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The microbiota influences the Drosophila melanogaster life history strategy
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
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Latitude as a co‐driver of human gut microbial diversity?
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Simultaneous Inference in General Parametric Models
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Diversity and function of the avian gut microbiota
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Human Genetics Shape the Gut Microbiome
inferredcites →https://doi.org/10.1016/j.celrep.2015.01.018openalex-snapshot
Microbes Promote Amino Acid Harvest to Rescue Undernutrition in Drosophila
inferredcites →https://doi.org/10.1016/j.celrep.2015.08.004openalex-snapshot
Distinct Shifts in Microbiota Composition during Drosophila Aging Impair Intestinal Function and Drive Mortality
inferredcites →https://doi.org/10.1016/j.chom.2016.04.017openalex-snapshot
Genetic Determinants of the Gut Microbiome in UK Twins
inferredcites →https://doi.org/10.1016/j.chom.2017.08.013openalex-snapshot
Host Genetic Control of the Oral Microbiome in Health and Disease
inferredcites →https://doi.org/10.1016/j.chom.2018.06.001openalex-snapshot
Bacterial Adaptation to the Host's Diet Is a Key Evolutionary Force Shaping Drosophila-Lactobacillus Symbiosis
inferredcites →https://doi.org/10.1016/j.cmet.2007.06.006openalex-snapshot
Increased Internal and External Bacterial Load during Drosophila Aging without Life-Span Trade-Off
inferredcites →https://doi.org/10.1016/j.cmet.2011.07.012openalex-snapshot
Lactobacillus plantarum Promotes Drosophila Systemic Growth by Modulating Hormonal Signals through TOR-Dependent Nutrient Sensing
inferredcites →https://doi.org/10.1016/j.cub.2017.05.034openalex-snapshot
Probabilistic Invasion Underlies Natural Gut Microbiome Stability
inferredcites →https://doi.org/10.1016/j.jinsphys.2008.04.008openalex-snapshot
Changes in body melanisation and desiccation resistance in highland vs. lowland populations of D. melanogaster
inferredcites →https://doi.org/10.1016/j.jinsphys.2017.05.005openalex-snapshot
Physiological responses of insects to microbial fermentation products: Insights from the interactions between Drosophila and acetic acid
inferredcites →https://doi.org/10.1016/j.mib.2016.04.010openalex-snapshot
Are you my symbiont? Microbial polymorphic toxins and antimicrobial compounds as honest signals of beneficial symbiotic defensive traits
inferredcites →https://doi.org/10.1016/j.mib.2017.05.012openalex-snapshot
Host–microbiota interactions in Caenorhabditis elegans and their significance
inferredcites →https://doi.org/10.1016/j.smim.2006.10.002openalex-snapshot
Use of axenic animals in studying the adaptation of mammals to their commensal intestinal microbiota
inferredcites →https://doi.org/10.1016/j.tem.2010.11.002openalex-snapshot
Obesity and nutrient sensing TOR pathway in flies and vertebrates: Functional conservation of genetic mechanisms
inferredcites →https://doi.org/10.1016/j.tig.2015.05.006openalex-snapshot
Revisiting classic clines in Drosophila melanogaster in the age of genomics
inferredcites →https://doi.org/10.1016/s0140-6736(17)30566-4openalex-snapshot
Evolution, human-microbe interactions, and life history plasticity
inferredcites →https://doi.org/10.1016/s0169-5347(02)02578-8openalex-snapshot
The physiology/life-history nexus
inferredcites →https://doi.org/10.1038/hdy.1981.99openalex-snapshot
Latitudinal relationships of esterase-6 and phosphoglucomutase gene frequencies in Drosophila melanogaster
inferredcites →https://doi.org/10.1038/ismej.2011.139openalex-snapshot
An improved Greengenes taxonomy with explicit ranks for ecological and evolutionary analyses of bacteria and archaea
inferredcites →https://doi.org/10.1038/ismej.2011.82openalex-snapshot
Impact of training sets on classification of high-throughput bacterial 16s rRNA gene surveys
inferredcites →https://doi.org/10.1038/ismej.2013.86openalex-snapshot
The inconstant gut microbiota of Drosophila species revealed by 16S rRNA gene analysis
inferredcites →https://doi.org/10.1038/ismej.2015.142openalex-snapshot
