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同时进行 Cyathostomins 的蛋白质组指纹图谱和分子分析。

Concurrent Proteomic Fingerprinting and Molecular Analysis of Cyathostomins.

机构信息

Institute for Parasitology and Tropical Veterinary Medicine, Department of Veterinary Medicine, Freie Universität Berlin, 14163, Berlin, Germany.

Institute for Animal Hygiene and Environmental Health, Department of Veterinary Medicine, Freie Universität Berlin, 14163, Berlin, Germany.

出版信息

Proteomics. 2019 Apr;19(7):e1800290. doi: 10.1002/pmic.201800290.

DOI:10.1002/pmic.201800290
PMID:30786147
Abstract

Rapid, cost-effective, efficient, and reliable helminth species identification is of considerable importance to understand host-parasite interactions, clinical disease, and drug resistance. Cyathostomins (Nematoda: Strongylidae) are considered to be the most important equine parasites, yet research on this group is hampered by the large number of 50 morphologically differentiated species, their occurrence in mixed infections with often more than 10 species and the difficulties associated with conventional identification methods. Here, MALDI-TOF MS, previously successfully applied to identify numerous organisms, is evaluated and compared with conventional and molecular genetic approaches. A simple and robust protocol for protein extraction and subsequent DNA isolation allowing molecular confirmation of proteomic findings is developed, showing that MALDI-TOF MS can discriminate adult stages of the two closely related cyathostomin species Cylicostephanus longibursatus and Cylicostephanus minutus. Intraspecific variability of proteomic profiles within morphospecies demonstrated an identification of morphospecies with an accuracy of close to 100%. In contrast, three genospecies within C. minutus and sex-specific profiles within both morphospecies could not be reliably discriminated using MALDI-TOF MS. In conclusion, MALDI-TOF MS complemented by the molecular protocol is a reliable and efficient approach for cyathostomin species identification.

摘要

快速、经济、高效且可靠的寄生虫种鉴定对于理解宿主-寄生虫相互作用、临床疾病和耐药性至关重要。Cyathostomins(线虫:Strongylidae)被认为是最重要的马属寄生虫,但由于大量形态上分化的物种、它们与通常超过 10 种的混合感染以及与传统鉴定方法相关的困难,对该组的研究受到了阻碍。在这里,MALDI-TOF MS 被评估并与传统和分子遗传方法进行了比较,MALDI-TOF MS 以前已成功应用于鉴定许多生物体。开发了一种简单而稳健的蛋白质提取和随后的 DNA 分离方案,允许对蛋白质组学发现进行分子确认,结果表明 MALDI-TOF MS 可以区分两种密切相关的 Cyathostomin 物种 Cyclostephanus longibursatus 和 Cyclostephanus minutus 的成虫阶段。形态种内蛋白质组图谱的种内变异性表明,形态种的鉴定准确性接近 100%。相比之下,无法使用 MALDI-TOF MS 可靠地区分 C. minutus 中的三个基因种和两个形态种中的性别特异性图谱。总之,MALDI-TOF MS 辅以分子方案是一种可靠且高效的 Cyathostomin 种鉴定方法。

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