首页> 美国卫生研究院文献>Ecology and Evolution >A new fast real‐time PCR method for the identification of three sibling Apodemus species (A. sylvaticus A. flavicollis and A. alpicola) in Italy
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A new fast real‐time PCR method for the identification of three sibling Apodemus species (A. sylvaticus A. flavicollis and A. alpicola) in Italy

机译:一种新的快速实时PCR方法用于鉴定意大利的三个兄弟姐妹姬鼠(A.sylvaticusA.flavicollis和A.alpicola)

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摘要

The identification of field mice Apodemus flavicollis, Apodemus sylvaticus, and Apodemus alpicola represents a challenge for field scientists due to their highly overlapping morphological traits and habitats. Here, we propose a new fast real‐time PCR method to discriminate the three species by species‐specific TaqMan assays. Primers and probes were designed based on the alignment of 54 cyt‐b partial sequences from 25 different European countries retrieved from GenBank. TaqMan assays were then tested on 133 samples from three different areas of Italy. Real‐time PCR analysis showed 92 samples classified as A. flavicollis, 13 as A. sylvaticus, and 28 as A. alpicola. We did not observe any double amplification and DNA sequencing confirmed species assignment obtained by the TaqMan assays. The method is implementable on different matrices (ear tissues, tail, and blood). It can be used on dead specimens or on alive animals with minimally invasive sampling, and given the high sensitivity, the assay may be also suitable for degraded or low‐DNA samples. The method proved to work well to discriminate between the species analyzed. Furthermore, it gives clear results (amplified or not) and it does not require any postamplification handling of PCR product, reducing the time needed for the analyses and the risk of carryover contamination. It therefore represents a valuable tool for field ecologists, conservationists, and epidemiologists.
机译:由于田鼠的形态学特征和栖息地高度重叠,因此它们对田鼠Apodmus flavicollis,姬鼠Apodemus sylvaticus和Apodemus alpicola的鉴定对田间科学家构成了挑战。在这里,我们提出了一种新的快速实时PCR方法,通过物种特异性TaqMan分析来区分这三种物种。基于比对来自GenBank的25个不同欧洲国家的54 cyt-b部分序列,设计了引物和探针。然后,对来自意大利三个不同地区的133个样品进行了TaqMan分析。实时PCR分析显示,有92个样品被分类为黄曲霉,13个分类为圆叶曲霉和28个分类为拟南芥。我们没有观察到通过TaqMan分析获得的任何双重扩增和DNA测序证实的物种分配。该方法可在不同的矩阵(耳朵组织,尾巴和血液)上实现。它可以用最少的侵入性样品用于死亡标本或活着的动物,并且具有高灵敏度,该测定法也可能适用于降解或低DNA样品。实践证明该方法可以很好地区分所分析的物种。此外,它提供清晰的结果(是否扩增),并且不需要对PCR产物进行任何扩增后处理,从而减少了分析所需的时间和残留污染的风险。因此,它对于现场生态学家,保护主义者和流行病学家而言是一种有价值的工具。

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