Introduction

Autism Spectrum Disorders (ASD) are a class of neurodevelopmental disorders characterized by deficits in three domains including: impairments in social interactions, deficits in language and communication and increased stereotyped restrictive/repetitive behaviors and interests.1 Estimates of heritability among twin and sibling studies indicate a moderate genetic and a substantial environmental component to the etiology.2 Numerous reports have suggested that the maternal environment, particularly stressors that disrupt development in utero, has a significant role in the incidence of ASD.3, 4, 5 Of particular interest is the link between fetal gestation and the state of the maternal immune system activation during critical periods of development. Recent epidemiological reports suggest a strong association between periods of maternal immune activation, particularly during early pregnancy, and an increased risk of having a child with ASD.6, 7 Although these reports suggest a relationship between maternal immune activation and ASD, they have not yet been able to demonstrate a causal link.

Mouse models allow for translational studies of genetic and environmental contributions to neurodevelopmental disorders that can potentially establish plausible etiologies in clinical populations. For example, numerous mouse models of maternal immune activation have demonstrated that maternal viral and bacterial infection alters offspring behavior8, 9, 10, resulting in ASD-like phenotypes.11 In addition, transgenic mutant mice and inbred strains have been examined to investigate possible genetic contributions to ASD-like behaviors.12, 13, 14 These studies led to the discovery of the BTBR T+ tf/J (BTBR) mouse as an inbred strain predisposed to exhibit ASD-like behaviors compared with those of the species-typical C57BL/6J (C57) mouse.15 These behaviors include reduced levels of reciprocal social interactions,16 a lack of species-typical sociability,15 unusual repertoire of ultrasonic vocalizations17 and significantly higher levels of repetitive self-grooming.15

Although mouse models have successfully identified genetic and maternal environmental factors that contribute to ASD independently, few studies have considered how these two factors work in combination. It is important to fill this gap in our knowledge, given the recent emphasis on understanding the importance of gene x environment interactions in human populations.18 Previous studies investigating the role of maternal immune activation on offspring development have only examined the effects on a single mouse strain,8, 10, 11, 19 with few studies considering how genetic differences contribute to the behavioral phenotype.20, 21 Moreover, while the BTBR mouse has been shown to exhibit behavioral patterns thought to be relevant to the core domains of ASD,15 it is unknown whether these behaviors can be further exacerbated by the effects of environmental insults, such as maternal immune system activation.

The BTBR mouse exhibits aberrant immune responses that may contribute to its characteristic phenotype.22 This link between immune system dysregulation and ASD-like behaviors parallels human clinical research reporting atypical immune system responses in individuals with ASD.23 For example, children with ASD have increased levels of several cytokines in the plasma, including interleukin (IL)-1 and IL-6.24 Moreover, production of the proinflammatory cytokine tumor necrosis factor (TNF)α is increased in response to in vitro stimulation of peripheral blood mononuclear cells from children with ASD, and this response is associated with increases in repetitive stereotypical behaviors.25 Given this link between immune system dysregulation and ASD, as well as the important role genetic makeup plays in susceptibility, it is important to take these factors into account when using animal models to elucidate the etiology of ASD. More specifically in mouse models, it is important to consider how the effects of environmental insults, such as maternal immune activation may be dependent on genetic variations across strains. To this end, it is hypothesized that maternal immune activation will further exacerbate ASD-like behaviors and immune dysregulation in a mouse model with pre-existing genetic susceptibility to the behavioral phenotype (that is, BTBR). To test this, C57 and BTBR dams were exposed to the viral mimic polyinosinic-polycytidiylic acid (polyI:C) to activate the immune system during gestation, and the offspring were tested for ASD-like behaviors. Following behavioral testing, splenocytes were removed and measured for differences in cytokine release following in vitro immune stimulation.

Materials and methods

Animals

Male and female C57 (Jackson Laboratory, Sacramento, CA, USA) and BTBR (Jackson Laboratory, Bar Harbor Maine) mice were bred and maintained by the Center for Laboratory Animal Research, at University of California, Davis, and maintained at ambient room temperature on a 12 h light/dark cycle (light on at 0600 hours). Additionally, 129/SvImJ mice (Jackson Laboratory, Sacramento, CA) were used as stimulus mice for the three-chambered social approach task. Each strain was housed separately, and food and water were provided ad libitum. All behavioral procedures were performed during the first 4 h of the light cycle, and all procedures were performed with approval by the University of California, Davis Institutional Animal Care and Use Committee and in accordance with the guidelines provided by the National Institutes of Health Guide for the Care and Use of Laboratory Animals.

