On the public citation graph

Barrier Immune Effectors Are Maintained during Transition from Nurse to Forager in the Honey Bee

https://doi.org/10.1371/journal.pone.0054097

0 signed · 103 inferred · view as graph

Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.

Is this your work? Sign in with ORCID and put your name on the claims that are yours.

Claim with ORCID

Reference health. See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.

See reference health

What this work says

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

inferredcites →https://doi.org/10.1002/arch.20301openalex-snapshot

Trade‐off between immune stimulation and expression of storage protein genes

inferredcites →https://doi.org/10.1002/wsbm.73openalex-snapshot

Nutritional regulation of division of labor in honey bees: toward a systems biology perspective

inferredcites →https://doi.org/10.1007/978-3-540-70962-6_2openalex-snapshot

Infectious Disease Modeling and the Dynamics of Transmission

inferredcites →https://doi.org/10.1007/bf00299306openalex-snapshot

Adaptive significance of the age polyethism schedule in honeybee colonies

inferredcites →https://doi.org/10.1016/j.anbehav.2004.03.017openalex-snapshot

Worker nutrition and division of labour in honeybees

inferredcites →https://doi.org/10.1016/j.arr.2005.03.007openalex-snapshot

Intergenerational transfers may have decoupled physiological and chronological age in a eusocial insect

inferredcites →https://doi.org/10.1016/j.bbagen.2008.06.008openalex-snapshot

Age-related upregulation of Drosophila caudal gene via NF-κB in the adult posterior midgut

inferredcites →https://doi.org/10.1016/j.ecolmodel.2007.01.001openalex-snapshot

HoPoMo: A model of honeybee intracolonial population dynamics and resource management

inferredcites →https://doi.org/10.1016/j.exger.2004.02.010openalex-snapshot

Hormonal control of the yolk precursor vitellogenin regulates immune function and longevity in honeybees

inferredcites →https://doi.org/10.1016/j.exger.2005.08.004openalex-snapshot

Social reversal of immunosenescence in honey bee workers

inferredcites →https://doi.org/10.1016/j.febslet.2010.04.007openalex-snapshot

The curious case of aging plasticity in honey bees

inferredcites →https://doi.org/10.1016/j.it.2009.04.004openalex-snapshot

Mucosal immunosenescence: new developments and vaccines to control infectious diseases

inferredcites →https://doi.org/10.1016/j.it.2009.05.001openalex-snapshot

An evolutionary perspective on the mechanisms of immunosenescence

inferredcites →https://doi.org/10.1016/j.jinsphys.2008.07.016openalex-snapshot

The ontogeny of immunity: Development of innate immune strength in the honey bee (Apis mellifera)

inferredcites →https://doi.org/10.1016/j.jinsphys.2011.04.020openalex-snapshot

The ontogeny of immunity in the honey bee, Apis mellifera L. following an immune challenge

inferredcites →https://doi.org/10.1016/j.jip.2006.04.004openalex-snapshot

Beepath: An ordered quantitative-PCR array for exploring honey bee immunity and disease

inferredcites →https://doi.org/10.1016/j.jip.2008.06.010openalex-snapshot

The distribution of Paenibacillus larvae spores in adult bees and honey and larval mortality, following the addition of American foulbrood diseased brood or spore-contaminated honey in honey bee (Apis mellifera) colonies

inferredcites →https://doi.org/10.1016/j.micinf.2008.07.010openalex-snapshot

Immune reactions of insects on bacterial pathogens and mutualists

inferredcites →https://doi.org/10.1016/j.tim.2011.09.003openalex-snapshot

Bees brought to their knees: microbes affecting honey bee health

inferredcites →https://doi.org/10.1016/s0020-7519(97)00189-6openalex-snapshot

Multiparasite communities in animals and humans: frequency, structure and pathogenic significance

inferredcites →https://doi.org/10.1016/s0021-9258(19)61943-5openalex-snapshot

Acute transcriptional response of the honeybee peptide-antibiotics gene repertoire and required post-translational conversion of the precursor structures.

