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Microbiota and pathogens in an invasive bee: Megachile sculpturalis from native and invaded regions

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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/ece3.3758openalex-snapshot

Range expansion of the Asian native giant resin bee Megachile sculpturalis (Hymenoptera, Apoidea, Megachilidae) in France

inferredcites →https://doi.org/10.1002/ece3.5599openalex-snapshot

Linking pollen foraging of megachilid bees to their nest bacterial microbiota

inferredcites →https://doi.org/10.1007/0-387-30744-3_17openalex-snapshot

The Genus Bacillus—Insect Pathogens

inferredcites →https://doi.org/10.1007/bf00177048openalex-snapshot

Aerobic microorganisms associated with alfalfa leafcutter bees (megachile rotundata)

inferredcites →https://doi.org/10.1007/s00248-016-0838-1openalex-snapshot

Flowers and Wild Megachilid Bees Share Microbes

inferredcites →https://doi.org/10.1007/s00248-020-01549-yopenalex-snapshot

Environment Shapes the Microbiome of the Blue Orchard Bee, Osmia lignaria

inferredcites →https://doi.org/10.1007/s00248-021-01682-2openalex-snapshot

Endosymbiotic Bacteria Aid to Overcome Temperature Induced Stress in the Oriental Fruit Fly, Bactrocera dorsalis

inferredcites →https://doi.org/10.1007/s10340-018-0990-0openalex-snapshot

Common pathways by which non-native forest insects move internationally and domestically

inferredcites →https://doi.org/10.1007/s10530-012-0311-0openalex-snapshot

Alien parasite hitchhikes to Patagonia on invasive bumblebee

inferredcites →https://doi.org/10.1007/s10592-017-0937-7openalex-snapshot

Hunting for healthy microbiomes: determining the core microbiomes of Ceratina, Megalopta, and Apis bees and how they associate with microbes in bee collected pollen

inferredcites →https://doi.org/10.1007/s11274-018-2437-4openalex-snapshot

Antimicrobial peptides produced by Brevibacillus spp.: structure, classification and bioactivity: a mini review

inferredcites →https://doi.org/10.1016/b978-0-444-52149-1.00001-xopenalex-snapshot

Definition, Classification and Nomenclature of the Yeasts

inferredcites →https://doi.org/10.1016/j.actao.2020.103556openalex-snapshot

Bee hotels host a high abundance of exotic bees in an urban context

inferredcites →https://doi.org/10.1016/j.cois.2020.09.007openalex-snapshot

(More than) Hitchhikers through the network: the shared microbiome of bees and flowers

inferredcites →https://doi.org/10.1016/j.ejop.2020.125688openalex-snapshot

Comparison between Apicystis cryptica sp. n. and Apicystis bombi (Arthrogregarida, Apicomplexa): Gregarine parasites that cause fat body hypertrophism in bees

inferredcites →https://doi.org/10.1016/j.femsyr.2005.03.006openalex-snapshot

and , two new yeast species from the clade associated with solitary bees in the Atlantic rain forest of Brazil

inferredcites →https://doi.org/10.1016/j.fm.2020.103446openalex-snapshot

Volatile organic compounds from Starmerella bacillaris to control gray mold on apples and modulate cider aroma profile

inferredcites →https://doi.org/10.1016/j.funeco.2020.100973openalex-snapshot

The vectoring of Starmerella species and other yeasts by stingless bees in a Neotropical savanna

inferredcites →https://doi.org/10.1016/j.ijfoodmicro.2015.12.009openalex-snapshot

Microbial diversity and metabolite composition of Belgian red-brown acidic ales

inferredcites →https://doi.org/10.1016/j.jinsphys.2008.07.011openalex-snapshot

Gut bacterial communities in the Mediterranean fruit fly (Ceratitis capitata) and their impact on host longevity

inferredcites →https://doi.org/10.1016/j.jip.2016.05.002openalex-snapshot

Brevibacillus laterosporus inside the insect body: Beneficial resident or pathogenic outsider?

