基于钙调素基因的黑曲霉和塔宾曲霉聚合酶链反应(PCR)鉴定。

A Susca, G Stea, G Mulè, G Perrone
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引用次数: 51

摘要

黑曲霉和塔宾曲霉属于黑曲霉科,通常存在于植物产品和加工食品中,如葡萄、谷物、咖啡和衍生产品。这两个物种很难通过经典的形态学标准来区分,并且已知一些分离株会产生赭曲霉毒素a。准确识别这两个物种对于避免毒理学污染和相关风险的高估非常重要。建立了一种基于聚合酶链反应(PCR)的鉴定和检测方法,利用钙调蛋白基因测序获得的分子差异来鉴定黑曲霉和图宾曲霉。设计了两对物种特异性引物,并对其进行了PCR鉴定。每组引物产生的物种特异性PCR产物长度分别为505 bp(图宾沙蚤)和245 bp(黑沙蚤),可用于多重PCR检测。在25微升的PCR反应体积中,使用两种物种的纯总DNA,该检测的灵敏度约为10 pg DNA。本研究描述的方法代表了一种快速可靠的方法来评估食品中两种产氧物种的存在。
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Polymerase chain reaction (PCR) identification of Aspergillus niger and Aspergillus tubingensis based on the calmodulin gene.

Aspergillus niger and A. tubingensis, species belonging to section Nigri, are commonly found in plant products and processed food, such as grapes, cereals, coffee, and derived products. These two species are very difficult to differentiate by classical morphological criteria and some isolates are known to produce ochratoxin A. The exact identification of these two species is very important to avoid the overestimation of toxicological contamination and related risks. A polymerase chain reaction (PCR)-based identification and detection assay was developed as a tool to identify A. niger and A. tubingensis, using molecular differences obtained by sequencing the calmodulin gene. Two pairs of species-specific primers were designed and empirically evaluated for PCR identification of A. niger and A. tubingensis. Species-specific PCR products generated by each primer set were 505 bp (A. tubingensis) and 245 bp (A. niger) in length, which could be potentially useful for a multiplex PCR assay. The sensitivity of this assay was about 10 pg DNA in a 25-microl PCR reaction volume, using pure total DNA of the two species. The method described in this study represents a rapid and reliable procedure to assess the presence in food products of two ochratoxigenic species of section Nigri.

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