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Widespread dispersal of the microsporidian Nosema ceranae, an emergent pathogen of the western honey bee, Apis mellifera

https://doi.org/10.1016/j.jip.2007.02.014

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What this work says

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

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The Ribosomal RNA Gene Region ofNosema apis(Microspora): DNA Sequence for Small and Large Subunit rRNA Genes and Evidence of a Large Tandem Repeat Unit Size

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The Transmission of Deformed Wing Virus between Honeybees (Apis melliferaL.) by the Ectoparasitic MiteVarroa jacobsoniOud

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Biogeography and Taxonomy of Honeybees

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Plight of the bumble bee: Pathogen spillover from commercial to wild populations

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Pathogenicity and virulence

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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)

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Emerging pathogens: the epidemiology and evolution of species jumps

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Buzziness as usual? Questioning the global pollination crisis

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Pollinator diversity and crop pollination services are at risk

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The role of varroa mites in infections of Kashmir bee virus (KBV) and deformed wing virus (DWV) in honey bees

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Progress in invasion biology: predicting invaders

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/10.1016/s0966-842x(02)02428-9openalex-snapshot

Population biology of emerging and re-emerging pathogens

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:2006054openalex-snapshot

ANosema ceranaeisolate from the honeybeeApis mellifera

inferredcites →https://doi.org/10.1080/0005772x.1993.11099183openalex-snapshot

World Bee Health Report

inferredcites →https://doi.org/10.1080/0005772x.2002.11099532openalex-snapshot

Honey bee winter mortality in France in 1999 and 2000

inferredcites →https://doi.org/10.1080/00218839.1984.11100617openalex-snapshot

Nosema Apis, Sampling Techniques and Honey Yield

inferredcites →https://doi.org/10.1080/00218839.1999.11100998openalex-snapshot

Genetic variability amongNosema apisisolates

inferredcites →https://doi.org/10.1080/00218839.2003.11101080openalex-snapshot

African honey bees (Apis mellifera scutellata) and nosema (Nosema apis) infections

inferredcites →https://doi.org/10.1080/00218839.2006.11101355openalex-snapshot

Natural infections of Nosema ceranae in European honey bees

inferredcites →https://doi.org/10.1093/jee/85.1.47openalex-snapshot

Reduced Pollen Collection by Honey Bee (Hymenoptera: Apidae) Colonies Infected with Nosema apis and Sacbrood Virus

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/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

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Emerging Infectious Diseases of Wildlife-- Threats to Biodiversity and Human Health

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The Microsporidia and Microsporidiosis

inferredcites →https://doi.org/10.1128/9781555818227.ch4openalex-snapshot

Molecular Biology, Molecular Phylogeny, and Molecular Diagnostic Approaches to the Microsporidia

inferredcites →https://doi.org/10.1146/annurev.en.13.010168.001203openalex-snapshot

Honey Bee Pathology

inferredcites →https://doi.org/10.3896/ibra.1.45.4.13openalex-snapshot

Natural infections of Nosema ceranae in European honey bees

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Incoming claims: where this work appears in other papers’ reference lists and arguments.

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The comparison of rDNA spacer regions of Nosema ceranae isolates from different hosts and locations

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Nosema ceranae is a long-present and wide-spread microsporidian infection of the European honey bee (Apis mellifera) in the United States

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First detection of Nosema ceranae, a microsporidian parasite of European honey bees (Apis mellifera), in Canada and central USA

inferred← citeshttps://doi.org/10.1016/j.jip.2008.04.005openalex-snapshot

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inferred← citeshttps://doi.org/10.1016/j.jip.2008.12.001openalex-snapshot

Energetic stress in the honeybee Apis mellifera from Nosema ceranae infection

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Presence of Nosema ceranae in honeybees (Apis mellifera) in Uruguay

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Asymmetrical coexistence of Nosema ceranae and Nosema apis in honey bees

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Nosema ceranae in European honey bees (Apis mellifera)

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Effects at Nearctic north-temperate latitudes of indoor versus outdoor overwintering on the microsporidium Nosema ceranae and western honey bees (Apis mellifera)

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A multiplex PCR assay to diagnose and quantify Nosema infections in honey bees (Apis mellifera)

