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Immunosenescence and resistance to parasite infection in the honey bee, Apis mellifera
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/jemt.10409openalex-snapshot
Aging of the vertebrate immune system
inferredcites →https://doi.org/10.1006/anbe.2001.1786openalex-snapshot
Changes in lifetime immunocompetence in male and female Gryllus texensis (formerly G. integer): trade-offs between immunity and reproduction
inferredcites →https://doi.org/10.1007/978-94-024-1179-9_300286openalex-snapshot
Colony Collapse Disorder
inferredcites →https://doi.org/10.1016/j.anbehav.2004.05.005openalex-snapshot
How should behavioural ecologists interpret measurements of immunity?
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.jinsphys.2003.11.011openalex-snapshot
Estimating disease resistance in insects: phenoloxidase and lysozyme-like activity and disease resistance in the cricket Gryllus texensis
inferredcites →https://doi.org/10.1016/j.jinsphys.2008.04.013openalex-snapshot
Temporal patterns in immune responses to a range of microbial insults (Tenebrio molitor)
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.2010.01.009openalex-snapshot
The effects of age and social interactions on innate immunity in a leaf-cutting ant
inferredcites →https://doi.org/10.1016/j.jinsphys.2012.04.016openalex-snapshot
Differential expression of immune genes of adult honey bee (Apis mellifera) after inoculated by Nosema ceranae
inferredcites →https://doi.org/10.1016/j.jip.2004.07.004openalex-snapshot
In vivo dynamics of an immune response in the bumble bee Bombus terrestris
inferredcites →https://doi.org/10.1016/j.jip.2006.02.005openalex-snapshot
Nosema ceranae, a new microsporidian parasite in honeybees in Europe
inferredcites →https://doi.org/10.1016/j.jip.2006.11.001openalex-snapshot
Experimental infection of Apis mellifera honeybees with Nosema ceranae (Microsporidia)
inferredcites →https://doi.org/10.1016/j.jip.2007.02.014openalex-snapshot
Widespread dispersal of the microsporidian Nosema ceranae, an emergent pathogen of the western honey bee, Apis mellifera
inferredcites →https://doi.org/10.1016/j.jip.2007.07.010openalex-snapshot
Nosema ceranae is a long-present and wide-spread microsporidian infection of the European honey bee (Apis mellifera) in the United States
inferredcites →https://doi.org/10.1016/j.jip.2009.06.017openalex-snapshot
Nosema ceranae in European honey bees (Apis mellifera)
inferredcites →https://doi.org/10.1016/j.jip.2009.10.009openalex-snapshot
Genetic detection and quantification of Nosema apis and N. ceranae in the honey bee
inferredcites →https://doi.org/10.1016/j.jip.2010.10.003openalex-snapshot
Nosema ceranae, a new parasite in Thai honeybees
inferredcites →https://doi.org/10.1016/j.jip.2013.06.005openalex-snapshot
Emerging dangers: Deadly effects of an emergent parasite in a new pollinator host
inferredcites →https://doi.org/10.1016/j.vetpar.2010.02.010openalex-snapshot
Comparative virulence of Nosema ceranae and Nosema apis in individual European honey bees
inferredcites →https://doi.org/10.1016/s0960-9822(02)00808-4openalex-snapshot
Genome-Wide Transcript Profiles in Aging and Calorically Restricted Drosophila melanogaster
inferredcites →https://doi.org/10.1017/s0031182002002755openalex-snapshot
Activation of host constitutive immune defence by an intestinal trypanosome parasite of bumble bees
inferredcites →https://doi.org/10.1038/nature12977openalex-snapshot
Disease associations between honeybees and bumblebees as a threat to wild pollinators
inferredcites →https://doi.org/10.1038/sj.hdy.6800031openalex-snapshot
Heritability of immune function in the caterpillar Spodoptera littoralis
inferredcites →https://doi.org/10.1046/j.1420-9101.2003.00611.xopenalex-snapshot