inferredcites →https://doi.org/10.1016/s1532-0456(01)00226-5openalex-snapshot

Eicosanoids act in nodulation reactions to bacterial infections in newly emerged adult honey bees, Apis mellifera, but not in older foragers

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/nrmicro1098openalex-snapshot

Antimicrobial peptides: pore formers or metabolic inhibitors in bacteria?

inferredcites →https://doi.org/10.1038/nrmicro2029openalex-snapshot

Super-shedding and the link between human infection and livestock carriage of Escherichia coli O157

inferredcites →https://doi.org/10.1051/apido:2001122openalex-snapshot

Implications of horizontal and vertical pathogen transmission for honey bee epidemiology

inferredcites →https://doi.org/10.1051/apido:2008015openalex-snapshot

Validation of reference genes for gene expression studies in the honey bee,Apis mellifera, by quantitative real-time RT-PCR

inferredcites →https://doi.org/10.1051/apido:2008032openalex-snapshot

Horizontal transmission of Paenibacillus larvae spores between honey bee ( Apis mellifera ) colonies through robbing

inferredcites →https://doi.org/10.1073/pnas.0701909104openalex-snapshot

Vitellogenin, juvenile hormone, insulin signaling, and queen honey bee longevity

inferredcites →https://doi.org/10.1073/pnas.0904847106openalex-snapshot

Human gut microbiome adopts an alternative state following small bowel transplantation

inferredcites →https://doi.org/10.1073/pnas.1530303100openalex-snapshot

Rethinking the evolutionary theory of aging: Transfers, not births, shape senescence in social species

inferredcites →https://doi.org/10.1073/pnas.94.26.14614openalex-snapshot

Drosophila host defense: Differential induction of antimicrobial peptide genes after infection by various classes of microorganisms

inferredcites →https://doi.org/10.1093/jee/97.3.752openalex-snapshot

Bacterial Probiotics Induce an Immune Response in the Honey Bee (Hymenoptera: Apidae)

inferredcites →https://doi.org/10.1098/rspb.1994.0176openalex-snapshot

Shared use of flowers leads to horizontal pathogen transmission

inferredcites →https://doi.org/10.1111/j.1365-2435.2010.01753.xopenalex-snapshot

Disease ecology meets ecological immunology: understanding the links between organismal immunity and infection dynamics in natural populations

inferredcites →https://doi.org/10.1111/j.1365-2435.2010.01817.xopenalex-snapshot

Outdoor immunology: methodological considerations for ecologists

inferredcites →https://doi.org/10.1111/j.1365-2583.2006.00682.xopenalex-snapshot

Immune pathways and defence mechanisms in honey bees Apis mellifera

inferredcites →https://doi.org/10.1111/j.1365-294x.2010.04959.xopenalex-snapshot

A simple and distinctive microbiota associated with honey bees and bumble bees

inferredcites →https://doi.org/10.1111/j.1462-2920.2005.00893.xopenalex-snapshot

Diversity and phylotype consistency of bacteria in the guts of three bee species ( Apoidea ) at an oilseed rape field

inferredcites →https://doi.org/10.1111/j.1474-9726.2008.00370.xopenalex-snapshot

Functional analysis of the Drosophila immune response during aging

inferredcites →https://doi.org/10.1111/j.1474-9726.2008.00380.xopenalex-snapshot

Age‐related changes in Drosophila midgut are associated with PVF2, a PDGF/VEGF‐like growth factor

inferredcites →https://doi.org/10.1111/j.1474-9726.2010.00647.xopenalex-snapshot

Social context, stress, and plasticity of aging

inferredcites →https://doi.org/10.1111/j.1474-9728.2004.00106.xopenalex-snapshot

Immunity and aging: the enemy within?

