Suppr超能文献

兔源原生动物艾美耳球虫全转录组图谱。

Global transcriptome landscape of the rabbit protozoan parasite Eimeria stiedae.

机构信息

Department of Parasitology, College of Veterinary Medicine, Sichuan Agricultural University, Chengdu, 611130, Sichuan, China.

Institute of Animal Genetics and Breeding, College of Animal Science and Technology, Sichuan Agricultural University, Chengdu, 611130, Sichuan, China.

出版信息

Parasit Vectors. 2021 Jun 7;14(1):308. doi: 10.1186/s13071-021-04811-5.

Abstract

BACKGROUND

Coccidiosis caused by Eimeria stiedae is a widespread and economically significant disease of rabbits. The lack of studies on the life-cycle development and host interactions of E. stiedae at the molecular level has hampered our understanding of its pathogenesis.

METHODS

In this study, we present a comprehensive transcriptome landscape of E. stiedae to illustrate its dynamic development from unsporulated oocysts to sporulated oocysts, merozoites, and gametocytes, and to identify genes related to parasite-host interactions during parasitism using combined PacBio single-molecule real-time and Illumina RNA sequencing followed by bioinformatics analysis and qRT-PCR validation.

RESULTS

In total, 12,582 non-redundant full-length transcripts were generated with an average length of 1808 bp from the life-cycle stages of E. stiedae. Pairwise comparisons between stages revealed 8775 differentially expressed genes (DEGs) showing highly significant description changes, which compiled a snapshot of the mechanisms underlining asexual and sexual biology of E. stiedae including oocyst sporulation between unsporulated and sporulated oocysts; merozoite replication between sporulated oocysts and merozoites; and gametophyte development and gamete generation between merozoites and gametocytes. Further, 248 DEGs were grouped into nine series clusters and five groups by expression patterns, and showed that parasite-host interaction-related genes predominated in merozoites and gametocytes and were mostly involved in steroid biosynthesis and lipid metabolism and carboxylic acid. Additionally, co-expression analyses identified genes associated with development and host invasion in unsporulated and sporulated oocysts and immune interactions during gametocyte parasitism.

CONCLUSIONS

This is the first study, to our knowledge, to use the global transcriptome profiles to decipher molecular changes across the E. stiedae life cycle, and these results not only provide important information for the molecular characterization of E. stiedae, but also offer valuable resources to study other apicomplexan parasites with veterinary and public significance.

摘要

背景

由斯氏艾美耳球虫引起的球虫病是一种广泛且具有重要经济意义的兔病。由于缺乏对斯氏艾美耳球虫在分子水平上的生命周期发育和宿主相互作用的研究,我们对其发病机制的理解受到了阻碍。

方法

在本研究中,我们展示了斯氏艾美耳球虫的综合转录组图谱,以说明其从未孢子化卵囊到孢子化卵囊、裂殖子和配子体的动态发育,并通过结合 PacBio 单分子实时和 Illumina RNA 测序,以及生物信息学分析和 qRT-PCR 验证,鉴定寄生虫-宿主相互作用过程中与寄生虫相关的基因。

结果

从斯氏艾美耳球虫的生命周期阶段共产生了 12582 个非冗余全长转录本,平均长度为 1808bp。阶段之间的成对比较显示了 8775 个差异表达基因(DEGs),这些基因的表达变化具有高度显著性,这些基因的表达变化构成了斯氏艾美耳球虫无性和有性生物学的机制快照,包括未孢子化卵囊和孢子化卵囊之间的卵囊孢子形成;孢子化卵囊和裂殖子之间的裂殖子复制;以及裂殖子和配子体之间的配子体发育和配子生成。此外,248 个 DEG 按表达模式分为九个系列簇和五个组,表明寄生虫-宿主相互作用相关基因在裂殖子和配子体中占主导地位,主要涉及甾体生物合成和脂质代谢以及羧酸。此外,共表达分析鉴定了与未孢子化卵囊和孢子化卵囊发育和宿主入侵以及配子体寄生期间免疫相互作用相关的基因。

结论

据我们所知,这是首次使用全转录组谱来破译斯氏艾美耳球虫生命周期中的分子变化,这些结果不仅为斯氏艾美耳球虫的分子特征提供了重要信息,也为研究其他具有兽医和公共意义的锥虫寄生虫提供了有价值的资源。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e954/8186055/8bdcf02ecca0/13071_2021_4811_Fig1_HTML.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验