Cargando…
Genomic Sequencing Reveals the Diversity of Seminal Bacteria and Relationships to Reproductive Potential in Boar Sperm
A number of emerging studies suggest that pathogenic microorganisms in semen may cause a decline in the reproductive potential of spermatozoa, and the bacterial diversity and profile of ejaculated boar semen in different seasons are currently unknown. To explore the bacterial composition and changes...
Autores principales: | , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7438901/ https://www.ncbi.nlm.nih.gov/pubmed/32903829 http://dx.doi.org/10.3389/fmicb.2020.01873 |
_version_ | 1783572886220439552 |
---|---|
author | Zhang, Jing Liu, Huan Yang, Qiangzhen Li, Peifei Wen, Yi Han, Xuejun Li, Bushe Jiang, Hongju Li, Xinhong |
author_facet | Zhang, Jing Liu, Huan Yang, Qiangzhen Li, Peifei Wen, Yi Han, Xuejun Li, Bushe Jiang, Hongju Li, Xinhong |
author_sort | Zhang, Jing |
collection | PubMed |
description | A number of emerging studies suggest that pathogenic microorganisms in semen may cause a decline in the reproductive potential of spermatozoa, and the bacterial diversity and profile of ejaculated boar semen in different seasons are currently unknown. To explore the bacterial composition and changes in ejaculated boar semen from winter and summer, and the underlying mechanism of decline in sperm quality and fertility capacity in summer, 120 ejaculated semen samples were examined for bacterial communities using genomic sequencing technology, and the associations between microbial composition and sperm reproductive potential were investigated. The results showed that Proteobacteria (57.53%), Firmicutes (31.17%), Bacteroidetes (4.24%), and Actinobacteria (3.41%) are the dominant phyla in the ejaculated semen, and the dominant genera were Pseudomonas (34.41%) and Lactobacillus (19.93%), which belong to the phyla of Proteobacteria and Firmicutes, respectively. Interestingly, the higher diversity of bacteria in ejaculated semen of winter differs from that of summer semen, potentially due to seasonal changes related to changes in semen quality and sperm fertilizing capacity. Furthermore, the highly abundant Lactobacillus in winter samples were positively associated with sperm quality and reproductive performance obtained from sows inseminated with such semen samples, while in contrast, the highly abundant Pseudomonas in summer samples was negatively associated with sperm quality and reproductive potential. Additionally, our results strongly indicated that Lactobacillus is not only a potential probiotic for semen quality and fertility potential but also beneficial for restraining the negative influence of Pseudomonas. Overall, our findings significantly contribute to the current understanding of the phenotypes and etiology of male “summer infertility,” and may represent a frontier in male reproductive disorders and possible early prevention against pathogenic bacteria. |
format | Online Article Text |
id | pubmed-7438901 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-74389012020-09-03 Genomic Sequencing Reveals the Diversity of Seminal Bacteria and Relationships to Reproductive Potential in Boar Sperm Zhang, Jing Liu, Huan Yang, Qiangzhen Li, Peifei Wen, Yi Han, Xuejun Li, Bushe Jiang, Hongju Li, Xinhong Front Microbiol Microbiology A number of emerging studies suggest that pathogenic microorganisms in semen may cause a decline in the reproductive potential of spermatozoa, and the bacterial diversity and profile of ejaculated boar semen in different seasons are currently unknown. To explore the bacterial composition and changes in ejaculated boar semen from winter and summer, and the underlying mechanism of decline in sperm quality and fertility capacity in summer, 120 ejaculated semen samples were examined for bacterial communities using genomic sequencing technology, and the associations between microbial composition and sperm reproductive potential were investigated. The results showed that Proteobacteria (57.53%), Firmicutes (31.17%), Bacteroidetes (4.24%), and Actinobacteria (3.41%) are the dominant phyla in the ejaculated semen, and the dominant genera were Pseudomonas (34.41%) and Lactobacillus (19.93%), which belong to the phyla of Proteobacteria and Firmicutes, respectively. Interestingly, the higher diversity of bacteria in ejaculated semen of winter differs from that of summer semen, potentially due to seasonal changes related to changes in semen quality and sperm fertilizing capacity. Furthermore, the highly abundant Lactobacillus in winter samples were positively associated with sperm quality and reproductive performance obtained from sows inseminated with such semen samples, while in contrast, the highly abundant Pseudomonas in summer samples was negatively associated with sperm quality and reproductive potential. Additionally, our results strongly indicated that Lactobacillus is not only a potential probiotic for semen quality and fertility potential but also beneficial for restraining the negative influence of Pseudomonas. Overall, our findings significantly contribute to the current understanding of the phenotypes and etiology of male “summer infertility,” and may represent a frontier in male reproductive disorders and possible early prevention against pathogenic bacteria. Frontiers Media S.A. 2020-08-04 /pmc/articles/PMC7438901/ /pubmed/32903829 http://dx.doi.org/10.3389/fmicb.2020.01873 Text en Copyright © 2020 Zhang, Liu, Yang, Li, Wen, Han, Li, Jiang and Li. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Microbiology Zhang, Jing Liu, Huan Yang, Qiangzhen Li, Peifei Wen, Yi Han, Xuejun Li, Bushe Jiang, Hongju Li, Xinhong Genomic Sequencing Reveals the Diversity of Seminal Bacteria and Relationships to Reproductive Potential in Boar Sperm |
title | Genomic Sequencing Reveals the Diversity of Seminal Bacteria and Relationships to Reproductive Potential in Boar Sperm |
title_full | Genomic Sequencing Reveals the Diversity of Seminal Bacteria and Relationships to Reproductive Potential in Boar Sperm |
title_fullStr | Genomic Sequencing Reveals the Diversity of Seminal Bacteria and Relationships to Reproductive Potential in Boar Sperm |
title_full_unstemmed | Genomic Sequencing Reveals the Diversity of Seminal Bacteria and Relationships to Reproductive Potential in Boar Sperm |
title_short | Genomic Sequencing Reveals the Diversity of Seminal Bacteria and Relationships to Reproductive Potential in Boar Sperm |
title_sort | genomic sequencing reveals the diversity of seminal bacteria and relationships to reproductive potential in boar sperm |
topic | Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7438901/ https://www.ncbi.nlm.nih.gov/pubmed/32903829 http://dx.doi.org/10.3389/fmicb.2020.01873 |
work_keys_str_mv | AT zhangjing genomicsequencingrevealsthediversityofseminalbacteriaandrelationshipstoreproductivepotentialinboarsperm AT liuhuan genomicsequencingrevealsthediversityofseminalbacteriaandrelationshipstoreproductivepotentialinboarsperm AT yangqiangzhen genomicsequencingrevealsthediversityofseminalbacteriaandrelationshipstoreproductivepotentialinboarsperm AT lipeifei genomicsequencingrevealsthediversityofseminalbacteriaandrelationshipstoreproductivepotentialinboarsperm AT wenyi genomicsequencingrevealsthediversityofseminalbacteriaandrelationshipstoreproductivepotentialinboarsperm AT hanxuejun genomicsequencingrevealsthediversityofseminalbacteriaandrelationshipstoreproductivepotentialinboarsperm AT libushe genomicsequencingrevealsthediversityofseminalbacteriaandrelationshipstoreproductivepotentialinboarsperm AT jianghongju genomicsequencingrevealsthediversityofseminalbacteriaandrelationshipstoreproductivepotentialinboarsperm AT lixinhong genomicsequencingrevealsthediversityofseminalbacteriaandrelationshipstoreproductivepotentialinboarsperm |