Abstract
Autism spectrum disorder (ASD), a group of neurodevelopmental disorders characterized by social communication deficits and stereotyped behaviors, may be associated with changes to the gut microbiota. However, how gut commensal bacteria modulate brain function in ASD remains unclear. Here, we used chromodomain helicase DNA-binding protein 8 (CHD8) haploinsufficient mice as a model of ASD to elucidate the pathways through which the host and gut microbiota interact with each other. We found that increased levels of amino acid transporters in the intestines of the mouse model of ASD contribute to the high level of serum glutamine and the increased excitation/inhibition (E/I) ratio in the brain. In addition, elevated α-defensin levels in the haploinsufficient mice resulted in dysregulation of the gut microbiota characterized by a reduced abundance of Bacteroides. Furthermore, supplementation with Bacteroides uniformis improved the ASD-like behaviors and restored the E/I ratio in the brain by decreasing intestinal amino acid transport and the serum glutamine levels. Our study demonstrates associations between changes in the gut microbiota and amino acid transporters, and ASD-like behavioral and electrophysiology phenotypes, in a mouse model.
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Introduction
Autism spectrum disorder (ASD), a group of heterogeneous neurodevelopmental disorders, is characterized by deficits in social communication and repetitive and stereotyped behaviors1. The reported incidence of ASD in children and adolescents is 1 in 59 in the United States2,3. ASD is believed to be influenced by genetic factors, including many de novo mutations and copy number variations identified by trio-based sequencing4,5,6, and environmental factors, which may include the gut microbiota7. In recent years, accumulating studies have proven the effects of the gut microbiota on neural activities8.
The gut microbiota has been shown to modulate the neural function and central nervous system (CNS)-related behaviors in physiological and pathological conditions9. In both people with ASD and animal models, gut microbiota dysbiosis has been reported10,11, and probiotics may alleviate the symptoms12. Despite the importance of gut microbiota in modulating neural activities, how gut commensal bacteria interact with the brain in ASD is still unclear. Lactobaciullus reuteri was shown to modulate the oxytocinergic and dopaminergic signaling pathways through the vagus nerve in ASD mouse models10. In addition, the gut microbiota metabolite 5-aminovaleric acid could rescue ASD-like behaviors by decreasing the excitability of pyramidal neurons in layer V in BTBR mice13. However, the identity of pathways other than the vagus nerve axis and the neuroactive compounds that mediate the neural function of the gut microbiota are unknown.
Since Chd8, which encodes the chromatin remodeler CHD8, is one of the top genes associated with ASD and individuals with Chd8 mutations exhibit gastrointestinal defects, Chd8+/− mice can be used as an ASD animal model to study the role of the gut microbiota in ASD and the underlying communication between the gut microbiota and the brain. Herein, we provided evidence for how the gut microbiota communicates with the brain via the neuroactive pathway in a model of ASD. Increased intestinal amino acid transport contributes to the increased excitation/inhibition (E/I) ratio with the increased glutamate levels in the brain, and the gut microbiota can restore the E/I imbalance in the brain by decreasing intestinal amino acid transport.
Results
Chd8 +/− mice exhibit anatomical abnormalities and ASD-like behaviors
To generate a Chd8 gene-deficient mouse model of autism, we deleted 13 bp from the first exon of the Chd8 gene, resulting in a frameshift mutation and a premature stop codon in Chd8 (Fig. 1a). Since the first exon is before most mutation sites in ASD linked to Chd8 defects14, the mouse model carrying a frameshift mutation at this position can mimic the effect of Chd8 mutants in individuals with ASD. Given that Chd8 homozygous mutant mice were reported to be embryonic lethal15, we used heterozygous mice and genotyped them by specific PCR primers targeting the mutant allele (Supplementary Fig. 1a, b). Subsequently, to verify the validity of the model, we examined Chd8 expression at the protein level; there are two isoforms, a full-length protein (280 kDa) and a smaller isoform (110 kDa). At the embryonic stage, in which Chd8 expression is high, the Chd8+/− mice showed significantly reduced expression of the full-length CHD8 protein in the brains (the whole brain and cerebral cortex) and intestines (Fig. 1b and Supplementary Fig. 1c), while the 110 kDa isoform did not change significantly in the whole brain or the cerebral cortex (Supplementary Fig. 1c). At the adult stage, the expression of the full-length CHD8 protein was also reduced in both the hypothalamus (Fig. 1b) and the cerebral cortex (Supplementary Fig. 1d) but could not be detected in the small intestine. The adult hypothalamus and the cerebral cortex showed no significant change in the expression of the 110 kDa isoform (Supplementary Fig. 1d). The adult and embryonic small intestines showed no expression of the 110 kDa isoform.
Similar to patients with mutant Chd8 exhibiting macrocephaly14, the Chd8+/− mice showed increased brain weights, with the most significant increase observed in their cerebrum and cerebellum (Fig. 1c and Supplementary Fig. 1e). The Chd8+/− mice exhibited a shortened small intestine and colon length (Fig. 1d), a decreased weight of the small intestine contents (Supplementary Fig. 1e), and a trend towards decreased intestinal motility (Supplementary Fig. 1f). These observed abnormalities of the gastrointestinal tract were similar to those reported in humans, zebrafish, and mouse models with Chd8 mutations14,15. The Chd8+/− mice also displayed weight loss at weeks 4, 12, and 18 (Fig. 1e), which was consistent with prior studies showing that individuals with ASD and mouse models with mutations in Chd8 showed weight loss14,16. We evaluated the feeding behavior of Chd8+/− mice but found no significant changes in food intake (Supplementary Fig. 1g).
Next, we explored whether the Chd8+/− mice exhibited ASD-like behaviors, including impaired social interaction, anxiety, learning and memory deficits, stereotyped behavior, and depression. Social interaction was examined using a three-chamber test and a reciprocal social interaction test. The Chd8+/− mice exhibited normal sociability (Supplementary Fig. 1h) and abnormal social novelty preferences (Fig. 1f) in the three-chamber test and no significant social interaction deficits in the reciprocal social interaction test (Supplementary Fig. 1i), suggesting mildly impaired social interaction. Anxiety-like behavior was studied via an open-field test and a light/dark box test. The Chd8+/− mice showed a decreased proportion of time in the center in the open-field test (Fig. 1g and Supplementary Fig. 1j) and a significantly reduced duration in the light box in the light/dark box test (Fig. 1h), indicating obvious anxiety. Learning and memory were examined using a novel object recognition test. The Chd8+/− mice displayed no significant difference in the exploration time of the old and novel objects, demonstrating learning and memory deficits (Fig. 1i). Stereotyped behavior was explored through a self-grooming test and a marble-burying test. The Chd8+/− mice did not exhibit a significantly increased grooming time in the self-grooming test or a significant increase in buried marbles in the marble-burying test, indicating no significant difference in stereotyped behavior (Supplementary Fig. 1k). The Chd8+/− mice also showed no significant difference in total distance traveled or movement velocity in the open-field test (Supplementary Fig. 1l), indicating no significant abnormality in motor function. Depression was detected via the forced swimming test. The Chd8+/− mice displayed no significant increase in immobility time (Supplementary Fig. 1m). Female Chd8+/− mice showed ASD-like behaviors similar to those of the male Chd8+/− mice (Supplementary Fig. 1n–t). These results indicated that the Chd8+/− mice have ASD-like behaviors, including anxiety, impaired social interaction, and learning and memory deficits.
