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Cladosporium—Insect Relationships

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

inferredcites →https://doi.org/10.1002/ece3.3676openalex-snapshot

Mosquito vector‐associated microbiota: Metabarcoding bacteria and eukaryotic symbionts across habitat types in Thailand endemic for dengue and other arthropod‐borne diseases

inferredcites →https://doi.org/10.1002/ps.6235openalex-snapshot

Identification of natural pathogens from wild Drosophila suzukii

inferredcites →https://doi.org/10.1006/jipa.2000.4928openalex-snapshot

Susceptibility of Vespula vulgaris (Hymenoptera: Vespidae) to Generalist Entomopathogenic Fungi and Their Potential for Wasp Control

inferredcites →https://doi.org/10.1007/bf01103782openalex-snapshot

Studies on the mycotic inhabitants ofCulex pipiens collected from fresh water ponds in Egypt

inferredcites →https://doi.org/10.1007/s00203-022-03386-8openalex-snapshot

Identification of cuticle and midgut fungal microflora of phlebotomine sandflies collected in Tunisia

inferredcites →https://doi.org/10.1007/s00248-011-9962-0openalex-snapshot

Symbiotic Fungal Flora in Leaf Galls Induced by Illiciomyia yukawai (Diptera: Cecidomyiidae) and in Its Mycangia

inferredcites →https://doi.org/10.1007/s00248-014-0478-2openalex-snapshot

Microbial Associates of the Vine Mealybug Planococcus ficus (Hemiptera: Pseudococcidae) under Different Rearing Conditions

inferredcites →https://doi.org/10.1007/s00248-016-0864-zopenalex-snapshot

A Metabarcoding Survey on the Fungal Microbiota Associated to the Olive Fruit Fly

inferredcites →https://doi.org/10.1007/s00248-022-02140-3openalex-snapshot

Sources of Fungal Symbionts in the Microbiome of a Mobile Insect Host, Spodoptera frugiperda

inferredcites →https://doi.org/10.1007/s00248-023-02304-9openalex-snapshot

The wild solitary bees Andrena vaga, Anthophora plumipes, Colletes cunicularius, and Osmia cornuta microbiota are host specific and dominated by endosymbionts and environmental microorganisms

inferredcites →https://doi.org/10.1007/s00253-020-10968-3openalex-snapshot

The multifunctional lifestyles of Metarhizium: evolution and applications

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/s00442-011-2151-5openalex-snapshot

Differential effects of foliar endophytic fungi on insect herbivores attacking a herbaceous plant

inferredcites →https://doi.org/10.1007/s10482-008-9268-5openalex-snapshot

Yeasts and filamentous fungi carried by the gynes of leaf-cutting ants

inferredcites →https://doi.org/10.1007/s10482-016-0724-3openalex-snapshot

Prevalence of the genus Cladosporium on the integument of leaf-cutting ants characterized by 454 pyrosequencing

inferredcites →https://doi.org/10.1007/s10482-023-01887-0openalex-snapshot

Novel Metschnikowia yeasts from the gut of green lacewing in Japan

inferredcites →https://doi.org/10.1007/s10526-016-9769-5openalex-snapshot

Beauveria bassiana as an endophyte: a critical review on associated methodology and biocontrol potential

inferredcites →https://doi.org/10.1007/s10682-007-9196-2openalex-snapshot

Contribution of symbiotic mycangial fungi to larval nutrition of a leaf-rolling weevil

inferredcites →https://doi.org/10.1007/s11046-007-9020-0openalex-snapshot

In vitro susceptibility to fungicides by invertebrate-pathogenic and saprobic fungi

inferredcites →https://doi.org/10.1007/s11274-008-9914-0openalex-snapshot

Preliminary evaluation of Cladosporium cladosporioides (Fresen.) de Vries in laboratory conditions, as a potential candidate for biocontrol of Tetranychus urticae Koch

inferredcites →https://doi.org/10.1007/s11274-023-03780-4openalex-snapshot

Endophytic insect pathogenic fungi-host plant-herbivore mutualism: elucidating the mechanisms involved in the tripartite interactions

inferredcites →https://doi.org/10.1007/s11557-006-0039-2openalex-snapshot

Phylogeny and taxonomy of Cladosporium-like hyphomycetes, including Davidiella gen. nov., the teleomorph of Cladosporium s. str.

