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Gut Microbial and Metabolic Profiling Reveal the Lingering Effects of Infantile Iron Deficiency Unless Treated with
Jordi Mayneris-Perxachs1,2,3, Wellington Amaral4, Gabriele R Lubach4
1Department of Diabetes, Endocrinology and Nutrition, Josep Trueta University Hospital, Girona, Spain.
Insights
Infant iron deficiency (ID) can cause lasting metabolic and gut microbial changes. Early iron treatment is crucial to prevent these chronic effects and support infant health.
Area of Science:
- Pediatrics
- Nutritional Science
- Microbiome Research
Background:
- Iron deficiency (ID) is a global infant health concern.
- While treatable, some long-term effects of infant ID persist.
- Investigating metabolic and gut microbial consequences of infant ID is critical.
Purpose of the Study:
- To investigate the metabolic and gut microbial consequences of infant iron deficiency.
- To compare outcomes after natural recovery versus iron treatment in juvenile monkeys.
Main Methods:
- Utilized 1H nuclear magnetic resonance (NMR) spectroscopy for metabolomic profiling of urine and plasma.
- Characterized gut microbiota using 16S rRNA gene amplicon sequencing from rectal swabs.
- Analyzed urinary and plasma metabolic profiles and gut microbial composition.
Main Results:
- Monkeys recovering naturally from iron deficiency (pID) showed distinct urinary metabolic profiles, including higher maltose and lower microbial metabolites.
- Plasma metabolomics revealed persistent differences in energy metabolism, with pID monkeys relying more on anaerobic glycolysis.
- Microbial profiling identified increased Methanobrevibacter, Lachnobacterium, and Ruminococcus, and decreased Prevotella in pID monkeys compared to controls.
Conclusions:
- Lingering metabolic and microbial effects are evident after natural recovery from infant iron deficiency.
- Early detection and treatment of infant ID are vital to prevent chronic metabolic derangements.
- Iron dextran and B vitamin treatment (pID+Fe) ameliorated these long-term biochemical effects.
Scope:
Iron deficiency (ID) compromises the health of infants worldwide. Although readily treated with iron, concerns remain about the persistence of some effects. Metabolic and gut microbial consequences of infantile ID were investigated in juvenile monkeys after natural recovery (pID) from iron deficiency or post-treatment with iron dextran and B vitamins (pID+Fe).
Methods And Results:
Metabolomic profiling of urine and plasma is conducted with 1 H nuclear magnetic resonance (NMR) spectroscopy. Gut microbiota are characterized from rectal swabs by amplicon sequencing of the 16S rRNA gene. Urinary metabolic profiles of pID monkeys significantly differed from pID+Fe and continuously iron-sufficient controls (IS) with higher maltose and lower amounts of microbial-derived metabolites. Persistent differences in energy metabolism are apparent from the plasma metabolic phenotypes with greater reliance on anaerobic glycolysis in pID monkeys. Microbial profiling indicated higher abundances of Methanobrevibacter, Lachnobacterium, and Ruminococcus in pID monkeys and any history of ID resulted in a lower Prevotella abundance compared to the IS controls.
Conclusions:
Lingering metabolic and microbial effects are found after natural recovery from ID. These long-term biochemical derangements are not present in the pID+Fe animals emphasizing the importance of the early detection and treatment of early-life ID to ameliorate its chronic metabolic effects.
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