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First indication of acetylcholine-based communication in honeybee haemocytes and its modulation by a neonicotinoid insecticide

https://doi.org/10.1101/105700
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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/ps.1616openalex-snapshot
Applied aspects of neonicotinoid uses in crop protection
inferredcites →https://doi.org/10.1002/ps.373openalex-snapshot
Neonicotinoid insecticides alter diapause behavior and survival of overwintering white grubs (Coleoptera: Scarabaeidae)
inferredcites →https://doi.org/10.1007/s10646-012-0863-xopenalex-snapshot
Neonicotinoids in bees: a review on concentrations, side-effects and risk assessment
inferredcites →https://doi.org/10.1016/j.bcp.2009.06.011openalex-snapshot
Nicotine-induced upregulation of nicotinic receptors: Underlying mechanisms and relevance to nicotine addiction
inferredcites →https://doi.org/10.1016/j.dci.2016.07.003openalex-snapshot
The cholinergic immune regulation mediated by a novel muscarinic acetylcholine receptor through TNF pathway in oyster Crassostrea gigas
inferredcites →https://doi.org/10.1016/j.envint.2016.01.009openalex-snapshot
Are bee diseases linked to pesticides? — A brief review
inferredcites →https://doi.org/10.1016/j.fsi.2014.03.008openalex-snapshot
Acetylcholine modulates the immune response in Zhikong scallop Chlamys farreri
inferredcites →https://doi.org/10.1016/j.jinsphys.2016.01.001openalex-snapshot
The neonicotinoids thiacloprid, imidacloprid, and clothianidin affect the immunocompetence of honey bees (Apis mellifera L.)
inferredcites →https://doi.org/10.1016/j.lfs.2012.05.006openalex-snapshot
Critical roles of acetylcholine and the muscarinic and nicotinic acetylcholine receptors in the regulation of immune function
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/s0165-6147(00)01820-4openalex-snapshot
Neonicotinoids: insecticides acting on insect nicotinic acetylcholine receptors
inferredcites →https://doi.org/10.1021/acs.est.5b03459openalex-snapshot
Neonicotinoid Residues in Wildflowers, a Potential Route of Chronic Exposure for Bees
inferredcites →https://doi.org/10.1021/ar800131popenalex-snapshot
Molecular Recognition of Neonicotinoid Insecticides: The Determinants of Life or Death
inferredcites →https://doi.org/10.1021/jf000873copenalex-snapshot
Neonicotinoid Insecticides: Molecular Features Conferring Selectivity for Insect versus Mammalian Nicotinic Receptors
inferredcites →https://doi.org/10.1023/a:1007512121082openalex-snapshot
Expression of a Neuronal Nicotinic Acetylcholine Receptor in Insect and Mammalian Host Cell Systems
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/ncomms12459openalex-snapshot
Impacts of neonicotinoid use on long-term population changes in wild bees in England
inferredcites →https://doi.org/10.1038/nri1810openalex-snapshot
Neural regulation of innate immunity: a coordinated nonspecific host response to pathogens
inferredcites →https://doi.org/10.1038/srep24764openalex-snapshot
Neonicotinoids target distinct nicotinic acetylcholine receptors and neurons, leading to differential risks to bumblebees
inferredcites →https://doi.org/10.1038/srep26396openalex-snapshot
The simple neuroendocrine-immune regulatory network in oyster Crassostrea gigas mediates complex functions
inferredcites →https://doi.org/10.1073/pnas.1314923110openalex-snapshot
Neonicotinoid clothianidin adversely affects insect immunity and promotes replication of a viral pathogen in honey bees
inferredcites →https://doi.org/10.1093/nar/gks596openalex-snapshot
Primer3—new capabilities and interfaces
inferredcites →https://doi.org/10.1098/rsob.160059openalex-snapshot
An invertebrate-specific miRNA targeted the ancient cholinergic neuroendocrine system of oyster
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/10.1111/1365-2664.12689openalex-snapshot
Investigating the impacts of field‐realistic exposure to a neonicotinoid pesticide on bumblebee foraging, homing ability and colony growth
inferredcites →https://doi.org/10.1111/1744-7917.12324openalex-snapshot
Molecular characterization and expression profiles of nicotinic acetylcholine receptors in the rice striped stem borer, Chilo suppressalis (Lepidoptera: Crambidae)
inferredcites →https://doi.org/10.1126/science.1215025openalex-snapshot
Neonicotinoid Pesticide Reduces Bumble Bee Colony Growth and Queen Production
inferredcites →https://doi.org/10.1126/science.1215039openalex-snapshot
A Common Pesticide Decreases Foraging Success and Survival in Honey Bees
inferredcites →https://doi.org/10.1126/science.1255957openalex-snapshot
Bee declines driven by combined stress from parasites, pesticides, and lack of flowers
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/10.1146/annurev.ento.48.091801.112731openalex-snapshot
S ELECTIVE T OXICITY OF N EONICOTINOIDS A TTRIBUTABLE TO S PECIFICITY OF I NSECT AND M AMMALIAN N ICOTINIC R ECEPTORS
inferredcites →https://doi.org/10.1186/s12864-015-2150-8openalex-snapshot
The comprehensive immunomodulation of NeurimmiRs in haemocytes of oyster Crassostrea gigas after acetylcholine and norepinephrine stimulation
inferredcites →https://doi.org/10.1242/jeb.123612openalex-snapshot
The neonicotinoid clothianidin interferes with navigation of the solitary bee Osmia cornuta in a laboratory test
inferredcites →https://doi.org/10.1371/journal.pone.0030828openalex-snapshot
The Immunomodulation of Acetylcholinesterase in Zhikong Scallop Chlamys farreri
inferredcites →https://doi.org/10.1371/journal.pone.0091364openalex-snapshot
Neonicotinoids Interfere with Specific Components of Navigation in Honeybees
inferredcites →https://doi.org/10.1677/joe.0.1690429openalex-snapshot
Neuroendocrine regulation of autoimmune/inflammatory disease
inferredcites →https://doi.org/10.1890/120126openalex-snapshot
Threats to an ecosystem service: pressures on pollinators
inferredcites →https://doi.org/10.3896/ibra.1.53.5.11openalex-snapshot
Apis melliferahaemocytesin-vitro, What type of cells are they? Functional analysis before and after pupal metamorphosis

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.cbpa.2024.111735openalex-snapshot
Assessment of oxidative status, detoxification capacity and immune responsiveness in honey bees with ageing
inferred← citeshttps://doi.org/10.1038/s41598-019-46842-0openalex-snapshot
Differential expression of acetylcholinesterase 1 in response to various stress factors in honey bee workers
inferred← citeshttps://doi.org/10.1111/imb.12845openalex-snapshot
Acetylcholine titre regulation by non‐neuronal acetylcholinesterase 1 and its putative roles in honey bee physiology
inferred← citeshttps://doi.org/10.1371/journal.pone.0256581openalex-snapshot
Improved mitochondrial function corrects immunodeficiency and impaired respiration in neonicotinoid exposed bumblebees
inferred← citeshttps://doi.org/10.3390/insects10120420openalex-snapshot
Acetylcholine and Its Receptors in Honeybees: Involvement in Development and Impairments by Neonicotinoids
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