Maternal immune activation

Mice were mated overnight and females were checked daily for the presence of seminal plugs, noted as gestational day 0.5 (G0.5). On G12.5, pregnant female mice were weighed and injected with a single dose (20 mg/kg; i.p.) of polyI:C (Sigma Aldrich; St Louis, MO, USA) or saline vehicle as previously described.10 Each dam was returned to its cage and left undisturbed until the birth of its litter. All mice pups remained with the mother until weaning on postnatal day 21 (P21), at which time mice were group housed 3–4 per cage with same-sex littermates. One male and one female from each litter were used for all behavioral tests to reduce the likelihood of litter effects. There were a total of four possible conditions: C57-saline (n=16), C57-polyI:C (n=18), BTBR-saline (n=12) and BTBR-polyI:C (n=12).

Ultrasonic vocalizations

On postnatal day 6, mice were removed from the nest and placed in a 7.5 cm diameter holding cup in a sound-attenuated chamber. Ultrasonic vocalizations were recorded using a mini-3 bat detector tuned to 40 kHz and Ultravox software (Noldus Information Technology, Leesburg, VA, USA) set to detect ultrasonic vocalizations with durations greater than 10 ms as previously described.26, 27 An amplitude filter was used to eliminate extraneous peripheral noise. Only one male and female pup were tested from each litter, and pups were marked with non-toxic ink on their paws for identification and repeated recordings were taken on P6, P8, P10, P12 and P14.

Three-chamber social approach

Ten-week-old mice were tested for social preference using the automated three-chambered social approach apparatus.28, 29 Briefly, experimental mice were placed in the center chamber and allowed to habituate for 10 min followed by an additional 10 min of free exploration of all three chambers to confirm the absence of a side preference. Then, mice were returned to the center chamber while a novel 129/SvImJ mouse was placed under an inverted wire cup in one side chamber, and an identical empty wire cup was placed on the other side. Experimental mice were then given an additional 10 min to explore both chambers and measured for the time spent in each chamber. The chamber containing the novel mouse was counterbalanced to control for any bias in chamber preference. Experimental mice were video recorded during the social approach phase and later scored for the time they spent sniffing the novel mouse by two independent investigators blind to the treatments. A sociability score was calculated as the time in social chamber minus time in novel object chamber. All testing chambers were thoroughly cleaned with 70% ethanol in between each testing session.

Marble burying

One week following the social approach task, mice were habituated to clean Plexiglas cages (37 × 14 × 12.5 cm) filled with a 4 cm thick layer of clean corncob bedding for 10 min. Following habituation, animals were returned to their home cage and 15 glass marbles were laid out in five rows of three marbles placed equidistance apart. Mice were then returned to the cages and allowed to explore under dim illumination for 10 min. At the end of the 10 min period, animals were gently removed from the testing cages and the number of marbles buried was recorded. Only marbles covered by 75% or more bedding were counted as buried, as previously described.11

Grooming

Two days after marble burying, mice were observed for frequency of grooming behavior. Preliminary studies determined a significant alteration in grooming duration when bedding was placed in the cages. Therefore, all subsequent grooming measurements were made while mice were in an empty clean Plexiglas cage. Grooming times were analyzed as percent change from saline exposed C57 controls. Briefly, after 10 min of habituation, animals were video recorded for an additional 10 min and later scored for self-grooming behavior by two individuals blind to treatment conditions. Grooming was defined as time spent licking paws, washing the nose, face or scratching fur with any foot.

Cell stimulation

One week following behavior testing, mice were killed by cervical dislocation and spleens collected for tissue processing. Briefly, fresh spleens were homogenized using a dounce homogenizer to separate splenocytes from connective tissues and to generate cells in suspension. Cells were then pelleted and red blood cells lysed using ammonium chloride potassium lysis buffer. Cells (5 × 106 ml−1) were stimulated for 24 h in a complete Roswell Park Memorial Institute medium 1640 (Invitrogen, Carlsbad, CA, USA) media supplemented with 10% low endotoxin, heat inactivated fetal bovine serum (Invitrogen), 100 IU ml−1 penicillin, and 100 IU ml−1 streptomycin (Sigma, St Louis, MO, USA), 25 μg ml−1 gentimycin (Sigma), 50 μM 2-mecaptoethanol (Sigma) with media alone or media containing phorbol myristate acetate (PMA)/ionomycin (100 ng ml−1/100 uM). After 24 h, supernatants were collect and stored at −80 °C.

