中华检验医学杂志
中華檢驗醫學雜誌
중화검험의학잡지
CHINESE JOURNAL OF LABORATORY MEDICINE
2009年
4期
462-465
,共4页
吴荣辉%楼跃民%何建华%陈如昌%郭小妹%孙兰青%陈俊
吳榮輝%樓躍民%何建華%陳如昌%郭小妹%孫蘭青%陳俊
오영휘%루약민%하건화%진여창%곽소매%손란청%진준
螺杆菌%幽门%克拉霉素%抗药性%细菌%寡核苷酸序列分析
螺桿菌%幽門%剋拉黴素%抗藥性%細菌%寡覈苷痠序列分析
라간균%유문%극랍매소%항약성%세균%과핵감산서렬분석
Helicobacter pylori%Clarithromycin%Drug resistance,bacterial%Oligonucleofide array sequence analysis
目的 建立一种寡核苷酸微阵列检测幽门螺杆菌23S rRNA基因A2142G、A2143G及C2182T点突变的方法.方法 根据23S rRNA基因A2142G、A2143G及C2182T突变位点设计相应探针,样本经不对称PCR扩增后,其产物与芯片杂交.非荧光标记引物扩增PCR产物克隆至T载体,测序验证芯片结果,并结合临床最低抑菌浓度实验判断该方法的正确性.结果 寡核苷酸微阵列技术与测序检测幽门螺杆菌23S rRNA基因多态性结果完全一致.经培养及鉴定幽门螺杆菌阳性的54份标本,杂交结果显示A2142位点均为野生型(54/54);A2143G突变率为11.11%(6/54),尚未发现A2143C和A2143T的突变;C2182T突变率为12.96%(7/54),尚未发现C2182A和C2182G的突变,其余均为野生型,上述结果与菌株体外试验MIC结果完全一致.结论 建立一种寡核苷酸微阵列技术检测幽门螺杆菌克拉霉素耐药的23S rRNA基因多态性的方法,可以高通量并直接检测胃黏膜而不需进行细菌培养,推动个体化治疗方案的实施.
目的 建立一種寡覈苷痠微陣列檢測幽門螺桿菌23S rRNA基因A2142G、A2143G及C2182T點突變的方法.方法 根據23S rRNA基因A2142G、A2143G及C2182T突變位點設計相應探針,樣本經不對稱PCR擴增後,其產物與芯片雜交.非熒光標記引物擴增PCR產物剋隆至T載體,測序驗證芯片結果,併結閤臨床最低抑菌濃度實驗判斷該方法的正確性.結果 寡覈苷痠微陣列技術與測序檢測幽門螺桿菌23S rRNA基因多態性結果完全一緻.經培養及鑒定幽門螺桿菌暘性的54份標本,雜交結果顯示A2142位點均為野生型(54/54);A2143G突變率為11.11%(6/54),尚未髮現A2143C和A2143T的突變;C2182T突變率為12.96%(7/54),尚未髮現C2182A和C2182G的突變,其餘均為野生型,上述結果與菌株體外試驗MIC結果完全一緻.結論 建立一種寡覈苷痠微陣列技術檢測幽門螺桿菌剋拉黴素耐藥的23S rRNA基因多態性的方法,可以高通量併直接檢測胃黏膜而不需進行細菌培養,推動箇體化治療方案的實施.
목적 건립일충과핵감산미진렬검측유문라간균23S rRNA기인A2142G、A2143G급C2182T점돌변적방법.방법 근거23S rRNA기인A2142G、A2143G급C2182T돌변위점설계상응탐침,양본경불대칭PCR확증후,기산물여심편잡교.비형광표기인물확증PCR산물극륭지T재체,측서험증심편결과,병결합림상최저억균농도실험판단해방법적정학성.결과 과핵감산미진렬기술여측서검측유문라간균23S rRNA기인다태성결과완전일치.경배양급감정유문라간균양성적54빈표본,잡교결과현시A2142위점균위야생형(54/54);A2143G돌변솔위11.11%(6/54),상미발현A2143C화A2143T적돌변;C2182T돌변솔위12.96%(7/54),상미발현C2182A화C2182G적돌변,기여균위야생형,상술결과여균주체외시험MIC결과완전일치.결론 건립일충과핵감산미진렬기술검측유문라간균극랍매소내약적23S rRNA기인다태성적방법,가이고통량병직접검측위점막이불수진행세균배양,추동개체화치료방안적실시.
Objective To develop an oligonucleotide array to detect single nucleotide mutations in 23S rRNA gene.Methods Primers and probes targeting A2142G.A2143G and C2182T mutations in 23S rRNA gene were designed tp develop an oligonucleotide array.Samples were performed by an asymmetric PCR and the PCR products were hybridized with the specific DNA microarray chips.Non fluorescence-labeled PCR products were cloned into T vectors.The results of oligonucleofide array were confirmed by direct DNA sequencing and evaluated by minimal inhibitory concentration (MIC).Results The results obtained from oligonucleotide microarray were identical to those of direct sequencing.In 54 Helicobacter pylori samples,oligonucleotide microarray indicated that no A-to-C transition at 2142 was found,and the mutant rate of A2143G was 11.11 % (6/54),the mutant rate of C2182T was 12.96% (7/54).A2143C,A2143T,C2182A and C2182G mutations were not found.The other specimens were wild-type.All the above results were the same as that of MIC tests.Conclusions The oligonucleofide microarray is a reliable and accurate genotyping assay for clarithromycin-resistance of Helieobaeter pylofi.It is high-throughput screening method for gastric mucosa and improve the application of strategy for personalized therapy.