4.4 Article

Discrete role for maternal stress and gut microbes in shaping maternal and offspring immunity

Journal

NEUROBIOLOGY OF STRESS
Volume 21, Issue -, Pages -

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.ynstr.2022.100480

Keywords

Prenatal stress; Microbiome; Antibiotics; Antifungals; Antimicrobials; Immune

Categories

Funding

  1. Ohio State University
  2. [K08MH112892]
  3. [R21MH117552]
  4. [T32 NS105864]

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Psychosocial stress during pregnancy can affect the immune function of both mothers and offspring, and the gut microbiome may play a role in this process. This study reveals that maternal stress and antimicrobial treatment independently influence maternal and offspring immunity, with some distinct effects.
Psychosocial stress is prevalent during pregnancy, and is associated with immune dysfunction, both for the mother and the child. The gut microbiome has been implicated as a potential mechanism by which stress during pregnancy can impact both maternal and offspring immune function; however, the complex interplay between the gut microbiome and the immune system is not well-understood. Here, we leverage a model of antimicrobial -mediated gut microbiome reduction, in combination with a well-established model of maternal restraint stress, to investigate the independent effects of and interaction between maternal stress and the gut microbiome in shaping maternal and offspring immunity. First, we confirmed that the antimicrobial treatment reduced maternal gut bacterial load and altered fecal alpha and beta diversity, with a reduction in commensal microbes and an increase in the relative abundance of rare taxa. Prenatal stress also disrupted the gut microbiome, according to measures of both alpha and beta diversity. Furthermore, prenatal stress and antimicrobials independently induced systemic and gastrointestinal immune suppression in the dam with a concomitant increase in circulating corticosterone. While stress increased neutrophils in the maternal circulation, lymphoid cells and monocytes were not impacted by either stress or antimicrobial treatment. Although the fetal immune compartment was largely spared, stress increased circulating neutrophils and CD8 T cells, and antibiotics increased neutrophils and reduced T cells in the adult offspring. Altogether, these data indicate similar, but discrete, roles for maternal stress and gut microbes in influencing maternal and offspring immune function.

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