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Differentiation of banding patterns between Streptococcus mutans and Streptococcus sobrinus isolates in rep-PCR using ERIC primer

机译:使用ERIC引物在rep-PCR中区分变形链球菌和sobrinus链球菌分离株的条带模式

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Background:StreptococcusmutansandStreptococcussobrinusareconsideredtobeimportantbacterialspeciesintheinitiationofhumandentalcaries.Therefore,theestablishmentofareliablegenotypingmethodtodistinguishS.mutansfromS.sobrinusisofcentralimportance.Objective:Weassessedtheusefulnessofrepetitiveextragenicpalindromicpolymerasechainreaction(rep-PCR)usingERICprimerbandingpatternsindifferentiatingS.mutansandS.sobrinus.Design:FiveS.mutansandtwoS.sobrinusprototypestrainsand50clinicalisolates(38S.mutansserotypec,4S.sobrinusserotyped,and8S.sobrinusserotypeg)wereexamined.Thebandingpatternsofampliconsgeneratedwerecomparedamongtheprototypestrainsandclinicalisolates,tofindcommonbandsthatdistinguishS.mutansandS.sobrinus.Results:Multiplebandingpatternswereseenwithallstrainstested.TherepresentativestrainsofS.mutanstestedrevealedsixunique,strongbandsat2,000bp,1,700bp,1,400bp,1,100bp,850bp,and250bp,whereasS.sobrinushadsevenstrongbandsat2,000bp,1,800bp,1,100bp,900bp,800bp,600bp,and550bp.Thebandat1,100bpwastheonlybandthatwasobservedinbothS.mutansandS.sobrinus.Furthermore,mostclinicalS.mutansisolatesrevealedidenticalbandingpatterns.AllS.mutanshadampliconsat1,700bp,850bp,and250bp,whereasthoseofS.sobrinuswereat1,100bp,900bp,and800bp.Conclusions:Theseresultsindicatethatusingrep-PCRwiththeERICprimerscandistinguishbetweenS.mutansandS.sobrinus.Keywords:rep-PCR;mutansstreptococci;clinicalisolates;dentalcaries;amplicons(Published:2December2011)Citation:JournalofOralMicrobiology2011,3:7190-DOI:10.3402/jom.v3i0.7190
机译:背景:StreptococcusmutansandStreptococcussobrinusareconsideredtobeimportantbacterialspeciesintheinitiationofhumandentalcaries.Therefore,theestablishmentofareliablegenotypingmethodtodistinguishS.mutansfromS.sobrinusisofcentralimportance.Objective:Weassessedtheusefulnessofrepetitiveextragenicpalindromicpolymerasechainreaction(REP-PCR)usingERICprimerbandingpatternsindifferentiatingS.mutansandS.sobrinus.Design:FiveS.mutansandtwoS.sobrinusprototypestrainsand50clinicalisolates(38S.mutansserotypec,4S.sobrinusserotyped,and8S.sobrinusserotypeg)wereexamined.Thebandingpatternsofampliconsgeneratedwerecomparedamongtheprototypestrainsandclinicalisolates, tofindcommonbandsthatdistinguishS.mutansandS.sobrinus.Results:Multiplebandingpatternswereseenwithallstrainstested.TherepresentativestrainsofS.mutanstestedrevealedsixunique,strongbandsat2,000bp,1,700bp,1,400bp,1,100bp,850bp,and250bp,whereasS.sobrinushadsevenstrongbandsat2,000bp,1,800bp,1,100bp,900bp的,800bp的,600bp的,and550bp只有1,100bp的带宽bandthatwasobservedinbothS.mutansandS.sobrinus.Furthermore,mostclinicalS.mutansisolatesrevealedidenticalbandingpatterns.AllS.mutanshadampliconsat1,700bp,850bp,and250bp,whereasthoseofS.sobrinuswereat1,100bp,900bp的,and800bp.Conclusions:Theseresultsindicatethatusingrep-PCRwiththeERICprimerscandistinguishbetweenS.mutansandS.sobrinus.Keywords:REP-PCR; mutansstreptococci;临床分离株;牙齿保护剂; amplicons(发表时间:2011年12月2日)

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