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开发并验证了一种实时 PCR 检测方法,用于检测和定量土壤中的块菌。

Development and validation of a real-time PCR assay for detection and quantification of Tuber magnatum in soil.

机构信息

Dipartimento di Protezione e Valorizzazione Agroalimentare, Alma Mater Studiorum Università di Bologna, Bologna, Italy.

出版信息

BMC Microbiol. 2012 Jun 6;12:93. doi: 10.1186/1471-2180-12-93.

Abstract

BACKGROUND

Tuber magnatum, the Italian white truffle, is the most sought-after edible ectomycorrhizal mushroom. Previous studies report the difficulties of detecting its mycorrhizas and the widespread presence of its mycelium in natural production areas, suggesting that the soil mycelium could be a good indicator to evaluate its presence in the soil. In this study a specific real-time PCR assay using TaqMan chemistry was developed to detect and quantify T. magnatum in soil. This technique was then applied to four natural T. magnatum truffières located in different regions of Italy to validate the method under different environmental conditions.

RESULTS

The primer/probe sets for the detection and quantification of T. magnatum were selected from the ITS rDNA regions. Their specificity was tested in silico and using qualitative PCR on DNA extracted from 25 different fungal species. The T. magnatum DNA concentration was different in the four experimental truffières and higher in the productive plots. T. magnatum mycelium was however also detected in most of the non-productive plots. Ascoma production during the three years of the study was correlated with the concentration of T. magnatum DNA.

CONCLUSIONS

Taken together, these results suggest that the specific real-time PCR assay perfected in this study could be an useful tool to evaluate the presence and dynamics of this precious truffle in natural and cultivated truffières.

摘要

背景

块菌,意大利白松露菌,是最受欢迎的食用外生菌根真菌。先前的研究报告指出,检测其菌根和在自然生产区广泛存在的菌丝存在困难,这表明土壤菌丝可能是评估其在土壤中存在的良好指标。在这项研究中,使用 TaqMan 化学开发了一种特定的实时 PCR 检测方法,用于检测和定量土壤中的 T. magnatum。该技术随后应用于意大利四个不同地区的四个天然 T. magnatum 块菌产区,以在不同的环境条件下验证该方法。

结果

用于检测和定量 T. magnatum 的引物/探针集是从 ITS rDNA 区域中选择的。它们的特异性通过计算机模拟和对从 25 种不同真菌物种提取的 DNA 进行定性 PCR 进行了测试。四个实验块菌中的 T. magnatum DNA 浓度不同,在有产块菌的地块中浓度更高。然而,在大多数非产块菌地块中也检测到了 T. magnatum 菌丝。在研究的三年中,子实体的产生与 T. magnatum DNA 的浓度相关。

结论

综上所述,这些结果表明,本研究中完善的特定实时 PCR 检测方法可能是评估这种珍贵块菌在自然和栽培块菌产区中存在和动态的有用工具。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/61f6/3438110/046a8b295156/1471-2180-12-93-1.jpg

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