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Mitochondrial-targeting fungicide formulations exacerbate the effects of Nosema ceranae infection in the honeybee Apis mellifera

https://doi.org/10.2139/ssrn.6914468
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Effects of co-formulants on the absorption and secretion of active substances in plant protection products in vitro
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Nosema spp. infections cause no energetic stress in tolerant honeybees
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Mitochondrial defects associated with β-alanine toxicity: relevance to hyper-beta-alaninemia
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Exposure assessment of honeybees through study of hive matrices: analysis of selected pesticide residues in honeybees, beebread, and beeswax from French beehives by LC-MS/MS
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Oxidative stress and mitochondrial damage induced by a novel pesticide fluopimomide in Caenorhabditis elegans
inferredcites →https://doi.org/10.1007/s41348-021-00541-zopenalex-snapshot
Inert agricultural spray adjuvants may increase the adverse effects of selected insecticides on honey bees (Apis mellifera L.) under laboratory conditions
inferredcites →https://doi.org/10.1016/j.agee.2020.107167openalex-snapshot
Residues of currently used pesticides in soils and earthworms: A silent threat?
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Effects of ‘inactive’ ingredients on bees
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Progress in understanding molecular mechanisms and evolution of resistance to succinate dehydrogenase inhibiting (SDHI) fungicides in phytopathogenic fungi
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Agrochemicals: Insect declines in a warming world
inferredcites →https://doi.org/10.1016/j.ecoenv.2021.112841openalex-snapshot
The active ingredients of a mitotoxic fungicide negatively affect pollen consumption and worker survival in laboratory-reared honey bees (Apis mellifera)
inferredcites →https://doi.org/10.1016/j.envint.2015.12.011openalex-snapshot
Widespread contamination of wildflower and bee-collected pollen with complex mixtures of neonicotinoids and fungicides commonly applied to crops
inferredcites →https://doi.org/10.1016/j.envint.2022.107311openalex-snapshot
Fungicides and bees: a review of exposure and risk
inferredcites →https://doi.org/10.1016/j.envpol.2019.113443openalex-snapshot
Exposure of honey bee larvae to thiamethoxam and its interaction with Nosema ceranae infection in adult honey bees
inferredcites →https://doi.org/10.1016/j.envpol.2021.117720openalex-snapshot
A common fungicide, Pristine®, impairs olfactory associative learning performance in honey bees (Apis mellifera)
inferredcites →https://doi.org/10.1016/j.etap.2025.104676openalex-snapshot
Exposure to a widely used mito-toxic fungicide negatively affects hemolymph protein and vitellogenin levels in honey bees (Apis mellifera)
inferredcites →https://doi.org/10.1016/j.ijpara.2017.11.004openalex-snapshot
Chronic Nosema ceranae infection inflicts comprehensive and persistent immunosuppression and accelerated lipid loss in host Apis mellifera honey bees
inferredcites →https://doi.org/10.1016/j.jhazmat.2019.05.056openalex-snapshot
Fungicides chlorothanolin, azoxystrobin and folpet induce transcriptional alterations in genes encoding enzymes involved in oxidative phosphorylation and metabolism in honey bees (Apis mellifera) at sublethal concentrations
inferredcites →https://doi.org/10.1016/j.jhazmat.2024.134380openalex-snapshot
Interaction of acetamiprid, Varroa destructor, and Nosema ceranae in honey bees
inferredcites →https://doi.org/10.1016/j.jhazmat.2025.138175openalex-snapshot
Assessing the impact of co-exposure to succinate dehydrogenase inhibitor (SDHI) fungicides and the intestinal parasite Nosema ceranae in the honey bee Apis mellifera
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.jinsphys.2016.01.004openalex-snapshot
Effects of pollen dilution on infection of Nosema ceranae in honey bees
inferredcites →https://doi.org/10.1016/j.jinsphys.2023.104554openalex-snapshot
A mitotoxic fungicide alters post-ingestive glucose signals necessary for associative learning in honey bees
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.2008.12.001openalex-snapshot
Energetic stress in the honeybee Apis mellifera from Nosema ceranae infection
inferredcites →https://doi.org/10.1016/j.jip.2010.12.005openalex-snapshot
Pathological effects of the microsporidium Nosema ceranae on honey bee queen physiology (Apis mellifera)
inferredcites →https://doi.org/10.1016/j.jip.2012.01.004openalex-snapshot
Survival and immune response of drones of a Nosemosis tolerant honey bee strain towards N. ceranae infections
