肺炎支原体巢式PCR的优化ppt课件

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ComparisonofP1and16SrRNAgenesfordetectionofMycoplasmapneumoniaebyoptimizednestedPCRinadultpatientsinZhejiang,China汇报人:周子博

1Mycoplasmapneumoniaeisafrequentcauseofcommunity-acquiredpneumoniafor10-40%inchildrenandadults.BecauseofthetreatmentofM.pneumoniainfectionwithβ-lactamantibioticsisineffectiveandtheclinicalmanifestationsofM.pneumoniaeinfectionarecomplicatedandnonspecific,soarapid,sensitiveandspecificlaboratorytestisvitalforearlydiagnosisofM.pneumoniaeinfection.ConventionaltestsfordetectingM.pneumoniaehavetheirlimitations.Introduction

2IntroductionSeveralPCR-relatedmethodsprovideenhancedsensitivityandhavebeensuccessfullyappliedforresearchpurposessuchasnestedPCR.TheP1adhesiongeneandthe16SrRNAgenehavebeenutilizedwidelyinPCRtechniquesasthetargetsfordetectionofM.pneumoniae.Inthisstudy,wesoughttoidentifythemoresensitiveandspecifictarget(P1or16SrRNA)inM.pneumoniaedetectionandtoevaluatetheuseofnestedPCRforthediagnosisofMPinfectionfrompatientsinwhomM.pneumoniaewassuspected.

3MaterialsandmethodsStrainsandclinicalsamplesDNApreparationOrthogonalarraydesignOptimizationofsinglefactorconditionsNestedPCRsensitivitytestDetectionofclinicalsamples

4OrthogonalarraydesignFactorsLevels123Primer(μΜ)0.10.30.5Mg2+(mM)1.52.54Annealingtemperature(℃)58(54)60(56)62(58)DilutionmultipleNO50100Table1NestedPCRfactorsandtheirlevelsfororthogonalprojects(Theannealingtemperatureof16SrRNAgeneisexpressedinthebrackets)

5OrthogonalarraydesignFactorsReactionPrimer(μΜ)Mg2+(mM)AnnealingDilutionmultipletemperature(℃)10.11.558(54)NO20.12.560(56)5030.1462(58)10040.31.560(56)10050.32.562(58)NO60.3458(54)5070.51.562(58)5080.52.558(54)10090.5460(56)NOTable2OrthogonalarraydesignfornestedPCR(Theannealingtemperatureof16SrRNAgeneisexpressedinthebrackets)

6Figure1:ElectrophoresisanalysisofvariednestedPCRproductsofMycoplasmapneumoniaeFHwiththetargetoftheP1adhesion(16SrRNA)gene.M123456789100bp→150bp→←107bpM123456789144bp150bp→P1gene16SrRNA

7SinglefactorexperimentAtlast,wedeterminedthefinaloptimalnestedPCRreactionconditions:FortheP1gene,theoptimalcombinationofMg2+concentration3mM,primerconcentration0.3uM,annealingtemperature60℃,thefirstroundPCRproduct50-folddilution;Forthe16Sgene,themostexcellentcombinationofMg2+concentration3mM,primerconcentration0.3uM,annealingtemperature56℃,thefirstroundPCRproduct50-folddilution.P1gene16SrRNA

8NestedPCRsensitivitytestsensitivitiesofnestedPCRforM.pneumoniae:LaneM:DNAmarker.Lane1:20ngofM.pneumoniaeFHstrain;Lane2:10ng;Lane3:10-1ng;Lane4:10-2ng;Lane5:10-3ng;Lane6:10-4ng;Lane7:10-5ng;Lane8:10-6ng;Lane9:negativecontrol.M123456789P1gene:1pg12345678912345678916SrRNA;0.1pg

9DetectionofclinicalsamplesP1adhesiongene:(25/55;43.6%)

10Detectionofclinicalsamples16SrRNAgene(30/55;56.3%)

11discussionWiththedevelopmentofmolecularbiologytechniques,PCRtechnologyhasbecomethemostvaluablemethodforrapiddiagnosisofMycoplasmapneumoniaeinfection.BothP1adhesiongeneand16SrRNAgenearewidelyusedastargetsfordetectionofM.pneumoniaebyPCR.However,itisstillinconclusiveforwhichtargetisbetterandoureffortistofindthemostsuitableone.Inthisstudy,wejointedorthogonalexperimentandsinglefactorteststooptimizeseveralcrucialconditionsofnestedPCRandfinallyconcludedtheoptimumreactionconditionsofthetwotargets.Thenwedetectedthesensitivityofthetwotargetsonthebasisoftheoptimalconditionsandtheresultsshowedthatthe16SrRNAgeneismoresensitivethantheP1adhesiongene.Wealsopresentedastudybyusingclinicalspecimensfromadultpatientsandfoundthat16SrRNAgenehasahigherpositiveratethantheP1adhesiongene.Sothe16SrRNAgeneisthemostexcellenttargetfordetectionofM.pneumoniaebynestedPCR.

