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抗寄生虫因子TEP1在疟疾媒介冈比亚按蚊中的转基因表达。

Transgenic Expression of the Anti-parasitic Factor TEP1 in the Malaria Mosquito Anopheles gambiae.

作者信息

Volohonsky Gloria, Hopp Ann-Katrin, Saenger Mélanie, Soichot Julien, Scholze Heidi, Boch Jens, Blandin Stéphanie A, Marois Eric

机构信息

Université de Strasbourg, CNRS UPR9022, INSERM U963, Institut de Biologie Moléculaire et Cellulaire, Strasbourg, France.

Martin-Luther Universität Halle-Wittenberg, Institut für Genetik, Halle (Saale), Germany.

出版信息

PLoS Pathog. 2017 Jan 17;13(1):e1006113. doi: 10.1371/journal.ppat.1006113. eCollection 2017 Jan.

Abstract

Mosquitoes genetically engineered to be resistant to Plasmodium parasites represent a promising novel approach in the fight against malaria. The insect immune system itself is a source of anti-parasitic genes potentially exploitable for transgenic designs. The Anopheles gambiae thioester containing protein 1 (TEP1) is a potent anti-parasitic protein. TEP1 is secreted and circulates in the mosquito hemolymph, where its activated cleaved form binds and eliminates malaria parasites. Here we investigated whether TEP1 can be used to create malaria resistant mosquitoes. Using a GFP reporter transgene, we determined that the fat body is the main site of TEP1 expression. We generated transgenic mosquitoes that express TEP1r, a potent refractory allele of TEP1, in the fat body and examined the activity of the transgenic protein in wild-type or TEP1 mutant genetic backgrounds. Transgenic TEP1r rescued loss-of-function mutations, but did not increase parasite resistance in the presence of a wild-type susceptible allele. Consistent with previous reports, TEP1 protein expressed from the transgene in the fat body was taken up by hemocytes upon a challenge with injected bacteria. Furthermore, although maturation of transgenic TEP1 into the cleaved form was impaired in one of the TEP1 mutant lines, it was still sufficient to reduce parasite numbers and induce parasite melanization. We also report here the first use of Transcription Activator Like Effectors (TALEs) in Anopheles gambiae to stimulate expression of endogenous TEP1. We found that artificial elevation of TEP1 expression remains moderate in vivo and that enhancement of endogenous TEP1 expression did not result in increased resistance to Plasmodium. Taken together, our results reveal the difficulty of artificially influencing TEP1-mediated Plasmodium resistance, and contribute to further our understanding of the molecular mechanisms underlying mosquito resistance to Plasmodium parasites.

摘要

经过基因工程改造而对疟原虫产生抗性的蚊子是抗击疟疾的一种很有前景的新方法。昆虫免疫系统本身就是抗寄生虫基因的一个来源,有可能用于转基因设计。冈比亚按蚊含硫酯蛋白1(TEP1)是一种有效的抗寄生虫蛋白。TEP1分泌后在蚊子血淋巴中循环,其活化的裂解形式会结合并清除疟原虫。在此,我们研究了TEP1是否可用于培育抗疟疾蚊子。利用绿色荧光蛋白(GFP)报告转基因,我们确定脂肪体是TEP1表达的主要部位。我们培育了在脂肪体中表达TEP1r(TEP1的一种有效抗性等位基因)的转基因蚊子,并在野生型或TEP1突变基因背景下检测了转基因蛋白的活性。转基因TEP1r挽救了功能丧失突变,但在存在野生型易感等位基因的情况下并未增加对寄生虫的抗性。与之前的报道一致,脂肪体中转基因表达的TEP1蛋白在注射细菌刺激后会被血细胞摄取。此外,尽管转基因TEP1在其中一个TEP1突变系中成熟为裂解形式的过程受损,但仍足以减少寄生虫数量并诱导寄生虫黑化。我们在此还报告了首次在冈比亚按蚊中使用转录激活样效应因子(TALE)来刺激内源性TEP1的表达。我们发现,体内内源性TEP1表达的人工升高仍然适中,且内源性TEP1表达的增强并未导致对疟原虫抗性的增加。综上所述,我们的结果揭示了人工影响TEP1介导的对疟原虫抗性的困难,并有助于进一步加深我们对蚊子对疟原虫寄生虫抗性的分子机制的理解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7bf7/5240933/471f829a92a9/ppat.1006113.g001.jpg

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