inferredcites →https://doi.org/10.1007/s11557-008-0558-0openalex-snapshot

Yeast biodiversity in the guts of several pests on maize; comparison of three methods: classical isolation, cloning and DGGE

inferredcites →https://doi.org/10.1007/s11557-021-01760-2openalex-snapshot

Richness of Cladosporium in a tropical bat cave with the description of two new species

inferredcites →https://doi.org/10.1007/s11829-012-9194-3openalex-snapshot

A leaf-rolling weevil benefits from general saprophytic fungi in polysaccharide degradation

inferredcites →https://doi.org/10.1007/s12010-014-1325-0openalex-snapshot

An Alpha-Glucosidase Inhibitor from an Endophytic Cladosporium sp. with Potential as a Biocontrol Agent

inferredcites →https://doi.org/10.1007/s12600-013-0298-9openalex-snapshot

Insecticidal potential of an endophytic fungus, Cladosporium uredinicola, against Spodoptera litura

inferredcites →https://doi.org/10.1007/s12600-019-00734-1openalex-snapshot

Characterizing members of the Cladosporium cladosporioides species complex as fruit rot pathogens of red raspberries in the mid-Atlantic and co-occurrence with Drosophila suzukii (spotted wing drosophila)

inferredcites →https://doi.org/10.1007/s13199-017-0494-3openalex-snapshot

Fungal load in Bradysia agrestis, a phytopathogen-transmitting insect vector

inferredcites →https://doi.org/10.1007/s13199-019-00635-1openalex-snapshot

Functional roles of fungal endophytes in host fitness during stress conditions

inferredcites →https://doi.org/10.1007/s13199-020-00687-8openalex-snapshot

New insights into fungal diversity associated with Megaplatypus mutatus: gut mycobiota

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/10.1007/s13225-012-0157-xopenalex-snapshot

Fungi associated with Asphondylia (Diptera: Cecidomyiidae) galls on Sarcocornia quinqueflora and Tecticornia arbuscula (Chenopodiaceae)

inferredcites →https://doi.org/10.1007/s13225-013-0268-zopenalex-snapshot

Comparative analysis of the biodiversity of fungal endophytes in insect-induced galls and surrounding foliar tissue

inferredcites →https://doi.org/10.1007/s13355-018-0594-4openalex-snapshot

The developmental parameters of the minute brown scavenger beetle Dienerella argus (Coleoptera: Latridiidae)

inferredcites →https://doi.org/10.1007/s41348-022-00701-9openalex-snapshot

Insecticidal bioactive compounds derived from Cladosporium cladosporioides (Fresen.) G.A. de Vries and Acremonium zeylanicum (Petch) W. Gams & H.C. Evans

inferredcites →https://doi.org/10.1016/0022-2011(72)90087-0openalex-snapshot

Fungi isolated from the intestinal contents of foraging worker honey bees, Apis mellifera

inferredcites →https://doi.org/10.1016/0022-2011(81)90082-3openalex-snapshot

Some microbial contaminants and control agents in a diet and larvae of Heliothis spp

inferredcites →https://doi.org/10.1016/0022-474x(74)90025-3openalex-snapshot

Development and oviposition of Ahasverus advena (Waltl) (coleoptera, silvanidae) on seven species of fungi

inferredcites →https://doi.org/10.1016/0167-8809(86)90122-2openalex-snapshot

Assessment of the fungus Cladosporium oxysporum (Berk. and Curt.) as a potential biocontrol agent against certain homoptera

inferredcites →https://doi.org/10.1016/0965-1748(94)90023-xopenalex-snapshot

Prooxidant effects of phenolic acids on the generalist herbivore Helicoverpa zea (Lepidoptera: Noctuidae): Potential mode of action for phenolic compounds in plant anti-herbivore chemistry

inferredcites →https://doi.org/10.1016/j.apsoil.2007.12.001openalex-snapshot

Occurrence and diversity of insect-associated fungi in natural soils in China

inferredcites →https://doi.org/10.1016/j.biocontrol.2021.104634openalex-snapshot

Trichoderma as biocontrol agent against pests: New uses for a mycoparasite

inferredcites →https://doi.org/10.1016/j.cropro.2008.07.010openalex-snapshot

Insect-associated fungi in soils of field crops and orchards

inferredcites →https://doi.org/10.1016/j.fct.2023.113845openalex-snapshot

Mycotoxins on edible insects: Should we be worried?