12discussionInthisstudy,weadoptednestedPCRtocomparethetwotargets.ThesuperiorsensitivityisthemajoradvantageofnestedPCR.ThesensitivitycanbeincreasedbynestedPCRbecauseitinvolvesthereamplificationofaPCRproductwithasecondprimerset.NestedPCRmayleadtoa103-foldincreaseinsensitivitythansingle-stepPCR,asnestedPCRenablesthedetectionof1-100fgofDNA,andsingle-stepPCRassayscanonlydetect10-100pgofDNA.Abele-Hornetal.candetect30-100fgofM.pneumoniaeDNAbynestedPCR,andthesensitivityis103-foldbetterthanthatforsingle-stepPCRandexceedsthatforantigencaptureenzymeimmunoassayandcultureby104-to105-fold.

13discussionAlthoughnestedPCRisarapidandsensitivemethodforearlydiagnosisofM.pneumoniaeinfection,theimpactofnestedPCRreactionconditionsisnumerousanditistime-consumingtofindtheoptimalcondition.Whatismore,onlyonthebasisoftheoptimumconditionscanobtainamoreaccurateandobjectiveresults.SoweadoptedtheorthogonalarraydesigntooptimizeseveralcrucialfactorsaffectingthenestedPCRusingthestandardstrainofM.pneumoniae,sinceorthogonaltestdesigncangreatlyshortenthetestnumberandcanquicklyarriveatamoreappropriatereactioncondition.Thenwealsoutilizedacompletelysinglefactortestdesignbasedontheresultsoftheorthogonaldesign.Atlast,thefinaloptimalreactionconditionsofnestedPCRaredeterminedbyintegratedtheresultsofthemethodsabove,sothecomparisonoftheP1adhesiongeneandthe16SrRNAgeneprimersunderthisoptimalconditioncanbemoreobjectivethanthatofotherlaboratories.

14discussionInourstudy,OrthogonalarraydesignwasadoptedtooptimizefourcommonfactorsaffectingthenestedPCR,whichweretheconcentrationofprimersandMg2+,dilutionmultipleofthefirstroundPCRproduct,annealingtemperature.AllofthemarethecriticalelementintheperformanceofnestedPCR.Firstly,throughthetestwefoundthatexcessivelylowprimerconcentrationcanreducePCRyieldandexcessivelyhighprimerconcentrationincreasetheprobabilityofmisprimingandgenerationsofnon-specificPCRproducts.Secondly,formourexperiments,IfMg2+concentrationwastoolow,theyieldofPCRproductcouldbereduced,sinceTapDNApolymerasesareMg2+-dependentenzymeanditissensitivetotheconcentrationofMg2+.Thirdly,ourresultsshowsthatpoorspecificityofamplifiedbandappearsatlowannealingtemperature,andweakenedamplifiedbandsathighannealingtemperature.ForthespecificityofPCRmainlydependsonannealingtemperatureandimprovetheannealingtemperaturewithinacertainrangecanincreasethespecificityofthePCRreaction.Lastly,wealsofoundthatalotofnon-specificbandsappearifnotdilution,thatwasprobablybecausethetemplateconcentrationofsecondroundofPCRisexcessivelyhigh.

