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Impact of Escherichia coli Outer Membrane Vesicles on Sperm Function
Reproductive tract infections account for approximately 15% of male infertility cases. Escherichia coli (E. coli) represents the most frequently isolated bacterial strain in the semen of infertile men. All Gram-negative bacteria constitutively produce outer membrane vesicles (OMVs). The present stud...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9319964/ https://www.ncbi.nlm.nih.gov/pubmed/35890027 http://dx.doi.org/10.3390/pathogens11070782 |
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author | Folliero, Veronica Santonastaso, Marianna Dell’Annunziata, Federica De Franciscis, Pasquale Boccia, Giovanni Colacurci, Nicola De Filippis, Anna Galdiero, Massimiliano Franci, Gianluigi |
author_facet | Folliero, Veronica Santonastaso, Marianna Dell’Annunziata, Federica De Franciscis, Pasquale Boccia, Giovanni Colacurci, Nicola De Filippis, Anna Galdiero, Massimiliano Franci, Gianluigi |
author_sort | Folliero, Veronica |
collection | PubMed |
description | Reproductive tract infections account for approximately 15% of male infertility cases. Escherichia coli (E. coli) represents the most frequently isolated bacterial strain in the semen of infertile men. All Gram-negative bacteria constitutively produce outer membrane vesicles (OMVs). The present study proved, for the first time, the involvement of OMVs in human sperm function. E. coli OMVs were isolated by ultracentrifugation and characterized via sodium dodecyl sulfate–polyacrylamide gel electrophoresis (SDS-PAGE), transmission electron microscopy (TEM) and dynamic light scattering (DLS) analysis. Human sperm was exposed to OMVs (8 µg/mL) for different times (30, 45, 60 and 90 min). The vitality, motility, morphology, ROS level and DNA fragmentation of spermatozoa were evaluated. OMVs reduced the progressive motility and increased the immobile spermatozoa amount after 30 min of treatment. In addition, a significant increase in the percentage of intracellular ROS and sperm DNA fragmentation was recorded for each vesicular exposure time. These preliminary findings prove that OMVs contribute to altering human sperm function via two mechanisms: (i) impaired motility and (ii) DNA fragmentation. |
format | Online Article Text |
id | pubmed-9319964 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-93199642022-07-27 Impact of Escherichia coli Outer Membrane Vesicles on Sperm Function Folliero, Veronica Santonastaso, Marianna Dell’Annunziata, Federica De Franciscis, Pasquale Boccia, Giovanni Colacurci, Nicola De Filippis, Anna Galdiero, Massimiliano Franci, Gianluigi Pathogens Article Reproductive tract infections account for approximately 15% of male infertility cases. Escherichia coli (E. coli) represents the most frequently isolated bacterial strain in the semen of infertile men. All Gram-negative bacteria constitutively produce outer membrane vesicles (OMVs). The present study proved, for the first time, the involvement of OMVs in human sperm function. E. coli OMVs were isolated by ultracentrifugation and characterized via sodium dodecyl sulfate–polyacrylamide gel electrophoresis (SDS-PAGE), transmission electron microscopy (TEM) and dynamic light scattering (DLS) analysis. Human sperm was exposed to OMVs (8 µg/mL) for different times (30, 45, 60 and 90 min). The vitality, motility, morphology, ROS level and DNA fragmentation of spermatozoa were evaluated. OMVs reduced the progressive motility and increased the immobile spermatozoa amount after 30 min of treatment. In addition, a significant increase in the percentage of intracellular ROS and sperm DNA fragmentation was recorded for each vesicular exposure time. These preliminary findings prove that OMVs contribute to altering human sperm function via two mechanisms: (i) impaired motility and (ii) DNA fragmentation. MDPI 2022-07-10 /pmc/articles/PMC9319964/ /pubmed/35890027 http://dx.doi.org/10.3390/pathogens11070782 Text en © 2022 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 Folliero, Veronica Santonastaso, Marianna Dell’Annunziata, Federica De Franciscis, Pasquale Boccia, Giovanni Colacurci, Nicola De Filippis, Anna Galdiero, Massimiliano Franci, Gianluigi Impact of Escherichia coli Outer Membrane Vesicles on Sperm Function |
title | Impact of Escherichia coli Outer Membrane Vesicles on Sperm Function |
title_full | Impact of Escherichia coli Outer Membrane Vesicles on Sperm Function |
title_fullStr | Impact of Escherichia coli Outer Membrane Vesicles on Sperm Function |
title_full_unstemmed | Impact of Escherichia coli Outer Membrane Vesicles on Sperm Function |
title_short | Impact of Escherichia coli Outer Membrane Vesicles on Sperm Function |
title_sort | impact of escherichia coli outer membrane vesicles on sperm function |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9319964/ https://www.ncbi.nlm.nih.gov/pubmed/35890027 http://dx.doi.org/10.3390/pathogens11070782 |
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