inferredcites →https://doi.org/10.1016/j.foodres.2019.108527openalex-snapshot

Current knowledge on the microbiota of edible insects intended for human consumption: A state-of-the-art review

inferredcites →https://doi.org/10.1016/j.funbio.2019.09.009openalex-snapshot

Fungal community associated with adults of the chestnut gall wasp Dryocosmus kuriphilus after emergence from galls: Taxonomy and functional ecology

inferredcites →https://doi.org/10.1016/j.funbio.2020.09.008openalex-snapshot

The fungal community associated with the ambrosia beetle Xylosandrus compactus invading the mediterranean maquis in central Italy reveals high biodiversity and suggests environmental acquisitions

inferredcites →https://doi.org/10.1016/j.funeco.2009.02.003openalex-snapshot

Fungal associations in Asphondylia (Diptera: Cecidomyiidae) galls from Australia and South Africa: implications for biological control of invasive acacias

inferredcites →https://doi.org/10.1016/j.funeco.2015.08.006openalex-snapshot

Molecular analysis of the fungal microbiome associated with the olive fruit fly Bactrocera oleae

inferredcites →https://doi.org/10.1016/j.funeco.2017.04.007openalex-snapshot

Fungal communities associated with bark and ambrosia beetles trapped at international harbours

inferredcites →https://doi.org/10.1016/j.funeco.2017.06.006openalex-snapshot

Wood-inhabiting insects can function as targeted vectors for decomposer fungi

inferredcites →https://doi.org/10.1016/j.funeco.2019.02.004openalex-snapshot

Aedes albopictus mosquitoes host a locally structured mycobiota with evidence of reduced fungal diversity in invasive populations

inferredcites →https://doi.org/10.1016/j.funeco.2020.100991openalex-snapshot

Termites host specific fungal communities that differ from those in their ambient environments

inferredcites →https://doi.org/10.1016/j.ibiod.2012.10.015openalex-snapshot

Can arthropods act as vectors of fungal dispersion in heritage collections? A case study on the archive of the University of Coimbra, Portugal

inferredcites →https://doi.org/10.1016/j.ijfoodmicro.2015.10.028openalex-snapshot

Fungal dissemination by housefly (Musca domestica L.) and contamination of food commodities in rural areas of South Africa

inferredcites →https://doi.org/10.1016/j.jece.2023.110801openalex-snapshot

Ingestion preference and efficiencies of different polymerization types foam plastics by Tenebrio molitor larvae, associated with changes of both core gut bacterial and fungal microbiomes

inferredcites →https://doi.org/10.1016/j.jpba.2020.113787openalex-snapshot

Insects’ potential: Understanding the functional role of their gut microbiome

inferredcites →https://doi.org/10.1016/j.jspr.2023.102188openalex-snapshot

Efficacy of entomopathogenic fungi against three major stored insect pests, Rhyzopertha dominica, Sitophilus zeamais and Trogoderma granarium

inferredcites →https://doi.org/10.1016/j.pestbp.2016.01.004openalex-snapshot

Insecticidal potential of an endophytic Cladosporium velox against Spodoptera litura mediated through inhibition of alpha glycosidases

inferredcites →https://doi.org/10.1016/j.pestbp.2020.01.013openalex-snapshot

Avermectin stress varied structure and function of gut microbial community in Lymantria dispar asiatica (Lepidoptera: Lymantriidae) larvae

inferredcites →https://doi.org/10.1016/j.phytochem.2021.113021openalex-snapshot

Endophytic fungus Cladosporium tenuissimum DF11, an efficient inducer of tanshinone biosynthesis in Salvia miltiorrhiza roots

inferredcites →https://doi.org/10.1016/j.scienta.2013.05.009openalex-snapshot

Effect of soil tillage on natural occurrence of fungal entomopathogens associated to Prays oleae Bern.

inferredcites →https://doi.org/10.1016/j.scitotenv.2022.157941openalex-snapshot

Bees under interactive stressors: the novel insecticides flupyradifurone and sulfoxaflor along with the fungicide azoxystrobin disrupt the gut microbiota of honey bees and increase opportunistic bacterial pathogens

inferredcites →https://doi.org/10.1016/j.simyco.2015.10.001openalex-snapshot

Common but different: The expanding realm of Cladosporium

inferredcites →https://doi.org/10.1016/s0031-4056(24)00018-0openalex-snapshot

Effects of diet on the growth and reproduction of some Collembola in laboratory cultures

inferredcites →https://doi.org/10.1016/s0031-4056(24)01970-xopenalex-snapshot

Feeding biology of fungivorous insects from Danish cereal fields

inferredcites →https://doi.org/10.1016/s0367-2530(17)30787-9openalex-snapshot

The fruit-wasp route to toxic nectar in Epipactis orchids?

