IDDF2024-ABS-0172 A potential intestinal pathogen for autism spectrum disorder: fecal enterotoxigenic bacteroides fragilis

<h3>Background</h3> The gut microbiota is closely associated with autism spectrum disorders (ASD), but the specific microorganism involved is not well understood<i>. Bacteroides fragilis</i> has been implicated in ASD in rodent models, though the evidence is inconclusive. <i>B. fragilis</i> exhibits remarkable genetic diversity and can be categorized into enterotoxigenic <i>B. fragilis</i> (ETBF) or non-toxigenic <i>B. fragilis</i> (NTBF). We aimed to investigate the potential role of <i>B. fragilis</i> in the ASD population. <h3>Methods</h3> Fecal samples were collected from 70 individuals with ASD, 45 individuals with Tic disorder (TD) as disease controls, and 64 healthy controls (HC) for PCR analysis to identify <i>B. fragilis</i> and ETBF. In five ASD children who were ETBF (+) and received fecal microbiota transplantation (FMT) treatment, we compared the ETBF copy number by quantitative PCR before and after FMT. <h3>Results</h3> There was no significant difference in the detection of <i>B. fragilis</i> between the ASD, TD, and HC groups, whereas ETBF was higher in ASD than in TD (21.43% vs. 6.67%, <i>P</i> = 0.0335) and HC (21.43% vs. 7.81%, <i>P</i> = 0.0272) (IDDF2024-ABS-0172 Figure 1. Stacked histogram of B. <i>fragilis</i> and subtype in ASD TD and HC children). Among five ASD children who tested positive for ETBF and received FMT treatment, 80% (4/5) showed a clinical response, a 4.5-point decrease in the CARS-2 score. Four cases had a reduction in their CARS-2 score by 5.5-6.5 and a decrease in ETBF copy number by over 90%. One non-responding case had a 2-point decrease in their CARS-2 score and a 49.88% decrease in ETBF copy number (IDDF2024-ABS-0172 Figure 2. Cars 2 scores and fecal ETBF copy number was reduced after FMT treatment in five ASD children). <h3>Conclusions</h3> The detection rate of ETBF was higher in ASD than in TD and HC children. FMT efficacy was correlated with ETBF, which may be a predictor of FMT efficacy for ASD. ETBF is a potential intestinal pathogen and biomarker for diagnostic and therapeutic targets for ASD.

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Journal
Clinical Gastroenterology
Published
2024-08-01
DOI
https://doi.org/10.1136/gutjnl-2024-iddf.268
Primary Topic
Gut microbiota and health
Type
article
Field-Weighted Citation Impact
0.00
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article

IDDF2024-ABS-0172 A potential intestinal pathogen for autism spectrum disorder: fecal enterotoxigenic bacteroides fragilis

Jingshuang Yan, Yiyuan Li, Huijun Zhao, Xinjun Wang et al.
Clinical Gastroenterology
Gut microbiota and health
article

IDDF2024-ABS-0172 A potential intestinal pathogen for autism spectrum disorder: fecal enterotoxigenic bacteroides fragilis

Jingshuang Yan, Yiyuan Li, Huijun Zhao, Xinjun Wang, Mengqi Xu, Zikai Wang, Fei Pan, Wenjie Xi, Li‐Ping Zou, Huanlong Qin, Lihua Peng, Yunsheng Yang, Xi Luo
article en

Abstract

<h3>Background</h3> The gut microbiota is closely associated with autism spectrum disorders (ASD), but the specific microorganism involved is not well understood<i>. Bacteroides fragilis</i> has been implicated in ASD in rodent models, though the evidence is inconclusive. <i>B. fragilis</i> exhibits remarkable genetic diversity and can be categorized into enterotoxigenic <i>B. fragilis</i> (ETBF) or non-toxigenic <i>B. fragilis</i> (NTBF). We aimed to investigate the potential role of <i>B. fragilis</i> in the ASD population. <h3>Methods</h3> Fecal samples were collected from 70 individuals with ASD, 45 individuals with Tic disorder (TD) as disease controls, and 64 healthy controls (HC) for PCR analysis to identify <i>B. fragilis</i> and ETBF. In five ASD children who were ETBF (+) and received fecal microbiota transplantation (FMT) treatment, we compared the ETBF copy number by quantitative PCR before and after FMT. <h3>Results</h3> There was no significant difference in the detection of <i>B. fragilis</i> between the ASD, TD, and HC groups, whereas ETBF was higher in ASD than in TD (21.43% vs. 6.67%, <i>P</i> = 0.0335) and HC (21.43% vs. 7.81%, <i>P</i> = 0.0272) (IDDF2024-ABS-0172 Figure 1. Stacked histogram of B. <i>fragilis</i> and subtype in ASD TD and HC children). Among five ASD children who tested positive for ETBF and received FMT treatment, 80% (4/5) showed a clinical response, a 4.5-point decrease in the CARS-2 score. Four cases had a reduction in their CARS-2 score by 5.5-6.5 and a decrease in ETBF copy number by over 90%. One non-responding case had a 2-point decrease in their CARS-2 score and a 49.88% decrease in ETBF copy number (IDDF2024-ABS-0172 Figure 2. Cars 2 scores and fecal ETBF copy number was reduced after FMT treatment in five ASD children). <h3>Conclusions</h3> The detection rate of ETBF was higher in ASD than in TD and HC children. FMT efficacy was correlated with ETBF, which may be a predictor of FMT efficacy for ASD. ETBF is a potential intestinal pathogen and biomarker for diagnostic and therapeutic targets for ASD.

Clinical Gastroenterology
Tongji University (CN), Beijing Tongren Hospital (CN), Capital Medical University (CN), Chinese PLA General Hospital (CN), Shanghai Tenth People's Hospital (CN), Beijing Children’s Hospital (CN)
Zero hunger
Openalex Percentile: Top 71%
Gut microbiota and health
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