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The Imd Pathway Is Involved in Antiviral Immune Responses in Drosophila

https://doi.org/10.1371/journal.pone.0007436

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

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Differentiation of larval drosophila eye‐antennal Discs in Vitro

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Signals from the IL-1 Receptor Homolog, Toll, Can Activate an Immune Response in a Drosophila Hemocyte Cell Line

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Sequence Analysis of the Bicistronic Drosophila X Virus Genome Segment A and Its Encoded Polypeptides

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Viruses of Invertebrates

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A nonoccluded virus of the field crickets Teleogryllus oceanicus and T. commodus (Orthoptera: Gryllidae)

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Akt and foxo Dysregulation Contribute to Infection-Induced Wasting in Drosophila

inferredcites →https://doi.org/10.1016/j.cub.2006.11.026openalex-snapshot

Psidin Is Required in Drosophila Blood Cells for Both Phagocytic Degradation and Immune Activation of the Fat Body

inferredcites →https://doi.org/10.1016/j.virol.2008.04.021openalex-snapshot

West Nile virus infection of Drosophila melanogaster induces a protective RNAi response

inferredcites →https://doi.org/10.1016/s0092-8674(00)80172-5openalex-snapshot

The Dorsoventral Regulatory Gene Cassette spätzle/Toll/cactus Controls the Potent Antifungal Response in Drosophila Adults

inferredcites →https://doi.org/10.1016/s0952-7915(02)00018-3openalex-snapshot

Death and survival: viral regulation of TNF signaling pathways

inferredcites →https://doi.org/10.1016/s0960-9822(00)00569-8openalex-snapshot

Interactions between the cellular and humoral immune responses in Drosophila

inferredcites →https://doi.org/10.1016/s0960-9822(02)00873-4openalex-snapshot

Inducible Expression of Double-Stranded RNA Reveals a Role for dFADD in the Regulation of the Antibacterial Response in Drosophila Adults

inferredcites →https://doi.org/10.1016/s0965-1748(02)00092-9openalex-snapshot

Insect hemocytes and their role in immunity

inferredcites →https://doi.org/10.1016/s1097-2765(00)80392-5openalex-snapshot

Relish, a Central Factor in the Control of Humoral but Not Cellular Immunity in Drosophila

inferredcites →https://doi.org/10.1016/s1534-5807(01)00059-4openalex-snapshot

Drosophila Immune Deficiency (IMD) Is a Death Domain Protein that Activates Antibacterial Defense and Can Promote Apoptosis

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The crystal structure of cricket paralysis virus: the first view of a new virus family.

inferredcites →https://doi.org/10.1038/41131openalex-snapshot

A human homologue of the Drosophila Toll protein signals activation of adaptive immunity

inferredcites →https://doi.org/10.1038/79801openalex-snapshot

Role of Drosophila IKKγ in a Toll-independent antibacterial immune response

inferredcites →https://doi.org/10.1038/nature07712openalex-snapshot

Antiviral immunity in Drosophila requires systemic RNA interference spread

inferredcites →https://doi.org/10.1038/nature734openalex-snapshot

The Drosophila immune response against Gram-negative bacteria is mediated by a peptidoglycan recognition protein

inferredcites →https://doi.org/10.1038/nature735openalex-snapshot

Functional genomic analysis of phagocytosis and identification of a Drosophila receptor for E. coli

inferredcites →https://doi.org/10.1038/ng1314openalex-snapshot

A complementary transposon tool kit for Drosophila melanogaster using P and piggyBac

inferredcites →https://doi.org/10.1038/ni.1664openalex-snapshot

The DExD/H-box helicase Dicer-2 mediates the induction of antiviral activity in drosophila

inferredcites →https://doi.org/10.1038/ni1019openalex-snapshot

Entry is a rate-limiting step for viral infection in a Drosophila melanogaster model of pathogenesis

inferredcites →https://doi.org/10.1038/ni1237openalex-snapshot

The Jak-STAT signaling pathway is required but not sufficient for the antiviral response of drosophila

inferredcites →https://doi.org/10.1038/ni1335openalex-snapshot

Essential function in vivo for Dicer-2 in host defense against RNA viruses in drosophila

inferredcites →https://doi.org/10.1038/ni1356openalex-snapshot

PGRP-LC and PGRP-LE have essential yet distinct functions in the drosophila immune response to monomeric DAP-type peptidoglycan

inferredcites →https://doi.org/10.1038/ni1388openalex-snapshot

Host-pathogen interactions in drosophila: new tricks from an old friend

inferredcites →https://doi.org/10.1038/nri2194openalex-snapshot

The Drosophila systemic immune response: sensing and signalling during bacterial and fungal infections

inferredcites →https://doi.org/10.1038/sj.embor.7400073openalex-snapshot

Parasite‐specific immune response in adult Drosophila melanogaster: a genomic study

inferredcites →https://doi.org/10.1038/sj.onc.1208156openalex-snapshot

Increased expression of Drosophila tetraspanin, Tsp68C, suppresses the abnormal proliferation of ytr-deficient and Ras/Raf-activated hemocytes

inferredcites →https://doi.org/10.1042/0264-6021:3590099openalex-snapshot

A Drosophila haemocyte-specific protein, hemolectin, similar to human von Willebrand factor

inferredcites →https://doi.org/10.1046/j.1432-1033.2003.03725.xopenalex-snapshot

Pherokine‐2 and ‐3

inferredcites →https://doi.org/10.1046/j.1525-1373.2000.22335.xopenalex-snapshot

Tumor Necrosis Factor (TNF)-alpha and TNF Receptors in Viral Pathogenesis

inferredcites →https://doi.org/10.1073/pnas.0404952102openalex-snapshot

Drosophila peptidoglycan recognition protein LC (PGRP-LC) acts as a signal-transducing innate immune receptor

inferredcites →https://doi.org/10.1073/pnas.0409181102openalex-snapshot

The Toll pathway is important for an antiviral response in Drosophila

inferredcites →https://doi.org/10.1073/pnas.070357597openalex-snapshot

The phytopathogenic bacteria Erwinia carotovora infects Drosophila and activates an immune response