inferredcites →https://doi.org/10.1016/j.jip.2012.08.014openalex-snapshot
Nosema ceranae infection intensity highly correlates with temperature
inferredcites →https://doi.org/10.1016/j.jip.2013.01.002openalex-snapshot
Flight behavior and pheromone changes associated to Nosema ceranae infection of honey bee workers (Apis mellifera) in field conditions
inferredcites →https://doi.org/10.1016/j.jip.2013.05.006openalex-snapshot
Nosema ceranae induced mortality in honey bees (Apis mellifera) depends on infection methods
inferredcites →https://doi.org/10.1016/j.jip.2014.07.002openalex-snapshot
Differential proteomic analysis of midguts from Nosema ceranae-infected honeybees reveals manipulation of key host functions
inferredcites →https://doi.org/10.1016/j.jip.2020.107348openalex-snapshot
Honeybee gut microbiota dysbiosis in pesticide/parasite co-exposures is mainly induced by Nosema ceranae
inferredcites →https://doi.org/10.1016/j.meegid.2013.04.016openalex-snapshot
Comparative susceptibility of three Western honeybee taxa to the microsporidian parasite Nosema ceranae
inferredcites →https://doi.org/10.1016/j.pestbp.2014.12.026openalex-snapshot
The formulation makes the honey bee poison
inferredcites →https://doi.org/10.1016/j.pestbp.2015.09.015openalex-snapshot
Prochloraz and coumaphos induce different gene expression patterns in three developmental stages of the Carniolan honey bee (Apis mellifera carnica Pollmann)
inferredcites →https://doi.org/10.1016/j.pestbp.2016.06.007openalex-snapshot
Evaluation of the toxicity of fungicides to flight muscle mitochondria of bumblebee (Bombus terrestris L.)
inferredcites →https://doi.org/10.1016/j.pestbp.2025.106414openalex-snapshot
Insecticide and pathogens co-exposure induces histomorphology changes in midgut and energy metabolism disorders on Apis mellifera
inferredcites →https://doi.org/10.1016/j.rvsc.2021.01.001openalex-snapshot
Impact of Varroa destructor and associated pathologies on the colony collapse disorder affecting honey bees
inferredcites →https://doi.org/10.1016/j.scitotenv.2009.10.067openalex-snapshot
Interactions between effects of environmental chemicals and natural stressors: A review
inferredcites →https://doi.org/10.1016/j.scitotenv.2021.152847openalex-snapshot
Acute oral exposure to imidacloprid induces apoptosis and autophagy in the midgut of honey bee Apis mellifera workers
inferredcites →https://doi.org/10.1016/j.scitotenv.2022.156857openalex-snapshot
Lethal, sublethal, and combined effects of pesticides on bees: A meta-analysis and new risk assessment tools
inferredcites →https://doi.org/10.1016/j.scitotenv.2022.158814openalex-snapshot
Pesticide drift mitigation measures appear to reduce contamination of non-agricultural areas, but hazards to humans and the environment remain
inferredcites →https://doi.org/10.1016/j.scitotenv.2023.161637openalex-snapshot
Ecotoxicological effects of common fungicides on the eastern honeybee Apis cerana cerana (Hymenoptera)
inferredcites →https://doi.org/10.1016/j.teac.2026.e00300openalex-snapshot
Pesticide contamination in apicultural products: An updated and comprehensive review of analytical methods, occurrence, and safety concerns
inferredcites →https://doi.org/10.1016/j.vetmic.2012.09.012openalex-snapshot
Comparative study of Nosema ceranae (Microsporidia) isolates from two different geographic origins
inferredcites →https://doi.org/10.1017/s0031182024001446openalex-snapshot
Nosemosis negatively affects honeybee survival: experimental and meta-analytic evidence
inferredcites →https://doi.org/10.1021/acs.est.2c09591openalex-snapshot
Pesticide Residues in French Soils: Occurrence, Risks, and Persistence
inferredcites →https://doi.org/10.1038/35106579openalex-snapshot
Genome sequence and gene compaction of the eukaryote parasite Encephalitozoon cuniculi
inferredcites →https://doi.org/10.1038/s41467-023-43215-0openalex-snapshot
3D reconstructions of parasite development and the intracellular niche of the microsporidian pathogen Encephalitozoon intestinalis
inferredcites →https://doi.org/10.1038/s41598-021-88302-8openalex-snapshot
Peritrophic matrix-degrading proteins are dispensable virulence factors in a virulent Melissococcus plutonius strain
inferredcites →https://doi.org/10.1038/srep00326openalex-snapshot
Parasite-insecticide interactions: a case study of Nosema ceranae and fipronil synergy on honeybee
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/10.1073/pnas.2023989118openalex-snapshot
Insect decline in the Anthropocene: Death by a thousand cuts
inferredcites →https://doi.org/10.1093/jee/toad161openalex-snapshot
Toxicity of spray adjuvants and tank mix combinations used in almond orchards to adult honey bees ( Apis mellifera )