Cytokine analysis

The quantification of IL-6, IL-10, IL-17 and TNFα in supernatants was carried out using murine multiplexing bead immunoassays (Millipore, Billerica, MA, USA). Cytokine analysis was performed as recommended by the manufacturer’s specifications. Briefly, 25 μl of supernatant was incubated with antibody-coupled beads. After a series of washes, a biotinylated detection antibody was added to the beads, and the reaction mixture was detected by the addition of streptavidin–phycoerythrin. The bead sets were analyzed using a flow-based Luminex 100 suspension array system (Bio-Plex 200; Bio-Rad Laboratories, Hercules, CA, USA). Unknown sample cytokine concentrations were calculated by Bio-Plex Manager software using a standard curve derived from the known reference cytokine concentrations supplied by the manufacturer. A five-parameter model was used to calculate final concentrations and values are expressed in pg ml−1. The sensitivity of this assay allowed the detection of cytokine concentrations with the following limit of detection: IL-6 (1.7 pg ml−1), IL-10 (4.0 pg ml−1), IL-17 (0.4 pg ml−1) and TNFα (0.7 pg ml−1). Concentrations obtained below the limit of detection were assigned a value of limit of detection/2 for statistical comparisons. Supernatant aliquots had not undergone any previous freeze/thaw cycle.

Statistical analysis

Statistical analyses were carried out using SPSS version 20 (Chicago, IL, USA). For ultrasonic vocalizations, data were analyzed using repeated measures analysis of variance with strain, treatment and sex as between-subjects factors and postnatal day as within-subjects factor. For social sniff time, grooming, and marble burying tasks, three-way analysis of variance (strain × treatment × sex) was performed followed by least-square difference post hoc analysis when appropriate. For social approach data, initial chamber preference and the presence of a social preference were determined by separate paired-samples Student’s t-test for each strain-treatment group. Cytokine data were log transformed to allow for parametric analysis and analyzed by two-way analysis of variance (strain × treatment). Within-strain differences were analyzed using a priori planned comparisons. Cytokine concentrations were correlated with sociability scores, grooming and percent of marbles buried using spearman’s rho (see Supplementary Material). All statistical tests were two-tailed with the alpha set at 0.05.

Results

Ultrasonic vocalizations

The number of calls elicited by pups differed across postnatal days (F(4,53)=47.62, P<0.001) with fewer calls observed at older ages as shown in Figure 1a. There was a significant main effect for mouse strain, with BTBR offspring emitting more calls than C57 offspring (F(1,56)=29.37, P<0.001). There was also a significant day × treatment interaction (F(4,53)=2.77, P<0.05). Further analysis showed significant treatment effects on P8 (F(1,56)=4.54, P<0.05) and on P10 (F(1,56) =9.28, P<0.01). Individual group comparisons revealed that on P8 offspring of polyI:C-treated BTBR dams showed significantly increased numbers of ultrasonic vocalizations compared with BTBR offspring of saline-treated dams (P<0.05). This effect of polyI:C was not seen in offspring of C57 dams (P=0.60) (Figure 1b). By P10, both C57 (P<0.05) and BTBR (P<0.05) offspring whose dams were exposed to polyI:C during gestation displayed increased number of calls compared with offspring of saline-treated dams of either strain (Figure 1c). Interestingly, on P10 C57 mice of dams exposed to polyI:C elicited as many calls in a 2 min period as offspring of BTBR mice exposed to saline (59±8.26 and 66±9.88, respectively). These data depict a stepwise gene-environment interaction, in which strain or treatment independently increase the number of ultrasonic vocalizations but also have additive effects on pup-elicited calls. No significant sex differences were observed across any developmental time point (F(1,56)=0.07, P=0.79).

