Abstract

The gut harbours diverse and complex microbiota, which influence body health including nutrient metabolism, immune development, and protection from pathogens. Pregnancy is associated with immune and metabolic changes that might be related to microbiota compositional dynamics. We therefore investigated the colonic luminal bacteria community in Huanjiang mini-pigs fed diets with different nutrient levels from the first to third trimester of pregnancy. The concentrations of intestinal metabolites including short-chain fat acids, NH3-N, indole, skatole, and bioamines were also determined. We found that the colonic bacteria species richness estimators (Chao1 and ACE) decreased with increased gestational age. The dominant phyla identified were Firmicutes and Bacteroidetes; the dominant genera were Lactobacillus, Treponema, Ruminococcus, Clostridium, and Prevotella. In addition, microbiota displayed spatial and temporal heterogeneity in composition, diversity, and species abundance in different colonic segments from the first to third trimester of pregnancy. Furthermore, the bacterial metabolites also changed according to the diet used and the pregnancy stage. These findings suggest that colonic bacteria richness decreased as gestational age increased, and that the higher nutrient level diet increased the production of metabolites related to nitrogen metabolism. However, although the higher nutrient diet was associated with pregnancy syndrome, causal links remain to be determined.

Highlights

  • Uterine growth during gestation causes profound gastrointestinal tract modification, giving rise to altered gastric motility and intestinal transit time along with gastrointestinal disturbances[5]

  • Many dietary components including protein and amino acid-derived bacterial metabolites such as short-chain fatty acids, NH3-N, indole, skatole, and bioamines affect the relationship between gut microbiota and the intestinal mucosa, and this relationship might evolve according to life stage[17]

  • Complex oligosaccharides and indigestible fibre matter not absorbed in the upper intestinal tract are fermented by the colonic anaerobic microbial community to produce SCFAs18; short-chain fatty acids (SCFAs) can be produced from some luminal amino acids[19]

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Summary

Introduction

Uterine growth during gestation causes profound gastrointestinal tract modification, giving rise to altered gastric motility and intestinal transit time along with gastrointestinal disturbances[5]. Koren et al demonstrated that in humans, the gut microbiota composition during first trimester pregnancy is very similar to that of a healthy non-pregnant control group but becomes enriched in Proteobacteria and Actinobacteria during the third trimester[6]. These latter changes are similar to those detected in inflammatory bowel disease and www.nature.com/scientificreports/. Many dietary components including protein and amino acid-derived bacterial metabolites such as short-chain fatty acids, NH3-N, indole, skatole, and bioamines affect the relationship between gut microbiota and the intestinal mucosa, and this relationship might evolve according to life stage[17]. Colonic bacterial metabolites including short-chain fatty acids (SCFAs), NH3-N, indole, skatole, and bioamines were determined

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