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Lactobacilli extracellular vesicles: potential postbiotics to support the vaginal microbiota homeostasis

BACKGROUND: Lactobacillus species dominate the vaginal microflora performing a first-line defense against vaginal infections. Extracellular vesicles (EVs) released by lactobacilli are considered mediators of their beneficial effects affecting cellular communication, homeostasis, microbial balance, a...

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Autores principales: Croatti, Vanessa, Parolin, Carola, Giordani, Barbara, Foschi, Claudio, Fedi, Stefano, Vitali, Beatrice
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9664694/
https://www.ncbi.nlm.nih.gov/pubmed/36376912
http://dx.doi.org/10.1186/s12934-022-01963-6
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author Croatti, Vanessa
Parolin, Carola
Giordani, Barbara
Foschi, Claudio
Fedi, Stefano
Vitali, Beatrice
author_facet Croatti, Vanessa
Parolin, Carola
Giordani, Barbara
Foschi, Claudio
Fedi, Stefano
Vitali, Beatrice
author_sort Croatti, Vanessa
collection PubMed
description BACKGROUND: Lactobacillus species dominate the vaginal microflora performing a first-line defense against vaginal infections. Extracellular vesicles (EVs) released by lactobacilli are considered mediators of their beneficial effects affecting cellular communication, homeostasis, microbial balance, and host immune system pathways. Up to now, very little is known about the role played by Lactobacillus EVs in the vaginal microenvironment, and mechanisms of action remain poorly understood. RESULTS: Here, we hypothesized that EVs can mediate lactobacilli beneficial effects to the host by modulating the vaginal microbiota colonization. We recovered and characterized EVs produced by two vaginal strains, namely Lactobacillus crispatus BC5 and Lactobacillus gasseri BC12. EVs were isolated by ultracentrifugation and physically characterized by Nanoparticle Tracking Analysis (NTA) and Dynamic Light Scattering (DLS). EVs protein and nucleic acids (DNA and RNA) content was also evaluated. We explored the role of EVs on bacterial adhesion and colonization, using a cervical cell line (HeLa) as an in vitro model. Specifically, we evaluated the effect of EVs on the adhesion of both vaginal beneficial lactobacilli and opportunistic pathogens (i.e., Escherichia coli, Staphylococcus aureus, Streptococcus agalactiae, and Enterococcus faecalis). We demonstrated that EVs from L. crispatus BC5 and L. gasseri BC12 significantly enhanced the cellular adhesion of all tested lactobacilli, reaching the maximum stimulation effect on strains belonging to L. crispatus species (335% and 269% of average adhesion, respectively). At the same time, EVs reduced the adhesion of all tested pathogens, being EVs from L. gasseri BC12 the most efficient. CONCLUSIONS: Our observations suggest for the first time that EVs released by symbiotic Lactobacillus strains favor healthy vaginal homeostasis by supporting the colonization of beneficial species and preventing pathogens attachment. This study reinforces the concept of EVs as valid postbiotics and opens the perspective of developing postbiotics from vaginal strains to maintain microbiota homeostasis and promote women’s health.
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spelling pubmed-96646942022-11-15 Lactobacilli extracellular vesicles: potential postbiotics to support the vaginal microbiota homeostasis Croatti, Vanessa Parolin, Carola Giordani, Barbara Foschi, Claudio Fedi, Stefano Vitali, Beatrice Microb Cell Fact Research BACKGROUND: Lactobacillus species dominate the vaginal microflora performing a first-line defense against vaginal infections. Extracellular vesicles (EVs) released by lactobacilli are considered mediators of their beneficial effects affecting cellular communication, homeostasis, microbial balance, and host immune system pathways. Up to now, very little is known about the role played by Lactobacillus EVs in the vaginal microenvironment, and mechanisms of action remain poorly understood. RESULTS: Here, we hypothesized that EVs can mediate lactobacilli beneficial effects to the host by modulating the vaginal microbiota colonization. We recovered and characterized EVs produced by two vaginal strains, namely Lactobacillus crispatus BC5 and Lactobacillus gasseri BC12. EVs were isolated by ultracentrifugation and physically characterized by Nanoparticle Tracking Analysis (NTA) and Dynamic Light Scattering (DLS). EVs protein and nucleic acids (DNA and RNA) content was also evaluated. We explored the role of EVs on bacterial adhesion and colonization, using a cervical cell line (HeLa) as an in vitro model. Specifically, we evaluated the effect of EVs on the adhesion of both vaginal beneficial lactobacilli and opportunistic pathogens (i.e., Escherichia coli, Staphylococcus aureus, Streptococcus agalactiae, and Enterococcus faecalis). We demonstrated that EVs from L. crispatus BC5 and L. gasseri BC12 significantly enhanced the cellular adhesion of all tested lactobacilli, reaching the maximum stimulation effect on strains belonging to L. crispatus species (335% and 269% of average adhesion, respectively). At the same time, EVs reduced the adhesion of all tested pathogens, being EVs from L. gasseri BC12 the most efficient. CONCLUSIONS: Our observations suggest for the first time that EVs released by symbiotic Lactobacillus strains favor healthy vaginal homeostasis by supporting the colonization of beneficial species and preventing pathogens attachment. This study reinforces the concept of EVs as valid postbiotics and opens the perspective of developing postbiotics from vaginal strains to maintain microbiota homeostasis and promote women’s health. BioMed Central 2022-11-15 /pmc/articles/PMC9664694/ /pubmed/36376912 http://dx.doi.org/10.1186/s12934-022-01963-6 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Croatti, Vanessa
Parolin, Carola
Giordani, Barbara
Foschi, Claudio
Fedi, Stefano
Vitali, Beatrice
Lactobacilli extracellular vesicles: potential postbiotics to support the vaginal microbiota homeostasis
title Lactobacilli extracellular vesicles: potential postbiotics to support the vaginal microbiota homeostasis
title_full Lactobacilli extracellular vesicles: potential postbiotics to support the vaginal microbiota homeostasis
title_fullStr Lactobacilli extracellular vesicles: potential postbiotics to support the vaginal microbiota homeostasis
title_full_unstemmed Lactobacilli extracellular vesicles: potential postbiotics to support the vaginal microbiota homeostasis
title_short Lactobacilli extracellular vesicles: potential postbiotics to support the vaginal microbiota homeostasis
title_sort lactobacilli extracellular vesicles: potential postbiotics to support the vaginal microbiota homeostasis
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9664694/
https://www.ncbi.nlm.nih.gov/pubmed/36376912
http://dx.doi.org/10.1186/s12934-022-01963-6
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