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Differential side-effects of Bacillus thuringiensis bioinsecticide on non-target Drosophila flies

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What this work says

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

inferredcites →https://doi.org/10.1002/1521-4028(200205)42:2<105::aid-jobm105>3.0.co;2-sopenalex-snapshot

Toxicity of Bacillus thuringiensis and B. sphaericus to laboratory populations of Drosophila melanogaster (Diptera: Drosophilidae)

inferredcites →https://doi.org/10.1002/bimj.200810425openalex-snapshot

Simultaneous Inference in General Parametric Models

inferredcites →https://doi.org/10.1002/ece3.2185openalex-snapshot

The effect of diet and time after bacterial infection on fecundity, resistance, and tolerance in Drosophila melanogaster

inferredcites →https://doi.org/10.1002/etc.3583openalex-snapshot

Interactions between Bt crops and aquatic ecosystems: A review

inferredcites →https://doi.org/10.1002/jat.3252openalex-snapshot

An overview of the safety and biological effects of Bacillus thuringiensis Cry toxins in mammals

inferredcites →https://doi.org/10.1002/ps.4262openalex-snapshot

Fate of insecticidal Bacillus thuringiensis Cry protein in soil: differences between purified toxin and biopesticide formulation

inferredcites →https://doi.org/10.1006/plas.1999.1415openalex-snapshot

Refined, Circular Restriction Map of the Bacillus thuringiensis subsp. israelensis Plasmid Carrying the Mosquito Larvicidal Genes

inferredcites →https://doi.org/10.1007/978-3-319-56678-8_1openalex-snapshot

Bacillus thuringiensis Characterization: Morphology, Physiology, Biochemistry, Pathotype, Cellular, and Molecular Aspects

inferredcites →https://doi.org/10.1007/978-3-319-56678-8_10openalex-snapshot

Specificity and Cross-order Activity of Bacillus thuringiensis Pesticidal Proteins

inferredcites →https://doi.org/10.1007/978-3-319-56678-8_3openalex-snapshot

Bacillus thuringiensis Toxin Classification

inferredcites →https://doi.org/10.1007/978-3-319-56678-8_4openalex-snapshot

Insecticidal Proteins from Bacillus thuringiensis and Their Mechanism of Action

inferredcites →https://doi.org/10.1007/978-94-007-3021-2_2openalex-snapshot

Bacillus thuringiensis Applications in Agriculture

inferredcites →https://doi.org/10.1007/978-94-007-7796-5_2openalex-snapshot

Environmental and Economic Costs of the Application of Pesticides Primarily in the United States

inferredcites →https://doi.org/10.1007/978-94-017-1429-7_16openalex-snapshot

Industrial fermentation and formulation of entomopathogenic bacteria

inferredcites →https://doi.org/10.1007/978-94-017-1429-7_21openalex-snapshot

Bacterial control of vector-mosquitoes and black flies

inferredcites →https://doi.org/10.1007/bf00333733openalex-snapshot

The colonization of organges by the cosmopolitan Drosophila

inferredcites →https://doi.org/10.1007/bf00345697openalex-snapshot

Breeding site specificity in the domestic species of Drosophila

inferredcites →https://doi.org/10.1007/bf02146902openalex-snapshot

The toxic action ofbacillus thuringiensis ‘Exotoxin’ onDrosophila reared in yeast-containing and yeast-free media

inferredcites →https://doi.org/10.1007/s00248-007-9331-1openalex-snapshot

The Ecology of Bacillus thuringiensis on the Phylloplane: Colonization from Soil, Plasmid Transfer, and Interaction with Larvae of Pieris brassicae

inferredcites →https://doi.org/10.1007/s10460-007-9067-zopenalex-snapshot

Insecticide use: Contexts and ecological consequences

inferredcites →https://doi.org/10.1016/j.cbi.2016.06.003openalex-snapshot

Effects of pesticide mixtures in human and animal models: An update of the recent literature

inferredcites →https://doi.org/10.1016/j.cub.2011.06.033openalex-snapshot

Coordinating Growth and Maturation — Insights from Drosophila

inferredcites →https://doi.org/10.1016/j.ecoenv.2016.01.028openalex-snapshot

Chronic toxicity and physiological changes induced in the honey bee by the exposure to fipronil and Bacillus thuringiensis spores alone or combined

