Quantification of a glucocorticoid profile in non-pooled samples is pivotal in stress research across vertebrates

Vertebrates are faced continuously with a variety of potential stressful stimuli and react by a highly conserved endocrine stress response. An immediate catecholamine mediated response increases plasma glucose levels in order to prepare the organism for the "fight or flight" reaction. In addition, in a matter of minutes after this (nor) adrenaline release, glucocorticoids, in particular cortisol or corticosterone depending on the species, are released through activation of the hypothalamic-pituitary-interrenal (HPI) axis in fish or hypothalamic-pituitary-adrenal (HPA) axis in other vertebrates. These plasma glucocorticoids are well documented and widely used as biomarker for stress across vertebrates. In order to study the role of glucocorticoids in acute and chronic stress and gain in-depth insight in the stress axis (re)activity across vertebrates, it is pivotal to pin-point the involved molecules, to understand the mechanisms of how the latter are synthesized, regulated and excreted, and to grasp their actions on a plethora of biological processes. Furthermore, in-depth knowledge on the characteristics of the tissues as well as on the analytical methodologies available for glucocorticoid quantification is needed. This manuscript is to be situated in the multi-disciplinary research topic of glucocorticoid action across vertebrates which is linked to a wide range of research domains including but not limited to biochemistry, ecology, endocrinology, ethology, histology, immunology, morphology, physiology, and toxicology, and provides a solid base for all interested in stress, in particular glucocorticoid, related research. In this framework, internationally validated confirmation methods for quantification of a glucocorticoid profile comprising: (i) the dominant hormone; (ii) its direct precursors; (iii) its endogenously present phase I metabolites; and (iv) the most abundant more polar excreted exogenous phase I metabolites in non-pooled samples are pivotal

Quantification of a Glucocorticoid Profile in Non-pooled Samples Is Pivotal in Stress Research Across Vertebrates

Vertebrates are faced continuously with a variety of potential stressful stimuli and react by a highly conserved endocrine stress response. An immediate catecholamine mediated response increases plasma glucose levels in order to prepare the organism for the “fight or flight” reaction. In addition, in a matter of minutes after this (nor)adrenaline release, glucocorticoids, in particular cortisol or corticosterone depending on the species, are released through activation of the hypothalamic-pituitary-interrenal (HPI) axis in fish or hypothalamic-pituitary-adrenal (HPA) axis in other vertebrates. These plasma glucocorticoids are well documented and widely used as biomarker for stress across vertebrates. In order to study the role of glucocorticoids in acute and chronic stress and gain in-depth insight in the stress axis (re)activity across vertebrates, it is pivotal to pin-point the involved molecules, to understand the mechanisms of how the latter are synthesized, regulated and excreted, and to grasp their actions on a plethora of biological processes. Furthermore, in-depth knowledge on the characteristics of the tissues as well as on the analytical methodologies available for glucocorticoid quantification is needed. This manuscript is to be situated in the multi-disciplinary research topic of glucocorticoid action across vertebrates which is linked to a wide range of research domains including but not limited to biochemistry, ecology, endocrinology, ethology, histology, immunology, morphology, physiology, and toxicology, and provides a solid base for all interested in stress, in particular glucocorticoid, related research. In this framework, internationally validated confirmation methods for quantification of a glucocorticoid profile comprising: (i) the dominant hormone; (ii) its direct precursors; (iii) its endogenously present phase I metabolites; and (iv) the most abundant more polar excreted exogenous phase I metabolites in non-pooled samples are pivotal

Stress in wild and captive snakes : quantification, effects and the importance of management

As in other animals, distress and impaired welfare have a deleterious effect on the mental, physical and behavioral health of snakes in the wild and in captivity. Besides anthropogenic disturbance, the availability of food and shelter, the presence of predators, and environmental factors, such as seasonality and climatological changes, are important factors that affect the stress level and subsequent welfare in wild snake populations. In captive snakes, inappropriate management is the most prominent cause of chronic stress and impaired welfare. Chronic stress can be assumed by looking at the snake's behavior, but there is need for a standardized quantification method to pin-point more accurately (chronic) stress levels. The biomarker suitable in this framework is the level of corticosterone in plasma, feces and shed skin

Cortisol directly impacts Flavobacterium columnare in vitro growth characteristics

Teleost fish faced with stressful stimuli launch an endocrine stress response through activation of the hypothalamicpituitary-interrenal axis to release glucocorticoids, in particular cortisol, into the blood. For the majority of bacterial fish pathogens, stress is considered a key factor in disease outbreaks. Based upon studies in mammals, there is considerable evidence to suggest that, besides impairing the immune system, cortisol can have a direct effect on bacterial cells. Hitherto, this intriguing field of microbial endocrinology has remained largely unexplored in aquatic diseases. The present study investigated in vitro the impact of cortisol on phenotypic traits of the fresh water fish pathogen Flavobacterium columnare. Colonies obtained from the highly virulent (HV) isolates resulted in significantly larger and more spreading colonies compared to those from the low virulent (LV) isolates. High cortisol doses added displayed a direct effect on the bacterial cells and induced a significant decrease in colony size. An additional intriguing finding was the inverse relationship between cortisol concentrations added to the broth and the spreading character of colonies retrieved, with higher cortisol doses resulting in less rhizoid to rough and even smooth colony formation (the latter only in the LV trout isolate), suggesting a dose-response effect. The loss of the rhizoid appearance of the F. columnare colonies upon administration of cortisol, and hence the loss of motility, might indicate a phenotypic change to the biofilm state. These findings form the basis for further research on the impact of glucocorticoids on other virulence factors and biofilm formation of F. columnare

