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Visualizing germination of microbiota endospores in the mammalian gut
Transmission of bacterial endospores between the environment and people and the following germination in vivo play critical roles in both the deadly infections of some bacterial pathogens and the stabilization of the commensal microbiotas in humans. Our knowledge about the germination process of dif...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9543051/ https://www.ncbi.nlm.nih.gov/pubmed/36175402 http://dx.doi.org/10.1080/19490976.2022.2125737 |
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author | Xu, Ningning Lin, Liyuan Du, Yahui Lin, Huibin Song, Jia Yang, Chaoyong Wang, Wei |
author_facet | Xu, Ningning Lin, Liyuan Du, Yahui Lin, Huibin Song, Jia Yang, Chaoyong Wang, Wei |
author_sort | Xu, Ningning |
collection | PubMed |
description | Transmission of bacterial endospores between the environment and people and the following germination in vivo play critical roles in both the deadly infections of some bacterial pathogens and the stabilization of the commensal microbiotas in humans. Our knowledge about the germination process of different bacteria in the mammalian gut, however, is still very limited due to the lack of suitable tools to visually monitor this process. We proposed a two-step labeling strategy that can image and quantify the endospores’ germination in the recipient’s intestines. Endospores collected from donor’s gut microbiota were first labeled with fluorescein isothiocyanate and transplanted to mice via gavage. The recipient mice were then administered with Cyanine5-tagged D-amino acid to label all the viable bacteria, including the germinated endospores, in their intestines in situ. The germinated donor endospores could be distinguished by presenting two types of fluorescent signals simultaneously. The integrative use of cell-sorting, 16S rDNA sequencing, and fluorescence in situ hybridization (FISH) staining of the two-colored bacteria unveiled the taxonomic information of the donor endospores that germinated in the recipient’s gut. Using this strategy, we investigated effects of different germinants and pre-treatment interventions on their germination, and found that germination of different commensal bacterial genera was distinctly affected by various types of germinants. This two-color labeling strategy shows its potential as a versatile tool for visually monitoring endospore germination in the hosts and screening for new interventions to improve endospore-based therapeutics. |
format | Online Article Text |
id | pubmed-9543051 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-95430512022-10-08 Visualizing germination of microbiota endospores in the mammalian gut Xu, Ningning Lin, Liyuan Du, Yahui Lin, Huibin Song, Jia Yang, Chaoyong Wang, Wei Gut Microbes Research Paper Transmission of bacterial endospores between the environment and people and the following germination in vivo play critical roles in both the deadly infections of some bacterial pathogens and the stabilization of the commensal microbiotas in humans. Our knowledge about the germination process of different bacteria in the mammalian gut, however, is still very limited due to the lack of suitable tools to visually monitor this process. We proposed a two-step labeling strategy that can image and quantify the endospores’ germination in the recipient’s intestines. Endospores collected from donor’s gut microbiota were first labeled with fluorescein isothiocyanate and transplanted to mice via gavage. The recipient mice were then administered with Cyanine5-tagged D-amino acid to label all the viable bacteria, including the germinated endospores, in their intestines in situ. The germinated donor endospores could be distinguished by presenting two types of fluorescent signals simultaneously. The integrative use of cell-sorting, 16S rDNA sequencing, and fluorescence in situ hybridization (FISH) staining of the two-colored bacteria unveiled the taxonomic information of the donor endospores that germinated in the recipient’s gut. Using this strategy, we investigated effects of different germinants and pre-treatment interventions on their germination, and found that germination of different commensal bacterial genera was distinctly affected by various types of germinants. This two-color labeling strategy shows its potential as a versatile tool for visually monitoring endospore germination in the hosts and screening for new interventions to improve endospore-based therapeutics. Taylor & Francis 2022-09-29 /pmc/articles/PMC9543051/ /pubmed/36175402 http://dx.doi.org/10.1080/19490976.2022.2125737 Text en © 2022 The Author(s). Published with license by Taylor & Francis Group, LLC. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Paper Xu, Ningning Lin, Liyuan Du, Yahui Lin, Huibin Song, Jia Yang, Chaoyong Wang, Wei Visualizing germination of microbiota endospores in the mammalian gut |
title | Visualizing germination of microbiota endospores in the mammalian gut |
title_full | Visualizing germination of microbiota endospores in the mammalian gut |
title_fullStr | Visualizing germination of microbiota endospores in the mammalian gut |
title_full_unstemmed | Visualizing germination of microbiota endospores in the mammalian gut |
title_short | Visualizing germination of microbiota endospores in the mammalian gut |
title_sort | visualizing germination of microbiota endospores in the mammalian gut |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9543051/ https://www.ncbi.nlm.nih.gov/pubmed/36175402 http://dx.doi.org/10.1080/19490976.2022.2125737 |
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