Iron supplementation is a common approach to address iron deficiency with recommendations for women of childbearing age, particularly those at risk of iron deficiency. Because of its considerably higher absorption, ferrous sulphate is the common iron compound used in iron supplements. However, concerns about iron supplements arise from the knowledge that a large portion of the supplement consumed is not absorbed. This unabsorbed iron travels to the colon and, in preclinical studies, has been shown to promote the growth of enteric pathogens at the expense of beneficial commensal bacteria and increase infection risk, including the clinical incidence of diarrhea. The objective of this study is to compare the effects of iron as ferrous sulfate (FeSO4) or FeSO4-enriched Aspergillus oryzae (Ao iron) on the growth and virulence of common enteric pathogens using an in vitro fecal fermentation model. Stool samples will be collected from women of reproductive age following ingestion of an iron supplement as either FeSO4 or Ao iron. Stool samples will be spiked with common enteric pathogens, and outcome measures will be determined following in vitro fecal fermentation.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
BASIC_SCIENCE
Masking
DOUBLE
Enrollment
15
2 FeSO4 supplements containing 27 mg elemental iron/supplements (54 mg total iron)
2 Ao iron supplements containing 27 mg elemental iron/supplements (54 mg total iron)
Iowa State University
Ames, Iowa, United States
Concentration of iron taken up by enteric pathogens
Iron uptake of common enteric pathogens will be determined in stool following in vitro fecal fermentation.
Time frame: Time Frame: 0-24 hours
Growth of enteric pathogens measured by optical density
Growth of common enteric pathogens will be determined in stool following in vitro fecal fermentation.
Time frame: Time Frame: 0-24 hours
Gut microbiome composition and diversity
Gut microbiome composition will be determined in stool following in vitro fecal fermentation using 16S rRNA gene sequencing.
Time frame: Time Frame: 0-24 hours
Individual fecal short chain fatty acid (SCFA) concentration
Individual SCFAs will be determined in stool following in vitro fecal fermentation by liquid chromatography-mass spectrometry.
Time frame: Time Frame: 0-24 hours
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.