inferredcites →https://doi.org/10.1016/j.sajb.2009.07.016openalex-snapshot

Yeasts in floral nectar of some South African plants: Quantification and associations with pollinator type and sugar concentration

inferredcites →https://doi.org/10.1016/j.scitotenv.2020.140873openalex-snapshot

Gut microbial composition in different castes and developmental stages of the invasive hornet Vespa velutina nigrithorax

inferredcites →https://doi.org/10.1016/j.scitotenv.2022.154246openalex-snapshot

On the road: Anthropogenic factors drive the invasion risk of a wild solitary bee species

inferredcites →https://doi.org/10.1016/j.sjbs.2017.05.008openalex-snapshot

Characterization of gut bacterial flora of Apis mellifera from north-west Pakistan

inferredcites →https://doi.org/10.1016/j.syapm.2014.03.002openalex-snapshot

Rosenbergiella australoborealis sp. nov., Rosenbergiella collisarenosi sp. nov. and Rosenbergiella epipactidis sp. nov., three novel bacterial species isolated from floral nectar

inferredcites →https://doi.org/10.1016/s0065-308x(08)00607-6openalex-snapshot

Chapter 7 Parasites and Biological Invasions

inferredcites →https://doi.org/10.1016/s0723-2020(11)80453-4openalex-snapshot

Transfer of Acidiphilium facilis and Acidiphilium aminolytica to the Genus Acidocella gen. nov., and Emendation of the Genus Acidiphilium

inferredcites →https://doi.org/10.1016/s0740-0020(14)00320-7openalex-snapshot

International Journal of Food Microbiology

inferredcites →https://doi.org/10.1038/1811310b0openalex-snapshot

New Zealand Journal of Agricultural Research

inferredcites →https://doi.org/10.1038/nature01346openalex-snapshot

Introduced species and their missing parasites

inferredcites →https://doi.org/10.1038/ncomms14435openalex-snapshot

No saturation in the accumulation of alien species worldwide

inferredcites →https://doi.org/10.1038/nmeth.3869openalex-snapshot

DADA2: High-resolution sample inference from Illumina amplicon data

inferredcites →https://doi.org/10.1038/s41597-020-00669-xopenalex-snapshot

Global land use for 2015–2100 at 0.05° resolution under diverse socioeconomic and climate scenarios

inferredcites →https://doi.org/10.1038/s41598-018-19583-9openalex-snapshot

Stingless Bee Larvae Require Fungal Steroid to Pupate

inferredcites →https://doi.org/10.1038/s41598-018-19860-7openalex-snapshot

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

inferredcites →https://doi.org/10.1038/s41598-021-82573-xopenalex-snapshot

Composition and acquisition of the microbiome in solitary, ground-nesting alkali bees

inferredcites →https://doi.org/10.1038/sdata.2017.122openalex-snapshot

Climatologies at high resolution for the earth’s land surface areas

inferredcites →https://doi.org/10.1046/j.1365-294x.2001.01243.xopenalex-snapshot

Founder effect in an island population of bighorn sheep

inferredcites →https://doi.org/10.1080/0005772x.1986.11098855openalex-snapshot

The Introduction ofBombus Ruderatusto Chile for Red Clover Pollination

inferredcites →https://doi.org/10.1080/00288233.1972.10430553openalex-snapshot

The introduction of bumblebees into North Island, New Zealand

inferredcites →https://doi.org/10.1093/aesa/106.6.875openalex-snapshot

Annals of the Entomological Society of America

inferredcites →https://doi.org/10.1093/aobpla/plv036openalex-snapshot

Long-distance plant dispersal to North Atlantic islands: colonization routes and founder effect

inferredcites →https://doi.org/10.1093/ee/16.3.664openalex-snapshot

Introduction of the European Bee, Osmia cornuta, into California Almond Orchards (Hymenoptera: Megachilidae)

inferredcites →https://doi.org/10.1093/femsec/fiy218openalex-snapshot

Bacterial community structure and succession in nests of two megachilid bee genera

inferredcites →https://doi.org/10.1093/nar/gkn201openalex-snapshot

NCBI BLAST: a better web interface

inferredcites →https://doi.org/10.1098/rspb.2018.0789openalex-snapshot

The distribution of bacterial doubling times in the wild

inferredcites →https://doi.org/10.1099/ijs.0.052217-0openalex-snapshot

Rosenbergiella nectarea gen. nov., sp. nov., in the family Enterobacteriaceae, isolated from floral nectar

inferredcites →https://doi.org/10.1099/ijs.0.65117-0openalex-snapshot

Synonymy of the yeast genera Moniliella and Trichosporonoides and proposal of Moniliella fonsecae sp. nov. and five new species combinations

inferredcites →https://doi.org/10.1099/ijs.0.65230-0openalex-snapshot

Candida flosculorum sp. nov. and Candida floris sp. nov., two yeast species associated with tropical flowers

inferredcites →https://doi.org/10.1099/ijsem.0.002675openalex-snapshot

Starmerella camargoi f.a., sp. nov., Starmerella ilheusensis f.a., sp. nov., Starmerella litoralis f.a., sp. nov., Starmerella opuntiae f.a., sp. nov., Starmerella roubikii f.a., sp. nov. and Starmerella vitae f.a., sp. nov., isolated from flowers and bees, and transfer of related Candida species…

