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Critical windows of early-life microbiota disruption on behaviour, neuroimmune function, and neurodevelopment

  • Caoimhe M.K. Lynch
  • , Caitlin S.M. Cowan
  • , Thomaz F.S. Bastiaanssen
  • , Gerard M. Moloney
  • , Nigel Theune
  • , Marcel van de Wouw
  • , Eva Florensa Zanuy
  • , Ana Paula Ventura-Silva
  • , Martin G. Codagnone
  • , Francisca Villalobos-Manríquez
  • , Matilde Segalla
  • , Fatma Koc
  • , Catherine Stanton
  • , Paul Ross
  • , Timothy G. Dinan
  • , Gerard Clarke
  • , John F. Cryan
  • University College Cork
  • Teagasc - Irish Agriculture and Food Development Authority

Research output: Contribution to journalArticlepeer-review

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.

Original languageEnglish
Pages (from-to)309-327
Number of pages19
JournalBrain, Behavior, and Immunity
Volume108
DOIs
Publication statusPublished - Feb 2023

Keywords

  • Adolescence
  • Adulthood
  • Behaviour
  • Critical windows
  • Development
  • Early life
  • Gut microbiota
  • Immune
  • Microglia
  • Myelin

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