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Infections of Nosema ceranae in four different honeybee species

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Molecular diversity of the microsporidium Kneallhazia solenopsae reveals an expanded host range among fire ants in North America

inferred← citeshttps://doi.org/10.1016/j.jip.2010.08.004openalex-snapshot

Sudden deaths and colony population decline in Greek honey bee colonies

inferred← citeshttps://doi.org/10.1016/j.jip.2010.10.003openalex-snapshot

Nosema ceranae, a new parasite in Thai honeybees

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.2010.12.010openalex-snapshot

Morphology, molecular characteristics and prevalence of a Cystosporogenes species (Microsporidia) isolated from Agrilus anxius (Coleoptera: Buprestidae)

inferred← citeshttps://doi.org/10.1016/j.jip.2011.02.003openalex-snapshot

Prevalence and infection intensity of Nosema in honey bee (Apis mellifera L.) colonies in Virginia

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.2011.05.016openalex-snapshot

Nosema ceranae in drone honey bees (Apis mellifera)

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.2012.01.004openalex-snapshot

Survival and immune response of drones of a Nosemosis tolerant honey bee strain towards N. ceranae infections

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.2012.04.001openalex-snapshot

Low natural levels of Nosema ceranae in Apis mellifera queens

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.2013.01.001openalex-snapshot

Comparative development and tissue tropism of Nosema apis and Nosema ceranae

inferred← citeshttps://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

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.2013.06.005openalex-snapshot

Emerging dangers: Deadly effects of an emergent parasite in a new pollinator host

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.2014.06.004openalex-snapshot

Immunosenescence and resistance to parasite infection in the honey bee, Apis mellifera

inferred← citeshttps://doi.org/10.1016/j.jip.2014.12.006openalex-snapshot

Comparative virulence and competition between Nosema apis and Nosema ceranae in honey bees (Apis mellifera)

inferred← citeshttps://doi.org/10.1016/j.jip.2015.05.013openalex-snapshot

Bee pathogens found in Bombus atratus from Colombia: A case study

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.2016.11.002openalex-snapshot

Distribution and prevalence of Nosema apis and N. ceranae in temperate and subtropical eco-regions of Argentina

inferred← citeshttps://doi.org/10.1016/j.jip.2018.02.011openalex-snapshot

Gamma irradiation inactivates honey bee fungal, microsporidian, and viral pathogens and parasites

inferred← citeshttps://doi.org/10.1016/j.jip.2018.03.008openalex-snapshot

Infection dynamics of Nosema ceranae in honey bee midgut and host cell apoptosis

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.2020.107502openalex-snapshot

Identification and characterization of three microsporidian genera concurrently infecting a silkworm, Bombyx mori, in Brazil

inferred← citeshttps://doi.org/10.1016/j.jip.2020.107506openalex-snapshot

OneHealth implications of infectious diseases of wild and managed bees

inferred← citeshttps://doi.org/10.1016/j.jip.2026.108637openalex-snapshot

Nosema ceranae and honey bee-associated virus levels in commercial beekeeping operations across Southwestern Saudi Arabia

inferred← citeshttps://doi.org/10.1016/j.jip.2026.108725openalex-snapshot

Comparison of different matrices for the detection of honey bee pathogens: results from a Norwegian study

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.meegid.2015.01.002openalex-snapshot

Recent worldwide expansion of Nosema ceranae (Microsporidia) in Apis mellifera populations inferred from multilocus patterns of genetic variation

inferred← citeshttps://doi.org/10.1016/j.micpath.2024.107161openalex-snapshot

Honeybee defense mechanisms: Role of honeybee gut microbiota and antimicrobial peptides in maintaining colony health and preventing diseases

inferred← citeshttps://doi.org/10.1016/j.mimet.2008.07.007openalex-snapshot

Transformation of the Gram-positive honey bee pathogen, Paenibacillus larvae, by electroporation

inferred← citeshttps://doi.org/10.1016/j.mimet.2016.09.021openalex-snapshot

Viability and infectivity of fresh and cryopreserved Nosema ceranae spores

inferred← citeshttps://doi.org/10.1016/j.pestbp.2024.105772openalex-snapshot

A potential trade-off between offense and defense in honeybee innate immunity: Reduced phagocytosis in honeybee hemocytes correlates with a protective response after exposure to imidacloprid and amitraz