inferredcites →https://doi.org/10.1099/ijsem.0.002758openalex-snapshot

Lactobacillus micheneri sp. nov., Lactobacillus timberlakei sp. nov. and Lactobacillus quenuiae sp. nov., lactic acid bacteria isolated from wild bees and flowers

inferredcites →https://doi.org/10.1099/ijsem.0.003099openalex-snapshot

Moniliella floricola sp. nov., a species of black yeast isolated from flowers

inferredcites →https://doi.org/10.1111/(issn)1758-2229openalex-snapshot

Environmental Microbiology Reports

inferredcites →https://doi.org/10.1111/1462-2920.13037openalex-snapshot

Species coexistence in simple microbial communities: unravelling the phenotypic landscape of co‐occurring M etschnikowia species in floral nectar

inferredcites →https://doi.org/10.1111/1462-2920.13524openalex-snapshot

Bacterial microbiota associated with flower pollen is influenced by pollination type, and shows a high degree of diversity and species‐specificity

inferredcites →https://doi.org/10.1111/1574-6976.12025openalex-snapshot

The gut microbiota of insects – diversity in structure and function

inferredcites →https://doi.org/10.1111/j.1365-2672.2006.02914.xopenalex-snapshot

Bacillus species in the intestine of termites and other soil invertebrates

inferredcites →https://doi.org/10.1111/j.1461-0248.2004.00616.xopenalex-snapshot

Is invasion success explained by the enemy release hypothesis?

inferredcites →https://doi.org/10.1111/j.1469-7998.1992.tb04461.xopenalex-snapshot

Phenology of two territorial solitary bees, Anthidium manicatum and A. florentinum (Hymenoptera: Megachilidae)

inferredcites →https://doi.org/10.1111/j.1523-1739.2011.01707.xopenalex-snapshot

Effects of Invasive Parasites on Bumble Bee Declines

inferredcites →https://doi.org/10.1111/j.1567-1364.2001.tb00007.xopenalex-snapshot

Biogeography of the yeasts of ephemeral flowers and their insects

inferredcites →https://doi.org/10.1111/j.1758-2229.2012.00385.xopenalex-snapshot

Molecular detection of protozoan parasites infecting A pis mellifera colonies in J apan

inferredcites →https://doi.org/10.1111/nph.14809openalex-snapshot

Nectar‐inhabiting microorganisms influence nectar volatile composition and attractiveness to a generalist pollinator

inferredcites →https://doi.org/10.1111/plb.12957openalex-snapshot

Nectar yeasts enhance the interaction between Clematis akebioides and its bumblebee pollinator

inferredcites →https://doi.org/10.1126/science.1201618openalex-snapshot

Natural Microbe-Mediated Refractoriness to Plasmodium Infection in Anopheles gambiae

inferredcites →https://doi.org/10.1126/science.265.5175.1084openalex-snapshot

Virulence and Local Adaptation of a Horizontally Transmitted Parasite

inferredcites →https://doi.org/10.1128/aem.01560-13openalex-snapshot

The Carbohydrate Metabolism Signature of Lactococcus lactis Strain A12 Reveals Its Sourdough Ecosystem Origin

inferredcites →https://doi.org/10.1128/eissn.1098-5336openalex-snapshot

Applied and Environmental Microbiology

inferredcites →https://doi.org/10.1128/mbio.00503-21openalex-snapshot

A Bacterial Symbiont Protects Honey Bees from Fungal Disease

inferredcites →https://doi.org/10.1146/annurev-ento-120709-144836openalex-snapshot

The Alfalfa Leafcutting Bee,Megachile rotundata: The World's Most Intensively Managed Solitary Bee

inferredcites →https://doi.org/10.1146/annurev.ecolsys.34.011802.132355openalex-snapshot