inferredcites →https://doi.org/10.1126/sageke.2004.26.pe28openalex-snapshot

Epigenetic Regulation of Aging in Honeybee Workers

inferredcites →https://doi.org/10.1126/science.1058709openalex-snapshot

Commensal Host-Bacterial Relationships in the Gut

inferredcites →https://doi.org/10.1126/science.1069911openalex-snapshot

Influence of Gene Action Across Different Time Scales on Behavior

inferredcites →https://doi.org/10.1128/aem.01319-09openalex-snapshot

Presence and Prevalence of Viruses in Local and Migratory Honeybees ( Apis mellifera ) in Massachusetts

inferredcites →https://doi.org/10.1128/aem.07810-11openalex-snapshot

Establishment of Characteristic Gut Bacteria during Development of the Honeybee Worker

inferredcites →https://doi.org/10.1146/annurev.immunol.25.022106.141615openalex-snapshot

The Host Defense of Drosophila melanogaster

inferredcites →https://doi.org/10.1159/000086648openalex-snapshot

Antimicrobial Peptides in Drosophila: Structures,Activities and Gene Regulation

inferredcites →https://doi.org/10.1242/dmm.003970openalex-snapshot

Drosophila melanogaster as a model for human intestinal infection and pathology

inferredcites →https://doi.org/10.1242/jeb.01956openalex-snapshot

Nutritional status influences socially regulated foraging ontogeny in honey bees

inferredcites →https://doi.org/10.1371/journal.pgen.1002082openalex-snapshot

A Decline in p38 MAPK Signaling Underlies Immunosenescence in Caenorhabditis elegans

inferredcites →https://doi.org/10.1371/journal.pone.0006481openalex-snapshot

Colony Collapse Disorder: A Descriptive Study

inferredcites →https://doi.org/10.1371/journal.pone.0014357openalex-snapshot

RNA Viruses in Hymenopteran Pollinators: Evidence of Inter-Taxa Virus Transmission via Pollen and Potential Impact on Non-Apis Hymenopteran Species

inferredcites →https://doi.org/10.1371/journal.pone.0018491openalex-snapshot

A Quantitative Model of Honey Bee Colony Population Dynamics

inferredcites →https://doi.org/10.1371/journal.pone.0020656openalex-snapshot

Temporal Analysis of the Honey Bee Microbiome Reveals Four Novel Viruses and Seasonal Prevalence of Known Viruses, Nosema, and Crithidia

inferredcites →https://doi.org/10.1371/journal.pone.0032962openalex-snapshot

Characterization of the Active Microbiotas Associated with Honey Bees Reveals Healthier and Broader Communities when Colonies are Genetically Diverse

inferredcites →https://doi.org/10.1371/journal.pone.0036393openalex-snapshot

Distinctive Gut Microbiota of Honey Bees Assessed Using Deep Sampling from Individual Worker Bees

inferredcites →https://doi.org/10.1371/journal.pone.0037017openalex-snapshot

Gut Pathology and Responses to the Microsporidium Nosema ceranae in the Honey Bee Apis mellifera

inferredcites →https://doi.org/10.1371/journal.pone.0041250openalex-snapshot

Independent Studies Using Deep Sequencing Resolve the Same Set of Core Bacterial Species Dominating Gut Communities of Honey Bees

inferredcites →https://doi.org/10.1371/journal.pone.0043562openalex-snapshot

Pathogen Webs in Collapsing Honey Bee Colonies

inferredcites →https://doi.org/10.1371/journal.ppat.1000184openalex-snapshot

Discerning the Complexity of Community Interactions Using a Drosophila Model of Polymicrobial Infections

inferredcites →https://doi.org/10.1515/9780691206851openalex-snapshot

Parasites in Social Insects

inferredcites →https://doi.org/10.1603/ec10355openalex-snapshot

Cross-Species Infection of Deformed Wing Virus Poses a New Threat to Pollinator Conservation

inferredcites →https://doi.org/10.1673/031.008.3301openalex-snapshot

Reference Gene Selection for Insect Expression Studies Using Quantitative Real-Time PCR: The Head of the Honeybee,Apis mellifera, After a Bacterial Challenge