inferredcites →https://doi.org/10.1016/s1049-9644(03)00139-7openalex-snapshot

Microorganisms associated with field-collected Chrysoperla rufilabris (Neuroptera: Chrysopidae) adults with emphasis on yeast symbionts

inferredcites →https://doi.org/10.1016/s2095-3119(15)61145-5openalex-snapshot

Isolation, identification, derivatization and phytotoxic activity of secondary metabolites produced by Cladosporium oxysporum DH14, a locust-associated fungus

inferredcites →https://doi.org/10.1017/s0007485300008919openalex-snapshot

Interrelationship between an entomogenous fungus and two ant-homopteran (Hymenoptera: Formicidae-Hemiptera: Pseudococcidae & Aphididae) mutualisms on guava trees

inferredcites →https://doi.org/10.1017/s0007485300033320openalex-snapshot

Xyleborus morstatti Hag. (Coleoptera, Scolytidae), a Shot-hole Borer attacking Avocado Pear in the Seychelles

inferredcites →https://doi.org/10.1017/s0953756203007986openalex-snapshot

Mycobiota associated with the coffee berry borer (Hypothenemus hampei) in Mexico

inferredcites →https://doi.org/10.1021/np010390iopenalex-snapshot

New Metabolites from Sponge-Derived Fungi Curvularia lunata and Cladosporium herbarum

inferredcites →https://doi.org/10.1023/a:1006947524503openalex-snapshot

Mycoflora of cave cricket Troglophilus neglectus cadavers

inferredcites →https://doi.org/10.1023/a:1010905420001openalex-snapshot

Fungal flora of the digestive tract of 5 species of triatomines vectors of Trypanosoma cruzi, Chagas 1909

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/s41396-018-0174-1openalex-snapshot

Gut bacterial and fungal communities of the domesticated silkworm ( Bombyx mori ) and wild mulberry-feeding relatives

inferredcites →https://doi.org/10.1038/s41522-021-00212-9openalex-snapshot

Compartmentalization of bacterial and fungal microbiomes in the gut of adult honeybees

inferredcites →https://doi.org/10.1038/s41598-018-23671-1openalex-snapshot

A Lethal Fungus Infects the Chinese White Wax Scale Insect and Causes Dramatic Changes in the Host Microbiota

inferredcites →https://doi.org/10.1038/s41598-018-34127-xopenalex-snapshot

Bacterial and fungal gut communities of Agrilus mali at different developmental stages and fed different diets

inferredcites →https://doi.org/10.1038/s41598-022-17278-wopenalex-snapshot

The bacterial and fungal communities of the larval midgut of Spodoptera frugiperda (Lepidoptera: Noctuidae) varied by feeding on two cruciferous vegetables

inferredcites →https://doi.org/10.1046/j.1439-0418.2003.00662.xopenalex-snapshot

Natural incidence ofCladosporiumspp. as a bio‐control agent against whiteflies and aphids in Egypt

inferredcites →https://doi.org/10.1073/pnas.1103384108openalex-snapshot

Flowers of Cypripedium fargesii (Orchidaceae) fool flat-footed flies (Platypezidae) by faking fungus-infected foliage

inferredcites →https://doi.org/10.1080/09583157.2011.622036openalex-snapshot

Efficacy of aCladosporiumsp. fungus againstHelicoverpaarmigera(Lepidoptera: Noctuidae), other insect pests and beneficial insects of cotton

inferredcites →https://doi.org/10.1080/09583159409355315openalex-snapshot

Effect of some phytopathogenic fungi and their metabolites on growth ofHeliothis virescens(F.) and its host plants

inferredcites →https://doi.org/10.1080/09583159730613openalex-snapshot

Alternaria infectoria , a Promising Biological Control Agent for the Fig Wax Scale, Ceroplastes rusci (Homoptera: Coccidae), in Egypt

inferredcites →https://doi.org/10.1080/10889868.2019.1640183openalex-snapshot

Bioaugmentation of endosulfan contaminated soil in artificial bed treatment using selected fungal species

