Home About us Contact
|
Home About us Contact | ||
|
|
||
Individual Flies (individual + fly)
Selected AbstractsEvolutionary biology of starvation resistance: what we have learned from DrosophilaJOURNAL OF EVOLUTIONARY BIOLOGY, Issue 5 2007S. RION Abstract Most animals face periods of food shortage and are thus expected to evolve adaptations enhancing starvation resistance (SR). Most of our knowledge of the genetic and physiological bases of those adaptations, their evolutionary correlates and trade-offs, and patterns of within- and among-population variation, comes from studies on Drosophila. In this review, we attempt to synthesize the various facets of evolutionary biology of SR emerging from those studies. Heritable variation for SR is ubiquitous in Drosophila populations, allowing for large responses to experimental selection. Individual flies can also inducibly increase their SR in response to mild nutritional stress (dietary restriction). Both the evolutionary change and the physiological plasticity involve increased accumulation of lipids, changes in carbohydrate and lipid metabolism and reduction in reproduction. They are also typically associated with greater resistance to desiccation and oxidative stress, and with prolonged development and lifespan. These responses are increasingly seen as facets of a shift of the physiology towards a ,survival mode', which helps the animal to survive hard times. The last decade has seen a great progress in revealing the molecular bases of induced responses to starvation, and the first genes contributing to genetic variation in SR have been identified. In contrast, little progress has been made in understanding the ecological significance of SR in Drosophila; in particular it remains unclear to what extent geographical variation in SR reflect differences in natural selection acting on this trait rather than correlated responses to selection on other traits. Drosophila offers a unique opportunity for an integrated study of the manifold aspects of adaptation to nutritional stress. Given that at least some major molecular mechanisms of response to nutritional stress seem common to animals, the insights from Drosophila are likely to apply more generally than just to dipterans or insects. [source] Attention-like processes underlying optomotor performance in a Drosophila choice mazeDEVELOPMENTAL NEUROBIOLOGY, Issue 2 2007Bruno van Swinderen Abstract The authors present a novel paradigm for studying visual responses in Drosophila. An eight-level choice maze was found to reliably segregate fly populations according to their responses to moving stripes displayed on a computer screen. Visual responsiveness was robust in wild-type flies, and performance depended on salience effects such as stimulus color and speed. Analysis of individual fly choices in the maze revealed that stereotypy, or choice persistence, contributed significantly to a strain's performance. On the basis of these observations, the authors bred wild-type flies for divergent visual phenotypes by selecting individual flies displaying extreme stereotypy. Selected flies alternated less often in the sequential choice maze than unselected flies, showing that stereotypy could evolve across generations. The authors found that selection for increased stereotypy impaired flies' responsiveness to competing stimuli in tests for attention-like behavior in the maze. Visual selective attention was further investigated by electrophysiology, and it was found that increased stereotypy also impaired responsiveness to competing stimuli at the level of brain activity. Combined results present a comprehensive approach to studying visual responses in Drosophila, and show that behavioral performance involves attention-like processes that are variable among individuals and thus sensitive to artificial selection. © 2006 Wiley Periodicals, Inc. Develop Neurobiol 67: 129,145, 2007. [source] Companion planting , behaviour of the cabbage root fly on host plants and non-host plantsENTOMOLOGIA EXPERIMENTALIS ET APPLICATA, Issue 1 2005Kate Morley Abstract Six-hundred individual female cabbage root flies (Delia radicum L.) (Diptera: Anthomyiidae) were each observed for 20 min under laboratory conditions to record how they behaved after landing on a host or a non-host plant. Fly movements were recorded on host plants [cabbage ,Brassica oleracea var. capitata (Cruciferae)] and non-host plants [clover ,Trifolium subterraneum L. (Papilionaceae)] surrounded by bare soil and on cabbage surrounded by clover. The most frequently observed behaviours made by the flies were (1) hops/spiral flights and (2) walks/runs. In the bare soil situation, the 50 individual flies observed in each treatment made 66 hops/spiral flights on the cabbage and 94 on the clover. When the two plants were tested together the movements were not additive as, instead of the expected 160 hops/spiral flights in the mixed plant treatment, the flies made 210 hops/spiral flights when they landed initially on cabbage but only 130 when they landed initially on clover. Few of the flies that landed initially on clover moved onto the host plant, even though the host plant was only a few centimetres away. The duration of the individual walks and runs made by the cabbage root flies were similar on both the host and non-host plants. The only differences were the numbers of walks/runs made and the time the flies remained inactive. On the host plants, the females made four walks/runs, each of about 12 s duration, interspersed by rest periods that totalled 1.5 min. In contrast, on the non-host plants the females made 10 walks/runs, each of about 9 s duration, interspersed by rest periods that totalled 7 min. Therefore, after landing on a plant, the flies, on average, left the host plant after 2.25 min and the non-host plant after 8.5 min. Our conclusion is that the protracted time spent on the non-host plants is the