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通过系统生物学方法解析人类疟原虫生物学的复杂性。

Decrypting the complexity of the human malaria parasite biology through systems biology approaches.

作者信息

Chahine Zeinab, Le Roch Karine G

机构信息

Department of Molecular, Cell and Systems Biology, University of California Riverside, Riverside, CA, United States.

出版信息

Front Syst Biol. 2022;2. doi: 10.3389/fsysb.2022.940321. Epub 2022 Sep 16.

Abstract

The human malaria parasite, falciparum, is a unicellular protozoan responsible for over half a million deaths annually. With a complex life cycle alternating between human and invertebrate hosts, this apicomplexan is notoriously adept at evading host immune responses and developing resistance to all clinically administered treatments. Advances in omics-based technologies, increased sensitivity of sequencing platforms and enhanced CRISPR based gene editing tools, have given researchers access to more in-depth and untapped information about this enigmatic micro-organism, a feat thought to be infeasible in the past decade. Here we discuss some of the most important scientific achievements made over the past few years with a focus on novel technologies and platforms that set the stage for subsequent discoveries. We also describe some of the systems-based methods applied to uncover gaps of knowledge left through single-omics applications with the hope that we will soon be able to overcome the spread of this life-threatening disease.

摘要

人类疟原虫恶性疟原虫是一种单细胞原生动物,每年导致超过50万人死亡。这种顶复门原虫具有复杂的生命周期,在人类和无脊椎动物宿主之间交替,它以善于逃避宿主免疫反应和对所有临床应用的治疗产生耐药性而闻名。基于组学的技术进步、测序平台灵敏度的提高以及基于CRISPR的基因编辑工具的改进,使研究人员能够获取有关这种神秘微生物更深入、未开发的信息,这一成果在过去十年被认为是不可行的。在这里,我们讨论过去几年取得的一些最重要的科学成就,重点关注为后续发现奠定基础的新技术和平台。我们还描述了一些基于系统的方法,这些方法用于揭示单一组学应用留下的知识空白,希望我们很快能够战胜这种危及生命的疾病的传播。

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