Contribution of neutral processes to the assembly of gut microbial communities in the zebrafish over host development
inferredcites →https://doi.org/10.1038/ismej.2015.64openalex-snapshot
Dietary input of microbes and host genetic variation shape among-population differences in stickleback gut microbiota
inferredcites →https://doi.org/10.1038/ismej.2016.95openalex-snapshot
Differential specificity between closely related corals and abundant Endozoicomonas endosymbionts across global scales
inferredcites →https://doi.org/10.1038/nature11234openalex-snapshot
Structure, function and diversity of the healthy human microbiome
inferredcites →https://doi.org/10.1038/nature17626openalex-snapshot
The evolution of cooperation within the gut microbiota
inferredcites →https://doi.org/10.1038/nature17655openalex-snapshot
Normalizing the environment recapitulates adult human immune traits in laboratory mice
inferredcites →https://doi.org/10.1038/ncomms7312openalex-snapshot
Host genetic determinants of microbiota-dependent nutrition revealed by genome-wide analysis of Drosophila melanogaster
inferredcites →https://doi.org/10.1038/ng.3663openalex-snapshot
The effect of host genetics on the gut microbiome
inferredcites →https://doi.org/10.1038/nmeth.f.303openalex-snapshot
QIIME allows analysis of high-throughput community sequencing data
inferredcites →https://doi.org/10.1038/s41396-017-0020-xopenalex-snapshot
Microbial community assembly in wild populations of the fruit fly Drosophila melanogaster
inferredcites →https://doi.org/10.1038/s41598-017-04922-zopenalex-snapshot
Maternally-transmitted microbiota affects odor emission and preference in Drosophila larva
inferredcites →https://doi.org/10.1038/s41684-018-0065-0openalex-snapshot
The Drosophila model for microbiome research
inferredcites →https://doi.org/10.1038/sj.hdy.6800532openalex-snapshot
Genetic correlations, tradeoffs and environmental variation
inferredcites →https://doi.org/10.1038/sj.hdy.6886490openalex-snapshot
Desiccation and starvation resistance in Drosophila: patterns of variation at the species, population and intrapopulation levels
inferredcites →https://doi.org/10.1038/srep05437openalex-snapshot
Functional divergence in gastrointestinal microbiota in physically-separated genetically identical mice
inferredcites →https://doi.org/10.1038/srep15469openalex-snapshot
Live fast die young life history in females: evolutionary trade-off between early life mating and lifespan in female Drosophila melanogaster
inferredcites →https://doi.org/10.1051/agro:2006030openalex-snapshot
Symbiotic nitrogen fixation in legume nodules: process and signaling. A review
inferredcites →https://doi.org/10.1073/pnas.0405207101openalex-snapshot
Drosophila lifespan enhancement by exogenous bacteria
inferredcites →https://doi.org/10.1073/pnas.0805485105openalex-snapshot
An amino acid polymorphism in the couch potato gene forms the basis for climatic adaptation in Drosophila melanogaster
inferredcites →https://doi.org/10.1073/pnas.0900300106openalex-snapshot
Latitudinal variation in lifespan within species is explained by the metabolic theory of ecology
inferredcites →https://doi.org/10.1073/pnas.1007028107openalex-snapshot
Individuality in gut microbiota composition is a complex polygenic trait shaped by multiple environmental and host genetic factors
inferredcites →https://doi.org/10.1073/pnas.1206721109openalex-snapshot
Quantification of the relative roles of niche and neutral processes in structuring gastrointestinal microbiomes
inferredcites →https://doi.org/10.1073/pnas.1218525110openalex-snapshot
Animals in a bacterial world, a new imperative for the life sciences
inferredcites →https://doi.org/10.1073/pnas.1419659112openalex-snapshot
Rapid molecular evolution across amniotes of the IIS/TOR network
inferredcites →https://doi.org/10.1080/00275514.1987.12025370openalex-snapshot
Distribution of VA Mycorrhizal Fungi Along a Latitudinal Temperature Gradient
inferredcites →https://doi.org/10.1086/597611openalex-snapshot
A Quantitative Survey of Local Adaptation and Fitness Trade‐Offs
inferredcites →https://doi.org/10.1086/661780openalex-snapshot
Thermal Tolerance in Widespread and Tropical Drosophila Species: Does Phenotypic Plasticity Increase with Latitude?
