Jain R K, Pappu S S, Pappu H R, Culbreath A K, Todd J W
Department of Plant Pathology.
Department of Entomology.
Plant Dis. 1998 Aug;82(8):900-904. doi: 10.1094/PDIS.1998.82.8.900.
Tomato spotted wilt tospovirus (TSWV) is a major disease constraint to peanut, tomato, pepper, and tobacco production in Georgia. Rapid molecular diagnosis of TSWV infection in peanut and its molecular studies were severely hampered by the lack of practical and rapid procedures for the extraction and amplification of the genomic nucleic acid. To circumvent this technical constraint, we adapted an immunocapture-procedure (ICP) for enriching the peanut tissue extracts for TSWV, and combined the ICP with a single-buffer, one-tube reverse transcription polymerase chain reaction (RT-PCR) to achieve rapid and reliable amplification of TSWV sequences from peanut. Both leaf and root tissue of peanut provided PCR-quality templates. Immunocapture, RT, and PCR were done in the same tube, allowing higher throughput. The technique was applicable to a wide range of TSWV-susceptible crops such as tomato, pepper, tobacco, gloxinia, and impatiens. Primers derived from the nucleocapsid protein gene as well as from the large RNA of the viral genome were able to amplify the target sequences in a highly specific and reproducible manner. This approach facilitated rapid molecular typing of natural populations of TSWV in Georgia.
番茄斑萎病毒(TSWV)是佐治亚州花生、番茄、辣椒和烟草生产的主要病害限制因素。由于缺乏实用且快速的基因组核酸提取和扩增程序,花生中TSWV感染的快速分子诊断及其分子研究受到严重阻碍。为了克服这一技术限制,我们采用了一种免疫捕获程序(ICP)来富集花生组织提取物中的TSWV,并将ICP与单缓冲液、单管逆转录聚合酶链反应(RT-PCR)相结合,以实现从花生中快速可靠地扩增TSWV序列。花生的叶片和根组织都能提供适合PCR的模板。免疫捕获、逆转录和PCR在同一管中进行,从而实现了更高的通量。该技术适用于多种对TSWV敏感的作物,如番茄、辣椒、烟草、大岩桐和凤仙花。源自核衣壳蛋白基因以及病毒基因组大RNA的引物能够以高度特异性和可重复性的方式扩增目标序列。这种方法促进了佐治亚州TSWV自然种群的快速分子分型。