期刊论文详细信息
BMC Microbiology
Infant formula supplemented with low protein and high carbohydrate alters the intestinal microbiota in neonatal SD rats
Guicheng Huo2  Fengbo Cao2  Yi Qu1  Yaru Tang2  Wenguang Fan1 
[1] Hei LongJiang Polytechnic, Harbin 150111, China;Key Laboratory of Dairy Science, Ministry of Education, Northeast Agricultural University, Harbin 150030, China
关键词: Microbiota;    Human breast milk-fed;    Low-protein, High-carbohydrate infant formula-fed;    Breast-fed;    SD rats;   
Others  :  1137732
DOI  :  10.1186/s12866-014-0279-2
 received in 2014-04-08, accepted in 2014-10-30,  发布年份 2014
PDF
【 摘 要 】

Background

Infant 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.

Results

In 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.

Conclusions

This 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.

【 授权许可】

   
2014 Fan et al.; licensee BioMed Central Ltd.

【 预 览 】
附件列表
Files Size Format View
20150317185732113.pdf 2761KB PDF download
Figure 10. 23KB Image download
Figure 9. 62KB Image download
Figure 8. 82KB Image download
Figure 7. 28KB Image download
Figure 6. 25KB Image download
Figure 5. 81KB Image download
Figure 4. 29KB Image download
Figure 3. 16KB Image download
Figure 2. 42KB Image download
Figure 1. 63KB Image download
【 图 表 】

Figure 1.

Figure 2.

Figure 3.

Figure 4.

Figure 5.

Figure 6.

Figure 7.

Figure 8.

Figure 9.

Figure 10.