15discussionThesensitivityofnestedPCRwastestedbyusingserialdilutions(1:10)ofM.pneumoniaeDNA,ourresultssuggestedthatthe16SrRNAgeneprimersweremoresensitivethantheP1adhesiongeneprimers,asthe16SrRNAgeneprimerscandetectupto0.1pgofM.pneumoniaeDNAandtheP1geneprimerscandetect1pgofM.pneumoniaeDNAatmost.OurfindingsarewellconfirmedtothestudybyMohamedNouretal,whofoundthatthefragmentintensityaftervisualinspectionofgelswasalwayshigherwith16SrDNAprimersthanwiththosedirectedtoP1adhesiongene,thisshowedthattheamplificationofthe16SrRNAgenebynestedPCRweremoresensitiveforthedetectionofM.pneumoniae.Thiswasmainlybecausethepresenceofapproximately103copiesof16SrRNApermycoplasmacellandthehighdegreeofconservationoftherRNAgenesallowingahighlyfixationofprimersonthetargetandleadtoahigherPCRyield.Whatismore,duetotheRNAisdestroyedmorerapidlythantheDNAafterthedeathofthemycoplasmacell,detectionofRNAprovidesfurtherevidenceofviablemycoplasmasinthespecimen.K.Loensetal.thoughtthattheP1adhesiongeneprimerswerefoundtobemoresensitivethanthe16SrRNAones.However,theycometothisconclusionmerelybyspeculation,nottocomparetheboth.

16discussionAccordingtoourresultsfromclinicaltest,16SrRNAgeneprovedclearlytobethebesttargetforthispurpose,yieldingapositivePCRresultin56.3%ofcases,whilethepositiveratewas43.6%fortheP1adhesiongene.TheresultsalsoshowedthattherewasanexcellentcorrespondenceofpositivesubjectsdetectedbytheP1adhesiongeneand16SrRNAgeneprimers,andthecoincidencerateofthetwogeneprimerscanreach76.4%(42/55),forbothP1adhesiongeneand16SrRNAgeneweretheidealtargetsforPCRasbothofthemwerethehighlyconservativerepetitivesequence.ThemajordifficultiesfortheinterpretationofthePCRdatewerethediscordantresult,ninepatientswerepositivebythe16SrRNAgeneprimersbutnegativebytheP1adhesiongeneprimersandfourpatientswerepositivebytheP1adhesiongenebutnegativebythe16SrRNAones.Theformermainlybecausethe16SrRNAgeneprimersaremoresensitivethantheP1adhesiongene,asitcanbeprovedbythesensitivetestweaccomplishedbefore.ThelatterpossiblyduetotheP1adhesiongeneprimersarelessspecificthanthatof16SrRNAones.

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《肺炎支原体巢式PCR的优化ppt课件》由会员上传分享,免费在线阅读,更多相关内容在行业资料-天天文库

ComparisonofP1and16SrRNAgenesfordetectionofMycoplasmapneumoniaebyoptimizednestedPCRinadultpatientsinZhejiang,China汇报人:周子博

1Mycoplasmapneumoniaeisafrequentcauseofcommunity-acquiredpneumoniafor10-40%inchildrenandadults.BecauseofthetreatmentofM.pneumoniainfectionwithβ-lactamantibioticsisineffectiveandtheclinicalmanifestationsofM.pneumoniaeinfectionarecomplicatedandnonspecific,soarapid,sensitiveandspecificlaboratorytestisvitalforearlydiagnosisofM.pneumoniaeinfection.ConventionaltestsfordetectingM.pneumoniaehavetheirlimitations.Introduction

2IntroductionSeveralPCR-relatedmethodsprovideenhancedsensitivityandhavebeensuccessfullyappliedforresearchpurposessuchasnestedPCR.TheP1adhesiongeneandthe16SrRNAgenehavebeenutilizedwidelyinPCRtechniquesasthetargetsfordetectionofM.pneumoniae.Inthisstudy,wesoughttoidentifythemoresensitiveandspecifictarget(P1or16SrRNA)inM.pneumoniaedetectionandtoevaluatetheuseofnestedPCRforthediagnosisofMPinfectionfrompatientsinwhomM.pneumoniaewassuspected.

3MaterialsandmethodsStrainsandclinicalsamplesDNApreparationOrthogonalarraydesignOptimizationofsinglefactorconditionsNestedPCRsensitivitytestDetectionofclinicalsamples

4OrthogonalarraydesignFactorsLevels123Primer(μΜ)0.10.30.5Mg2+(mM)1.52.54Annealingtemperature(℃)58(54)60(56)62(58)DilutionmultipleNO50100Table1NestedPCRfactorsandtheirlevelsfororthogonalprojects(Theannealingtemperatureof16SrRNAgeneisexpressedinthebrackets)

