Prenatal and postnatal maternal contributions in the infection model of schizophrenia
Urs Meyer1, Severin Schwendener, Joram Feldon
1Laboratory of Behavioural Neurobiology, Swiss Federal Institute of Technology Zurich, Schorenstrasse 16, 8603, Schwerzenbach, Switzerland.
Insights
Prenatal immune challenge can lead to later psychosis, but postnatal maternal factors also play a role. Specifically, being raised by an immune-challenged mother can cause learning deficits in offspring, regardless of prenatal exposure.
Area of Science:
- Neuroscience
- Immunology
- Developmental Psychology
Background:
- Prenatal exposure to pathogens is linked to increased schizophrenia risk.
- Rodent studies support a link between prenatal immune challenge and later psychosis-related brain and behavioral changes.
- The impact of postnatal maternal factors on psychopathology following prenatal immune stimulation is poorly understood.
Purpose of the Study:
- To investigate the combined effects of prenatal immune challenge and postnatal maternal environment on offspring psychopathology.
- To determine the relative contributions of prenatal inflammatory events and postnatal maternal factors in precipitating juvenile and adult psychopathology.
- To utilize a cross-fostering design to disentangle these influences.
Main Methods:
- Pregnant mice were administered polyriboinosinic-polyribocytidilic acid (PolyI:C), a viral mimic, or vehicle on gestation day 9.
- Offspring were cross-fostered to surrogate mothers with either inflammatory or vehicle treatment during pregnancy.
- Latent inhibition (LI) was assessed in juvenile and adult offspring using classical and instrumental conditioning paradigms.
Main Results:
- Prenatal PolyI:C exposure did not affect juvenile LI but caused post-pubertal LI disruption, irrespective of postnatal rearing.
- Prenatal control offspring adopted by PolyI:C-treated mothers showed pre- and post-pubertal LI loss.
- Adoption by control mothers did not protect prenatally immune-challenged offspring from adult psychopathology.
Conclusions:
- Postnatal maternal inflammatory environment is sufficient to induce learning disabilities in offspring, even without prenatal immune challenge.
- Prenatal immune challenge leads to lasting deficits in learning and memory, which are not ameliorated by a healthy postnatal environment.
- These findings highlight the critical role of both prenatal and postnatal maternal factors in neurodevelopmental outcomes and psychopathology risk.
Abstract:
Epidemiological studies have indicated that the risk of schizophrenia is enhanced by prenatal maternal infection with viral or bacterial pathogens. Recent experimentation in rodents has yielded additional support for a causal relationship between prenatal immune challenge and the emergence of psychosis-related abnormalities in brain and behaviour in later life. However, little is known about the putative roles of maternal postnatal factors in triggering and modulating the emergence of psychopathology following prenatal immunological stimulation. Here, we aimed to dissect the relative contributions of prenatal inflammatory events and postnatal maternal factors in precipitating juvenile and adult psychopathology in the resulting offspring with a cross-fostering design. Pregnant mice were exposed to the viral mimic, polyriboinosinic-polyribocytidilic acid (PolyI:C; at 5 mg/kg, intravenously), or vehicle treatment on gestation day 9, and offspring born to PolyI:C- and vehicle-treated dams were then simultaneously cross-fostered to surrogate rearing mothers, which had either experienced inflammatory or vehicle treatment during pregnancy. Prenatal PolyI:C administration did not affect the expression of latent inhibition (LI) at a juvenile stage of development, but led to the post-pubertal emergence of LI disruption in both aversive classical and instrumental conditioning regardless of the postnatal rearing condition. In addition, deficits in conditioning as such led to a pre- and post-pubertal loss of LI in prenatal control animals that were adopted by PolyI:C-treated surrogate mothers. Our findings thus indicate that the adoption of prenatally immune-challenged neonates by control surrogate mothers does not possess any protective effects against the subsequent emergence of psychopathology in adulthood. At the same time, however, the present study highlights for the first time that the adoption of prenatal control animals by immune-challenged rearing mothers is sufficient to precipitate learning disabilities in the juvenile and adult offspring.
More Related Videos
Related Concept Videos
Biological Causes of Schizophrenia
Genetic Factors in Schizophrenia
The genetic basis of schizophrenia is strongly supported by family and twin studies.
Development of the Oral Microbiota
Gut-Brain Axis
Development of Immunocompetence
The initial cells that migrate from the fetal thymus settle within the skin and epithelial tissues lining the mouth, digestive tract, and in females, the uterus and vagina. These cells, including skin-based dendritic cells, serve as antigen-presenting cells, playing a key role in T cell activation.
Subsequent T...


