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Infant formula supplemented with low protein and high carbohydrate alters the intestinal microbiota in neonatal SD rats

Overview of attention for article published in BMC Microbiology, November 2014
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Title
Infant formula supplemented with low protein and high carbohydrate alters the intestinal microbiota in neonatal SD rats
Published in
BMC Microbiology, November 2014
DOI 10.1186/s12866-014-0279-2
Pubmed ID
Authors

Wenguang Fan, Yaru Tang, Yi Qu, Fengbo Cao, Guicheng Huo

Abstract

BackgroundInfant microbiota is influenced by numerous factors, such as delivery mode, environment, prematurity and diet (breast milk or formula) and last but not least, the diet composition. In the diet composition, protein and carbohydrate are very important for the growth of microbiota, many infant fomulas (different ratio protein/carbohydrate) can regulate the development of gut microbiota by different metabolism. The effect of low-protein, high-carbohydrate infant formula on the establishment of microbiota remains unclear, and the effect of human breast milk on the gut microbiota of the rats has also not been reported.ResultsIn a 7 d intervention, a total of 36 neonatal SD rats (14 d old) were randomly assigned to the following groups: (1) breast-fed group (A group); (2) low-protein, high-carbohydrate infant formula-fed group (B group); (3) human breast milk-fed group (C group). After 7 days, we selected 6 rats at random from each group to study. Microbial composition in the contents of the large intestines was analysed by Miseq Sequencing. Significantly different (p<0.05) microbial colonisation patterns were observed in the large intestines of breast-fed group from low-protein, high-carbohydrate infant formula-fed and human breast milk-fed rats, but the microbiota of low-protein, high-carbohydrate infant formula-fed group and human breast milk-fed group have high similarity. At the phylum level, the absolute quantity of Bacteroidetes, Firmicutes and Proteobacteria (p<0.001) significantly differentiated in breast-fed group from low- protein, high- carbohydrate infant formula-fed and human breast milk-fed groups. Lachnospiraceae, Bacteroidaceae, Porphyromonadaceae and Prevotellaceae were the 4 top families in breast-fed group, but the top 4 families in low-protein, high- carbohydrate infant formula-fed and human breast milk-fed groups were the same, which were Bacteroidaceae, Enterobacteriaceae, Porphyromonadaceae and Lachnospiraceae. At the genus level, Bacteroides was the most abundant division, their OTUS abundance in three groups was 14.91%, 35.94%, 43.24% respectively.ConclusionsThis study showed that infant formula closer resembling human milk was more different than rats¿ breast milk and led to a microbiota profile similar to that for human breast milk-fed neonates. The finding could support a new thinking to develop infant formulas, and provide much more details than what is known previously.

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Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 82 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 82 100%

Demographic breakdown

Readers by professional status Count As %
Researcher 13 16%
Student > Master 13 16%
Student > Bachelor 12 15%
Student > Ph. D. Student 7 9%
Student > Doctoral Student 4 5%
Other 12 15%
Unknown 21 26%
Readers by discipline Count As %
Nursing and Health Professions 17 21%
Agricultural and Biological Sciences 15 18%
Immunology and Microbiology 7 9%
Medicine and Dentistry 7 9%
Biochemistry, Genetics and Molecular Biology 5 6%
Other 6 7%
Unknown 25 30%
Attention Score in Context

Attention Score in Context

This research output has an Altmetric Attention Score of 1. This is our high-level measure of the quality and quantity of online attention that it has received. This Attention Score, as well as the ranking and number of research outputs shown below, was calculated when the research output was last mentioned on 29 September 2015.
All research outputs
#20,246,428
of 22,774,233 outputs
Outputs from BMC Microbiology
#2,685
of 3,184 outputs
Outputs of similar age
#303,359
of 362,510 outputs
Outputs of similar age from BMC Microbiology
#52
of 61 outputs
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