inferredcites →https://doi.org/10.1016/j.envpol.2015.09.046openalex-snapshot

Persistence of detectable insecticidal proteins from Bacillus thuringiensis (Cry) and toxicity after adsorption on contrasting soils

inferredcites →https://doi.org/10.1016/j.ibmb.2011.02.006openalex-snapshot

Bacillus thuringiensis: A story of a successful bioinsecticide

inferredcites →https://doi.org/10.1016/j.ibmb.2016.11.008openalex-snapshot

Expressing a moth abcc2 gene in transgenic Drosophila causes susceptibility to Bt Cry1Ac without requiring a cadherin-like protein receptor

inferredcites →https://doi.org/10.1016/j.jinsphys.2009.11.006openalex-snapshot

Protein and carbohydrate composition of larval food affects tolerance to thermal stress and desiccation in adult Drosophila melanogaster

inferredcites →https://doi.org/10.1016/j.jip.2013.05.010openalex-snapshot

Cross-order and cross-phylum activity of Bacillus thuringiensis pesticidal proteins

inferredcites →https://doi.org/10.1016/j.jip.2015.07.009openalex-snapshot

Insect pathogens as biological control agents: Back to the future

inferredcites →https://doi.org/10.1016/j.procbio.2005.07.015openalex-snapshot

Recent advances in downstream processing and formulations of Bacillus thuringiensis based biopesticides

inferredcites →https://doi.org/10.1016/j.scitotenv.2016.02.096openalex-snapshot

No association between the use of Bti for mosquito control and the dynamics of non-target aquatic invertebrates in French coastal and continental wetlands

inferredcites →https://doi.org/10.1016/j.soilbio.2003.08.009openalex-snapshot

Persistence of toxins and cells of Bacillus thuringiensis subsp. kurstaki introduced in sprays to Sardinia soils

inferredcites →https://doi.org/10.1016/j.toxicon.2006.11.022openalex-snapshot

Mode of action of Bacillus thuringiensis Cry and Cyt toxins and their potential for insect control

inferredcites →https://doi.org/10.1021/acs.est.6b03056openalex-snapshot

Low-Dose Effects: Nonmonotonic Responses for the Toxicity of a Bacillus thuringiensis Biocide to Daphnia magna

inferredcites →https://doi.org/10.1023/a:1017569318401openalex-snapshot

Genetic analysis of extended lifespan in Drosophila melanogaster III. On the relationship between artificially selected and wild stocks

inferredcites →https://doi.org/10.1038/s41598-017-10801-4openalex-snapshot

Effects of purified or plant-produced Cry proteins on Drosophila melanogaster (Diptera: Drosophilidae) larvae

inferredcites →https://doi.org/10.1046/j.1365-2672.2001.01315.xopenalex-snapshot

Assessment of toxic potential of local JordanianBacillus thuringiensisstrains onDrosophila melanogasterandCulexsp. (Diptera)

inferredcites →https://doi.org/10.1046/j.1440-1703.2000.00328.xopenalex-snapshot

Coexistence of drosophilid flies: Aggregation, patch size diversity and parasitism

inferredcites →https://doi.org/10.1051/agro:2007054openalex-snapshot

Bacillus thuringiensis: applications in agriculture and insect resistance management. A review

inferredcites →https://doi.org/10.1073/pnas.1521741113openalex-snapshot

Midgut microbiota and host immunocompetence underlie Bacillus thuringiensis killing mechanism

inferredcites →https://doi.org/10.1073/pnas.79.22.6951openalex-snapshot

Transfer of Bacillus thuringiensis plasmids coding for delta-endotoxin among strains of B. thuringiensis and B. cereus.

inferredcites →https://doi.org/10.1093/jee/tow062openalex-snapshot

Biological Activity of Bacillus thuringiensis in Drosophila suzukii (Diptera: Drosophilidae)

inferredcites →https://doi.org/10.1111/1365-2664.12422openalex-snapshot

Microbial communities and nutrient dynamics in experimental microcosms are altered after the application of a high dose of Bti

inferredcites →https://doi.org/10.1111/j.1095-8312.1991.tb00594.xopenalex-snapshot