inferredcites →https://doi.org/10.1073/pnas.1035902100openalex-snapshot

Caspase-mediated processing of the Drosophila NF-κB factor Relish

inferredcites →https://doi.org/10.1073/pnas.95.24.14337openalex-snapshot

Analysis of the Drosophila host defense in domino mutant larvae, which are devoid of hemocytes

inferredcites →https://doi.org/10.1074/jbc.m304802200openalex-snapshot

Immune Activation of NF-κB and JNK Requires Drosophila TAK1

inferredcites →https://doi.org/10.1074/jbc.m313856200openalex-snapshot

Differential Activation of the NF-κB-like Factors Relish and Dif in Drosophila melanogaster by Fungi and Gram-positive Bacteria

inferredcites →https://doi.org/10.1093/embo-reports/kvd073openalex-snapshot

The Drosophila caspase Dredd is required to resist Gram‐negative bacterial infection

inferredcites →https://doi.org/10.1093/emboj/21.11.2568openalex-snapshot

The Toll and Imd pathways are the major regulators of the immune response in Drosophila

inferredcites →https://doi.org/10.1093/genetics/147.2.623openalex-snapshot

Drosophila Immunity: Analysis of Larval Hemocytes by P-Element-Mediated Enhancer Trap

inferredcites →https://doi.org/10.1093/oxfordjournals.aje.a118408openalex-snapshot

A SIMPLE METHOD OF ESTIMATING FIFTY PER CENT ENDPOINTS12

inferredcites →https://doi.org/10.1096/fj.06-7907comopenalex-snapshot

Infection‐induced proteolysis of PGRP‐LC controls the IMD activation and melanization cascades in Drosophila

inferredcites →https://doi.org/10.1098/rspb.1998.0324openalex-snapshot

Phylogeny and PCR–based classification of Wolbachia strains using wsp gene sequences

inferredcites →https://doi.org/10.1099/0022-1317-35-2-393openalex-snapshot

End-point Dilution and Plaque Assay Methods for Titration of Cricket Paralysis Virus in Cultured Drosophila Cells

inferredcites →https://doi.org/10.1099/vir.0.83684-0openalex-snapshot

Induction of host defence responses by Drosophila C virus

inferredcites →https://doi.org/10.1101/gad.1482006openalex-snapshot

The RNA silencing endonuclease Argonaute 2 mediates specific antiviral immunity in Drosophila melanogaster

inferredcites →https://doi.org/10.1101/gad.203301openalex-snapshot

Mutations in the Drosophila dTAK1 gene reveal a conserved function for MAPKKKs in the control of rel/NF-κB-dependent innate immune responses

inferredcites →https://doi.org/10.1101/gad.856901openalex-snapshot

The antibacterial arm of the Drosophila innate immune response requires an IκB kinase

inferredcites →https://doi.org/10.1111/j.1420-9101.2006.01267.xopenalex-snapshot

Alternative measures of response to Pseudomonas aeruginosa infection in Drosophila melanogaster

inferredcites →https://doi.org/10.1111/j.1462-5822.2006.00688.xopenalex-snapshot

RNAi is an antiviral immune response against a dsRNA virus in Drosophila melanogaster

inferredcites →https://doi.org/10.1126/science.1070216openalex-snapshot

Requirement for a Peptidoglycan Recognition Protein (PGRP) in Relish Activation and Antibacterial Immune Responses in Drosophila

inferredcites →https://doi.org/10.1126/science.1092447openalex-snapshot

Genetic Basis of Natural Variation in D. melanogaster Antibacterial Immunity

inferredcites →https://doi.org/10.1126/science.1125694openalex-snapshot

RNA Interference Directs Innate Immunity Against Viruses in Adult Drosophila

inferredcites →https://doi.org/10.1126/science.1162418openalex-snapshot

Wolbachia and Virus Protection in Insects

inferredcites →https://doi.org/10.1126/science.288.5475.2376openalex-snapshot

Malaria Parasite Development in a Drosophila Model

inferredcites →https://doi.org/10.1128/aem.02248-07openalex-snapshot

Drosophila melanogaster Mounts a Unique Immune Response to the Rhabdovirus Sigma virus

inferredcites →https://doi.org/10.1128/jvi.75.2.996-1003.2001openalex-snapshot

Central Role of Hemocytes in Autographa californica M Nucleopolyhedrovirus Pathogenesis in Heliothis virescens and Helicoverpa zea

inferredcites →https://doi.org/10.1159/000149489openalex-snapshot

Cricket Paralysis Virus Replicates in Cultured Drosophila Cells

inferredcites →https://doi.org/10.1159/000149886openalex-snapshot

The Isolation of Cricket Paralysis Virus from the Emperor Gum Moth, Antheraea eucalypti Scott, and its Infectivity towards a Range of Insect Species

inferredcites →https://doi.org/10.1201/9780203734322-10openalex-snapshot

Identification, Pathology, Structure, and Replication of Insect Picornaviruses

inferredcites →https://doi.org/10.1242/dev.27.2.353openalex-snapshot

Cell lines derived from late embryonic stages of Drosophila melanogaster

inferredcites →https://doi.org/10.1242/dmm.000307openalex-snapshot

Models of infectious diseases in the fruit fly Drosophila melanogaster

inferredcites →https://doi.org/10.1371/journal.pbio.1000002openalex-snapshot

The Bacterial Symbiont Wolbachia Induces Resistance to RNA Viral Infections in Drosophila melanogaster

inferredcites →https://doi.org/10.1371/journal.ppat.0030026openalex-snapshot

A Specific Primed Immune Response in Drosophila Is Dependent on Phagocytes

inferredcites →https://doi.org/10.1371/journal.ppat.0030041openalex-snapshot

Drosophila eiger Mutants Are Sensitive to Extracellular Pathogens

inferredcites →https://doi.org/10.1371/journal.ppat.1000098openalex-snapshot

The Aedes aegypti Toll Pathway Controls Dengue Virus Infection

inferredcites →https://doi.org/10.1534/genetics.107.083782openalex-snapshot

Identification of Drosophila Mutants Altering Defense of and Endurance to Listeria monocytogenes Infection

inferredcites →https://doi.org/10.1534/genetics.107.085449openalex-snapshot

Genetic Variation Affecting Host–Parasite Interactions: Different Genes Affect Different Aspects of Sigma Virus Replication and Transmission in Drosophila melanogaster

