Gut microbiota as a modulator of circadian neural development in the honey bee model.
KORU, Y. B.; Beer, K.; Ruggieri, A. A.; Rodriguez-Cordero, J. A.; Aviles-Rios, E.; Anderson, M.; Citron-Rodriguez, E. A.; Montes-Mercado, A.; De Jesus-Cortes, H.; Giannoni-Guzman, M. A.; Perez Claudio, E.; Courtney, E. C.; Andujar-Sierra, C. L.; Strubbe-Nieves, A.; Ortiz-Alvarado, Y.; Doke, M. A.; Ortiz-Zuazaga, H.; Moore, D.; Giordano, R.; Ghezzi, A.; Scheiner, R.; Giray, T.; Agosto-Rivera, J. L.
Show abstract
Disruption in gut microbiota during the early postnatal period can disrupt normal neural development and result in long-term behavioral alterations1. Similar to other neural systems, the circadian clock mechanism continues to mature after birth2, yet how microbial disturbances in the early period influence the onset of circadian rhythms and the development of central clock mechanisms remains poorly understood. Here we studied whether early-life gut dysbiosis affects the ontogeny of behavioral circadian rhythms and the maturation of clock neurons using the honey bee (Apis mellifera), a model organism that shares features of postnatal development of behavioral circadian rhythm and clock system3-5 with humans6. Our findings demonstrate that antibiotic-treated and gnotobiotic-reared bees display reduced rhythmicity compared to controls. These treatments also impair the development of the circadian pacemaker, marked by fewer Pigment-Dispersing Factor (PDF)-expressing neurons. Additionally, antibiotic exposure increased the expression of the Insulin-like Growth Factor Binding Protein Acid Labile Subunit (IGFALS) in early ages, which stabilizes the IGF-1/27, a hormone important for neurodevelopmental processes42. Together, these results identify gut microbiota as a modulator of circadian development. Our work provides an understanding of how early-life microbial disruptions influence the development of circadian rhythms, providing information that may extend to other animals, including humans.
Matching journals
The top 4 journals account for 50% of the predicted probability mass.
Similar papers in this journal
- The opposing Chloride Cotransporters KCC and NKCC control locomotor activity inconstant light and during long days. 93%
- Recognition of distinct sleep states in Drosophila uncovers previously obscured homeostatic and circadian control of sleep. 92%
- Polyamine elevation and nitrogen stress are toxic hallmarks of chronic sleep loss in Drosophila melanogaster 92%
Similar papers in this journal
Similar papers in this journal
Similar papers in this journal
- Lifespan prolonging mechanisms and insulin upregulation without fat accumulation in long-lived reproductives of a higher termite 93%
- Trade-offs between sperm viability and immune protein expression in honey bee queens (Apis mellifera) 92%
- Gut microbiota-mediated lipid accumulation as a driver of evolutionary adaptation to blue light toxicity in Drosophila 91%
"Similar papers" are the closest papers from that journal in the model's embedding space. They show what the match is built on, but the ranking comes mostly from a classifier over the whole training set, not from these examples alone.