Aedes aegypti Beta-1,3-Glucan-Binding Protein Inhibits Dengue and ZIKA Virus Replication
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Chun-Xiao Li | D. Xing | T. Zhao | Di Wang | Xiaoxue Xie | Bo Li | Guorui Liang | Xiaoli Chen | Xinyu Zhou
[1] S. Dong,et al. Aedes aegypti Argonaute 2 controls arbovirus infection and host mortality , 2023, Nature communications.
[2] A. Johnpaul,et al. Plasma β-1,3 Glucan Binding Protein Mediated Opsono-Phagocytosis by Hemocytes In Vitro of Marine Mussel Perna viridis. , 2023, DNA and cell biology.
[3] Chun-Xiao Li,et al. Mosquito CYP4C21 knockout reduces dengue virus and Zika virus replication in Aedes aegypti cells , 2023, Biosafety and Health.
[4] A. Tassanakajon,et al. Heat Shock Protein 70 Is a Damage-Associated Molecular Pattern That by Binding to Lipopolysaccharide and β-1,3-Glucan–Binding Protein Activates the Prophenoloxidase System in Shrimp , 2022, The Journal of Immunology.
[5] J. Zafar,et al. Combined transcriptomic and proteomic analysis of developmental features in the immune system of Plutella xylostella during larva-to-adult metamorphosis. , 2022, Genomics.
[6] Da-Wei Huang,et al. Genome-Wide Analysis of Gene Families of Pattern Recognition Receptors in Fig Wasps (Hymenoptera, Chalcidoidea) , 2021, Genes.
[7] Guodong Wang,et al. Full-length transcriptome sequencing of Heliocidaris crassispina using PacBio single-molecule real-time. , 2021, Fish & shellfish immunology.
[8] G. Dimopoulos,et al. Mosquito transgenesis for malaria control. , 2021, Trends in parasitology.
[9] C. Tu,et al. Comparative Analysis of Adelphocoris suturalis Jakovlev (Hemiptera: Miridae) Immune Responses to Fungal and Bacterial Pathogens , 2021, Frontiers in Physiology.
[10] P. Oliveira,et al. Rhodnius prolixus uses the peptidoglycan recognition receptor rpPGRP-LC/LA to detect Gram-negative bacteria and activate the IMD pathway , 2020, Current research in insect science.
[11] A. York. Zika virus enhances dengue risk , 2020, Nature Reviews Microbiology.
[12] D. Missé,et al. JNK pathway restricts DENV2, ZIKV and CHIKV infection by activating complement and apoptosis in mosquito salivary glands , 2020, PLoS pathogens.
[13] T. Zhao,et al. Transcriptome analysis of Aedes aegypti Aag2 cells in response to dengue virus-2 infection , 2020, Parasites & Vectors.
[14] M. Riehle,et al. Exposure of Anopheles mosquitoes to trypanosomes reduces reproductive fitness and enhances susceptibility to Plasmodium , 2020, PLoS neglected tropical diseases.
[15] Renli Zhang,et al. A mosquito salivary protein promotes flavivirus transmission by activation of autophagy , 2020, Nature Communications.
[16] Hong Yang,et al. Genomic landscape and genetic manipulation of the black soldier fly Hermetia illucens, a natural waste recycler , 2019, Cell Research.
[17] N. Buchon,et al. Methods for the study of innate immunity in Drosophila melanogaster , 2019, Wiley interdisciplinary reviews. Developmental biology.
[18] S. Hay,et al. The current and future global distribution and population at risk of dengue , 2019, Nature Microbiology.
[19] Zuo-Kun Shi,et al. Aedes aegypti HPX8C modulates immune responses against viral infection , 2019, PLoS neglected tropical diseases.
[20] S. Rutz,et al. Ribonucleoprotein Transfection for CRISPR/Cas9‐Mediated Gene Knockout in Primary T Cells , 2018, Current protocols in immunology.
[21] T. Yeh,et al. Dengue virus non-structural protein 1: a pathogenic factor, therapeutic target, and vaccine candidate , 2018, Journal of Biomedical Science.
[22] Yongliang Fan,et al. The genomic and functional landscapes of developmental plasticity in the American cockroach , 2018, Nature Communications.
[23] A. Raikhel,et al. The bacterium Wolbachia exploits host innate immunity to establish a symbiotic relationship with the dengue vector mosquito Aedes aegypti , 2017, The ISME Journal.
[24] D. Shin,et al. The Effect of West Nile Virus Infection on the Midgut Gene Expression of Culex pipiens quinquefasciatus Say (Diptera: Culicidae) , 2016, Insects.
[25] J. Charlwood,et al. Molecular evolution and population genetics of a Gram-negative binding protein gene in the malaria vector Anopheles gambiae (sensu lato) , 2016, Parasites & Vectors.
[26] Simon I Hay,et al. The global burden of dengue: an analysis from the Global Burden of Disease Study 2013. , 2016, The Lancet. Infectious diseases.
[27] Leslie B Vosshall,et al. Genome engineering with CRISPR-Cas9 in the mosquito Aedes aegypti. , 2015, Cell reports.
[28] A. Raikhel,et al. Wolbachia induces reactive oxygen species (ROS)-dependent activation of the Toll pathway to control dengue virus in the mosquito Aedes aegypti , 2011, Proceedings of the National Academy of Sciences.
[29] Haobo Jiang,et al. Recognition of microbial molecular patterns and stimulation of prophenoloxidase activation by a β-1,3-glucanase-related protein in Manduca sexta larval plasma. , 2011, Insect biochemistry and molecular biology.
[30] M. Blaxter,et al. The components of the Daphnia pulex immune system as revealed by complete genome sequencing , 2009, BMC Genomics.
[31] Zhiyong Xi,et al. The Aedes aegypti Toll Pathway Controls Dengue Virus Infection , 2008, PLoS pathogens.
[32] B. Lemaître,et al. The host defense of Drosophila melanogaster. , 2007, Annual review of immunology.
[33] Dominique Ferrandon,et al. Dual Detection of Fungal Infections in Drosophila via Recognition of Glucans and Sensing of Virulence Factors , 2006, Cell.
[34] N. Gay,et al. Sensing of Gram‐positive bacteria in Drosophila: GNBP1 is needed to process and present peptidoglycan to PGRP‐SA , 2006, The EMBO journal.
[35] J. Royet. Infectious non-self recognition in invertebrates: lessons from Drosophila and other insect models. , 2004, Molecular immunology.
[36] S. Sinkins,et al. Male-specific insecticide resistance and mosquito transgene dispersal. , 2004, Trends in parasitology.
[37] B. Beutler. Innate immunity: an overview. , 2004, Molecular immunology.
[38] M. Belvin,et al. Dual Activation of the Drosophila Toll Pathway by Two Pattern Recognition Receptors , 2003, Science.
[39] Yuzhen Lu,et al. Pattern recognition receptors in Drosophila immune responses. , 2019, Developmental and comparative immunology.