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Outcome of Colonization of Apis mellifera by Nosema ceranae

https://doi.org/10.1128/aem.00270-07
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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1006/jipa.1993.1103openalex-snapshot
In Vitro Germination of Nosema apis (Microspora: Nosematidae) Spores and Its Effect on Their αα-Trehalose/d-Glucose Ratio
inferredcites →https://doi.org/10.1016/0022-2011(71)90002-4openalex-snapshot
Ultrastructural changes in the hypopharyngeal glands of worker honey bees infected by Nosema apis
inferredcites →https://doi.org/10.1016/j.jip.2005.10.012openalex-snapshot
Specific and sensitive detection of Nosema bombi (Microsporidia: Nosematidae) in bumble bees (Bombus spp.; Hymenoptera: Apidae) by PCR of partial rRNA gene sequences
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/s0022-2011(02)00175-1openalex-snapshot
Detection of Thelohania solenopsae (Microsporidia: Thelohaniidae) in Solenopsis invicta (Hymenoptera: Formicidae) by multiplex PCR
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/10.1023/a:1006456720416openalex-snapshot
Varroa jacobsoni (Acari: Varroidae) is more than one species
inferredcites →https://doi.org/10.1051/apido:2003063openalex-snapshot
Nosema apis infection in worker and queen Apis mellifera
inferredcites →https://doi.org/10.1051/apido:2006045openalex-snapshot
Protein profiles of testes, seminal vesicles and accessory glands of honey bee pupae and their relation to the ecdysteroid titer
inferredcites →https://doi.org/10.1051/apido:2006054openalex-snapshot
ANosema ceranaeisolate from the honeybeeApis mellifera
inferredcites →https://doi.org/10.1079/joh2006364openalex-snapshot
Hosts and parasites as aliens
inferredcites →https://doi.org/10.1080/0005772x.1993.11099149openalex-snapshot
Nosema Apis —A Parasite in the Honey Bee Colony
inferredcites →https://doi.org/10.1080/0005772x.2002.11099532openalex-snapshot
Honey bee winter mortality in France in 1999 and 2000
inferredcites →https://doi.org/10.1080/00218839.2005.11101179openalex-snapshot
Honey bee nosema disease in the Republic of Turkey
inferredcites →https://doi.org/10.1080/00218839.2006.11101355openalex-snapshot
Natural infections of Nosema ceranae in European honey bees
inferredcites →https://doi.org/10.1111/j.1550-7408.2005.00057.xopenalex-snapshot
Complete rRNA Gene Sequences Reveal that the Microsporidium Nosema bombi Infects Diverse Bumblebee (Bombus spp.) Hosts and Contains Multiple Polymorphic Sites
inferredcites →https://doi.org/10.1111/j.1744-7348.1953.tb01093.xopenalex-snapshot
THE INFLUENCE OF INFECTION WITH NOSEMA APIS ON THE ACTIVITIES AND LONGEVITY OF THE WORKER HONEYBEE
inferredcites →https://doi.org/10.1128/9781555818227.ch4openalex-snapshot
Molecular Biology, Molecular Phylogeny, and Molecular Diagnostic Approaches to the Microsporidia
inferredcites →https://doi.org/10.1128/aem.62.3.1102-1106.1996openalex-snapshot
Relief of amplification inhibition in PCR with bovine serum albumin or T4 gene 32 protein
inferredcites →https://doi.org/10.1128/jcm.39.2.485-493.2001openalex-snapshot
Purification and Characterization of PCR-Inhibitory Components in Blood Cells
inferredcites →https://doi.org/10.1146/annurev.en.13.010168.001203openalex-snapshot
Honey Bee Pathology
inferredcites →https://doi.org/10.1653/0015-4040(2004)087[0085:sdovim]2.0.co;2openalex-snapshot
SIMULTANEOUS DETECTION OF VAIRIMORPHA INVICTAE (MICROSPORIDIA: BURENELLIDAE) AND THELOHANIA SOLENOPSAE (MICROSPORIDIA: THELOHANIIDAE) IN FIRE ANTS BY PCR

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.2020.12.003zenodo-depositor-declared
Workflow of Lotmaria passim isolation: Experimental infection with a low-passage strain causes higher honeybee mortality rates than the PRA-403 reference strain
inferred← citeshttps://doi.org/10.1002/9781118395264.ch18openalex-snapshot
Culture and Propagation of Microsporidia
inferred← citeshttps://doi.org/10.1002/9781119569831.ch19openalex-snapshot
HONEY BEES
inferred← citeshttps://doi.org/10.1002/pmic.202400075openalex-snapshot
What proteomics has taught us about honey bee ( Apis mellifera ) health and disease
inferred← citeshttps://doi.org/10.1002/ps.2188openalex-snapshot
An exposure study to assess the potential impact of fipronil in treated sunflower seeds on honey bee colony losses in Spain
inferred← citeshttps://doi.org/10.1002/rcm.8980openalex-snapshot
Matrix‐assisted laser desorption/ionization mass spectrometry biotyping, an approach for deciphering and assessing the identity of the honeybee pathogen Nosema
inferred← citeshttps://doi.org/10.1002/vms3.70917openalex-snapshot
Extracts From Grapefruit ( Citrus paradisi ) Peel via Microwave‐Assisted and Conventional Extractions: Evaluation of Nosema Infection and Toxicity in Honey Bees