inferredcites →https://doi.org/10.1080/13102818.2019.1695541openalex-snapshot

Identification and application of a fungal biocontrol agent Cladosporium cladosporioides against Bemisia tabaci

inferredcites →https://doi.org/10.1080/15572536.2007.11832595openalex-snapshot

Patterns in the occurrence of saprophytic fungi carried by arthropods caught in traps baited with rotted wood and dung

inferredcites →https://doi.org/10.1080/21501203.2013.841299openalex-snapshot

Rearing and storage in mung beans reduce medically significant molds by the seed beetle,Callosobruchus maculatus(Coleoptera: Chrysomelidae), utilized in science classrooms

inferredcites →https://doi.org/10.1088/1755-1315/1060/1/012093openalex-snapshot

Isolation and Identification of Entomopathogenic Fungi from of Green Peach Aphid Myzus Persicae and Evaluation of Their Activity for Insect Control

inferredcites →https://doi.org/10.1088/issn.1755-1315openalex-snapshot

IOP Conference Series: Earth and Environmental Science

inferredcites →https://doi.org/10.1093/aesa/80.2.251openalex-snapshot

Microorganisms Associated with Cotton Fleahopper, Pseudatomoscelis seriatus (Heteroptera: Miridae)

inferredcites →https://doi.org/10.1093/ee/12.1.245openalex-snapshot

Fungus Found in Galls of Adelges abietis (L.) (Homoptera: Adelgidae): Identification, Within-Tree Distribution, and Possible Impact on Insect Survival 1

inferredcites →https://doi.org/10.1093/ee/3.6.965openalex-snapshot

Survival of Springtails Hypogastrura tullbergi and Proisotoma minuta on Fungal and Bacterial Diets 1

inferredcites →https://doi.org/10.1093/ee/nvaa060openalex-snapshot

Effect of Bacterial and Fungal Microbiota Removal on the Survival and Development of Bryophagous Beetles

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/nvy028openalex-snapshot

A New Gall Midge Species of Asphondylia (Diptera: Cecidomyiidae) Inducing Flower Galls on Clinopodium nepeta (Lamiaceae) From Europe, Its Phenology, and Associated Fungi

inferredcites →https://doi.org/10.1093/ee/nvy167openalex-snapshot

Associations BetweenDrosophila suzukii(Diptera: Drosophilidae) and Fungi in Raspberries

inferredcites →https://doi.org/10.1093/femsec/fiac148openalex-snapshot

High density polyethylene (HDPE) biodegradation by the fungus Cladosporium halotolerans

inferredcites →https://doi.org/10.1093/jee/64.1.3openalex-snapshot

Fungus as Food for Some Stored-Product Insects1

inferredcites →https://doi.org/10.1093/jee/64.2.398openalex-snapshot

Interactions Between a Springtail, Hypogastrura tullbergi, and Soil-Borne Fungi12

inferredcites →https://doi.org/10.1093/jee/77.1.110openalex-snapshot

Behavioral Response of the Larger Black Flour Beetle (Coleoptera: Tenebrionidae) to Olfactory Cues from Food Sources

inferredcites →https://doi.org/10.1093/jme/tjad097openalex-snapshot

Microplastic ingestion perturbs the microbiome of Aedes albopictus (Diptera: Culicidae) and Aedes aegypti

inferredcites →https://doi.org/10.1101/2021.01.28.428626openalex-snapshot

Amplicon sequencing of variable 16S rRNA and ITS2 regions reveal honeybee susceptibility to diseases resulted of their dietary preferences under anthropogenic landforms

inferredcites →https://doi.org/10.1111/1365-2435.14177openalex-snapshot

Complex plant quality—microbiota–population interactions modulate the response of a specialist herbivore to the defence of its host plant

inferredcites →https://doi.org/10.1111/1462-2920.14915openalex-snapshot

Who is eating fructose within the Aedes albopictus gut microbiota?