Phenotypic signatures of urbanization are scale-dependent : a multi-trait study on a classic urban exploiter

Understanding at which spatial scales anthropogenic selection pressures operate most strongly is a prerequisite for efficient conservation and management of urban biodiversity. Heterogeneity in findings on the strength and direction of urbanization effects may result from a lack of consensus on which spatial scales are most adequate when studying biotic effects of urbanization. Therefore, here, using the house sparrow (Passer domesticus) as model, we test the hypothesis that more than one spatial scale will explain variation among phenotypic stress markers. By applying a unique hierarchical sampling design enabling us to differentiate between local and regional effects of urbanization, we here show that the strength and direction of relationships with the percentage of built-up area - a simple structural measure of urbanization - vary among phenotypic stress markers and across the spatial range over which urbanization is measured. While inverse relationships with scaled body mass and bill height of adult house sparrows (Passer domesticus) were strongest when the degree of urbanization was quantified at city-level, similar relationships with corticosterone concentrations in feathers were only detected at the scale of individual home ranges. In contrast, tarsus length, wing length, and two measures of feather development were not significantly related to urbanization at any spatial scale. As the suite of phenotypic stress markers applied in this study revealed signatures of urbanization over a broad spatial range, we conclude that measures aimed at mitigating impacts of urbanization on free-ranging populations should best be implemented at multiple spatial scales too

Bayesian uncertainty quantification framework for wake model calibration and validation with historical wind farm power data

The expected growth in wind energy capacity requires efficient and accurate models for wind farm layout optimization, control, and annual energy predictions. Although analytical wake models are widely used for these applications, several model components must be better understood to improve their accuracy. To this end, we propose a Bayesian uncertainty quantification framework for physics-guided data-driven model enhancement. The framework incorporates turbulence-related aleatoric uncertainty in historical wind farm data, epistemic uncertainty in the empirical parameters, and systematic uncertainty due to unmodelled physics. We apply the framework to the wake expansion parameterization in the Gaussian wake model and employ historical power data of the Westermost Rough offshore wind farm. We find that the framework successfully distinguishes the three sources of uncertainty in the joint posterior distribution of the parameters. On the one hand, the framework allows for wake model calibration by selecting the maximum a posteriori estimators for the empirical parameters. On the other hand, it facilitates model validation by separating the measurement error and the model error distribution. In addition, the model adequacy and the effect of unmodelled physics are assessable via the posterior parameter uncertainty and correlations. Consequently, we believe that the Bayesian uncertainty quantification framework can be used to calibrate and validate existing and upcoming physics-guided models

Modulation of innate immune-related genes and glucocorticoid synthesis in gnotobiotic full-sibling European sea bass (Dicentrarchus labrax) larvae challenged with Vibrio anguillarum

Although several efforts have been made to describe the immunoendocrine interaction in fish, there are no studies to date focusing on the characterization of the immune response and glucocorticoid synthesis using the host-pathogen interaction on larval stage as an early developmental stage model of study. Therefore, the aim of this study was to evaluate the glucocorticoid synthesis and the modulation of stress-and innate immune-related genes in European sea bass (Dicentrarchus labrax) larvae challenged with Vibrio anguillarum. For this purpose, we challenged by bath full-sibling gnotobiotic sea bass larvae with 107 CFU mL(-1) of V. anguillarum strain HI 610 on day 5 post-hatching (dph). The mortality was monitored up to the end of the experiment [120 hours post-challenge (hpc)]. While no variations were registered in non-challenged larvae maintained under gnotobiotic conditions (93.20% survival at 120 hpc), in the challenged group a constant and sustained mortality was observed from 36 hpc onward, dropping to 18.31% survival at 120 hpc. Glucocorticoid quantification and expression analysis of stress-and innate immunity-related genes were carried out in single larvae. The increase of cortisol, cortisone and 20 beta-dihydrocortisone was observed at 120 hpc, although did not influence upon the modulation of stress-related genes (glucocorticoid receptor 1 [gr1], gr2, and heat shock protein 70 [hsp70]). On the other hand, the expression of lysozyme, transferrin, and il-10 differentially increased at 120 hpc together with a marked upregulation of the pro-inflammatory cytokines (il-1 beta and il-8) and hepcidin, suggesting a late activation of defense mechanisms against V. anguillarum. Importantly, this response coincided with the lowest survival observed in challenged groups. Therefore, the increase in markers associated with glucocorticoid synthesis together with the upregulation of genes associated with the anti-inflammatory response suggests that in larvae infected with V. anguillarum a pro-inflammatory response at systemic level takes place, which then leads to the participation of other physiological mechanisms at systemic level to counteract the effect and the consequences of such response. However, this late systemic response could be related to the previous high mortality observed in sea bass larvae challenged with V. anguillarum