inferredcites →https://doi.org/10.1093/jee/tov195openalex-snapshot
Assessing Honey Bee (Hymenoptera: Apidae) Foraging Populations and the Potential Impact of Pesticides on Eight U.S. Crops
inferredcites →https://doi.org/10.1093/jee/tov251openalex-snapshot
Effects of Oral Exposure to Fungicides on Honey Bee Nutrition and Virus Levels
inferredcites →https://doi.org/10.1098/rsbl.2009.0986openalex-snapshot
Diet effects on honeybee immunocompetence
inferredcites →https://doi.org/10.1098/rspb.2006.3721openalex-snapshot
Importance of pollinators in changing landscapes for world crops
inferredcites →https://doi.org/10.1111/1365-2664.13811openalex-snapshot
Parasites and pesticides act antagonistically on honey bee health
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/brv.12140openalex-snapshot
The return of metabolism: biochemistry and physiology of the pentose phosphate pathway
inferredcites →https://doi.org/10.1111/brv.12206openalex-snapshot
Interactive effects of pesticide exposure and pathogen infection on bee health – a critical analysis
inferredcites →https://doi.org/10.1111/cmi.12240openalex-snapshot
Strategies for maximizing ATP supply in the microsporidian E ncephalitozoon cuniculi : direct binding of mitochondria to the parasitophorous vacuole and clustering of the mitochondrial porin VDAC
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/10.1111/j.1550-7408.2004.tb00166.xopenalex-snapshot
Relationship between the Host Cell Mitochondria and the Parasitophorous Vacuole in Cells Infected with Encephalitozoon Microsporidia
inferredcites →https://doi.org/10.1126/science.1251817openalex-snapshot
Defaunation in the Anthropocene
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/10.1128/aem.00532-09openalex-snapshot
Bacillus thuringiensis Bel Protein Enhances the Toxicity of Cry1Ac Protein to Helicoverpa armigera Larvae by Degrading Insect Intestinal Mucin
inferredcites →https://doi.org/10.1146/annurev-ento-011613-162005openalex-snapshot
Honey Bee Toxicology
inferredcites →https://doi.org/10.1177/0300985819864302openalex-snapshot
Nosema apis and Nosema ceranae Tissue Tropism in Worker Honey Bees ( Apis mellifera )
inferredcites →https://doi.org/10.1186/s13567-016-0335-zopenalex-snapshot
Sublethal effects of acaricides and Nosema ceranae infection on immune related gene expression in honeybees
inferredcites →https://doi.org/10.1242/jeb.01956openalex-snapshot
Nutritional status influences socially regulated foraging ontogeny in honey bees
inferredcites →https://doi.org/10.1242/jeb.245180openalex-snapshot
Contrasting effects of fungicide and herbicide active ingredients and their formulations on bumblebee learning and behaviour
inferredcites →https://doi.org/10.12688/openreseurope.20475.2openalex-snapshot
Soil contamination in Europe unveiled: A review of pesticides and metabolites to watch
inferredcites →https://doi.org/10.1289/ehp.9374openalex-snapshot
Unidentified Inert Ingredients in Pesticides: Implications for Human and Environmental Health
inferredcites →https://doi.org/10.1371/journal.pone.0009754openalex-snapshot
High Levels of Miticides and Agrochemicals in North American Apiaries: Implications for Honey Bee Health
inferredcites →https://doi.org/10.1371/journal.pone.0021550openalex-snapshot
Exposure to Sublethal Doses of Fipronil and Thiacloprid Highly Increases Mortality of Honeybees Previously Infected by Nosema ceranae
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.0058165openalex-snapshot
Physiological and Behavioral Changes in Honey Bees (Apis mellifera) Induced by Nosema ceranae Infection
inferredcites →https://doi.org/10.1371/journal.pone.0070182openalex-snapshot
Crop Pollination Exposes Honey Bees to Pesticides Which Alters Their Susceptibility to the Gut Pathogen Nosema ceranae
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.0225743openalex-snapshot
Fungicides, herbicides and bees: A systematic review of existing research and methods
inferredcites →https://doi.org/10.1371/journal.ppat.1008580openalex-snapshot
A growing pandemic: A review of Nosema parasites in globally distributed domesticated and native bees
inferredcites →https://doi.org/10.3389/fphys.2024.1440531openalex-snapshot
Molecular identification of two thioredoxin genes and their function in antioxidant defense in Arma chinensis diapause
inferredcites →https://doi.org/10.3389/fpubh.2016.00092openalex-snapshot
Toxicological Risks of Agrochemical Spray Adjuvants: Organosilicone Surfactants May Not Be Safe
inferredcites →https://doi.org/10.5802/crbiol.37openalex-snapshot
Insect decline: immediate action is needed
inferredcites →https://doi.org/10.7717/peerj.6325openalex-snapshot
Response of adult honey bees treated in larval stage with prochloraz to infection with Nosema ceranae
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