Competition on a divided and ephemeral resource: a cage experiment

inferredcites →https://doi.org/10.1111/j.1365-2664.2010.01821.xopenalex-snapshot

Red flag for green spray: adverse trophic effects of Bti on breeding birds

inferredcites →https://doi.org/10.1111/j.1420-9101.2007.01405.xopenalex-snapshot

Evolutionary biology of starvation resistance: what we have learned from Drosophila

inferredcites →https://doi.org/10.1111/j.1420-9101.2010.02094.xopenalex-snapshot

Effects of inbreeding on aversive learning in Drosophila

inferredcites →https://doi.org/10.1111/j.1439-0469.1994.tb00470.xopenalex-snapshot

An eight year phenological study of a local drosophilid community in Central Chile

inferredcites →https://doi.org/10.1111/j.1474-9726.2010.00560.xopenalex-snapshot

Dietary restriction affects lifespan but not cognitive aging in Drosophila melanogaster

inferredcites →https://doi.org/10.1111/j.1552-6909.2009.01092.xopenalex-snapshot

Pesticides and Health Risks

inferredcites →https://doi.org/10.1111/j.1742-4658.2009.07275.xopenalex-snapshot

Analysis of the region for receptor binding and triggering of oligomerization on Bacillus thuringiensis Cry1Aa toxin

inferredcites →https://doi.org/10.1126/science.290.5494.1166openalex-snapshot

Survival for Immunity: The Price of Immune System Activation for Bumblebee Workers

inferredcites →https://doi.org/10.1128/aem.63.12.4883-4890.1997openalex-snapshot

Extended screening by PCR for seven cry-group genes from field-collected strains of Bacillus thuringiensis

inferredcites →https://doi.org/10.1128/aem.68.10.5082-5095.2002openalex-snapshot

Complete Sequence and Organization of pBtoxis, the Toxin-Coding Plasmid ofBacillus thuringiensissubsp.israelensis

inferredcites →https://doi.org/10.1128/mmbr.62.3.775-806.1998openalex-snapshot

Bacillus thuringiensis and Its Pesticidal Crystal Proteins

inferredcites →https://doi.org/10.1186/s13071-016-1514-5openalex-snapshot

Effects of larvicidal and larval nutritional stresses on Anopheles gambiae development, survival and competence for Plasmodium falciparum

inferredcites →https://doi.org/10.1371/journal.pone.0156560openalex-snapshot

Activation of Bt Protoxin Cry1Ac in Resistant and Susceptible Cotton Bollworm

inferredcites →https://doi.org/10.1371/journal.ppat.1000905openalex-snapshot

Environmental Factors Determining the Epidemiology and Population Genetic Structure of the Bacillus cereus Group in the Field

inferredcites →https://doi.org/10.1603/ipm10010openalex-snapshot

Drosophila suzukii (Diptera: Drosophilidae): Invasive Pest of Ripening Soft Fruit Expanding its Geographic Range and Damage Potential

inferredcites →https://doi.org/10.2165/00139709-200423030-00003openalex-snapshot

Glyphosate Poisoning

inferredcites →https://doi.org/10.2307/2411114openalex-snapshot

Density-Dependent Natural Selection in Drosophila: Evolution of Growth Rate and Body Size

inferredcites →https://doi.org/10.2903/j.efsa.2012.2540openalex-snapshot

Conclusion on the peer review of the pesticide risk assessment of the active substanceBacillus thuringiensissubsp.kurstaki (strains ABTS 351, PB 54, SA 11, SA 12, EG 2348)

inferredcites →https://doi.org/10.2903/j.efsa.2016.4524openalex-snapshot

Risks for public health related to the presence of Bacillus cereus and other Bacillus spp. including Bacillus thuringiensis in foodstuffs

inferredcites →https://doi.org/10.3389/fpls.2015.00283openalex-snapshot

The food and environmental safety of Bt crops

inferredcites →https://doi.org/10.3390/toxins6123296openalex-snapshot

Bacillus thuringiensis Toxins: An Overview of Their Biocidal Activity

inferredcites →https://doi.org/10.3406/bsef.2012.3076openalex-snapshot

Les Drosophiles de la région Rhône-Alpes (Diptera, Drosophilidae)

inferredcites →https://doi.org/10.3929/ethz-b-000105397openalex-snapshot

Fitting Linear Mixed-Effects Models Using lme4

What points at this work

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

inferred← citeshttps://doi.org/10.3390/insects11100697openalex-snapshot

Bacillus thuringiensis Bioinsecticides Induce Developmental Defects in Non-Target Drosophila melanogaster Larvae

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