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Varroa Mites Drive Honey Bee Pathogen Dynamics

https://doi.org/10.2139/ssrn.5374508
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Reduced parasite burden in feral honeybee colonies
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Seasonal dynamics and co‐occurrence patterns of honey bee pathogens revealed by high‐throughput RT‐qPCR analysis
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The Transmission of Deformed Wing Virus between Honeybees (Apis melliferaL.) by the Ectoparasitic MiteVarroa jacobsoniOud
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Ontogenesis of the mite Varroa jacobsoni Oud. in worker brood of the honeybee Apis mellifera L. under natural conditions
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Ontogenesis of the mite Varroa jacobsoni Oud. in drone brood of the honeybee Apis mellifera L. under natural conditions
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Physiology of reproductive worker honey bees (Apis mellifera): insights for the development of the worker caste
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Varroa destructor parasitism reduces hemocyte concentrations and prophenol oxidase gene expression in bees from two populations
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Picornavirales, a proposed order of positive-sense single-stranded RNA viruses with a pseudo-T = 3 virion architecture
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Spatial clusters of Varroa destructor control strategies in Europe
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The Dicistroviridae: An emerging family of invertebrate viruses
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Crowding honeybee colonies in apiaries can increase their vulnerability to the deadly ectoparasite Varroa destructor
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Cellular immunity in Apis mellifera: studying hemocytes brings light about bees skills to confront threats
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Varroa resistance in Apis cerana: a review
inferredcites →https://doi.org/10.1007/s13592-025-01147-2openalex-snapshot
Seasonal variations of the five main honey bee viruses in a three-year longitudinal survey
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Worker nutrition and division of labour in honeybees
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Honey bee colony losses and associated viruses
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Hormonal control of the yolk precursor vitellogenin regulates immune function and longevity in honeybees
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Social reversal of immunosenescence in honey bee workers
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Honey bee survival mechanisms against the parasite Varroa destructor: a systematic review of phenotypic and genomic research efforts
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Adult honeybees (Apis mellifera L.) abandon hemocytic, but not phenoloxidase-based immunity
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)
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The ontogeny of immunity in the honey bee, Apis mellifera L. following an immune challenge
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Horizontal and vertical transmission of viruses in the honey bee, Apis mellifera
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Chronic bee paralysis: A disease and a virus like no other?
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The Acute bee paralysis virus–Kashmir bee virus–Israeli acute paralysis virus complex
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Biology and control of Varroa destructor
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Widespread distribution of honey bee-associated pathogens in native bees and wasps: Trends in pathogen prevalence and co-occurrence
inferredcites →https://doi.org/10.1016/j.pt.2020.04.004openalex-snapshot
Varroa destructor: A Complex Parasite, Crippling Honey Bees Worldwide
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Genome sequence heterogeneity of Lake Sinai Virus found in honey bees and Orf1/RdRP-based polymorphisms in a single host
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Coevolution while you wait: Varroa jacobsoni, a new parasite of western honeybees
inferredcites →https://doi.org/10.1016/s0932-4739(96)80059-9openalex-snapshot
Nosema ceranae n. sp. (Microspora, Nosematidae), morphological and molecular characterization of a microsporidian parasite of the Asian honey bee Apis cerana (Hymenoptera, Apidae)
inferredcites →https://doi.org/10.1017/s0031182006000710openalex-snapshot
Effects of parasitization by Varroa destructor on survivorship and physiological traits of Apis mellifera in correlation with viral incidence and microbial challenge
inferredcites →https://doi.org/10.1038/s41467-024-44915-xopenalex-snapshot
Life-history stage determines the diet of ectoparasitic mites on their honey bee hosts
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Regional patterns and climatic predictors of viruses in honey bee (Apis mellifera) colonies over time
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The German bee monitoring project: a long term study to understand periodically high winter losses of honey bee colonies
inferredcites →https://doi.org/10.1051/apido:19900304openalex-snapshot
Preference for drone brood cells by Varroa jacobsoni Oud in colonies of Apis mellifera carnica
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:2007040openalex-snapshot
Honey bee colonies that have survived Varroa destructor
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.1818371116openalex-snapshot
Varroa destructor feeds primarily on honey bee fat body tissue and not hemolymph
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The Biology and Behaviour of Drones
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Weight Loss and Other Damage to Developing Worker Honeybees from Infestation with Varroa Jacobsoni
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Honeybee Paralysis: Its Natural Spread and its Diminished Incidence in England and Wales
inferredcites →https://doi.org/10.1080/00218839.1993.11101302openalex-snapshot
Invasion ofVarroa jacobsonsinto honey bee brood cells: a matter of chance or choice?