Chd8 +/- mice exhibit an increased E/I ratio
The Chd8+/− mice exhibited ASD-like behaviors, but the etiology of these behaviors remains unknown. Given that oxytocin was associated with ASD and that ASD mouse models showed decreased oxytocin levels7,17, we investigated the oxytocin levels in the Chd8+/− mice. Immunofluorescence analysis did not show a significant difference in the level of oxytocin in the hypothalamic paraventricular nuclei (PVN) and the supraoptic nuclei (SON) (Supplementary Fig. 2a). In addition to the change in oxytocin, an E/I imbalance is one of the etiologies of ASD. An E/I imbalance has been reported in humans and several ASD animal models18,19,20. To evaluate the E/I imbalance in the Chd8+/− mice, we tested the miniature excitatory postsynaptic currents (mEPSCs) and the miniature inhibitory postsynaptic currents (mIPSCs) of pyramidal cells in neocortical layer V and observed an increased mEPSC frequency and a decreased mIPSC frequency but no significant differences in the amplitudes of the mEPSCs and mIPSCs (Fig. 2a, b). These results suggested that the Chd8+/− mice exhibit an E/I imbalance with an increased E/I ratio.
Next, we explored the mechanism underlying the E/I imbalance. Given that some amino acids can act as excitatory or inhibitory neurotransmitters or as neurotransmitter precursors and thus affect the E/I imbalance, we examined the levels of twenty-two common amino acids in the brain using a targeted metabolomics assay. The Chd8+/− mice showed increased levels of glutamate and glutamine and decreased levels of tryptophan and histidine in the brains (Supplementary Fig. 2b). Furthermore, the Chd8+/− mouse brains showed an increased glutamate/GABA ratio (Supplementary Fig. 2b), corroborating the finding of an increased E/I ratio at the neural circuit level (Fig. 2a, b). To explore these changes in different parts of the brain, we examined the glutamate, glutamine, and GABA levels in the cerebrum, brain stem, and cerebrum and found that the cerebrum displayed the most significant changes (Fig. 2c and Supplementary Fig. 2c).
Among the above amino acids, glutamate was selected, as it is the major excitatory neurotransmitter in the brain, and elevated glutamate levels indicate increased excitability21. We next explored the reasons for the increased glutamate level in the brain. Since glutamate cannot pass through the brain–blood barrier (BBB)22, this amino acid is synthesized in situ in the brain by the conversion of other substances23 (Supplementary Fig. 2d). Glutamate can be reversibly generated from glutamine, GABA, and αKG. We found an elevated level of glutamine and no significant differences in the αKG (Supplementary Fig. 2e) and GABA levels (Supplementary Fig. 2b, c), suggesting that the increased glutamate level in the brain might result from an increase in glutamine.
We next explored the reasons for the increased glutamine level in the brain; this change may be due to the conversion of other substances in the brain as well as the transport of serum glutamine to the brain via the BBB. We first focused on factors outside the brain that can influence the glutamine level in the brain, including the expression levels of neutral amino acid transporters at the BBB and the serum glutamine concentration. We examined the gene expression of the large neutral amino acid transporter LAT1 (SLC7A5)24,25 by single-cell RNA-seq (scRNA-seq) and found no significant difference in the expression level of Slc7a5 in endothelial cells of the Chd8+/− mice (Supplementary Fig. 2f, g). To test the serum glutamine level, we performed targeted metabolomics assays for twenty-two amino acids, including glutamine. The Chd8+/− mice showed significantly increased serum levels of glutamine and tryptophan (Fig. 2d and Supplementary Fig. 2h). These results suggest that increased serum glutamine in the Chd8+/− mice may contribute to the increased E/I ratio characterized by elevated glutamate levels and glutamate/GABA ratios.
Increased expression of intestinal amino acid transporters may contribute to the elevated serum amino acid levels of the Chd8 +/− mice
We subsequently explored the mechanisms underlying the elevated levels of serum glutamine and tryptophan in the Chd8+/− mice. Intestinal transport of amino acids to the blood is one of the main sources of amino acids in the serum. Therefore, we examined the expression of amino acid transporters in the small intestines using bulk RNA-seq. The Chd8+/− mice showed elevated expression of intestinal amino acid transporters (Fig. 2e and Supplementary Fig. 3a). Among these transporters, the neutral amino acid transporters responsible for glutamine and tryptophan transport were examined (Supplementary Fig. 3b). We found elevated expression levels of Slc6a19, Slc7a8, and Slc7a15 (Supplementary Fig. 3b) and validated them using quantitative PCR (qPCR) analyses (Supplementary Fig. 3c). We further verified the expression levels of amino acid transporters in intestinal epithelial cells using scRNA-seq experiments and observed increased expression levels of the three selected intestinal amino acid transporters and increased numbers of cells expressing these transporters (Fig. 2f–h and Supplementary Fig. 3d, e). Subsequently, we selected Slc6a19 and Slc7a8, two highly expressed transporters on the apical and basal lateral membranes of the intestinal epithelium, respectively, for protein detection. Both Western blot and immunofluorescence experiments confirmed the increased protein expression of the two transporters in the Chd8+/− mice (Fig. 2i, j). These results indicated that the increased expression of amino acid transporters in intestinal epithelial cells may lead to elevated serum amino acid levels in the Chd8+/− mice.
Since abnormal expression of intestinal amino acid transporters affects serum amino acid levels as well as fecal amino acid levels26, we next examined the levels of amino acids in the feces. Interestingly, we found that the levels of five amino acids, including glutamine and tryptophan, were significantly reduced in the feces of the Chd8+/− mice (Supplementary Fig. 3f). These results suggest that high expression of intestinal amino acid transporters may lead to more amino acids being absorbed in the serum and fewer amino acids being retained in the feces.
The gut microbiota is dysregulated in the Chd8 +/− mice
Given the reported role of the gut microbiota in ASD, we investigated the gut microbiota in the Chd8+/− mice. We performed metagenomic sequencing on the fecal DNA of adult mice to examine the gut microbiota. The beta diversity showed a substantial difference between the two groups of mice (Fig. 3a and Supplementary Fig. 4a). Furthermore, the Chd8+/− mice showed a significantly reduced abundance of Bacteroides, while the levels of other genera remained largely unchanged (Fig. 3b). In addition, at the species level, the abundances of Bacteroides uniformis, Bacteroides acidifaciens and Bacteroides vulgatus were significantly reduced in the Chd8+/− mice, with B. uniformis showing the largest fold change (Fig. 3c, d). Moreover, the alpha diversity and the microbiota composition at the phylum level did not differ significantly between the two groups of mice (Supplementary Fig. 4b, c).
To explore how changes in the gut microbiota affected the metabolism of intestinal contents, we performed a microbiota functional analysis. A total of 301 Kyoto Encyclopedia of Genes and Genomes (KEGG) orthologs (KOs) were found to be significantly enriched or depleted, most of which were involved in amino acid metabolism and metabolic signaling pathways (Supplementary Fig. 4d–f). Notably, eight KOs related to amino acids were significantly depleted in the Chd8+/− mice (Supplementary Fig. 4f), suggesting that the decreased amino acid levels in the feces of the Chd8+/− mice might be due to dysregulated gut microbiota.
We next investigated the presence of other metabolic changes in the intestines in addition to dysregulated gut microbiota. Short-chain fatty acids (SCFAs) have been associated with the gut–brain axis27, but the two groups of mice showed no significant changes in the SCFA levels in their feces (Supplementary Fig. 4g). Intestinal barrier dysfunction and BBB damage were also reported as mechanisms of gut–brain communication28,29, but the Chd8+/− mice did not exhibit increased intestinal permeability (Supplementary Fig. 4h) or BBB permeability (Supplementary Fig. 4i). These results indicated that the Chd8+/− mice showed a disturbance in the gut microbiota including a decreased abundance of Bacteroides.
