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1.
Proc Biol Sci ; 290(2006): 20231305, 2023 09 13.
Artículo en Inglés | MEDLINE | ID: mdl-37700658

RESUMEN

Mechanisms aimed at recovering from heat-induced damages are closely associated with the ability of ectotherms to survive exposure to stressful temperatures. Autophagy, a ubiquitous stress-responsive catabolic process, has recently gained renewed attention as one of these mechanisms. By increasing the turnover of cellular structures as well as the clearance of long-lived protein and protein aggregates, the induction of autophagy has been linked to increased tolerance to a range of abiotic stressors in diverse ectothermic organisms. However, whether a link between autophagy and heat-tolerance exists in insect models remains unclear despite broad ecophysiological implications thereof. Here, we explored the putative association between autophagy and heat-tolerance using Drosophila melanogaster as a model. We hypothesized that (i) heat-stress would cause an increase of autophagy in flies' tissues, and (ii) rapamycin exposure would trigger a detectable autophagic response in adults and increase their heat-tolerance. In line with our hypothesis, we report that flies exposed to heat-stress present signs of protein aggregation and appear to trigger an autophagy-related homoeostatic response as a result. We further show that rapamycin feeding causes the systemic effect associated with target of rapamycin (TOR) inhibition, induces autophagy locally in the fly gut, and increases the heat-stress tolerance of individuals. These results argue in favour of a substantial contribution of autophagy to the heat-stress tolerance mechanisms of insects.


Asunto(s)
Drosophila melanogaster , Termotolerancia , Animales , Calor , Autofagia , Temperatura
2.
Insects ; 13(4)2022 Mar 23.
Artículo en Inglés | MEDLINE | ID: mdl-35447757

RESUMEN

Here we aimed to assess whether variation in (1) developmental temperature and (2) transport conditions influenced the low-temperature performance and flight ability of false codling moth (FCM) adults in an SIT programme. To achieve the first aim, larvae were exposed to either a (control) (constant 25 °C), a cold treatment (constant 15 °C) or a fluctuating thermal regime (FTR) (25 °C for 12 h to 15 °C for 12 h) for 5 days, whereafter larvae were returned to 25 °C to pupate and emerge. After adult emergence, critical thermal minimum, chill coma recovery time, life history traits and laboratory flight ability were scored. For the second aim, adult FCM were exposed to 4 or 25 °C with or without vibrations to simulate road transportation. After the pre-treatments, flight ability, spontaneous behaviour (i.e., muscle coordination by monitoring whether the moth moved out of a defined circle or not) and chill coma recovery time were determined. The first experiment showed that FTR led to enhanced cold tolerance, increased flight performance and high egg-laying capacity with minimal costs. The second experiment showed that transport conditions currently in use did not appear to adversely affect flight and low-temperature performance of FCM. These results are important for refining conditions prior to and during release for maximum field efficacy in an SIT programme for FCM.

3.
Curr Res Insect Sci ; 2: 100048, 2022.
Artículo en Inglés | MEDLINE | ID: mdl-36683956

RESUMEN

Insects have the ability to readily adapt to changes in environmental conditions, however the strength of local environmental adaptation signals under divergent conditions and the occurrence of trait inertia after relaxation of selection, remains poorly understood, especially for traits of climate stress resistance (CSR) and their phenotypic plasticity. The strength of environmental adaptation signals depend on several selection pressures present in the local environment, while trait inertia often occurs when there is a weakening or removal of a source of selection. Here, using Drosophila melanogaster, we asked whether signals of adaptation in CSR traits (critical thermal limits, heat and chill survival and, desiccation and starvation resistance) persist after exposure to laboratory culture for different durations (two vs. ten generations) across four climatically distinct populations. We show that culture duration has large effects on CSR traits and can both amplify or dilute signals of local adaptation. Effects were however dependent upon interactions between the source population, acclimation (adult acclimation at either 18 °C, 23 °C or 28 °C) conditions and the sex of the flies. Trait plasticity is markedly affected by the interaction between the source population, the specific acclimation conditions employed, and the duration in the laboratory. Therefore, a complex matrix of dynamic CSR trait responses is shown in space and time. Given these strong interaction effects, 'snapshot' estimates of environmental adaptation can result in misleading conclusions about the fitness consequences of climate variability.

4.
J Insect Physiol ; 140: 104403, 2022 07.
Artículo en Inglés | MEDLINE | ID: mdl-35667397

RESUMEN

Cold acclimation may enhance low temperature flight ability, and salt loading can alter an insects' cold tolerance by affecting their ability to maintain ion balance in the cold. Presently however, it remains unclear if dietary salt impacts thermal acclimation of flight ability in insects. Here, we examined the effect of a combination of dietary salt loading (either NaCl or KCl) and low temperature exposure on the flight ability of Drosophila melanogaster at low (15 °C) and benign (optimal, 22 °C) temperatures. Additionally, we determined whether dietary salt supplementation translates into increased K+ and Na+ levels in the bodies of D. melanogaster. Lastly, we determined whether salt supplementation impacts body mass and wing morphology, to ascertain whether any changes in flight ability were potentially driven by flight-related morphometric variation. In control flies, we find that cold acclimation enhances low temperature flight ability over non-acclimated flies confirming the beneficial acclimation hypothesis. By contrast, flies supplemented with KCl that were cold acclimated and tested at a cold temperature had the lowest flight ability, suggesting that excess dietary KCl during development negates the beneficial cold acclimation process that would have otherwise taken place. Overall, the NaCl-supplemented flies and the control group had the greatest flight ability, whilst those fed a KCl-supplemented diet had the lowest. Dietary salt supplementation translated into increased Na+ and K+ concentration in the body tissues of flies, confirming that dietary shifts are reflected in changes in body composition and are not simply regulated out of the body by homeostasis over the course of development. Flies fed with a KCl-supplemented diet tended to be larger with larger wings, whilst those reared on the control or NaCl-supplemented diet were smaller with smaller wings. Additionally, the flies with greater flight ability tended to be smaller and have lower wing loading. In conclusion, dietary salts affected wing morphology as well as ion balance, and dietary KCl seemed to have a detrimental effect on cold acclimation responses of flight ability in D. melanogaster.


Asunto(s)
Drosophila melanogaster , Cloruro de Sodio Dietético , Aclimatación/fisiología , Animales , Frío , Suplementos Dietéticos , Drosophila melanogaster/fisiología , Sodio , Cloruro de Sodio/farmacología
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