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1.
BMC Genomics ; 22(1): 158, 2021 Mar 06.
Artículo en Inglés | MEDLINE | ID: mdl-33676394

RESUMEN

BACKGROUND: Maternal hormones, like testosterone, can strongly influence developing offspring, even generating long-term organizational effects on adult behavior; yet, the mechanisms facilitating these effects are still unclear. Here, we experimentally elevated prenatal testosterone in the eggs of zebra finches (Taeniopygia guttata) and measured male aggression in adulthood along with patterns of neural gene expression (RNA-seq) and DNA methylation (MethylC-Seq) in two socially relevant brain regions (hypothalamus and nucleus taenia of the amygdala). We used enrichment analyses and protein-protein interaction networks to find candidate processes and hub genes potentially affected by the treatment. We additionally identified differentially expressed genes that contained differentially methylated regions. RESULTS: We found that males from testosterone-injected eggs displayed more aggressive behaviors compared to males from control eggs. Hundreds of genes were differentially expressed, particularly in the hypothalamus, including potential aggression-related hub genes (e.g., brain derived neurotrophic factor). There were also enriched processes with well-established links to aggressive phenotypes (e.g., somatostatin and glutamate signaling). Furthermore, several highly connected genes identified in protein-protein interaction networks also showed differential methylation, including adenylate cyclase 2 and proprotein convertase 2. CONCLUSIONS: These results highlight genes and processes that may play an important role in mediating the effects of prenatal testosterone on long-term phenotypic outcomes, thereby providing insights into the molecular mechanisms that facilitate hormone-mediated maternal effects.


Asunto(s)
Pinzones , Testosterona , Agresión , Animales , Pinzones/genética , Hipotálamo , Masculino , Vitaminas
2.
Artículo en Inglés | MEDLINE | ID: mdl-29531144

RESUMEN

Human activities create novel food resources that can alter wildlife-pathogen interactions. If resources amplify or dampen, pathogen transmission probably depends on both host ecology and pathogen biology, but studies that measure responses to provisioning across both scales are rare. We tested these relationships with a 4-year study of 369 common vampire bats across 10 sites in Peru and Belize that differ in the abundance of livestock, an important anthropogenic food source. We quantified innate and adaptive immunity from bats and assessed infection with two common bacteria. We predicted that abundant livestock could reduce starvation and foraging effort, allowing for greater investments in immunity. Bats from high-livestock sites had higher microbicidal activity and proportions of neutrophils but lower immunoglobulin G and proportions of lymphocytes, suggesting more investment in innate relative to adaptive immunity and either greater chronic stress or pathogen exposure. This relationship was most pronounced in reproductive bats, which were also more common in high-livestock sites, suggesting feedbacks between demographic correlates of provisioning and immunity. Infection with both Bartonella and haemoplasmas were correlated with similar immune profiles, and both pathogens tended to be less prevalent in high-livestock sites, although effects were weaker for haemoplasmas. These differing responses to provisioning might therefore reflect distinct transmission processes. Predicting how provisioning alters host-pathogen interactions requires considering how both within-host processes and transmission modes respond to resource shifts.This article is part of the theme issue 'Anthropogenic resource subsidies and host-parasite dynamics in wildlife'.


Asunto(s)
Infecciones por Bartonella/veterinaria , Quirópteros/inmunología , Inmunidad Innata , Infecciones por Mycoplasma/veterinaria , Reproducción/fisiología , Inmunidad Adaptativa , Animales , Bartonella/inmunología , Infecciones por Bartonella/epidemiología , Infecciones por Bartonella/inmunología , Infecciones por Bartonella/microbiología , Belice/epidemiología , Quirópteros/microbiología , Ingestión de Alimentos/fisiología , Femenino , Interacciones Huésped-Patógeno/inmunología , Inmunoglobulina G , Ganado/fisiología , Linfocitos/inmunología , Linfocitos/microbiología , Masculino , Mycoplasma/inmunología , Infecciones por Mycoplasma/epidemiología , Infecciones por Mycoplasma/inmunología , Infecciones por Mycoplasma/microbiología , Neutrófilos/inmunología , Neutrófilos/microbiología , Perú/epidemiología , Dinámica Poblacional
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