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多重RT-PCR结合植物mRNA特异性内参检测草莓属植物中四种蚜虫传播的草莓病毒。

Multiplex RT-PCR detection of four aphid-borne strawberry viruses in Fragaria spp. in combination with a plant mRNA specific internal control.

作者信息

Thompson J R, Wetzel S, Klerks M M, Vasková D, Schoen C D, Spak J, Jelkmann W

机构信息

BBA, Institut für Pflanzenschutz im Obstbau, Schwabenheimer Strasse 101, D-69221, Dossenheim, Germany.

出版信息

J Virol Methods. 2003 Aug;111(2):85-93. doi: 10.1016/s0166-0934(03)00164-2.

Abstract

The principal aphid-borne viruses infecting Strawberry (Fragaria spp.) Strawberry crinkle virus (SCV), Strawberry mild yellow edge virus (SMYEV), Strawberry mottle virus (SMoV) and Strawberry vein banding virus (SVBV) can cause serious crop losses. In this paper, a multiplex reverse transcriptase polymerase chain reaction (RT-PCR) method is described for the simultaneous detection of all four viruses in combination with a plant mRNA specific internal control which can be used as an indicator of the effectiveness of the extraction and RT-PCR. In total, 18 strawberry isolates infected naturally were analysed by this method. Every combination of RNA virus was able to be detected and a full complement of all four viruses were found together in three isolates, all taken from wild strawberry (Fragaria chiloensis (L.) Duch.) in Chile. The upper detection limit for the four viruses was at an extract dilution of 1/200. The broad applicability of the RNA specific internal control primers-which produced a PCR fragment of the expected size in 25 of 27 plant species tested-combined with improvements, made in extraction methods described provides potentially a standard method for comparable RT-PCR analyses in a wide variety of plant species.

摘要

主要的蚜虫传播病毒感染草莓(草莓属)——草莓皱缩病毒(SCV)、草莓轻型黄边病毒(SMYEV)、草莓斑驳病毒(SMoV)和草莓脉带病毒(SVBV),可导致严重的作物损失。本文描述了一种多重逆转录聚合酶链反应(RT-PCR)方法,用于同时检测这四种病毒,并结合一种植物mRNA特异性内部对照,该对照可用作提取和RT-PCR有效性的指标。总共用该方法分析了18个自然感染的草莓分离株。RNA病毒的每种组合都能被检测到,并且在三个分离株中同时发现了全部四种病毒,所有这些分离株均取自智利的野生草莓(智利草莓(Fragaria chiloensis (L.) Duch.))。这四种病毒的检测上限为提取物稀释1/200。RNA特异性内部对照引物在27种测试植物中的25种中产生了预期大小的PCR片段,其广泛适用性与所述提取方法的改进相结合,可能为多种植物物种的可比RT-PCR分析提供一种标准方法。

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