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.4561311openalex-extracted

Analysis of X-Ray Irradiation Effects on the Mortality Values and Hemolymph Immune Cell Composition of Apis Mellifera and its Parasite, Varroa Destructor

inferred← citeshttps://doi.org/10.1002/ps.70106openalex-snapshot

Immune priming of honey bees protects against a major microsporidian pathogen

inferred← citeshttps://doi.org/10.1007/s00253-016-7870-4openalex-snapshot

Beneficial microorganisms for honey bees: problems and progresses

inferred← citeshttps://doi.org/10.1007/s12602-024-10248-wopenalex-snapshot

Probiotic Potential of Bacillus Subtilis Strain I3: Antagonistic Activity Against Chalkbrood Pathogen and Pesticide Degradation for Enhancing Honeybee Health

inferred← citeshttps://doi.org/10.1007/s13592-014-0279-0openalex-snapshot

Apis mellifera hemocytes generate increased amounts of nitric oxide in response to wounding/encapsulation

inferred← citeshttps://doi.org/10.1007/s13592-015-0418-2openalex-snapshot

Cellular immunity in Apis mellifera: studying hemocytes brings light about bees skills to confront threats

inferred← citeshttps://doi.org/10.1007/s13592-024-01135-yopenalex-snapshot

Topical exposure of honey bee queens to heat-inactivated Israeli acute paralysis virus does not protect their offspring against active infection

inferred← citeshttps://doi.org/10.1007/s13592-026-01278-0openalex-snapshot

Influence of bee pollen supplement on health and immunity of the honeybee Apis mellifera L

inferred← citeshttps://doi.org/10.1016/j.aspen.2025.102519openalex-snapshot

Ecological interactions among plants, honeybees, and microbes: implications for sustainable ecosystems

inferred← citeshttps://doi.org/10.1016/j.cbpb.2021.110679openalex-snapshot

Cuticle melanization and the expression of immune-related genes in the honeybee Apis mellifera (Hymenoptera: Apidae) adult workers

inferred← citeshttps://doi.org/10.1016/j.chroma.2014.11.041openalex-snapshot

A sensitive quantification of the peptide apidaecin 1 isoforms in single bee tissues using a weak cation exchange pre-separation and nanocapillary liquid chromatography coupled with mass spectrometry

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

Single and mixed-species trypanosome and microsporidia infections elicit distinct, ephemeral cellular and humoral immune responses in honey bees

inferred← citeshttps://doi.org/10.1016/j.ecoenv.2023.115754openalex-snapshot

Variation in the physiological response of adult worker bees of different ages (Apis mellifera L.) to pyraclostrobin stress

inferred← citeshttps://doi.org/10.1016/j.exger.2019.02.005openalex-snapshot

Immunosenescence in honey bees (Apis mellifera L.) is caused by intrinsic senescence and behavioral physiology

inferred← citeshttps://doi.org/10.1016/j.ibmb.2020.103368openalex-snapshot

The IRE1 pathway regulates honey bee Unfolded Protein Response gene expression

inferred← citeshttps://doi.org/10.1016/j.ibmb.2021.103667openalex-snapshot

Halofuginone triggers a transcriptional program centered on ribosome biogenesis and function in honey bees

inferred← citeshttps://doi.org/10.1016/j.jip.2017.07.005openalex-snapshot

Relative abundance of deformed wing virus, Varroa destructor virus 1, and their recombinants in honey bees (Apis mellifera) assessed by kmer analysis of public RNA-Seq data

inferred← citeshttps://doi.org/10.1016/j.jip.2017.09.006openalex-snapshot

Chinese Sacbrood virus infection in Asian honey bees (Apis cerana cerana) and host immune responses to the virus infection

inferred← citeshttps://doi.org/10.1016/j.jip.2024.108109openalex-snapshot

Analysis of X-ray irradiation effects on the mortality values and hemolymph immune cell composition of Apis mellifera and its parasite, Varroa destructor

