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一种TaqMan检测法可准确检测和定量分析引起番茄枯萎病和腐烂病的病原菌。

A TaqMan Assay Allows an Accurate Detection and Quantification of spp., the Causal Agents of Tomato Wilt and Rot Diseases.

作者信息

Campos Maria Doroteia, Varanda Carla, Patanita Mariana, Amaro Ribeiro Joana, Campos Catarina, Materatski Patrick, Albuquerque André, Félix Maria do Rosário

机构信息

MED-Mediterranean Institute for Agriculture, Environment and Development & CHANGE-Global Change and Sustainability Institute, Institute for Advanced Studies and Research, Universidade de Évora, Pólo da Mitra, Ap. 94, 7006-554 Évora, Portugal.

MED-Mediterranean Institute for Agriculture, Environment and Development & CHANGE-Global Change and Sustainability Institute, Departamento de Fitotecnia, Escola de Ciências e Tecnologia, Universidade de Évora, Pólo da Mitra, Ap. 94, 7006-554 Évora, Portugal.

出版信息

Biology (Basel). 2023 Feb 8;12(2):268. doi: 10.3390/biology12020268.

Abstract

In tomato plants, spp. have been increasingly associated with several wilt and rot diseases that are responsible for severe yield losses. Here, we present a real-time PCR TaqMan MGB (Minor Groove Binder) assay to detect and discriminate spp. from other fungal species that affect tomato plants. The methodology used is based on the selective amplification of the internal transcribed spacer (ITS) region of spp. This assay revealed to be highly specific and sensitive for species, targeting only the 29 isolates from the 45 tested isolates associated to tomato diseases. Sensitivity was assessed with serial dilutions of genomic DNA, with the limit of detection of 3.05 pg. An absolute DNA quantification method was also established, based on the determination of the absolute number of target copies. Finally, the effectiveness of the assay was successfully validated with the detection and quantification of spp. in potentially infected tomato plants from an experimental field and in control plants grown under controlled conditions. The established methodology allows a reliable, sensitive, and reproducible estimation of accumulation in infected tomato plants, gaining new insights for disease control and providing an additional tool in the screening of resistant plants.

摘要

在番茄植株中,[具体物种]越来越多地与几种枯萎病和腐烂病相关联,这些病害会导致严重的产量损失。在此,我们提出一种实时荧光定量PCR TaqMan MGB(小沟结合物)检测方法,用于从影响番茄植株的其他真菌物种中检测和区分[具体物种]。所使用的方法基于对[具体物种]内部转录间隔区(ITS)区域的选择性扩增。该检测方法对[具体物种]具有高度特异性和敏感性,仅针对45个与番茄病害相关的测试分离株中的29个[具体物种]分离株。通过对[具体物种]基因组DNA的系列稀释来评估敏感性,检测限为3.05 pg。还基于靶标拷贝数的绝对测定建立了一种绝对DNA定量方法。最后,通过对来自试验田的潜在感染番茄植株和在受控条件下生长的对照植株中的[具体物种]进行检测和定量,成功验证了该检测方法的有效性。所建立的方法能够可靠、灵敏且可重复地估计感染番茄植株中[具体物种]的积累情况,为病害控制提供了新的见解,并为抗性植株的筛选提供了额外的工具。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/67c9/9953614/4b1f13c75294/biology-12-00268-g001.jpg

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