Effects of Introduced Bees on Native Ecosystems

inferredcites →https://doi.org/10.1146/ecolsys.693openalex-snapshot

Annual Review of Ecology, Evolution, and Systematics

inferredcites →https://doi.org/10.1155/2018/5862437openalex-snapshot

Insights into Brevibacillus borstelensis AK1 through Whole Genome Sequencing: A Thermophilic Bacterium Isolated from a Hot Spring in Saudi Arabia

inferredcites →https://doi.org/10.1155/2020/6906921openalex-snapshot

Bacterial Composition, Community Structure, and Diversity in Apis nigrocincta Gut

inferredcites →https://doi.org/10.1155/8472openalex-snapshot

International Journal of Microbiology

inferredcites →https://doi.org/10.1186/s12862-020-01729-xopenalex-snapshot

Evidence for multiple introductions of an invasive wild bee species currently under rapid range expansion in Europe

inferredcites →https://doi.org/10.1186/s13059-014-0550-8openalex-snapshot

Moderated estimation of fold change and dispersion for RNA-seq data with DESeq2

inferredcites →https://doi.org/10.1303/aez.2010.7openalex-snapshot

Impacts of non-native bumblebees in Western Europe and North America

inferredcites →https://doi.org/10.1371/journal.pone.0061217openalex-snapshot

phyloseq: An R Package for Reproducible Interactive Analysis and Graphics of Microbiome Census Data

inferredcites →https://doi.org/10.1371/journal.pone.0078296openalex-snapshot

Diverse Microbiota Identified in Whole Intact Nest Chambers of the Red Mason Bee Osmia bicornis (Linnaeus 1758)

inferredcites →https://doi.org/10.1371/journal.pone.0081475openalex-snapshot

Genetic Variability of the Neogregarine Apicystis bombi, an Etiological Agent of an Emergent Bumblebee Disease

inferredcites →https://doi.org/10.1371/journal.pone.0123911openalex-snapshot

Caste-Specific Differences in Hindgut Microbial Communities of Honey Bees (Apis mellifera)

inferredcites →https://doi.org/10.1371/journal.pone.0236042openalex-snapshot

Dispersal patterns of an introduced wild bee, Megachile sculpturalis Smith, 1853 (Hymenoptera: Megachilidae) in European alpine countries

inferredcites →https://doi.org/10.14806/ej.17.1.200openalex-snapshot

Cutadapt removes adapter sequences from high-throughput sequencing reads

inferredcites →https://doi.org/10.1603/0013-8746(2008)101[140:braain]2.0.co;2openalex-snapshot

Bee Richness and Abundance in New York City Urban Gardens

inferredcites →https://doi.org/10.1890/12-1810.1openalex-snapshot

Do invasive species perform better in their new ranges?

inferredcites →https://doi.org/10.2147/ccidopenalex-snapshot

Clinical, Cosmetic and Investigational Dermatology

inferredcites →https://doi.org/10.2147/ccid.s329569openalex-snapshot

Founder Effects Contribute to the Population Genetic Structure of the Major Dermatophytosis Pathogen Trichophyton rubrum on Hainan Island, China

inferredcites →https://doi.org/10.2317/0022-8567-85.4.384openalex-snapshot

Occupation of Active Xylocopa virginica Nests by the Recently Invasive Megachile sculpturalis in Upstate New York

inferredcites →https://doi.org/10.2317/0022-8567-85.4.387openalex-snapshot

Aggressive Eviction of the Eastern Carpenter Bee (Xylocopa virginica (Linnaeus)) from its Nest by the Giant Resin Bee (Megachile sculpturalis Smith)

inferredcites →https://doi.org/10.2317/kentopenalex-snapshot

Journal of the Kansas Entomological Society

inferredcites →https://doi.org/10.25221/fee.395.2openalex-snapshot

First record of the invasive giant resin bee Megachile (Callomegachile) sculpturalis Smith, 1853 (Hymenoptera: Megachilidae) in the Crimea

inferredcites →https://doi.org/10.3389/fevo.2021.781470openalex-snapshot

The Holobiont as a Key to the Adaptation and Conservation of Wild Bees in the Anthropocene

inferredcites →https://doi.org/10.3389/fmicb.2017.02291openalex-snapshot

The Gut Entomotype of Red Palm Weevil Rhynchophorus ferrugineus Olivier (Coleoptera: Dryophthoridae) and Their Effect on Host Nutrition Metabolism

inferredcites →https://doi.org/10.3389/fmicb.2019.00004openalex-snapshot

Comparative Genome Analysis of Lactococcus lactis Indicates Niche Adaptation and Resolves Genotype/Phenotype Disparity

inferredcites →https://doi.org/10.3389/fmicb.2020.599911openalex-snapshot

Lenzimycins A and B, Metabolites With Antibacterial Properties From Brevibacillus sp. Associated With the Dung Beetle Onthophagus lenzii

inferredcites →https://doi.org/10.3390/insects12060545openalex-snapshot

Nesting, Sex Ratio and Natural Enemies of the Giant Resin Bee in Relation to Native Species in Europe

