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Host switching by an ambrosia beetle fungal mutualist: Mycangial colonization of indigenous beetles by the invasive laurel wilt fungal pathogen

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What this work says

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

inferredcites →https://doi.org/10.1007/253.1432-0614openalex-snapshot
Applied Microbiology and Biotechnology
inferredcites →https://doi.org/10.1007/s00248-018-1188-yopenalex-snapshot
Partnerships Between Ambrosia Beetles and Fungi: Lineage-Specific Promiscuity Among Vectors of the Laurel Wilt Pathogen, Raffaelea lauricola
inferredcites →https://doi.org/10.1007/s00253-018-9037-yopenalex-snapshot
Identification of the Achilles heels of the laurel wilt pathogen and its beetle vector
inferredcites →https://doi.org/10.1007/s00253-020-10762-1openalex-snapshot
High efficiency transformation and mutant screening of the laurel wilt pathogen, Raffaelea lauricola
inferredcites →https://doi.org/10.1007/s00253-021-11268-0openalex-snapshot
Fungal mutualisms and pathosystems: life and death in the ambrosia beetle mycangia
inferredcites →https://doi.org/10.1007/s10530-017-1427-zopenalex-snapshot
No rest for the laurels: symbiotic invaders cause unprecedented damage to southern USA forests
inferredcites →https://doi.org/10.1007/s13199-017-0514-3openalex-snapshot
Nutritional symbionts of a putative vector, Xyleborus bispinatus, of the laurel wilt pathogen of avocado, Raffaelea lauricola
inferredcites →https://doi.org/10.1007/s13199-021-00776-2openalex-snapshot
Phoretic and internal transport of Raffaelea lauricola by different species of ambrosia beetle associated with avocado trees
inferredcites →https://doi.org/10.1016/j.fgb.2014.10.014openalex-snapshot
Discordant phylogenies suggest repeated host shifts in the Fusarium–Euwallacea ambrosia beetle mutualism
inferredcites →https://doi.org/10.1016/j.fgb.2019.103269openalex-snapshot
Members of the Euwallacea fornicatus species complex exhibit promiscuous mutualism with ambrosia fungi in Taiwan
inferredcites →https://doi.org/10.1016/j.funbio.2017.08.004openalex-snapshot
Wood decay fungus Flavodon ambrosius (Basidiomycota: Polyporales) is widely farmed by two genera of ambrosia beetles
inferredcites →https://doi.org/10.1016/j.funeco.2016.07.002openalex-snapshot
Mutualism with aggressive wood-degrading Flavodon ambrosius (Polyporales) facilitates niche expansion and communal social structure in Ambrosiophilus ambrosia beetles
inferredcites →https://doi.org/10.1016/j.funeco.2016.10.008openalex-snapshot
Ambrosia beetle Premnobius cavipennis (Scolytinae: Ipini) carries highly divergent ascomycotan ambrosia fungus, Afroraffaelea ambrosiae gen. nov. et sp. nov. (Ophiostomatales)
inferredcites →https://doi.org/10.1016/j.funeco.2018.03.006openalex-snapshot
Multiple evolutionary origins lead to diversity in the metabolic profiles of ambrosia fungi
inferredcites →https://doi.org/10.1016/s1369-5274(00)00191-0openalex-snapshot
Dimorphism in fungal pathogens: Candida albicans and Ustilago maydis—similar inputs, different outputs
inferredcites →https://doi.org/10.1038/ismej.2014.115openalex-snapshot
The ambrosia symbiosis is specific in some species and promiscuous in others: evidence from community pyrosequencing
inferredcites →https://doi.org/10.1038/s41396-020-0593-7openalex-snapshot
Lipids and small metabolites provisioned by ambrosia fungi to symbiotic beetles are phylogeny-dependent, not convergent
inferredcites →https://doi.org/10.1080/00275514.2017.1400353openalex-snapshot
New Meredithiella species from mycangia of Corthylus ambrosia beetles suggest genus-level coadaptation but not species-level coevolution
inferredcites →https://doi.org/10.1080/00275514.2020.1755209openalex-snapshot
Four mycangium types and four genera of ambrosia fungi suggest a complex history of fungus farming in the ambrosia beetle tribe Xyloterini
inferredcites →https://doi.org/10.1080/14787210.2017.1290524openalex-snapshot
Candida albicans morphology: still in focus
inferredcites →https://doi.org/10.1086/273542openalex-snapshot
Transactions of the Kansas Academy of Science for 1881-2
inferredcites →https://doi.org/10.1093/ee/nvw070openalex-snapshot
Fungal Associates of theXylosandrus compactus(Coleoptera: Curculionidae, Scolytinae) Are Spatially Segregated on the Insect Body
inferredcites →https://doi.org/10.1093/ee/nvx151openalex-snapshot
Rearing Xyleborus volvulus (Coleoptera: Curculionidae) on Media Containing Sawdust from Avocado or Silkbay, With or Without Raffaelea lauricola (Ophiostomatales: Ophiostomataceae)
