Abstract

BackgroundThe hyper-prolificacy Meishan gilts achieved a superior endometrial gland development (EGD) than white crossbred gilts during the ovary-independent period (before 60 d of age). Then, the EGD continues under the management of ovary-derived steroid hormones that regulated by gut microbiota (after 60 d of age). However, whether Meishan gilts’ superiority in EGD lasting to the ovary-dependent period (after 60 d of age) and the role of gut microbiota in this period both remain unclear.MethodsMeishan gilts and Landrace x Yorkshire (LxY) gilts were raised under the same housing and feeding conditions until sexual maturity and then we compared their EGD and gut microbiota. Meanwhile, we transplanted fecal microbiota from Meishan gilts to L×Y gilts to explore the role of gut microbiota in EGD. We sampled plasma every 3 weeks and collected the uterus, ovary, liver, and rectal feces after the sacrifice. We then determined the hormone concentrations and expressions of the EGD-related genes. We also profiled the gut microbiota using 16S rDNA sequencing and metabolites of plasma and liver tissue using untargeted metabolomics. Finally, the correlation analysis and significant test was conducted between FMT-shifted gut microbes and EGD-related indices.ResultsMeishan gilts have larger endometrial gland area (P < 0.001), longer uterine horn length (P < 0.01) but lighter uterine horn weight (P < 0.05), a distinctive gut microbiota compared with L×Y gilts. Fecal microbiota transplantation (FMT) increased endometrial gland area (P < 0.01). FMT markedly shifted the metabolite profiles of both liver and plasma, and these differential metabolites enriched in steroid hormone biosynthesis pathway. FMT increased estradiol and insulin-like growth factor 1 but decreased progesterone dynamically. FMT also increased the expression of the EGD-related genes estrogen receptor 1 gene, epithelial cadherin, and forkhead box protein A2. There is a significant correlation between FMT-shifted gut microbes and EGD-related indices.ConclusionSexually matured Meishan gilts achieved a superior EGD than LxY gilts. Meanwhile, gut microbiota contribute to the EGD potentially via regulating of steroid hormones during the ovary-dependent period.

Highlights

  • The hyper-prolificacy Meishan gilts achieved a superior endometrial gland development (EGD) than white crossbred gilts during the ovary-independent period

  • Meishan gilts have distinct uterine characters and gut microbiota compared with Landrace x Yorkshire (LxY) gilts Under the same housing and feeding conditions, Meishan gilts have larger (P < 0.001) endometrial gland area normaled to the endometrial area (Fig. 1a-b) and longer (P < 0.01 for left uterine horn and P < 0.001 for right uterine horn) uterine horn length (Fig. 1c) but lighter (P < 0.05) uterine horn weight (Fig. 1d) compared with Landrace × Yorkshire (L×Y) gilts at the age of third estrus

  • Further taxon analysis showed that Meishan gilts’ gut harbored more bacteria of phyla Actinobacteria Firmicutes, Fibrobacteres, Lentisphaerae, and Synergistetes but fewer bacteria of phyla Bacteroidetes and WPS-2 compared with L×Y gilts

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Summary

Introduction

The hyper-prolificacy Meishan gilts achieved a superior endometrial gland development (EGD) than white crossbred gilts during the ovary-independent period (before 60 d of age). The EGD continues under the management of ovary-derived steroid hormones that regulated by gut microbiota (after 60 d of age). Whether Meishan gilts’ superiority in EGD lasting to the ovary-dependent period (after 60 d of age) and the role of gut microbiota in this period both remain unclear. Progesterone can inhibit estradiol actions in stimulation of uterine epithelial proliferation through epithelial progesterone receptors [5, 7]. This relationship between estradiol and progesterone may regulate the endometrial gland development and uterine function

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