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.2139/ssrn.4097512openalex-extracted

Heightened Immune Surveillance in Drosophila Melanogaster Populations Selected for Faster Development and Extended Longevity

inferred← citeshttps://doi.org/10.1002/9781118924846.app1openalex-snapshot

APPENDIX A

inferred← citeshttps://doi.org/10.1002/arch.21436openalex-snapshot

Cloning and analysis of peptidoglycan recognition protein‐LC and immune deficiency from the diamondback moth, Plutella xylostella

inferred← citeshttps://doi.org/10.1002/npp2.70043openalex-snapshot

Innate immunity shapes the persistent transmission of plant viruses by insect vectors

inferred← citeshttps://doi.org/10.1002/ps.70587openalex-snapshot

Defensin1, an IMD pathway antiviral peptide, inhibits rice gall dwarf virus propagation in leafhoppers

inferred← citeshttps://doi.org/10.1007/82_2010_107openalex-snapshot

NF-κB/Rel Proteins and the Humoral Immune Responses of Drosophila melanogaster

inferred← citeshttps://doi.org/10.1007/978-1-61779-037-9_1openalex-snapshot

Defense and Counterdefense in the RNAi-Based Antiviral Immune System in Insects

inferred← citeshttps://doi.org/10.1007/978-3-031-64292-0_17openalex-snapshot

Viral Infections and Host Immunity: Lessons Learned from Model Organisms

inferred← citeshttps://doi.org/10.1007/978-3-319-94075-5_9openalex-snapshot

Mosquitoes as Arbovirus Vectors: From Species Identification to Vector Competence

inferred← citeshttps://doi.org/10.1007/s00018-017-2453-9openalex-snapshot

Innate and intrinsic antiviral immunity in Drosophila

inferred← citeshttps://doi.org/10.1007/s00705-012-1223-0openalex-snapshot

Infection of honey bees with acute bee paralysis virus does not trigger humoral or cellular immune responses

inferred← citeshttps://doi.org/10.1007/s11033-026-12386-6openalex-snapshot

Transcriptomic analysis of oriental tea tortrix infected with male-killing virus

inferred← citeshttps://doi.org/10.1007/s11274-015-1901-7openalex-snapshot

Molecular cloning and characterization of gloverin from the diamondback moth, Plutella xylostella L. and its interaction with bacterial membrane

inferred← citeshttps://doi.org/10.1007/s13337-014-0217-9openalex-snapshot

Antiviral responses of arthropod vectors: an update on recent advances

inferred← citeshttps://doi.org/10.1016/b978-0-12-387680-5.00001-xopenalex-snapshot

Of Insects and Viruses

inferred← citeshttps://doi.org/10.1016/b978-0-12-416028-6.00003-7openalex-snapshot

Secondary Sexual Traits, Immune Response, Parasites, and Pathogens

inferred← citeshttps://doi.org/10.1016/b978-0-12-803252-7.00010-2openalex-snapshot

Aedes aegypti Immune Responses to Dengue Virus

inferred← citeshttps://doi.org/10.1016/b978-0-323-95424-2.00004-2openalex-snapshot

Insect-associated viruses: Effects on host immunity and fitness

inferred← citeshttps://doi.org/10.1016/bs.ai.2018.08.002openalex-snapshot

The Fly Way of Antiviral Resistance and Disease Tolerance

inferred← citeshttps://doi.org/10.1016/bs.aiip.2017.02.001openalex-snapshot

Exploiting Innate Immunity for Biological Pest Control

inferred← citeshttps://doi.org/10.1016/bs.aivir.2017.10.006openalex-snapshot

Antiviral Immune Response and the Route of Infection in Drosophila melanogaster

inferred← citeshttps://doi.org/10.1016/bs.pmbts.2020.01.005openalex-snapshot

Drosophila as a model to understand autophagy deregulation in human disorders

inferred← citeshttps://doi.org/10.1016/j.antiviral.2014.05.013openalex-snapshot

Antiviral defense in shrimp: From innate immunity to viral infection

inferred← citeshttps://doi.org/10.1016/j.aquaculture.2020.734969openalex-snapshot

Interleukin-17 suppresses grass carp reovirus infection in Ctenopharyngodon idellus kidney cells by activating NF-κB signaling

inferred← citeshttps://doi.org/10.1016/j.aspen.2019.07.014openalex-snapshot

Role of Toll-receptors in the inhibition of BmNPV proliferation and their interplay with antimicrobial seroin proteins in Bombyx mori

inferred← citeshttps://doi.org/10.1016/j.aspen.2022.101895openalex-snapshot

Effects of exposure to trace pyriproxyfen on the intestinal bacterial diversity and immune signal pathways of silkworm (Bombyx mori) larvae

inferred← citeshttps://doi.org/10.1016/j.bbrc.2015.03.013openalex-snapshot

DIP1 plays an antiviral role against DCV infection in Drosophila melanogaster

inferred← citeshttps://doi.org/10.1016/j.cbpb.2017.10.002openalex-snapshot

Molecular cloning and analysis of PGRP-L1 and IMD from silkworm Bombyx mori

inferred← citeshttps://doi.org/10.1016/j.ceb.2015.07.003openalex-snapshot

Drosophila immune cell migration and adhesion during embryonic development and larval immune responses

inferred← citeshttps://doi.org/10.1016/j.celrep.2018.05.029openalex-snapshot

Analysis of Drosophila STING Reveals an Evolutionarily Conserved Antimicrobial Function

inferred← citeshttps://doi.org/10.1016/j.celrep.2022.111143openalex-snapshot

A dRASSF-STRIPAK-Imd-JAK/STAT axis controls antiviral immune response in Drosophila

inferred← citeshttps://doi.org/10.1016/j.celrep.2024.113973openalex-snapshot

The circular RNA circATP8B(2) regulates ROS production and antiviral immunity in Drosophila

inferred← citeshttps://doi.org/10.1016/j.chom.2012.08.011openalex-snapshot

Transcriptional Pausing Controls a Rapid Antiviral Innate Immune Response in Drosophila

inferred← citeshttps://doi.org/10.1016/j.chom.2018.05.022openalex-snapshot

Inflammation-Induced, STING-Dependent Autophagy Restricts Zika Virus Infection in the Drosophila Brain