inferredcites →https://doi.org/10.3390/insects7040069openalex-snapshot

Positive and Negative Impacts of Non-Native Bee Species around the World

inferredcites →https://doi.org/10.3390/jof7110917openalex-snapshot

Elucidation of the Natural Function of Sophorolipids Produced by Starmerella bombicola

inferredcites →https://doi.org/10.3390/microorganisms8071029openalex-snapshot

Metschnikowia pulcherrima and Related Pulcherrimin-Producing Yeasts: Fuzzy Species Boundaries and Complex Antimicrobial Antagonism

inferredcites →https://doi.org/10.3897/bdj.3.e6733openalex-snapshot

The Giant Resin Bee, Megachile sculpturalis Smith: New Distributional Records for the Mid- and Gulf-south USA

inferredcites →https://doi.org/10.47446/osmia3.3openalex-snapshot

Premières données sur la présence de l’abeille asiatique Megachile (Callomegachile) sculpturalis Smith (Hymenoptera, Megachilidae) en Europe

inferredcites →https://doi.org/10.47446/osmia9.4openalex-snapshot

Actualisation des connaissances sur l’abeille Megachile sculpturalis SMITH, 1853 en France et en Europe (Hymenoptera : Megachilidae)

inferredcites →https://doi.org/10.5167/uzh-139381openalex-snapshot

Climatologies at high resolution for the earth’s land surface areas

inferredcites →https://doi.org/10.5169/seals-986133openalex-snapshot

Die Blattschneiderbiene Megachile sculpturalis Smith, 1853 (Hymenoptera, Apidae) nun auch in der Schweiz

inferredcites →https://doi.org/10.5281/zenodo.5537058openalex-snapshot

FURTHER RANGE EXPANSION OF THE SCULPTURED RESIN BEE (MEGACHILE SCULPTURALIS) IN SERBIA AND BOSNIA & HERZEGOVINA

inferredcites →https://doi.org/10.7717/peerj.8822openalex-snapshot

Draft genome of Rosenbergiella nectarea strain 8N4T provides insights into the potential role of this species in its plant host

What points at this work

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

inferred← citeshttps://doi.org/10.3897/neobiota.98.145939zenodo-depositor-declared

The role of microbiomes in animal invasions: a scoping review

inferred← citeshttps://doi.org/10.1002/arch.70183openalex-snapshot

Immune Response and Gut Microbiota Shift in the Red Palm Weevil ( Rhynchophorus ferrugineus ) Infected With Entomopathogenic Fungus, Beauveria bassiana , Reveal Host‐Pathogen Interactions

inferred← citeshttps://doi.org/10.1007/978-3-031-76742-5_10openalex-snapshot

Bee Microbiomes: Unveiling Diversity and Social Dynamics in Managed and Wild Bees

inferred← citeshttps://doi.org/10.1007/s10530-024-03312-7openalex-snapshot

On the occurrence of the neogregarine Apicystis bombi (Apicomplexa) in South America: an unassembled puzzle

inferred← citeshttps://doi.org/10.1007/s13592-024-01077-5openalex-snapshot

Distribution widening of a ground-nesting social bee across Europe favored by climate change and urban setting

inferred← citeshttps://doi.org/10.1016/j.syapm.2025.126648openalex-snapshot

Carnimonas bestiolae sp. nov. and Cernens ardua gen. nov., sp. nov.: new halotolerant bacteria from the invasive solitary bee Megachile sculpturalis

inferred← citeshttps://doi.org/10.1016/j.syapm.2026.126776openalex-snapshot

Lactobacillus apisdorsatae sp. nov. from the giant honeybee (Apis dorsata), Lactobacillus pollinatoris sp. nov. and Lactobacillus xylocopae sp. nov., from the carpenter bee (Xylocopa violacea)

inferred← citeshttps://doi.org/10.1093/jambio/lxad303openalex-snapshot

A case study of the diet-microbiota-parasite interplay in bumble bees

inferred← citeshttps://doi.org/10.1101/2023.11.02.565352openalex-snapshot

Microbial Metamorphosis: Symbiotic bacteria and fungi proliferate during diapause and may enhance overwintering survival in a solitary bee

inferred← citeshttps://doi.org/10.1111/eva.70234openalex-snapshot

Environment and Pollen Diversity Differentially Affect the Gut Microbiomes of Introduced Honeybees and Bumblebees

inferred← citeshttps://doi.org/10.1128/msystems.00603-25openalex-snapshot

Extremely distinct microbial communities in closely related leafhopper subfamilies: Typhlocybinae and Eurymelinae (Cicadellidae, Hemiptera)

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