inferredcites →https://doi.org/10.1093/femsre/fuv035openalex-snapshot
Fungal dimorphism: the switch from hyphae to yeast is a specialized morphogenetic adaptation allowing colonization of a host
inferredcites →https://doi.org/10.1094/pdis-01-13-0056-feopenalex-snapshot
Destructive Tree Diseases Associated with Ambrosia and Bark Beetles: Black Swan Events in Tree Pathology?
inferredcites →https://doi.org/10.1094/pdis-08-11-0633openalex-snapshot
Laurel Wilt, Caused by Raffaelea lauricola, is Confirmed in Miami-Dade County, Center of Florida's Commercial Avocado Production
inferredcites →https://doi.org/10.1094/pdis-92-2-0215openalex-snapshot
A Fungal Symbiont of the Redbay Ambrosia Beetle Causes a Lethal Wilt in Redbay and Other Lauraceae in the Southeastern United States
inferredcites →https://doi.org/10.1094/php-12-16-0070-rpopenalex-snapshot
Recovery Plan for Laurel Wilt of Avocado, Caused by Raffaelea lauricola
inferredcites →https://doi.org/10.1094/phyto-01-10-0032openalex-snapshot
Quantification of Propagules of the Laurel Wilt Fungus and Other Mycangial Fungi from the Redbay Ambrosia Beetle,Xyleborus glabratus
inferredcites →https://doi.org/10.1098/rspb.2018.2127openalex-snapshot
A selective fungal transport organ (mycangium) maintains coarse phylogenetic congruence between fungus-farming ambrosia beetles and their symbionts
inferredcites →https://doi.org/10.1111/1574-6941.12026openalex-snapshot
Abundance and dynamics of filamentous fungi in the complex ambrosia gardens of the primitively eusocial beetleXyleborinus saxeseniiRatzeburg (Coleoptera: Curculionidae, Scolytinae)
inferredcites →https://doi.org/10.1111/efp.12134openalex-snapshot
Responses of swamp bay, Persea palustris, and avocado, Persea americana, to various concentrations of the laurel wilt pathogen, Raffaelea lauricola
inferredcites →https://doi.org/10.1111/ens.12353openalex-snapshot
Non‐destructive observation of the mycangia of Euwallacea interjectus (Blandford) (Coleoptera: Curculionidae: Scolytinae) using X‐ray computed tomography
inferredcites →https://doi.org/10.1111/j.1365-3059.2011.02564.xopenalex-snapshot
Responses of avocado to laurel wilt, caused by Raffaelea lauricola
inferredcites →https://doi.org/10.1111/j.1558-5646.2010.01055.xopenalex-snapshot
REPEATED EVOLUTION OF CROP THEFT IN FUNGUS-FARMING AMBROSIA BEETLES
inferredcites →https://doi.org/10.1111/mec.14394openalex-snapshot
Know your farmer: Ancient origins and multiple independent domestications of ambrosia beetle fungal cultivars
inferredcites →https://doi.org/10.1146/annurev-ento-031616-035105openalex-snapshot
The Ambrosia Symbiosis: From Evolutionary Ecology to Practical Management
inferredcites →https://doi.org/10.1371/journal.pone.0236653openalex-snapshot
Micro-computed tomography permits enhanced visualization of mycangia across development and between sexes in Euwallacea ambrosia beetles
inferredcites →https://doi.org/10.1371/journal.ppat.1004608openalex-snapshot
Dimorphism in Fungal Pathogens of Mammals, Plants, and Insects
inferredcites →https://doi.org/10.21273/horttech.20.1.234openalex-snapshot
Potential Economic Impact of Laurel Wilt Disease on the Florida Avocado Industry
inferredcites →https://doi.org/10.2307/3626562openalex-snapshot
Ecology of Ambrosia Fungi and Their Dissemination by Beetles
inferredcites →https://doi.org/10.3390/f8020048openalex-snapshot
Laurel Wilt in Natural and Agricultural Ecosystems: Understanding the Drivers and Scales of Complex Pathosystems
inferredcites →https://doi.org/10.3390/pathogens10050528openalex-snapshot
Unique Attributes of the Laurel Wilt Fungal Pathogen, Raffaelea lauricola, as Revealed by Metabolic Profiling
inferredcites →https://doi.org/10.3852/10-417openalex-snapshot
Isolations from the redbay ambrosia beetle, Xyleborus glabratus , confirm that the laurel wilt pathogen, Raffaelea lauricola , originated in Asia
inferredcites →https://doi.org/10.3852/15-133openalex-snapshot
Geographic variation in mycangial communities of Xyleborus glabratus
inferredcites →https://doi.org/10.4236/ajps.2013.43a092openalex-snapshot
An Uncertain Future for American Lauraceae: A Lethal Threat from Redbay Ambrosia Beetle and Laurel Wilt Disease (A Review)
inferredcites →https://doi.org/10.7551/mitpress/13600.001.0001openalex-snapshot
The Convergent Evolution of Agriculture in Humans and Insects
inferredcites →https://doi.org/10.7551/mitpress/13600.003.0013openalex-snapshot
Mycangia Define the Diverse Ambrosia Beetle–Fungus Symbioses