5OrthogonalarraydesignFactorsReactionPrimer(μΜ)Mg2+(mM)AnnealingDilutionmultipletemperature(℃)10.11.558(54)NO20.12.560(56)5030.1462(58)10040.31.560(56)10050.32.562(58)NO60.3458(54)5070.51.562(58)5080.52.558(54)10090.5460(56)NOTable2OrthogonalarraydesignfornestedPCR(Theannealingtemperatureof16SrRNAgeneisexpressedinthebrackets)

6Figure1:ElectrophoresisanalysisofvariednestedPCRproductsofMycoplasmapneumoniaeFHwiththetargetoftheP1adhesion(16SrRNA)gene.M123456789100bp→150bp→←107bpM123456789144bp150bp→P1gene16SrRNA

7SinglefactorexperimentAtlast,wedeterminedthefinaloptimalnestedPCRreactionconditions:FortheP1gene,theoptimalcombinationofMg2+concentration3mM,primerconcentration0.3uM,annealingtemperature60℃,thefirstroundPCRproduct50-folddilution;Forthe16Sgene,themostexcellentcombinationofMg2+concentration3mM,primerconcentration0.3uM,annealingtemperature56℃,thefirstroundPCRproduct50-folddilution.P1gene16SrRNA

8NestedPCRsensitivitytestsensitivitiesofnestedPCRforM.pneumoniae:LaneM:DNAmarker.Lane1:20ngofM.pneumoniaeFHstrain;Lane2:10ng;Lane3:10-1ng;Lane4:10-2ng;Lane5:10-3ng;Lane6:10-4ng;Lane7:10-5ng;Lane8:10-6ng;Lane9:negativecontrol.M123456789P1gene:1pg12345678912345678916SrRNA;0.1pg

9DetectionofclinicalsamplesP1adhesiongene:(25/55;43.6%)

10Detectionofclinicalsamples16SrRNAgene(30/55;56.3%)

11discussionWiththedevelopmentofmolecularbiologytechniques,PCRtechnologyhasbecomethemostvaluablemethodforrapiddiagnosisofMycoplasmapneumoniaeinfection.BothP1adhesiongeneand16SrRNAgenearewidelyusedastargetsfordetectionofM.pneumoniaebyPCR.However,itisstillinconclusiveforwhichtargetisbetterandoureffortistofindthemostsuitableone.Inthisstudy,wejointedorthogonalexperimentandsinglefactorteststooptimizeseveralcrucialconditionsofnestedPCRandfinallyconcludedtheoptimumreactionconditionsofthetwotargets.Thenwedetectedthesensitivityofthetwotargetsonthebasisoftheoptimalconditionsandtheresultsshowedthatthe16SrRNAgeneismoresensitivethantheP1adhesiongene.Wealsopresentedastudybyusingclinicalspecimensfromadultpatientsandfoundthat16SrRNAgenehasahigherpositiveratethantheP1adhesiongene.Sothe16SrRNAgeneisthemostexcellenttargetfordetectionofM.pneumoniaebynestedPCR.

12discussionInthisstudy,weadoptednestedPCRtocomparethetwotargets.ThesuperiorsensitivityisthemajoradvantageofnestedPCR.ThesensitivitycanbeincreasedbynestedPCRbecauseitinvolvesthereamplificationofaPCRproductwithasecondprimerset.NestedPCRmayleadtoa103-foldincreaseinsensitivitythansingle-stepPCR,asnestedPCRenablesthedetectionof1-100fgofDNA,andsingle-stepPCRassayscanonlydetect10-100pgofDNA.Abele-Hornetal.candetect30-100fgofM.pneumoniaeDNAbynestedPCR,andthesensitivityis103-foldbetterthanthatforsingle-stepPCRandexceedsthatforantigencaptureenzymeimmunoassayandcultureby104-to105-fold.

13discussionAlthoughnestedPCRisarapidandsensitivemethodforearlydiagnosisofM.pneumoniaeinfection,theimpactofnestedPCRreactionconditionsisnumerousanditistime-consumingtofindtheoptimalcondition.Whatismore,onlyonthebasisoftheoptimumconditionscanobtainamoreaccurateandobjectiveresults.SoweadoptedtheorthogonalarraydesigntooptimizeseveralcrucialfactorsaffectingthenestedPCRusingthestandardstrainofM.pneumoniae,sinceorthogonaltestdesigncangreatlyshortenthetestnumberandcanquicklyarriveatamoreappropriatereactioncondition.Thenwealsoutilizedacompletelysinglefactortestdesignbasedontheresultsoftheorthogonaldesign.Atlast,thefinaloptimalreactionconditionsofnestedPCRaredeterminedbyintegratedtheresultsofthemethodsabove,sothecomparisonoftheP1adhesiongeneandthe16SrRNAgeneprimersunderthisoptimalconditioncanbemoreobjectivethanthatofotherlaboratories.

