Literature DB >> 15269386

Population structure and genetic variability within isolates of Grapevine fanleaf virus from a naturally infected vineyard in France: evidence for mixed infection and recombination.

Emmanuelle Vigne1, Marc Bergdoll2, Sébastien Guyader3, Marc Fuchs1.   

Abstract

The nematode-borne Grapevine fanleaf virus, from the genus Nepovirus in the family Comoviridae, causes severe degeneration of grapevines in most vineyards worldwide. We characterized 347 isolates from transgenic and conventional grapevines from two vineyard sites in the Champagne region of France for their molecular variant composition. The population structure and genetic diversity were examined in the coat protein gene by IC-RT-PCR-RFLP analysis with EcoRI and StyI, and nucleotide sequencing, respectively. RFLP data suggested that 55 % (191 of 347) of the isolates had a population structure consisting of one predominant variant. Sequencing data of 51 isolates representing the different restrictotypes confirmed the existence of mixed infection with a frequency of 33 % (17 of 51) and showed two major predominant haplotypes representing 71 % (60 of 85) of the sequence variants. Comparative nucleotide diversity among population subsets implied a lack of genetic differentiation according to host (transgenic vs conventional) or field site for most restrictotypes (17 of 18 and 13 of 18) and for haplotypes in most phylogenetic groups (seven of eight and six of eight), respectively. Interestingly, five of the 85 haplotypes sequenced had an intermediate divergence (0.036-0.066) between the lower (0.005-0.028) and upper range (0.083-0.138) of nucleotide variability, suggesting the occurrence of homologous RNA recombination. Sequence alignments clearly indicated a mosaic structure for four of these five variants, for which recombination sites were identified and parental lineages proposed. This is the first in-depth characterization of the population structure and genetic diversity in a nepovirus.

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Year:  2004        PMID: 15269386     DOI: 10.1099/vir.0.79904-0

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


  17 in total

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Authors:  John J Dennehy; Nicholas A Friedenberg; Yul W Yang; Paul E Turner
Journal:  Appl Environ Microbiol       Date:  2006-03       Impact factor: 4.792

4.  Distinct viral populations differentiate and evolve independently in a single perennial host plant.

Authors:  Chiraz Jridi; Jean-François Martin; Véronique Marie-Jeanne; Gérard Labonne; Stéphane Blanc
Journal:  J Virol       Date:  2006-03       Impact factor: 5.103

5.  Genetic diversity and biological characterization of sugarcane streak mosaic virus isolates from Iran.

Authors:  Zohreh Moradi; Mohsen Mehrvar; Ehsan Nazifi
Journal:  Virusdisease       Date:  2018-06-07

6.  Population genetic analysis of potato virus X based on the CP gene sequence.

Authors:  Mohammad Hajizadeh; Nemat Sokhandan-Bashir
Journal:  Virusdisease       Date:  2017-02-06

7.  The 50 distal amino acids of the 2AHP homing protein of Grapevine fanleaf virus elicit a hypersensitive reaction on Nicotiana occidentalis.

Authors:  Isabelle R Martin; Emmanuelle Vigne; François Berthold; Véronique Komar; Olivier Lemaire; Marc Fuchs; Corinne Schmitt-Keichinger
Journal:  Mol Plant Pathol       Date:  2017-05-15       Impact factor: 5.663

8.  Molecular Characterization of Phylogenetically Distinct Isolates of Grapevine fanleaf virus from Iran Based on 2A(HP) Gene.

Authors:  Nemat Sokhandan-Bashir; Azam Hooshmand; Afsaneh Delpasand-Khabazi
Journal:  Indian J Virol       Date:  2012-03-04

9.  Host species-dependent population structure of a pollen-borne plant virus, Cherry leaf roll virus.

Authors:  Kathrin Rebenstorf; Thierry Candresse; Marie Josée Dulucq; Carmen Büttner; Christian Obermeier
Journal:  J Virol       Date:  2006-03       Impact factor: 5.103

10.  An evolutionary analysis of the Secoviridae family of viruses.

Authors:  Jeremy R Thompson; Nitin Kamath; Keith L Perry
Journal:  PLoS One       Date:  2014-09-02       Impact factor: 3.240

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