inferred← citeshttps://doi.org/10.1016/j.chom.2019.12.006openalex-snapshot

lncRNA Sensing of a Viral Suppressor of RNAi Activates Non-canonical Innate Immune Signaling in Drosophila

inferred← citeshttps://doi.org/10.1016/j.coi.2010.01.007openalex-snapshot

Innate antiviral immunity in Drosophila

inferred← citeshttps://doi.org/10.1016/j.cois.2014.07.005openalex-snapshot

Mosquito immune responses to arbovirus infections

inferred← citeshttps://doi.org/10.1016/j.cois.2015.04.016openalex-snapshot

Antiviral defense mechanisms in honey bees

inferred← citeshttps://doi.org/10.1016/j.cois.2017.05.002openalex-snapshot

West Nile virus and its vectors

inferred← citeshttps://doi.org/10.1016/j.cois.2024.101222openalex-snapshot

Tripartite interactions between viruses, parasites, and mosquitoes

inferred← citeshttps://doi.org/10.1016/j.coviro.2016.09.005openalex-snapshot

Discovery of novel targets for antivirals: learning from flies

inferred← citeshttps://doi.org/10.1016/j.cub.2024.05.009openalex-snapshot

Viral infection disrupts intestinal homeostasis via Sting-dependent NF-κB signaling in Drosophila

inferred← citeshttps://doi.org/10.1016/j.cvfa.2021.06.007openalex-snapshot

Honey Bee (Apis mellifera) Immunity

inferred← citeshttps://doi.org/10.1016/j.dci.2010.08.013openalex-snapshot

Litopenaeus vannamei tumor necrosis factor receptor-associated factor 6 (TRAF6) responds to Vibrio alginolyticus and white spot syndrome virus (WSSV) infection and activates antimicrobial peptide genes

inferred← citeshttps://doi.org/10.1016/j.dci.2011.08.007openalex-snapshot

Regulation of Drosophila-virus interaction

inferred← citeshttps://doi.org/10.1016/j.dci.2013.05.001openalex-snapshot

WITHDRAWN: Overview of Drosophila immunity: A historical perspective

inferred← citeshttps://doi.org/10.1016/j.dci.2013.05.002openalex-snapshot

Viruses and antiviral immunity in Drosophila

inferred← citeshttps://doi.org/10.1016/j.dci.2013.05.014openalex-snapshot

The Drosophila IMD pathway in the activation of the humoral immune response

inferred← citeshttps://doi.org/10.1016/j.dci.2013.05.017openalex-snapshot

Immune competence in insect eggs depends on the extraembryonic serosa

inferred← citeshttps://doi.org/10.1016/j.dci.2013.07.004openalex-snapshot

Characterization of an immune deficiency homolog (IMD) in shrimp (Fenneropenaeus chinensis) and crayfish (Procambarus clarkii)

inferred← citeshttps://doi.org/10.1016/j.dci.2013.08.018openalex-snapshot

Overview of Drosophila immunity: A historical perspective

inferred← citeshttps://doi.org/10.1016/j.dci.2015.05.004openalex-snapshot

Plasmodium berghei induced priming in Anopheles albimanus independently of bacterial co-infection

inferred← citeshttps://doi.org/10.1016/j.dci.2017.11.011openalex-snapshot

The Single von Willebrand factor C-domain protein (SVC) coding gene is not involved in the hymenoptaecin upregulation after Israeli acute paralysis virus (IAPV) injection in the bumblebee Bombus terrestris

inferred← citeshttps://doi.org/10.1016/j.dci.2017.12.025openalex-snapshot

Antiviral systems in vector mosquitoes

inferred← citeshttps://doi.org/10.1016/j.dci.2018.12.010openalex-snapshot

The Aedes aegypti IMD pathway is a critical component of the mosquito antifungal immune response

inferred← citeshttps://doi.org/10.1016/j.dci.2020.103985openalex-snapshot

Sensing and signalling viral infection in drosophila

inferred← citeshttps://doi.org/10.1016/j.dci.2021.104010openalex-snapshot

Genetic determinants of antiviral immunity in dipteran insects – Compiling the experimental evidence

inferred← citeshttps://doi.org/10.1016/j.dci.2021.104012openalex-snapshot

The antiviral immunity of ticks against transmitted viral pathogens

inferred← citeshttps://doi.org/10.1016/j.fsi.2014.11.015openalex-snapshot

Activation of PmRelish from Penaeus monodon by yellow head virus

inferred← citeshttps://doi.org/10.1016/j.fsi.2019.02.062openalex-snapshot

Potential immunomodulatory and protective effects of the Arthrospira-based dietary supplement on shrimp intestinal immune defenses

inferred← citeshttps://doi.org/10.1016/j.heliyon.2022.e12090openalex-snapshot

Heightened immune surveillance in Drosophila melanogaster populations selected for faster development and extended longevity

inferred← citeshttps://doi.org/10.1016/j.ibmb.2011.09.008openalex-snapshot

Differential inhibition of BmRelish1-dependent transcription in lepidopteran cells by bracovirus ankyrin-repeat proteins

inferred← citeshttps://doi.org/10.1016/j.ibmb.2012.04.003openalex-snapshot

The transcriptome of Spodoptera exigua larvae exposed to different types of microbes

inferred← citeshttps://doi.org/10.1016/j.ibmb.2023.103947openalex-snapshot

BmCPV replication is suppressed by the activation of the NF-κB/autophagy pathway through the interaction of vsp21 translated by vcircRNA_000048 with ubiquitin carboxyl-terminal hydrolase

inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2021.11.201openalex-snapshot

Bombyx mori Akirin hijacks a viral peptide vSP27 encoded by BmCPV circRNA and activates the ROS-NF-κB pathway against viral infection

inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2023.123482openalex-snapshot

Transcriptome analysis reveals that knocking out BmNPV iap2 induces apoptosis by inhibiting the oxidative phosphorylation pathway

inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2025.146178openalex-snapshot

