Comparative analysis of phosphorylated proteomes between plerocercoid and adult Spirometra mansoni reveals phosphoproteomic profiles of the medical tapeworm.

IF 3 2区 医学 Q1 PARASITOLOGY
Yong Yan Liu, Rui Jie Wang, Si Si Ru, Fei Gao, Wei Liu, Xi Zhang
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Abstract

Background: Plerocercoid larvae of the tapeworm Spirometra mansoni can infect both humans and animals, leading to severe parasitic zoonosis worldwide. Despite ongoing research efforts, our understanding of the developmental process of S. mansoni remains inadequate. To better characterize posttranslational regulation associated with parasite growth, development, and reproduction, a comparative phosphoproteomic study was conducted on the plerocercoid and adult stages of S. mansoni.

Methods: In this study, site-specific phosphoproteomic analysis was conducted via 4D label-free quantitative analysis technology to obtain primary information about the overall phosphorylation status of plerocercoids and adults.

Results: A total of 778 differentially abundant proteins (DAPs) were detected between adults and plerocercoids, of which 704 DAPs were upregulated and only 74 were downregulated. DAPs involved in metabolic activity were upregulated in plerocercoid larvae compared with adults, whereas DAPs associated with binding were upregulated in adults. Gene Ontology (GO) and Kyoto Encyclopedia of Genes (KEGG) analyses indicated that most DAPs involved in signal transduction and environmental information processing pathways were highly active in adults. DAPs upregulated in the plerocercoid group were enriched mainly in metabolic activities. The kinases PKACA, GSK3B, and smMLCK closely interact, suggesting potential active roles in the growth and development of S. mansoni.

Conclusions: The dataset presented in this study offers a valuable resource for forthcoming research on signaling pathways as well as new insights into functional studies on the molecular mechanisms of S. mansoni.

疟原虫和曼氏螺旋绦虫成虫磷酸化蛋白质组的比较分析揭示了医学绦虫的磷酸化蛋白质组特征。
背景:曼氏螺旋绦虫(Spirometra mansoni)的疟原虫幼虫可感染人类和动物,导致全球范围内严重的人畜共患寄生虫病。尽管研究工作一直在进行,但我们对曼氏螺旋绦虫发育过程的了解仍然不足。为了更好地描述与寄生虫的生长、发育和繁殖相关的翻译后调控,我们对曼氏沙门氏菌的稚虫期和成虫期进行了磷酸化蛋白质组学比较研究:在这项研究中,通过 4D 无标记定量分析技术进行了位点特异性磷酸化蛋白质组分析,以获得有关稚虫和成虫整体磷酸化状态的主要信息:结果:共检测到 778 个差异丰富蛋白(DAPs),其中 704 个上调,74 个下调。与成虫相比,参与代谢活动的 DAPs 在桡足类幼虫中上调,而与结合相关的 DAPs 在成虫中上调。基因本体(GO)和京都基因百科全书(KEGG)分析表明,大多数参与信号转导和环境信息处理途径的 DAPs 在成虫体内高度活跃。桡足类中上调的 DAPs 主要集中在代谢活动中。激酶 PKACA、GSK3B 和 smMLCK 密切相互作用,表明它们在曼氏沙门氏菌的生长发育过程中可能发挥着积极作用:本研究提供的数据集为即将开展的信号通路研究提供了宝贵的资源,也为曼氏沙门氏菌分子机制的功能研究提供了新的见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Parasites & Vectors
Parasites & Vectors 医学-寄生虫学
CiteScore
6.30
自引率
9.40%
发文量
433
审稿时长
1.4 months
期刊介绍: Parasites & Vectors is an open access, peer-reviewed online journal dealing with the biology of parasites, parasitic diseases, intermediate hosts, vectors and vector-borne pathogens. Manuscripts published in this journal will be available to all worldwide, with no barriers to access, immediately following acceptance. However, authors retain the copyright of their material and may use it, or distribute it, as they wish. Manuscripts on all aspects of the basic and applied biology of parasites, intermediate hosts, vectors and vector-borne pathogens will be considered. In addition to the traditional and well-established areas of science in these fields, we also aim to provide a vehicle for publication of the rapidly developing resources and technology in parasite, intermediate host and vector genomics and their impacts on biological research. We are able to publish large datasets and extensive results, frequently associated with genomic and post-genomic technologies, which are not readily accommodated in traditional journals. Manuscripts addressing broader issues, for example economics, social sciences and global climate change in relation to parasites, vectors and disease control, are also welcomed.
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