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多头绦虫基因组揭示了对多头蚴病的寄生机制和控制的理解。

The genome of tapeworm Taenia multiceps sheds light on understanding parasitic mechanism and control of coenurosis disease.

机构信息

State Key Laboratory of Veterinary Etiological Biology, Key Laboratory of Veterinary Parasitology of Gansu Province, Lanzhou Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Lanzhou, China.

Agricultural Genomic Institute, Chinese Academy of Agricultural Sciences, Shenzhen, China.

出版信息

DNA Res. 2018 Oct 1;25(5):499-510. doi: 10.1093/dnares/dsy020.

Abstract

Coenurosis, caused by the larval coenurus of the tapeworm Taenia multiceps, is a fatal central nervous system disease in both sheep and humans. Though treatment and prevention options are available, the control of coenurosis still faces presents great challenges. Here, we present a high-quality genome sequence of T. multiceps in which 240 Mb (96%) of the genome has been successfully assembled using Pacbio single-molecule real-time (SMRT) and Hi-C data with a N50 length of 44.8 Mb. In total, 49.5 Mb (20.6%) repeat sequences and 13, 013 gene models were identified. We found that Taenia spp. have an expansion of transposable elements and recent small-scale gene duplications following the divergence of Taenia from Echinococcus, but not in Echinococcus genomes, and the genes underlying environmental adaptability and dosage effect tend to be over-retained in the T. multiceps genome. Moreover, we identified several genes encoding proteins involved in proglottid formation and interactions with the host central nervous system, which may contribute to the adaption of T. multiceps to its parasitic life style. Our study not only provides insights into the biology and evolution of T. multiceps, but also identifies a set of species-specific gene targets for developing novel treatment and control tools for coenurosis.

摘要

多头蚴病由多头绦虫的幼虫多头蚴引起,是绵羊和人类中枢神经系统的一种致命疾病。尽管有治疗和预防措施,但多头蚴病的控制仍然面临巨大挑战。在这里,我们提供了多头绦虫的高质量基因组序列,使用 Pacbio 单分子实时 (SMRT) 和 Hi-C 数据成功组装了 240 Mb(96%)的基因组,N50 长度为 44.8 Mb。总共鉴定出 49.5 Mb(20.6%)的重复序列和 13013 个基因模型。我们发现,在多头绦虫与细粒棘球绦虫分化后,多头绦虫有转座元件的扩张和近期的小规模基因复制,但在细粒棘球绦虫基因组中没有,而与环境适应性和剂量效应相关的基因往往在多头绦虫基因组中过度保留。此外,我们鉴定了一些编码与节片形成和与宿主中枢神经系统相互作用相关蛋白的基因,这可能有助于多头绦虫适应其寄生生活方式。我们的研究不仅深入了解了多头绦虫的生物学和进化,还为开发针对多头蚴病的新型治疗和控制工具确定了一组种特异性基因靶标。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8dc4/6191302/1cb4fa6fba03/dsy020f1.jpg

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