中华实验和临床病毒学杂志
中華實驗和臨床病毒學雜誌
중화실험화림상병독학잡지
CHINESE JOURNAL OF EXPERIMENTAL AND CLINICAL VIROLOGY
2014年
5期
321-323
,共3页
李阿茜%李伟红%李建东%张硕%曲靖%李川%张全福%梁米芳%李德新
李阿茜%李偉紅%李建東%張碩%麯靖%李川%張全福%樑米芳%李德新
리아천%리위홍%리건동%장석%곡정%리천%장전복%량미방%리덕신
扎伊尔型埃博拉病毒%核蛋白%糖蛋白%实时荧光逆转录聚合酶链反应
扎伊爾型埃博拉病毒%覈蛋白%糖蛋白%實時熒光逆轉錄聚閤酶鏈反應
찰이이형애박랍병독%핵단백%당단백%실시형광역전록취합매련반응
Zaire Ebolavirus%Nucleoprotein%Glycoprotein%Real-time Revers trenscriptase polymerase chain reaction
目的 建立扎伊尔型埃博拉病毒的核酸检测方法,以期用于埃博拉出血热临床标本的检测.方法 针对扎伊尔型埃博拉病毒核蛋白和糖蛋白基因设计引物和探针,建立单重和双重实时荧光RT-PCR检测方法,利用体外转录病毒RNA和埃博拉病毒系列参考品RNA评价其敏感性,利用马尔堡病毒、健康人、登革热患者和发热伴血小板减少综合征患者血清评价其特异性.结果 所建立的实时荧光RT-PCR检测方法扩增效率在95%~105%,可特异性地检测扎伊尔型埃博拉病毒核蛋白和糖蛋白基因,与马尔堡病毒、登革热和发热伴血小板减少综合征病毒均无交叉反应,体外转录的病毒RNA可检出10~100拷贝/μl.双重检测方法通过细胞培养的扎伊尔型埃博拉病毒RNA验证,可检出100 pfu/ml病毒.结论 本研究建立的检测扎伊尔型埃博拉病毒的实时荧光RT-PCR方法具有良好的特异性和敏感性,可用于埃博拉出血热临床标本的检测.
目的 建立扎伊爾型埃博拉病毒的覈痠檢測方法,以期用于埃博拉齣血熱臨床標本的檢測.方法 針對扎伊爾型埃博拉病毒覈蛋白和糖蛋白基因設計引物和探針,建立單重和雙重實時熒光RT-PCR檢測方法,利用體外轉錄病毒RNA和埃博拉病毒繫列參攷品RNA評價其敏感性,利用馬爾堡病毒、健康人、登革熱患者和髮熱伴血小闆減少綜閤徵患者血清評價其特異性.結果 所建立的實時熒光RT-PCR檢測方法擴增效率在95%~105%,可特異性地檢測扎伊爾型埃博拉病毒覈蛋白和糖蛋白基因,與馬爾堡病毒、登革熱和髮熱伴血小闆減少綜閤徵病毒均無交扠反應,體外轉錄的病毒RNA可檢齣10~100拷貝/μl.雙重檢測方法通過細胞培養的扎伊爾型埃博拉病毒RNA驗證,可檢齣100 pfu/ml病毒.結論 本研究建立的檢測扎伊爾型埃博拉病毒的實時熒光RT-PCR方法具有良好的特異性和敏感性,可用于埃博拉齣血熱臨床標本的檢測.
목적 건립찰이이형애박랍병독적핵산검측방법,이기용우애박랍출혈열림상표본적검측.방법 침대찰이이형애박랍병독핵단백화당단백기인설계인물화탐침,건립단중화쌍중실시형광RT-PCR검측방법,이용체외전록병독RNA화애박랍병독계렬삼고품RNA평개기민감성,이용마이보병독、건강인、등혁열환자화발열반혈소판감소종합정환자혈청평개기특이성.결과 소건립적실시형광RT-PCR검측방법확증효솔재95%~105%,가특이성지검측찰이이형애박랍병독핵단백화당단백기인,여마이보병독、등혁열화발열반혈소판감소종합정병독균무교차반응,체외전록적병독RNA가검출10~100고패/μl.쌍중검측방법통과세포배양적찰이이형애박랍병독RNA험증,가검출100 pfu/ml병독.결론 본연구건립적검측찰이이형애박랍병독적실시형광RT-PCR방법구유량호적특이성화민감성,가용우애박랍출혈열림상표본적검측.
Objective To establish a method for Zaire Ebolavirus (ZEBOV) RNA detection and laboratory diagnosis of suspected ZEBOV infected cases.Methods Primers/probe sets for Nucleoprotein (NP) and Glycoprotein(GP) detection were designed and used to develop monoplex and duplex real-time RT-PCR assays.The sensitivity was evaluated by in vitro transcribed RNA and ZEBOV RNA reference,and the specificity was identified by Marburg virus,healthy human sera and sera from Dengue fever patients and Severe fever with thrombocytopenia syndrome (SFTS) patients.Results The developed real-time RT-PCR assay scould be used for ZEBOV NP and GP detection specifically,and the amplification efficiency was 95% -105%.There was no cross reaction with Marburg virus,Dengue fever virus and SFTS virus.The sensitivity was evaluated with serial dilutions of synthesized viral RNAs,and the results showed that in vitro transcribed RNA of 10-100 copies/μl could be detected.The developed duplex assay was further verified with extracted RNA of ZEBOV collected from cell culture,and viruses in titer of 100 pfu/ml could be successfully detected.Conclusion Real-time RT-PCR assays for ZEBOV detection were established in this study,and proved to be specific and sensitive,which can be used for laboratory detection of suspected human Ebola hemorrhagic fever cases.