Increased level of alpha defensins contributes to gut microbiota dysbiosis
We further explored how the host influenced the dysbiosis of gut microbiota in the Chd8+/− mice. Given that defensins, short peptides produced by intestinal Paneth cells, play a pivotal role in maintaining the homeostasis of the gut microbiota30, we screened eight common defensins expressed in the small intestine. The Chd8+/− mice showed elevated expression of Defa1 and Defa2 (Fig. 3e) but unchanged levels of the other six defensins (Supplementary Fig. 4j). Since the protein levels of defensin α1 were higher than those of defensin α2 in the contents of the small intestine, cecum, and colon of the Chd8+/+ mice (Fig. 3f), we focused on defensin α1. We found that the Chd8+/− mice exhibited increased protein levels of defensin α1 in the small intestinal and colonic contents (Fig. 3g).
To determine whether the increased defensin α1 level was sufficient to cause gut microbiota dysbiosis in the Chd8+/− mice, we treated the Chd8+/+ mice by gavage with defensin α1 every day for 8 consecutive days and examined the gut microbiota in their feces (Fig. 3h). The defensin α1-gavaged mice showed an increased abundance of Firmicutes (P = 0.027) (Fig. 3i), and the beta diversity at the genus level showed a significant difference between the two groups of mice (Fig. 3j and Supplementary Fig. 4k). The Chd8+/− mice showed a decrease in the abundance of Bacteroides in the gut microbiota, but this decrease was not found in the defensin α1-treated mice (Supplementary Fig. 4l). The Bray-Curtis (BC) distance and the Euclidean distance between the defensin α1-treated mice and the Chd8+/+ mice (D_W) was slightly greater than that between the defensin α1-treated mice and the Chd8+/− mice (D_K) (Fig. 3k and Supplementary Fig. 4m). In addition, the BC distance and the Euclidean distance between the water-treated mice and the Chd8+/− mice (H_K) were greater than that between the water-treated mice and the Chd8+/+ mice (H_W) (Supplementary Fig. 4n). These results indicate that the shifts in gut microbiota caused by defensin α1 treatment are partially towards ASD-like microbiota. To detect whether the influence of defensins on the microbiota, especially the level of B. uniformis, was a cumulative effect of multiple defensins, we treated the Chd8+/+ mice with defensin α1 and α2 every day by gavage for 8 consecutive days (Fig. 3l). We found that the defensin α1 and α2-treated mice showed a slightly decreased level of B. uniformis in their feces (Fig. 3l).
To further investigate the role of alpha defensins in the gut microbiota, especially the level of B. uniformis, we decreased the level of alpha defensins in the intestine of Chd8+/− mice by using an inhibitor of matrix metalloproteinase (MMP), GM6001 (Fig. 3m), since alpha defensin precursors are cleaved and activated by MMP731,32. We found that Chd8+/− mice intraperitoneally injected with GM6001 showed increased intestinal alpha defensin levels and decreased B. uniformis abundance (Fig. 3n and Supplementary Fig. 4o, p). Taken together, these results indicated that increased levels of alpha defensins contribute to gut microbiota dysbiosis, especially the level of B. uniformis, in the Chd8+/− mice.
In addition to defensins, intestinal inflammation can cause gut microbiota dysbiosis33,34. We further examined eight intestinal inflammatory cytokines related to the microbiota and found that the levels of six proinflammatory cytokines increased (Fig. 3o). The Chd8+/− mice showed increased levels of intestinal inflammatory cytokines but unchanged serum inflammatory cytokines (Supplementary Fig. 4q), suggesting that the altered microbial composition in Chd8+/− mice may be related to intestinal inflammation. Since dysbiosis in the gut microbiota can also lead to inflammation33, gut microbiota dysbiosis and increased inflammation in Chd8+/− mice may reinforce each other.
B. uniformis improves the ASD-like behaviors and restores E/I imbalance in the Chd8 +/− mice
To reveal whether the dysregulated gut microbiota would affect the behaviors of Chd8+/− mice, we co-housed the Chd8+/+ and Chd8+/− mice after weaning in a 3:1 ratio (Fig. 4a), since it has been reported that housing conditions may impact both the microbiota and behaviors of animals7. After co-housing the mice for 4 weeks, we checked the gut microbiome and the behaviors of Chd8+/+ mice, Chd8+/− mice, and co-housed Chd8+/− mice (Fig. 4a). We used the abundance change of B. uniformis as an indicator of the microbiota changes (Supplementary Fig. 5a), since it showed the largest change fold and a significantly reduced level in Chd8+/− mice (Fig. 3c, d). We found that co-housed Chd8+/− mice showed an increased level of B. uniformis in their feces compared with Chd8+/− mice (Fig. 4b). For behavioral tests, co-housing improved the anxiety-like behavior (Fig. 4c) and social interaction behavior (Fig. 4d), but failed to improve the learning and memory deficits of Chd8+/− mice (Supplementary Fig. 5b). These results indicate the pivotal role of the gut microbiota in the ASD-like phenotypes of the Chd8+/− mice.
Next, to clarify the role of B. uniformis in the ASD-like phenotypes of the Chd8+/- mice, we treated weaned Chd8+/− mice by gavage with B. uniformis every 3 days for 4 weeks and then examined the effects of this treatment (Fig. 4e). Following gavage, the Chd8+/− mice showed an increased B. uniformis level in their feces (Supplementary Fig. 5c) but their anatomical abnormalities, including those in their body weight, brain weight, and cerebrum weight, were not changed (Supplementary Fig. 5d). Subsequently, we conducted a three-chamber test to detect the effects of recovery of B. uniformis on the social behavior of the Chd8+/− mice and found that the impaired social interaction, one of the core phenotypes of ASD models, was improved (Fig. 4f). We also performed open-field and light/dark box tests to detect the effects of recovery of B. uniformis on the anxiety-like behavior of the Chd8+/− mice. Following gavage with B. uniformis, the Chd8+/− mice showed an increased proportion of time in the center in the open-field test and a significantly increased time in the light box in the light/dark box test (Fig. 4g, h), indicating the decreased anxiety-like behavior. The novel object recognition test revealed that B. uniformis failed to improve the learning and memory deficits in the Chd8+/− mice (Supplementary Fig. 5e). In addition, B. uniformis treatment did not impact the locomotor behaviors of Chd8+/− mice (Supplementary Fig. 5f).
In addition to behavioral phenotypes, the E/I imbalance of the Chd8+/− mice was also recovered by reducing the frequency of the mEPSCs (Fig. 4i, j). We further examined the effect of B. uniformis on the glutamate, GABA, and glutamine levels in the brains of the Chd8+/− mice since changes in glutamate levels and the glutamate/GABA ratio were one of the causes and manifestations of the E/I imbalance. B. uniformis reduced the glutamate and glutamine levels and the glutamate/GABA ratio in the cerebrum and the whole brain of the Chd8+/− mice (Fig. 4k and Supplementary Fig. 5g–i). Taken together, these results indicated that B. uniformis can improve the ASD-like behaviors and restore E/I imbalance in the Chd8+/− mice.
B. uniformis restores intestinal amino acid transporter levels
The elevated serum glutamine level is believed to be one of the reasons for the increased glutamine level in the brain. To examine how B. uniformis affected the serum levels of amino acids, especially glutamine and tryptophan, we performed a targeted metabolomics assay for amino acids. We found that B. uniformis reduced the serum glutamine and tryptophan levels in the Chd8+/− mice without affecting the other amino acids (Fig. 5a and Supplementary Fig. 6a). To explore the effect of B. uniformis on the intestinal amino acid transporters of the Chd8+/− mice, we performed RNA-seq analysis of small intestinal cells. For the dysregulated intestinal genes, supplementation with B. uniformis decreased the differences between the Chd8+/− and Chd8+/+ mice (Fig. 5b, c). In terms of enriched pathways of differentially expressed (DE) genes, supplementation with B. uniformis reduced the expression of intestinal amino acid transporters in the Chd8+/− mice but not to the same level as that in the Chd8+/+ mice (Fig. 5d and Supplementary Fig. 6b–d). In terms of individual gene expression, the expression levels of Slc6a19, Slc7a8, and Slc7a15, three highly expressed neutral amino acid transporters in the Chd8+/− mice, were reduced (Supplementary Fig. 6e), and these results were confirmed by qPCR assays (Supplementary Fig. 6f). At the protein level, SLC6A19 and SLC7A8 expression was also reduced by B. uniformis (Fig. 5e, f). Furthermore, supplementation with B. uniformis affected the fecal amino acid levels, in which the reduced fecal levels of several amino acids in the Chd8+/− mice were partially restored by supplementation with B. uniformis (Supplementary Fig. 6g). These results revealed that B. uniformis reduces the serum levels of amino acids by inhibiting intestinal amino acid transporter expression in the Chd8+/− mice.
