Maternal antibiotics disrupt microbiome, behavior, and temperature regulation in unexposed infant mice

Christopher Harshaw1, Sayuri Kojima2, Cara L Wellman2

  • 1Department of Psychology, University of New Orleans, New Orleans, Louisiana, USA.

Insights

Maternal antibiotic exposure disrupts offspring gut microbiota and thermoregulation, impacting early autism spectrum disorder (ASD)-relevant behaviors. These disruptions suggest potential metabolic confounders in early-life antibiotic studies.

Area of Science:

  • Microbiology
  • Neuroscience
  • Developmental Biology

Background:

  • Maternal antibiotic exposure can alter the maternal-offspring microbiome transfer.
  • Early-life dysbiosis is linked to neurodevelopmental disorders, including autism spectrum disorder (ASD).
  • Limited research exists on the preweaning behavioral effects of maternal antibiotic exposure in rodent models.

Purpose of the Study:

  • To investigate the impact of maternal antibiotic exposure on ASD-relevant behaviors in preweaning mice.
  • To assess thermoregulatory competence in offspring exposed to maternal antibiotics.
  • To explore potential links between thermoregulation, microbiome disruption, and behavioral changes.

Main Methods:

  • Antibiotic treatment of C57BL/6J mouse dams during gestation and early lactation.
  • Assay of offspring behaviors: ultrasonic vocalizations (USVs) during maternal separation, huddling, and home orientation.
  • Measurement of pup thermoregulatory competence.

Main Results:

  • Offspring of antibiotic-treated dams exhibited altered USV production and huddling behavior.
  • Thermoregulatory deficiencies were observed in pups from antibiotic-exposed dams, particularly at younger ages.
  • Behavioral differences were partially attributable to thermoregulatory deficits.

Conclusions:

  • Early-life maternal antibiotic exposure disrupts the microbiome, thermoregulation, and behavior in offspring.
  • Thermoregulatory impairments may underlie some observed behavioral alterations.
  • Metabolic effects could confound the interpretation of behavioral changes following early-life antibiotic exposure.

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