Grabensteiner Elvira, Bakonyi Tamás, Ritter Wolfgang, Pechhacker Hermann, Nowotny Norbert
Clinic for Avian, Reptile and Fish Medicine, Clinical Department for Farm Animals and Herd Health Management, University of Veterinary Medicine, Vienna, A-1210 Vienna, Austria.
J Invertebr Pathol. 2007 Mar;94(3):222-5. doi: 10.1016/j.jip.2006.11.006. Epub 2007 Jan 4.
A single-step multiple-target (multiplex) reverse transcription-PCR (RT-PCR) was developed for the simultaneous detection and differentiation of three economically important viruses of the honeybee Apis mellifera L.: Acute bee paralysis virus (ABPV), Black queen cell virus (BQCV) and Sacbrood virus (SBV). Three compatible sets of primers, specific for each virus, were designed in conserved regions of the viral genomes for use in a one-step (single tube) RT-PCR assay. The individual RT-PCR assays and the combined multiplex assay were optimized for highest sensitivity and specificity. The multiplex RT-PCR assay was tested on field samples collected from Austrian honeybee colonies. All three viruses were detected, and their identity was confirmed by sequencing of the PCR products. The described multiplex RT-PCR proved to be an accurate tool for rapid simultaneous detection of ABPV, BQCV and SBV directly in honeybee specimens.
开发了一种单步多靶标(多重)逆转录聚合酶链反应(RT-PCR),用于同时检测和区分蜜蜂(西方蜜蜂)的三种重要经济病毒:急性蜜蜂麻痹病毒(ABPV)、黑蜂王台病毒(BQCV)和囊状幼虫病毒(SBV)。针对每种病毒设计了三套兼容的引物,这些引物位于病毒基因组的保守区域,用于一步法(单管)RT-PCR检测。对单个RT-PCR检测和组合多重检测进行了优化,以实现最高的灵敏度和特异性。对从奥地利蜜蜂蜂群采集的田间样本进行了多重RT-PCR检测。检测到了所有三种病毒,并通过对PCR产物进行测序确认了它们的身份。所描述的多重RT-PCR被证明是一种直接在蜜蜂样本中快速同时检测ABPV、BQCV和SBV的准确工具。