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Infection-Related Declines in Chill Coma Recovery and Negative Geotaxis in Drosophila melanogaster

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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/dvg.1020110204openalex-snapshot
Genetic alteration of normal aging processes is responsible for extended longevity in Drosophila
inferredcites →https://doi.org/10.1007/s10522-007-9086-6openalex-snapshot
Hormetic effects of repeated exposures to cold at young age on longevity, aging and resistance to heat or cold shocks in Drosophila melanogaster
inferredcites →https://doi.org/10.1007/s10522-008-9206-yopenalex-snapshot
Cold stress increases resistance to fungal infection throughout life in Drosophila melanogaster
inferredcites →https://doi.org/10.1007/s10522-009-9250-2openalex-snapshot
Combined effects of suppressing live yeast and of a cold pretreatment on longevity, aging and resistance to several stresses in Drosophila melanogaster
inferredcites →https://doi.org/10.1007/s10522-010-9309-0openalex-snapshot
A cold stress applied at various ages can increase resistance to heat and fungal infection in aged Drosophila melanogaster flies
inferredcites →https://doi.org/10.1007/s11064-010-0198-zopenalex-snapshot
Attenuation of Rotenone-Induced Mitochondrial Oxidative Damage and Neurotoxicty in Drosophila melanogaster Supplemented with Creatine
inferredcites →https://doi.org/10.1016/0022-1910(72)90157-6openalex-snapshot
Effects of carbon dioxide anaesthesia on Drosophila melanogaster
inferredcites →https://doi.org/10.1016/0022-1910(94)90093-0openalex-snapshot
Cold-shock and chilling tolerance in Drosophila
inferredcites →https://doi.org/10.1016/0531-5565(80)90061-3openalex-snapshot
Metabolic changes in ageing Drosophila melanogaster
inferredcites →https://doi.org/10.1016/j.bbrc.2009.12.053openalex-snapshot
Fatty acids of membrane phospholipids in Drosophila melanogaster lines showing rapid and slow recovery from chill coma
inferredcites →https://doi.org/10.1016/j.coi.2011.11.003openalex-snapshot
Pioneering immunology: insect style
inferredcites →https://doi.org/10.1016/j.cub.2006.08.052openalex-snapshot
Akt and foxo Dysregulation Contribute to Infection-Induced Wasting in Drosophila
inferredcites →https://doi.org/10.1016/j.cub.2007.03.049openalex-snapshot
Interactions between circadian rhythm and immunity in Drosophila melanogaster
inferredcites →https://doi.org/10.1016/j.exger.2005.02.005openalex-snapshot
Rapid iterative negative geotaxis (RING): a new method for assessing age-related locomotor decline in
inferredcites →https://doi.org/10.1016/j.exger.2006.08.008openalex-snapshot
Are functional and demographic senescence genetically independent?
inferredcites →https://doi.org/10.1016/j.jinsphys.2004.05.004openalex-snapshot
Dissecting chill coma recovery as a measure of cold resistance: evidence for a biphasic response in Drosophila melanogaster
inferredcites →https://doi.org/10.1016/j.jinsphys.2006.07.001openalex-snapshot
The effects of carbon dioxide anesthesia and anoxia on rapid cold-hardening and chill coma recovery in Drosophila melanogaster
inferredcites →https://doi.org/10.1016/j.jinsphys.2010.08.008openalex-snapshot
Survival rate and expression of Heat-shock protein 70 and Frost genes after temperature stress in Drosophila melanogaster lines that are selected for recovery time from temperature coma
inferredcites →https://doi.org/10.1016/j.jinsphys.2010.09.003openalex-snapshot
The effects of CO2 and chronic cold exposure on fecundity of female Drosophila melanogaster
inferredcites →https://doi.org/10.1016/j.jinsphys.2010.10.004openalex-snapshot
Mechanisms underlying insect chill-coma
inferredcites →https://doi.org/10.1016/j.neuro.2009.08.012openalex-snapshot
Neuroprotective efficacy of Bacopa monnieri against rotenone induced oxidative stress and neurotoxicity in Drosophila melanogaster
inferredcites →https://doi.org/10.1038/186124d0openalex-snapshot
Biochemical and Biophysical Research Communications
inferredcites →https://doi.org/10.1038/nri2432openalex-snapshot
Two ways to survive infection: what resistance and tolerance can teach us about treating infectious diseases
inferredcites →https://doi.org/10.1038/nri3169openalex-snapshot
Living in the liver: hepatic infections
inferredcites →https://doi.org/10.1073/pnas.0307605101openalex-snapshot
Similar gene expression patterns characterize aging and oxidative stress in Drosophila melanogaster
inferredcites →https://doi.org/10.1073/pnas.0405775102openalex-snapshot
Longer lifespan, altered metabolism, and stress resistance in Drosophila from ablation of cells making insulin-like ligands
inferredcites →https://doi.org/10.1073/pnas.0502240102openalex-snapshot
Drosophila host defense after oral infection by an entomopathogenic Pseudomonas species