inferred← citeshttps://doi.org/10.1007/978-3-030-13947-6_4openalex-snapshot
Welfare of Managed Honey Bees
inferred← citeshttps://doi.org/10.1007/978-3-030-93306-7_4openalex-snapshot
Factors That Determine Microsporidia Infection and Host Specificity
inferred← citeshttps://doi.org/10.1007/978-981-95-9139-8_4openalex-snapshot
Behavior and Ecology of Pollinators: Focus on Honeybees
inferred← citeshttps://doi.org/10.1007/s00114-015-1298-zopenalex-snapshot
Stable genetic diversity despite parasite and pathogen spread in honey bee colonies
inferred← citeshttps://doi.org/10.1007/s00114-020-1670-5openalex-snapshot
Occurrence of virus, microsporidia, and pesticide residues in three species of stingless bees (Apidae: Meliponini) in the field
inferred← citeshttps://doi.org/10.1007/s00248-015-0594-7openalex-snapshot
Seasonal Variation of Honeybee Pathogens and its Association with Pollen Diversity in Uruguay
inferred← citeshttps://doi.org/10.1007/s00248-016-0880-zopenalex-snapshot
Characterization of Nosema ceranae Genetic Variants from Different Geographic Origins
inferred← citeshttps://doi.org/10.1007/s00248-017-0975-1openalex-snapshot
Nosema ceranae in South American Native Stingless Bees and Social Wasp
inferred← citeshttps://doi.org/10.1007/s00248-018-1268-zopenalex-snapshot
Genetic and Genome Analyses Reveal Genetically Distinct Populations of the Bee Pathogen Nosema ceranae from Thailand
inferred← citeshttps://doi.org/10.1007/s00248-020-01538-1openalex-snapshot
Impact of Nutritional Stress on Honeybee Gut Microbiota, Immunity, and Nosema ceranae Infection
inferred← citeshttps://doi.org/10.1007/s00248-022-02014-8openalex-snapshot
Effect of Chronic Exposure to Sublethal Doses of Imidacloprid and Nosema ceranae on Immunity, Gut Microbiota, and Survival of Africanized Honey Bees
inferred← citeshttps://doi.org/10.1007/s00253-010-2573-8openalex-snapshot
Honey bee pathology: current threats to honey bees and beekeeping
inferred← citeshttps://doi.org/10.1007/s00436-010-1875-1openalex-snapshot
Effect of bacterial metabolites on microsporidian Nosema ceranae and on its host Apis mellifera
inferred← citeshttps://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)
inferred← citeshttps://doi.org/10.1007/s00436-011-2566-2openalex-snapshot
Genetic variation and widespread dispersal of Nosema ceranae in Apis mellifera apiaries from Argentina
inferred← citeshttps://doi.org/10.1007/s00436-011-2640-9openalex-snapshot
Comparative analysis of detection limits and specificity of molecular diagnostic markers for three pathogens (Microsporidia, Nosema spp.) in the key pollinators Apis mellifera and Bombus terrestris
inferred← citeshttps://doi.org/10.1007/s00436-011-2760-2openalex-snapshot
Critical aspects of the Nosema spp. diagnostic sampling in honey bee (Apis mellifera L.) colonies
inferred← citeshttps://doi.org/10.1007/s00436-012-2875-0openalex-snapshot
Nosema ceranae an emergent pathogen of Apis mellifera in Chile
inferred← citeshttps://doi.org/10.1007/s00436-012-3195-0openalex-snapshot
The microsporidian parasites Nosema ceranae and Nosema apis are widespread in honeybee (Apis mellifera) colonies across Scotland
inferred← citeshttps://doi.org/10.1007/s00436-015-4733-3openalex-snapshot
Higher prevalence and levels of Nosema ceranae than Nosema apis infections in Canadian honey bee colonies
inferred← citeshttps://doi.org/10.1007/s00436-015-4761-zopenalex-snapshot
Are commercial probiotics and prebiotics effective in the treatment and prevention of honeybee nosemosis C?
inferred← citeshttps://doi.org/10.1007/s00436-020-06915-wopenalex-snapshot
Development of a loop-mediated isothermal amplification (LAMP) and a direct LAMP for the specific detection of Nosema ceranae, a parasite of honey bees
inferred← citeshttps://doi.org/10.1007/s00436-021-07381-8openalex-snapshot
Vairimorpha ceranae was the only detected microsporidian species from Iranian honey bee colonies: a molecular and phylogenetic study
inferred← citeshttps://doi.org/10.1007/s00705-022-05458-yopenalex-snapshot
Silent threat in honey bee colonies: infection dynamics and molecular epidemiological assessment of black queen cell virus in Turkey
inferred← citeshttps://doi.org/10.1007/s10340-024-01829-3openalex-snapshot
Colonies under dysbiosis benefit from oxalic acid application: the role of landscape and beekeeping practices in microbiota response to treatment
inferred← citeshttps://doi.org/10.1007/s11033-024-10087-6openalex-snapshot
NcPTP2, a polar tube protein, interacts with spore wall protein in the parasitic microsporidian Nosema ceranae
inferred← citeshttps://doi.org/10.1007/s11259-022-10036-3openalex-snapshot
Biocontrol potential of Apilactobacillus kunkeei EIR/BG-1 against infectious diseases in honey bees (Apis mellifera L.)
