Variations of genes copy number in populations of Bluetongue-virus

Viruses have the largest diversity of genome architectures. Among them, segmented viruses possess a genome divided in several chromosomes or segments, encapsidated together. The most prevalent hypothesis to expia in the evolution of this genome organisation is an increased ability for genetic exchanges. Recently a hypothesis has suggested that this genome organisation could have evolved to favour the regulation of gene copy number and thus gene expression at the population level. ln an infected host, a viral population is composed of different genotypes, including defective genotypes lacking specific segments. Under this new hypothesis, the segment copy number in the population differs among segments, and consequently among the genes they bear. This situation would lead to a differential expression of viral genes at the host level, influencing phenotype. Our study aims to test whether variations in segment copy number exist in populations of Bluetongue virus, whose genome harbour a segment number among the highest described. Bluetongue virus follows a complex life cycle involving compulsory alternation between insect vectors and ruminants. This virus could thus use different segment copy numbers to differentially regulate gene expression in its highly unrelated hasts. To test our hypothesis, we designed a QPCR assay for each of the 10 genomic segments in order to monitor quantitative variations in different hosts. We first isolated a BTV genotype (BTV4 serotype) from sheeps infected in Corsica in 2017. This isolate was used to infect two different cell lines, a mammalian line (VERO) and an insect cell line (KC). Gene copy number variation in segmented genome virus could be a key mechanism underlying their high adaptive capacity and supporting an alternative way of adaptation to host alternation. This study is a prelude to Bluetongue virus gene copy number variation monitoring with time, space and environmental variations.

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Main Authors: Moreau, Yannis, Breard, Emmanuel, Gil, Patricia, Loire, Etienne, Gutierrez, Serafin
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Published: ESEB
Online Access:http://agritrop.cirad.fr/588868/
http://agritrop.cirad.fr/588868/1/ID588868.pdf
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spelling dig-cirad-fr-5888682018-10-26T16:14:10Z http://agritrop.cirad.fr/588868/ http://agritrop.cirad.fr/588868/ Variations of genes copy number in populations of Bluetongue-virus. Moreau Yannis, Breard Emmanuel, Gil Patricia, Loire Etienne, Gutierrez Serafin. 2018. . Montpellier : ESEB, Résumé, 1 p. Joint Congress on Evolutionary Biology, Montpellier, France, 19 Août 2018/22 Août 2018.https://oral-and-poster-abstracts.europa-group.com/index/slide/abstract/1981 <https://oral-and-poster-abstracts.europa-group.com/index/slide/abstract/1981> Researchers Variations of genes copy number in populations of Bluetongue-virus Moreau, Yannis Breard, Emmanuel Gil, Patricia Loire, Etienne Gutierrez, Serafin eng 2018 ESEB Viruses have the largest diversity of genome architectures. Among them, segmented viruses possess a genome divided in several chromosomes or segments, encapsidated together. The most prevalent hypothesis to expia in the evolution of this genome organisation is an increased ability for genetic exchanges. Recently a hypothesis has suggested that this genome organisation could have evolved to favour the regulation of gene copy number and thus gene expression at the population level. ln an infected host, a viral population is composed of different genotypes, including defective genotypes lacking specific segments. Under this new hypothesis, the segment copy number in the population differs among segments, and consequently among the genes they bear. This situation would lead to a differential expression of viral genes at the host level, influencing phenotype. Our study aims to test whether variations in segment copy number exist in populations of Bluetongue virus, whose genome harbour a segment number among the highest described. Bluetongue virus follows a complex life cycle involving compulsory alternation between insect vectors and ruminants. This virus could thus use different segment copy numbers to differentially regulate gene expression in its highly unrelated hasts. To test our hypothesis, we designed a QPCR assay for each of the 10 genomic segments in order to monitor quantitative variations in different hosts. We first isolated a BTV genotype (BTV4 serotype) from sheeps infected in Corsica in 2017. This isolate was used to infect two different cell lines, a mammalian line (VERO) and an insect cell line (KC). Gene copy number variation in segmented genome virus could be a key mechanism underlying their high adaptive capacity and supporting an alternative way of adaptation to host alternation. This study is a prelude to Bluetongue virus gene copy number variation monitoring with time, space and environmental variations. conference_item info:eu-repo/semantics/conferenceObject Conference info:eu-repo/semantics/publishedVersion http://agritrop.cirad.fr/588868/1/ID588868.pdf text Cirad license info:eu-repo/semantics/openAccess https://agritrop.cirad.fr/mention_legale.html https://oral-and-poster-abstracts.europa-group.com/index/slide/abstract/1981 info:eu-repo/semantics/altIdentifier/purl/https://oral-and-poster-abstracts.europa-group.com/index/slide/abstract/1981
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description Viruses have the largest diversity of genome architectures. Among them, segmented viruses possess a genome divided in several chromosomes or segments, encapsidated together. The most prevalent hypothesis to expia in the evolution of this genome organisation is an increased ability for genetic exchanges. Recently a hypothesis has suggested that this genome organisation could have evolved to favour the regulation of gene copy number and thus gene expression at the population level. ln an infected host, a viral population is composed of different genotypes, including defective genotypes lacking specific segments. Under this new hypothesis, the segment copy number in the population differs among segments, and consequently among the genes they bear. This situation would lead to a differential expression of viral genes at the host level, influencing phenotype. Our study aims to test whether variations in segment copy number exist in populations of Bluetongue virus, whose genome harbour a segment number among the highest described. Bluetongue virus follows a complex life cycle involving compulsory alternation between insect vectors and ruminants. This virus could thus use different segment copy numbers to differentially regulate gene expression in its highly unrelated hasts. To test our hypothesis, we designed a QPCR assay for each of the 10 genomic segments in order to monitor quantitative variations in different hosts. We first isolated a BTV genotype (BTV4 serotype) from sheeps infected in Corsica in 2017. This isolate was used to infect two different cell lines, a mammalian line (VERO) and an insect cell line (KC). Gene copy number variation in segmented genome virus could be a key mechanism underlying their high adaptive capacity and supporting an alternative way of adaptation to host alternation. This study is a prelude to Bluetongue virus gene copy number variation monitoring with time, space and environmental variations.
format conference_item
author Moreau, Yannis
Breard, Emmanuel
Gil, Patricia
Loire, Etienne
Gutierrez, Serafin
spellingShingle Moreau, Yannis
Breard, Emmanuel
Gil, Patricia
Loire, Etienne
Gutierrez, Serafin
Variations of genes copy number in populations of Bluetongue-virus
author_facet Moreau, Yannis
Breard, Emmanuel
Gil, Patricia
Loire, Etienne
Gutierrez, Serafin
author_sort Moreau, Yannis
title Variations of genes copy number in populations of Bluetongue-virus
title_short Variations of genes copy number in populations of Bluetongue-virus
title_full Variations of genes copy number in populations of Bluetongue-virus
title_fullStr Variations of genes copy number in populations of Bluetongue-virus
title_full_unstemmed Variations of genes copy number in populations of Bluetongue-virus
title_sort variations of genes copy number in populations of bluetongue-virus
publisher ESEB
url http://agritrop.cirad.fr/588868/
http://agritrop.cirad.fr/588868/1/ID588868.pdf
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AT loireetienne variationsofgenescopynumberinpopulationsofbluetonguevirus
AT gutierrezserafin variationsofgenescopynumberinpopulationsofbluetonguevirus
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