Multiplex detection of Phytophthora spp. using the Fluidigm platform

Q4 Agricultural and Biological Sciences USDA Forest Service - Research Papers PNW-RP Pub Date : 2020-12-01 DOI:10.2478/frp-2020-0019
K. Sikora, T. Oszako, K. Kubiak, J. Nowakowska, T. Malewski
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Abstract

Abstract The genus Phytophthora plays an important role not only in agriculture but also in forest ecosystems. As the number of known Phytophthora species continues to grow, identifying new isolates in this genus has become increasingly challenging even by DNA sequencing. Therefore, the development of proper techniques for detection and identification is crucial for monitoring and control of these pathogens in the forestry sector. In recent years, new molecular methods using innovative approaches have indeed been developed. However, the majority of these methods was designed to detect single Phytophthora species. Techniques that are able to target multiple species would offer advantages, especially for the assessment of Phytophthora diversity in the environment. This paper describes a multiplex assay for the identification of eight Phytophthora isolates, down to the species level, based on a Fluidigm platform employing pyrosequencing. The obtained results showed that for an accurate determination of the species, it is sufficient to know the sequence of two markers, ITS and COX1. The sensitivity of this test is sufficient to identify Phytophthora in a pure culture. Unfortunately, analysis based on a pyrosequencing platform does not provide enough data to simultaneous identify multiple Phytophthora species in samples collected in the field. This problem could be resolved in the future by sequencing using more efficient platforms like Illumina or IonTorrent.
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利用Fluidigm平台对疫霉菌进行多重检测
疫霉属(Phytophthora)不仅在农业中发挥重要作用,而且在森林生态系统中也发挥着重要作用。随着已知疫霉菌种类的数量不断增长,即使通过DNA测序,在该属中鉴定新的分离株也变得越来越具有挑战性。因此,发展适当的检测和鉴定技术对于监测和控制林业部门的这些病原体至关重要。近年来,使用创新方法的新分子方法确实得到了发展。然而,这些方法大多被设计用于检测单一的疫霉物种。能够针对多个物种的技术将提供优势,特别是对环境中疫霉多样性的评估。本文描述了一种基于Fluidigm平台采用焦磷酸测序的多重检测方法,用于鉴定8种疫霉菌分离物,直至物种水平。结果表明,为了准确地确定该物种,只要知道ITS和COX1两个标记的序列就足够了。该试验的灵敏度足以在纯培养物中鉴定疫霉菌。不幸的是,基于焦磷酸测序平台的分析不能提供足够的数据来同时鉴定田间采集的样品中的多个疫霉菌物种。这个问题可以在未来通过使用更高效的测序平台如Illumina或IonTorrent来解决。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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USDA Forest Service - Research Papers PNW-RP
USDA Forest Service - Research Papers PNW-RP Agricultural and Biological Sciences-Forestry
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