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Published on: October 10, 2025
Cesarean delivery may affect the early biodiversity of intestinal bacteria
Giacomo Biasucci1, Belinda Benenati, Lorenzo Morelli
1Department of Paediatrics and Neonatology, "Guglielmo da Saliceto Hospital," Piacenza, Italy. g.biasucci@ausl.pc.it
Insights
Mode of delivery significantly impacts infant gut microbiota. Cesarean delivery results in less diverse intestinal bacteria and lacks Bifidobacteria compared to vaginal births, affecting early immune development.
Area of Science:
- Microbiology
- Neonatal immunology
- Gut microbiome research
Background:
- The neonatal gastrointestinal tract is colonized by microorganisms post-birth, primarily from the mother.
- Early gut microbiota composition is crucial for the development of the neonatal immune system.
- The mode of delivery is a potential factor influencing initial microbial colonization.
Purpose of the Study:
- To investigate the relationship between the mode of delivery and the intestinal bacterial ecosystem in newborns.
- To analyze the impact of cesarean section versus vaginal delivery on neonatal gut microbiota composition.
Main Methods:
- Molecular biology techniques, including PCR-denaturing gradient gel electrophoresis and PCR-temperature gradient gel electrophoresis.
- Specific amplification of key bacterial groups: Bifidobacterium, Ruminococcus, and Bacteroides species.
- Analysis of intestinal bacterial composition on day 3 of life in infants born via vaginal delivery and cesarean section.
Main Results:
- Infants delivered by cesarean section exhibited a less diverse intestinal microbiota compared to vaginally delivered infants.
- The gut microbiota of neonates born via cesarean delivery was characterized by a significant absence of Bifidobacteria species.
- Vaginally delivered neonates showed predominant bacterial groups like Bifidobacterium longum and Bifidobacterium catenulatum, despite individual variations.
Conclusions:
- The mode of delivery profoundly influences the composition of the intestinal microbiota in early life.
- Findings suggest a link between delivery mode, microbiota composition, and potential immune system development.
- Further research is needed to explore microbiota modulation in cesarean-delivered neonates and the role of microbiological tools in clinical trials.
Abstract:
The gastrointestinal tract of neonates becomes colonized immediately after birth with environmental microorganisms, mainly from the mother; strong evidence suggests that the early composition of the microbiota of neonates plays an important role for the postnatal development of the immune system. The present study was designed to evaluate by means of a molecular biology approach the relation between the intestinal ecosystem of the newborn and the mode of delivery. The intestinal bacterial composition on d 3 of life was investigated in 23 infants born by vaginal delivery and in 23 infants delivered by cesarean section. PCR-denaturing gradient gel electrophoresis and PCR-temperature gradient gel electrophoresis have been utilized, together with the specific amplifications for 10 Bifidobacterium species, 3 Ruminococcus species, and Bacteroides. The intestinal microbiota of neonates delivered by cesarean delivery appears to be less diverse, in terms of bacteria species, than the microbiota of vaginally delivered infants. The intestinal microbiota after cesarean delivery is characterized by an absence of Bifidobacteria species. Vaginally delivered neonates, even if they showed individual microbial profiles, were characterized by predominant groups such as B. longum and B. catenulatum. Our data demonstrate that the mode of delivery has a deep impact on the composition of the intestinal microbiota at the very beginning of human life. This study opens the path to further investigations to confirm the link between microbiota composition and immune system development and to identify tools for the modulation of the intestinal microbiota of cesarean-delivered neonates. Additionally, we underline the importance of adequate microbiological tools used to support clinically relevant trials, if intestinal microbiota is considered as a study outcome.
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