Laboratory of Virology-Centre for Plant Virus Research, Institute of Experimental Botany of the Czech Academy of Sciences, Rozvojová 263, 165 02 Prague, Czech Republic.
Department of Experimental Plant Biology, Faculty of Science, Charles University in Prague, Albertov 6, 128 43 Prague, Czech Republic.
Viruses. 2022 Jan 31;14(2):298. doi: 10.3390/v14020298.
Reverse transcription PCR (RT-PCR) is a popular method for detecting RNA viruses in plants. RT-PCR is usually performed in a classical two-step procedure: in the first step, cDNA is synthesized by reverse transcriptase (RT), followed by PCR amplification by a thermostable polymerase in a separate tube in the second step. However, one-step kits containing multiple enzymes optimized for RT and PCR amplification in a single tube can also be used. Here, we describe an RT-PCR single-enzyme assay based on an RTX DNA polymerase that has both RT and polymerase activities. The expression plasmid pET_RTX_(exo-) was transferred to various genotypes that either compensated for codon bias (Rosetta-gami 2) or contained additional chaperones to promote solubility (BL21 (DE3) with plasmids pKJE8 or pTf2). The RTX enzyme was then purified and used for the RT-PCR assay. Several purified plant viruses (TMV, PVX, and PVY) were used to determine the efficiency of the assay compared to a commercial one-step RT-PCR kit. The RT-PCR assay with the RTX enzyme was validated for the detection of viruses from different genera using both total RNA and crude sap from infected plants. The detection endpoint of RTX-PCR for purified TMV was estimated to be approximately 0.01 pg of the whole virus per 25 µL reaction, corresponding to 6 virus particles/µL. Interestingly, the endpoint for detection of TMV from crude sap was also 0.01 pg per reaction in simulated crude plant extracts. The longest RNA fragment that could be amplified in a one-tube arrangement was 2379 bp long. The longest DNA fragment that could be amplified during a 10s extension was 6899 bp long. In total, we were able to detect 13 viruses from 11 genera using RTX-PCR. For each virus, two to three specific fragments were amplified. The RT-PCR assay using the RTX enzyme described here is a very robust, inexpensive, rapid, easy to perform, and sensitive single-enzyme assay for the detection of plant viruses.
逆转录聚合酶链反应(RT-PCR)是一种常用于检测植物中 RNA 病毒的方法。RT-PCR 通常在经典的两步法中进行:第一步,用逆转录酶(RT)合成 cDNA,然后在第二步中,在单独的试管中用热稳定聚合酶进行 PCR 扩增。然而,也可以使用包含在单个试管中针对 RT 和 PCR 扩增进行优化的多种酶的一步试剂盒。在这里,我们描述了一种基于具有 RT 和聚合酶活性的 RTX DNA 聚合酶的 RT-PCR 单酶检测方法。表达质粒 pET_RTX_(exo-)被转移到各种基因型中,这些基因型要么补偿密码子偏倚(Rosetta-gami 2),要么包含额外的伴侣蛋白以促进可溶性(带有质粒 pKJE8 或 pTf2 的 BL21 (DE3))。然后纯化 RTX 酶并用于 RT-PCR 检测。使用几种纯化的植物病毒(TMV、PVX 和 PVY)来确定与商业一步 RT-PCR 试剂盒相比,该测定的效率。使用来自不同属的总 RNA 和感染植物的粗提物验证了使用 RTX 酶的 RT-PCR 检测。纯化的 TMV 的 RTX-PCR 检测终点估计约为 25µL 反应中每 0.01pg 整个病毒,相当于 6 个病毒颗粒/µL。有趣的是,来自粗提物的 TMV 的检测终点在模拟的粗植物提取物中也是 0.01pg/反应。在单管排列中可以扩增的最长 RNA 片段长 2379bp。在 10s 延伸过程中可以扩增的最长 DNA 片段长 6899bp。总共,我们能够使用 RTX-PCR 从 11 个属中检测到 13 种病毒。对于每种病毒,都可以扩增 2 到 3 个特定片段。这里描述的使用 RTX 酶的 RT-PCR 检测是一种非常稳健、廉价、快速、易于操作和灵敏的单酶检测植物病毒的方法。