1. Mosquito Defense Strategies against Viral Infection
Gong Cheng, Yang Liu, Penghua Wang, Xiaoping Xiao 
Trends in Parasitology 
Volume 32, Issue 3, Pages (March 2016)
DOI: /j.pt
Copyright © 2015 Elsevier Ltd Terms and Conditions

2. Figure 1
Key Figure: Schematic Overview of Mosquito Antiviral Mechanisms
Mosquitoes ingest an arbovirus-infected blood meal into the midgut. After replication in the midgut epithelial cells, the virus escapes into the hemolymph and subsequently spreads via the hemolymph circulation to the fat body, muscles, salivary glands, and neural tissue. Mosquitoes have evolved systemic (A) and tissue-specific (B–E) antiviral mechanisms to limit viral propagation to a tolerable level. (A) The insect Toll and Imd pathways (left) are closely related to the mammalian Toll-like receptor (TLR) and tumor necrosis factor (TNF) pathways. The viral pattern recognition receptors in the Toll and Imd pathways are unknown. The Toll pathway uses viral pattern recognition to initiate an extracellular signaling cascade for the maturation of Spatzle (Spz), which is a ligand that binds the Toll receptor. The intracellular signaling pathway is mediated by Myd88 and results in the translocation of the NF-κB-like factor Rel1 to the nucleus to initiate downstream transcription. In the Imd pathway, there is an unknown pattern recognition receptor that binds viruses to recruit the adaptor molecules Imd and FADD, which results in activation of a NF-kB-like factor, Rel2. The activated Rel2 translocates to the nucleus to induce the transcription of immune genes such as multiple AMPs. The functional information of the siRNA pathway (center) was obtained from Drosophila studies. Briefly, viral siRNAs are generated by double-stranded RNA (dsRNA) either as viral replication intermediates or as part of RNA viral genomes. Dicer-2 (Dcr2) acts as the pattern recognition receptor to recognize the dsRNA. R2D2 is a protein containing two dsRNA-binding domains (R2) and is associated with Dcr2 (D2), which is required to initiate the subsequent antiviral defense. The long dsRNA is processed into siRNAs that are approximately 21–23bp in length. The siRNAs are then incorporated into the RNA-induced silencing complex (RISC) to specifically recognize viral sequences and degrade viral mRNAs and genomes. The activation of the Drosophila JAK–STAT pathway (right) is initiated by the recognition of the extracellular unpaired ligand Upd by the transmembrane receptor Domeless (Dome). Dome is an ortholog of the mammalian type I cytokine receptor. The ligand–receptor interaction undergoes a conformational change that causes the autophosphorylation of Hop, which is a homolog of the mammalian JAK kinase. Activated Hop subsequently phosphorylates Dome, leading to the phosphorylation and dimerization of STAT. The activated STAT dimer translocates into the nucleus and activates the transcription of specific target genes. Orthologs of the core JAK–STAT pathway components have been identified in mosquitoes. In addition to their systemic antiviral mechanisms, mosquitoes also contain the following specific antiviral responses in various tissues: RNAi/Toll/JAK–STAT pathways and microbiota in the midgut (B), the PO system and complement-like cascade in the hemolymph/hemocytes (C), and multiple antiviral effectors in the salivary glands (D) and neural system (E). Broken arrows represent secreted processes; unbroken arrows represent signaling processes. Abbreviations: AaHig, Aedes aegypti Hikaru genki; AaMCR, A. aegypti macroglobulin complement-related factor; AaSR-C, A. aegypti scavenger receptor-C; AMP, antimicrobial peptide; AnkP, ankyrin repeat-containing protein; CEC, cecropin; Cyst, cystatin; FADD, Fas-associated death domain-containing protein; Imd, immune deficiency factor; Myd88, myeloid differentiation primary response gene 88; NF-κB, nuclear factor kappa light chain enhancer of activated B cells; PO, phenoloxidase; PRR, pattern recognition receptor; STAT, signal transduction and activators of transcription; viRNA, virus-induced RNA; Vir-1, virus-induced RNA-1.
Trends in Parasitology  , DOI: ( /j.pt )
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