inferred← citeshttps://doi.org/10.1007/s11259-024-10383-3openalex-snapshot
Current status of Nosema spp. infection cases in apis mellifera in eurasian countries and Ptp3 gene haplotypes in the Republic of Tatarstan, Russia
inferred← citeshttps://doi.org/10.1007/s11686-024-00887-yopenalex-snapshot
Prevalence and Phylogenetic Network Analysis of Nosema apis and Nosema ceranae Isolates from Honeybee Colonies in Türkiye
inferred← citeshttps://doi.org/10.1007/s11829-022-09918-9openalex-snapshot
Can the exotic pathogen Nosema ceranae affect the amount of Cucurbita maxima pollen grains transported by the native bee Eucera fervens?
inferred← citeshttps://doi.org/10.1007/s12595-016-0188-5openalex-snapshot
Effect of Some Honeybee Diseases on Seasonal Mortality of Apis mellifera intermissa in Algeria Apiaries
inferred← citeshttps://doi.org/10.1007/s12602-022-10025-7openalex-snapshot
Beneficial Bacteria and Plant Extracts Promote Honey Bee Health and Reduce Nosema ceranae Infection
inferred← citeshttps://doi.org/10.1007/s13592-011-0003-2openalex-snapshot
The stability and effectiveness of fumagillin in controlling Nosema ceranae (Microsporidia) infection in honey bees (Apis mellifera) under laboratory and field conditions
inferred← citeshttps://doi.org/10.1007/s13592-011-0076-yopenalex-snapshot
In vivo evaluation of antiparasitic activity of plant extracts on Nosema ceranae (Microsporidia)
inferred← citeshttps://doi.org/10.1007/s13592-012-0121-5openalex-snapshot
Patterns of Apis mellifera infestation by Nosema ceranae support the parasite hypothesis for the evolution of extreme polyandry in eusocial insects
inferred← citeshttps://doi.org/10.1007/s13592-012-0147-8openalex-snapshot
Detection of Nosema apis and N. ceranae in honeybee bottom scraps and frass in naturally infected hives
inferred← citeshttps://doi.org/10.1007/s13592-013-0203-zopenalex-snapshot
Characteristics of Nosema ceranae infection in Serbian honey bee colonies
inferred← citeshttps://doi.org/10.1007/s13592-013-0241-6openalex-snapshot
Nosema ceranae and RNA viruses in European and Africanized honeybee colonies (Apis mellifera) in Uruguay
inferred← citeshttps://doi.org/10.1007/s13592-015-0375-9openalex-snapshot
European isolates of the Microsporidia Nosema apis and Nosema ceranae have similar virulence in laboratory tests on European worker honey bees
inferred← citeshttps://doi.org/10.1007/s13592-015-0394-6openalex-snapshot
Microscopic and molecular detection of Nosema spp. in honeybees of Turkey
inferred← citeshttps://doi.org/10.1007/s13592-015-0401-yopenalex-snapshot
Prevalence of Nosema species in a feral honey bee population: a 20-year survey
inferred← citeshttps://doi.org/10.1007/s13592-015-0409-3openalex-snapshot
Evaluation of Fumagilin-B® and other potential alternative chemotherapies against Nosema ceranae-infected honeybees (Apis mellifera) in cage trial assays
inferred← citeshttps://doi.org/10.1007/s13592-015-0411-9openalex-snapshot
The effect of dicyclohexylamine and fumagillin on Nosema ceranae-infected honey bee (Apis mellifera) mortality in cage trial assays
inferred← citeshttps://doi.org/10.1007/s13592-018-0589-8openalex-snapshot
The first detection of Nosema ceranae (Microsporidia) in the small hive beetle, Aethina tumida Murray (Coleoptera: Nitidulidae)
inferred← citeshttps://doi.org/10.1007/s13592-020-00733-wopenalex-snapshot
Phoretic mites on South American bumblebees (Bombus spp.) as parasite carriers: a historical input
inferred← citeshttps://doi.org/10.1007/s13592-020-00831-9openalex-snapshot
Environmental conditions and beekeeping practices associated with Nosema ceranae presence in Argentina
inferred← citeshttps://doi.org/10.1007/s13592-023-01037-5openalex-snapshot
Effectiveness of an ethanol extract of jet black ant nests for combatting nosemosis in apiary honey bees
inferred← citeshttps://doi.org/10.1007/s13592-024-01132-1openalex-snapshot
The effects of diet enhancement on the health of commercial bumblebee colonies
inferred← citeshttps://doi.org/10.1007/s13592-025-01156-1openalex-snapshot
Nutritional landscape of managed honey bee colonies in Mexico
inferred← citeshttps://doi.org/10.1007/s13592-025-01242-4openalex-snapshot
Mitigating the impacts of nutritional stress on honey bee colonies located in monoculture Eucalyptus plantations
inferred← citeshttps://doi.org/10.1007/s13592-026-01254-8openalex-snapshot
Curative effects of gallic acid in honey bees (Apis mellifera) infected with Nosema ceranae
inferred← citeshttps://doi.org/10.1007/s13592-026-01291-3openalex-snapshot
Scientific note on the non-specific amplification of honey bee pathogens in a non-target host: the European beewolf (Philanthus triangulum)
inferred← citeshttps://doi.org/10.1007/s13744-025-01352-9openalex-snapshot
Infestation by Phorid Flies Disrupts Behavior and Immune Function in Honey Bees Monitored by Radio-frequency Identification
inferred← citeshttps://doi.org/10.1007/s42360-021-00393-5openalex-snapshot
Rapid Identification of Corynespora cassiicola by multiplex PCR
inferred← citeshttps://doi.org/10.1007/s43538-022-00062-9openalex-snapshot
Honey bee pathogenesis posing threat to its global population: a short review
inferred← citeshttps://doi.org/10.1016/b978-0-08-088504-9.00327-5openalex-snapshot
Genetic Basis of Disease Resistance in the Honey Bee (Apis mellifera L.)