【 参考文献 】
  • [1]Bjorksten B: The gut microbiota: a complex ecosystem. Clin Exp Allergy 2006, 36:1215-1217.
  • [2]Ley RE, Lozupone CA, Hamady M, Knight R, Gordon JI: Worlds within worlds: evolution of the vertebrate gut microbiota. Nat Rev Microbiol 2008, 6:776-788.
  • [3]Rawls JF, Samuel BS, Gordon JI: Gnotobiotic zebrafish reveal evolutionarily conserved responses to the gut microbiota. Proc Natl Acad Sci U S A 2004, 101:4596-4601.
  • [4]Young VB: The intestinal microbiota in health and disease. Curr Opin Gastroenterol 2012, 28:63-69.
  • [5]Flint HJ, Bayer EA, Rincon MT, Lamed R, White BA: Polysaccharide utilization by gut bacteria: potential for new insights from genomic analysis. Nat Rev Microbiol 2008, 6(2):121-131.
  • [6]Kong Y, Teather R, Forster R: Composition, spatial distribution, and diversity of the bacterial communities in the rumen of cows fed different forages. FEMS Microbiol Ecol 2010, 74:612-622.
  • [7]Morelli L: Postnatal development of intestinal microflora as influenced by infant nutrition. J Nutr 2008, 138:1791S-1795S.
  • [8]Harmsen HJ, Wildeboer-Veloo AC, Raangs GC, Wagendorp AA, Klijn N, Bindels JG, Welling GW: Analysis of intestinal flora development in breast-fed and formula-fed infants by using molecular identification and detection methods. J Pediatr Gastroenterol Nutr 2000, 30:61-67.
  • [9]Fox PF: Indigenous enzymes in milk. In Advanced dairy chemistry—1 proteins. Edited by Fox PF. McSweeney PLH, Springer US; 2003:467-471.
  • [10]Newburg DS: Oligosaccharides in human milk and bacterial colonization. J Pediatr Gastroenterol Nutr 2000, 30(Suppl 2):S8-S17.
  • [11]Li R, Rock VJ, Grummer-Strawn L: Changes in public attitudes toward breastfeeding in the United States, 1999–2003. J Am Diet Assoc 2007, 107:122-127.
  • [12]Jost R, Maire J-C, Maynard F, Secretin M-C: Aspects of whey protein usage in infant nutrition, a brief review. Int J Food Sci Technol 1999, 34:533-542.
  • [13]Mace K, Steenhout P, Klassen P, Donnet A: Protein quality and quantity in cow's milk-based formula for healthy term infants: past, present and future. Nestle Nutr Workshop Ser Paediatr Program 2006, 58:189-203.
  • [14]Embleton ND, Cooke RJ: Protein requirements in preterm infants: effect of different levels of protein intake on growth and body composition. Pediatr Res 2005, 58:855-860.
  • [15]Thureen P, Heird WC: Protein and energy requirements of the preterm/low birthweight (LBW) infant. Pediatr Res 2005, 57:95R-98R.
  • [16]Chatelais L, Jamin A, Gras-Le Guen C, Lalles JP, Le Huerou-Luron I, Boudry G: The level of protein in milk formula modifies ileal sensitivity to LPS later in life in a piglet model. PLoS One 2011, 6:e19594.
  • [17]Hascoet JM, Hubert C, Rochat F, Legagneur H, Gaga S, Emady-Azar S, Steenhout PG: Effect of formula composition on the development of infant gut microbiota. J Pediatr Gastroenterol Nutr 2011, 52:756-762.
  • [18][http://CRAN.R-project.org/package=vegan] webcite Oksanen J, Blanchet FG, Kindt R, Legendre P, Minchin PR, O’Hara RB, Simpson GL, Solymos P, Stevens MH, Wagner H: Vegan: Community Ecology Package. R package version 2.0-5.. In ᅟ. ; 2012. .
  • [19]Lonnerdal B: Nutritional and physiologic significance of human milk proteins. Am J Clin Nutr 2003, 77:1537S-1543S.
  • [20]Russell WR, Gratz SW, Duncan SH, Holtrop G, Ince J, Scobbie L, Duncan G, Johnstone AM, Lobley GE, Wallace RJ, Duthie GG, Flint HJ: High-protein, reduced-carbohydrate weight-loss diets promote metabolite profiles likely to be detrimental to colonic health. Am J Clin Nutr 2011, 93:1062-1072.
  • [21]Andriamihaja M, Davila AM, Eklou-Lawson M, Petit N, Delpal S, Allek F, Blais A, Delteil C, Tome D, Blachier F: Colon luminal content and epithelial cell morphology are markedly modified in rats fed with a high-protein diet. Am J Physiol Gastrointest Liver Physiol 2010, 299:G1030-G1037.
  • [22]Nyangale EP, Mottram DS, Gibson GR: Gut microbial activity, implications for health and disease: the potential role of metabolite analysis. J Proteome Res 2012, 11(12):5573-5585.
  • [23]Kong XF, Wu GY, Liao YP, Hou ZP, Liu HJ, Yin FG, Li TJ, Huang RL, Zhang YM, Deng D, Kang P, Wang RX, Tang ZY, Yang CB, Deng ZY, Xiong H, Chu WY, Ruan Z, Xie MY, Yin YL: Effects of Chinese herbal ultra-fine powder as a dietary additive on growth performance, serum metabolites and intestinal health in early-weaned piglets. Livest Sci 2007, 108:272-275.