inferredcites →https://doi.org/10.1093/aesa/86.5.545openalex-snapshot
Identification of Aphid (Homoptera: Aphididae) Species and Clones by Random Amplified Polymorphic DNA
inferredcites →https://doi.org/10.1093/bioinformatics/btp636openalex-snapshot
PyNAST: a flexible tool for aligning sequences to a template alignment
inferredcites →https://doi.org/10.1093/bioinformatics/btq461openalex-snapshot
Search and clustering orders of magnitude faster than BLAST
inferredcites →https://doi.org/10.1093/biomet/33.3.183openalex-snapshot
ON THE USE OF MATRICES IN CERTAIN POPULATION MATHEMATICS
inferredcites →https://doi.org/10.1093/femsre/fux030openalex-snapshot
Lifestyles in transition: evolution and natural history of the genus Lactobacillus
inferredcites →https://doi.org/10.1093/molbev/msr064openalex-snapshot
Molecular Basis of Adaptive Shift in Body Size in Drosophila melanogaster: Functional and Sequence Analyses of the Dca Gene
inferredcites →https://doi.org/10.1098/rsbl.2013.1037openalex-snapshot
Geographical variation of human gut microbial composition
inferredcites →https://doi.org/10.1098/rsbl.2015.0469openalex-snapshot
Consumption of dietary sugar by gut bacteria determinesDrosophilalipid content
inferredcites →https://doi.org/10.1098/rspb.1998.0324openalex-snapshot
Phylogeny and PCR–based classification of Wolbachia strains using wsp gene sequences
inferredcites →https://doi.org/10.1098/rspb.2015.0209openalex-snapshot
Early-late life trade-offs and the evolution of ageing in the wild
inferredcites →https://doi.org/10.1098/rstb.2010.0208openalex-snapshot
Personality and the emergence of the pace-of-life syndrome concept at the population level
inferredcites →https://doi.org/10.1101/232959openalex-snapshot
High-dimensional microbiome interactions shape host fitness
inferredcites →https://doi.org/10.1111/1365-2656.12709openalex-snapshot
The microbiota of diapause: How host–microbe associations are formed after dormancy in an aquatic crustacean
inferredcites →https://doi.org/10.1111/1462-2920.12570openalex-snapshot
Microbiology of sugar‐rich environments: diversity, ecology and system constraints
inferredcites →https://doi.org/10.1111/evo.12546openalex-snapshot
A highly pleiotropic amino acid polymorphism in the Drosophila insulin receptor contributes to life-history adaptation
inferredcites →https://doi.org/10.1111/geb.12582openalex-snapshot
Plant mycorrhizal status, but not type, shifts with latitude and elevation in Europe
inferredcites →https://doi.org/10.1111/j.1365-294x.2012.05731.xopenalex-snapshot
Genome‐wide patterns of latitudinal differentiation among populations of D rosophila melanogaster from N orth A merica
inferredcites →https://doi.org/10.1111/j.1420-9101.2010.02110.xopenalex-snapshot
A comprehensive assessment of geographic variation in heat tolerance and hardening capacity in populations of Drosophila melanogaster from eastern Australia
inferredcites →https://doi.org/10.1111/j.1462-2920.2011.02511.xopenalex-snapshot
Low‐diversity bacterial community in the gut of the fruitfly Drosophila melanogaster
inferredcites →https://doi.org/10.1111/j.1469-7998.1990.tb04316.xopenalex-snapshot
Living fast and dying young: A comparative analysis of life‐history variation among mammals
inferredcites →https://doi.org/10.1111/j.1558-5646.2008.00351.xopenalex-snapshot
REPRODUCTIVE DIAPAUSE AND LIFE-HISTORY CLINES IN NORTH AMERICAN POPULATIONS OF DROSOPHILA MELANOGASTER
inferredcites →https://doi.org/10.1111/jbi.12795openalex-snapshot