We next explored whether the increased levels of amino acid transporters were due to the genetic mutation or the changes of the microbiome in Chd8+/− mice. We transferred the feces from Chd8+/+ and Chd8+/− mice separately to the germ-free (GF) mice (Supplementary Fig. 6h) and then measured the level of amino acid transporters in the small intestines after fecal microbiota transplantation. We observed a slight decrease of B. uniformis in mice transferred with the feces of Chd8+/− mice (Supplementary Fig. 6i), but no significant alterations of amino acid transporters slc6a19 and slc7a8 in mRNA (Supplementary Fig. 6j) or protein level (Supplementary Fig. 6k), suggesting that dysbiotic gut microbiota alone cannot increase the expression of intestinal amino acid transporters without genetic mutation.
An inhibitor of intestinal amino acid transporters restores ASD-like phenotypes
We next explored whether B. uniformis-mediated modulation of intestinal amino acid transport could restore the ASD-like phenotypes in the Chd8+/− mice. First, we aimed to increase intestinal amino acid transport in the Chd8+/+ mice and investigate whether these mice exhibited ASD-like phenotypes featuring an increased E/I ratio. The Chd8+/+ mice were supplemented with glutamine for 2 weeks to increase the intestinal supply of glutamine (Supplementary Fig. 7a), but the serum glutamine level was not increased, even supplemented with the high concentration of glutamine (Supplementary Fig. 7b). Considering the influence of intestinal amino acid transporters on the serum levels of amino acids, we detected the expression of intestinal amino acid transporters. We found that a high concentration of glutamine in the drinking water reduced the expression of amino acid transporters to some extent (Supplementary Fig. 7c, d). Next, we intended to reduce intestinal amino acid transport in the Chd8+/− mice and investigated whether ASD-like phenotypes characterized by an increased E/I ratio were alleviated. In addition to the expression level, the activity of intestinal amino acid transporters affects amino acid transport. S-benzyl-L-cysteine35 and nimesulide36 have been previously reported to inhibit the intestinal amino acid transporter SLC6A19 at the cellular level (Fig. 6a). We added these two drugs to the drinking water of the Chd8+/+ mice and tested the drugs’ inhibitory effect 2 weeks later, using the serum glutamine level as an indicator (Fig. 6b). We found that both drugs could reduce the serum glutamine level and that the inhibitory effect of S-benzyl-L-cysteine was stronger than that of nimesulide (Fig. 6c). Subsequently, we investigated the effect of S-benzyl-L-cysteine on the glutamine and glutamate levels in the brain. We found that S-benzyl-L-cysteine reduced the level of glutamine, but not glutamate, in the brain of the Chd8+/+ mice (Fig. 6d).
To explore the effect on the Chd8+/− mice, we added S-benzyl-L-cysteine in the drinking water of weaning Chd8+/− mice for 4 weeks and performed behavioral tests at the age of 8 weeks (Fig. 6e). S-benzyl-L-cysteine failed to recover the learning and memory deficits of the Chd8+/− mice (Supplementary Fig. 7e) but improved their impaired social interaction and anxiety (Fig. 6f–h), similar to the effect of B. uniformis. Furthermore, we found that S-benzyl-L-cysteine, similar to B. uniformis, could reduce the serum glutamine levels as well as the glutamine and glutamate levels and the glutamate/GABA ratio in the cerebrum of the Chd8+/− mice (Fig. 6i). S-benzyl-L-cysteine did not significantly affect the Chd8+/− mouse body weight, whole brain weight or cerebrum weight (Supplementary Fig. 7f). These results indicated that the restoration of the ASD-like phenotypes in the Chd8+/− mice by B. uniformis may be achieved by suppressing the expression of their intestinal amino acid transporters.
Discussion
The microbiota–gut–brain axis, a bidirectional communication pathway linking the gut and brain, plays an important role in neuropsychiatric disorders. Nonetheless, the role of the microbiota–gut–brain axis in ASD is still unclear. Our study focused on analyzing the mutual interactions between the host and the gut microbiota in the development of ASD and our results support a role of intestinal amino acid transporters in the regulation of host neural activities by the gut microbiota in a mouse model of ASD-like behavior (Fig. 7).
We observed gut microbiota dysbiosis characterized by a reduced abundance of Bacteroides in the Chd8+/− mice, in consistent with previous studies that the gut microbiota in ASD exhibits a significant decrease in a large variety of probiotics, such as Lactobacillus and Bacteroides7,37,38. The supplementation of Bacteroides fragilis to the offspring of maternal immune activation mouses has shown beneficial effects on the CNS-related behaviors of the host38. Our study found that several species in Bacteroides exhibited reduced abundance in the Chd8+/− mice, and B. uniformis can rescue the ASD-relevant phenotypes and E/I imbalance. Furthermore, we found a slightly increased abundance of Lachnospiraceae bacterium A4 in the Chd8+/− mice. Lachnospiraceae bacterium A4 has reportedly inhibited Th2‐cell differentiation in lamina propria, which is important in the host mucosal T-cell responses39,40. How Lachnospiraceae bacterium A4 influences the host in the Chd8+/− mice and whether it affects the host neural activities by modulating mucosal immunity still need further investigation.
The host can regulate the gut microbiota through several direct or indirect pathways, among which antimicrobial peptides are one of the most direct ones41. We identified that an increased level of α-defensins contributed to gut microbiota dysbiosis in the Chd8+/− mice, in agreement with previous research demonstrating that α-defensins play a pivotal role in governing the intestinal microbial ecology42. Furthermore, defensins and CHD8 are expressed at different developmental stages in the intestine. Therefore, the regulation of defensins by CHD8 may be through indirect pathways. Extensive studies have shown that the Wnt-signaling pathway transcription factor Tcf-4 is required to express most α-defensins, and this process is independent of the gut microbiota43,44,45. Moreover, CHD8 is required for maintaining Wnt signaling in mouse cortical neurons46. Whether CHD8 modulates elevated levels of defensins by influencing the Wnt/Tcf-4 remains to be clarified. In addition, we observed a slightly decreased intestinal transit in Chd8+/− mice. Since the change in gastrointestinal transit is supposed to affect the delivery rate of nutrients to the gut microbiota41, the host may regulate the gut microbiota indirectly by changing the luminal environment in Chd8+/− mice.
We observed that the Chd8+/− mice show an E/I imbalance characterized by an increased glutamate/GABA ratio caused by elevated glutamate and glutamine levels in the brain. Except for the elevated glutamate and glutamine levels, gamma-glutamylated amino acid levels in the brain, which the gut microbiota can also modulate, reportedly have been associated with glutamate/GABA ratio47. Whether B. uniformis affects the glutamate/GABA ratio by regulating gamma-glutamylated amino acids in the brain needs further studies. In this study, we focused on the effect of intestinal abnormalities on the E/I imbalance. Notably, we found that B. uniformis partially restored the E/I imbalance at the neural circuit level, suggesting that abnormal synaptic transmission triggered by host defects in the brain remains an important contributor to the E/I imbalance.