inferred← citeshttps://doi.org/10.1016/j.apjtb.2016.11.004openalex-snapshot
Molecular identification of Nosema species in provinces of Fars, Chaharmahal and Bakhtiari and Isfahan (Southwestern Iran)
inferred← citeshttps://doi.org/10.1016/j.aspen.2019.08.006openalex-snapshot
Protective potential of Chinese herbal extracts against microsporidian Nosema ceranae, an emergent pathogen of western honey bees, Apis mellifera L.
inferred← citeshttps://doi.org/10.1016/j.aspen.2021.05.006openalex-snapshot
Screening of anti-nosemosis active compounds based on the structure-activity correlation
inferred← citeshttps://doi.org/10.1016/j.biocontrol.2020.104213openalex-snapshot
Nosema maddoxi (Microsporidia: Nosematidae) in brown marmorated stink bug, Halyomorpha halys (Hemiptera: Pentatomidae), populations in the United States
inferred← citeshttps://doi.org/10.1016/j.chemosphere.2015.12.030openalex-snapshot
Effects of Nosema ceranae and thiametoxam in Apis mellifera: A comparative study in Africanized and Carniolan honey bees
inferred← citeshttps://doi.org/10.1016/j.chroma.2008.03.019openalex-snapshot
Trace analysis of fumagillin in honey by liquid chromatography-diode array–electrospray ionization mass spectrometry
inferred← citeshttps://doi.org/10.1016/j.cvex.2020.01.001openalex-snapshot
Common and Emerging Infectious Diseases of Honeybees (Apis mellifera)
inferred← citeshttps://doi.org/10.1016/j.dib.2021.107019openalex-snapshot
Dataset of the next-generation sequencing of variable 16S rRNA from bacteria and ITS2 regions from fungi and plants derived from honeybees kept under anthropogenic landscapes
inferred← citeshttps://doi.org/10.1016/j.ecoenv.2023.115427openalex-snapshot
Sulfoxaflor effects depend on the interaction with other pesticides and Nosema ceranae infection in the honey bee (Apis mellifera)
inferred← citeshttps://doi.org/10.1016/j.ejop.2018.01.007openalex-snapshot
A novel TaqMan ® assay for Nosema ceranae quantification in honey bee, based on the protein coding gene Hsp70
inferred← citeshttps://doi.org/10.1016/j.ejop.2022.125935openalex-snapshot
Specific detection and quantification of three microsporidia infecting bees, Nosema apis, Nosema ceranae, and Nosema bombi, using probe-based real-time PCR
inferred← citeshttps://doi.org/10.1016/j.exppara.2012.08.018openalex-snapshot
The prevalence of Acarapis woodi in Spanish honey bee (Apis mellifera) colonies
inferred← citeshttps://doi.org/10.1016/j.foodchem.2015.01.111openalex-snapshot
Stability of dicyclohexylamine and fumagillin in honey
inferred← citeshttps://doi.org/10.1016/j.heliyon.2020.e04599openalex-snapshot
Mathematical modelling of population and food storage dynamics in a honey bee colony infected with Nosema ceranae
inferred← citeshttps://doi.org/10.1016/j.ijpara.2011.10.005openalex-snapshot
Diversity of Nosema associated with bumblebees (Bombus spp.) from China
inferred← citeshttps://doi.org/10.1016/j.ijpara.2019.04.002openalex-snapshot
The levels of natural Nosema spp. infection in Apis mellifera iberiensis brood stages
inferred← citeshttps://doi.org/10.1016/j.ijpara.2024.11.008openalex-snapshot
Production and characterization of monoclonal antibodies for specific detection of Nosema ceranae and Nosema apis in beehive samples
inferred← citeshttps://doi.org/10.1016/j.jinsphys.2010.05.016openalex-snapshot
Parasitic infection leads to decline in hemolymph sugar levels in honeybee foragers
inferred← citeshttps://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
inferred← citeshttps://doi.org/10.1016/j.jinsphys.2012.07.010openalex-snapshot
Gas chromatography–mass spectrometry metabolite profiling of worker honey bee (Apis mellifera L.) hemolymph for the study of Nosema ceranae infection
inferred← citeshttps://doi.org/10.1016/j.jinsphys.2017.12.010openalex-snapshot
Impact of Nosema ceranae and Nosema apis on individual worker bees of the two host species (Apis cerana and Apis mellifera) and regulation of host immune response
inferred← citeshttps://doi.org/10.1016/j.jinsphys.2021.104237openalex-snapshot
Immunity and physiological changes in adult honey bees (Apis mellifera) infected with Nosema ceranae: The natural colony environment
inferred← citeshttps://doi.org/10.1016/j.jip.2008.04.005openalex-snapshot
Does fumagillin control the recently detected invasive parasite Nosema ceranae in western honey bees (Apis mellifera)?