inferredcites →https://doi.org/10.1111/1744-7917.12729openalex-snapshot

Diversity and dynamics of microbial communities in brown planthopper at different developmental stages revealed by high‐throughput amplicon sequencing

inferredcites →https://doi.org/10.1111/1744-7917.12799openalex-snapshot

Diversity of fungal isolates from fungus‐growing termite Macrotermes barneyi and characterization of bioactive compound from Xylaria escharoidea

inferredcites →https://doi.org/10.1111/aab.12360openalex-snapshot

First report of the gall midge Asphondylia serpylli on thyme (Thymus vulgaris), and identification of the associated fungal symbiont

inferredcites →https://doi.org/10.1111/eea.13217openalex-snapshot

Biological and molecular characterization of Cladosporium sp. and Acremonium zeylanicum as biocontrol agents of Aphis fabae in a tri‐trophic system

inferredcites →https://doi.org/10.1111/j.1439-0329.2007.00535.xopenalex-snapshot

Associations between Pityogenes bidentatus and fungi in young managed Scots pine stands in Poland

inferredcites →https://doi.org/10.1111/j.1439-0418.2007.01194.xopenalex-snapshot

Fungal flora associated with Tomicus piniperda L. in an area close to a timber yard in southern Poland

inferredcites →https://doi.org/10.1111/j.1439-0507.2007.01470.xopenalex-snapshot

The giant Madagascar hissing‐cockroach (Gromphadorhina portentosa) as a source of antagonistic moulds: concerns arising from its use in a public setting

inferredcites →https://doi.org/10.1111/j.1440-6055.2008.00655.xopenalex-snapshot

Microbial population and diversity on the exoskeletons of four insect species associated with gorse (Ulex europaeus L.)

inferredcites →https://doi.org/10.1111/jen.12624openalex-snapshot

Entomopathogenic fungi naturally infecting the eucalypt bronze bug,Thaumastocoris peregrinus(Heteroptera: Thaumastocoridae), in Uruguay

inferredcites →https://doi.org/10.1111/mec.13741openalex-snapshot

Midgut fungal and bacterial microbiota of Aedes triseriatus and Aedes japonicus shift in response to La Crosse virus infection

inferredcites →https://doi.org/10.1111/mec.14332openalex-snapshot

An exceptional family: Ophiocordyceps‐allied fungus dominates the microbiome of soft scale insects (Hemiptera: Sternorrhyncha: Coccidae)

inferredcites →https://doi.org/10.1111/mec.15281openalex-snapshot

Angiosperm to Gymnosperm host‐plant switch entails shifts in microbiota of theWelwitschiabug,Probergrothius angolensis(Distant, 1902)

inferredcites →https://doi.org/10.1111/mec.16436openalex-snapshot

Phylogenetic conservatism of mycoparasitism and its contribution to pathogen antagonism

inferredcites →https://doi.org/10.1128/msphere.00267-23openalex-snapshot

Geographical survey of the mycobiome and microbiome of Southern California glassy-winged sharpshooters

inferredcites →https://doi.org/10.1128/spectrum.01009-23openalex-snapshot

Altitude as a key environmental factor shaping microbial communities of tea green leafhoppers ( Matsumurasca onukii )

inferredcites →https://doi.org/10.1139/b87-083openalex-snapshot

Fungi associated with Onychiurus subtenuis (Collembola) in an aspen woodland

inferredcites →https://doi.org/10.1146/annurev-ento-031616-035105openalex-snapshot

The Ambrosia Symbiosis: From Evolutionary Ecology to Practical Management

inferredcites →https://doi.org/10.1186/s13071-016-1763-3openalex-snapshot

Isolation of fungi from dead arthropods and identification of a new mosquito natural pathogen

inferredcites →https://doi.org/10.1186/s40168-019-0748-9openalex-snapshot

Microbial communities of the house fly Musca domestica vary with geographical location and habitat

inferredcites →https://doi.org/10.1186/s40168-023-01702-yopenalex-snapshot

Different roles of host and habitat in determining the microbial communities of plant-feeding true bugs

inferredcites →https://doi.org/10.1186/s41938-018-0030-7openalex-snapshot

Pathogenicity of three entomopathogenic fungi, to the aphid species, Metopolophium dirhodum (Walker) (Hemiptera: Aphididae), and their Alkaline protease activities

inferredcites →https://doi.org/10.1186/s41938-023-00685-0openalex-snapshot

Novel isolate of Cladosporium subuliforme and its potential to control Asian citrus psyllid, Diaphorina citri Kuwayama (Hemiptera: Liviidae)

inferredcites →https://doi.org/10.1186/s42523-021-00135-yopenalex-snapshot

Parasitism by endoparasitoid wasps alters the internal but not the external microbiome in host caterpillars

