Roy Subha Deep, Ramasamy Selvarajan, Obbineni Jagan M
School of Biosciences and Technology, Vellore Institute of Technology, Vellore, Tamil Nadu India.
School of Agricultural Innovations and Advanced Learning, Vellore Institute of Technology, Vellore, Tamil Nadu India.
Virusdisease. 2024 Jun;35(2):357-376. doi: 10.1007/s13337-024-00863-0. Epub 2024 May 11.
Precise and timely diagnosis of plant viruses is a prerequisite for the implementation of efficient management strategies, considering factors like globalization of trade and climate change facilitating the spread of viruses that lead to agriculture yield losses of billions yearly worldwide. Symptomatic diagnosis alone may not be reliable due to the diverse symptoms and confusion with plant abiotic stresses. It is crucial to detect plant viruses accurately and reliably and do so with little time. A complete understanding of the various detection methods is necessary to achieve this. Enzyme-linked immunosorbent assay (ELISA), has become more popular as a method for detecting viruses but faces limitations such as antibody availability, cost, sample volume, and time. Advanced techniques like polymerase chain reaction (PCR) have surpassed ELISA with its various sensitive variants. Over the last decade, nucleic acid-based molecular methods have gained popularity and have quickly replaced other techniques, such as serological techniques for detecting plant viruses due to their specificity and accuracy. Hence, this review enables the reader to understand the strengths and weaknesses of each molecular technique starting with PCR and its variations, along with various isothermal amplification followed by DNA microarrays, and next-generation sequencing (NGS). As a result of the development of new technologies, NGS is becoming more and more accessible and cheaper, and it looks possible that this approach will replace others as a favoured approach for carrying out regular diagnosis. NGS is also becoming the method of choice for identifying novel viruses.
The online version contains supplementary material available at 10.1007/s13337-024-00863-0.
考虑到贸易全球化和气候变化等因素促进了病毒传播,导致全球每年农业产量损失数十亿美元,准确及时地诊断植物病毒是实施有效管理策略的前提条件。仅靠症状诊断可能不可靠,因为症状多样且易与植物非生物胁迫混淆。准确、可靠且快速地检测植物病毒至关重要。要做到这一点,全面了解各种检测方法是必要的。酶联免疫吸附测定(ELISA)作为一种检测病毒的方法已变得更受欢迎,但面临抗体可用性、成本、样本量和时间等限制。像聚合酶链反应(PCR)这样的先进技术及其各种敏感变体已超越了ELISA。在过去十年中,基于核酸的分子方法因其特异性和准确性而受到欢迎,并迅速取代了其他技术,如检测植物病毒的血清学技术。因此,本综述使读者能够了解从PCR及其变体开始的每种分子技术的优缺点,以及各种等温扩增技术,随后是DNA微阵列和下一代测序(NGS)。由于新技术的发展,NGS越来越容易获得且成本更低,这种方法有可能取代其他方法成为常规诊断的首选方法。NGS也正成为鉴定新型病毒的首选方法。
在线版本包含可在10.1007/s13337-024-00863-0获取的补充材料。