FISH-Flow Cytometry Reveals Microbiome-Wide Changes in Post-Translational Modification and Altered Microbial Abundance Among Children with Inflammatory Bowel Disease

Pathogens. 2024 Dec 13;13(12):1102. doi: 10.3390/pathogens13121102.

Abstract

Metaproteomic analysis of microbiome post-translation modifications (PTMm) is challenging, and little is known about the effects of inflammation on the bacterial PTM landscape in IBD. Here, we adapted and optimised fluorescence in situ hybridisation-flow cytometry (FISH-FC) to study microbiome-wide tyrosine phosphorylation (p-Tyr) in children with and without inflammatory bowel disease (IBD). Microbial p-Tyr signal was significantly higher in children with IBD, compared to those without. Faecalibacterium prausnitzii, Bacteroidota, Gammaproteobacteria and Bifidobacteria tended to be more abundant in IBD than in non-IBD control children but there were only minor differences in p-Tyr among these bacterial communities in those with and without IBD. p-Tyr was significantly lower in non-IBD children older than 9 yrs compared with those less than 9 yrs, and the effect was seen in all four bacterial subgroups studied. The opposite trend was seen in patients with IBD. p-Tyr overall is higher in children with IBD but the effects of inflammation on p-Tyr vary according to the bacterial community. The overall microbiome p-Tyr signal changes with age in healthy children. FISH-FC can be used to study the microbiome-wide PTM landscape.

Keywords: FISH–flow cytometry; child; inflammatory bowel disease; microbiome; post-translational modification; tyrosine phosphorylation.

MeSH terms

  • Adolescent
  • Bacteria / classification
  • Bacteria / genetics
  • Bacteria / isolation & purification
  • Bacteria / metabolism
  • Child
  • Child, Preschool
  • Feces / microbiology
  • Female
  • Flow Cytometry* / methods
  • Gastrointestinal Microbiome*
  • Humans
  • In Situ Hybridization, Fluorescence* / methods
  • Inflammatory Bowel Diseases* / immunology
  • Inflammatory Bowel Diseases* / microbiology
  • Male
  • Microbiota
  • Phosphorylation
  • Protein Processing, Post-Translational*
  • Tyrosine / metabolism

Substances

  • Tyrosine