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用于检测和区分三种猫蠕形螨的系统发育关系及新的基因工具

Phylogenetic relationships and new genetic tools for the detection and discrimination of the three feline Demodex mites.

作者信息

Silbermayr Katja, Horvath-Ungerboeck Christa, Eigner Barbara, Joachim Anja, Ferrer Lluis

机构信息

Institute of Parasitology, Department of Pathobiology, Vetmeduni Vienna, Vienna, Austria,

出版信息

Parasitol Res. 2015 Feb;114(2):747-52. doi: 10.1007/s00436-014-4243-8. Epub 2014 Dec 3.

Abstract

Two feline Demodex mite species have been described as causative agents of feline demodicosis, until recently a third species was detected. We provide an updated analysis on the phylogenetic relationship of Demodex mites. In addition, we present the first qPCR assay for the detection and differentiation of all three feline mite species in a single reaction. Specimen of Demodex cati, Demodex gatoi, and the recently discovered third species were collected from skin scrapings and fecal flotation for DNA extraction, conventional PCR, sequencing, and alignment. A total of 24 sequences of the partial 16S rRNA gene were used to estimate the evolutionary divergence in a p-distance model and a maximum likelihood phylogenetic tree. For the qPCR assay, new primers and fluorescent probes for the simultaneous detection of all three feline Demodex mites were designed. A consensus fragment of 351 bp was phylogenetically analyzed. The third species sequence of our study shares 98.6 % similarity to the available sequence in GenBank®. It is most similar to D. gatoi (82.41 %) and most distant to the canine Demodex injai (78.28 %). In contrast, D. gatoi is most similar to human Demodex brevis (87.01 %). The multiplex qPCR detected and discriminated the three different mite species in one reaction. The detection limit is ≤1.4 ng of mite DNA. The three feline Demodex species have distinct genotypes and did not cluster in one genetic clade. The species differentiation and assessment of evolutionary relationships will ultimately support correct diagnostics and treatment approaches.

摘要

两种猫蠕形螨已被描述为猫蠕形螨病的病原体,直到最近又发现了第三种。我们提供了关于蠕形螨系统发育关系的最新分析。此外,我们还展示了首个在单一反应中检测和区分所有三种猫螨的qPCR检测方法。从皮肤刮屑和粪便漂浮物中收集猫蠕形螨、加氏蠕形螨和最近发现的第三种螨的样本,用于DNA提取、常规PCR、测序和比对。共使用24个部分16S rRNA基因序列,在p距离模型和最大似然系统发育树中估计进化分歧。对于qPCR检测,设计了用于同时检测所有三种猫蠕形螨的新引物和荧光探针。对一个351 bp的共有片段进行了系统发育分析。我们研究中的第三种螨的序列与GenBank®中可用序列的相似度为98.6%。它与加氏蠕形螨最相似(82.41%),与犬蠕形螨最不相似(78.28%)。相比之下,加氏蠕形螨与人类毛囊蠕形螨最相似(87.01%)。多重qPCR在一个反应中检测并区分了三种不同的螨。检测限为≤1.4 ng螨DNA。三种猫蠕形螨具有不同的基因型,并未聚集在一个遗传分支中。物种区分和进化关系评估最终将有助于正确的诊断和治疗方法。

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