We observed that several, but not all, neutral amino acids changed their serum levels in Chd8+/− mice. One possible reason may be due to the fact that not all the neutral amino acid transporters were increased in the intestine. Among the nine neutral amino acid transporters, six of them maintained unchanged expression, while three (Slc6a19, Slc7a8, and Slc7a15) showed increased expression levels. Another possible explanation may be related to the homeostasis of serum amino acid levels. Besides intestinal amino acid transporters, some other pathways, including intra-organ exchange of amino acids48 and transport of amino acids from the kidney, are also involved in maintaining serum amino acid levels49. Moreover, the transporter preference for some specific amino acids50 and the concentration of substrates in intestinal contents, may also contribute to the uptake of amino acids in intestines. SLC6A19 is one of the major neutral amino acid transporters in the intestine and absorbs most of the diet amino acids51. Our study revealed that the inhibitor of SLC6A19 (S-benzyl-L-cysteine) could reduce serum amino acid levels, which led to decreased amino acid levels in the brain and restored the ASD phenotypes in Chd8+/- mice. However, there is still a possibility that the absorbed S-benzyl-L-cysteine might affect the brain amino acid levels by directly inhibiting the amino acid transporters in the brain. In addition, alternative mechanisms may also exist, such as via vagus nerve and/or neural active microbial metabolites. Future studies are still needed to elucidate the interplay between intestinal amino acid transport and the CNS. Our study suggests that intestinal interventions (e.g., probiotics, inhibitors of intestinal amino acid transporters) may serve as a potential target for development of therapy for ASD.
Methods
Mouse maintenance and breeding
The mice were maintained in the animal facility at the Institute of Microbiology, Chinese Academy of Sciences, under specific pathogen-free conditions. The temperature was kept at 22 ± 1 °C with a relative humidity of 30–70%, and the dark/light cycle was 12 h:12 h (lights on at 7:00 a.m.). The mice were fed with chow diet (SPF-F01-001, SPF Biotechnology Co., Ltd (Beijing, China)). The mice were bred by crossing male heterozygous Chd8+/− mice with female wild-type mice (C57BL/6J). Mice that were crossed for more than three generations were used for experiments. Unless stated otherwise, male mice or samples from male mice were used in the experiments. After weaning, Chd8+/+ and Chd8+/− mice were housed separately by genotype unless stated otherwise.
Animal ethics statements
All animal experiments were performed in accordance with the National Institute of Health Guide for the Care and Use of Laboratory Animals. All procedures were approved by the Animal Ethics Committee at the Institute of Zoology, Chinese Academy of Sciences.
Generation of Chd8 mutant mice
The Chd8 mutant mouse model was established by the Nanjing Biomedical Research Institute of Nanjing University (NBRI, China). Briefly, gRNA was designed to target exon 1 in the mouse Chd8 gene. Cas9 mRNA and gRNA were injected into mouse zygotes (C57BL/6J). The mice of generation F0 were genotyped by sequencing with a primer specific for exon 1 (Chd8-exon 1-R1). The mouse carrying a 13 bp deletion in exon 1 was selected as the founder and was imported to the animal facility at the Institute of Microbiology, Chinese Academy of Sciences. The founder was crossed with wild-type female mice to generate F1 mice. All F1 mice were genotyped by sequencing (Chd8-exon1-R1), and male mice carrying the desired mutations were kept and crossed with wild-type female mice to generate F2 mice. F2 and other generations of mice were genotyped with PCR primers specific for the 13 bp deletion allele (Chd8-mut-F1/Chd8-mut-R1). The sequences of primers were provided in Supplementary Table.
Behavioral tests
The test mice were handled for 3 consecutive days before the experiments. All behavioral tests were performed between 8:00 a.m. and 19:00 p.m. in the behavioral test room, where the mice were transferred at least 1 h in advance for acclimation. Male mice aged 8–14 weeks were selected and divided into three cohorts for behavioral tests. Each cohort was used to perform 3–4 behavioral tests. Each behavioral test had results from at least two cohorts.
Open-field test
The open-field test was performed in an automated AniLab Eight-Box Locomotor Test Station (AniLab Scientific Instruments Co., Ltd., Ningbo, China). The mouse was introduced to the center of the arena (40 cm × 40 cm) and allowed to explore for 30 min. Total distance traveled, time in the center (24 cm × 24 cm), and movement velocity were recorded using LabState software (AniLab Scientific Instruments Co., Ltd.)52. These data were calculated across a total of 30 min and every 10 min (the first 10 min (1st), the second 10 min (2nd), and the last 10 min (3rd)).
Light/dark box test
A test mouse was placed in the center of the dark box and allowed to freely explore both chambers for 5 min. The percentage of time spent in the light box was calculated as the index of anxiety-related behavior52.
Three-chamber social interaction test
The three-chamber social interaction test was performed as previously described with minor modifications53,54. Briefly, the arena [60 cm (L) × 40 cm (W) × 30 cm (H)] was horizontally separated into three equal-sized chambers by transparent dividers with a square opening in each divider to let the mouse move freely in the three chambers. A stainless cylinder with steel bars was placed in the middle of each left and right chamber. In the first session, the test mouse was introduced to the middle chamber center and moved freely for 10 min. In the second session (social ability session), an age- and sex-matched stranger C57BL/6J mouse (M1) previously habituated to the cylinder was placed in the center of the right chamber, while an object in another cylinder (object) was placed in the center of the left chamber. The test mouse was then allowed to explore freely for 10 min. The movement of the mouse was recorded by a camera over the arena. The interaction time was defined as the time spent sniffing the cylinder when the nose was directly oriented towards the cylinder. The percentages of interaction time in the social ability session were calculated as M1/(M1 + Object) and Object/(M1 + Object), and the preference index was (M1-Object)/(M1 + Object). For the third session (social novelty preference session), another age- and sex-matched stranger C57BL/6J mouse (M2) previously habituated to the cylinder was placed in the center of the right chamber, while M1 was placed in the center of the left chamber. The test mouse was then allowed to explore freely for 10 min. The percentages of interaction time in the social novelty preference session were calculated as M1/(M1 + M2) and M2/(M1 + M2), and the preference index was calculated as (M2 − M1)/(M2 + M1).
Novel object recognition test
The novel object recognition test was performed as previously described with slight modifications55. Briefly, the mouse was placed in the arena (30 × 40 × 30 cm) to explore two identical objects (circular cone or rectangle pyramid) that were 5 cm away from the sidewall and 25 cm away from each other. Ten min later, the mouse was returned to the home cage. One hour later, one familiar object (Old Object) and one novel object (Novel Object) were placed in the arena where the two identical objects were located previously. Then, the mouse was introduced to the arena to explore for five min. The movement of the mouse was recorded by a camera over the arena. The contact time was defined as the time spent sniffing the object when the nose was directly oriented toward the object. The percentages of interaction time were calculated as Old Object/(Novel Object + Old Object) and Novel Object/(Novel Object + Old Object), and the preference index was calculated as (Novel Object − Old Object)/(Novel Object + Old Object).
Reciprocal social interaction test
The reciprocal social interaction test was performed as previously described with minor alterations7. Briefly, a pair of age-, sex-, and body weight-matched unfamiliar mice with the same genotype was placed in the arena (30 × 40 × 25 cm) for 5 min. The movement of the mouse was recorded by a camera over the arena. The time spent in close social interaction (nose-to-nose sniffing, nose-to-anus sniffing, touching, close following, and/or crawling over/under each other) was calculated by a human observer blind to the experimental design.
Marble-burying test
The marble-burying test was performed as previously described18. The test mouse was placed in an arena containing 20 black marbles sitting on 5 cm of fresh bedding. After 20 min, the mouse was removed, and marbles with at least half of their depth covered were considered buried.
