Enzyme-Linked Immunosorbent Assay-Format Tissue Culture Infectious Dose-50 Test for Titrating Dengue Virus 英文参考文献.docVIP
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Enzyme-Linked Immunosorbent Assay-Format Tissue Culture Infectious Dose-50 Test for Titrating Dengue Virus 英文参考文献
Enzyme-LinkedImmunosorbentAssay-FormatTissue
CultureInfectiousDose-50TestforTitratingDengue
Virus
JieLi1,2,Dong-meiHu1,2,Xi-xiaDing1,2,YueChen1,2,Yu-xianPan1,2,Li-wenQiu1,2,Xiao-yanChe1,2
*
1CenterforClinicalLaboratory,ZhujiangHospital,SouthernMedicalUniversity,Guangzhou,People’sRepublicofChina,2KeyLaboratoryofPreventionandControlof
EmergingInfectiousDiseasesofGuangdongHigherEducationInstitutes,Guangzhou,People’sRepublicofChina
Abstract
Adenguenonstructuralprotein1(NS1)antigencaptureenzyme-linkedimmunosorbentassay(ELISA)-basedtissueculture
infectiousdose-50(TCID50)test(TCID50-ELISA)wasdevelopedasanalternativetothestandardplaqueassayfortitrating
denguevirus. Virustitersobtained byTCID50-ELISAwerecomparable tothoseobtainedby theplaque assayandbythe
traditionalTCID50-cytopathiceffect(CPE)test(TCID50-CPE),withabetterreproducibilityandalowercoefficientofvariation.
QuantitativecomparisonofTCID50-ELISAandTCID50-CPEresultedinacorrelationcoefficientof0.976.Moreover,thisnew
methodshowedawiderapplicationtoC6/36,VeroE6,BHK-21,andVerocellscomparedwithothertitrationmethods.In
summary,thenovelTCID50-ELISAmethoddescribedhereprovidesamorereliableandmoreaccuratealternativecompared
totheplaqueassayandTCID50-CPEfortitrationofdenguevirus.
Citation:LiJ,HuD-m,DingX-x,ChenY,PanY-x,etal.(2011)Enzyme-LinkedImmunosorbentAssay-FormatTissueCultureInfectiousDose-50TestforTitrating
DengueVirus.PLoSONE6(7):e22553.doi:10.1371/journal.pone.0022553
Editor:PedroLagerbladOliveira,UniversidadeFederaldoRiodeJaneiro,Brazil
ReceivedMarch11,2011;AcceptedJune24,2011;PublishedJuly25,2011
Copyright:?2011Lietal.Thisisanopen-accessarticledistributedunderthetermsoftheCreativeCommonsAttributionLicense,whichpermitsunrestricted
use,distribution,andreproductioninanymedium,providedtheoriginalauthorandsourcearecredited.
Funding: This work was supported by grantfrom the National Outstanding Young Scientist Foundation of China, grant 2009ZX10004-306 of the
NationalScienceandTechnologyMajorProjectofChina,a
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