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
2008年
4期
305-307
,共3页
孟庆玲%郭子杰%曹经瑗%毕胜利
孟慶玲%郭子傑%曹經瑗%畢勝利
맹경령%곽자걸%조경원%필성리
肝炎病毒,甲型%病毒浓缩%病毒检测%逆转录聚合酶链反应
肝炎病毒,甲型%病毒濃縮%病毒檢測%逆轉錄聚閤酶鏈反應
간염병독,갑형%병독농축%병독검측%역전록취합매련반응
Hepatitis A virus%Virus concentration%Virus detection%Reverse transcriptase polymerase reaction
目的 建立水、贝类、血液及唾液中甲型肝炎病毒核酸RT-PCR检测方法.方法 加入一定量甲肝病毒到贝类、水、血液及唾液标本中,贝类经研磨后,PEG沉淀浓缩;水直接经PEG沉淀浓缩;以上标本及血液、唾液标本用Trizol试剂提取核酸,套式RT-PCR检测甲肝病毒核酸.引物位于甲肝病毒结构区VP1-2A区.结果病毒培养液中能检测到0.1 TCID50甲肝病毒;水、血清及唾液中能检测到1TCID50甲肝病毒;毛蚶中能检测到1-10TCID50甲肝病毒.某地甲肝病毒污染的水及患者血清标本中检测到了甲肝病毒核酸,并进行了序列分析比对.结论 本研究建立的不同标本中甲型肝炎病毒核酸RT-PCR检测方法,敏感、特异、快速,具有广泛的应用价值,将为甲肝的溯源研究及分子流行病学研究打下理论基础及提供技术支撑.
目的 建立水、貝類、血液及唾液中甲型肝炎病毒覈痠RT-PCR檢測方法.方法 加入一定量甲肝病毒到貝類、水、血液及唾液標本中,貝類經研磨後,PEG沉澱濃縮;水直接經PEG沉澱濃縮;以上標本及血液、唾液標本用Trizol試劑提取覈痠,套式RT-PCR檢測甲肝病毒覈痠.引物位于甲肝病毒結構區VP1-2A區.結果病毒培養液中能檢測到0.1 TCID50甲肝病毒;水、血清及唾液中能檢測到1TCID50甲肝病毒;毛蚶中能檢測到1-10TCID50甲肝病毒.某地甲肝病毒汙染的水及患者血清標本中檢測到瞭甲肝病毒覈痠,併進行瞭序列分析比對.結論 本研究建立的不同標本中甲型肝炎病毒覈痠RT-PCR檢測方法,敏感、特異、快速,具有廣汎的應用價值,將為甲肝的溯源研究及分子流行病學研究打下理論基礎及提供技術支撐.
목적 건립수、패류、혈액급타액중갑형간염병독핵산RT-PCR검측방법.방법 가입일정량갑간병독도패류、수、혈액급타액표본중,패류경연마후,PEG침정농축;수직접경PEG침정농축;이상표본급혈액、타액표본용Trizol시제제취핵산,투식RT-PCR검측갑간병독핵산.인물위우갑간병독결구구VP1-2A구.결과병독배양액중능검측도0.1 TCID50갑간병독;수、혈청급타액중능검측도1TCID50갑간병독;모감중능검측도1-10TCID50갑간병독.모지갑간병독오염적수급환자혈청표본중검측도료갑간병독핵산,병진행료서렬분석비대.결론 본연구건립적불동표본중갑형간염병독핵산RT-PCR검측방법,민감、특이、쾌속,구유엄범적응용개치,장위갑간적소원연구급분자류행병학연구타하이론기출급제공기술지탱.
Objective To develop an extraction and concentration method for the detection of hepatitis Avirus (HAV) in shellfish, water, serum and saliva samples by nested RT-PCR. Methods HAV were artificially inoculated into the above samples, calm sample was extracted using glycine buffer pH9.5, PEG precipitation;water sample was PEG precipitated directly; then all the samples including serum and saliva samples were extracted using Trizol regent, followed by nested RT-PCR detection using primers from HAV VPI-2A region. Results The detection limit for HAV in cultured cell lysis was 0.1TCID50; in water, serum or salva sample was 1TCID50 respectively, in calm sample was 1-10 TCID50. HAV RNA was detected in water and sera samples collected from the HAV outbreak region, sequenced and analysis. Conclusion The method developed here is convenient,specific and capable of detecting low levels of HAV in different samples, would be useful for diagnostic laboratories in order to perform HAV analysis in cases of foedbome infections or for molecular epidemiology investigation of HAV outbreaks.