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利用基因组学和基因组生物学来理解疟疾生物学。

Harnessing genomics and genome biology to understand malaria biology.

机构信息

Department of Immunology and Infectious Disease, Harvard School of Public Health, 665 Huntington Avenue, Boston, Massachusetts 02115, USA.

出版信息

Nat Rev Genet. 2012 Apr 12;13(5):315-28. doi: 10.1038/nrg3187.

DOI:10.1038/nrg3187
PMID:22495435
Abstract

Malaria is an important human disease and is the target of a global eradication campaign. New technological and informatics advancements in population genomics are being leveraged to identify genetic loci under selection in the malaria parasite and to find variants that are associated with key clinical phenotypes, such as drug resistance. This article provides a timely Review of how population-genetics-based strategies are being applied to Plasmodium falciparum both to identify genetic loci as key targets of interventions and to develop monitoring and surveillance tools that are crucial for the successful elimination and eradication of malaria.

摘要

疟疾是一种重要的人类疾病,也是全球消除运动的目标。人口基因组学中的新技术和信息学进展正在被利用来识别疟原虫中受选择影响的遗传基因座,并找到与关键临床表型(如耐药性)相关的变异。本文及时地综述了基于种群遗传学的策略如何应用于恶性疟原虫,以确定遗传基因座作为干预的关键靶点,并开发监测和监督工具,这对于成功消除和根除疟疾至关重要。

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Using CF11 cellulose columns to inexpensively and effectively remove human DNA from Plasmodium falciparum-infected whole blood samples.使用 CF11 纤维素柱从恶性疟原虫感染的全血样本中廉价且有效地去除人 DNA。
Malar J. 2012 Feb 10;11:41. doi: 10.1186/1475-2875-11-41.
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Imaging of Plasmodium liver stages to drive next-generation antimalarial drug discovery.
Genetic structure of apical membrane antigen-1 in Plasmodium falciparum isolates from Pakistan.
巴基斯坦疟原虫分离株顶膜抗原-1 的遗传结构。
Parasites Hosts Dis. 2024 Aug;62(3):302-312. doi: 10.3347/PHD.24028. Epub 2024 Aug 26.
4
Hyper-diverse antigenic variation and resilience to transmission-reducing intervention in falciparum malaria.恶性疟原虫的抗原高度多样化变异和对降低传播干预的恢复能力。
Nat Commun. 2024 Aug 26;15(1):7343. doi: 10.1038/s41467-024-51468-6.
5
From multiplicity of infection to force of infection for sparsely sampled populations at high transmission.从高传播率下稀疏抽样人群的感染复数到感染力
medRxiv. 2025 Mar 19:2024.02.12.24302148. doi: 10.1101/2024.02.12.24302148.
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