Age-related decline in humoral immune function in Collared Flycatchers
inferredcites →https://doi.org/10.1051/apido/2009046openalex-snapshot
Nosemasp. influences flight behavior of infected honey bee (Apis mellifera) foragers
inferredcites →https://doi.org/10.1051/apido/2010046openalex-snapshot
A standardised protocol for measuring phenoloxidase and prophenoloxidase in the honey bee, Apis mellifera
inferredcites →https://doi.org/10.1051/apido:2007037openalex-snapshot
Nosema ceranaehas infectedApis melliferain Europe since at least 1998 and may be more virulent thanNosema apis
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/10.1073/pnas.94.1.338openalex-snapshot
Heterogeneities in the transmission of infectious agents: Implications for the design of control programs
inferredcites →https://doi.org/10.1093/oso/9780198506201.003.0001openalex-snapshot
Ecology of wildlife diseases
inferredcites →https://doi.org/10.1093/oso/9780198506201.003.0002openalex-snapshot
Heterogeneities in macroparasite infections: patterns and processes
inferredcites →https://doi.org/10.1098/rspb.2006.3482openalex-snapshot
Senescence effects in an extremely long-lived bird: the grey-headed albatross Thalassarche chrysostoma
inferredcites →https://doi.org/10.1111/1365-2664.12134openalex-snapshot
The T rojan hives: pollinator pathogens, imported and distributed in bumblebee colonies
inferredcites →https://doi.org/10.1111/j.1365-2435.2008.01419.xopenalex-snapshot
Ageing in a eusocial insect: molecular and physiological characteristics of life span plasticity in the honey bee
inferredcites →https://doi.org/10.1111/j.1420-9101.2006.01158.xopenalex-snapshot
MHC class I variation associates with parasite resistance and longevity in tropical pythons
inferredcites →https://doi.org/10.1111/j.1420-9101.2007.01424.xopenalex-snapshot
Phenotypic plasticity of immune defence linked with foraging activity in the ant Cataglyphis velox
inferredcites →https://doi.org/10.1111/j.1462-2920.2008.01687.xopenalex-snapshot
How natural infection by Nosema ceranae causes honeybee colony collapse
inferredcites →https://doi.org/10.1111/j.1462-2920.2009.01953.xopenalex-snapshot
Immune suppression in the honey bee ( Apis mellifera ) following infection by Nosema ceranae ( Microsporidia )
inferredcites →https://doi.org/10.1111/j.1462-2920.2009.02123.xopenalex-snapshot
Interactions between Nosema microspores and a neonicotinoid weaken honeybees ( Apis mellifera )
inferredcites →https://doi.org/10.1139/cjz-79-12-2176openalex-snapshot
Effects of age and gender on immune function of dragonflies (Odonata, Lestidae) from a wild population
inferredcites →https://doi.org/10.1146/annurev.ecolsys.31.1.367openalex-snapshot
Temporal Variation in Fitness Components and Population Dynamics of Large Herbivores
inferredcites →https://doi.org/10.1186/1742-4933-10-12openalex-snapshot
Immunosenescence in vertebrates and invertebrates
inferredcites →https://doi.org/10.1371/journal.pone.0030641openalex-snapshot
Pervasiveness of Parasites in Pollinators
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.ppat.1003083openalex-snapshot
A Strong Immune Response in Young Adult Honeybees Masks Their Increased Susceptibility to Infection Compared to Older Bees
inferredcites →https://doi.org/10.2307/2389786openalex-snapshot
Is Accelerated Senescence a Cost of Reproduction?
inferredcites →https://doi.org/10.3896/ibra.1.49.1.11openalex-snapshot
Does infection by Nosema ceranae cause “Colony Collapse Disorder” in honey bees ( Apis mellifera )?
inferredcites →https://doi.org/10.55782/ane-2000-1323openalex-snapshot
Senescence and learning in honeybee (Apis mellifera) workers
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1016/j.ijppaw.2015.10.001zenodo-depositor-declared
Do managed bees drive parasite spread and emergence in wild bees?