Figure 1
figure 1

Number of calls elicited during pup separation. (a) BTBR pups elicited more calls than C57 mice throughout postnatal development (*P<0.05). (b) On postnatal day 8, only BTBR offspring of polyI:C-treated dams produced more calls than offspring of saline-treated dams (*P<0.05). (c) On postnatal day 10, both C57 and BTBR mice exposed to polyI:C during gestation produced a significantly greater number of calls compared with saline-exposed controls of the same strain (*P<0.05).

Social approach

During the initial habituation phase of the social approach task there were no preferences for either empty side chamber (chamber 1 versus chamber 3) across either strain or treatment groups (Figure 2a). Although the BTBR offspring of polyI:C-exposed dams appeared to show a slight preference for chamber three, this preference was not statistically significant (t(13)=1.63, P=0.129). As shown in Figure 2b, C57 mice whose dams were exposed to saline during gestation showed a strong preference for the chamber housing a novel mouse (t(14)=6.03, P<0.001). In contrast, C57 offspring born from polyI:C-exposed dams displayed decreased preference for the chamber containing the novel mouse. However the preference for the novel mouse chamber was still significantly greater than for the chamber containing the object (t(17)=3.21, P<0.01). In contrast, BTBR offspring whose dams were exposed to saline failed to display a preference for the chamber with the novel mouse over the chamber with the object (that is, lack of preference for social stimuli) (t(11)=0.02, P=0.99). A similar asocial behavior was observed in BTBR offspring of dams exposed to polyI:C (t(11)=−1.47, P=0.17), (Figure 2b).

Figure 2
figure 2

Maternal immune activation decreases social approach and social sniff. (a) No significant chamber preferences were found during the initial habituation period. (b) C57 offspring from saline and polyI:C-exposed dams showed significant preferences for the chamber with the novel mouse (*P<0.05), although the magnitude of preference was lower in the C57-polyI:C group. BTBR offspring from both saline and polyI:C-treated dams failed to show a preference for the chamber with the novel mouse. (c) Analysis of sociability scores showed that C57 offspring of polyI:C-treated dams were significantly less social than C57 mice from saline-treated dams (*P<0.05). Although BTBR mice from both saline and polyI:C treatment dams had reduced sociability scores compared with C57-saline controls (*P<0.05), no differences were observed between BTBR treatment groups. (d) C57 offspring of polyI:C-exposed dams showed less social sniff time than C57 offspring of saline-exposed C57 dams (*P<0.05). Both groups of BTBR offspring also showed less social sniff time than C57 offspring of saline-exposed C57 dams (*P<0.05). No significant differences were found in social sniff times between BTBR mice of either treatment condition.

The sociability score, a measure of the magnitude of preference for a social stimulus, was determined by the difference between the time spent in the chamber with a novel mouse minus the time spent in the chamber with a novel object.30 A three-way analysis of variance revealed significant strain (F(1,56)=22.63, P<0.001) and treatment (F(1,56)=5.20, P<0.05) effects. The main effect for sex was not statistically significant (F(1, 56)=0.01, P=0.91). Post hoc analysis revealed a significant decrease in the sociability score for C57 offspring from dams exposed to polyI:C compared with offspring of saline-treated C57 dams (P<0.05) (Figure 2c). Interestingly, BTBR offspring from polyI:C-treated dams displayed significantly lower sociability scores compared with C57 offspring from both polyI:C (P<0.01) and saline (P<0.01)-treated dams.

Finally, Figure 1d shows that the time spent social sniffing was significantly different between strains (F(1,56)=6.66, P<0.05) and treatment groups (F(1,56)=4.25, P<0.05). These differences occurred independent of sex (F(1,56)=0.001, P>0.97). Post hoc analysis revealed that C57 offspring of dams exposed to polyI:C during development spent significantly less time sniffing the novel mouse compared with C57 offspring of saline exposed dams (P<0.05). Similarly, both groups of BTBR offspring spent less time sniffing the novel mouse compared with C57 offspring of saline-treated dams (P<0.05). No differences were observed between BTBR treatment groups.

Marble burying

During the 10 min marble burying task (Figure 3), offspring of BTBR dams buried a larger percent of marbles than offspring of C57 dams (F(1,56)=51.66, P<0.001). In addition, offspring of dams exposed to polyI:C buried a larger percent of marbles than offspring of dams exposed to saline (F(1,56)=10.48, P<0.01). Within mouse strain comparisons showed that C57 offspring of dams exposed to polyI:C buried a higher percent of marbles than offspring of saline-exposed dams (P<0.05). Despite this increase, C57 offspring of polyI:C-exposed dams buried fewer marbles compared with BTBR offspring of saline-exposed dams (P<0.05). Finally, BTBR offspring of polyI:C-exposed dams buried a higher percentage of marbles compared with all other groups (P<0.05 for all comparisons) (Figure 3).