SePGRP-SA promotes antiviral immunity in Spodoptera exigua via Toll pathway activation

inferred← citeshttps://doi.org/10.1016/j.immuni.2018.07.013openalex-snapshot

The Kinase IKKβ Regulates a STING- and NF-κB-Dependent Antiviral Response Pathway in Drosophila

inferred← citeshttps://doi.org/10.1016/j.immuni.2018.08.003openalex-snapshot

Insects Go on a STING Operation to Tackle Intracellular Invaders

inferred← citeshttps://doi.org/10.1016/j.jinsphys.2012.07.004openalex-snapshot

Beyond RNAi: Antiviral defense strategies in Drosophila and mosquito

inferred← citeshttps://doi.org/10.1016/j.jinsphys.2013.03.010openalex-snapshot

Effect of larval density and Sindbis virus infection on immune responses in Aedes aegypti

inferred← citeshttps://doi.org/10.1016/j.jinsphys.2019.03.004openalex-snapshot

Short-term persistence precedes pathogenic infection: Infection kinetics of cricket paralysis virus in silkworm-derived Bm5 cells

inferred← citeshttps://doi.org/10.1016/j.jip.2018.02.012openalex-snapshot

Discovery of anti-viral molecules and their vital functions in Bombyx mori

inferred← citeshttps://doi.org/10.1016/j.jip.2018.04.006openalex-snapshot

The IMD pathway regulates lysozyme-like proteins (LLPs) in the silkmoth Antheraea mylitta

inferred← citeshttps://doi.org/10.1016/j.jip.2019.107207openalex-snapshot

Identification and function of a lebocin-like gene from the Chinese oak silkworm, Antheraea pernyi

inferred← citeshttps://doi.org/10.1016/j.jip.2025.108483openalex-snapshot

Antiviral activity of curcumin against Israeli acute paralysis virus in Apis mellifera: Screening and mechanistic study

inferred← citeshttps://doi.org/10.1016/j.jmb.2013.10.006openalex-snapshot

Insect Antiviral Innate Immunity: Pathways, Effectors, and Connections

inferred← citeshttps://doi.org/10.1016/j.mib.2014.05.006openalex-snapshot

Induced antiviral innate immunity in Drosophila

inferred← citeshttps://doi.org/10.1016/j.mib.2016.05.002openalex-snapshot

The diversity of insect antiviral immunity: insights from viruses

inferred← citeshttps://doi.org/10.1016/j.molimm.2018.12.021openalex-snapshot

Peptidoglycan recognition proteins in insect immunity

inferred← citeshttps://doi.org/10.1016/j.molimm.2019.02.011openalex-snapshot

Modulation of antiviral immunity by the ichnovirus HdIV in Spodoptera frugiperda

inferred← citeshttps://doi.org/10.1016/j.pt.2015.09.009openalex-snapshot

Mosquito Defense Strategies against Viral Infection

inferred← citeshttps://doi.org/10.1016/j.tim.2017.12.005openalex-snapshot

Antiviral Immunity and Virus-Mediated Antagonism in Disease Vector Mosquitoes

inferred← citeshttps://doi.org/10.1016/j.virol.2019.12.001openalex-snapshot

Drosophila immunity against natural and nonnatural viral pathogens

inferred← citeshttps://doi.org/10.1016/j.virol.2025.110462openalex-snapshot

Immunity responses as checkpoints for efficient transmission of begomoviruses by whiteflies

inferred← citeshttps://doi.org/10.1016/j.ydbio.2014.12.001openalex-snapshot

Heixuedian (heix), a potential melanotic tumor suppressor gene, exhibits specific spatial and temporal expression pattern during drosophila hematopoiesis

inferred← citeshttps://doi.org/10.1017/s0007485321000821openalex-snapshot

The dietary arachidonic acid improved growth and immunity of honey bee (Apis mellifera ligustica)

inferred← citeshttps://doi.org/10.1038/ncomms14401openalex-snapshot

Infection-derived lipids elicit an immune deficiency circuit in arthropods

inferred← citeshttps://doi.org/10.1038/nprot.2015.071openalex-snapshot

Analysis of resistance and tolerance to virus infection in Drosophila

inferred← citeshttps://doi.org/10.1038/nri3763openalex-snapshot

Immunity in Drosophila melanogaster — from microbial recognition to whole-organism physiology

inferred← citeshttps://doi.org/10.1038/s41418-022-01038-4openalex-snapshot

Drosophila caspases as guardians of host-microbe interactions

inferred← citeshttps://doi.org/10.1038/s41467-025-61139-9openalex-snapshot

Mosquito immune cells enhance dengue and Zika virus infection in Aedes aegypti

inferred← citeshttps://doi.org/10.1038/s41559-022-01697-zopenalex-snapshot

Innate immune pathways act synergistically to constrain RNA virus evolution in Drosophila melanogaster

inferred← citeshttps://doi.org/10.1038/s41598-017-06623-zopenalex-snapshot

Virus and dsRNA-triggered transcriptional responses reveal key components of honey bee antiviral defense

inferred← citeshttps://doi.org/10.1038/s41598-017-17270-9openalex-snapshot

Vitamin K2 Prevents Lymphoma in Drosophila

inferred← citeshttps://doi.org/10.1038/s41598-019-38559-xopenalex-snapshot

Peroxisome-associated Sgroppino links fat metabolism with survival after RNA virus infection in Drosophila

inferred← citeshttps://doi.org/10.1038/s41598-021-89922-wopenalex-snapshot

PmAP2-β depletion enhanced activation of the Toll signaling pathway during yellow head virus infection in the black tiger shrimp Penaeus monodon

inferred← citeshttps://doi.org/10.1038/s44318-026-00761-9openalex-snapshot

FADD is recruited to activated STING oligomers to initiate caspase-mediated NF-κB activation in Drosophila melanogaster

inferred← citeshttps://doi.org/10.1038/srep12758openalex-snapshot

The heat shock response restricts virus infection in Drosophila

inferred← citeshttps://doi.org/10.1038/srep34200openalex-snapshot

Differential expression pattern of Vago in bumblebee (Bombus terrestris), induced by virulent and avirulent virus infections

inferred← citeshttps://doi.org/10.1038/srep36254openalex-snapshot

Understanding the immune system architecture and transcriptome responses to southern rice black-streaked dwarf virus in Sogatella furcifera

inferred← citeshttps://doi.org/10.1073/pnas.1116932108openalex-snapshot

Wolbachia induces reactive oxygen species (ROS)-dependent activation of the Toll pathway to control dengue virus in the mosquito Aedes aegypti

