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松苗红斑病菌(Phytophthora pluvialis)的分子检测,松苗红斑病的致病因子。

Molecular detection of Phytophthora pluvialis, the causal agent of red needle cast in Pinus radiata.

机构信息

Scion, New Zealand Forest Research Institute Ltd., Private Bag 3020, Rotorua 3046, New Zealand.

Scion, New Zealand Forest Research Institute Ltd., Private Bag 3020, Rotorua 3046, New Zealand.

出版信息

J Microbiol Methods. 2021 Oct;189:106299. doi: 10.1016/j.mimet.2021.106299. Epub 2021 Aug 8.

Abstract

BACKGROUND

Phytophthora pluvialis was first described in 2013 and is the causal agent of red needle cast (RNC) in Pinus radiata as well as infection in Douglas fir (Pseudotsuga menziesii). A species-specific PCR is necessary for detection of this pathogen and diagnosis of RNC.

OBJECTIVE

To design and validate a species-specific molecular assay for P. pluvialis using isolates from infected pine needles.

METHODS

Species-specific PCR primers were generated from the ras-related GTP-binding protein 1 gene (ypt1) gene sequence, concentrating on DNA regions unique to P. pluvialis, and real-time and quantitative polymerase chain reaction (qPCR) were used to detect P. pluvialis from both artificially inoculated and naturally infected samples.

RESULTS

The species-specific PCR assay was generated following P. pluvialis DNA sequence analysis. In vitro tests of the specificity of the probe-based, quantitative, polymerase chain reaction (qPCR) assay showed that no amplification was observed with other Phytophthora species including other closely-related clade 3 species, or with fungal species associated with pine or with pine DNA. The limit of detection of the qPCR assay was 2 pg/μl. When the qPCR assay was used to detect P. pluvialis in artificially-inoculated and naturally infected P. radiata needles, a PCR product was detected in all inoculated samples; the mean concentration ranges of P. pluvialis DNA in the inoculated and naturally infected samples tested were 5.9-124.5 pg/μl and 8.1-340.2 pg/μl, respectively. The assays described herein were used with serological diagnostic strips, providing the ability to identify to species level.

CONCLUSIONS

The assay described herein detects P. pluvialis with high specificity and sensitivity from a range of DNA samples, including those extracted from infected plant material and serological diagnostic strips. The ability to detect and identify P. pluvialis, from infected tissues directly, provides value and practicality to diagnostics, biosecurity and research.

摘要

背景

疫霉属 Pluvialis 于 2013 年首次被描述,是辐射松红针枯梢病菌,也是道格拉斯枞(Pseudotsuga menziesii)感染病菌。该病原体的检测和红针枯梢病的诊断需要使用物种特异性 PCR。

目的

利用感病松针中的分离株,为疫霉属 Pluvialis 设计并验证一种物种特异性分子检测方法。

方法

根据 ras 相关 GTP 结合蛋白 1 基因(ypt1)序列,生成物种特异性 PCR 引物,重点关注疫霉属 Pluvialis 特有的 DNA 区域,并使用实时定量聚合酶链反应(qPCR)检测人工接种和自然感染的样本中的疫霉属 Pluvialis。

结果

对疫霉属 Pluvialis DNA 序列进行分析后,生成了物种特异性 PCR 检测方法。基于探针的定量聚合酶链反应(qPCR)检测方法的特异性体外试验表明,与其他疫霉属物种(包括密切相关的 3 谱系物种)、与松属相关的真菌物种或松属 DNA 均无扩增。qPCR 检测方法的检测限为 2pg/μl。当 qPCR 检测方法用于检测人工接种和自然感染的辐射松针中的疫霉属 Pluvialis 时,所有接种样本均检测到 PCR 产物;接种和自然感染样本中疫霉属 Pluvialis DNA 的平均浓度范围分别为 5.9-124.5pg/μl 和 8.1-340.2pg/μl。本文描述的检测方法与血清学诊断条带一起使用,能够鉴定到种水平。

结论

该方法具有较高的特异性和灵敏度,可从多种 DNA 样本中检测到疫霉属 Pluvialis,包括从感染植物材料和血清学诊断条带中提取的样本。能够直接从感染组织中检测和鉴定疫霉属 Pluvialis,为诊断、生物安全和研究提供了价值和实用性。

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