Latitudinal variation in the symbiotic dinoflagellate Symbiodinium of the common reef zoantharian Palythoa tuberculosa on the Saudi Arabian coast of the Red Sea
inferredcites →https://doi.org/10.1111/jeb.12480openalex-snapshot
Trade‐off of ovarian lipids and total body lipids for fecundity and starvation resistance in tropical populations of Drosophila melanogaster
inferredcites →https://doi.org/10.1111/mec.13455openalex-snapshot
Secondary contact and local adaptation contribute to genome‐wide patterns of clinal variation in Drosophila melanogaster
inferredcites →https://doi.org/10.1111/mec.14232openalex-snapshot
A genomic investigation of ecological differentiation between free‐living and Drosophila ‐associated bacteria
inferredcites →https://doi.org/10.1111/mec.14413openalex-snapshot
How gut transcriptional function of Drosophila melanogaster varies with the presence and composition of the gut microbiota
inferredcites →https://doi.org/10.1111/oik.03900openalex-snapshot
Life history and eco‐evolutionary dynamics in light of the gut microbiota
inferredcites →https://doi.org/10.1126/science.1109523openalex-snapshot
A Rapid Shift in a Classic Clinal Pattern in Drosophila Reflecting Climate Change
inferredcites →https://doi.org/10.1126/science.1212782openalex-snapshot
Drosophila Microbiome Modulates Host Developmental and Metabolic Homeostasis via Insulin Signaling
inferredcites →https://doi.org/10.1126/science.aad2602openalex-snapshot
The ecology of the microbiome: Networks, competition, and stability
inferredcites →https://doi.org/10.1128/aem.00062-07openalex-snapshot
Naive Bayesian Classifier for Rapid Assignment of rRNA Sequences into the New Bacterial Taxonomy
inferredcites →https://doi.org/10.1128/aem.00662-18openalex-snapshot
Bacterial Methionine Metabolism Genes Influence Drosophila melanogaster Starvation Resistance
inferredcites →https://doi.org/10.1128/aem.01043-13openalex-snapshot
Development of a Dual-Index Sequencing Strategy and Curation Pipeline for Analyzing Amplicon Sequence Data on the MiSeq Illumina Sequencing Platform
inferredcites →https://doi.org/10.1128/aem.01442-15openalex-snapshot
The Host as the Driver of the Microbiota in the Gut and External Environment of Drosophila melanogaster
inferredcites →https://doi.org/10.1128/aem.02120-06openalex-snapshot
Geographical Distribution and Diversity of Bacteria Associated with Natural Populations of Drosophila melanogaster
inferredcites →https://doi.org/10.1128/aem.02742-13openalex-snapshot
Interspecies Interactions Determine the Impact of the Gut Microbiota on Nutrient Allocation in Drosophila melanogaster
inferredcites →https://doi.org/10.1128/aem.03301-15openalex-snapshot
Host Genetic Control of the Microbiota Mediates the Drosophila Nutritional Phenotype
inferredcites →https://doi.org/10.1128/mbio.00155-18openalex-snapshot
The Drosophila melanogaster Gut Microbiota Provisions Thiamine to Its Host
inferredcites →https://doi.org/10.1128/mbio.00860-13openalex-snapshot
Frequent Replenishment Sustains the Beneficial Microbiome of Drosophila melanogaster
inferredcites →https://doi.org/10.1128/mbio.01114-18openalex-snapshot
Monoassociation with Lactobacillus plantarum Disrupts Intestinal Homeostasis in Adult Drosophila melanogaster
inferredcites →https://doi.org/10.1128/mbio.01117-13openalex-snapshot
Dual Role for Inflammasome Sensors NLRP1 and NLRP3 in Murine Resistance to Toxoplasma gondii
inferredcites →https://doi.org/10.1128/mbio.01631-14openalex-snapshot
Metagenome-Wide Association of Microbial Determinants of Host Phenotype in Drosophila melanogaster
inferredcites →https://doi.org/10.1128/mbio.02284-14openalex-snapshot
