Genetic Control of Canine Leishmaniasis Genome-Wide Association Study and Genomic Selection Analysis 英文参考文献.docVIP
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Genetic Control of Canine Leishmaniasis Genome-Wide Association Study and Genomic Selection Analysis 英文参考文献
GeneticControlofCanineLeishmaniasis:Genome-Wide
AssociationStudyandGenomicSelectionAnalysis
JavierQuilez1,2*,Vero′nicaMart?′nez1,2,JohnA.Woolliams4,ArmandSanchez1,2,3,RicardoPong-Wong4,
LornaJ.Kennedy5,RupertJ.Quinnell6,WilliamE.R.Ollier5,XavierRoura7,Llu?′sFerrer7,LauraAltet2,3,
OlgaFrancino2,3
1DepartamentdeGene`ticaAnimal,CentredeRecercaenAgrigeno`mica(CRAG),UniversitatAuto`nomadeBarcelona,Barcelona,Spain,2DepartamentdeCie`nciaAnimali
delsAliments,FacultatdeVeterina`ria, UniversitatAuto`nomadeBarcelona,Barcelona,Spain,3ServeiVeterinarideGene`ticaMolecular,DepartamentdeCie`nciaAnimali
dels Aliments, Facultat de Veterina`ria, Universitat Auto`noma de Barcelona, Barcelona, Spain, 4The Roslin Institute and R(D)SVS, University of Edinburgh, Easter Bush,
Scotland,UnitedKingdom,5CentreforIntegratedGenomicMedicalResearch(CIGMR),UniversityofManchester,StopfordBuilding,OxfordRoad,Manchester,United
Kingdom,6InstituteofIntegrativeandComparativeBiology,UniversityofLeeds,Leeds,UnitedKingdom,7HospitalCl?′nicVeterinari,UniversitatAuto`nomadeBarcelona,
Barcelona,Spain
Abstract
Background:Thecurrentdiseasemodelforleishmaniasissuggeststhatonlyaproportionofinfectedindividualsdevelop
clinicaldisease,whileothersareasymptomaticallyinfectedduetoimmunecontrolofinfection.Thefactorsthatdetermine
whether individuals progress to clinical disease following Leishmania infection are unclear, although previous studies
suggest a role for host genetics. Our hypothesis was that canine leishmaniasis is a complex disease with multiple loci
responsiblefortheprogressionofthediseasefromLeishmaniainfection.
Methodology/Principal Findings: Genome-wide association and genomic selection approaches were applied to a
population-basedcase-controldatasetof219dogsfromasinglebreed(Boxer)genotypedfor,170,000SNPs.Firstly,we
aimed to identify individual disease loci; secondly, we quantified the genetic component of the observed phenotypic
variance;andthirdly,wetestedwhethergenome-wideSNPdatacouldaccuratelypredic
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