inferred← citeshttps://doi.org/10.1016/j.jip.2008.12.001openalex-snapshot
Energetic stress in the honeybee Apis mellifera from Nosema ceranae infection
inferred← citeshttps://doi.org/10.1016/j.jip.2009.03.006openalex-snapshot
Presence of Nosema ceranae in honeybees (Apis mellifera) in Uruguay
inferred← citeshttps://doi.org/10.1016/j.jip.2009.05.012openalex-snapshot
Asymmetrical coexistence of Nosema ceranae and Nosema apis in honey bees
inferred← citeshttps://doi.org/10.1016/j.jip.2009.06.017openalex-snapshot
Nosema ceranae in European honey bees (Apis mellifera)
inferred← citeshttps://doi.org/10.1016/j.jip.2009.10.009openalex-snapshot
Genetic detection and quantification of Nosema apis and N. ceranae in the honey bee
inferred← citeshttps://doi.org/10.1016/j.jip.2010.01.009openalex-snapshot
Effects at Nearctic north-temperate latitudes of indoor versus outdoor overwintering on the microsporidium Nosema ceranae and western honey bees (Apis mellifera)
inferred← citeshttps://doi.org/10.1016/j.jip.2010.06.001openalex-snapshot
A multiplex PCR assay to diagnose and quantify Nosema infections in honey bees (Apis mellifera)
inferred← citeshttps://doi.org/10.1016/j.jip.2010.06.005openalex-snapshot
Infections of Nosema ceranae in four different honeybee species
inferred← citeshttps://doi.org/10.1016/j.jip.2010.10.010openalex-snapshot
Distribution of Nosema ceranae in the European honeybee, Apis mellifera in Japan
inferred← citeshttps://doi.org/10.1016/j.jip.2011.05.012openalex-snapshot
Phylogenetic analysis of Nosema ceranae isolated from European and Asian honeybees in Northern Thailand
inferred← citeshttps://doi.org/10.1016/j.jip.2011.07.003openalex-snapshot
Polar tube protein gene diversity among Nosema ceranae strains derived from a Greek honey bee health study
inferred← citeshttps://doi.org/10.1016/j.jip.2011.09.009openalex-snapshot
Nosema ceranae in age cohorts of the western honey bee (Apis mellifera)
inferred← citeshttps://doi.org/10.1016/j.jip.2011.11.001openalex-snapshot
Comparison of within hive sampling and seasonal activity of Nosema ceranae in honey bee colonies
inferred← citeshttps://doi.org/10.1016/j.jip.2012.01.002openalex-snapshot
External and internal detection of Nosema ceranae on honey bees using real-time PCR
inferred← citeshttps://doi.org/10.1016/j.jip.2012.01.007openalex-snapshot
Linking evolutionary lineage with parasite and pathogen prevalence in the Iberian honey bee
inferred← citeshttps://doi.org/10.1016/j.jip.2012.02.014openalex-snapshot
Further evidence of an oriental origin for Nosema ceranae (Microsporidia: Nosematidae)
inferred← citeshttps://doi.org/10.1016/j.jip.2012.06.008openalex-snapshot
Asymptomatic presence of Nosema spp. in Spanish commercial apiaries
inferred← citeshttps://doi.org/10.1016/j.jip.2012.08.014openalex-snapshot
Nosema ceranae infection intensity highly correlates with temperature
inferred← citeshttps://doi.org/10.1016/j.jip.2013.01.004openalex-snapshot
Molecular differentiation of Nosema apis and Nosema ceranae based on species–specific sequence differences in a protein coding gene
inferred← citeshttps://doi.org/10.1016/j.jip.2013.01.005openalex-snapshot
Improving molecular discrimination of Nosema apis and Nosema ceranae
inferred← citeshttps://doi.org/10.1016/j.jip.2013.09.002openalex-snapshot
Nosema ceranae has been present in Brazil for more than three decades infecting Africanized honey bees
inferred← citeshttps://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
inferred← citeshttps://doi.org/10.1016/j.jip.2015.07.019openalex-snapshot
The influence of Nosema (Microspora: Nosematidae) infection on honey bee (Hymenoptera: Apidae) defense against Varroa destructor (Mesostigmata: Varroidae)
inferred← citeshttps://doi.org/10.1016/j.jip.2016.07.001openalex-snapshot
Species-specific diagnostics of Apis mellifera trypanosomatids: A nine-year survey (2007–2015) for trypanosomatids and microsporidians in Serbian honey bees
inferred← citeshttps://doi.org/10.1016/j.jip.2016.11.001openalex-snapshot
Nosema ceranae is an old resident of honey bee (Apis mellifera) colonies in Mexico, causing infection levels of one million spores per bee or higher during summer and fall
inferred← citeshttps://doi.org/10.1016/j.jip.2017.08.012openalex-snapshot
Antifungal activity of the essential oil obtained from Cryptocarya alba against infection in honey bees by Nosema ceranae
inferred← citeshttps://doi.org/10.1016/j.jip.2018.09.007openalex-snapshot
Impact of the microsporidian Nosema ceranae on the gut epithelium renewal of the honeybee, Apis mellifera
inferred← citeshttps://doi.org/10.1016/j.jip.2021.107671openalex-snapshot
Effect of feeding chitosan or peptidoglycan on Nosema ceranae infection and gene expression related to stress and the innate immune response of honey bees (Apis mellifera)
inferred← citeshttps://doi.org/10.1016/j.jip.2021.107688openalex-snapshot
Natural extracts as potential control agents for Nosema ceranae infection in honeybees, Apis mellifera
inferred← citeshttps://doi.org/10.1016/j.jip.2024.108074openalex-snapshot
