Evidence map›Paper›PMID 42343222›Full record

ArticleBMC microbiology2026

Gut bacterial characteristics in children with autism spectrum disorder according to symptom severity: a cross-sectional study.

Aliye Aili, Zumureti Yimin, Nadire Maiming, Yilijiang Tuhongjiang, Jiazila Paerhati, Xayida Aini, Asimuguli Kelimu, Rena Maimaiti

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Article in BMC microbiology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

Authors and funding

8 authors.

Aliye AiliDepartment of Child and Maternal Health, School of Public Health, Xinjiang Medical University, Urumqi, 830011, PR China.
Zumureti YiminDepartment of Child Health Care, The First Affiliated Hospital of Xinjiang Medical University, Urumqi, 830011, PR China.
Nadire MaimingUrumqi Center for Disease Control and Prevention (Urumqi Health Supervision Institute), Urumqi, 830011, PR China.
Yilijiang TuhongjiangXinjiang Uygur autonomous region Children's Hospital, Urumqi, 830011, PR China.
Jiazila PaerhatiYining Center for Disease Control and Prevention (Yining Health Supervision Institute), Yining, 835000, PR China.
Xayida AiniDepartment of Child and Maternal Health, School of Public Health, Xinjiang Medical University, Urumqi, 830011, PR China.
Asimuguli KelimuDepartment of Child and Maternal Health, School of Public Health, Xinjiang Medical University, Urumqi, 830011, PR China. 370645504@qq.com.
Rena MaimaitiDepartment of Child Health Care, The First Affiliated Hospital of Xinjiang Medical University, Urumqi, 830011, PR China. krena95@aliyun.com.

Funding

Tianshan Talent Project - Medical and Health High-Level Talent Training Program TSYC202301A013
6 · The paper itself

Abstract

backgroundAutism spectrum disorder (ASD) is associated with alterations in gut microbiota. The gut-brain axis, which involves bidirectional communication between the gastrointestinal tract and the central nervous system, has been implicated in the pathophysiology of ASD. This study aimed to investigate the relationship between gut microbiota characteristics and symptom severity in children with ASD.

methodsThis cross-sectional study enrolled a total of 81 children with ASD aged 3-12 years, who were divided into mild-to-moderate (n = 35) and severe (n = 46) groups based on Childhood Autism Rating Scale scores. Fecal samples were collected for 16 S rRNA gene sequencing. Alpha diversity, beta diversity, and species composition were analyzed using R software. Linear Discriminant Analysis Effect Size (LEfSe) with a threshold of LDA score ≥ 2.0 and P < 0.05 was used to identify differentially abundant taxa.

resultsThe severe ASD group showed significantly lower Shannon index [4.04 (3.74-4.33) vs. 3.82 (3.40-4.23); P = 0.047] and Simpson index [0.95 (0.93-0.96) vs. 0.92 (0.90-0.96); P = 0.012] compared with the mild-to-moderate ASD group. Beta diversity analysis revealed significant separation between groups (PERMANOVA, R² = 0.048, P = 0.003). At the phylum level, the severe ASD group showed decreased Firmicutes (56.92%→47.46%) and increased Proteobacteria (5.92%→14.46%). At the family level, Enterobacteriaceae was increased (4.64%→13.08%), while Selenomonadaceae (2.64%→0.80%), Veillonellaceae (3.99%→2.70%), and Coriobacteriaceae (3.90%→2.36%) were decreased. At the genus level, Klebsiella showed a 2.8-fold increase (1.81%→5.06%), while Faecalibacterium (14.81%→11.84%) and Dialister (2.85%→1.95%) were decreased. LEfSe identified 11 differentially abundant taxa (LDA score ≥ 2.0, P < 0.05), with 10 taxa enriched in the mild-to-moderate ASD group, including Firmicutes (LDA = 4.69, P = 0.003), Coriobacteriia (LDA = 3.95, P = 0.026), Coriobacteriales (LDA = 3.95, P = 0.026), Bacteroides ovatus (LDA = 3.10, P = 0.048), and Sutterella (LDA = 2.65, P = 0.030), and several uncultured taxa. Only Fusobacteriaceae (family) was enriched in the severe ASD group (LDA = 3.40, P = 0.043).

conclusionsGut bacterial dysbiosis in ASD children is characterized by reduced diversity and altered composition, with more pronounced abnormalities in the severe ASD group. However, this study only evaluated bacterial communities (not fungi or viruses), and the cross-sectional design does not support causal inferences. These findings suggest that microbiota modulation may represent a potential therapeutic approach for ASD, though causal relationships remain to be established in longitudinal studies.

Indexed as

Autism Spectrum DisorderBacteriaGastrointestinal MicrobiomeChildChild, PreschoolCross-Sectional StudiesDNA, BacterialFecesFemaleHumansMalePhylogenyRNA, Ribosomal, 16SSequence Analysis, DNASeverity of Illness IndexDNA, BacterialRNA, Ribosomal, 16S16S rRNA sequencingAutism spectrum disorderChildhood Autism Rating Scale (CARS)Gut-brain axisGut microbiotaSymptom severity

Identifiers

PMID42343222
PMCPMC13540246

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.