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挖掘人类宿主代谢组以增进对疟疾传播的理解。

Mining the Human Host Metabolome Toward an Improved Understanding of Malaria Transmission.

作者信息

Joice Cordy Regina

机构信息

Department of Biology, Wake Forest University, Winston-Salem, NC, United States.

Department of Microbiology and Immunology, Wake Forest School of Medicine, Winston-Salem, NC, United States.

出版信息

Front Microbiol. 2020 Feb 14;11:164. doi: 10.3389/fmicb.2020.00164. eCollection 2020.

DOI:10.3389/fmicb.2020.00164
PMID:32117175
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7033509/
Abstract

The big data movement has led to major advances in our ability to assess vast and complex datasets related to the host and parasite during malaria infection. While host and parasite genomics and transcriptomics are often the focus of many computational efforts in malaria research, metabolomics represents another big data type that has great promise for aiding our understanding of complex host-parasite interactions that lead to the transmission of malaria. Recent analyses of the complement of metabolites present in human blood, skin and breath suggest that host metabolites play a critical role in the transmission cycle of malaria. Volatile compounds released through breath and skin serve as attractants to mosquitoes, with malaria-infected hosts appearing to have unique profiles that further increase host attractiveness. Inside the host, fluctuations in the levels of certain metabolites in blood may trigger increased production of transmission-competent sexual stages (gametocytes), setting the stage for enhanced transmission of malaria from human to mosquito. Together, these recent discoveries suggest that metabolites of human blood, skin and breath play critical roles in malaria transmission. This review discusses recent advances in this area, with a focus on metabolites that have been identified to play a role in malaria transmission and methods that may lead to an improved understanding of malaria transmission.

摘要

大数据运动已使我们在评估与疟疾感染期间宿主和寄生虫相关的庞大而复杂数据集的能力方面取得了重大进展。虽然宿主和寄生虫基因组学及转录组学常常是疟疾研究中许多计算工作的重点,但代谢组学代表了另一种大数据类型,对于帮助我们理解导致疟疾传播的复杂宿主-寄生虫相互作用具有巨大前景。最近对人类血液、皮肤和呼出气体中存在的代谢物补充物进行的分析表明,宿主代谢物在疟疾传播周期中起着关键作用。通过呼出气体和皮肤释放的挥发性化合物充当蚊子的引诱剂,感染疟疾的宿主似乎具有独特的特征,这进一步增加了宿主的吸引力。在宿主体内,血液中某些代谢物水平的波动可能会触发具有传播能力的有性阶段(配子体)产量的增加,为疟疾从人类向蚊子的传播增强奠定基础。总之,这些最新发现表明,人类血液、皮肤和呼出气体中的代谢物在疟疾传播中起着关键作用。本综述讨论了该领域的最新进展,重点关注已确定在疟疾传播中起作用的代谢物以及可能有助于更好理解疟疾传播的方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c439/7033509/228e04da2e02/fmicb-11-00164-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c439/7033509/228e04da2e02/fmicb-11-00164-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c439/7033509/228e04da2e02/fmicb-11-00164-g001.jpg

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本文引用的文献

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Plasmodium falciparum sexual differentiation in malaria patients is associated with host factors and GDV1-dependent genes.疟原虫在疟疾患者中的有性分化与宿主因素和 GDV1 依赖性基因有关。
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