Richman A M, Dimopoulos G, Seeley D, Kafatos F C
European Molecular Biology Laboratory, Meyerhofstrasse 1, 69117 Heidelberg, Germany.
EMBO J. 1997 Oct 15;16(20):6114-9. doi: 10.1093/emboj/16.20.6114.
Innate immune-related gene expression in the major disease vector mosquito Anopheles gambiae has been analyzed following infection by the malaria parasite, Plasmodium berghei. Substantially increased levels of mRNAs encoding the antibacterial peptide defensin and a putative Gram-negative bacteria-binding protein (GNBP) are observed 20-30 h after ingestion of an infected blood-meal, at a time which indicates that this induction is a response to parasite invasion of the midgut epithelium. The induction is dependent upon the ingestion of infective, sexual-stage parasites, and is not due to opportunistic co-penetration of resident gut micro-organisms into the hemocoel. The response is activated following infection both locally (in the midgut) and systemically (in remaining tissues, presumably fat body and/or hemocytes). The observation that Plasmodium can trigger a molecularly defined immune response in the vector constitutes an important advance in our understanding of parasite-vector interactions that are potentially involved in malaria transmission, and extends knowledge of the innate immune system of insects to encompass responses to protozoan parasites.
在感染疟原虫伯氏疟原虫后,对主要疾病传播媒介冈比亚按蚊中与先天免疫相关的基因表达进行了分析。在摄入感染性血餐后20 - 30小时,观察到编码抗菌肽防御素和一种假定的革兰氏阴性菌结合蛋白(GNBP)的mRNA水平大幅增加,这表明这种诱导是对寄生虫侵入中肠上皮的一种反应。这种诱导依赖于摄入感染性的有性阶段寄生虫,而不是由于常驻肠道微生物偶然共同侵入血腔。感染后,局部(在中肠)和全身(在其余组织,可能是脂肪体和/或血细胞)都会激活这种反应。疟原虫能够在媒介中引发分子明确的免疫反应这一观察结果,是我们对可能参与疟疾传播的寄生虫 - 媒介相互作用理解的重要进展,并将昆虫先天免疫系统的知识扩展到包括对原生动物寄生虫的反应。