Self-grooming test
The self-grooming test was performed as previously described18. The test mouse was placed in a clean arena to explore freely for 20 min. Self-grooming behavior was recorded in the second 10 min, as the first 10 min was considered the habituation phase.
Forced swimming
The test mouse was placed in a plastic cylinder (height of 30 cm and diameter of 20 cm) filled with water (25 ± 1 °C, 15 cm in depth) and allowed to swim freely for five min. The movement of the mouse was recorded by a camera directly above the cylinder, and the immobility time during the 5 min was calculated by an observer blind to the genotypes. Immobile behavior was defined as motionless floating in the water with little movement56.
Metabolomics assay
Sample preparation
Fecal samples were collected, immediately frozen in liquid nitrogen and stored at −80 °C until use. Frozen feces were thawed on ice and resuspended in Milli-Q water (3 µl/mg) on ice. Water extraction of feces was performed by centrifugation (4 °C, 15871 rcf, 20 min), and the sample was stored at −80 °C. Fifty microliters of fecal water was removed, and 150 µl of methanol was added. The mixture was vortexed and stored at 4 °C for 1 h before centrifugation (4 °C, 15871 rcf, 20 min). The fecal samples for the metabolomics assay were obtained and stored at −80 °C until use.
The brain samples were harvested, immediately frozen in liquid nitrogen and stored at −80 °C until use. The brain tissues were homogenized in methanol (10 μl/mg). After centrifugation (4 °C, 15871 rcf, 20 min), the supernatant was stored as the brain sample for the metabolomics assay at −80 °C until use57.
Blood was collected from the mouse eyes and was stored undisturbed at room temperature for 20 min before centrifugation (2000 rcf, 10 min). Fifty microliters of supernatant was removed, and 150 µl of methanol was added. The mixture was vortexed and stored at 4 °C for 1 h before centrifugation (4 °C, 15871 rcf, 20 min). The serum sample for metabolomics was obtained and stored at −80 °C until use.
Targeted metabolomics assay for amino acids and SCFAs
Metabolomics assays were performed on an ABSciex QTRAP 6500 mass spectrometer interfaced with a Waters ACQUITY UPLC equipped with a BEH C18 column (2.1 × 100 mm, 1.7 μm; Waters). Amino acids and SCFAs were monitored in multiple reaction monitoring modes using characteristic parent-daughter ion transitions at m/z ratios for each amino acid and SCFA. Several concentrations of amino acids and SCFA standards were used for quantification.
mEPSC and mIPSC recording
mEPSC and mIPSC recordings were performed as previously described with minor modifications18,58. Briefly, adult mice (8–9 weeks) were anesthetized by chloral hydrate and transcardially perfused with aCSF containing: 185 mM Sucrose, 2.5 mM KCl, 1.2 mM NaH2PO4, 25 mM NaHCO3, 25 mM D-Glucose, 0.5 mM CaCl2, and 10 mM MgSO4. After decapitation, the brain was quickly removed, and coronal slices (300 μm) of the medial prefrontal cortex were prepared. The slices were incubated in aCSF for 1 h before mEPSC and mIPSC recording. All solutions were bubbled with 95% O2 and 5% CO2.
Pyramidal cells of medial prefrontal cortex layer V were visualized under an IR-DIC microscope. Whole-cell recordings were obtained using a patch electrode filled with intracellular solution (for mEPSCs, 140 mM K-gluconate, 2 mM MgCl2, 10 mM HEPES, 8 mM KCl, 2 mM Na2-ATP, 0.2 mM NaGTP, pH 7.3; for mIPSCs, 140 mM CsCl, 2 mM MgCl2, 10 mM HEPES, 1.1 mM EGTA, 2 mM Na2-ATP, 0.1 mM CaCl, pH 7.3). Perfusion solution containing 1 μM TTX, 10 μM NBQX, and 50 μM DAP5 was used to block excitatory synaptic transmission in mIPSC recordings. In the mEPSC recordings, 1 μM TTX, 10 μM bicuculline, and 50 μM DAP5 were added in aCSF. The membrane potential of pyramidal neurons was held at −70 mV.
B. uniformis administration
B. uniformis D2-69 was grown anaerobically on Gifu Anaerobic Broth (GAM Broth) in anaerobic tubes at 37 °C. For gavage, the bacteria were centrifuged in an anaerobic tube and suspended in anaerobic PBS to a concentration of 5 × 108 colony forming units (CFU)/ml59. The B. uniformis suspension was removed from the anaerobic tube and immediately administered to the mice orally by gavage (0.1 ml for mice aged 4–5 weeks; 0.2 ml for mice older than 5 weeks).
GM6001 administration
GM6001 (Abcam, Cat # ab120845) was dissolved in DMSO (10 mg/ml) as the stock solution and stored at −80 °C until use. Before administrating to mice, the stock or DMSO was further diluted with four times 10% Tween 20 (v/v, diluted in normal saline) to make a final DMSO concentration of 20%. Adult mice (8–9 weeks) were intraperitoneally injected with diluted GM6001 (5 ml/kg BW) or diluted DMSO (5 ml/kg BW) every day for 5 consecutive days60,61. After the last injection, feces were collected before the mice were sacrificed.
Drug administration
For glutamine administration, glutamine (13 mg/ml or 25 mg/ml) was supplemented in the drinking water of the mice62. For S-benzyl-L-cysteine administration, it was dissolved in water at a concentration of 20 mmol/l. NaOH was added to help dissolve the chemical, and the pH was adjusted to 8.563. For nimesulide administration, suspensions of nimesulide were prepared in 0.05% carboxy methyl cellulose at a concentration of 0.65 mg/ml64. The drug solutions were sterilized with a 0.22 μm membrane before being given to the mice, and the solutions were changed twice a week.
Fecal microbiota transplantation
Feces from Chd8+/+ and Chd8+/− mice have been collected immediately into 3 ml cryoprotectant buffer (normal saline containing 30% glycerin and 0.1% L-cysteine) to the final volume of 4 ml. The feces were dispersed in the cryoprotectant buffer anaerobically and then passed through a 70 μm cell strainer anaerobically. The filtrate was stored at −80 °C until use.
Germ-free mice were separated into two groups according to their body weight (Day 0) and gavaged with fecal filtrate from Chd8+/+ and Chd8+/− mice separately three times (Day 0, Day 1, Day 3). Two weeks after the first gavage (Day 14), the mice were sacrificed, and their tissues were obtained.
Enzyme-linked immunosorbent assay (ELISA)
The small intestinal contents, cecal contents, and colonic contents were harvested and suspended in Milli-Q water (3 µl/mg) on ice before centrifugation (4 °C, 15871 rcf, 20 min). The supernatant was used for defensin α1 and defensin α2 detection using ELISA kits (JL48732 and JL48735, Jianglaibio, Shanghai, China) according to the manufacturer’s instructions.
Immunofluorescence
For preparation of intestinal cross sections, mouse ileal segments were harvested, and the debris in the lumen was flushed with ice-cold EBSS (SL6160, Coolaber, China). Tissue sections were fixed in 4% paraformaldehyde (PFA) for 1 h before dehydration for 2 h each in 20% and 30% sucrose. Dehydrated tissues were frozen in OCT and cut 10 μm thick using a cryostat (Leica CM1950, Germany).
For preparation of coronal sections of the brain, a mouse was transcardially perfused with normal saline followed by 4% PFA immediately. The brain was removed and fixed with 4% PFA overnight before dehydration for 24 h in 20% and 30% sucrose. Dehydrated tissues were frozen in OCT and cut 30 μm thick using a cryostat (Leica CM1950, Germany).