Figure 3
figure 3

Marble burying behavior. BTBR offspring buried significantly more marbles than C57 offspring (P<0.001). In addition, offspring of C57 and BTBR dams exposed to polyI:C buried more marbles than same strain offspring of dams exposed to saline (*P<0.05).

Grooming

Time spent grooming for C57 offspring of saline-exposed dams was used as a baseline (that is, 100%) and percent change in grooming from this baseline was calculated for the other groups as shown in Figure 4. Statistical analysis showed a significant difference in grooming between strains, with BTBR offspring showing more grooming than C57 offspring (F(1,56)=3.93, P<0.05). There was also a significant sex by treatment interaction (F(1,56)=5.17, P<0.05), and therefore data for male and female offspring are presented separately in Figures 4a and b, respectively. As shown in Figure 4a, male BTBR offspring of polyI:C-exposed dams showed significantly more grooming than male BTBR offspring of saline-exposed dams (P<0.05). This effect of polyI:C exposure was not significant in male C57 offspring or in female BTBR or C57 offspring.

Figure 4
figure 4

Maternal immune activation and sex-specific increases in grooming. (a) Overall, male BTBR offspring showed more grooming than male C57 offspring (P<0.05). BTBR offspring of polyI:C-treated dams showed significantly more grooming than BTBR offspring from saline-treated dams. The apparent difference between treatment groups of C57 mice did not reach significance. (b) Overall, female BTBR offspring showed significantly more grooming than female C57 offspring (*P<0.05). However, for females there were no significant treatment effects on grooming for either strain.

Dynamic immune response

Analysis of splenocyte responses to stimulation by phorbol myristate acetate/ionomycin, revealed significant increases in immune response between mice strains (IL-6, F(1,45)=16.53, P<0.001; IL-10, F(1,45)=20.60, P<0.001; IL-17, F(1,45)=18.91, P<0.001; and TNFα, F(1,45)=18.91, P<0.001), with BTBR mice expressing increased concentrations of all cytokines measured (Figure 5). While maternal polyI:C exposure had no effect on IL-6 production in either strain (Figure 5a), a significant strain × treatment interaction was observed in the release of IL-17 (F(1,45)=5.44, P<0.05) (Figure 5b), and increases of IL-10 (F(1, 45)=3.29, P=0.08) and of TNFα (F(1,45)=3.16, P=0.08) approached statistical significance (Figures 5c and d). Planned comparisons for polyI:C treatment effects within strain showed that offspring of polyI:C-treated BTBR dams produced greater levels of IL-17 (t(22)=2.82, P<0.05) and IL-10 (t(22)=2.02, P=0.05) compared with offspring of BTBR-saline controls, while the increase in TNFα was not significant (t(22)=1.82, P=0.08). For C57 offspring, maternal exposure to polyI:C did not affect release of any of the four cytokines measured. Concentrations of all four cytokines measured were significantly correlated with marble burying and grooming behavior, but not sociability scores (see Supplementary Table S1). These associations were most apparent across strains (see Supplementary Figures S2–S4).

Figure 5
figure 5

Dysregulated cytokine responses in offspring of polyI:C-treated dams. (a) IL-6 levels were significantly higher in BTBR than C57 offspring (*P<0.05). (b) IL-17 levels were significantly elevated in BTBR offspring versus C57 mice (*P<0.05) and levels were higher in BTBR-polyI:C offspring than BTBR-saline offspring (**P<0.05). (c) BTBR mice expressed greater concentrations of IL-10 compared with C57 mice and increased levels of IL-10 in BTBR offspring of polyI:C-treated dams compared with BTBR mice of saline-exposed dams approached significance (§P=0.05). (d) Both BTBR treatment groups expressed higher concentrations of TNFα compared with C57 mice with even greater increases observed in BTBR offspring of polyI:C-treated dams, though not statistically significance (§P=0.08).

