Merkling Sarah Hélène, Raquin Vincent, Dabo Stéphanie, Henrion-Lacritick Annabelle, Blanc Hervé, Moltini-Conclois Isabelle, Frangeul Lionel, Varet Hugo, Saleh Maria-Carla, Lambrechts Louis
Institut Pasteur, Insect-Virus Interactions Unit, UMR2000, CNRS, 75015 Paris, France.
Institut Pasteur, Viruses and RNA Interference Unit, UMR3569, CNRS, 75015 Paris, France.
iScience. 2020 Feb 21;23(2):100870. doi: 10.1016/j.isci.2020.100870.
Diseases caused by mosquito-borne viruses have been on the rise for the last decades, and novel methods aiming to use laboratory-engineered mosquitoes that are incapable of carrying viruses have been developed to reduce pathogen transmission. This has stimulated efforts to identify optimal target genes that are naturally involved in mosquito antiviral defenses or required for viral replication. Here, we investigated the role of a member of the Tudor protein family, Tudor-SN, upon dengue virus infection in the mosquito Aedes aegypti. Tudor-SN knockdown reduced dengue virus replication in the midgut of Ae. aegypti females. In immunofluorescence assays, Tudor-SN localized to the nucleolus in both Ae. aegypti and Aedes albopictus cells. A reporter assay and small RNA profiling demonstrated that Tudor-SN was not required for RNA interference function in vivo. Collectively, these results defined a novel proviral role for Tudor-SN upon early dengue virus infection of the Ae. aegypti midgut.
在过去几十年中,由蚊媒病毒引起的疾病一直在增加,为减少病原体传播,人们已开发出旨在利用无法携带病毒的实验室工程蚊子的新方法。这激发了人们努力寻找自然参与蚊子抗病毒防御或病毒复制所需的最佳靶基因。在此,我们研究了都铎蛋白家族成员都铎-SN在埃及伊蚊感染登革病毒时所起的作用。敲低都铎-SN可减少登革病毒在埃及伊蚊雌性中肠中的复制。在免疫荧光试验中,都铎-SN定位于埃及伊蚊和白纹伊蚊细胞的核仁。一项报告基因检测和小RNA分析表明,都铎-SN在体内的RNA干扰功能中并非必需。总体而言,这些结果确定了都铎-SN在埃及伊蚊中肠早期感染登革病毒时具有一种新的病毒促进作用。