Zhao Bo, Lucas Keira J, Saha Tusar T, Ha Jisu, Ling Lin, Kokoza Vladimir A, Roy Sourav, Raikhel Alexander S
Department of Entomology and Institute for Integrative Genome Biology, University of California Riverside, Riverside, California, United States of America.
Graduate Program in Genetics, Genomics and Bioinformatics, University of California Riverside, Riverside, California, United States of America.
PLoS Genet. 2017 Aug 7;13(8):e1006943. doi: 10.1371/journal.pgen.1006943. eCollection 2017 Aug.
The yellow fever mosquito Aedes aegypti is the major vector of arboviruses, causing numerous devastating human diseases, such as dengue and yellow fevers, Chikungunya and Zika. Female mosquitoes need vertebrate blood for egg development, and repeated cycles of blood feeding are tightly linked to pathogen transmission. The mosquito's posterior midgut (gut) is involved in blood digestion and also serves as an entry point for pathogens. Thus, the mosquito gut is an important tissue to investigate. The miRNA aae-miR-275 (miR-275) has been shown to be required for normal blood digestion in the female mosquito; however, the mechanism of its action has remained unknown. Here, we demonstrate that miR-275 directly targets and positively regulates sarco/endoplasmic reticulum Ca2+ adenosine triphosphatase, which is implicated in active transport of Ca2+ from the cytosol to the sarco/endoplasmic reticulum. We utilized a combination of the gut-specific yeast transcription activator protein Gal4/upstream activating sequence (Gal4/UAS) system and miRNA Tough Decoy technology to deplete the endogenous level of miR-275 in guts of transgenic mosquitoes. This gut-specific reduction of miR-275 post blood meal decreased SERCA mRNA and protein levels of the digestive enzyme late trypsin. It also resulted in a significant reduction of gut microbiota. Moreover, the decrease of miR-275 and SERCA correlated with defects in the Notch signaling pathway and assembly of the gut actin cytoskeleton. The adverse phenotypes caused by miR-275 silencing were rescued by injections of miR-275 mimic. Thus, we have discovered that miR-275 directly targets SERCA, and the maintenance of its level is critical for multiple gut functions in mosquitoes.
黄热病媒介埃及伊蚊是虫媒病毒的主要传播媒介,可引发众多毁灭性的人类疾病,如登革热、黄热病、基孔肯雅热和寨卡病毒病。雌蚊需要摄取脊椎动物血液以促进卵子发育,而反复的吸血周期与病原体传播紧密相关。蚊子的中肠后部(肠道)参与血液消化,也是病原体的侵入点。因此,蚊子肠道是一个重要的研究组织。微小RNA aae-miR-275(miR-275)已被证明是雌蚊正常血液消化所必需的;然而,其作用机制仍不清楚。在此,我们证明miR-275直接靶向并正向调节肌浆/内质网Ca2+ 三磷酸腺苷酶,该酶参与将Ca2+ 从细胞质主动转运至肌浆/内质网。我们利用肠道特异性酵母转录激活蛋白Gal4/上游激活序列(Gal4/UAS)系统和微小RNA Tough Decoy技术相结合,来降低转基因蚊子肠道中内源性miR-275的水平。血餐后肠道中miR-275的这种特异性降低,减少了消化酶晚期胰蛋白酶的SERCA mRNA和蛋白质水平。这也导致肠道微生物群显著减少。此外,miR-275和SERCA的减少与Notch信号通路缺陷和肠道肌动蛋白细胞骨架组装有关。通过注射miR-275模拟物可挽救由miR-275沉默引起的不良表型。因此,我们发现miR-275直接靶向SERCA,其水平的维持对蚊子肠道的多种功能至关重要。