Related Experiment Video
Updated: Dec 7, 2025

Quantitative Polymerase Chain Reaction-based Analyses of Murine Intestinal Microbiota After Oral Antibiotic Treatment
Published on: November 17, 2018
Effects of changes on gut microbiota in children with acute Kawasaki disease
Jie Shen1, Yinghe Ding1, Zuocheng Yang1
1Department of Pediatrics, The Third Xiangya Hospital, Central South University, Changsha, Hunan Province, China.
Insights
Gut microbiota diversity is reduced in children with Kawasaki disease (KD). Specific bacteria like Bacteroidetes and Dorea are less abundant in KD patients, suggesting a link between gut health and KD.
Area of Science:
- Microbiology
- Pediatrics
- Immunology
Background:
- Kawasaki disease (KD) is a childhood illness with unknown causes.
- Current KD research focuses on genetics, infections, and immunity.
- The role of gut microbiota in KD pathogenesis is largely unexplored.
Purpose of the Study:
- To investigate the correlation between gut microbiota and Kawasaki disease.
- To compare gut microbial composition in children with KD and healthy controls.
Main Methods:
- High-throughput sequencing of fecal samples to analyze bacterial taxonomic content.
- Comparison of gut microbiota diversity, richness, and composition between KD and control groups.
- Analysis of routine blood tests and immunoglobulin levels.
Main Results:
- Significantly reduced gut microbiota richness and diversity in children with KD compared to controls.
- Lower abundance of Bacteroidetes and Dorea in KD patients.
- Decreased levels of Immunoglobulin A (IgA) and Immunoglobulin G (IgG) in KD patients.
Conclusions:
- Gut microbiota dysbiosis is present in acute Kawasaki disease.
- Reduced Dorea, a hydrogen-producing bacterium, is a novel finding in KD.
- Intestinal microecology may play a role in KD etiology and pathogenesis, offering diagnostic potential.
Background:
Kawasaki disease (KD) is an acute febrile illness of early childhood. The exact etiology of the disease remains unknown. At present, research on KD is mostly limited to susceptibility genes, infections, and immunity. However, research on the correlation between gut microbiota and KD is rare.
Methods:
Children with a diagnosis of acute KD and children undergoing physical examination during the same period were included. At the time of admission, the subjects' peripheral venous blood and feces were collected. Faecal samples were analyzed for bacterial taxonomic content via high-throughput sequencing. The abundance, diversity, composition, and characteristic differences of the gut microbiota in KD and healthy children were compared by alpha diversity, beta diversity, linear discriminant analysis and LDA effect size analysis. Blood samples were used for routine blood examination, biochemical analysis, and immunoglobulin quantitative detection.
Results:
Compared with the control group, the community richness and structure of gut microbiota in the KD group was significantly reduced (Chao1 richness estimator, mean 215.85 in KD vs. mean 725.76 in control, p < 0.01; Shannon diversity index, mean 3.32 in KD vs. mean 5.69 in control, p < 0.05). LEfSe analysis identified two strains of bacteria significantly associated with KD: Bacteroidetes and Dorea. Bacteroidetes were enriched in healthy children (mean 0.16 in KD vs. mean 0.34 in control, p < 0.05). Dorea was also enriched in healthy children but rarely existed in children with KD (mean 0.002 in KD vs. mean 0.016 in control, p < 0.05). Compared with the control, IgA and IgG in the KD group decreased (IgA, median 0.68 g/L in KD vs. median 1.06 g/L in control, p < 0.001; IgG, median 6.67 g/L in KD vs. median 9.71 g/L in control, p < 0.001), and IgE and IgM levels were not significantly changed.
Conclusions:
Dysbiosis of gut microbiota occurs in children with acute KD and may be related to the etiology or pathogenesis of KD. It is worth noting that for the first time, we found that Dorea, a hydrogen-producing bacterium, was significantly reduced in children with acute KD. Overall, our results provide a theoretical basis for the prevention or diagnosis of KD based on intestinal microecology.
More Related Videos
Related Concept Videos
Anatomy of the Intestines
Small Intestines
The small intestine is an ~7 meter-long tube with an inner diameter of just 2.5 cm. Since most nutrients are absorbed here, the inner lining of the...
Drugs Affecting GI Tract Motility: Antimicrobials as Antidiarrheal Agents
Pharmacokinetics in Pediatric Patients: Overview and Drug Absorption

