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寄生虫清除的遗传控制导致对伯氏疟原虫ANKA感染的抗性并赋予免疫力。

Genetic control of parasite clearance leads to resistance to Plasmodium berghei ANKA infection and confers immunity.

作者信息

Campino S, Bagot S, Bergman M-L, Almeida P, Sepúlveda N, Pied S, Penha-Gonçalves C, Holmberg D, Cazenave P-A

机构信息

Instituto Gulbenkian de Ciência, Oeiras, Portugal.

出版信息

Genes Immun. 2005 Aug;6(5):416-21. doi: 10.1038/sj.gene.6364219.

Abstract

Unprecedented cure after infection with the lethal Plasmodium berghei ANKA was observed in an F2 progeny generated by intercrossing the wild-derived WLA and the laboratory C57BL/6 mouse strains. Resistant mice were able to clear parasitaemia and establish immunity. The observed resistance was disclosed as a combinatorial effect of genetic factors derived from the two parental strains. Genetic mapping of survival time showed that the WLA allele at a locus on chromosome 1 (colocalizing with Berghei resistance 1 (Berr1), a locus associated with resistance to experimental cerebral malaria) increases the probability to resist early death. Also, the C57Bl/6 allele at a novel locus on chromosome 9 (Berr3) confers overall resistance to this lethal Plasmodium infection. This report underlines the value of using wild-derived mouse strains to identify novel genetic factors in the aetiology of disease phenotypes, and provides a unique model for studying parasite clearance and immunity associated with malaria.

摘要

在通过野生来源的WLA和实验室C57BL/6小鼠品系杂交产生的F2后代中,观察到感染致死性伯氏疟原虫ANKA后出现了前所未有的治愈情况。抗性小鼠能够清除寄生虫血症并建立免疫力。观察到的抗性被揭示为来自两个亲本品系的遗传因素的组合效应。生存时间的遗传图谱显示,1号染色体上一个位点的WLA等位基因(与伯氏抗性1(Berr1)共定位,Berr1是一个与实验性脑型疟疾抗性相关的位点)增加了抵抗早期死亡的概率。此外,9号染色体上一个新位点(Berr3)的C57Bl/6等位基因赋予了对这种致死性疟原虫感染的总体抗性。本报告强调了利用野生来源的小鼠品系来识别疾病表型病因学中新型遗传因素的价值,并为研究与疟疾相关的寄生虫清除和免疫提供了一个独特的模型。

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