inferred← citeshttps://doi.org/10.1073/pnas.1205231109openalex-snapshot

Secreted Vago restricts West Nile virus infection in Culex mosquito cells by activating the Jak-STAT pathway

inferred← citeshttps://doi.org/10.1073/pnas.1517124112openalex-snapshot

FOXO regulates RNA interference in Drosophila and protects from RNA virus infection

inferred← citeshttps://doi.org/10.1073/pnas.1808905116openalex-snapshot

p47 licenses activation of the immune deficiency pathway in the tick Ixodes scapularis

inferred← citeshttps://doi.org/10.1073/pnas.2511857122openalex-snapshot

The integrated stress response suppresses antiviral RNA interference by autophagy-mediated degradation of the RNA-induced silencing complex

inferred← citeshttps://doi.org/10.1073/pnas.2613025123openalex-snapshot

Splicing suppression alters the STING transcription start site to attenuate antiviral innate immunity

inferred← citeshttps://doi.org/10.1074/jbc.ra117.000194openalex-snapshot

Stimulator of interferon genes (STING) provides insect antiviral immunity by promoting Dredd caspase–mediated NF-κB activation

inferred← citeshttps://doi.org/10.1080/19336934.2022.2149204openalex-snapshot

The role of micro RNAs (miRNAs) in the regulation of Drosophila melanogaster’s innate immunity

inferred← citeshttps://doi.org/10.1080/21505594.2025.2549497openalex-snapshot

Investigating the differential microRNAs expression in young and aged Drosophila melanogaster following Flock House Virus infection

inferred← citeshttps://doi.org/10.1080/22221751.2019.1599302openalex-snapshot

Endogenous non-retroviral elements in genomes of Aedes mosquitoes and vector competence

inferred← citeshttps://doi.org/10.1093/gbe/evag034openalex-snapshot

Predictors of Protein Evolution in the drosophilid Immune System

inferred← citeshttps://doi.org/10.1093/nar/gkaf715openalex-snapshot

A U3 snoRNA is required for the regulation of chromatin dynamics and antiviral response in Drosophila melanogaster

inferred← citeshttps://doi.org/10.1097/qco.0000000000000342openalex-snapshot

The potential role of Wolbachia in controlling the transmission of emerging human arboviral infections

inferred← citeshttps://doi.org/10.1098/rsob.120075openalex-snapshot

Drosophila as a model system to unravel the layers of innate immunity to infection

inferred← citeshttps://doi.org/10.1098/rsob.200246openalex-snapshot

Temperature modulates immune gene expression in mosquitoes during arbovirus infection

inferred← citeshttps://doi.org/10.1098/rsob.220146openalex-snapshot

Lipopolysaccharide detection by the innate immune system may be an uncommon defence strategy used in nature

inferred← citeshttps://doi.org/10.1098/rspb.2010.1517openalex-snapshot

Within and transgenerational immune priming in an insect to a DNA virus

inferred← citeshttps://doi.org/10.1099/jgv.0.001741openalex-snapshot

The antiviral role of NF-κB-mediated immune responses and their antagonism by viruses in insects

inferred← citeshttps://doi.org/10.1099/vir.0.057422-0openalex-snapshot

Understanding the Wolbachia-mediated inhibition of arboviruses in mosquitoes: progress and challenges

inferred← citeshttps://doi.org/10.1099/vir.0.064766-0openalex-snapshot

Genomic diversity in European Spodoptera exigua multiple nucleopolyhedrovirus isolates

inferred← citeshttps://doi.org/10.1101/2020.05.14.096024openalex-snapshot

Recurrent evolution of two competing haplotypes in an insect DNA virus

inferred← citeshttps://doi.org/10.1101/2021.01.13.425146openalex-snapshot

Aedes aegypti Aag-2 culture cells enter endoreplication process upon pathogen challenge

inferred← citeshttps://doi.org/10.1101/2023.11.16.567400openalex-snapshot

Viral infection disrupts intestinal homeostasis via Sting-dependent NF-kB signaling

inferred← citeshttps://doi.org/10.1101/2024.04.03.587950openalex-snapshot

Mosquito immune cells enhance dengue and Zika virus dissemination in Aedes aegypti

inferred← citeshttps://doi.org/10.1111/1744-7917.13158openalex-snapshot

Antiviral function of peptidoglycan recognition protein in Spodoptera exigua (Lepidoptera: Noctuidae)

inferred← citeshttps://doi.org/10.1111/1744-7917.70180openalex-snapshot

Phase separation and phosphorylation of sfCactin orchestrate antiviral defense against Southern rice black‐streaked dwarf virus in Sogatella furcifera

inferred← citeshttps://doi.org/10.1111/1748-5967.70053openalex-snapshot

Adaptation Mechanisms of Drosophila melanogaster and Drosophila suzukii to Their Distinct Habitats

inferred← citeshttps://doi.org/10.1111/febs.13235openalex-snapshot

Drosophila blood cells and their role in immune responses

inferred← citeshttps://doi.org/10.1111/imb.12166openalex-snapshot

Molecular interactions and immune responses between Maize fine streak virus and the leafhopper vector Graminella nigrifrons through differential expression and RNA interference

inferred← citeshttps://doi.org/10.1111/imb.12681openalex-snapshot

Target antifungal peptides of immune signalling pathways in silkworm, Bombyx mori , against Beauveria bassiana

inferred← citeshttps://doi.org/10.1111/imb.70006openalex-snapshot

Modulation of DNA methyltransferases ( DNMTs ) in Spodoptera frugiperda (Sf9) cells following AcMNPV infection, and its effects on the virus‐cell interaction

inferred← citeshttps://doi.org/10.1111/j.1365-2583.2010.01060.xopenalex-snapshot

Analysis of expressed sequence tags from Maize mosaic rhabdovirus ‐infected gut tissues of Peregrinus maidis reveals the presence of key components of insect innate immunity

inferred← citeshttps://doi.org/10.1111/j.1462-5822.2011.01649.xopenalex-snapshot

Innate immune control of West Nile virus infection

inferred← citeshttps://doi.org/10.1111/j.1600-065x.2010.00985.xopenalex-snapshot

Intracellular immune responses of dipteran insects

inferred← citeshttps://doi.org/10.1111/j.1600-065x.2012.01096.xopenalex-snapshot

NF‐κB: where did it come from and why?