Inactivation of Nosema spp. with zinc phthalocyanine
inferred← citeshttps://doi.org/10.1016/j.jip.2024.108185openalex-snapshot
Symbiont-mediated antisense RNA delivery controls Nosema ceranae infections in Apis mellifera
inferred← citeshttps://doi.org/10.1016/j.jip.2025.108333openalex-snapshot
Propolis can reduce Nosema ceranae infection and enhance the immune response in honey bees, without disrupting the gut microbiota
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.jip.2026.108735openalex-snapshot
Molecular detection of Paenibacillus larvae, Melissococcus plutonius and Vairimorpha spp., in historical honey samples from South Brazil
inferred← citeshttps://doi.org/10.1016/j.jip.2026.108758openalex-snapshot
Bombus terrestris as a suboptimal host for Vairimorpha (Nosema) ceranae: Evidence of limited intracellular development following experimental exposure
inferred← citeshttps://doi.org/10.1016/j.jksus.2016.05.005openalex-snapshot
First detection of Nosema sp., microsporidian parasites of honeybees (Apis mellifera) in Riyadh city, Saudi Arabia
inferred← citeshttps://doi.org/10.1016/j.jviromet.2013.12.006openalex-snapshot
Identification of Kashmir bee virus in France using a new RT-PCR method which distinguishes closely related viruses
inferred← citeshttps://doi.org/10.1016/j.meegid.2014.02.008openalex-snapshot
Presence of Nosema ceranae associated with honeybee queen introductions
inferred← citeshttps://doi.org/10.1016/j.mimet.2021.106183openalex-snapshot
An international inter-laboratory study on Nosema spp. spore detection and quantification through microscopic examination of crushed honey bee abdomens
inferred← citeshttps://doi.org/10.1016/j.parint.2021.102361openalex-snapshot
Prevalence of Nosema species infections in Apis cerana japonica and Apis mellifera honeybees in the Tohoku region of Japan
inferred← citeshttps://doi.org/10.1016/j.pestbp.2019.11.006openalex-snapshot
A Pediococcus strain to rescue honeybees by decreasing Nosema ceranae- and pesticide-induced adverse effects
inferred← citeshttps://doi.org/10.1016/j.prevetmed.2021.105322openalex-snapshot
Plant-based supplement containing B-complex vitamins can improve bee health and increase colony performance
inferred← citeshttps://doi.org/10.1016/j.rbe.2018.04.001openalex-snapshot
Spores of Paenibacillus larvae, Ascosphaera apis, Nosema ceranae and Nosema apis in bee products supervised by the Brazilian Federal Inspection Service
inferred← citeshttps://doi.org/10.1016/j.rvsc.2011.08.002openalex-snapshot
The growing prevalence of Nosema ceranae in honey bees in Spain, an emerging problem for the last decade
inferred← citeshttps://doi.org/10.1016/j.rvsc.2012.03.006openalex-snapshot
Low prevalence of honeybee viruses in Spain during 2006 and 2007
inferred← citeshttps://doi.org/10.1016/j.rvsc.2026.106245openalex-snapshot
A large-scale, longitudinal study on the epidemiology of Nosema (=Vairimorpha) ceranae and black queen cell virus (BQCV) in Apis mellifera colonies across the Italian agroecosystems
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2019.134208openalex-snapshot
The toxic unit approach as a risk indicator in honey bees surveillance programmes: A case of study in Apis mellifera iberiensis
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2026.181785openalex-snapshot
“Pollen diets influence gut microbiota composition and colony development in native South American bumblebees”
inferred← citeshttps://doi.org/10.1016/j.sjbs.2017.01.054openalex-snapshot
Geographical distribution and molecular detection of Nosema ceranae from indigenous honey bees of Saudi Arabia
inferred← citeshttps://doi.org/10.1016/j.sjbs.2018.11.017openalex-snapshot
Nosema ceranae infection in honeybee samples from Tuscanian Archipelago (Central Italy) investigated by two qPCR methods
inferred← citeshttps://doi.org/10.1016/j.sjbs.2019.11.012openalex-snapshot
Twenty-five-year study of Nosema spp. in honey bees (Apis mellifera) in Serbia
inferred← citeshttps://doi.org/10.1016/j.tim.2011.09.003openalex-snapshot
Bees brought to their knees: microbes affecting honey bee health
inferred← citeshttps://doi.org/10.1016/j.vetpar.2010.02.010openalex-snapshot
Comparative virulence of Nosema ceranae and Nosema apis in individual European honey bees
inferred← citeshttps://doi.org/10.1016/j.vetpar.2012.12.004openalex-snapshot
Susceptibility of four different honey bee species to Nosema ceranae
inferred← citeshttps://doi.org/10.1016/j.zool.2016.03.007openalex-snapshot
Parasite resistance and tolerance in honeybees at the individual and social level
inferred← citeshttps://doi.org/10.1016/s2222-1808(15)60980-xopenalex-snapshot
Molecular epidemiology and geographical distribution of Nosema ceranae in honeybees, Northern Thailand
inferred← citeshttps://doi.org/10.1016/s2222-1808(16)61163-5openalex-snapshot
Development and evaluation of loop-mediated isothermal amplification for rapid detection of Nosema ceranae in honeybee
inferred← citeshttps://doi.org/10.1017/s0031182010000235openalex-snapshot
Behavioural fever in infected honeybees: parasitic manipulation or coincidental benefit?