For immunofluorescence staining, brain or ileal sections were permeabilized with 0.3% Triton in 5% BSA (V900933, Sigma, USA) diluted in PBS for 1 h at room temperature for staining. The permeabilized sections were incubated with primary antibodies: anti-SLC6A19 (1:1000, ab180516, Abcam), anti-SLC7A8 (1:1000, ab75610, Abcam), or anti-oxytocin (1:2000, 20068, ImmunoStar) before washing and incubation with secondary antibodies (1:500, A-11012, Thermo Fisher Scientific) and DAPI (C1002, Beyotime, Haimen, China). The sections were washed again and mounted with Fluoromount-G (0100-01, Southern Biotech, USA) on slides with coverslips. The slides were stored in the dark at 4 °C until they were imaged using a spinning disk confocal super-resolution microscope (SpinSR10, Olympus, Tokyo, Japan). ImageJ software (NIH) was used for image processing and quantification.
Western blot
Tissues were homogenized in lysis buffer (P0013B, Beyotime, Haimen, China) containing protease inhibitor cocktail (P0013B, Beyotime, Haimen, China). The homogenates were centrifuged (4 °C, 15871 rcf, 20 min), and the supernatant was collected. Approximately 20 μg of proteins was loaded on a Tris-glycine gel. Proteins were transferred onto PVDF membranes, blocked, and stained overnight using the following primary antibodies: anti-CHD8 (1:1000, ab114126, Abcam), HRP-conjugated anti-GAPDH (1:5000, BE0034, Easybio, Beijing, China), anti-SLC6A19 (1:5000, ab180516, Abcam), and anti-SLC7A8 (1:5000, ab75610, Abcam). Membranes were washed and stained with HRP-conjugated secondary antibodies (1:5000, BE0101 and BE0102, Easybio, Beijing, China) before washing and development with enhanced chemiluminescence (ECL) substrate for Western blotting (BE6706, Easybio, Beijing, China).
Bulk RNA-seq
Total RNA was extracted from the small intestines of 12-week-old mice using TRIzol (Invitrogen) according to the manufacturer’s instructions. There were three, three and five mice in the KN, KB and WN groups, respectively (WN: Chd8+/+ mice gavaged with PBS; KN: Chd8+/− mice gavaged with PBS; KB: Chd8+/− mice gavaged with B. uniformis). mRNA sequencing libraries were prepared and sequenced on the NovaSeq6000 platform (Illumina), generating an average of 20 million paired-end reads per sample.
scRNA-seq
Adult mice (12 weeks) were anesthetized and decapitated, and the brain and small intestine were removed immediately and submerged in ice-cold aCSF and D-HANKS, respectively. Single cells from the brain were harvested using an Adult Brain Dissociation Kit (130–107-677, Miltenyi Biotec, Germany) according to the manufacturer’s instructions. Single cells from the small intestine were obtained by digestion with papain (0.8 U/ml, Sigma, P3125), DNase I (50 U/ml, Coolaber, CD4871), FBS (20 μl/ml, Gibco), collagenase I (31.25 U/ml, Sigma, C0130), and collagenase IV (31.25 U/ml, Sigma, C5138). Single-cell suspensions of freshly isolated cells were then resuspended in PBS containing 0.04% ultrapure BSA. scRNA-seq libraries were prepared using Chromium Single-Cell 3' Reagent Kits v2 (10× Genomics) according to the manufacturer’s instructions. The target cell recovery for each library was 7000. Generated libraries were sequenced on an Illumina HiSeq2500 system (Beijing Institutes of Life Science, Chinese Academy of Science).
Whole-genome shotgun metagenomic sequencing and 16S rRNA sequencing
Microbial DNA was extracted from the frozen fecal samples using a TIANamp Stool DNA kit (DP328, Tiangen Biotech, Beijing, China) according to the manufacturer’s instructions. The DNA quality and concentration were measured by agarose gel electrophoresis and a Qubit fluorometer (Life Technologies, Waltham, MA) before downstream high-throughput sequencing.
To explore the gut microbiota of the Chd8+/+ and Chd8+/− mice, we performed metagenomic sequencing on frozen fecal samples. There were 11 Chd8+/− mice and 12 Chd8+/+ mice in each group. Extracted DNA was fragmented and used to construct a genomic library with an average insert size of ~280 bp and then sequenced by NovaSeq6000 (Illumina).
To study the effect of the increased defensin α1 expression on the gut microbiota, we performed 16S rRNA sequencing on frozen fecal samples from the Chd8+/+ mice gavaged with defensin α1 or water. There were ten mice in each group. For 16S rRNA sequencing, variable regions 3 and 4 (V3–V4) of the 16S rRNA gene were amplified using the 241F and 805R primers. The purified V3–V4 amplicons were sequenced on a HiSeq2500 platform (Illumina, San Diego, CA) with paired-end 250 bp sequencing.
Transcriptome and metagenome analyses
scRNA-seq data analysis
Data produced by scRNA-seq were processed with Cell Ranger (version 3.1.0) software65. In detail, this program was used to demultiplex the FASTQ reads and align them to the mouse reference genome (mm10) with default parameters. The result contains a digital gene expression (DEG) matrix for each sample, with the number of unique molecular identifiers (UMIs) collapsing for each gene. Next, the DEG matrix was subjected to Scanpy (version 1.6.0)66. Quality control was performed, and cells with more than 6000 or less than 200 detected genes and cells with a mitochondrial transcription ratio >5% were discarded. In addition, cell doublets were discarded after identification using the scrublet tool. After log(x + 1)-transformation, size factors were estimated using Scran v1.16.0, and normalization was performed67. Data were then removed based on batch effects and biological covariates with Harmony (version 0.0.5)68. Next, cells were divided into unsupervised clusters using graph-based clustering of the PCA reduced data with the Louvain algorithm after computing the nearest neighbor graph to partition the cells. The results were visualized by uniform approximation and projection (UMAP, version 0.4.6). Finally, the resulting coordinates of UMAP and cluster tags for each cell were assigned to the expression matrix after the size factor correction step for downstream analysis. DE genes between groups in each cluster were detected using the Wilcoxon rank-sum test in diffxpy.api in Scanpy. Adjusted P values were separately evaluated for each cell subset comparison using the Benjamini–Hochberg correction. Finally, cells were partitioned into epithelial, stromal, neuronal, endothelial and immune compartments based on the expression of canonical cell type-specific markers.
Bulk RNA-seq data analysis
For bulk RNA-seq data, transcripts were mapped and quantified using the HISAT2 (version 2.0.5)-StringTie (version 1.3.4) pipeline69. A total of 20,413 genes supported by more than five reads in 20% of the samples were selected for downstream analysis. Differential expression analysis was performed by DESeq2 (version 1.24.0)70. There were 560 and 475 DE genes in KB_WN and KN_WN, respectively, under a strict threshold of adjusted P < 0.01 and |log2(cf)| > 0.585, and then, these DE genes were used in Gene Ontology term enrichment analysis (GOEA). A total of 13,611 highly expressed genes with an average FPKM greater than 1 were used in gene set enrichment analysis (GSEA). GSEA and GOEA were performed with clusterProfiler (version 3.12.0)71. The results of GOEA were visualized in GOplot (version 1.0.2). Euclidean distance was calculated based on the FPKM of DE genes in the three groups to compare the function dist (method = “euclidean”) in R. The Mann–Whitney test was performed in R to compare the difference in Euclidean distance between different groups.
Taxonomic analysis
For metagenomic sequencing data, cutadapt (version 1.14) was used for adaptor and quality trimming. Mouse DNA was removed using BowTie2 (version 2.3.2) to map the reads against the mouse reference genome. Ten million reads were randomly selected from each sample to ensure the consistency of data size in different samples. Quantitative taxonomic profiling was carried out using DIAMOND (version 0.9.24) by aligning reads to the NR database with the −f 102 parameter72,73.