Discussion

Although heritability of ASD is substantial, the discordance rate in ASD among monozygotic twins is also large,2, 31, 32, 33, 34, 35 making it apparent that genetic factors alone cannot account for the incidence of ASD. Instead, it is likely that an interaction between genetic predisposition and environmental insult during early prenatal or postnatal development contributes to the etiology of ASD. The current results document previously reported differences between C57 and BTBR mouse strains in several behaviors relevant to autism, including increased pup ultrasonic vocalizations,17 reduced social approach, and more self-grooming behaviors in the BTBR.15 In addition, the present results also show that a single polyI:C injection on gestational day 12.5 can increase vocalizations, impair social behaviors and increase marble burying, with many of these effects being substantially more robust in BTBR mice. However, polyI:C-induced changes were not observed during the social approach task in BTBR mice. This observation is likely due to a floor effect as BTBR mice inherently lack social preference in the three-chambered social approach task. Interestingly, the behavioral deficits observed after maternal immune activation on C57 mice closely resembled the phenotype of typical BTBR mice (that is, BTBR-saline). These findings demonstrate that either genetic predisposition or environmental factors may have similar effects on behavior, but the combination of genetic predisposition (that is, BTBR mouse strain) and exposure to an environmental insult (that is, polyI:C) appears to be synergistic resulting in greater behavioral impairment than from either factor alone. Therefore, the complex spectrum of behavioral symptoms observed in human ASD populations may be due to the contributions of genetic, environment and to the additive effects of these factors.

Previous research in mouse models relevant to ASD has underscored the importance of both genetic makeup and the environment in the development of ASD-like behaviors. For example, systematic phenotyping of ASD-like behaviors across mouse strains has revealed a spectrum of behavioral responses dependent on genetic background.12, 13, 36 These studies identified the BTBR strain as a model organism that exhibits behavioral deficits modeling all three core domains of ASD.15 Similarly, studies have used mouse models to examine the effects of viral and bacterial infection on offspring behavior (for review see9). For example, Malkova et al.11 demonstrated a direct link between maternal polyI:C exposure and the expression of ASD-like behaviors in exposed offspring. Many of the behavioral outcomes observed in offspring of dams exposed to polyI:C in the current report are in line with previously reported findings, including deficits in social interaction and increased marble burying. However, increased grooming and more frequent ultrasonic vocalization calls are not in agreement. These difference may reflect variations in methodological approaches between reports including differences in the dose, developmental dates when injected, and the number of exposures to polyI:C. In addition, it is important to highlight the different approaches to mitigating litter effects between prior maternal immune activation studies and the current findings. One plausible explanation for discrepancies in the behavioral outcomes observed in the current study and prior reports may be due to the finding that maternal immune activation alters gene expression differently for each pup within a single litter.37 This notion would suggest that the effects of maternal polyI:C exposure on offspring behavior are dependent on additional factors and warrants further investigation into the mechanisms linking maternal immune activation to the expression of ASD-like behaviors.

Activation of the maternal immune system results in a cascade of inflammatory responses that are dependent on the pathogenic agent. The viral mimic polyI:C is a toll-like receptor 3 agonist that stimulates maternal immune responses resulting in behavioral alterations that are mediated through an IL-6 dependent pathway.8 Blockade of IL-6 activity by administering anti-IL-6 antibodies inhibits the generation of social deficits in offspring of polyI:C-treated dams.10 Moreover, pregnant dams injected with IL-6 produce offspring exhibiting a phenotype similar to offspring of polyI:C-treated mothers, suggesting that polyI:C and IL-6 alter offspring behavior through a conserved signaling pathway.8 In both polyI:C and IL-6 treatment regimens, IL-6 activity mediates changes in hormone growth factors important for appropriate development.8 Moreover, maternal exposure to polyI:C alters synaptic protein expression and downregulates specific N-Methyl-D-aspartate (NMDA) receptor subunits in the offspring38, suggesting a disruption in proper neuronal connectivity and an imbalance in excitatory/inhibitory inputs,39 two pathologies associated with ASD.40, 41

