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Sperm Microbiota and Its Impact on Semen Parameters

Compared to its female counterpart, the microbiota of the male genital tract has not been studied extensively. With this study, we aimed to evaluate the bacterial composition of seminal fluid and its impact on sperm parameters. We hypothesized that a dysbiotic microbiota composition may have an infl...

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Autores principales: Baud, David, Pattaroni, Céline, Vulliemoz, Nicolas, Castella, Vincent, Marsland, Benjamin J., Stojanov, Milos
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6379293/
https://www.ncbi.nlm.nih.gov/pubmed/30809218
http://dx.doi.org/10.3389/fmicb.2019.00234
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author Baud, David
Pattaroni, Céline
Vulliemoz, Nicolas
Castella, Vincent
Marsland, Benjamin J.
Stojanov, Milos
author_facet Baud, David
Pattaroni, Céline
Vulliemoz, Nicolas
Castella, Vincent
Marsland, Benjamin J.
Stojanov, Milos
author_sort Baud, David
collection PubMed
description Compared to its female counterpart, the microbiota of the male genital tract has not been studied extensively. With this study, we aimed to evaluate the bacterial composition of seminal fluid and its impact on sperm parameters. We hypothesized that a dysbiotic microbiota composition may have an influence on sperm quality. Semen samples of 26 men with normal spermiogram and 68 men with at least one abnormal spermiogram parameter were included in the study. Samples were stratified based on total sperm count, spermatozoa concentration, progressive motility, total motility and spermatozoa morphology. Microbiota profiling was performed using 16S rRNA gene amplicons sequencing and total bacterial load was determined using a panbacterial quantitative PCR. Semen samples broadly clustered into three microbiota profiles: Prevotella-enriched, Lactobacillus-enriched, and polymicrobial. Prevotella-enriched samples had the highest bacterial load (p < 0.05). Network analysis identified three main co-occurrence modules, among which two contained bacteria commonly found in the vaginal flora. Genera from the same module displayed similar oxygen requirements, arguing for the presence of different ecological niches for bacteria that colonize semen through the passage. Contrary to our hypothesis, shifts in overall microbiota composition (beta-diversity) did not correlate with spermiogram parameters. Similarly, we did not find any difference in microbial richness or diversity (alpha-diversity). Differential abundance testing, however, revealed three specific genera that were significantly enriched or depleted in some of the sperm quality groups (p < 0.05). Prevotella relative abundance was increased in samples with defective sperm motility while Staphylococcus was increased in the corresponding control group. In addition, we observed an increased relative abundance of Lactobacillus in samples with normal sperm morphology. Our study indicates that overall bacterial content of sperm might not play a major role in male infertility. Although no major shifts in microbiota composition or diversity were found, the differential abundance of specific bacterial genera in the sperm suggests that a small subset of microbes might impact the spermatozoal physiology during sperm transition, more specifically motility and morphology. Further studies are required to challenge this finding and develop potential strategies to induce the formation of a healthy seminal microbiota.
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spelling pubmed-63792932019-02-26 Sperm Microbiota and Its Impact on Semen Parameters Baud, David Pattaroni, Céline Vulliemoz, Nicolas Castella, Vincent Marsland, Benjamin J. Stojanov, Milos Front Microbiol Microbiology Compared to its female counterpart, the microbiota of the male genital tract has not been studied extensively. With this study, we aimed to evaluate the bacterial composition of seminal fluid and its impact on sperm parameters. We hypothesized that a dysbiotic microbiota composition may have an influence on sperm quality. Semen samples of 26 men with normal spermiogram and 68 men with at least one abnormal spermiogram parameter were included in the study. Samples were stratified based on total sperm count, spermatozoa concentration, progressive motility, total motility and spermatozoa morphology. Microbiota profiling was performed using 16S rRNA gene amplicons sequencing and total bacterial load was determined using a panbacterial quantitative PCR. Semen samples broadly clustered into three microbiota profiles: Prevotella-enriched, Lactobacillus-enriched, and polymicrobial. Prevotella-enriched samples had the highest bacterial load (p < 0.05). Network analysis identified three main co-occurrence modules, among which two contained bacteria commonly found in the vaginal flora. Genera from the same module displayed similar oxygen requirements, arguing for the presence of different ecological niches for bacteria that colonize semen through the passage. Contrary to our hypothesis, shifts in overall microbiota composition (beta-diversity) did not correlate with spermiogram parameters. Similarly, we did not find any difference in microbial richness or diversity (alpha-diversity). Differential abundance testing, however, revealed three specific genera that were significantly enriched or depleted in some of the sperm quality groups (p < 0.05). Prevotella relative abundance was increased in samples with defective sperm motility while Staphylococcus was increased in the corresponding control group. In addition, we observed an increased relative abundance of Lactobacillus in samples with normal sperm morphology. Our study indicates that overall bacterial content of sperm might not play a major role in male infertility. Although no major shifts in microbiota composition or diversity were found, the differential abundance of specific bacterial genera in the sperm suggests that a small subset of microbes might impact the spermatozoal physiology during sperm transition, more specifically motility and morphology. Further studies are required to challenge this finding and develop potential strategies to induce the formation of a healthy seminal microbiota. Frontiers Media S.A. 2019-02-12 /pmc/articles/PMC6379293/ /pubmed/30809218 http://dx.doi.org/10.3389/fmicb.2019.00234 Text en Copyright © 2019 Baud, Pattaroni, Vulliemoz, Castella, Marsland and Stojanov. 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
Baud, David
Pattaroni, Céline
Vulliemoz, Nicolas
Castella, Vincent
Marsland, Benjamin J.
Stojanov, Milos
Sperm Microbiota and Its Impact on Semen Parameters
title Sperm Microbiota and Its Impact on Semen Parameters
title_full Sperm Microbiota and Its Impact on Semen Parameters
title_fullStr Sperm Microbiota and Its Impact on Semen Parameters
title_full_unstemmed Sperm Microbiota and Its Impact on Semen Parameters
title_short Sperm Microbiota and Its Impact on Semen Parameters
title_sort sperm microbiota and its impact on semen parameters
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6379293/
https://www.ncbi.nlm.nih.gov/pubmed/30809218
http://dx.doi.org/10.3389/fmicb.2019.00234
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