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The innate immune system of kissing bugs, vectors of chagas disease

机译:亲吻虫子的天生免疫系统,赤曲病的载体

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摘要

Kissing bugs have long served as models to study many aspects of insect physiology. They also serve as vectors for the parasite Trypanosoma cruzi that causes Chagas disease in humans. The overall success of insects is due, in part, to their ability to recognize parasites and pathogens as non-self and to eliminate them using their innate immune system. This immune system comprises physical barriers, cellular responses (phagocytosis, nodulation and encapsulation), and humoral factors (antimicrobial peptides and the prophenoloxidase cascade). Trypanosomn cruzi survives solely in the gastrointestinal (GI) tract of the vector; if it migrates to the hemocoel it is eliminated. Kissing bugs may not mount a vigorous immune response in the GI tract to avoid eliminating obligate symbiotic microbes on which they rely for survival. Here we describe the current knowledge of innate immunity in kissing bugs and new opportunities using genomic and transcriptomic approaches to study the complex triatomine-trypanosome-microbiome interactions.
机译:亲吻虫子长期以来担任模型,以研究昆虫生理学的许多方面。它们还用作寄生虫胰蛋白酶瘤Cruzi的载体,导致人类的Chagas病。昆虫的总体成功部分地部分地取决于他们将寄生虫和病原体识别为非自我并使用先天免疫系统消除它们的能力。该免疫系统包括物理屏障,细胞应答(吞噬作用,染色和包封)和体液因子(抗微生物肽和丙甲酸钠酶梯形)。锥虫Cruzi仅在载体的胃肠道(GI)道中存活;如果它迁移到血管块,则会被删除。亲吻虫子可能无法在GI流动中升起剧烈的免疫反应,以避免消除他们依赖于生存的迫使共生微生物。在这里,我们描述了利用基因组和转录组的方法来研究复杂的三角瘤 - 锥虫组微生物组相互作用,描述了目前对亲吻错误和新机会的先天免疫知识。

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