Department of Virology, Parasitology and Immunology, Laboratory of Parasitology, Faculty of Veterinary Medicine, Ghent University, Merelbeke, Belgium.
VIB Department of Medical Protein Research, Receptor Research laboratories, Nuclear Receptor Lab, Faculty of Medicine and Health Sciences, Ghent University, Ghent, Belgium.
Sci Rep. 2017 Aug 17;7(1):8520. doi: 10.1038/s41598-017-08590-x.
The protozoan parasite Giardia is a highly prevalent intestinal pathogen with a wide host range. Data obtained in mice, cattle and humans revealed the importance of IL-17A in the development of a protective immune response against Giardia. The aim of this study was to further unravel the protective effector mechanisms triggered by IL-17A following G. muris infection in mice, by an RNA-sequencing approach. C57BL/6 WT and C57BL/6 IL-17RA KO mice were orally infected with G. muris cysts. Three weeks post infection, intestinal tissue samples were collected for RNA-sequencing, with samples from uninfected C57BL/6 WT and C57BL/6 IL-17RA KO animals serving as negative controls. Differential expression analysis showed that G. muris infection evoked the transcriptional upregulation of a wide array of genes, mainly in animals with competent IL-17RA signaling. IL-17RA signaling induced the production of various antimicrobial peptides, such as angiogenin 4 and α- and β-defensins and regulated complement activation through mannose-binding lectin 2. The expression of the receptor that regulates the secretion of IgA into the intestinal lumen, the polymeric immunoglobulin receptor, was also dependent on IL-17RA signaling. Interestingly, the transcriptome data showed for the first time the involvement of the circadian clock in the host response following Giardia infection.
原虫寄生虫贾第虫是一种广泛宿主范围的高度流行肠道病原体。在小鼠、牛和人类中获得的数据表明,IL-17A 在针对贾第虫的保护性免疫反应的发展中具有重要作用。本研究旨在通过 RNA 测序方法进一步揭示 IL-17A 在 G. muris 感染后引发的保护性效应机制。C57BL/6 WT 和 C57BL/6 IL-17RA KO 小鼠经口感染 G. muris 包囊。感染后 3 周,收集肠道组织样本进行 RNA 测序,未感染的 C57BL/6 WT 和 C57BL/6 IL-17RA KO 动物的样本作为阴性对照。差异表达分析表明,G. muris 感染引发了广泛基因的转录上调,主要在具有有效 IL-17RA 信号的动物中。IL-17RA 信号诱导多种抗菌肽的产生,如血管生成素 4 和 α-和 β-防御素,并通过甘露糖结合凝集素 2 调节补体激活。调节 IgA 分泌到肠腔的受体,即多聚免疫球蛋白受体的表达也依赖于 IL-17RA 信号。有趣的是,转录组数据首次显示了生物钟在贾第虫感染后宿主反应中的参与。