  • [24]Heo JM, Kim JC, Hansen CF, Mullan BP, Hampson DJ, Pluske JR: Effects of feeding low protein diets to piglets on plasma urea nitrogen, faecal ammonia nitrogen, the incidence of diarrhoea and performance after weaning. Arch Anim Nutr 2008, 62:343-358.
  • [25]Williams BA, Bosch MW, Awati A, Konstantinov SR, Smidt H, Akkermans ADL, Verstegen MWA, Tamminga S: In vitro assessment of gastrointestinal tract (GIT) fermentation in pigs: Fermentable substrates and microbial activity. Anim Res 2005, 54:191-201.
  • [26]Lallès J-P, Bosi P, Smidt H, Stokes CR: Weaning-A challenge to gut physiologists. Livest Sci 2007, 108:82-93.
  • [27]Srinivasan M, Laychock SG, Hill DJ, Patel MS: Neonatal nutrition: metabolic programming of pancreatic islets and obesity. Exp Biol Med 2003, 228:15-23.
  • [28]Srinivasan M, Song F, Aalinkeel R, Patel MS: Molecular adaptations in islets from neonatal rats reared artificially on a high carbohydrate milk formula. J Nutr Biochem 2001, 12:575-584.
  • [29]Backhed F, Ley RE, Sonnenburg JL, Peterson DA, Gordon JI: Host-bacterial mutualism in the human intestine. Science (New York, NY) 2005, 307:1915-1920.
  • [30]Qin J, Li R, Raes J, Arumugam M, Burgdorf KS, Manichanh C, Nielsen T, Pons N, Levenez F, Yamada T, Mende DR, Li J, Xu J, Li S, Li D, Cao J, Wang B, Liang H, Zheng H, Xie Y, Tap J, Lepage P, Bertalan M, Batto JM, Hansen T, Le Paslier D, Linneberg A, Nielsen HB, Pelletier E, Renault P, et al.: A human gut microbial gene catalogue established by metagenomic sequencing. Nature 2010, 464:59-65.
  • [31]Claesson MJ, Cusack S, O'Sullivan O, Greene-Diniz R, de Weerd H, Flannery E, Marchesi JR, Falush D, Dinan T, Fitzgerald G, Stanton C, van Sinderen D, O'Connor M, Harnedy N, O'Connor K, Henry C, O'Mahony D, Fitzgerald AP, Shanahan F, Twomey C, Hill C, Ross RP, O'Toole PW: Composition, variability, and temporal stability of the intestinal microbiota of the elderly. Proc Natl Acad Sci U S A 2011, 108(Suppl 1):4586-4591.
  • [32]Verschuere L, Rombaut G, Sorgeloos P, Verstraete W: Probiotic bacteria as biological control agents in aquaculture. Microbiol Mol Biol Rev 2000, 64:655-671.
  • [33]Fernandez L, Langa S, Martin V, Maldonado A, Jimenez E, Martin R, Rodriguez JM: The human milk microbiota: origin and potential roles in health and disease. Pharmacol Res 2013, 69:1-10.
  • [34]Sinkiewicz G, Ljunggren L: Occurrence of Lactobacillus reuteri in human breast milk. Microb Ecol Health Dis 2008, 20:122-126.
  • [35]Ventura M, Canchaya C, Tauch A, Chandra G, Fitzgerald GF, Chater KF, van Sinderen D: Genomics of actinobacteria: tracing the evolutionary history of an ancient phylum. Microbiol Mol Biol Rev 2007, 71:495-548.
  • [36]Benno Y, Sawada K, Mitsuoka T: The intestinal microflora of infants: composition of fecal flora in breast-fed and bottle-fed infants. Microbiol Immunol 1984, 28:975-986.
  • [37]Penders J, Thijs C, Vink C, Stelma FF, Snijders B, Kummeling I, van den Brandt PA, Stobberingh EE: Factors influencing the composition of the intestinal microbiota in early infancy. Pediatrics 2006, 118:511-521.
  • [38]Palmer C, Bik EM, DiGiulio DB, Relman DA, Brown PO: Development of the human infant intestinal microbiota. PLoS Biol 2007, 5:e177.
  • [39]Turnbaugh PJ, Hamady M, Yatsunenko T, Cantarel BL, Duncan A, Ley RE, Sogin ML, Jones WJ, Roe BA, Affourtit JP, Egholm M, Henrissat B, Heath AC, Knight R, Gordon JI: A core gut microbiome in obese and lean twins. Nature 2009, 457:480-484.
  • [40]Schloss PD, Westcott SL, Ryabin T, Hall JR, Hartmann M, Hollister EB, Lesniewski RA, Oakley BB, Parks DH, Robinson CJ, Sahl JW, Stres B, Thallinger GG, Van Horn DJ, Weber CF: Introducing mothur: open-source, platform-independent, community-supported software for describing and comparing microbial communities. Appl Environ Microbiol 2009, 75:7537-7541.
  • [41]Jami E, Israel A, Kotser A, Mizrahi I: Exploring the bovine rumen bacterial community from birth to adulthood. The ISME Journal 2013, 7:1069-1079.
  • [42]Fouts DE, Szpakowski S, Purushe J, Torralba M, Waterman RC, MacNeil MD, Alexander LJ, Nelson KE: Next generation sequencing to define prokaryotic and fungal diversity in the bovine rumen. PloS one 2011, 7:e48289.
  文献评价指标  
  下载次数:76次 浏览次数:7次