Application of a Neutral Community Model To Assess Structuring of the Human Lung Microbiome
inferredcites →https://doi.org/10.1146/annurev-micro-091313-103654openalex-snapshot
The Importance of Microbes in Animal Development: Lessons from the Squid-Vibrio Symbiosis
inferredcites →https://doi.org/10.1146/annurev.genet.42.110807.091427openalex-snapshot
Molecular Determinants of a Symbiotic Chronic Infection
inferredcites →https://doi.org/10.1186/s12864-016-3307-9openalex-snapshot
The Drosophila transcriptional network is structured by microbiota
inferredcites →https://doi.org/10.1186/s13059-015-0759-1openalex-snapshot
Host genetic variation impacts microbiome composition across human body sites
inferredcites →https://doi.org/10.1242/jeb.101725openalex-snapshot
Gut microbiota dictates the metabolic response ofDrosophilato diet
inferredcites →https://doi.org/10.1242/jeb.151522openalex-snapshot
Lactobacillus plantarum favors the early emergence of fit and fertile adult Drosophila upon chronic undernutrition
inferredcites →https://doi.org/10.1371/journal.pbio.2005710openalex-snapshot
Drosophila melanogaster establishes a species-specific mutualistic interaction with stable gut-colonizing bacteria
inferredcites →https://doi.org/10.1371/journal.pgen.1004775openalex-snapshot
Genomic Evidence of Rapid and Stable Adaptive Oscillations over Seasonal Time Scales in Drosophila
inferredcites →https://doi.org/10.1371/journal.pone.0009490openalex-snapshot
FastTree 2 – Approximately Maximum-Likelihood Trees for Large Alignments
inferredcites →https://doi.org/10.1371/journal.pone.0036765openalex-snapshot
Impact of the Resident Microbiota on the Nutritional Phenotype of Drosophila melanogaster
inferredcites →https://doi.org/10.1371/journal.pone.0070749openalex-snapshot
Host Species and Environmental Effects on Bacterial Communities Associated with Drosophila in the Laboratory and in the Natural Environment
inferredcites →https://doi.org/10.1371/journal.pone.0134643openalex-snapshot
The Gut Microbiota of Wild Mice
inferredcites →https://doi.org/10.1371/journal.pone.0140301openalex-snapshot
Genome-Wide Association Studies of the Human Gut Microbiota
inferredcites →https://doi.org/10.1515/9781400881376openalex-snapshot
The Theory of Island Biogeography
inferredcites →https://doi.org/10.1534/genetics.110.123059openalex-snapshot
Genomic Differentiation Between Temperate and Tropical Australian Populations ofDrosophila melanogaster
inferredcites →https://doi.org/10.1554/05-115.1openalex-snapshot
GEOGRAPHIC VARIATION IN DIAPAUSE INCIDENCE, LIFE-HISTORY TRAITS, AND CLIMATIC ADAPTATION IN DROSOPHILA MELANOGASTER
inferredcites →https://doi.org/10.1890/07-1162.1openalex-snapshot
ECOLOGICAL GENETICS IN THE NORTH ATLANTIC: ENVIRONMENTAL GRADIENTS AND ADAPTATION AT SPECIFIC LOCI
inferredcites →https://doi.org/10.32614/cran.package.rcompanionopenalex-snapshot
rcompanion: Functions to Support Extension Education Program Evaluation
inferredcites →https://doi.org/10.3354/meps244017openalex-snapshot
Molecular diversity of symbiotic algae at the latitudinal margins of their distribution: dinoflagellates of the genus Symbiodinium in corals and sea anemones
inferredcites →https://doi.org/10.3389/fmicb.2014.00576openalex-snapshot
In vivo function and comparative genomic analyses of the Drosophila gut microbiota identify candidate symbiosis factors
inferredcites →https://doi.org/10.3389/fmicb.2017.02414openalex-snapshot
Plant Phylogeny and Life History Shape Rhizosphere Bacterial Microbiome of Summer Annuals in an Agricultural Field
