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Genotyping of a microsatellite locus to differentiate clinical Ostreid herpesvirus 1 specimens
Ostreid herpesvirus 1 (OsHV-1) is a DNA virus belonging to the Malacoherpesviridae family from the Herpesvirales order. OsHV-1 has been associated with mortality outbreaks in different bivalve species including the Pacific cupped oyster, Crassostrea gigas. Since 2008, massive mortality events have b...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3897894/ https://www.ncbi.nlm.nih.gov/pubmed/24410800 http://dx.doi.org/10.1186/1297-9716-45-3 |
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author | Renault, Tristan Tchaleu, Gwenaëlle Faury, Nicole Moreau, Pierrick Segarra, Amélie Barbosa-Solomieu, Valérie Lapègue, Sylvie |
author_facet | Renault, Tristan Tchaleu, Gwenaëlle Faury, Nicole Moreau, Pierrick Segarra, Amélie Barbosa-Solomieu, Valérie Lapègue, Sylvie |
author_sort | Renault, Tristan |
collection | PubMed |
description | Ostreid herpesvirus 1 (OsHV-1) is a DNA virus belonging to the Malacoherpesviridae family from the Herpesvirales order. OsHV-1 has been associated with mortality outbreaks in different bivalve species including the Pacific cupped oyster, Crassostrea gigas. Since 2008, massive mortality events have been reported among C. gigas in Europe in relation to the detection of a variant of OsHV-1, called μVar. Since 2009, this variant has been mainly detected in France. These results raise questions about the emergence and the virulence of this variant. The search for association between specific virus genetic markers and clinical symptoms is of great interest and the characterization of the genetic variability of OsHV-1 specimens is an area of growing interest. Determination of nucleotide sequences of PCR-amplified virus DNA fragments has already been used to characterize OsHV-1 specimens and virus variants have thus been described. However, the virus DNA sequencing approach is time-consuming in the high-scale format. Identification and genotyping of highly polymorphic microsatellite loci appear as a suitable approach. The main objective of the present study was the development of a genotyping method in order to characterise clinical OsHV-1 specimens by targeting a particular microsatellite locus located in the ORF4 area. Genotyping results were compared to sequences already available. An excellent correlation was found between the detected genotypes and the corresponding sequences showing that the genotyping approach allowed an accuraté discrimination between virus specimens. |
format | Online Article Text |
id | pubmed-3897894 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-38978942014-01-23 Genotyping of a microsatellite locus to differentiate clinical Ostreid herpesvirus 1 specimens Renault, Tristan Tchaleu, Gwenaëlle Faury, Nicole Moreau, Pierrick Segarra, Amélie Barbosa-Solomieu, Valérie Lapègue, Sylvie Vet Res Research Ostreid herpesvirus 1 (OsHV-1) is a DNA virus belonging to the Malacoherpesviridae family from the Herpesvirales order. OsHV-1 has been associated with mortality outbreaks in different bivalve species including the Pacific cupped oyster, Crassostrea gigas. Since 2008, massive mortality events have been reported among C. gigas in Europe in relation to the detection of a variant of OsHV-1, called μVar. Since 2009, this variant has been mainly detected in France. These results raise questions about the emergence and the virulence of this variant. The search for association between specific virus genetic markers and clinical symptoms is of great interest and the characterization of the genetic variability of OsHV-1 specimens is an area of growing interest. Determination of nucleotide sequences of PCR-amplified virus DNA fragments has already been used to characterize OsHV-1 specimens and virus variants have thus been described. However, the virus DNA sequencing approach is time-consuming in the high-scale format. Identification and genotyping of highly polymorphic microsatellite loci appear as a suitable approach. The main objective of the present study was the development of a genotyping method in order to characterise clinical OsHV-1 specimens by targeting a particular microsatellite locus located in the ORF4 area. Genotyping results were compared to sequences already available. An excellent correlation was found between the detected genotypes and the corresponding sequences showing that the genotyping approach allowed an accuraté discrimination between virus specimens. BioMed Central 2014 2014-01-10 /pmc/articles/PMC3897894/ /pubmed/24410800 http://dx.doi.org/10.1186/1297-9716-45-3 Text en Copyright © 2014 Renault et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Renault, Tristan Tchaleu, Gwenaëlle Faury, Nicole Moreau, Pierrick Segarra, Amélie Barbosa-Solomieu, Valérie Lapègue, Sylvie Genotyping of a microsatellite locus to differentiate clinical Ostreid herpesvirus 1 specimens |
title | Genotyping of a microsatellite locus to differentiate clinical Ostreid herpesvirus 1 specimens |
title_full | Genotyping of a microsatellite locus to differentiate clinical Ostreid herpesvirus 1 specimens |
title_fullStr | Genotyping of a microsatellite locus to differentiate clinical Ostreid herpesvirus 1 specimens |
title_full_unstemmed | Genotyping of a microsatellite locus to differentiate clinical Ostreid herpesvirus 1 specimens |
title_short | Genotyping of a microsatellite locus to differentiate clinical Ostreid herpesvirus 1 specimens |
title_sort | genotyping of a microsatellite locus to differentiate clinical ostreid herpesvirus 1 specimens |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3897894/ https://www.ncbi.nlm.nih.gov/pubmed/24410800 http://dx.doi.org/10.1186/1297-9716-45-3 |
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