inferredcites →https://doi.org/10.1098/rspb.2006.3721openalex-snapshot
Importance of pollinators in changing landscapes for world crops
inferredcites →https://doi.org/10.1098/rspb.2017.2140openalex-snapshot
The worldwide importance of honey bees as pollinators in natural habitats
inferredcites →https://doi.org/10.1099/vir.0.80470-0openalex-snapshot
Complete sequence of a picorna-like virus of the genus Iflavirus replicating in the mite Varroa destructor
inferredcites →https://doi.org/10.1099/vir.0.80824-0openalex-snapshot
Intricate transmission routes and interactions between picorna-like viruses (Kashmir bee virus and sacbrood virus) with the honeybee host and the parasitic varroa mite
inferredcites →https://doi.org/10.1099/vir.0.81401-0openalex-snapshot
RT-PCR analysis of Deformed wing virus in honeybees (Apis mellifera) and mites (Varroa destructor)
inferredcites →https://doi.org/10.1111/1462-2920.12426openalex-snapshot
Bees under stress: sublethal doses of a neonicotinoid pesticide and pathogens interact to elevate honey bee mortality across the life cycle
inferredcites →https://doi.org/10.1111/j.1462-2920.2008.01687.xopenalex-snapshot
How natural infection by Nosema ceranae causes honeybee colony collapse
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Crithidia mellificae n. sp. an Acidophilic Trypanosomatid of the Honey Bee Apis mellifera
inferredcites →https://doi.org/10.1111/j.1758-2229.2009.00014.xopenalex-snapshot
Honeybee colony collapse due to Nosema ceranae in professional apiaries
inferredcites →https://doi.org/10.1111/jeu.12209openalex-snapshot
Characterization of Two Species of Trypanosomatidae from the Honey Bee Apis mellifera: Crithidia mellificae Langridge and McGhee, and Lotmaria passim n. gen., n. sp.
inferredcites →https://doi.org/10.1111/mec.13185openalex-snapshot
Multiple host shifts by the emerging honeybee parasite, Varroa jacobsoni
inferredcites →https://doi.org/10.1126/science.1146498openalex-snapshot
A Metagenomic Survey of Microbes in Honey Bee Colony Collapse Disorder
inferredcites →https://doi.org/10.1126/science.aac9976openalex-snapshot
Deformed wing virus is a recent global epidemic in honeybees driven by Varroa mites
inferredcites →https://doi.org/10.1128/aem.03097-09openalex-snapshot
Five-Year Cohort Study of Nosema spp. in Germany: Does Climate Shape Virulence and Assertiveness of Nosema ceranae ?
inferredcites →https://doi.org/10.1128/aem.72.1.606-611.2006openalex-snapshot
Prevalence and Transmission of Honeybee Viruses
inferredcites →https://doi.org/10.1128/jvi.01786-20openalex-snapshot
Direct Evidence for Infection of Varroa destructor Mites with the Bee-Pathogenic Deformed Wing Virus Variant B, but Not Variant A, via Fluorescence In Situ Hybridization Analysis
inferredcites →https://doi.org/10.1146/annurev-ento-010715-023731openalex-snapshot
Ecology of Varroa destructor , the Major Ectoparasite of the Western Honey Bee, Apis mellifera
inferredcites →https://doi.org/10.1146/annurev-virology-092818-015700openalex-snapshot
Deformed Wing Virus in Honeybees and Other Insects
inferredcites →https://doi.org/10.1146/annurev.ento.45.1.519openalex-snapshot
Parasitic Mites of Honey Bees: Life History, Implications, and Impact
inferredcites →https://doi.org/10.1186/s12917-015-0386-9openalex-snapshot
Vertical transmission of honey bee viruses in a Belgian queen breeding program
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.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.0066415openalex-snapshot
Antibacterial Immune Competence of Honey Bees (Apis mellifera) Is Adapted to Different Life Stages and Environmental Risks
inferredcites →https://doi.org/10.1371/journal.pone.0150362openalex-snapshot
How Honey Bee Colonies Survive in the Wild: Testing the Importance of Small Nests and Frequent Swarming
inferredcites →https://doi.org/10.1371/journal.pone.0227264openalex-snapshot
Detection of amitraz resistance and reduced treatment efficacy in the Varroa Mite, Varroa destructor, within commercial beekeeping operations
inferredcites →https://doi.org/10.1371/journal.ppat.1004230openalex-snapshot
A Virulent Strain of Deformed Wing Virus (DWV) of Honeybees (Apis mellifera) Prevails after Varroa destructor-Mediated, or In Vitro, Transmission
inferredcites →https://doi.org/10.21105/joss.01686openalex-snapshot
Welcome to the Tidyverse
inferredcites →https://doi.org/10.3389/fmicb.2020.00943openalex-snapshot
Bee Viruses: Routes of Infection in Hymenoptera
inferredcites →https://doi.org/10.3390/v7072789openalex-snapshot
Genome Characterization, Prevalence and Distribution of a Macula-Like Virus from Apis mellifera and Varroa destructor
inferredcites →https://doi.org/10.3390/vetsci7040166openalex-snapshot
Factors Associated with Honey Bee Colony Losses: A Mini-Review
inferredcites →https://doi.org/10.3896/ibra.1.49.1.01openalex-snapshot
Honey bee colony losses
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/10.3896/ibra.1.52.4.22openalex-snapshot
Standard methods for virus research in Apis mellifera
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Norwegian honey bees surviving Varroa destructor miteinfestations by means of natural selection
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