What points at this work

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

inferred← citeshttps://doi.org/10.3897/mycokeys.110.129228zenodo-depositor-declared
Thyridium lauri sp. nov. (Thyridiaceae, Thyridiales): a new pathogenic fungal species of bay laurel from Italy
inferred← citeshttps://doi.org/10.1007/s11157-024-09709-zopenalex-snapshot
Chemical interactions under the bark: bark-, ambrosia-, and wood-boring beetles and their microbial associates
inferred← citeshttps://doi.org/10.1016/j.aspen.2023.102137openalex-snapshot
Detection of native-alien populations of Anisandrus dispar (Fabricius, 1792) in Europe
inferred← citeshttps://doi.org/10.1016/j.funbio.2025.101665openalex-snapshot
Phylogeny and ecological roles shaping yeast-hyphae morphogenesis in Ophiostomataceae
inferred← citeshttps://doi.org/10.1016/j.isci.2025.113281openalex-snapshot
Spatial organization within social ambrosia beetle nests limits spread of infectious disease
inferred← citeshttps://doi.org/10.1016/j.xpro.2026.104375openalex-snapshot
Protocol for spatial sampling and monitoring infection disease dynamics and pathogen spread in social ambrosia beetle colonies
inferred← citeshttps://doi.org/10.1111/1462-2920.70364openalex-snapshot
Fulfilling Koch‐Like Postulates for Animal Fungal Mutualists: New Fungal Symbionts and Gallery and Mycangial Colonisation by Xyleborus affinis Ambrosia Fungi
inferred← citeshttps://doi.org/10.1128/aem.00818-24openalex-snapshot
A strong priority effect in the assembly of a specialized insect-microbe symbiosis
inferred← citeshttps://doi.org/10.1186/s12864-026-12931-4openalex-snapshot
Carrying the seeds of your crop: fungal genetic networks activated during colonization of the ambrosia beetle symbiotic organ
inferred← citeshttps://doi.org/10.1186/s40694-026-00217-zopenalex-snapshot
Genetic tools for transformation of Xyleborus ambrosia beetle fungal symbionts
inferred← citeshttps://doi.org/10.32473/edis-fr475-2024openalex-snapshot
The Redbay Ambrosia Beetle and Laurel Wilt
inferred← citeshttps://doi.org/10.3390/insects16060644openalex-snapshot
Cell Structure of the Preoral Mycangia of Xyleborus (Coleoptera: Curculiondiae) Ambrosia Beetles
inferred← citeshttps://doi.org/10.3390/jof11030184openalex-snapshot
Fungi That Live Within Animals: Application of Cell Cytometry to Examine Fungal Colonization of Ambrosia Beetle (Xyleborus sp.) Mycangia
inferred← citeshttps://doi.org/10.3390/jof9121175openalex-snapshot
Characterization of Terpenoids from the Ambrosia Beetle Symbiont and Laurel Wilt Pathogen Harringtonia lauricola
inferred← citeshttps://doi.org/10.64898/2026.04.23.720448openalex-snapshot
Fulfilling Koch-like postulates for animal fungal mutualists: New fungal symbionts and gallery and mycangial colonization by Xyleborus affinis ambrosia fungi
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