中华微生物学和免疫学杂志
中華微生物學和免疫學雜誌
중화미생물학화면역학잡지
CHINESE JOURNAL OF MICROBIOLOGY AND IMMUNOLOGY
2010年
4期
382-386
,共5页
易海华%何广会%房超%宋阳威%徐波%孙慧宇%王云飞%王伟%徐政%赵金伟
易海華%何廣會%房超%宋暘威%徐波%孫慧宇%王雲飛%王偉%徐政%趙金偉
역해화%하엄회%방초%송양위%서파%손혜우%왕운비%왕위%서정%조금위
金黄葡萄球菌%环介导等温扩增技术%快速检测
金黃葡萄毬菌%環介導等溫擴增技術%快速檢測
금황포도구균%배개도등온확증기술%쾌속검측
Staphyloccocus aureus%Loop-mediated isothermal amplification%Rapid detection
目的 探索建立一种快速的、简单的检测金黄葡萄球菌的环介导等温基因扩增方法(100p-mediated isothermal amplification,LAMP).方法 针对金黄葡萄球菌clfA基因保守序列,根据LAMP方法的原理,设计LAMP检测反应体系和程序,对方法的特异性、灵敏度、重复性及初始拷贝数的对数值与反应时间(荧光信号值为1×10~4时对应的时间)之间的线性关系进行评估.结果 使用LAMP方法可以在0.5 h内获得检测结果,LAMP检测技术的灵敏度高出经典PCR技术10倍以上,与其他相关致病菌无交叉反应,平均试验间变异系数小于5%,反应时间与模板浓度有良好的线性关系(r~2=0.9501),LAMP法检测临床样本中金黄葡萄球菌的灵敏度为100%,特异度为94.4%,符合性为96.6%.结论 该方法快速、灵敏、特异、操作简单、设备要求低的特点适合基层医疗卫生机构和现场查验机构的广泛应用.
目的 探索建立一種快速的、簡單的檢測金黃葡萄毬菌的環介導等溫基因擴增方法(100p-mediated isothermal amplification,LAMP).方法 針對金黃葡萄毬菌clfA基因保守序列,根據LAMP方法的原理,設計LAMP檢測反應體繫和程序,對方法的特異性、靈敏度、重複性及初始拷貝數的對數值與反應時間(熒光信號值為1×10~4時對應的時間)之間的線性關繫進行評估.結果 使用LAMP方法可以在0.5 h內穫得檢測結果,LAMP檢測技術的靈敏度高齣經典PCR技術10倍以上,與其他相關緻病菌無交扠反應,平均試驗間變異繫數小于5%,反應時間與模闆濃度有良好的線性關繫(r~2=0.9501),LAMP法檢測臨床樣本中金黃葡萄毬菌的靈敏度為100%,特異度為94.4%,符閤性為96.6%.結論 該方法快速、靈敏、特異、操作簡單、設備要求低的特點適閤基層醫療衛生機構和現場查驗機構的廣汎應用.
목적 탐색건립일충쾌속적、간단적검측금황포도구균적배개도등온기인확증방법(100p-mediated isothermal amplification,LAMP).방법 침대금황포도구균clfA기인보수서렬,근거LAMP방법적원리,설계LAMP검측반응체계화정서,대방법적특이성、령민도、중복성급초시고패수적대수치여반응시간(형광신호치위1×10~4시대응적시간)지간적선성관계진행평고.결과 사용LAMP방법가이재0.5 h내획득검측결과,LAMP검측기술적령민도고출경전PCR기술10배이상,여기타상관치병균무교차반응,평균시험간변이계수소우5%,반응시간여모판농도유량호적선성관계(r~2=0.9501),LAMP법검측림상양본중금황포도구균적령민도위100%,특이도위94.4%,부합성위96.6%.결론 해방법쾌속、령민、특이、조작간단、설비요구저적특점괄합기층의료위생궤구화현장사험궤구적엄범응용.
Objective To develop a method of loop-mediated isothermal amplification(LAMP) to Staphyloccocus aureus rapidly, specifically, sensitively and simply suited for the primary health agency. Methods According to conserved nucleotide of Staphyloccocus aureus and principle of LAMP, we designed a set of LAMP primers and set up an LAMP reaction system. We evaluated the specificity, sensitivity and re-peatability of the method. In addition,we evaluated the linearity between initial template copies 1g value and reaction time (the time when the fluorescent value is 1×10~4). Results The optimal assay showed that it was no cross-reaction with other closely related members of pathogens, and was 10 times more sensitive than PCR. The coefficient of variance between tests was less than 5% ,and the kinetics curves showed a good line-arity between initial template copies lg value and reaction time(r~2=0. 9501). The detection activity could be finished within 1 h with the sensitivity of LAMP was 100% and the specificity was 94.4%, and the accuracy was 96.6%. Conclusion These findings demonstrated that the LAMP had the potential clinical application for detection and differentiation of Staphyloccocus aureus in the public health agency for its sensitive, specific and simple feature.