes representatives with either mono- or bipartite positive-strand ssRNA genomes. Closteroviruses are transmitted semipersistently by insects from three families of Homoptera, in infected plants are associated with phloem tissue, and demonstrate an astonishing genetic diversity that suggests extensive, on-going evolution. Phylogenetic analyses of their replicative genes as well as the conserved HSP70 demonstrate that closteroviruses co-evolved with their insect vectors, resulting in three major lineages, i.e. aphid-, mealybug-, and whitefly-transmitted viruses. Closteroviruses apparently represent an ancient and diverse virus family that may pose threats to agriculture and needs serious attention.
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            The family Closteroviridae revised.

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              Genomic and biological analysis of Grapevine leafroll-associated virus 7 reveals a possible new genus within the family Closteroviridae.

              Deep sequencing analysis of an asymptomatic grapevine revealed a virome containing five RNA viruses and a viroid. Of these, Grapevine leafroll-associated virus 7 (GLRaV-7), an unassigned closterovirus, was by far the most prominently represented sequence in the analysis. Graft-inoculation of the infection to another grape variety confirmed the lack of the leafroll disease symptoms, even though GLRaV-7 could be detected in the inoculated indicator plants. A 16,496 nucleotide-long genomic sequence of this virus was determined from the deep sequencing data. Its genome architecture and the sequences encoding its nine predicted proteins were compared with those of other closteroviruses. The comparison revealed that two other viruses, Little cherry virus-1 and Cordyline virus-1 formed a well supported phylogenetic cluster with GLRaV-7. Copyright © 2011 Elsevier B.V. All rights reserved.
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                Author and article information

                Journal
                Front Microbiol
                Front Microbiol
                Front. Microbiol.
                Frontiers in Microbiology
                Frontiers Media S.A.
                1664-302X
                05 March 2013
                2013
                : 4
                : 39
                Affiliations
                Department of Plant and Environmental Protection Sciences, College of Tropical Agriculture and Human Resources, University of Hawaii Honolulu, HI, USA
                Author notes

                Edited by: Giovanni P. Martelli, University of Bari “Aldo Moro”, Italy

                Reviewed by: Marc Fuchs, Cornell University, USA; Pasquale Saldarelli, Istituto di Virologia Vegetale CNR, Italy

                *Correspondence: Michael J. Melzer, Department of Plant and Environmental Protection Sciences, College of Tropical Agriculture and Human Resources, University of Hawaii, 3190 Maile Way, St. John 310, Honolulu, HI 96822, USA. e-mail: melzer@ 123456hawaii.edu

                GenBank Accessions: JQ599282, JQ599283, JQ599284

                This article was submitted to Frontiers in Virology, a specialty of Frontiers in Microbiology.

                Article
                10.3389/fmicb.2013.00039
                3588190
                23467405
                6bfbbf43-9120-400e-84f8-1de90443f743
                Copyright © Melzer, Sugano, Uchida, Borth, Kawate and Hu.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in other forums, provided the original authors and source are credited and subject to any copyright notices concerning any third-party graphics etc.

                History
                : 31 December 2012
                : 15 February 2013
                Page count
                Figures: 2, Tables: 2, Equations: 0, References: 19, Pages: 6, Words: 0
                Categories
                Microbiology
                Original Research Article

                Microbiology & Virology
                pyrosequencing,closteroviridae,velarivirus, cordyline,ti ringspot
                Microbiology & Virology
                pyrosequencing, closteroviridae, velarivirus, cordyline, ti ringspot

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