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首页> 外文期刊>African Journal of Biotechnology >Detection of potato leafroll virus isolated from potato fields in Tehran province in aphids by immunocapture reverse transcription polymerase chain reaction
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Detection of potato leafroll virus isolated from potato fields in Tehran province in aphids by immunocapture reverse transcription polymerase chain reaction

机译:免疫捕获逆转录聚合酶链反应检测德黑兰马铃薯田中马铃薯叶卷病毒

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摘要

The surveys conducted during 2006 and 2007 revealed the infection of the virus in potato fields in Tehran province. Due to the important roll of aphids in transmission of the virus, immunocapture reverse transcription polymerase chain reaction (IC-RT-PCR) and reverse transcription polymerase chain reaction (RT-PCR) was developed using potato leafroll virus?(PLRV) specific antibodies and specific primer pair (20 mer) located in the virus capsid gene to detect the virus in aphids. A 336-bp PCR product was detected from aphids (Myzus persicae) which had been fed on PLRV-infected plants. The PCR band was specific to PLRV as determined in PLRV-infected plants. This inquiry shows that this method is applicable to assess viroliferous nature of aphids in yellow -pan traps during season.
机译:2006年至2007年进行的调查显示,该病毒在德黑兰省的马铃薯田中受到感染。由于蚜虫在病毒传播中起着重要的作用,因此利用马铃薯卷叶病毒(PLRV)特异性抗体和免疫印迹技术开发了免疫捕获逆转录聚合酶链反应(IC-RT-PCR)和逆转录聚合酶链反应(RT-PCR)。位于病毒衣壳基因中的特异性引物对(20聚体),用于检测蚜虫中的病毒。从蚜虫(Myzus persicae)中检测到336bp的PCR产物,该蚜虫已经喂食了PLRV感染的植物。如在感染PLRV的植物中确定的,PCR带对PLRV具有特异性。该查询表明该方法适用于评估季节内黄盆陷井中蚜虫的有毒性质。

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