inferred← citeshttps://doi.org/10.1111/sji.12170openalex-snapshot

JAK/STAT Pathway in Drosophila Immunity

inferred← citeshttps://doi.org/10.1128/9781555819194.ch5openalex-snapshot

Advances in Myeloid-Like Cell Origins and Functions in the Model OrganismDrosophila melanogaster

inferred← citeshttps://doi.org/10.1128/cmr.00045-12openalex-snapshot

West Nile Virus: Biology, Transmission, and Human Infection

inferred← citeshttps://doi.org/10.1128/jvi.00177-24openalex-snapshot

Regulation of ubiquitination and antiviral activity of Cactin by deubiquitinase Usp14 in Drosophila

inferred← citeshttps://doi.org/10.1128/jvi.00238-16openalex-snapshot

Analysis of the Contribution of Hemocytes and Autophagy to Drosophila Antiviral Immunity

inferred← citeshttps://doi.org/10.1128/jvi.00254-18openalex-snapshot

Bub1 Facilitates Virus Entry through Endocytosis in a Model of Drosophila Pathogenesis

inferred← citeshttps://doi.org/10.1128/jvi.00463-15openalex-snapshot

The 5′ Untranslated Region of a Novel Infectious Molecular Clone of the Dicistrovirus Cricket Paralysis Virus Modulates Infection

inferred← citeshttps://doi.org/10.1128/jvi.01443-18openalex-snapshot

Induction and Suppression of NF-κB Signalling by a DNA Virus of Drosophila

inferred← citeshttps://doi.org/10.1128/jvi.01779-16openalex-snapshot

Disruption of Stress Granule Formation by the Multifunctional Cricket Paralysis Virus 1A Protein

inferred← citeshttps://doi.org/10.1128/jvi.01985-19openalex-snapshot

Mitochondrial and Innate Immunity Transcriptomes from Spodoptera frugiperda Larvae Infected with the Spodoptera frugiperda Ascovirus

inferred← citeshttps://doi.org/10.1128/jvi.02320-14openalex-snapshot

Drosophila C Virus Systemic Infection Leads to Intestinal Obstruction

inferred← citeshttps://doi.org/10.1128/jvi.03360-12openalex-snapshot

An Antiviral Role for Antimicrobial Peptides during the Arthropod Response to Alphavirus Replication

inferred← citeshttps://doi.org/10.1128/mbio.01378-23openalex-snapshot

Regulation of phase separation and antiviral activity of Cactin by glycolytic enzyme PGK via phosphorylation in Drosophila

inferred← citeshttps://doi.org/10.1128/mbio.01469-24openalex-snapshot

Protein-coding circular RNA enhances antiviral immunity via JAK/STAT pathway in Drosophila

inferred← citeshttps://doi.org/10.1128/mbio.02209-20openalex-snapshot

Endogenous Viral Element-Derived Piwi-Interacting RNAs (piRNAs) Are Not Required for Production of Ping-Pong-Dependent piRNAs from Diaphorina citri Densovirus

inferred← citeshttps://doi.org/10.1128/microbiolspec.mchd-0038-2016openalex-snapshot

Advances in Myeloid-Like Cell Origins and Functions in the Model OrganismDrosophila melanogaster

inferred← citeshttps://doi.org/10.1186/1471-2164-11-303openalex-snapshot

Massively parallel pyrosequencing-based transcriptome analyses of small brown planthopper (Laodelphax striatellus), a vector insect transmitting rice stripe virus (RSV)

inferred← citeshttps://doi.org/10.1186/1743-422x-10-210openalex-snapshot

Transcriptional profiling of Drosophila S2 cells in early response to Drosophila C virus

inferred← citeshttps://doi.org/10.1186/s12864-025-12421-zopenalex-snapshot

Integrated transcriptomic and metabolomic analysis reveal metabolic responses of Eriocheir sinensis to Aeromonas hydrophila infection

inferred← citeshttps://doi.org/10.1186/s12864-026-12902-9openalex-snapshot

Persistent viral infection in the Drosophila fat body is associated with immune activation at the single cell level

inferred← citeshttps://doi.org/10.1186/s12866-018-1296-3openalex-snapshot

Coevolution of hytrosaviruses and host immune responses

inferred← citeshttps://doi.org/10.1186/s12866-018-1298-1openalex-snapshot

RNA interference-based antiviral immune response against the salivary gland hypertrophy virus in Glossina pallidipes

inferred← citeshttps://doi.org/10.1242/jcs.064592openalex-snapshot

Drosophilacellular immunity: a story of migration and adhesion

inferred← citeshttps://doi.org/10.1242/jeb.097766openalex-snapshot

Immunogene and viral transcript dynamics during parasitic Varroa destructor mite infection of developing honey bee (Apis mellifera) pupae

inferred← citeshttps://doi.org/10.1371/journal.pgen.1003633openalex-snapshot

Sociogenomics of Cooperation and Conflict during Colony Founding in the Fire Ant Solenopsis invicta

inferred← citeshttps://doi.org/10.1371/journal.pone.0010678openalex-snapshot

Dengue Virus Inhibits Immune Responses in Aedes aegypti Cells

inferred← citeshttps://doi.org/10.1371/journal.pone.0015361openalex-snapshot

Innate Immune Responses of Drosophila melanogaster Are Altered by Spaceflight

inferred← citeshttps://doi.org/10.1371/journal.pone.0077263openalex-snapshot

Non-Specific dsRNA-Mediated Antiviral Response in the Honey Bee

inferred← citeshttps://doi.org/10.1371/journal.pone.0112092openalex-snapshot

A Drosophila Toolkit for the Visualization and Quantification of Viral Replication Launched from Transgenic Genomes

inferred← citeshttps://doi.org/10.1371/journal.pone.0223438openalex-snapshot

Comparison of transcriptomes of an orthotospovirus vector and non-vector thrips species

inferred← citeshttps://doi.org/10.1371/journal.ppat.1002722openalex-snapshot

Polydnavirus Ank Proteins Bind NF-κB Homodimers and Inhibit Processing of Relish

inferred← citeshttps://doi.org/10.1371/journal.ppat.1002735openalex-snapshot

Synergistic Parasite-Pathogen Interactions Mediated by Host Immunity Can Drive the Collapse of Honeybee Colonies

