[Age distribution characteristics of intestinal segmented filamentous bacteria and their relationship with intestinal

Wei-Rong Liu1, Xiao-Li Shu, Wei-Zhong Gu

  • 1Department of Gastroenterology, Children's Hospital, Zhejiang University School of Medicine, Hangzhou 310003, China. mizu@zju.edu.cn.

Insights

Intestinal segmented filamentous bacteria (SFB) colonization is common in young children, peaking under age three. SFB presence correlates with increased intestinal secretory IgA but reduced IL-17A cells in the terminal ileum.

Area of Science:

  • Microbiology
  • Immunology
  • Pediatrics

Background:

  • Segmented filamentous bacteria (SFB) are commensal microorganisms residing in the rodent gut, known to influence host immunity.
  • The role and prevalence of SFB in human intestinal ecosystems, particularly in children, remain less understood.
  • Understanding SFB's age-related distribution and its impact on developing mucosal immunity is crucial for pediatric health research.

Purpose of the Study:

  • To determine the age-specific prevalence of intestinal SFB in a pediatric cohort.
  • To investigate the association between SFB colonization and key markers of intestinal mucosal immunity, including secretory IgA (sIgA) and T helper cell-related cytokines.
  • To explore the relationship between SFB and the expression of transcription factors (T-bet, FOXP3, ROR-γt) involved in T cell differentiation.

Main Methods:

  • Collected fecal samples from 177 children and ileocecal fluid from 47 children for SFB detection via real-time PCR.
  • Quantified secretory immunoglobulin A (sIgA) concentration using enzyme-linked immunosorbent assay.
  • Assessed the density of interleukin 17A (IL-17A) cells and intraepithelial lymphocytes, along with T-bet, FOXP3, and ROR-γt expression in terminal ileum mucosa via immunohistochemistry.

Main Results:

  • The overall prevalence of intestinal SFB was 19.2%, with significantly higher rates in children under three years old (40-47%).
  • SFB-positive children exhibited significantly higher levels of intestinal sIgA compared to SFB-negative children.
  • While intraepithelial lymphocytes and key transcription factor expressions were similar, SFB-positive children showed a significant reduction in IL-17A cells in the terminal ileum.

Conclusions:

  • Intestinal SFB colonization in children is strongly age-dependent, with a high colonization rate observed in those under three years of age.
  • SFB colonization is associated with enhanced intestinal sIgA secretion, suggesting an impact on humoral immunity.
  • A notable finding is the reduced presence of IL-17A-producing cells in the terminal ileum of SFB-colonized children, indicating a potential modulation of Th17-mediated immunity.
Abstract

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