inferredcites →https://doi.org/10.1371/journal.pone.0038137openalex-snapshot

Purification and Characterization of a Novel Chlorpyrifos Hydrolase from Cladosporium cladosporioides Hu-01

inferredcites →https://doi.org/10.1371/journal.pone.0047205openalex-snapshot

Biodegradation of Chlorpyrifos and Its Hydrolysis Product 3,5,6-Trichloro-2-Pyridinol by a New Fungal Strain Cladosporium cladosporioides Hu-01

inferredcites →https://doi.org/10.1371/journal.pone.0089295openalex-snapshot

Interactions between a Sap Beetle, Sabal Palm, Scale Insect, Filamentous Fungi and Yeast, with Discovery of Potential Antifungal Compounds

inferredcites →https://doi.org/10.1371/journal.pone.0134542openalex-snapshot

Diversity, Bacterial Symbionts and Antibacterial Potential of Gut-Associated Fungi Isolated from the Pantala flavescens Larvae in China

inferredcites →https://doi.org/10.1371/journal.pone.0170782openalex-snapshot

Cladosporium cladosporioides and Cladosporium pseudocladosporioides as potential new fungal antagonists of Puccinia horiana Henn., the causal agent of chrysanthemum white rust

inferredcites →https://doi.org/10.1371/journal.pone.0194899openalex-snapshot

Investigation of the seasonal microbiome of Anopheles coluzzii mosquitoes in Mali

inferredcites →https://doi.org/10.1371/journal.pone.0284393openalex-snapshot

Filamentous fungal associates of the alder bark beetle, Alniphagus aspericollis, including an undescribed species of Neonectria

inferredcites →https://doi.org/10.1371/journal.ppat.1011497openalex-snapshot

Fusarium phytopathogens as insect mutualists

inferredcites →https://doi.org/10.1515/jppr-2015-0011openalex-snapshot

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inferredcites →https://doi.org/10.1590/1519-6984.166681openalex-snapshot

Potential of endophytic fungi as biocontrol agents of Duponchelia fovealis (Zeller) (Lepidoptera:Crambidae)

inferredcites →https://doi.org/10.1590/1519-6984.260039openalex-snapshot

Diversity and enzymatic capabilities of fungi associated with the digestive tract of larval stages of a shredder insect in Cerrado and Amazon Forest, Brazil

inferredcites →https://doi.org/10.1590/1519-6984.265681openalex-snapshot

Diversity of cellulolytic and xylanolytic fungi associated with the digestive tract of aquatic insect larvae in streams of the Amazon Forest and Cerrado in Brazil

inferredcites →https://doi.org/10.1590/1809-4392202000902openalex-snapshot

Cultivable cellulolytic fungi isolated from the gut of Amazonian aquatic insects

inferredcites →https://doi.org/10.1590/s0074-02762002000800007openalex-snapshot

Isolation of fungi in Musca domestica Linnaeus, 1758 (Diptera: Muscidae) captured at two natural breeding grounds in the municipality of Seropédica, Rio de Janeiro, Brazil

inferredcites →https://doi.org/10.1603/0013-8746(2004)097[0492:mawtcb]2.0.co;2openalex-snapshot

Mycobiota Associated with the Coffee Berry Borer (Coleoptera: Scolytidae) and Its Galleries in Fruit

inferredcites →https://doi.org/10.1603/0013-8746(2007)100[703:fifiag]2.0.co;2openalex-snapshot

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inferredcites →https://doi.org/10.1603/an13164openalex-snapshot

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inferredcites →https://doi.org/10.1603/en11090openalex-snapshot

Fungi Associated With Scolytogenes birosimensis (Coleoptera: Curculionidae) Infesting Pittosporum tobira

inferredcites →https://doi.org/10.1603/en12001openalex-snapshot

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inferredcites →https://doi.org/10.1649/553openalex-snapshot

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inferredcites →https://doi.org/10.18311/jbc/2020/24775openalex-snapshot

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inferredcites →https://doi.org/10.18641/jbc/27/2/45549openalex-snapshot

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inferredcites →https://doi.org/10.19263/redia-104.21.14openalex-snapshot

