Silva Gonçalo, Oyekanmi Joshua, Nkere Chukwuemeka K, Bömer Moritz, Kumar P Lava, Seal Susan E
Natural Resources Institute, University of Greenwich, Chatham Maritime, Kent, ME4 4TB, UK.
International Institute of Tropical Agriculture (IITA), Oyo Road, PMB 5320, Ibadan, Nigeria.
Anal Biochem. 2018 Apr 1;546:17-22. doi: 10.1016/j.ab.2018.01.019. Epub 2018 Jan 31.
Potyviruses (genus Potyvirus; family Potyviridae) are widely distributed and represent one of the most economically important genera of plant viruses. Therefore, their accurate detection is a key factor in developing efficient control strategies. However, this can sometimes be problematic particularly in plant species containing high amounts of polysaccharides and polyphenols such as yam (Dioscorea spp.). Here, we report the development of a reliable, rapid and cost-effective detection method for the two most important potyviruses infecting yam based on reverse transcription-recombinase polymerase amplification (RT-RPA). The developed method, named 'Direct RT-RPA', detects each target virus directly from plant leaf extracts prepared with a simple and inexpensive extraction method avoiding laborious extraction of high-quality RNA. Direct RT-RPA enables the detection of virus-positive samples in under 30 min at a single low operation temperature (37 °C) without the need for any expensive instrumentation. The Direct RT-RPA tests constitute robust, accurate, sensitive and quick methods for detection of potyviruses from recalcitrant plant species. The minimal sample preparation requirements and the possibility of storing RPA reagents without cold chain storage, allow Direct RT-RPA to be adopted in minimally equipped laboratories and with potential use in plant clinic laboratories and seed certification facilities worldwide.
马铃薯Y病毒属病毒(马铃薯Y病毒属;马铃薯Y病毒科)分布广泛,是对经济影响最为重大的植物病毒属之一。因此,其准确检测是制定有效防控策略的关键因素。然而,这有时可能会出现问题,尤其是在含有大量多糖和多酚的植物物种中,如山药(薯蓣属)。在此,我们报告了一种基于逆转录重组酶聚合酶扩增(RT-RPA)技术,用于检测侵染山药的两种最重要马铃薯Y病毒属病毒的可靠、快速且经济高效的检测方法。所开发的方法名为“直接RT-RPA”,可直接从用简单且廉价的提取方法制备的植物叶片提取物中检测每种目标病毒,避免了高质量RNA的繁琐提取过程。直接RT-RPA能够在单一低温操作温度(37°C)下,30分钟内检测出病毒阳性样本,且无需任何昂贵的仪器设备。直接RT-RPA检测构成了从难处理的植物物种中检测马铃薯Y病毒属病毒的强大、准确、灵敏且快速的方法。对样本制备要求极低,且RPA试剂无需冷链储存,这使得直接RT-RPA能够在设备简陋的实验室中采用,并有望在全球植物临床实验室和种子认证机构中使用。