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Industrial bees: when agricultural intensification doesn’t impact local disease prevalence

https://doi.org/10.1101/428656
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Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1006/anbe.1996.0068openalex-snapshot
Temporal polyethism and behavioural canalization in the honey bee,Apis mellifera
inferredcites →https://doi.org/10.1007/s00285-016-0973-9openalex-snapshot
Disease eradication on large industrial farms
inferredcites →https://doi.org/10.1007/s00436-011-2292-9openalex-snapshot
Comparison of the energetic stress associated with experimental Nosema ceranae and Nosema apis infection of honeybees (Apis mellifera)
inferredcites →https://doi.org/10.1007/s11692-010-9089-0openalex-snapshot
Intensive Farming: Evolutionary Implications for Parasites and Pathogens
inferredcites →https://doi.org/10.1007/s13592-015-0361-2openalex-snapshot
Crowding honeybee colonies in apiaries can increase their vulnerability to the deadly ectoparasite Varroa destructor
inferredcites →https://doi.org/10.1007/s13592-016-0443-9openalex-snapshot
Distance between honey bee Apis mellifera colonies regulates populations of Varroa destructor at a landscape scale
inferredcites →https://doi.org/10.1007/s13592-016-0453-7openalex-snapshot
Fine scale population genetic structure of Varroa destructor, an ectoparasitic mite of the honey bee (Apis mellifera)
inferredcites →https://doi.org/10.1016/bs.aivir.2018.02.008openalex-snapshot
Emerging Viruses in Bees: From Molecules to Ecology
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.ijppaw.2015.10.001openalex-snapshot
Do managed bees drive parasite spread and emergence in wild bees?
inferredcites →https://doi.org/10.1016/j.jip.2009.06.011openalex-snapshot
A historical review of managed honey bee populations in Europe and the United States and the factors that may affect them
inferredcites →https://doi.org/10.1016/j.jip.2010.06.004openalex-snapshot
The occurrence of Melissococcus plutonius in healthy colonies of Apis mellifera and the efficacy of European foulbrood control measures
inferredcites →https://doi.org/10.1016/j.jip.2014.06.004openalex-snapshot
Immunosenescence and resistance to parasite infection in the honey bee, Apis mellifera
inferredcites →https://doi.org/10.1016/j.jtbi.2017.03.009openalex-snapshot
Stress-mediated Allee effects can cause the sudden collapse of honey bee colonies
inferredcites →https://doi.org/10.1016/j.prevetmed.2014.04.002openalex-snapshot
Risk factors associated with the presence of Varroa destructor in honey bee colonies from east-central Argentina
inferredcites →https://doi.org/10.1016/j.sjbs.2014.09.020openalex-snapshot
New approach for determination of an optimum honeybee colony’s carrying capacity based on productivity and nectar secretion potential of bee forage species
inferredcites →https://doi.org/10.1016/j.tree.2005.04.026openalex-snapshot
Buzziness as usual? Questioning the global pollination crisis
inferredcites →https://doi.org/10.1016/j.tree.2010.01.007openalex-snapshot
Global pollinator declines: trends, impacts and drivers
inferredcites →https://doi.org/10.1016/s0025-5564(02)00108-6openalex-snapshot
Reproduction numbers and sub-threshold endemic equilibria for compartmental models of disease transmission
inferredcites →https://doi.org/10.1017/s0021859600035103openalex-snapshot
The drifting of honey-bees
inferredcites →https://doi.org/10.1017/s0031182014001243openalex-snapshot
Horizontal transmission of a parasite is influenced by infected host phenotype and density
inferredcites →https://doi.org/10.1017/s003118201500092xopenalex-snapshot
The adaptive evolution of virulence: a review of theoretical predictions and empirical tests
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/s41559-017-0246-zopenalex-snapshot
Ecological and evolutionary approaches to managing honeybee disease
inferredcites →https://doi.org/10.1038/s41598-017-05596-3openalex-snapshot
The virulent, emerging genotype B of Deformed wing virus is closely linked to overwinter honeybee worker loss
inferredcites →https://doi.org/10.1046/j.1365-2664.2001.00662.xopenalex-snapshot
The role of Varroa and viral pathogens in the collapse of honeybee colonies: a modelling approach
inferredcites →https://doi.org/10.1051/apido/2009027openalex-snapshot
Biodiversity, conservation and current threats to European honeybees
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:2003048openalex-snapshot
The behaviour of drifted Cape honeybee workers (Apis mellifera capensis): predisposition for social parasitism?