inferred← citeshttps://doi.org/10.1017/s0031182013001133openalex-snapshot
New insights on the genetic diversity of the honeybee parasiteNosema ceranaebased onmultilocussequence analysis
inferred← citeshttps://doi.org/10.1017/s0031182013001790openalex-snapshot
High levels of genetic diversity inNosema ceranaewithinApis melliferacolonies
inferred← citeshttps://doi.org/10.1017/s0031182020001481openalex-snapshot
A new isolate ofNosema fumiferanae(Microsporidia: Nosematidae) from the date mothApomyelois(Ectomyelois)ceratoniae, Zeller, 1839 (Lepidoptera: Pyralidae)
inferred← citeshttps://doi.org/10.1017/s1742758417000212openalex-snapshot
Prevalence of common honey bee pathogens at selected apiaries in Kenya, 2013/2014
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/10.1021/jf4055374openalex-snapshot
Fumagillin: An Overview of Recent Scientific Advances and Their Significance for Apiculture
inferred← citeshttps://doi.org/10.1038/s41598-018-23678-8openalex-snapshot
Porphyrins inactivate Nosema spp. microsporidia
inferred← citeshttps://doi.org/10.1038/s41598-019-46453-9openalex-snapshot
Impact of nutritional stress on the honeybee colony health
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/s41598-020-57909-8openalex-snapshot
Direct and sensitive detection of a microsporidian parasite of bumblebees using loop-mediated isothermal amplification (LAMP)
inferred← citeshttps://doi.org/10.1038/s41598-020-68420-5openalex-snapshot
Bioactivity studies of porphyrinoids against microsporidia isolated from honeybees
inferred← citeshttps://doi.org/10.1038/s41598-020-74209-3openalex-snapshot
Nosema ceranae causes cellular immunosuppression and interacts with thiamethoxam to increase mortality in the stingless bee Melipona colimana
inferred← citeshttps://doi.org/10.1038/s41598-022-18534-9openalex-snapshot
Effect of amide protoporphyrin derivatives on immune response in Apis mellifera
inferred← citeshttps://doi.org/10.1038/s41598-023-38905-0openalex-snapshot
Geographic population structure of the honeybee microsporidian parasite Vairimorpha (Nosema) ceranae in the South West Indian Ocean
inferred← citeshttps://doi.org/10.1038/s41598-025-11303-4openalex-snapshot
The in vitro potential of non-thermal atmospheric pressure plasma against Nosema ceranae infection in honeybees (Apis mellifera)
inferred← citeshttps://doi.org/10.1038/s42003-023-04587-7openalex-snapshot
Significant, but not biologically relevant: Nosema ceranae infections and winter losses of honey bee colonies
inferred← citeshttps://doi.org/10.1038/srep10565openalex-snapshot
Consequences of Nosema apis infection for male honey bees and their fertility
inferred← citeshttps://doi.org/10.1051/apido/2008065openalex-snapshot
Nosema ceranae infects honey bees ( Apis mellifera ) and contaminates honey in Australia
inferred← citeshttps://doi.org/10.1051/apido/2009039openalex-snapshot
Behavioral changes mediated by hunger in honeybees infected withNosema ceranae
inferred← citeshttps://doi.org/10.1051/apido/2009070openalex-snapshot
Effect of thymol and resveratrol administered with candy or syrup on the development of Nosema ceranae and on the longevity of honeybees ( Apis mellifera L.) in laboratory conditions
inferred← citeshttps://doi.org/10.1051/apido/2009076openalex-snapshot
Varroa destructor is the main culprit for the death and reduced populations of overwintered honey bee ( Apis mellifera ) colonies in Ontario, Canada
inferred← citeshttps://doi.org/10.1051/apido/2010010openalex-snapshot
Research strategies to improve honeybee health in Europe
inferred← citeshttps://doi.org/10.1051/apido/2010014openalex-snapshot
The German bee monitoring project: a long term study to understand periodically high winter losses of honey bee colonies
inferred← citeshttps://doi.org/10.1051/apido/2010019openalex-snapshot
Nosema ceranaein Europe: an emergent type C nosemosis
inferred← citeshttps://doi.org/10.1051/apido/2010030openalex-snapshot
The microsporidian Nosema ceranae, the antibiotic Fumagilin-B®, and western honey bee (Apis mellifera) colony strength
inferred← citeshttps://doi.org/10.1051/apido/2010034openalex-snapshot
Dominance of Nosema ceranae in honey bees in the Balkan countries in the absence of symptoms of colony collapse disorder
inferred← citeshttps://doi.org/10.1051/apido/2010045openalex-snapshot
Molecular detection of Nosema ceranae and N. apis from Turkish honey bees
inferred← citeshttps://doi.org/10.1051/apido/2010047openalex-snapshot
Evaluation of colony losses in Israel in relation to the incidence of pathogens and pests
inferred← citeshttps://doi.org/10.1051/apido:2008022openalex-snapshot
Screening of natural compounds for the control of nosema disease in honeybees ( Apis mellifera )
inferred← citeshttps://doi.org/10.1051/apido:2008040openalex-snapshot
Analytical sensitivity and specificity of a RT-PCR for the diagnosis and characterization of the spatial distribution of three Apis mellifera viral diseases in Spain
