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隧道尽头的一盏灯:一种用于快速、现场部署的南洋杉细菌性枯萎病病原体(Phytophthora agathidicida)检测方法。

A LAMP at the end of the tunnel: A rapid, field deployable assay for the kauri dieback pathogen, Phytophthora agathidicida.

机构信息

Bio-Protection Research Centre, Massey University, Palmerston North, New Zealand.

School of Fundamental Sciences, Massey University, Palmerston North, New Zealand.

出版信息

PLoS One. 2020 Jan 24;15(1):e0224007. doi: 10.1371/journal.pone.0224007. eCollection 2020.

Abstract

The root rot causing oomycete, Phytophthora agathidicida, threatens the long-term survival of the iconic New Zealand kauri. Currently, testing for this pathogen involves an extended soil bioassay that takes 14-20 days and requires specialised staff, consumables, and infrastructure. Here we describe a loop-mediated isothermal amplification (LAMP) assay for the detection of P. agathidicida that targets a portion of the mitochondrial apocytochrome b coding sequence. This assay has high specificity and sensitivity; it did not cross react with a range of other Phytophthora isolates and detected as little as 1 fg of total P. agathidicida DNA or 116 copies of the target locus. Assay performance was further investigated by testing plant tissue baits from flooded soil samples using both the extended soil bioassay and LAMP testing of DNA extracted from baits. In these comparisons, P. agathidicida was detected more frequently using the LAMP test. In addition to greater sensitivity, by removing the need for culturing, the hybrid baiting plus LAMP approach is more cost effective than the extended soil bioassay and, importantly, does not require a centralised laboratory facility with specialised staff, consumables, and equipment. Such testing will allow us to address outstanding questions about P. agathidicida. For example, the hybrid approach could enable monitoring of the pathogen beyond areas with visible disease symptoms, allow direct evaluation of rates and patterns of spread, and allow the effectiveness of disease control to be evaluated. The hybrid LAMP bioassay also has the potential to empower local communities to evaluate the pathogen status of local kauri stands, providing information for disease management and conservation initiatives.

摘要

引起根腐病的卵菌,即疫霉属(Phytophthora)的银莲花无性型(Phytophthora agathidicida),威胁着新西兰标志性的罗汉松的长期生存。目前,对这种病原体的检测需要进行为期 14-20 天的延长土壤生物测定,并且需要专业人员、耗材和基础设施。在这里,我们描述了一种针对线粒体细胞色素 b 编码序列部分的环介导等温扩增(LAMP)检测方法,用于检测 P. agathidicida。该检测方法具有高特异性和灵敏度;它与一系列其他疫霉属分离株没有交叉反应,并且可以检测到低至 1 fg 的总 P. agathidicida DNA 或 116 个目标基因座的拷贝数。通过使用延长土壤生物测定和从诱饵中提取的 DNA 的 LAMP 测试来测试来自水淹土壤样本的植物组织诱饵,进一步研究了该检测方法的性能。在这些比较中,使用 LAMP 测试更频繁地检测到 P. agathidicida。除了更高的灵敏度外,通过去除培养的需要,杂交诱饵加 LAMP 方法比延长土壤生物测定更具成本效益,并且重要的是,它不需要具有专业人员、耗材和设备的集中式实验室设施。这种检测将使我们能够解决关于 P. agathidicida 的悬而未决的问题。例如,该杂交方法可以使我们能够在有可见疾病症状的区域之外监测病原体,直接评估传播的速度和模式,并评估疾病控制的有效性。杂交 LAMP 生物测定也有可能使当地社区能够评估当地罗汉松林的病原体状况,为疾病管理和保护倡议提供信息。

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