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Altered Gut Microbiota and Predicted Immune Dysregulation in Early Childhood SARS-CoV-2 Infection
Dong Hyun Kim1, Byung Ok Kwak1,2, Ky Young Cho2
1Department of Pediatrics, Inha University College of Medicine, 27, Inhang-ro, Jung-gu, Incheon 22332, Republic of Korea.
Insights
Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection in young children disrupts the gut microbiome, causing dysbiosis. This imbalance suppresses crucial immune pathways, potentially affecting long-term immune development.
Area of Science:
- Microbiology
- Immunology
- Pediatrics
Background:
- The gut microbiome is vital for immune regulation, especially during rapid development in early childhood.
- Limited data exist on how severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection impacts the pediatric gut microbiome.
- Understanding these changes is crucial for assessing potential long-term health consequences.
Purpose of the Study:
- To characterize gut microbiome alterations in infants and toddlers with coronavirus disease 2019 (COVID-19).
- To investigate associated changes in immune-related pathways.
- To explore the implications for immune development in early childhood.
Main Methods:
- 16S rRNA gene sequencing of stool samples from 18 children under 2 with COVID-19 and 7 healthy controls.
- Analysis of gut microbiome composition, diversity (alpha and beta diversity), and predicted functional pathways.
- Comparison between COVID-19-affected children and healthy controls.
Main Results:
- COVID-19 was associated with increased Bacteroidota and Bacillota, and decreased Actinomycetota and Pseudomonadota.
- Specific genera like *Bifidobacterium*, *Escherichia*, and *Streptococcus* were more abundant, while *Faecalibacterium*, *Clostridium*, and *Ruminococcus* were less abundant in COVID-19 cases.
- Reduced alpha diversity and altered beta diversity indicated gut dysbiosis. Predictive analysis showed downregulated immune pathways (IL-17, NLR, TLR signaling).
Conclusions:
- SARS-CoV-2 infection in early childhood induces gut dysbiosis.
- The infection suppresses critical immune signaling pathways, potentially impairing mucosal immunity and viral clearance.
- These early-life microbial disruptions may have lasting effects on immune system development.
Abstract:
The gut microbiome plays a key role in immune regulation. Young children experience rapid microbiome development, yet data on its alteration during severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection remain limited. This study aimed to characterize gut microbiome changes and immune-related pathway alterations in young children with coronavirus disease 2019 (COVID-19). Eighteen children under 2 years old with confirmed SARS-CoV-2 infection and seven healthy controls were enrolled between December 2021 and June 2022. Stool samples were analyzed using 16S rRNA gene sequencing. In children with COVID-19, the gut microbiome exhibited an increase in Bacteroidota and Bacillota, whereas Actinomycetota and Pseudomonadota were reduced, with higher abundances of Bifidobacterium, Escherichia, and Streptococcus and lower abundances of Faecalibacterium, Clostridium, and Ruminococcus compared with healthy controls. Children with COVID-19 exhibited reduced alpha diversity, indicating microbial dysbiosis, and significant differences in beta diversity compared with healthy controls. Predictive functional analysis revealed downregulation of key immune-related pathways, such as interleukin-17, NOD-like receptor, and Toll-like signaling, which may impact mucosal immunity and viral clearance in children with COVID-19. SARS-CoV-2 infection in early childhood is associated with gut dysbiosis and the suppression of key immune pathways. These findings highlight the potential long-term impact of early-life microbial disruptions on immune development.
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