inferred← citeshttps://doi.org/10.1080/0005772x.2019.1699007openalex-snapshot
Biotic Stressors Affecting Key Apiaries in Argentina
inferred← citeshttps://doi.org/10.1080/00218839.2015.1101240openalex-snapshot
Confirmation ofNosema ceranaein New Zealand and a phylogenetic comparison ofNosemaspp. strains
inferred← citeshttps://doi.org/10.1080/00218839.2016.1144975openalex-snapshot
Infectivity ofNosema ceranaeisolates from different hosts and immune response in honey beesApis melliferaandApis cerana
inferred← citeshttps://doi.org/10.1080/00218839.2016.1175731openalex-snapshot
Prevalence and distribution of honey bee pests and pathogens in Uruguay
inferred← citeshttps://doi.org/10.1080/00218839.2016.1189676openalex-snapshot
A pest and disease survey of the isolated Norfolk Island honey bee (Apis mellifera) population
inferred← citeshttps://doi.org/10.1080/00218839.2017.1327936openalex-snapshot
Detection of Nosema spp. spore contamination in commercial Apis mellifera bee pollens of Thailand
inferred← citeshttps://doi.org/10.1080/00218839.2017.1343020openalex-snapshot
Biochemical status of feral honey bees (Apis mellifera) infested with various pathogens
inferred← citeshttps://doi.org/10.1080/00218839.2017.1348714openalex-snapshot
Oral administration of essential oils and main components: Study on honey bee survival and Nosema ceranae development
inferred← citeshttps://doi.org/10.1080/00218839.2018.1494892openalex-snapshot
Genetic diversity and prevalence of Varroa destructor, Nosema apis, and N. ceranae in managed honey bee (Apis mellifera) colonies in the Caribbean island of Dominica, West Indies
inferred← citeshttps://doi.org/10.1080/00218839.2018.1517989openalex-snapshot
Nosema ceranae contamination in bee keeping material: the use of ozone as disinfection method
inferred← citeshttps://doi.org/10.1080/00218839.2019.1614737openalex-snapshot
First molecular detection of Nosema ceranae in Azerbaijan
inferred← citeshttps://doi.org/10.1080/00218839.2019.1632148openalex-snapshot
Nosema ceranae, the most common microsporidium infecting Apis mellifera in the main beekeeping regions of China since at least 2005
inferred← citeshttps://doi.org/10.1080/00218839.2019.1676999openalex-snapshot
Prevalence and geographical distribution of Nosema apis and Nosema ceranae in apiaries of Northwest Mexico using a duplex real-time PCR with melting-curve analysis
inferred← citeshttps://doi.org/10.1080/00218839.2020.1736782openalex-snapshot
Glyphosate-based herbicides and Nosema sp. microsporidia reduce honey bee (Apis mellifera L.) survivability under laboratory conditions
inferred← citeshttps://doi.org/10.1080/00218839.2020.1749451openalex-snapshot
Nosema ceranae and RNA viruses in honey bee populations of Cuba
inferred← citeshttps://doi.org/10.1080/00218839.2021.1880760openalex-snapshot
Interactions between sublethal doses of thiamethoxam and Nosema ceranae in the honey bee, Apis mellifera
inferred← citeshttps://doi.org/10.1080/00218839.2021.1888537openalex-snapshot
Can pollen supplementation mitigate the impact of nutritional stress on honey bee colonies?
inferred← citeshttps://doi.org/10.1080/00218839.2021.1889803openalex-snapshot
Estimation of honey bee colony infection with Nosema ceranae and Varroa destructor using fluorescence spectroscopy in combination with differential scanning calorimetry of honey samples
inferred← citeshttps://doi.org/10.1080/00218839.2021.1994261openalex-snapshot
Coexistence between selected pathogens in honey bee workers
inferred← citeshttps://doi.org/10.1080/00218839.2021.2008706openalex-snapshot
Prevalence of nosemosis in honey bees (Apis mellifera L., 1758) of the Hatay province in Turkey
inferred← citeshttps://doi.org/10.1080/00218839.2021.2013423openalex-snapshot
No effect of abscisic and p-coumaric acids as food supplements and stimulants of the immunological system of Africanized hybrids of Apis mellifera
inferred← citeshttps://doi.org/10.1080/00218839.2022.2055265openalex-snapshot
Presence of Lotmaria passim , Crithidia mellificae and Nosema spp. in differently aged Apis mellifera brood
inferred← citeshttps://doi.org/10.1080/00218839.2022.2083846openalex-snapshot
A new duplex qPCR assay for the quantification of honey bee ( Apis mellifera ) parasites Nosema ceranae and Nosema apis tested with low dose experimental exposure
inferred← citeshttps://doi.org/10.1080/00218839.2022.2106089openalex-snapshot
Detection of honey bee viruses in apiaries in Southern Brazil through two standardized multiplex RT-PCR
inferred← citeshttps://doi.org/10.1080/00218839.2023.2169368openalex-snapshot
Evaluation of oxalic acid with glycerin efficacy against Varroa destructor (Varroidae): a four year assay
inferred← citeshttps://doi.org/10.1080/00218839.2023.2190066openalex-snapshot
Honey bee viruses in solitary bees in South America: simultaneous detection and prevalence
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