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Published on: March 25, 2016
Critical windows of early-life microbiota disruption on behaviour, neuroimmune function, and neurodevelopment
Caoimhe M K Lynch1, Caitlin S M Cowan2, Thomaz F S Bastiaanssen1
1APC Microbiome Ireland, University College Cork, Ireland; Department of Anatomy & Neuroscience, University College Cork, Ireland.
Insights
Targeted antibiotic use in early life disrupts the gut microbiome, impacting adolescent brain development, immune cells, and anxiety-related behaviors, with lasting effects into adulthood.
Area of Science:
- Microbiology
- Neuroscience
- Developmental Biology
Background:
- Early-life gut microbiota influences neurodevelopment and behavior.
- Antibiotic exposure in early life is linked to increased risk of immune and metabolic diseases.
- Previous studies show long-term effects of antibiotic-induced microbial disruption, but not targeted depletion during critical windows.
Purpose of the Study:
- To investigate the impact of targeted antibiotic-induced microbiota depletion during specific early-life developmental windows on later-life physiology and behavior.
- To understand how disrupting the gut microbiome during critical developmental periods affects neurodevelopmental outcomes.
Main Methods:
- Administered a broad-spectrum oral antibiotic cocktail to mice during three critical windows: postnatal (PN), pre-weaning (PreWean), or post-weaning (Wean).
- Assessed effects on caecal microbiome structure and function, circulating immune cells, neurophysiology (myelin gene expression, microglial morphology), and behavior (anxiety, social, depressive-like, memory) in later life.
Main Results:
- Targeted microbiota disruption during early life, particularly during weaning, caused enduring effects on the caecal microbiome into adolescence.
- Microbial disruption altered circulating immune cells and neurophysiology, including myelin-related gene expression in the prefrontal cortex and microglial morphology in the basolateral amygdala.
- Observed sex- and time-dependent effects on anxiety-related behaviors, with limited impact on social behavior and memory.
Conclusions:
- Early-life gut microbiota plays a crucial role during critical developmental windows.
- Targeted perturbations of the gut microbiota can have subtle but long-lasting effects on brain physiology and behavior into adolescence and adulthood.
Abstract:
Numerous studies have emphasised the importance of the gut microbiota during early life and its role in modulating neurodevelopment and behaviour. Epidemiological studies have shown that early-life antibiotic exposure can increase an individual's risk of developing immune and metabolic diseases. Moreover, preclinical studies have shown that long-term antibiotic-induced microbial disruption in early life can have enduring effects on physiology, brain function and behaviour. However, these studies have not investigated the impact of targeted antibiotic-induced microbiota depletion during critical developmental windows and how this may be related to neurodevelopmental outcomes. Here, we addressed this gap by administering a broad-spectrum oral antibiotic cocktail (ampicillin, gentamicin, vancomycin, and imipenem) to mice during one of three putative critical windows: the postnatal (PN; P2-9), pre-weaning (PreWean; P12-18), or post-weaning (Wean; P21-27) developmental periods and assessed the effects on physiology and behaviour in later life. Our results demonstrate that targeted microbiota disruption during early life has enduring effects into adolescence on the structure and function of the caecal microbiome, especially for antibiotic exposure during the weaning period. Further, we show that microbial disruption in early life selectively alters circulating immune cells and modifies neurophysiology in adolescence, including altered myelin-related gene expression in the prefrontal cortex and altered microglial morphology in the basolateral amygdala. We also observed sex and time-dependent effects of microbiota depletion on anxiety-related behavioural outcomes in adolescence and adulthood. Antibiotic-induced microbial disruption had limited and subtle effects on social behaviour and did not have any significant effects on depressive-like behaviour, short-term working, or recognition memory. Overall, this study highlights the importance of the gut microbiota during critical windows of development and the subtle but long-term effects that microbiota-targeted perturbations can have on brain physiology and behaviour.
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