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.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.sjbs.2017.01.010openalex-snapshot

Prevalence of the microsporidian Nosema ceranae in honeybee (Apis mellifera) apiaries in Central Italy

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.synbio.2024.07.003openalex-snapshot

Liposome-based RNAi delivery in honeybee for inhibiting parasite Nosema ceranae

inferred← citeshttps://doi.org/10.1016/j.vetmic.2015.02.003openalex-snapshot

Evidence of the synergistic interaction of honey bee pathogens Nosema ceranae and Deformed wing virus

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.ympev.2016.03.015openalex-snapshot

Population genetic structure and long-distance dispersal of a recently expanding migratory bird

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/10.1017/s0031182009991818openalex-snapshot

The ecology and evolution of microsporidian parasites

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/s0031182014001243openalex-snapshot

Horizontal transmission of a parasite is influenced by infected host phenotype and density

inferred← citeshttps://doi.org/10.1017/s0031182015000840openalex-snapshot

A descriptive study of the prevalence of parasites and pathogens in Chinese black honeybees

inferred← citeshttps://doi.org/10.1017/s0031182020001018openalex-snapshot

Cross-infectivity of honey and bumble bee-associated parasites across three bee families

inferred← citeshttps://doi.org/10.1017/s0031182024001446openalex-snapshot

Nosemosis negatively affects honeybee survival: experimental and meta-analytic evidence

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/nrmicro.2016.43openalex-snapshot

Gut microbial communities of social bees

inferred← citeshttps://doi.org/10.1038/s41467-018-07426-0openalex-snapshot

Characterisation of the British honey bee metagenome

inferred← citeshttps://doi.org/10.1038/s41467-020-15919-0openalex-snapshot

Chronic bee paralysis as a serious emerging threat to honey bees

inferred← citeshttps://doi.org/10.1038/s41538-025-00464-1openalex-snapshot

Honey bulk DNA metagenomic analysis to identify honey biological composition and monitor honey bee pathogens

inferred← citeshttps://doi.org/10.1038/s41559-017-0246-zopenalex-snapshot

Ecological and evolutionary approaches to managing honeybee disease

inferred← citeshttps://doi.org/10.1038/s41598-018-19860-7openalex-snapshot

Social status shapes the bacterial and fungal gut communities of the honey bee

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/s41598-020-68420-5openalex-snapshot

Bioactivity studies of porphyrinoids against microsporidia isolated from honeybees

inferred← citeshttps://doi.org/10.1038/s41598-021-90615-7openalex-snapshot

Identification of pathogens in the invasive hornet Vespa velutina and in native Hymenoptera (Apidae, Vespidae) from SW-Europe

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/s41598-024-51514-9openalex-snapshot

Prevalence and distribution of Varroa destructor and Nosema spp. in symptomatic honey bee colonies across the USA from 2015 to 2022

inferred← citeshttps://doi.org/10.1038/s41598-024-67796-yopenalex-snapshot

Exploring the interactions between Nosema ceranae infection and the honey bee gut microbiome

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/srep00326openalex-snapshot

Parasite-insecticide interactions: a case study of Nosema ceranae and fipronil synergy on honeybee

inferred← citeshttps://doi.org/10.1038/srep10982openalex-snapshot

The cost of promiscuity: sexual transmission of Nosema microsporidian parasites in polyandrous honey bees

inferred← citeshttps://doi.org/10.1038/srep22042openalex-snapshot

Parasite infection accelerates age polyethism in young honey bees

inferred← citeshttps://doi.org/10.1038/srep22626openalex-snapshot

Effects of Nosema apis, N. ceranae, and coinfections on honey bee (Apis mellifera) learning and memory

inferred← citeshttps://doi.org/10.1039/c8lc01342jopenalex-snapshot

Rapid imaging, detection, and quantification of Nosema ceranae spores in honey bees using mobile phone-based fluorescence microscopy

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/2009046openalex-snapshot

Nosemasp. influences flight behavior of infected honey bee (Apis mellifera) foragers

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/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

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