The effect of avian brood parasitism on physiological responses of host nestlings.

Avian obligate brood parasites lay their eggs in the nests of other species that may provide care for the foreign offspring. Brood parasitism often imparts substantial fitness losses upon host nestlings when they are raised alongside the typically more competitive, larger, and older parasitic chick(s). Whereas fitness costs due to reduced host offspring survival in parasitized broods have been studied in detail, the physiological changes in host nestlings caused by parasitic nestmate(s) are less well known. We compared prothonotary warbler (Protonotaria citrea) nestlings, a host of the nest-sharing brown-headed cowbird (Molothrus ater), in experimentally parasitized vs. non-parasitized broods. Our aim was to determine whether cohabitation with brood parasitic young impacted host nestling baseline corticosterone plasma concentrations, immune responses, body condition, and mortality. Corticosterone levels and body condition of host nestlings were similar between nests with or without a cowbird nestmate, whereas host immune responses were lower and nestling mortality was greater in parasitized broods, irrespective of variation in brood size or total brood mass. We detected no trade-offs of baseline corticosterone levels with either immune responses or with body condition. These results suggest that this host species' nestlings experience some adverse fitness-relevant physiological effects in parasitized broods, but are also resilient in other aspects when coping with brood parasitism.

Inducible and Conditional Stimulation of Adult Hippocampal Neurogenesis Rescues Cadmium-Induced Impairments of Adult Hippocampal Neurogenesis and Hippocampus-Dependent Memory in Mice.

Cadmium (Cd) is a heavy metal and an environmental pollutant. However, the full spectrum of its neurotoxicity and the underlying mechanisms are not completely understood. Our previous studies demonstrated that Cd exposure impairs adult hippocampal neurogenesis and hippocampus-dependent memory in mice. This study aims to determine if these adverse effects of Cd exposure can be mitigated by genetically and conditionally enhancing adult neurogenesis. To address this issue, we utilized the transgenic constitutive active MEK5 (caMEK5) mouse strain we previously developed and characterized. This mouse strain enables us to genetically and conditionally activate adult neurogenesis by administering tamoxifen to induce expression of a caMEK5 in adult neural stem/progenitor cells, which stimulates adult neurogenesis through activation of the endogenous extracellular signal-regulated kinase 5 mitogen-activated protein kinase pathway. The caMEK5 mice were exposed to 0.6 mg/l Cd through drinking water for 38 weeks. Once impairment of memory was confirmed, tamoxifen was administered to induce caMEK5 expression and to activate adult neurogenesis. Behavior tests were conducted at various time points to monitor hippocampus-dependent memory. Upon completion of the behavior tests, brain tissues were collected for cellular studies of adult hippocampal neurogenesis. We report here that Cd impaired hippocampus-dependent spatial memory and contextual fear memory in mice. These deficits were rescued by the tamoxifen induction of caMEK5 expression. Furthermore, Cd inhibition of adult hippocampal neurogenesis was also reversed. This rescue experiment provides strong evidence for a direct link between Cd-induced impairments of adult hippocampal neurogenesis and hippocampus-dependent memory.

Physiological responses of host parents to rearing an avian brood parasite: An experimental study.

Raising an obligate avian brood parasite is costly for host parents because it redirects valuable parental resources from one's own offspring to genetically unrelated young. The costs of raising a brood parasite may be mediated by physiological stressors for foster parents if it requires greater or biased parental effort compared to raising non-parasitized broods. For example, upregulating glucocorticoid hormones or reducing immune responses may mediate a trade-off between resource allocation to a current brood versus future reproductive opportunities, but published data on parasitized hosts' physiology are scarce. Here we used an experimental approach to test if host parents respond to the presence of brood parasitic young through dynamic changes in their own physiology. We conducted our experiments with parasitic brown-headed cowbirds (Molothrus ater) fostered into nests of host prothonotary warblers (Protonotaria citrea). Relative to parents caring for non-parasitized control broods, parasitism increased baseline corticosterone levels and reduced body mass in adult male, but not in female, hosts. Immune responses to a novel antigen were depressed in both parents of parasitized broods compared to parents of non-parasitized broods. Additionally, we found that immune function increased along the breeding season regardless of treatment. These experiments also confirmed prior observational data that parasitized adult males have reduced return rates to breeding sites in years subsequent to raising cowbirds. The findings demonstrate diverse physiological effects of parasitism on the foster parents in our particular host-brood parasite system, yet we found no evidence of individual trade-offs between endocrine and immune responses of adult hosts.

Maternal experience with predation risk influences genome-wide embryonic gene expression in threespined sticklebacks (Gasterosteus aculeatus).

There is growing evidence for nongenetic effects of maternal experience on offspring. For example, previous studies have shown that female threespined stickleback fish (Gasterosteus aculeatus) exposed to predation risk produce offspring with altered behavior, metabolism and stress physiology. Here, we investigate the effect of maternal exposure to predation risk on the embryonic transcriptome in sticklebacks. Using RNA-sequencing we compared genome-wide transcription in three day post-fertilization embryos of predator-exposed and control mothers. There were hundreds of differentially expressed transcripts between embryos of predator-exposed mothers and embryos of control mothers including several non-coding RNAs. Gene Ontology analysis revealed biological pathways involved in metabolism, epigenetic inheritance, and neural proliferation and differentiation that differed between treatments. Interestingly, predation risk is associated with an accelerated life history in many vertebrates, and several of the genes and biological pathways that were identified in this study suggest that maternal exposure to predation risk accelerates the timing of embryonic development. Consistent with this hypothesis, embryos of predator-exposed mothers were larger than embryos of control mothers. These findings point to some of the molecular mechanisms that might underlie maternal effects.

A test of maternal programming of offspring stress response to predation risk in threespine sticklebacks.

Non-genetic maternal effects are widespread across taxa and challenge our traditional understanding of inheritance. Maternal experience with predators, for example, can have lifelong consequences for offspring traits, including fitness. Previous work in threespine sticklebacks showed that females exposed to simulated predation risk produced eggs with higher cortisol content and offspring with altered anti-predator behavior. However, it is unknown whether this maternal effect is mediated via the offspring glucocorticoid stress response and if it is retained over the entire lifetime of offspring. Therefore, we tested the hypothesis that maternal exposure to simulated predation risk has long-lasting effects on the cortisol response to simulated predation risk in stickleback offspring. We measured circulating concentrations of cortisol before (baseline), 15 min after, and 60 min after exposure to a simulated predation risk. We compared adult offspring of predator-exposed mothers and control mothers in two different social environments (alone or in a group). Relative to baseline, offspring plasma cortisol was highest 15 min after exposure to simulated predation risk and decreased after 60 min. Offspring of predator-exposed mothers differed in the cortisol response to simulated predation risk compared to offspring of control mothers. In general, females had higher cortisol than males, and fish in a group had lower cortisol than fish that were by themselves. The buffering effect of the social environment did not differ between maternal treatments or between males and females. Altogether the results show that while a mother's experience with simulated predation risk might affect the physiological response of her adult offspring to a predator, sex and social isolation have much larger effects on the stress response to predation risk in sticklebacks.