Quantitative Real-Time PCR Assays To Identify and Quantify Fecal <i>Bifidobacterium</i> Species in Infants Receiving a Prebiotic Infant Formula
Количественные методы ПЦР в реальном времени для идентификации и количественного определения видов Bifidobacterium в фекалиях младенцев, получающих детскую смесь с пребиотиками
2005-05-01
SCID: 54.1/srnkby3k
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5′ nuclease assaysBifidobacterium speciesfecal microbiotaprebiotic infant formulaquantitative real-time PCR
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Abstract (AI)
A healthy intestinal microbiota is considered to be important for priming of the infants' mucosal and systemic immunity. Breast-fed infants typically have an intestinal microbiota dominated by different Bifidobacterium species. It has been described that allergic infants have different levels of specific Bifidobacterium species than healthy infants. For the accurate quantification of Bifidobacterium adolescentis, Bifidobacterium angulatum, Bifidobacterium bifidum, Bifidobacterium breve, Bifidobacterium catenulatum, Bifidobacterium dentium, Bifidobacterium infantis, and Bifidobacterium longum in fecal samples, duplex 5' nuclease assays were developed. The assays, targeting rRNA gene intergenic spacer regions, were validated and compared with conventional PCR and fluorescent in situ hybridization methods. The 5' nuclease assays were subsequently used to determine the relative amounts of different Bifidobacterium species in fecal samples from infants receiving a standard formula or a standard formula supplemented with galacto- and fructo-oligosaccharides (OSF). A breast-fed group was studied in parallel as a reference. The results showed a significant increase in the total amount of fecal bifidobacteria (54.8% +/- 9.8% to 73.4% +/- 4.0%) in infants receiving the prebiotic formula (OSF), with a diversity of Bifidobacterium species similar to breast-fed infants. The intestinal microbiota of infants who received a standard formula seems to resemble a more adult-like distribution of bifidobacteria and contains relatively more B. catenulatum and B. adolescentis (2.71% +/- 1.92% and 8.11% +/- 4.12%, respectively, versus 0.15% +/- 0.11% and 1.38% +/- 0.98% for the OSF group). In conclusion, the specific prebiotic infant formula used induces a fecal microbiota that closely resembles the microbiota of breast-fed infants also at the level of the different Bifidobacterium species.
Key Findings
1
Duplex 5′ nuclease quantitative PCR assays were developed and validated to accurately identify and quantify eight Bifidobacterium species in infant fecal samples.
2
Infants receiving prebiotic formula exhibited Bifidobacterium species diversity similar to that of breast-fed infants.
3
Prebiotic formula supplementation with galacto- and fructo-oligosaccharides significantly increased total fecal bifidobacteria from 54.8% ± 9.8% to 73.4% ± 4.0%.
4
Standard-formula infants had relatively higher proportions of B. catenulatum and B. adolescentis than prebiotic-formula infants, consistent with a more adult-like bifidobacterial distribution.
5
The assays targeted rRNA gene intergenic spacer regions and were compared with conventional PCR and fluorescent in situ hybridization methods.
Research Object
Fecal Bifidobacterium species in infants receiving standard or prebiotic-supplemented formula, with breast-fed infants as a reference
Research Subject
The species composition and relative abundance of fecal bifidobacteria, and their alteration by galacto- and fructo-oligosaccharide-supplemented formula
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2005-05-01
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