For 16S rRNA-seq data, raw sequencing data were analyzed using QIIME2 (version: 2020.2.0)74. First, raw reads were denoised, dereplicated, merged, and finally processed by DADA2 in QIIME275. For taxonomy annotation, following the recommendations of the QIIME2 (https://docs.qiime2.org/2021.8/tutorials/overview/), we used the blast-based classification method (classify-consensus-blast) to compare the representative sequence to a reference database of sequences with known taxonomic composition (Greengenes 99% OTUs database (version:13_8). The microbial profile table was then exported as a text file for subsequent analyses.
For diversity analysis, first the microbial table was normalized by total sum reads with the function of transform(transform = “compositional”) in the R package microbiome (version 1.6.0). Alpha diversity was analyzed by function diversity in the R package vegan (version 2.5.6), and statistical significance was calculated by the Mann–Whitney test in R. For beta analysis, principal component analysis (PCA) was performed by the prcomp function in R and was visualized with the R package ggbioplot (version 0.55). Multivariate analysis of variance using distance matrices (PERMANOVA) was performed using the adonis(permutations = 9999,method = “bray”) function in the vegan package. Analysis of similarities test (ANOSIM) was also used to detect the degree of separation between groups by the anosim(permutations = 9999,distance = “bray”) function in the vegan package. The BC distances of the two groups of samples were also compared by Mann–Whitney test. And we also reanalyzed the beta diversity and distance based on the centered log-ratio transformed Euclidean distances by using transform(transform = “clr”). We obtained results with altered significance but consistent trends.
For differential analysis of metagenomic data, the highly reliable microbiota supported by more than 10 reads in 10% of the samples was selected by the Mann–Whitney test in R. All P values were adjusted for multiple testing by the Benjamini–Hochberg approach by the function p.adjust(method = “BH”) in R. DESeq2 was used in the differential analysis of the 16S rRNA data. Discriminant microbial features between the study groups were determined using linear discriminant analysis (LDA) effect size (LEfSE) on the Galaxy platform (https://galaxy.medunigraz.at, P < 0.05, LDA score >3.0).
Functional analysis of metagenomic data
Functional profiling was performed with HUMAnN2 (version 0.11.1)76, which aligned reads to selected databases (KEGG, GO and COG) using BLAST or other alignment tools to characterize functional profiles. In total, we identified 5220 KOs, and to facilitate comparisons between groups, we normalized the abundance of KOs to copies per million (CPM). Differential abundance analysis was carried out on the 2781 KOs with a mean CPM > 1. Then, 301 KOs (Mann–Whitney test, P < 0.05) were used for functional enrichment analysis in the R package clusterProfiler. The relationship between KEGG pathways and KOs was downloaded from the KEGG database. The result was visualized in the R package GOplot (version 1.0.2).
qPCR analysis
Total RNA isolated from mouse intestines was used for cDNA preparation using a Hifair® II 1st Strand cDNA Synthesis Kit (11121ES60, Yeasen, Shanghai, China). Real-time PCR analysis was performed using Hieff® qPCR SYBR Green Master Mix (11203ES03, Yeasen, Shanghai, China) in a StepOne PLus Real-Time PCR system instrument (Applied Biosystems) to determine the expression levels of defensin genes (Defa1, Defa2, Defa4, Reg3a, Reg3b, Reg3g, Lyz1, Defb3), amino acid transporter genes (Slc6a19, Slc7a8, Slc7a15), intestinal tight junction genes (Ocln, Cldn1, Tjp1), and the Gapdh gene. The sequences of primers were provided in Supplementary Table 1.
Intestinal permeability assay
The assay was based on intestinal permeability towards 4 kDa fluorescein isothiocyanate-conjugated dextran (FITC-dextran) as previously described77. Briefly, the mice were fasted for 4 h and injected with FITC-dextran (600 mg/kg body weight, 80 mg/ml in PBS) by gavage. The mice were sacrificed 4 h later, and FITC-dextran concentration in the serum was determined with a fluorescence spectrophotometer (excitation at 485 nm and emission at 535 nm; Infinite 200 PRO, Tecan) according to the standard curve.
Blood–brain barrier (BBB) integrity detection
Adult mice (8–9 weeks) were administrated Evans blue dye (2% w/v; intraperitoneal injection; 10 ml/kg BW) in normal saline. Two hours later, mice were transcardially perfused with ice-cold normal saline immediately and brain obtained. Cortex was removed and placed in 50% (w/v, in distilled water) ice-cold trichloroacetic acid (1 ml/0.2 g tissue) before homogenization. The homogenates were incubated at 4°C for 30 min, followed by centrifugation (4 °C, 15871 rcf, 20 min). Evans blue concentration in the supernatant was determined with a fluorescence spectrophotometer (excitation at 540 nm and emission at 680 nm; Infinite 200 PRO, Tecan) according to the standard curve.
Assessment of feeding behavior
Adult mice (11 weeks) were housed in groups of two to four animals per cage. Body weight and food consumption were monitored once a week over 6 weeks. Weekly body weight was shown as the average value during the week. The food intake of mice was calculated as the weight of food pellets consumed per kg body weight for each cage78.
Gastrointestinal transit test
Adult mice were injected with 200 µl of charcoal marker (10% charcoal and 5% gum arabic dissolved in water) by gavage after food deprivation for 12 h with free access to water. The mice were sacrificed by cervical dislocation 30 min later, and the intestine from the pyloric junction to the ileocecal junction was removed for measurement of the total length of the intestine and the distance traveled by the charcoal marker. Gastrointestinal transit is expressed as the distance traveled by the charcoal marker and the percentage of distance traveled by the charcoal marker relative to the total length of the small intestine15,79.
Multiplexed determination of cytokines
Colon samples were harvested and frozen in liquid nitrogen immediately and stored at −80 °C until use. Colon samples were homogenized in lysis buffer (P0013B, Beyotime, Haimen, China) containing protease inhibitor cocktail (P0013B, Beyotime, Haimen, China) on ice for protein extraction. The homogenates were centrifuged (4 °C, 15871 rcf, 20 min), and the supernatant was collected as colonic protein samples. The serum samples were obtained and stored as described above. The levels of eight cytokines of interest (IL-1β, IL-4, IL-6, IL-22, IL-10, IL-12p70, IL-17A, and IL-33) in the serum and colon were measured using a personalized Milliplex Map kit (Millipore) following the manufacturer’s instructions. The concentrations of cytokines in the colon were normalized to the protein concentrations of the samples.
Reporting summary
Further information on research design is available in the Nature Research Reporting Summary linked to this article.
Data availability
The raw sequence data reported in this study have been deposited in the Genome Sequence Archive (GSA) in National Genomics Data Center, Beijing Institute of Genomics (China National Center for Bioinformation), Chinese Academy of Sciences under the accession code PRJCA007907. In detail, the 16S rRNA and metagenomic sequencing data have been deposited under the accession code CRA005819. The bulk RNA-seq data have been deposited under the accession code CRA005826. The scRNA-sequencing data have been deposited under the accession code CRA005899. The remaining data generated in this study are provided in the Supplementary Information. Source data are provided with this paper.
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Acknowledgements
This work was supported by grants from National Natural Science Foundation of China (32025009, 32001082), the National Key R&D Program (2021YFA1301000, 2021YFC2300017), and the Strategic Priority Research Program of Chinese Academy of Sciences (XDB38020300).
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F.Z. conceived the project. Y.Y., Z.Z., Y.H., C.L., and S.L. performed the experiments and generated the sequencing data. Y.Y., B.Z., and P.J. performed the data analysis. Y.Y. and F.Z. wrote the paper with the contribution of all authors.
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Yu, Y., Zhang, B., Ji, P. et al. Changes to gut amino acid transporters and microbiome associated with increased E/I ratio in Chd8+/− mouse model of ASD-like behavior. Nat Commun 13, 1151 (2022). https://doi.org/10.1038/s41467-022-28746-2
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DOI: https://doi.org/10.1038/s41467-022-28746-2
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