inferredcites →https://doi.org/10.1051/apido:2006069openalex-snapshot
Spatial distribution of Melissococcus plutonius in adult honey bees collected from apiaries and colonies with and without symptoms of European foulbrood
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:2008032openalex-snapshot
Horizontal transmission of Paenibacillus larvae spores between honey bee ( Apis mellifera ) colonies through robbing
inferredcites →https://doi.org/10.1051/apido:200819openalex-snapshot
Infection rate based on quantitative real-time PCR ofMelissococcus plutonius, the causal agent of European foulbrood, in honeybee colonies before and after apiary sanitation
inferredcites →https://doi.org/10.1073/pnas.1208059110openalex-snapshot
Zoonosis emergence linked to agricultural intensification and environmental change
inferredcites →https://doi.org/10.1080/00034983.1912.11687060openalex-snapshot
The Morphology and Life History ofNosema Apisand the Significance of its Various Stages in the so-called ‘Isle of Wight’ Disease in Bees(Microsporidiosis)
inferredcites →https://doi.org/10.1080/00218839.1965.11100119openalex-snapshot
Drifting of Honeybees in Commercial Apiaries 1. Effect of Various Environmental Factors
inferredcites →https://doi.org/10.1080/00218839.1966.11100147openalex-snapshot
Drifting of Honeybees in Commercial Apiaries. III. Effect of Apiary Layout
inferredcites →https://doi.org/10.1080/00218839.1968.11100185openalex-snapshot
Drifting of Honeybees in Commercial Apiaries. IV. Further Studies of the Effect of Apiary Layout
inferredcites →https://doi.org/10.1080/00218839.1991.11101235openalex-snapshot
Drifting behaviour of drone honey bees (Apis melliferaL.) in commercial apiaries
inferredcites →https://doi.org/10.1080/00218839.1994.11100873openalex-snapshot
The effect of drifting honey bees on the spread of American foulbrood infections
inferredcites →https://doi.org/10.1080/00218839.2016.1245396openalex-snapshot
Risk factors associated with the abundance ofNosemaspp. in apiaries located in temperate and subtropical conditions after honey harvest
inferredcites →https://doi.org/10.1080/00218839.2016.1251081openalex-snapshot
Epidemiology, risk factors and varroa mite control in the Estonian honey bee population
inferredcites →https://doi.org/10.1093/ee/nvx155openalex-snapshot
Vegetation Management and Host Density Influence Bee–Parasite Interactions in Urban Gardens
inferredcites →https://doi.org/10.1098/rsos.160444openalex-snapshot
Age structure is critical to the population dynamics and survival of honeybee colonies
inferredcites →https://doi.org/10.1098/rspb.2016.0811openalex-snapshot
Elevated virulence of an emerging viral genotype as a driver of honeybee loss
inferredcites →https://doi.org/10.1098/rstb.2012.0086openalex-snapshot
What limits the evolutionary emergence of pathogens?
inferredcites →https://doi.org/10.1111/1365-2656.12345openalex-snapshot
A sting in the spit: widespread cross‐infection of multiple RNA viruses across wild and managed bees
inferredcites →https://doi.org/10.1111/1365-2664.12112openalex-snapshot
REVIEW: Towards a systems approach for understanding honeybee decline: a stocktaking and synthesis of existing models
inferredcites →https://doi.org/10.1111/1365-2664.12385openalex-snapshot
REVIEW: Emerging viral disease risk to pollinating insects: ecological, evolutionary and anthropogenic factors
inferredcites →https://doi.org/10.1111/eva.12342openalex-snapshot
Potential drivers of virulence evolution in aquaculture
inferredcites →https://doi.org/10.1111/j.1439-0310.1992.tb00844.xopenalex-snapshot
Colony Integration in Honey Bees: Mechanisms of Behavioral Reversion
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.1558-5646.2012.01803.xopenalex-snapshot
VACCINATION AND REDUCED COHORT DURATION CAN DRIVE VIRULENCE EVOLUTION: MAREK’S DISEASE VIRUS AND INDUSTRIALIZED AGRICULTURE
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/10.1126/science.aac9976openalex-snapshot
Deformed wing virus is a recent global epidemic in honeybees driven by Varroa mites
inferredcites →https://doi.org/10.1186/2049-9957-3-2openalex-snapshot
In an interconnected world: joint research priorities for the environment, agriculture and infectious disease
inferredcites →https://doi.org/10.1371/journal.pone.0072016openalex-snapshot
Influence of Pollen Nutrition on Honey Bee Health: Do Pollen Quality and Diversity Matter?
inferredcites →https://doi.org/10.1371/journal.pone.0110237openalex-snapshot
Effects of Infection on Honey Bee Population Dynamics: A Model
inferredcites →https://doi.org/10.1371/journal.pone.0133228openalex-snapshot
Pathogens as Predictors of Honey Bee Colony Strength in England and Wales
inferredcites →https://doi.org/10.1371/journal.pone.0143805openalex-snapshot
A Mathematical Model of Intra-Colony Spread of American Foulbrood in European Honeybees (Apis mellifera L.)
inferredcites →https://doi.org/10.1371/journal.pone.0172591openalex-snapshot
A pan-European epidemiological study reveals honey bee colony survival depends on beekeeper education and disease control
inferredcites →https://doi.org/10.1371/journal.ppat.1004816openalex-snapshot
Prospective Large-Scale Field Study Generates Predictive Model Identifying Major Contributors to Colony Losses
inferredcites →https://doi.org/10.1515/9781400841035openalex-snapshot
Modeling Infectious Diseases in Humans and Animals
inferredcites →https://doi.org/10.2307/j.ctvcm4gk0openalex-snapshot
Modeling Infectious Diseases in Humans and Animals
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.1.52.1.08openalex-snapshot
Standard epidemiological methods to understand and improveApis mellifera health
inferredcites →https://doi.org/10.7326/0003-4819-117-2-174_4openalex-snapshot
Infectious Diseases of Humans: Dynamics and Control

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inferred← citeshttps://doi.org/10.1098/rspb.2023.1965openalex-snapshot
Signatures of adaptive decreased virulence of deformed wing virus in an isolated population of wild honeybees ( Apis mellifera )
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