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Published on: September 18, 2016
Intestinal microbiota of infants with colic: development and specific signatures
Carolina de Weerth1, Susana Fuentes, Philippe Puylaert
1Montessorilaan 3, PO Box 9104, 6500 HE, Nijmegen, Netherlands. c.deweerth@psych.ru.nl
Insights
Infant colic is linked to distinct gut microbial signatures in early life, with lower diversity and altered bacterial groups like Proteobacteria. These findings may enable early diagnostics and targeted therapies for excessive crying.
Area of Science:
- Microbiology
- Infant Health
- Gastroenterology
Background:
- Infant colic, characterized by excessive crying, affects a significant portion of newborns.
- The role of the gut microbiota in infant colic is an area of ongoing research.
Purpose of the Study:
- To conduct a comprehensive analysis of the fecal microbiota in infants with colic compared to controls during the first 100 days of life.
- To identify specific microbial signatures associated with infant colic.
Main Methods:
- Phylogenetic microarray analysis of microbial DNA from over 200 fecal samples.
- Comparison of microbiota composition and diversity between 12 infants with colic and 12 age-matched controls.
Main Results:
- Infants with colic exhibited significantly lower microbial diversity and stability in the early weeks of life compared to controls.
- A notable increase in Proteobacteria (over twofold) and a decrease in Bifidobacteria and Lactobacilli were observed in infants with colic.
- Colic correlated positively with specific Proteobacteria (e.g., Escherichia, Klebsiella) and negatively with Bacteroidetes and Firmicutes phyla.
Conclusions:
- Distinct microbial signatures are present in the first weeks of life in infants who develop colic.
- These findings suggest potential for early diagnostic markers for colic.
- The identified microbial patterns may inform the development of specific therapeutic interventions for excessive crying in infants.
Objectives:
To provide a comprehensive analysis of the fecal microbiota in infants with colic, as compared with control infants, during their first 100 days of life.
Methods:
Microbial DNA of >200 samples from 12 infants with colic and 12 age-matched control infants was extracted and hybridized to a phylogenetic microarray.
Results:
Microbiota diversity gradually increased after birth only in the control group; moreover, in the first weeks, the diversity of the colic group was significantly lower than that of the control group. The stability of the successive samples also appeared to be significantly lower in the infants with colic for the first weeks. Further analyses revealed which bacterial groups were responsible for colic-related differences in microbiota at age 1 or 2 weeks, the earliest ages with significant differences. Proteobacteria were significantly increased in infants with colic compared with control infants, with a relative abundance that was more than twofold. In contrast, bifidobacteria and lactobacilli were significantly reduced in infants with colic. Moreover, the colic phenotype correlated positively with specific groups of proteobacteria, including bacteria related to Escherichia, Klebsiella, Serratia, Vibrio, Yersinia, and Pseudomonas, but negatively with bacteria belonging to the Bacteroidetes and Firmicutes phyla, the latter of which includes some lactobacilli and canonical groups known to produce butyrate and lactate.
Conclusions:
The results indicate the presence of microbial signatures in the first weeks of life in infants who later develop colic. These microbial signatures may be used to understand the excessive crying. The results offer opportunities for early diagnostics as well as for developing specific therapies.
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