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Adaptive response to iterative passages of five Lactobacillus species in simulated vaginal fluid
BACKGROUND: Microbiome and metagenomic studies have given rise to a new understanding of microbial colonization of various human tissues and their ability to impact our health. One human microbiome growing in notoriety, the vaginal microbiome, stands out given its importance for women’s health, and...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7653816/ https://www.ncbi.nlm.nih.gov/pubmed/33172400 http://dx.doi.org/10.1186/s12866-020-02027-8 |
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author | Brandt, Katelyn Barrangou, Rodolphe |
author_facet | Brandt, Katelyn Barrangou, Rodolphe |
author_sort | Brandt, Katelyn |
collection | PubMed |
description | BACKGROUND: Microbiome and metagenomic studies have given rise to a new understanding of microbial colonization of various human tissues and their ability to impact our health. One human microbiome growing in notoriety, the vaginal microbiome, stands out given its importance for women’s health, and is peculiar in terms of its relative bacterial composition, including its simplicity and typical domination by a small number of Lactobacillus species. The loss of Lactobacillus dominance is associated with disorders such as bacterial vaginosis, and efforts are now underway to understand the ability of Lactobacillus species to colonize the vaginal tract and adapt to this dynamic and acidic environment. Here, we investigate how various Lactobacillus species often isolated from the vaginal and intestinal cavities genomically and transcriptionally respond to iterative growth in simulated vaginal fluid. RESULTS: We determined the genomes and transcriptomes of L. acidophilus, L. crispatus, L. fermentum, L. gasseri, and L. jensenii and compared profiles after 50, 100, 500, and 1000 generations of iterative passages in synthetic vaginal fluid. In general, we identified relatively few genetic changes consisting of single nucleotide polymorphisms, with higher counts occurring more frequently in non-vaginal isolated species. Transcriptional profiles were more impacted over time and tended to be more extensive for species that typically do not dominate the vaginal tract, reflecting a more extensive need to adapt to a less familiar environment. CONCLUSIONS: This study provides insights into how vaginal and non-vaginal Lactobacillus species respond and adapt to a simulated vaginal environment. Overall, trends indicate high genomic stability for all species involved, with more variability in the transcriptome especially for non-dominant species of the vaginal tract. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12866-020-02027-8. |
format | Online Article Text |
id | pubmed-7653816 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-76538162020-11-16 Adaptive response to iterative passages of five Lactobacillus species in simulated vaginal fluid Brandt, Katelyn Barrangou, Rodolphe BMC Microbiol Research Article BACKGROUND: Microbiome and metagenomic studies have given rise to a new understanding of microbial colonization of various human tissues and their ability to impact our health. One human microbiome growing in notoriety, the vaginal microbiome, stands out given its importance for women’s health, and is peculiar in terms of its relative bacterial composition, including its simplicity and typical domination by a small number of Lactobacillus species. The loss of Lactobacillus dominance is associated with disorders such as bacterial vaginosis, and efforts are now underway to understand the ability of Lactobacillus species to colonize the vaginal tract and adapt to this dynamic and acidic environment. Here, we investigate how various Lactobacillus species often isolated from the vaginal and intestinal cavities genomically and transcriptionally respond to iterative growth in simulated vaginal fluid. RESULTS: We determined the genomes and transcriptomes of L. acidophilus, L. crispatus, L. fermentum, L. gasseri, and L. jensenii and compared profiles after 50, 100, 500, and 1000 generations of iterative passages in synthetic vaginal fluid. In general, we identified relatively few genetic changes consisting of single nucleotide polymorphisms, with higher counts occurring more frequently in non-vaginal isolated species. Transcriptional profiles were more impacted over time and tended to be more extensive for species that typically do not dominate the vaginal tract, reflecting a more extensive need to adapt to a less familiar environment. CONCLUSIONS: This study provides insights into how vaginal and non-vaginal Lactobacillus species respond and adapt to a simulated vaginal environment. Overall, trends indicate high genomic stability for all species involved, with more variability in the transcriptome especially for non-dominant species of the vaginal tract. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12866-020-02027-8. BioMed Central 2020-11-10 /pmc/articles/PMC7653816/ /pubmed/33172400 http://dx.doi.org/10.1186/s12866-020-02027-8 Text en © The Author(s) 2020 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/. The Creative Commons Public Domain Dedication waiver (http://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 Article Brandt, Katelyn Barrangou, Rodolphe Adaptive response to iterative passages of five Lactobacillus species in simulated vaginal fluid |
title | Adaptive response to iterative passages of five Lactobacillus species in simulated vaginal fluid |
title_full | Adaptive response to iterative passages of five Lactobacillus species in simulated vaginal fluid |
title_fullStr | Adaptive response to iterative passages of five Lactobacillus species in simulated vaginal fluid |
title_full_unstemmed | Adaptive response to iterative passages of five Lactobacillus species in simulated vaginal fluid |
title_short | Adaptive response to iterative passages of five Lactobacillus species in simulated vaginal fluid |
title_sort | adaptive response to iterative passages of five lactobacillus species in simulated vaginal fluid |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7653816/ https://www.ncbi.nlm.nih.gov/pubmed/33172400 http://dx.doi.org/10.1186/s12866-020-02027-8 |
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