inferred← citeshttps://doi.org/10.1002/arch.21405openalex-snapshot
Induction of stress‐ and immune‐associated genes in the Indian meal moth Plodia interpunctella against envenomation by the ectoparasitoid Bracon hebetor
inferred← citeshttps://doi.org/10.1002/ece3.1668openalex-snapshot
Aging in personal and social immunity: do immune traits senesce at the same rate?
inferred← citeshttps://doi.org/10.1002/pmic.202100224openalex-snapshot
Molecular histoproteomy by MALDI mass spectrometry imaging to uncover markers of the impact of Nosema on Apis mellifera
inferred← citeshttps://doi.org/10.1007/978-3-030-93306-7_7openalex-snapshot
Nosema apis and N. ceranae Infection in Honey bees: A Model for Host-Pathogen Interactions in Insects
inferred← citeshttps://doi.org/10.1007/978-3-319-64597-1_4-1openalex-snapshot
Using Insects as Models of Immunosenescence
inferred← citeshttps://doi.org/10.1007/978-3-319-99375-1_4openalex-snapshot
Using Insects as Models of Immunosenescence
inferred← citeshttps://doi.org/10.1007/s00040-024-00946-7openalex-snapshot
Newly emerged bumblebees are highly susceptible to gut parasite infection
inferred← citeshttps://doi.org/10.1007/s13592-017-0535-1openalex-snapshot
Nosema ceranae disease of the honey bee (Apis mellifera)
inferred← citeshttps://doi.org/10.1007/s13592-026-01270-8openalex-snapshot
Developmental and behavioral modulation of humoral immunity in the stingless bee Frieseomelitta varia
inferred← citeshttps://doi.org/10.1007/s13744-015-0308-3openalex-snapshot
Temporal Variation in Immune Components of the White Grub Phyllophaga polyphylla (Bates) (Coleoptera: Melolonthidae)
inferred← citeshttps://doi.org/10.1016/j.aspen.2017.01.017openalex-snapshot
Analysis of the whole developmental period reveals stage-specific gene expression profiles of the Indianmeal moth, Plodia interpunctella
inferred← citeshttps://doi.org/10.1016/j.aspen.2020.09.009openalex-snapshot
Differentiated transcriptional regulation before and after death in Indianmeal moth Plodia interpunctella
inferred← citeshttps://doi.org/10.1016/j.dci.2015.12.006openalex-snapshot
Insect immunology and hematopoiesis
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.ijpara.2020.03.005openalex-snapshot
Honey bee survival mechanisms against the parasite Varroa destructor: a systematic review of phenotypic and genomic research efforts
inferred← citeshttps://doi.org/10.1016/j.jinsphys.2024.104629openalex-snapshot
Immune response in paper wasp workers: Task matters more than age
inferred← citeshttps://doi.org/10.1016/j.jinsphys.2024.104720openalex-snapshot
Physiological trade-offs in male social insects: Interactions among infection, immunity, fertility, size, and age in honey bee drones
inferred← citeshttps://doi.org/10.1016/j.jip.2016.04.004openalex-snapshot
Influence of mating and age on susceptibility of the beetle Anoplophora glabripennis to the fungal pathogen Metarhizium brunneum
inferred← citeshttps://doi.org/10.1016/j.jip.2025.108352openalex-snapshot
Microalgae functional feed additives strengthen immunity and increase longevity in honey bees
inferred← citeshttps://doi.org/10.1016/j.jip.2026.108706openalex-snapshot
Feeding the disease: The impact of nutritional supplementation on Nosema (Vairimorpha) infection in honey bees (Apis mellifera)
inferred← citeshttps://doi.org/10.1016/j.pt.2019.03.008openalex-snapshot
Host Age Effects in Invertebrates: Epidemiological, Ecological, and Evolutionary Implications
inferred← citeshttps://doi.org/10.1017/s0031182014001243openalex-snapshot
Horizontal transmission of a parasite is influenced by infected host phenotype and density
inferred← citeshttps://doi.org/10.1017/s0031182023001130openalex-snapshot
Increased virulence due to multiple infection in Daphnia leads to limited growth in 1 of 2 co-infecting microsporidian parasites
inferred← citeshttps://doi.org/10.1021/acs.jproteome.0c00658openalex-snapshot
