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基于孢子捕捉器和定量聚合酶链反应检测和估算孢子载量方法的开发

Development of a Method for Detecting and Estimating Spore Loads Based on Spore Traps and qPCR.

作者信息

Jiménez-Zapata Diana L, Quiroga-Pérez Manuela, Quiroz-Yepes Manuela, Marulanda-Tobón Alejandro, Álvarez Javier C, Mosquera-López Sandra

机构信息

Division of Natural Systems and Sustainability, School of Applied Sciences and Engineering, EAFIT University, Medellín 050021, Colombia.

CIBIOP Research Group, School of Applied Sciences and Engineering, EAFIT University, Medellín 050021, Colombia.

出版信息

J Fungi (Basel). 2022 Dec 28;9(1):47. doi: 10.3390/jof9010047.

Abstract

Frosty pod rot, caused by Moniliophthora roreri, is the most damaging disease of cacao in Latin America and, to better comprehend its epidemiology, we must understand its dissemination and proliferation. However, we do not know how M. roreri spores loads fluctuate in time and space due to the lack of a reliable technique to quantify M. roreri spores in the fields. Therefore, we developed a method that relies on spore traps and qPCR to detect and quantify M. roreri spore loads. This study demonstrated that the qPCR protocol can detect down to 0.025 ng of M. roreri DNA and quantify between 0.006 ng and 60 ng. Moreover, it demonstrated that qPCR protocol can detect and quantify DNA extracted from spore suspension and spore traps containing at least 2.9 × 104 M. roreri spores. However, the variability of the estimates for spore samples was high. Finally, we described a spore-trap device designed to carry spore traps in the field. The qPCR protocol and spore-trap device here developed will help in the understanding of the M. roreri dissemination patterns since they can be used to assess the environmental loads of M. roreri spore in cacao fields.

摘要

由可可球二孢菌引起的霜霉病是拉丁美洲对可可危害最大的病害,为了更好地理解其流行病学,我们必须了解其传播和扩散情况。然而,由于缺乏一种可靠的田间定量可可球二孢菌孢子的技术,我们并不清楚该病菌孢子数量在时间和空间上是如何波动的。因此,我们开发了一种基于孢子捕捉器和定量聚合酶链反应(qPCR)的方法来检测和定量可可球二孢菌的孢子数量。本研究表明,该qPCR方法能够检测低至0.025纳克的可可球二孢菌DNA,并能对0.006纳克至60纳克的DNA进行定量。此外,研究还表明,该qPCR方法能够检测和定量从孢子悬浮液以及含有至少2.9×10⁴个可可球二孢菌孢子的孢子捕捉器中提取的DNA。然而,孢子样本估计值的变异性很高。最后,我们描述了一种用于在田间携带孢子捕捉器的装置。此处开发的qPCR方法和孢子捕捉器装置将有助于了解可可球二孢菌的传播模式,因为它们可用于评估可可田间可可球二孢菌孢子的环境数量。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/84f9/9862605/85bed470f178/jof-09-00047-g001.jpg

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