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高分辨率单细胞测序疟疾寄生虫。

High-Resolution Single-Cell Sequencing of Malaria Parasites.

机构信息

Genetics Department, Texas Biomedical Research Institute, San Antonio, Texas.

Malawi-Wellcome-Liverpool-Wellcome Trust Clinical Research Programme, Chichiri, Blantyre, Malawi.

出版信息

Genome Biol Evol. 2017 Dec 1;9(12):3373-3383. doi: 10.1093/gbe/evx256.

Abstract

Single-cell genomics is a powerful tool for determining the genetic architecture of complex communities of unicellular organisms. In areas of high transmission, malaria patients are often challenged by the activities of multiple Plasmodium falciparum lineages, which can potentiate pathology, spread drug resistance loci, and also complicate most genetic analysis. Single-cell sequencing of P. falciparum would be key to understanding infection complexity, though efforts are hampered by the extreme nucleotide composition of its genome (∼80% AT-rich). To counter the low coverage achieved in previous studies, we targeted DNA-rich late-stage parasites by Fluorescence-Activated Cell Sorting and whole genome sequencing. Our method routinely generates accurate, near-complete capture of the 23 Mb P. falciparum genome (mean breadth of coverage 90.7%) at high efficiency. Data from 48 single-cell genomes derived from a polyclonal infection sampled in Chikhwawa, Malawi allowed for unambiguous determination of haplotype diversity and recent meiotic events, information that will aid public health efforts.

摘要

单细胞基因组学是确定单细胞生物复杂群落遗传结构的有力工具。在高传播地区,疟疾患者经常受到多种恶性疟原虫系的活动挑战,这可能会加剧病理学、传播耐药性基因座,并使大多数遗传分析复杂化。恶性疟原虫的单细胞测序对于理解感染的复杂性至关重要,尽管由于其基因组(约 80%的富含 AT)的极端核苷酸组成,这方面的工作受到了阻碍。为了克服之前研究中覆盖率低的问题,我们通过荧光激活细胞分选和全基因组测序,靶向富含 DNA 的晚期寄生虫。我们的方法通常能够以高效率准确地捕获 23 Mb 的恶性疟原虫基因组(平均覆盖广度为 90.7%),近乎完整。从马拉维奇克瓦瓦采集的多克隆感染中获得的 48 个单细胞基因组的数据,能够明确确定单倍型多样性和最近的减数分裂事件,这些信息将有助于公共卫生工作。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7874/5737330/dc630bc00cba/evx256f1.jpg

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