mechanism that disrupts insects from finding host plants in diverse plantings. Hence, the flies were arrested by non-host plants rather than being repelled or deterred as suggested in earlier studies. [source] Isolation and molecular characterization of Musca domestica delta-9 desaturase sequencesINSECT MOLECULAR BIOLOGY, Issue 6 2002A. L. Eigenheer Abstract We have isolated fatty acyl-CoA desaturase cDNA (Mdomd9) and genomic sequences from the housefly, Musca domestica. Two ,1.66 kb cDNAs were recovered. They had identical coding regions and 3, untranslated regions (UTRs), but differed in their 5, UTRs. The open reading frame encodes a 380 amino acid (aa) protein with 82% identity to Drosophila melanogaster desat1, and significant (> 50%) identity with other insect delta-9 desaturases. Functional analyses in a yeast expression system confirmed the cDNA encodes a ,9 desaturase. Northern analysis indicated two transcripts of 1.7 and 2.9 kb that hybridized specifically to the open reading frame. PCR amplification of genomic templates revealed three intron sites that are conserved among other insect species. Southern analysis of genomic DNA indicated at least two desaturase gene copies per haploid genome. There is a high degree of polymorphism, most of which appears to be due to variable intron sequences; curiously, individual flies had varying morphs of intron II and intron III. Together, the data suggest that there are more ,9 desaturase alleles within the population studied than there are loci within the genome, and support other studies suggesting that insect fatty acyl-CoA desaturases are a dynamically evolving gene family. [source] The fruit fly PUB: a phagostimulation unit bioassay system to quantitatively measure ingestion of baits by individual fliesJOURNAL OF APPLIED ENTOMOLOGY, Issue 9-10 2004D. Nestel Abstract:, A bioassay to investigate quantitative phagostimulation and ingestion physiology of baits on individual fruit flies is presented. The study was undertaken using two fruit fly species: the Mediterranean fruit fly (Ceratitis capitata), a cosmopolitan insect pest, and the Ethiopian fruit fly (Dacus ciliatus), a quarantine insect in Israel. Our model bait suspension included spinosad as the toxic agent, and 1% yeast hydrolysate with 10% sucrose as phagostimulant. A preliminary toxicology study showed that the two fruit flies are highly sensitive to low concentrations of spinosad baited with this phagostimulant. The maximum concentration needed to kill 90% of the female flies was 4.2 and 8.5 p.p.m. for C. capitata and D. ciliatus, respectively. The bioassay was able to detect the ingestion of low volumes (e.g. 1 ,l) of tested solutions. The bioassay was also able to detect differences in intake of different concentrations of spinosad solutions and relate ingestion to fruit fly mortality. Additionally, the bioassay was sensitive enough to highlight differences in intake related to the physiological status of the fruit fly and fly species. The bioassay can also be used to follow ingestion kinetics of baits. We expect that this bioassay will contribute in the exploration of more efficient bait systems for fruit flies. [source] Vector competence of South African Culicoides species for bluetongue virus serotype 1 (BTV-1) with special reference to the effect of temperature on the rate of virus replication in C. imicola and C. bolitinosMEDICAL AND VETERINARY ENTOMOLOGY, Issue 1 2002J. T. Paweska Abstract. The oral susceptibility of 22 South African livestock associated Culicoides species to infection with bluetongue virus serotype 1 (BTV-1) and its replication rate in C. imicola Kieffer and C. bolitinos Meiswinkel (Diptera: Ceratopogonidae) over a range of different incubation periods and temperatures are reported. Field-collected Culicoides were fed on sheep blood containing 7.5 log10TCID50/mL of BTV-1, and then held at constant different temperatures. Virus replication was measured over time by assaying individual flies in BHK-21 cells using a microtitration procedure. Regardless of the incubation temperatures (10, 15, 18, 23.5 and 30°C) the mean virus titre/midge, infection rates (IR) and the proportion of infected females with transmission potential (TP = virus titre/midge ,,3 log10 TCID50) were found to be significantly higher in C. bolitinos than in C. imicola. Results from days 4,10 post-infection (dpi), at 15,30°C, shows that the mean IR and TP values in C. bolitinos ranged from 36.7 to 87.8%, and from 8.4 to 87.7%, respectively; in C. imicola the respective values were 11.0,13.7% and 0,46.8%. In both species the highest IR was recorded at 25°C and the highest TP at 30°C. The time required for the development of TP in C. bolitinos ranged from 2 dpi at 25°C to 8 dpi at 15°C. In C. imicola it ranged from 4 dpi at 30°C to 10 dpi at 23.5°C; no individuals with TP were detected at 15°C. There was no evidence of virus replication in flies held at 10°C. When, at various points of incubation, individual flies were transferred from 10°C to 23.5°C and then assayed 4,10 days later, virus was recovered from both species. The mean virus titres/midge, and proportion of individuals with TP and IR, were again significantly higher in C. bolitinos than in C. imicola. Also the infection prevalence in C. magnus Colaço was higher than in C. imicola. Low infection prevalences were found in C. bedfordi Ingram & Macfie, C. leucostictus Kieffer, C. pycnostictus Ingram & Macfie, C. gulbenkiani Caeiro and C. milnei Austen. BTV-1 was not detected in 14 other Culicoides species tested; however, some of these were tested in limited numbers. The present study indicates a multivector potential for BTV transmission in South Africa. In C. imicola and C. bolitinos the replication rates are distinct and are significantly influenced by temperature. These findings are discussed in relation to the epidemiology of bluetongue in South Africa. [source] | ||||||||||