Proteomics of Anatomical Sections of the Gut of Nosema-Infected Western Honeybee (Apis mellifera) Reveals Different Early Responses to Nosema spp. Isolates
inferred← citeshttps://doi.org/10.1038/s41598-019-50974-8openalex-snapshot
Microsporidia Nosema spp. – obligate bee parasites are transmitted by air
inferred← citeshttps://doi.org/10.1038/s41598-025-06939-1openalex-snapshot
Developmental transcriptomics reveals stage-specific immune gene expression profiles in Spodoptera frugiperda
inferred← citeshttps://doi.org/10.1038/srep10982openalex-snapshot
The cost of promiscuity: sexual transmission of Nosema microsporidian parasites in polyandrous honey bees
inferred← citeshttps://doi.org/10.1093/jee/tow103openalex-snapshot
Approaches and Challenges to Managing Nosema (Microspora: Nosematidae) Parasites in Honey Bee (Hymenoptera: Apidae) Colonies
inferred← citeshttps://doi.org/10.1101/428656openalex-snapshot
Industrial bees: when agricultural intensification doesn’t impact local disease prevalence
inferred← citeshttps://doi.org/10.1111/1365-2656.12433openalex-snapshot
Immunosenescence and the ability to survive bacterial infection in the red flour beetle Tribolium castaneum
inferred← citeshttps://doi.org/10.1111/1365-2664.13461openalex-snapshot
Industrial bees: The impact of apicultural intensification on local disease prevalence
inferred← citeshttps://doi.org/10.1111/1462-2920.14103openalex-snapshot
Nosema ceranae in Apis mellifera : a 12 years postdetection perspective
inferred← citeshttps://doi.org/10.1111/1748-5967.12286openalex-snapshot
Sex‐biased gene expression during the adult stage of the Indian meal moth Plodia interpunctella
inferred← citeshttps://doi.org/10.1111/eea.12902openalex-snapshot
Infectivity and virulence of Nosema ceranae (Microsporidia) isolates obtained from various Apis mellifera morphotypes
inferred← citeshttps://doi.org/10.1111/een.13204openalex-snapshot
Host condition and pathogen identity influence bacterial infection survival in the common eastern firefly, Photinus pyralis
inferred← citeshttps://doi.org/10.1111/jeb.13721openalex-snapshot
Immune priming depends on age, sex and Wolbachia in the interaction between Armadillidium vulgare and Salmonella
inferred← citeshttps://doi.org/10.1186/s12711-023-00844-9openalex-snapshot
Unravelling the genetic variability of host resilience to endo- and ectoparasites in Nellore commercial herds
inferred← citeshttps://doi.org/10.1186/s12936-015-0912-zopenalex-snapshot
Mosquito age and avian malaria infection
inferred← citeshttps://doi.org/10.1371/journal.pone.0167752openalex-snapshot
Sepsis and Hemocyte Loss in Honey Bees (Apis mellifera) Infected with Serratia marcescens Strain Sicaria
inferred← citeshttps://doi.org/10.1371/journal.ppat.1009270openalex-snapshot
Transferrin-mediated iron sequestration suggests a novel therapeutic strategy for controlling Nosema disease in the honey bee, Apis mellifera
inferred← citeshttps://doi.org/10.1515/jas-2015-0025openalex-snapshot
Expression of the Prophenoloxidase Gene and Phenoloxidase Activity, During the Development of Apis Mellifera Brood Infected with Varroa Destructor
inferred← citeshttps://doi.org/10.21203/rs.3.rs-154711/v1openalex-snapshot
Unraveling the genetic variability of host resilience to endo and ectoparasites under natural infestation, in Nellore cattle
inferred← citeshttps://doi.org/10.21203/rs.3.rs-154711/v2openalex-snapshot
Unraveling the genetic variability of host resilience to endo and ectoparasites under natural infestation, in Nellore cattle
inferred← citeshttps://doi.org/10.21203/rs.3.rs-4990584/v1openalex-snapshot
Comparative gene expression analyses reveal developmental stage dependent immune adaptations of Spodoptera frugiperda
inferred← citeshttps://doi.org/10.21203/rs.3.rs-757584/v1openalex-snapshot
Gut and Colony Microbiota of Honey Bees Apis mellifera: Social Immunity, Opportunistic Disease and Survival Overwinter.