The finding that a transient activation of the maternal immune system during gestation can produce lasting changes in offspring behavior underscores the importance of the prenatal environment on brain development and the emergence of complex behaviors. The gestational period is a time of critical development when perturbations can alter neuronal migration, differentiation and connectivity across the brain.42 Therefore, it is not surprising that environmental insults can produce differential effects on the brain depending on when the insult occurs during development. Indeed, maternal treatment with polyI:C has previously been shown to elicit distinct phenotypes in offspring dependent on whether the immune activating agent was given early or late in gestation. For example, offspring of dams exposed to polyI:C on gestational day 9 exhibit impaired sensorimotor gating, whereas mice from dams injected with polyI:C on gestational day 17 are characterized by impairments in working memory.19 BTBR and C57 mice in the current report were exposed to polyI:C on gestational day 12.5, a time point previously shown to result in autism-like behaviors in mouse offspring.10 These differences in behavioral phenotypes produced when the immune activating agent is introduced early, middle or late in gestation highlight the importance of critical developmental windows and demonstrate the diverse behavioral outcomes that can be produced with a single environmental insult.

In addition to the temporal onset of exposure to environmental agents, genetic makeup may also contribute to the expression of ASD-like behaviors and its underlying pathophysiology. In this study, we found that the effects of maternal immune activation were more pronounced in the BTBR strain when compared with the C57 strain, supporting the notion that the effects of maternal immune activation are dependent on pre-existing genetic factors. This finding warrants careful consideration of the genetic variations between strains that may give rise to their distinct phenotypes. To date, the genetic links to the BTBR’s ASD-like behavioral profile are not well-understood and likely due to multiple genetic factors. One potential gene candidate that may contribute to the additive effects observed in the current report is the Disrupted In Schizophrenia 1 (Disc1) gene. BTBR mice are an inbred strain derived from the 129 mouse,43, 44, 45 a strain known to lack the Disc1 gene.46 Transgenic mice possessing a mutant form of Disc1 show increased anxiety, depression and social behavior deficits when born from dams exposed to polyI:C during gestation,47 demonstrating the important role that gene × environment interactions play in behavioral outputs. These Disc1 mutant mice were also reported to express altered cytokine levels that were futher disrupted when their dams were exposed to polyI:C. Similarly, BTBR mice in the current report produced greater release of IL-6, IL-17, IL-10 and TNFα when challenged with phorbol myristate acetate/ionomycin compared with C57 mice, and these increases were further exacerbated in offspring of dams whose immune system was activated during gestation by polyI:C. While our findings follow similar trends to previous reports,47 these similarities must be met with caution as the studies differ in the timing of polyI:C exposure. Interestingly, one report suggested that maternal immune activation is associated with the increase of IL-6 and IL-17 production in C57 offspring.48 However, in the current study, C57 offspring of polyI:C-treated dams tested as adults failed to exhibit alterations in IL-6 production, a finding consistent with other reports demonstrating altered cytokine levels in periadolescence but not adult offspring of maternal immune activated dams.49

The potential contributions of peripheral cytokine dysregulation on central nervous system function is an area of research that is gaining attention in the study of neurodevelopmental disorders. Cytokine receptors are expressed in the brain and exhibit region-specific difference in their distribution patterns across development.50, 51 Although cytokine proteins do not readily penetrate the blood brain barrier, there are several mechanisms that are proposed to mediate cytokine signaling between the periphery and the brain. These pathways include active transport through the blood–brain barrier,52 activation of peripheral nerve fibers (for example, vagus nerve) that innervate cytokine releasing cells in the brain,53 and recruiting peripheral immune cells (that is, monocytes/macrophages) into the brain.54 Although cytokines were originally identified as immune-specific signaling molecules, it is becoming increasingly apparent that their release can modulate neuronal function. For example, IL-6 and TNFα modulate serotonin production through the activation of indoleamine-2,3-dioxygenase55, and TNFα release can alter both glutamate release and reuptake.56, 57 In mice, disruption of cytokine signaling through receptor blockade or gene deletion produces cytokine-specific changes in ASD-related behaviors, including memory deficits and social withdrawal (for review see23). Together, the complex interplay between immune and neural signaling along with our reported association between behavioral deficits and cytokine concentrations warrant future research on immune-related treatment strategies to target ASD-like behaviors.

In summary, our findings demonstrate the additive effects of genetic predisposition and maternal polyI:C exposure on the severity of ASD-like behaviors in mice. Moreover, maternal immune activation potentiates immune responses in offspring in a strain-dependent manner. These data further indicate the need to consider how genetic predisposition may exacerbate or protect against the effects of environmental insults in the etiology of ASD and underscore the importance of strain selection in the use of rodent models of neurodevelopmental disorders.