14discussionInourstudy,OrthogonalarraydesignwasadoptedtooptimizefourcommonfactorsaffectingthenestedPCR,whichweretheconcentrationofprimersandMg2+,dilutionmultipleofthefirstroundPCRproduct,annealingtemperature.AllofthemarethecriticalelementintheperformanceofnestedPCR.Firstly,throughthetestwefoundthatexcessivelylowprimerconcentrationcanreducePCRyieldandexcessivelyhighprimerconcentrationincreasetheprobabilityofmisprimingandgenerationsofnon-specificPCRproducts.Secondly,formourexperiments,IfMg2+concentrationwastoolow,theyieldofPCRproductcouldbereduced,sinceTapDNApolymerasesareMg2+-dependentenzymeanditissensitivetotheconcentrationofMg2+.Thirdly,ourresultsshowsthatpoorspecificityofamplifiedbandappearsatlowannealingtemperature,andweakenedamplifiedbandsathighannealingtemperature.ForthespecificityofPCRmainlydependsonannealingtemperatureandimprovetheannealingtemperaturewithinacertainrangecanincreasethespecificityofthePCRreaction.Lastly,wealsofoundthatalotofnon-specificbandsappearifnotdilution,thatwasprobablybecausethetemplateconcentrationofsecondroundofPCRisexcessivelyhigh.

15discussionThesensitivityofnestedPCRwastestedbyusingserialdilutions(1:10)ofM.pneumoniaeDNA,ourresultssuggestedthatthe16SrRNAgeneprimersweremoresensitivethantheP1adhesiongeneprimers,asthe16SrRNAgeneprimerscandetectupto0.1pgofM.pneumoniaeDNAandtheP1geneprimerscandetect1pgofM.pneumoniaeDNAatmost.OurfindingsarewellconfirmedtothestudybyMohamedNouretal,whofoundthatthefragmentintensityaftervisualinspectionofgelswasalwayshigherwith16SrDNAprimersthanwiththosedirectedtoP1adhesiongene,thisshowedthattheamplificationofthe16SrRNAgenebynestedPCRweremoresensitiveforthedetectionofM.pneumoniae.Thiswasmainlybecausethepresenceofapproximately103copiesof16SrRNApermycoplasmacellandthehighdegreeofconservationoftherRNAgenesallowingahighlyfixationofprimersonthetargetandleadtoahigherPCRyield.Whatismore,duetotheRNAisdestroyedmorerapidlythantheDNAafterthedeathofthemycoplasmacell,detectionofRNAprovidesfurtherevidenceofviablemycoplasmasinthespecimen.K.Loensetal.thoughtthattheP1adhesiongeneprimerswerefoundtobemoresensitivethanthe16SrRNAones.However,theycometothisconclusionmerelybyspeculation,nottocomparetheboth.

16discussionAccordingtoourresultsfromclinicaltest,16SrRNAgeneprovedclearlytobethebesttargetforthispurpose,yieldingapositivePCRresultin56.3%ofcases,whilethepositiveratewas43.6%fortheP1adhesiongene.TheresultsalsoshowedthattherewasanexcellentcorrespondenceofpositivesubjectsdetectedbytheP1adhesiongeneand16SrRNAgeneprimers,andthecoincidencerateofthetwogeneprimerscanreach76.4%(42/55),forbothP1adhesiongeneand16SrRNAgeneweretheidealtargetsforPCRasbothofthemwerethehighlyconservativerepetitivesequence.ThemajordifficultiesfortheinterpretationofthePCRdatewerethediscordantresult,ninepatientswerepositivebythe16SrRNAgeneprimersbutnegativebytheP1adhesiongeneprimersandfourpatientswerepositivebytheP1adhesiongenebutnegativebythe16SrRNAones.Theformermainlybecausethe16SrRNAgeneprimersaremoresensitivethantheP1adhesiongene,asitcanbeprovedbythesensitivetestweaccomplishedbefore.ThelatterpossiblyduetotheP1adhesiongeneprimersarelessspecificthanthatof16SrRNAones.

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