植物保护
植物保護
식물보호
PLANT PROTECTION
2014年
6期
116-121,125
,共7页
胡加谊%罗志文%李向宏%范鸿雁%周朋%章绍延%张治礼%刘志昕%何凡
鬍加誼%囉誌文%李嚮宏%範鴻雁%週朋%章紹延%張治禮%劉誌昕%何凡
호가의%라지문%리향굉%범홍안%주붕%장소연%장치례%류지흔%하범
菠萝凋萎相关病毒-1%TaqMan探针%实时荧光定量RT-PCR%检测
菠蘿凋萎相關病毒-1%TaqMan探針%實時熒光定量RT-PCR%檢測
파라조위상관병독-1%TaqMan탐침%실시형광정량RT-PCR%검측
PMWaV-1%TaqMan probe%real-time fluorescent quantitative RT-PCR%detection
菠萝凋萎相关病毒-1(Pineapplemealybugwiltassociatedvirus-1,PMWaV-1)是田间检出率最高的菠萝凋萎病毒。本研究根据PMWaV-1 CP基因保守序列设计特异性TaqMan探针和引物,建立并优化了PMWaV-1实时荧光定量RT-PCR检测方法。优化后的反应体系制备的标准曲线为y=-3.307×log x+38.18,相关系数r2为0.998。试验结果表明,该方法能特异性地检测PMWaV-1,对PMWaV-2、3和阴性对照均无反应;最低检测限达到40拷贝。重复性试验表明批内和批间变异系数均小于1.98%,是一种操作简便、特异性强、灵敏度高、重复性较好的PMWaV-1定量检测方法。样品检测结果表明PMWaV-1在菠萝植株老叶、嫩叶和吸芽中的病毒含量呈递减趋势。
菠蘿凋萎相關病毒-1(Pineapplemealybugwiltassociatedvirus-1,PMWaV-1)是田間檢齣率最高的菠蘿凋萎病毒。本研究根據PMWaV-1 CP基因保守序列設計特異性TaqMan探針和引物,建立併優化瞭PMWaV-1實時熒光定量RT-PCR檢測方法。優化後的反應體繫製備的標準麯線為y=-3.307×log x+38.18,相關繫數r2為0.998。試驗結果錶明,該方法能特異性地檢測PMWaV-1,對PMWaV-2、3和陰性對照均無反應;最低檢測限達到40拷貝。重複性試驗錶明批內和批間變異繫數均小于1.98%,是一種操作簡便、特異性彊、靈敏度高、重複性較好的PMWaV-1定量檢測方法。樣品檢測結果錶明PMWaV-1在菠蘿植株老葉、嫩葉和吸芽中的病毒含量呈遞減趨勢。
파라조위상관병독-1(Pineapplemealybugwiltassociatedvirus-1,PMWaV-1)시전간검출솔최고적파라조위병독。본연구근거PMWaV-1 CP기인보수서렬설계특이성TaqMan탐침화인물,건립병우화료PMWaV-1실시형광정량RT-PCR검측방법。우화후적반응체계제비적표준곡선위y=-3.307×log x+38.18,상관계수r2위0.998。시험결과표명,해방법능특이성지검측PMWaV-1,대PMWaV-2、3화음성대조균무반응;최저검측한체도40고패。중복성시험표명비내화비간변이계수균소우1.98%,시일충조작간편、특이성강、령민도고、중복성교호적PMWaV-1정량검측방법。양품검측결과표명PMWaV-1재파라식주로협、눈협화흡아중적병독함량정체감추세。
Pineapple mealybug wilt associated virus-1 (PMWaV-1 )highly infected pineapple in growing region in Hainan Province. A method of real-time fluorescent quantitative RT-PCR was established and optimized by using TaqMan probe and specific primers according to conserved sequence from the coat protein(CP)gene of PMWaV-1 . The standard curve of the method was y= -3.307×log x+38.18,r2= 0.998. The results showed that the meth-od was specific to PMWaV-1 and minimum detectable copies were 40. Both the variation coefficient of intra-assay and inter-assay for the method were less than 1.98% . Therefore,the established real-time fluorescent quantitative RT-PCR is a sample,specific,sensitive and reproducible method for PMWaV-1 detection. Detection analysis indi-cated that the content of PMWaV-1 in old leaves,younger leaves and suckers went down gradually.