Iron fortification adversely affects the gut microbiome, increases pathogen abundance and induces intestinal inflammation in Kenyan infants

Обогащение железом оказывает неблагоприятное воздействие на микробиом кишечника, увеличивает численность патогенов и вызывает воспаление кишечника у младенцев в Кении
Tanja Jaeggi, Guus A. M. Kortman, Diego Moretti, Christophe Chassard, Penny Holding, Alexandra Dostal, Jos Boekhorst, Harro M. Timmerman, Dorine W. Swinkels, Harold Tjalsma, Jane Njenga, Alice Mwangi, Jane Kvalsvig, Christophe Lacroix, Michael Zimmermann
2014-08-20

Kenyan infantsinfant gut microbiomeintestinal inflammationiron fortificationpathogenic enterobacteria
BACKGROUND: In-home iron fortification for infants in developing countries is recommended for control of anaemia, but low absorption typically results in >80% of the iron passing into the colon. Iron is essential for growth and virulence of many pathogenic enterobacteria. We determined the effect of high and low dose in-home iron fortification on the infant gut microbiome and intestinal inflammation. METHODS: We performed two double-blind randomised controlled trials in 6-month-old Kenyan infants (n=115) consuming home-fortified maize porridge daily for 4 months. In the first, infants received a micronutrient powder (MNP) containing 2.5 mg iron as NaFeEDTA or the MNP without iron. In the second, they received a different MNP containing 12.5 mg iron as ferrous fumarate or the MNP without the iron. The primary outcome was gut microbiome composition analysed by 16S pyrosequencing and targeted real-time PCR (qPCR). Secondary outcomes included faecal calprotectin (marker of intestinal inflammation) and incidence of diarrhoea. We analysed the trials separately and combined. RESULTS: At baseline, 63% of the total microbial 16S rRNA could be assigned to Bifidobacteriaceae but there were high prevalences of pathogens, including Salmonella Clostridium difficile, Clostridium perfringens, and pathogenic Escherichia coli. Using pyrosequencing, +FeMNPs increased enterobacteria, particularly Escherichia/Shigella (p=0.048), the enterobacteria/bifidobacteria ratio (p=0.020), and Clostridium (p=0.030). Most of these effects were confirmed using qPCR; for example, +FeMNPs increased pathogenic E. coli strains (p=0.029). +FeMNPs also increased faecal calprotectin (p=0.002). During the trial, 27.3% of infants in +12.5 mgFeMNP required treatment for diarrhoea versus 8.3% in -12.5 mgFeMNP (p=0.092). There were no study-related serious adverse events in either group. CONCLUSIONS: In this setting, provision of iron-containing MNPs to weaning infants adversely affects the gut microbiome, increasing pathogen abundance and causing intestinal inflammation. TRIAL REGISTRATION NUMBER: NCT01111864.
1
At baseline, Bifidobacteriaceae comprised 63% of assigned microbial sequences, but enteric pathogens including Salmonella, Clostridium difficile, Clostridium perfringens, and pathogenic Escherichia coli were prevalent.
2
Diarrhoea treatment was more frequent with 12.5 mg iron than without iron (27.3% versus 8.3%), although the difference was not statistically significant and no serious study-related adverse events occurred.
3
Iron supplementation increased pathogenic E. coli strains and fecal calprotectin, indicating expansion of pathogens and increased intestinal inflammation.
4
Iron-containing micronutrient powders increased enterobacteria, particularly Escherichia/Shigella, the enterobacteria-to-bifidobacteria ratio, and Clostridium abundance.
5
Two double-blind randomized trials in 115 Kenyan infants evaluated 2.5 mg and 12.5 mg daily iron fortification for four months.

The gut microbiome and intestinal environment of 6-month-old Kenyan infants receiving in-home iron-fortified maize porridge

The effects of high- and low-dose iron fortification on gut microbiome composition, pathogen abundance, intestinal inflammation, and diarrhoea incidence

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2014-08-20
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Tanja Jaeggi
Guus A. M. Kortman
Diego Moretti
Christophe Chassard
Penny Holding
Alexandra Dostal
Jos Boekhorst
Harro M. Timmerman
Dorine W. Swinkels
Harold Tjalsma
Jane Njenga
Alice Mwangi
Jane Kvalsvig
Christophe Lacroix
Michael Zimmermann
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