inferredcites →https://doi.org/10.3791/54219openalex-snapshot
Rearing the Fruit Fly Drosophila melanogaster Under Axenic and Gnotobiotic Conditions
inferredcites →https://doi.org/10.3945/jn.115.222380openalex-snapshot
Acidic Food pH Increases Palatability and Consumption and Extends Drosophila Lifespan
inferredcites →https://doi.org/10.4049/jimmunol.1700453openalex-snapshot
Of Mice, Dirty Mice, and Men: Using Mice To Understand Human Immunology
inferredcites →https://doi.org/10.5860/choice.30-4983openalex-snapshot
The evolution of life histories: theory and analysis
inferredcites →https://doi.org/10.7554/elife.18855openalex-snapshot
Metabolite exchange between microbiome members produces compounds that influence Drosophila behavior
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1007/s10682-020-10068-8openalex-snapshot
Environmental specificity in Drosophila-bacteria symbiosis affects host developmental plasticity
inferred← citeshttps://doi.org/10.1073/pnas.1809349115openalex-snapshot
Microbiome interactions shape host fitness
inferred← citeshttps://doi.org/10.1073/pnas.1907787116openalex-snapshot
Microbiome composition shapes rapid genomic adaptation of Drosophila melanogaster
inferred← citeshttps://doi.org/10.1098/rspb.2019.1911openalex-snapshot
Parallel changes in gut microbiome composition and function during colonization, local adaptation and ecological speciation
inferred← citeshttps://doi.org/10.1101/2020.09.21.306779openalex-snapshot
Host evolutionary history and ecological context modulate the adaptive potential of the microbiome
inferred← citeshttps://doi.org/10.1101/736843openalex-snapshot
Parallel changes in gut microbiome composition and function in parallel local adaptation and speciation
inferred← citeshttps://doi.org/10.1111/1758-2229.12826openalex-snapshot
Common structuring principles of the Drosophila melanogaster microbiome on a continental scale and between host and substrate
inferred← citeshttps://doi.org/10.1111/mec.15939openalex-snapshot
Allelic polymorphism at foxo contributes to local adaptation in Drosophila melanogaster
inferred← citeshttps://doi.org/10.1128/aem.00305-20openalex-snapshot
Genetic Influences of the Microbiota on the Life Span of Drosophila melanogaster
inferred← citeshttps://doi.org/10.1128/mbio.01496-19openalex-snapshot
Why Evolve Reliance on the Microbiome for Timing of Ontogeny?
inferred← citeshttps://doi.org/10.33016/nextjournal.csi.kv6mmq6tbda4eelcehkxsopenalex-snapshot
Microbiome interactions shape host fitness
inferred← citeshttps://doi.org/10.3410/f.736618952.793565848openalex-snapshot
Faculty Opinions recommendation of Microbiome composition shapes rapid genomic adaptation of Drosophila melanogaster.
inferred← citeshttps://doi.org/10.7287/peerj.8097v0.1/reviews/1openalex-snapshot
Peer Review #1 of "The microbiota of Drosophila suzukii influences the larval development of Drosophila melanogaster (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.8097v0.1/reviews/2openalex-snapshot
Peer Review #2 of "The microbiota of Drosophila suzukii influences the larval development of Drosophila melanogaster (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.8097v0.1/reviews/3openalex-snapshot
Peer Review #3 of "The microbiota of Drosophila suzukii influences the larval development of Drosophila melanogaster (v0.1)"
inferred← citeshttps://doi.org/10.7717/peerj.8097openalex-snapshot
The microbiota of Drosophila suzukii influences the larval development of Drosophila melanogaster
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