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本文引用的文献

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Submicroscopic infection in Plasmodium falciparum-endemic populations: a systematic review and meta-analysis.恶性疟原虫流行地区的亚显微感染:一项系统评价与荟萃分析。
J Infect Dis. 2009 Nov 15;200(10):1509-17. doi: 10.1086/644781.
3
Heritability of antibody isotype and subclass responses to Plasmodium falciparum antigens.抗体同种型和亚类对疟原虫抗原反应的遗传力。
PLoS One. 2009 Oct 8;4(10):e7381. doi: 10.1371/journal.pone.0007381.
4
The impact of pedigree structure on heritability estimates.系谱结构对遗传力估计值的影响。
Hum Hered. 2009;68(4):243-51. doi: 10.1159/000228922. Epub 2009 Jul 22.
5
A world malaria map: Plasmodium falciparum endemicity in 2007.一幅世界疟疾地图:2007年恶性疟原虫的流行情况
PLoS Med. 2009 Mar 24;6(3):e1000048. doi: 10.1371/journal.pmed.1000048.
6
A global network for investigating the genomic epidemiology of malaria.一个用于调查疟疾基因组流行病学的全球网络。
Nature. 2008 Dec 11;456(7223):732-7. doi: 10.1038/nature07632.
7
Heritability of P. falciparum and P. vivax malaria in a Karen population in Thailand.泰国克伦族人群中恶性疟原虫和间日疟原虫疟疾的遗传度。
PLoS One. 2008;3(12):e3887. doi: 10.1371/journal.pone.0003887. Epub 2008 Dec 8.
8
Genetics of susceptibility to malaria related phenotypes.疟疾相关表型易感性的遗传学
Infect Genet Evol. 2009 Jan;9(1):97-103. doi: 10.1016/j.meegid.2008.10.008. Epub 2008 Oct 31.
9
Heritability of human hookworm infection in Papua New Guinea.巴布亚新几内亚人体钩虫感染的遗传力。
Parasitology. 2008 Oct;135(12):1407-15. doi: 10.1017/S0031182008004976.
10
Genetic determination and linkage mapping of Plasmodium falciparum malaria related traits in Senegal.塞内加尔恶性疟原虫疟疾相关性状的遗传决定及连锁图谱分析
PLoS One. 2008 Apr 23;3(4):e2000. doi: 10.1371/journal.pone.0002000.

疟疾寄生虫密度在乌干达农村社区的遗传性。

Heritability of Plasmodium parasite density in a rural Ugandan community.

机构信息

Department of Infectious and Tropical Diseases, London School of Hygiene and Tropical Medicine, London, United Kingdom.

出版信息

Am J Trop Med Hyg. 2010 Nov;83(5):990-5. doi: 10.4269/ajtmh.2010.10-0049.

DOI:10.4269/ajtmh.2010.10-0049
PMID:21036825
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2963957/
Abstract

Many factors influence variation in Plasmodium infection levels, including parasite/host genetics, immunity, and exposure. Here, we examine the roles of host genetics and exposure in determining parasite density, and test whether effects differ with age. Data for 1,711 residents of an eastern Ugandan community were used in pedigree-based variance component analysis. Heritability of parasite density was 13% (P < 0.001) but was not significant after controlling for shared household. Allowing variance components to vary between children (< 16 years) and adults (≥ 16 years) revealed striking age differences; 26% of variation could be explained by additively acting genes in children (P < 0.001), but there was no genetic involvement in adults. Domestic environment did not explain variation in children and explained 5% in adults (P = 0.09). Genetic effects are an important determinant of parasite density in children in this population, consistent with previous quantitative genetic studies of Plasmodium parasitaemia, although differences in environmental exposure play a lesser role.

摘要

许多因素会影响疟原虫感染水平的变化,包括寄生虫/宿主遗传、免疫和暴露。在这里,我们研究了宿主遗传和暴露在决定寄生虫密度中的作用,并检验了其作用是否随年龄而变化。在基于家系的方差成分分析中,我们使用了乌干达东部一个社区的 1711 名居民的数据。寄生虫密度的遗传率为 13%(P<0.001),但在控制了共享家庭因素后,这一数字并不显著。允许方差成分在儿童(<16 岁)和成人(≥16 岁)之间变化,揭示了惊人的年龄差异;在儿童中,可由累加作用基因解释的变异为 26%(P<0.001),而在成人中则没有遗传参与。家庭环境并不能解释儿童的变异,只能解释 5%的成人变异(P=0.09)。遗传效应是该人群中儿童寄生虫密度的重要决定因素,与之前对疟原虫感染的定量遗传研究一致,尽管环境暴露的差异所起的作用较小。