inferredcites →https://doi.org/10.1073/pnas.91.14.6428openalex-snapshot
Host cell responses to Listeria monocytogenes infection include differential transcription of host stress genes involved in signal transduction.
inferredcites →https://doi.org/10.1086/419555openalex-snapshot
Seasonal Changes in Immune Function
inferredcites →https://doi.org/10.1093/emboj/21.11.2568openalex-snapshot
The Toll and Imd pathways are the major regulators of the immune response in Drosophila
inferredcites →https://doi.org/10.1093/icb/icr019openalex-snapshot
Leptin as a Physiological Mediator of Energetic Trade-Offs in Ecoimmunology: Implications for Disease
inferredcites →https://doi.org/10.1096/fj.05-5709comopenalex-snapshot
Causative role of oxidative stress in a Drosophila model of Friedreich ataxia
inferredcites →https://doi.org/10.1098/rspb.2001.1636openalex-snapshot
Immune challenge affects basal metabolic activity in wintering great tits
inferredcites →https://doi.org/10.1111/j.1365-2583.2005.00589.xopenalex-snapshot
Cold hardening and transcriptional change in Drosophila melanogaster
inferredcites →https://doi.org/10.1111/j.1365-2583.2012.01133.xopenalex-snapshot
Temperature stress affects the expression of immune response genes in the alfalfa leafcutting bee, Megachile rotundata
inferredcites →https://doi.org/10.1111/j.1558-5646.2008.00516.xopenalex-snapshot
EXPERIMENTAL EVOLUTION SHOWSDROSOPHILA MELANOGASTERRESISTANCE TO A MICROSPORIDIAN PATHOGEN HAS FITNESS COSTS
inferredcites →https://doi.org/10.1126/science.1214935openalex-snapshot
Disease Tolerance as a Defense Strategy
inferredcites →https://doi.org/10.1155/2012/583792openalex-snapshot
Recent Advances in the Use ofDrosophila melanogasteras a Model to Study Immunopathogenesis of Medically Important Filamentous Fungi
inferredcites →https://doi.org/10.1155/2012/967852openalex-snapshot
New Insight into Immunity and Immunopathology of Rickettsial Diseases
inferredcites →https://doi.org/10.1155/8472openalex-snapshot
International Journal of Microbiology
inferredcites →https://doi.org/10.1155/cdiopenalex-snapshot
Clinical and Developmental Immunology
inferredcites →https://doi.org/10.1159/000212612openalex-snapshot
A Longitudinal Study of the Effects of Age on Spontaneous Locomotor Activity in Drosophila melanogaster
inferredcites →https://doi.org/10.1186/1471-2148-8-76openalex-snapshot
The evolutionary costs of immunological maintenance and deployment
inferredcites →https://doi.org/10.1242/jeb.051003openalex-snapshot
Knocking down expression of Hsp22 and Hsp23 by RNA interference affects recovery from chill coma in Drosophila melanogaster
inferredcites →https://doi.org/10.1242/jeb.059535openalex-snapshot
Divergent transcriptomic responses to repeated and single cold exposures in Drosophila melanogaster
inferredcites →https://doi.org/10.1371/journal.pbio.1000150openalex-snapshot
The Role of Anorexia in Resistance and Tolerance to Infections in Drosophila
inferredcites →https://doi.org/10.1371/journal.pone.0010925openalex-snapshot
Functional Characterization of the Frost Gene in Drosophila melanogaster: Importance for Recovery from Chill Coma
inferredcites →https://doi.org/10.1371/journal.ppat.0020056openalex-snapshot
Prevalence of Local Immune Response against Oral Infection in a Drosophila/Pseudomonas Infection Model
inferredcites →https://doi.org/10.4161/fly.8051openalex-snapshot
Cross-generational fitness effects of infection in Drosophila melanogaster

What points at this work

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

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inferred← citeshttps://doi.org/10.1007/s00442-015-3529-6openalex-snapshot
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Fast drosophila enterocyte regrowth after infection involves a reverse metabolic flux driven by an amino acid transporter
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Analysis of survival, gene expression and behavior following chill-coma in the medfly Ceratitis capitata: Effects of population heterogeneity and age
inferred← citeshttps://doi.org/10.1016/j.jinsphys.2016.10.009openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.jtherbio.2018.03.021openalex-snapshot
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Flash sintering of ZrO2–SnO2–ZrSnO4 composite nanofibers: Fabrication, properties, and biochemical effects in Drosophila melanogaster
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Therapeutic evaluation of Martynia annua derived carbon dots in epileptic Drosophila model
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inferred← citeshttps://doi.org/10.1093/icb/ict004openalex-snapshot
Cross-tolerance and Cross-talk in the Cold: Relating Low Temperatures to Desiccation and Immune Stress in Insects
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