XYLOSANDRUS COMPACTUS AND LIPARTHRUM COLCHICUM (COLEOP- TERA SCOLYTINAE) IN TUSCANY: A PRELIMINARY SCREENING OF ASSOCIATED FUNGI

inferredcites →https://doi.org/10.19263/redia-105.22.25openalex-snapshot

FUNGI OBTAINED FROM OLIVE TWIG DIEBACK AND ADULTS OF THE ALIEN PEST XYLOSANDRUS COMPACTUS (EICHHOFF) (COLEOPTERA CURCULIONIDAE SCOLYTINAE)

inferredcites →https://doi.org/10.21608/eajbsa.2012.14287openalex-snapshot

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inferredcites →https://doi.org/10.21608/eajbsa.2021.198978openalex-snapshot

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inferredcites →https://doi.org/10.21608/jppp.2005.238696openalex-snapshot

VIRULENCE AND ENZYMATIC ACTIVITIES OF SOME ENTOMOPATHOGENIC FUNGI AGAINST WHITEFLIES AND APHIDS ..

inferredcites →https://doi.org/10.21608/jppp.2005.238989openalex-snapshot

INTERACTIONS AMONG THE ENTOMOPATHOGENIC FUNGUS, Cladosporium uridenicolla SPEG., AND TWO WHITEFLIES BENEFICIAL INSECTS, Eretmocerus mundus MERCERT AND Coccienlla undecimpunctata L.: FROM AN IPM PROSPECTIVE

inferredcites →https://doi.org/10.21608/jppp.2017.46947openalex-snapshot

Biodiversity of Entomopathogenic Fungi Naturally Infecting Cabbage Aphid, Brevicoryne brassicae. L.

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Isolation, Characterization and Insecticidal Activity of Methylene Chloride Extract of Cladosporium cladosporioides Secondary Metabolites against Aphis gossypii (Glov.)

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inferredcites →https://doi.org/10.3114/sim0003openalex-snapshot

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inferredcites →https://doi.org/10.3161/15052249pje2020.68.1.002openalex-snapshot

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inferredcites →https://doi.org/10.3389/ffunb.2022.918052openalex-snapshot

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inferredcites →https://doi.org/10.3389/fmicb.2015.00185openalex-snapshot

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inferredcites →https://doi.org/10.3389/fmicb.2020.00300openalex-snapshot

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inferredcites →https://doi.org/10.3389/fmicb.2020.557980openalex-snapshot

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inferredcites →https://doi.org/10.3389/fmicb.2020.568853openalex-snapshot

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inferredcites →https://doi.org/10.3389/fmicb.2020.577268openalex-snapshot

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inferredcites →https://doi.org/10.3389/fmicb.2021.634503openalex-snapshot

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inferredcites →https://doi.org/10.3389/fmicb.2021.818787openalex-snapshot

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inferredcites →https://doi.org/10.3389/fmicb.2022.964735openalex-snapshot

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inferredcites →https://doi.org/10.3390/insects12121119openalex-snapshot

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inferredcites →https://doi.org/10.3390/insects4040631openalex-snapshot

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inferredcites →https://doi.org/10.3390/jof10010078openalex-snapshot

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inferredcites →https://doi.org/10.3390/jof7100863openalex-snapshot

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inferredcites →https://doi.org/10.3390/jof8030286openalex-snapshot

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inferredcites →https://doi.org/10.3390/jof9020163openalex-snapshot

Mycophagy: A Global Review of Interactions between Invertebrates and Fungi

inferredcites →https://doi.org/10.3390/microorganisms10010045openalex-snapshot

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inferredcites →https://doi.org/10.3390/microorganisms10010096openalex-snapshot

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inferredcites →https://doi.org/10.3390/microorganisms11020440openalex-snapshot

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inferredcites →https://doi.org/10.3390/microorganisms11041086openalex-snapshot

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inferredcites →https://doi.org/10.3390/microorganisms8060795openalex-snapshot

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inferredcites →https://doi.org/10.3390/molecules26133959openalex-snapshot

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inferredcites →https://doi.org/10.3390/molecules26247568openalex-snapshot

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inferredcites →https://doi.org/10.3390/pathogens10030369openalex-snapshot

New Cladosporium Species from Normal and Galled Flowers of Lamiaceae

inferredcites →https://doi.org/10.3390/pathogens10030381openalex-snapshot

Amplicon Sequencing of Variable 16S rRNA from Bacteria and ITS2 Regions from Fungi and Plants, Reveals Honeybee Susceptibility to Diseases Results from Their Forage Availability under Anthropogenic Landscapes

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

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