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Microbiome–Metabolome Reveals the Contribution of the Gut–Testis Axis to Sperm Motility in Sheep (Ovis aries)
SIMPLE SUMMARY: Healthy sperm viability, the core of male fertility, affects the sustainability of livestock breeding. Several studies have shown a strong link between male sperm motility and gut microbial regulation of the host metabolome, testicular function, and gut microbiota. However, few studi...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10044597/ https://www.ncbi.nlm.nih.gov/pubmed/36978536 http://dx.doi.org/10.3390/ani13060996 |
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author | Wang, Mingming Ren, Chunhuan Wang, Penghui Cheng, Xiao Chen, Yale Huang, Yafeng Chen, Jiahong Sun, Zhipeng Wang, Qiangjun Zhang, Zijun |
author_facet | Wang, Mingming Ren, Chunhuan Wang, Penghui Cheng, Xiao Chen, Yale Huang, Yafeng Chen, Jiahong Sun, Zhipeng Wang, Qiangjun Zhang, Zijun |
author_sort | Wang, Mingming |
collection | PubMed |
description | SIMPLE SUMMARY: Healthy sperm viability, the core of male fertility, affects the sustainability of livestock breeding. Several studies have shown a strong link between male sperm motility and gut microbial regulation of the host metabolome, testicular function, and gut microbiota. However, few studies have examined the association between the gut microbiome, host metabolome, and testicular function. In this study, the microbiome and metabolome of adult sheep with significantly different sperm viabilities were analyzed. Our results confirm that gut microorganisms and metabolites differ significantly in sheep with different sperm viabilities and are strongly correlated among themselves and with sperm viability. Thus, our study provides new insights into weak spermatozoa in rams. ABSTRACT: A close association exists among testicular function, gut microbiota regulation, and organismal metabolism. In this study, serum and seminal plasma metabolomes, and the rumen microbiome of sheep with significant differences in sperm viability, were explored. Serum and seminal plasma metabolomes differed significantly between high-motility (HM) and low-motility (LM) groups of sheep, and 39 differential metabolites closely related to sperm motility in sheep were found in seminal plasma metabolomes, while 35 were found in serum samples. A 16S rRNA sequence analysis showed that the relative abundance of HM and LM rumen microorganisms, such as Ruminococcus and Quinella, was significantly higher in the HM group, whereas genera such as Rikenellaceae_RC9_gut_group and Lactobacillus were enriched in the mid-LM group. Serum hormone assays revealed that serum follicle-stimulating hormone (FSH) and MT levels were significantly lower in the LM group than in the HM group, whereas serum glucocorticoid (GC) levels were higher in the LM group than in the HM group, and they all affected sperm motility in sheep. Ruminococcus and other rumen microorganisms were positively correlated with sperm motility, whereas Lactobacillus was negatively correlated with FSH and GCs levels. Our findings suggest that rumen microbial activity can influence the host metabolism and hormone levels associated with fertility in sheep. |
format | Online Article Text |
id | pubmed-10044597 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-100445972023-03-29 Microbiome–Metabolome Reveals the Contribution of the Gut–Testis Axis to Sperm Motility in Sheep (Ovis aries) Wang, Mingming Ren, Chunhuan Wang, Penghui Cheng, Xiao Chen, Yale Huang, Yafeng Chen, Jiahong Sun, Zhipeng Wang, Qiangjun Zhang, Zijun Animals (Basel) Article SIMPLE SUMMARY: Healthy sperm viability, the core of male fertility, affects the sustainability of livestock breeding. Several studies have shown a strong link between male sperm motility and gut microbial regulation of the host metabolome, testicular function, and gut microbiota. However, few studies have examined the association between the gut microbiome, host metabolome, and testicular function. In this study, the microbiome and metabolome of adult sheep with significantly different sperm viabilities were analyzed. Our results confirm that gut microorganisms and metabolites differ significantly in sheep with different sperm viabilities and are strongly correlated among themselves and with sperm viability. Thus, our study provides new insights into weak spermatozoa in rams. ABSTRACT: A close association exists among testicular function, gut microbiota regulation, and organismal metabolism. In this study, serum and seminal plasma metabolomes, and the rumen microbiome of sheep with significant differences in sperm viability, were explored. Serum and seminal plasma metabolomes differed significantly between high-motility (HM) and low-motility (LM) groups of sheep, and 39 differential metabolites closely related to sperm motility in sheep were found in seminal plasma metabolomes, while 35 were found in serum samples. A 16S rRNA sequence analysis showed that the relative abundance of HM and LM rumen microorganisms, such as Ruminococcus and Quinella, was significantly higher in the HM group, whereas genera such as Rikenellaceae_RC9_gut_group and Lactobacillus were enriched in the mid-LM group. Serum hormone assays revealed that serum follicle-stimulating hormone (FSH) and MT levels were significantly lower in the LM group than in the HM group, whereas serum glucocorticoid (GC) levels were higher in the LM group than in the HM group, and they all affected sperm motility in sheep. Ruminococcus and other rumen microorganisms were positively correlated with sperm motility, whereas Lactobacillus was negatively correlated with FSH and GCs levels. Our findings suggest that rumen microbial activity can influence the host metabolism and hormone levels associated with fertility in sheep. MDPI 2023-03-09 /pmc/articles/PMC10044597/ /pubmed/36978536 http://dx.doi.org/10.3390/ani13060996 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Wang, Mingming Ren, Chunhuan Wang, Penghui Cheng, Xiao Chen, Yale Huang, Yafeng Chen, Jiahong Sun, Zhipeng Wang, Qiangjun Zhang, Zijun Microbiome–Metabolome Reveals the Contribution of the Gut–Testis Axis to Sperm Motility in Sheep (Ovis aries) |
title | Microbiome–Metabolome Reveals the Contribution of the Gut–Testis Axis to Sperm Motility in Sheep (Ovis aries) |
title_full | Microbiome–Metabolome Reveals the Contribution of the Gut–Testis Axis to Sperm Motility in Sheep (Ovis aries) |
title_fullStr | Microbiome–Metabolome Reveals the Contribution of the Gut–Testis Axis to Sperm Motility in Sheep (Ovis aries) |
title_full_unstemmed | Microbiome–Metabolome Reveals the Contribution of the Gut–Testis Axis to Sperm Motility in Sheep (Ovis aries) |
title_short | Microbiome–Metabolome Reveals the Contribution of the Gut–Testis Axis to Sperm Motility in Sheep (Ovis aries) |
title_sort | microbiome–metabolome reveals the contribution of the gut–testis axis to sperm motility in sheep (ovis aries) |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10044597/ https://www.ncbi.nlm.nih.gov/pubmed/36978536 http://dx.doi.org/10.3390/ani13060996 |
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