Table 1.
Insect metabolomics studies
Insect order | Species | Research topic | Sample type | Techniques utilised | Conclusions |
---|---|---|---|---|---|
Diptera | Aedes aegyti | Juvenile hormone regulation | Solvent extract | HPLC‐FD* | Mevalonate and juvenile hormone pathways are highly dynamic and linked to reproductive physiology1 |
Belgica antarctica | Temperature stress response | Solvent extract | GC‐MS | Freezing and desiccation are associated with increases in metabolites associated with carbohydrate metabolism and a decrease in free amino acids2. Shifts in metabolite pools are associated with changes in gene regulation related to dehydration3 | |
Chymomyza costata | Cryopreservation | Solvent extract, biofluid | GC‐MS, LC‐MS | Survival of cryopreservation is associated with increased proline levels in larval tissues4 | |
Drosophila melanogaster | Metabolomic profiling | Solvent extract, biofluid | GC‐MS, LC‐MS | Cold shock disturbs short‐ and long‐term cellular homeostasis5 , 6 , 7 , 8. Inbreeding, both in the absence and the presence of temperature stress, alters metabolic processes9. Lower rates of glycolysis occur in adapted flies undergoing hypoxia10 , 11 , 12. Age‐related decline of hypoxia tolerance is linked to reduced recovery of mitochondrial respiration13. >230 metabolites profiled across four Drosophila subspecies14 , 15. Bowman‐Birk inhibitor disrupts energy metabolism16. Long‐term cold acclimation modifies the larval metabolome12. Absolute quantification of 28 phospholipids17. Larvae with the y mutation have altered lysine metabolism18. CO2 exposure causes metabolic changes during short term recovery19. Infection by Listeria monocytogenes results in loss of energy store regulation20. Developmental and adult cold acclimation strongly promoted cold tolerance and restored metabolic homeostasis21 | |
Temperature stress responses | |||||
CO₂ anaesthesia | |||||
Bacterial infection | |||||
Hypoxia | |||||
Drosophila montana | Temperature stress responses | Solvent extract | GC‐MS, LC‐MS | Seasonal variations in thermoperiod are correlated with differential expression of myo‐inositol, proline and trehalose22 | |
Sarcophaga crassipalpis | Temperature stress response | Solvent extract | GC‐MS, 1D NMR | Rapid cold‐hardening elevates glycolysis associated metabolites whilst reducing levels of aerobic metabolic intermediates23 | |
Hemiptera | Aphids (multiple species) | Trehalose analysis | Solvent extract, biofluid | 1D NMR | High concentrations of trehalose are present in aphid hemolymph24. Removal of bacterial–insect symbiosis reduced expression of dietary metabolites, including essential amino acids25 |
Insect–bacterial symbiosis | |||||
Hymenoptera | Apis mellifera | Nosema ceranae infection | Solvent extract, biofluid | GC‐MS, LC‐MS | Exposure to infectious pathogens and neonicotinoid pesticides results in altered larval and adult metabolism26 , 27 |
Pesticide exposure | |||||
Praon volucre | Diapause induction | Solvent extract | GC‐MS | Cold acclimation eliminated cryo‐stress associated homeostatic perturbations28 | |
Venturia canescens | Temperature stress responses | Solvent extract | GC‐MS | Increases in cold tolerance are associated with the accumulation of cryoprotective metabolites29 | |
Lepidoptera | Helicoverpa armigera | Diapause induction | Solvent extract | GC‐MS, MALDI‐TOF | Diapause induces metabolic alterations associated with photoperiodic information and energy storage30 |
Manduca sexta | Host parasitism | Biofluid | 1D NMR | Insect parasitism enhances glucogenesis induction and halts lipogenesis31 , 32. Concentrations of small molecule metabolites change alongside larval development33 | |
Spodoptera frugiperda | Metabolomic profiling | Solvent extract | LC‐MS | Identification of major pathways associated with cellular protein productivity34 | |
Trichoplusia ni | Metabolomic profiling | Solvent extract | LC‐MS | Major pathways associated with cellular protein productivity identified34 | |
Orthoptera | Chorthippus (multiple species) | Metabolomic profiling | Solvent extract | GC‐MS | Determination of water soluble and lipid components of abdomial secretions of grasshoppers35 , 36 |
Locusta migratoria | Developmental phase transition | Solvent extract | 1D NMR | Onset of solitary‐group behavioural phase transitions are regulated by carnitine expression37 | |
Schistocerca gregaria | Social behaviour | Biofluid | 1D NMR | Concentrations of trehalose and lipids were lower in the haemolymph of crowd‐reared than in solitary‐reared nymphs38 | |
Phasmatodea | Anisomorpha buprestoides | Venom analysis | Biofluid | 1D, 2D NMR | Stick insect defence secretions contain high levels of glucose, lysine, histodine, serotonin and sorbitol39 |
Peruphasma schultei | Venom analysis | Biofluid | 1D NMR | Individual insects produce different stereoisomeric mixtures40 | |
Plecoptera | Dinocras cephalotes | Hypoxia | Solvent extract | 1D NMR/DI‐MS | Metabolic shifts associated with heat stress are more pronounced under hypoxia41 |
*High‐Performance Liquid Chromatography with Fluorescence Detection.
1Rivera‐Perez et al. (2014); 2Michaud et al. (2008); 3Teets et al. (2012); 4Koštál et al. (2011b); 5Malmendal et al. (2006); 6Overgaard et al. (2007); 7Malendal et al. (2013); 8Williams et al. (2014); 9Pedersen et al. (2008); 10Feala et al. (2008); 11Feala et al. (2009); 12Koštál et al. (2011a); 13Coquin et al. (2008); 14Kamleh et al. (2008); 15Kamleh et al. (2009); 16Li et al. (2010); 17Hammad et al. (2011); 18Bratty et al. (2012); 19Colinet & Renault (2012); 20Chambers et al. (2012); 21Colinet et al. (2012a); 22Vesala et al. (2012); 23Michaud & Denlinger (2007); 24Moriwaki et al. (2003); 25Wang et al. (2010); 26Aliferis et al. (2012); 27Derecka et al. (2013); 28Colinet et al. (2012b); 29Foray et al. (2013); 30Zhang et al. (2012); 31Thompson et al., (1990); 32Thompson (2001); 33Phalaraksh et al. (2008); 34Monteiro et al. (2014); 35Buszewska‐Forajta et al. (2014b); 36Buszewska‐Forajta et al. (2014a); 37Wu et al. (2012); 38Lenz et al. (2001); 39Zhang et al. (2007); 40Dossey et al. (2006); 41Verberk et al. (2013).