Low iron availability in continuous in vitro colonic fermentations induces strong dysbiosis of the child gut microbial consortium and a decrease in main metabolites.
Low iron availability in continuous in vitro colonic fermentations induces strong dysbiosis of the child gut microbial consortium and a decrease in main metabolites.
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连续的体外结肠发酵中铁的低可用性会诱导儿童肠道微生物联盟的强大营养不良,而主代谢产物的降低。
DOI:
10.1111/j.1574-6941.2012.01461.x
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发表时间:
2013-01
影响因子:
4.2
通讯作者:
Lacroix C
中科院分区:
文献类型:
--
作者:
Dostal A;Fehlbaum S;Chassard C;Zimmermann MB;Lacroix C
Iron (Fe) deficiency affects an estimated 2 billion people worldwide and Fe supplements are a common corrective strategy. The impact of Fe deficiency and Fe supplementation on the complex microbial community of the child gut was studied using in vitro colonic fermentation models inoculated with immobilized fecal microbiota. Chyme media (all Fe chelated by 2,2’-dipyridyl to 26.5 mg Fe L-1) mimicking Fe deficiency and supplementation were continuously fermented. Fermentation effluent samples were analyzed daily on the microbial composition and metabolites by qPCR, 16S rRNA gene 454-pyrosequencing and HPLC. Low Fe conditions (1.56 mg Fe L-1) significantly decreased acetate concentrations and subsequent Fe supplementation (26.5 mg Fe L-1) restored acetate production. High Fe following normal Fe conditions had no impact on the gut microbiota composition and metabolic activity. During very low Fe conditions (0 . 9 m g F e L-1 or Fe chelated b y 2,2’-dipyridyl), a decrease of Roseburia spp./Eubacterium rectale, Clostridium Cluster IV members and Bacteroides spp. was observed while Lactobacillus spp. and Enterobacteriaceae increased consistent with a decrease of butyrate (-84%) and propionate (-55%). The strong dysbiosis of the gut microbiota together with decrease of main gut microbiota metabolites observed with very low iron conditions could weaken the barrier effect of the microbiota and negatively impact gut health.
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影响因子:
1.9
作者:
HOVE, H;NORDGAARDANDERSEN, I;MORTENSEN, PB
通讯作者:
MORTENSEN, PB
影响因子:
64.8
作者:
Fukuda, Shinji;Toh, Hidehiro;Ohno, Hiroshi
通讯作者:
Ohno, Hiroshi
影响因子:
3.7
作者:
Andersson, Anders F.;Lindberg, Mathilda;Jakobsson, Hedvig;Backhed, Fredrik;Nyren, Pal;Engstrand, Lars
通讯作者:
Engstrand, Lars
影响因子:
4
作者:
Cleusix, V.;Lacroix, C.;Le Blay, G.
通讯作者:
Le Blay, G.
影响因子:
3.6
作者:
Balamurugan, Ramadass;Mary, R. Regina;Ramakrishna, Balakrishnan S.
通讯作者:
Ramakrishna, Balakrishnan S.