inferred← citeshttps://doi.org/10.1371/journal.ppat.1003914openalex-snapshot

Genome-Wide RNAi Screen Identifies Broadly-Acting Host Factors That Inhibit Arbovirus Infection

inferred← citeshttps://doi.org/10.1371/journal.ppat.1004034openalex-snapshot

pelo Is Required for High Efficiency Viral Replication

inferred← citeshttps://doi.org/10.1371/journal.ppat.1004507openalex-snapshot

The Toll-Dorsal Pathway Is Required for Resistance to Viral Oral Infection in Drosophila

inferred← citeshttps://doi.org/10.1371/journal.ppat.1007020openalex-snapshot

p38b and JAK-STAT signaling protect against Invertebrate iridescent virus 6 infection in Drosophila

inferred← citeshttps://doi.org/10.1371/journal.ppat.1011044openalex-snapshot

Investigating the outcomes of virus coinfection within and across host species

inferred← citeshttps://doi.org/10.1371/journal.ppat.1012828openalex-snapshot

White spot syndrome virus immediate-early protein (wsv100) antagonizes the NF-κB pathway to inhibit innate immune response in shrimp

inferred← citeshttps://doi.org/10.14288/1.0058465openalex-snapshot

Analysis of the host-pathogen proteomics of Israeli Acute Paralysis Virus in the honey bee using mass spectrometry

inferred← citeshttps://doi.org/10.1534/g3.118.200872openalex-snapshot

A Transgenic Flock House Virus Replicon Reveals an RNAi Independent Antiviral Mechanism Acting inDrosophilaFollicular Somatic Cells

inferred← citeshttps://doi.org/10.1534/genetics.113.150854openalex-snapshot

The Innate Immune Response Transcription Factor Relish Is Necessary for Neurodegeneration in a Drosophila Model of Ataxia-Telangiectasia

inferred← citeshttps://doi.org/10.21775/9781912530083.03openalex-snapshot

Sensing Viral Infections in Insects: A Dearth of Pathway Receptors

inferred← citeshttps://doi.org/10.21775/9781912530083.05openalex-snapshot

Dicistrovirus-Host Molecular Interactions

inferred← citeshttps://doi.org/10.21775/cimb.034.031openalex-snapshot

Sensing Viral Infections in Insects: A Dearth of Pathway Receptors

inferred← citeshttps://doi.org/10.21775/cimb.034.083openalex-snapshot

Dicistrovirus-Host Molecular Interactions

inferred← citeshttps://doi.org/10.25560/6358openalex-snapshot

Anti-viral immunity in Anopheles gambiae mosquitoes

inferred← citeshttps://doi.org/10.31390/gradschool_dissertations.1179openalex-snapshot

Identification and Characterization of a Relish-type NF-kB, DvRelish in Dermacentor variabilis, the American Dog Tick

inferred← citeshttps://doi.org/10.3389/978-2-88971-890-0openalex-snapshot

Unconventional Animal Models in Infectious Disease Research

inferred← citeshttps://doi.org/10.3389/fcimb.2013.00103openalex-snapshot

Drosophila at the intersection of infection, inflammation, and cancer

inferred← citeshttps://doi.org/10.3389/fcimb.2017.00258openalex-snapshot

NF-κB-Like Signaling Pathway REL2 in Immune Defenses of the Malaria Vector Anopheles gambiae

inferred← citeshttps://doi.org/10.3389/fcimb.2020.00214openalex-snapshot

Drosophila as a Model Organism in Host–Pathogen Interaction Studies

inferred← citeshttps://doi.org/10.3389/fcimb.2025.1538459openalex-snapshot

Unveiling Wolbachia transcriptomic signature in the arboviral vector Aedes aegypti

inferred← citeshttps://doi.org/10.3389/fcimb.2025.1621846openalex-snapshot

Drosophila melanogaster as a model system for studying the effects of porcine rotavirus on intestinal immunity

inferred← citeshttps://doi.org/10.3389/fimmu.2019.00776openalex-snapshot

Distinct Functions of Bombyx mori Peptidoglycan Recognition Protein 2 in Immune Responses to Bacteria and Viruses

inferred← citeshttps://doi.org/10.3389/fimmu.2022.904862openalex-snapshot

A Versatile Hemolin With Pattern Recognitional Contributions to the Humoral Immune Responses of the Chinese Oak Silkworm Antheraea pernyi

inferred← citeshttps://doi.org/10.3389/finsc.2021.749781openalex-snapshot

The Honey Bee Gene Bee Antiviral Protein-1 Is a Taxonomically Restricted Antiviral Immune Gene

inferred← citeshttps://doi.org/10.3389/fitd.2022.762132openalex-snapshot

Trans-Generational Symbiont Transmission Reduced at High Temperatures in a West Nile Virus Vector Mosquito Culex quinquefasciatus

inferred← citeshttps://doi.org/10.3389/fmicb.2017.00223openalex-snapshot

Tick Humoral Responses: Marching to the Beat of a Different Drummer

inferred← citeshttps://doi.org/10.3389/fmicb.2018.01040openalex-snapshot

Viral Determinants and Vector Competence of Zika Virus Transmission

inferred← citeshttps://doi.org/10.3389/fmicb.2021.773211openalex-snapshot

Vector Specificity of Arbovirus Transmission

inferred← citeshttps://doi.org/10.3389/fmicb.2024.1380647openalex-snapshot

Wolbachia endosymbionts in Drosophila regulate the resistance to Zika virus infection in a sex dependent manner

inferred← citeshttps://doi.org/10.3389/fphys.2013.00319openalex-snapshot

The possible impact of persistent virus infection on the function of the RNAi machinery in insects: a hypothesis

inferred← citeshttps://doi.org/10.3390/biom13071159openalex-snapshot

Recognition of Arboviruses by the Mosquito Immune System

inferred← citeshttps://doi.org/10.3390/books978-3-03921-517-1openalex-snapshot

Family Iridoviridae Molecular and Ecological Studies of a Family Infecting Invertebrates and Ectothermic Vertebrates

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