inferred← citeshttps://doi.org/10.3389/fimmu.2024.1404766openalex-snapshot
Extensive influence of microsporidian infection on sucrose solution consumption, antioxidant enzyme activity, cell structure, and lifespan of Asian honeybees
inferred← citeshttps://doi.org/10.3389/fphys.2023.1198070openalex-snapshot
Overlapping exposure effects of pathogen and dimethoate on honeybee (Apis mellifera Linnaeus) metabolic rate and longevity
inferred← citeshttps://doi.org/10.3390/insects10120417openalex-snapshot
Age and Method of Inoculation Influence the Infection of Worker Honey Bees (Apis mellifera) by Nosema ceranae
inferred← citeshttps://doi.org/10.3390/insects13030308openalex-snapshot
Functional Properties and Antimicrobial Activity from Lactic Acid Bacteria as Resources to Improve the Health and Welfare of Honey Bees
inferred← citeshttps://doi.org/10.3390/jof8050424openalex-snapshot
Recent Advances in the Biocontrol of Nosemosis in Honey Bees (Apis mellifera L.)
inferred← citeshttps://doi.org/10.51458/bstd.2023.37openalex-snapshot
Defensive Behaviors of the Central Highland Honeybees, Apis mellifera bandasii against Varroa destructor in Ethiopia
inferred← citeshttps://doi.org/10.6084/m9.figshare.24603456openalex-snapshot
Additional file 1 of Unravelling the genetic variability of host resilience to endo- and ectoparasites in Nellore commercial herds
inferred← citeshttps://doi.org/10.6084/m9.figshare.24604007openalex-snapshot
Additional file 2 of Unravelling the genetic variability of host resilience to endo- and ectoparasites in Nellore commercial herds
inferred← citeshttps://doi.org/10.6084/m9.figshare.26643202openalex-snapshot
Additional file 3 of Unravelling the genetic variability of host resilience to endo- and ectoparasites in Nellore commercial herds
inferred← citeshttps://doi.org/10.6084/m9.figshare.26643205openalex-snapshot
Additional file 4 of Unravelling the genetic variability of host resilience to endo- and ectoparasites in Nellore commercial herds
inferred← citeshttps://doi.org/10.6084/m9.figshare.26643208openalex-snapshot
Additional file 5 of Unravelling the genetic variability of host resilience to endo- and ectoparasites in Nellore commercial herds
inferred← citeshttps://doi.org/10.6084/m9.figshare.26643211openalex-snapshot
Additional file 6 of Unravelling the genetic variability of host resilience to endo- and ectoparasites in Nellore commercial herds
inferred← citeshttps://doi.org/10.70675/a26081ebz8871z46f2za5f1z35c22ef19688openalex-snapshot
Division of labor in anti-parasite defense strategies in ant colonies
inferred← citeshttps://doi.org/10.70675/e73cfc0bz8c50z4c8czbc73z76b9321e40b1openalex-snapshot
Analyse de l'immunoprotéome de l'abeille en réponse à différents stress environnementaux
inferred← citeshttps://doi.org/10.7717/peerj.522openalex-snapshot
The relationship between managed bees and the prevalence of parasites in bumblebees
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