inferred← citeshttps://doi.org/10.1016/j.micpath.2017.10.006openalex-snapshot

Immune responses in the haemolymph and antimicrobial peptide expression in the abdomen of Apis mellifera challenged with Spiroplasma melliferum CH-1

inferred← citeshttps://doi.org/10.1038/nrmicro.2016.43openalex-snapshot

Gut microbial communities of social bees

inferred← citeshttps://doi.org/10.1080/00218839.2015.1109919openalex-snapshot

Antimicrobial peptides: a key component of honey bee innate immunity

inferred← citeshttps://doi.org/10.1080/15476286.2015.1128063openalex-snapshot

Negligible uptake and transfer of diet-derived pollen microRNAs in adult honey bees

inferred← citeshttps://doi.org/10.1093/jee/tox193openalex-snapshot

Nectar and Pollen Phytochemicals Stimulate Honey Bee (Hymenoptera: Apidae) Immunity to Viral Infection

inferred← citeshttps://doi.org/10.1159/000550255openalex-snapshot

Clodronate Liposomes Untangle the Role of Hemocytes in Apis mellifera Response to Temperature Variation and Microbial Infection

inferred← citeshttps://doi.org/10.1186/s43088-025-00596-zopenalex-snapshot

Effect of thymol and propolis extract on genotoxicity, biochemical activities and expression profile of some genes on honey bee, Apis mellifera, infected with Vairimorpha (Nosema) ceranae

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.0108486openalex-snapshot

Honey Bee Hemocyte Profiling by Flow Cytometry

inferred← citeshttps://doi.org/10.1371/journal.pone.0187079openalex-snapshot

Immune related gene expression in worker honey bee (Apis mellifera carnica) pupae exposed to neonicotinoid thiamethoxam and Varroa mites (Varroa destructor)

inferred← citeshttps://doi.org/10.1371/journal.pone.0220703openalex-snapshot

Influence of chronic exposure to thiamethoxam and chronic bee paralysis virus on winter honey bees

inferred← citeshttps://doi.org/10.1515/jas-2017-0007openalex-snapshot

Effects of Lactobacillus Johnsonii AJ5 Metabolites on Nutrition, Nosema Ceranae Development and Performance of Apis Mellifera L.

inferred← citeshttps://doi.org/10.2478/jas-2020-0009openalex-snapshot

Effects of Bacterial Cell-Free Supernatant on Nutritional Parameters of Apis Mellifera and Their Toxicity Against Varroa Destructor

inferred← citeshttps://doi.org/10.3390/insects16060593openalex-snapshot

Immune Gene Expression and Locomotor Activity in Response to Vairimorpha ceranae Infection Across Five Honey Bee Subspecies

inferred← citeshttps://doi.org/10.3390/insects9030079openalex-snapshot

Does the Pollen Diet Influence the Production and Expression of Antimicrobial Peptides in Individual Honey Bees?

inferred← citeshttps://doi.org/10.3390/microorganisms8081146openalex-snapshot

Dynamics of the Honeybee (Apis mellifera) Gut Microbiota Throughout the Overwintering Period in Canada

inferred← citeshttps://doi.org/10.51970/jasp.1266441openalex-snapshot

Vairimorpha (Nosema) Parazitinin Antimikrobiyal Peptidler Aracılığıyla Bal Arılarının Hümoral Bağışıklığına Etkileri

inferred← citeshttps://doi.org/10.70675/69169268z4f8az41a3z8125z3ef5ded0ff95openalex-snapshot

Rôle des intéractions virus/ pesticides dans le déclin des abeilles

Editorial review for independent work. ICSAC — the Institute for Complexity Science and Advanced Computing — runs a structured editorial panel for researchers publishing outside journals, and publishes on CiteStamp rails. Submission is free and goes through ORCID: icsacinstitute.org/submit.