Cargando…

Disentangling the link between zebrafish diet, gut microbiome succession, and Mycobacterium chelonae infection

BACKGROUND: Despite the long-established importance of zebrafish (Danio rerio) as a model organism and their increasing use in microbiome-targeted studies, relatively little is known about how husbandry practices involving diet impact the zebrafish gut microbiome. Given the microbiome’s important ro...

Descripción completa

Detalles Bibliográficos
Autores principales: Sieler, Michael J., Al-Samarrie, Colleen E., Kasschau, Kristin D., Varga, Zoltan M., Kent, Michael L., Sharpton, Thomas J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10413624/
https://www.ncbi.nlm.nih.gov/pubmed/37563644
http://dx.doi.org/10.1186/s42523-023-00254-8
_version_ 1785087171749740544
author Sieler, Michael J.
Al-Samarrie, Colleen E.
Kasschau, Kristin D.
Varga, Zoltan M.
Kent, Michael L.
Sharpton, Thomas J.
author_facet Sieler, Michael J.
Al-Samarrie, Colleen E.
Kasschau, Kristin D.
Varga, Zoltan M.
Kent, Michael L.
Sharpton, Thomas J.
author_sort Sieler, Michael J.
collection PubMed
description BACKGROUND: Despite the long-established importance of zebrafish (Danio rerio) as a model organism and their increasing use in microbiome-targeted studies, relatively little is known about how husbandry practices involving diet impact the zebrafish gut microbiome. Given the microbiome’s important role in mediating host physiology and the potential for diet to drive variation in microbiome composition, we sought to clarify how three different dietary formulations that are commonly used in zebrafish facilities impact the gut microbiome. We compared the composition of gut microbiomes in approximately 60 AB line adult (129- and 214-day-old) zebrafish fed each diet throughout their lifespan. RESULTS: Our analysis finds that diet has a substantial impact on the composition of the gut microbiome in adult fish, and that diet also impacts the developmental variation in the gut microbiome. We further evaluated how 214-day-old fish microbiome compositions respond to exposure of a common laboratory pathogen, Mycobacterium chelonae, and whether these responses differ as a function of diet. Our analysis finds that diet determines the manner in which the zebrafish gut microbiome responds to M. chelonae exposure, especially for moderate and low abundance taxa. Moreover, histopathological analysis finds that male fish fed different diets are differentially infected by M. chelonae. CONCLUSIONS: Overall, our results indicate that diet drives the successional development of the gut microbiome as well as its sensitivity to exogenous exposure. Consequently, investigators should carefully consider the role of diet in their microbiome zebrafish investigations, especially when integrating results across studies that vary by diet. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s42523-023-00254-8.
format Online
Article
Text
id pubmed-10413624
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-104136242023-08-11 Disentangling the link between zebrafish diet, gut microbiome succession, and Mycobacterium chelonae infection Sieler, Michael J. Al-Samarrie, Colleen E. Kasschau, Kristin D. Varga, Zoltan M. Kent, Michael L. Sharpton, Thomas J. Anim Microbiome Research BACKGROUND: Despite the long-established importance of zebrafish (Danio rerio) as a model organism and their increasing use in microbiome-targeted studies, relatively little is known about how husbandry practices involving diet impact the zebrafish gut microbiome. Given the microbiome’s important role in mediating host physiology and the potential for diet to drive variation in microbiome composition, we sought to clarify how three different dietary formulations that are commonly used in zebrafish facilities impact the gut microbiome. We compared the composition of gut microbiomes in approximately 60 AB line adult (129- and 214-day-old) zebrafish fed each diet throughout their lifespan. RESULTS: Our analysis finds that diet has a substantial impact on the composition of the gut microbiome in adult fish, and that diet also impacts the developmental variation in the gut microbiome. We further evaluated how 214-day-old fish microbiome compositions respond to exposure of a common laboratory pathogen, Mycobacterium chelonae, and whether these responses differ as a function of diet. Our analysis finds that diet determines the manner in which the zebrafish gut microbiome responds to M. chelonae exposure, especially for moderate and low abundance taxa. Moreover, histopathological analysis finds that male fish fed different diets are differentially infected by M. chelonae. CONCLUSIONS: Overall, our results indicate that diet drives the successional development of the gut microbiome as well as its sensitivity to exogenous exposure. Consequently, investigators should carefully consider the role of diet in their microbiome zebrafish investigations, especially when integrating results across studies that vary by diet. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s42523-023-00254-8. BioMed Central 2023-08-10 /pmc/articles/PMC10413624/ /pubmed/37563644 http://dx.doi.org/10.1186/s42523-023-00254-8 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This 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/) .
spellingShingle Research
Sieler, Michael J.
Al-Samarrie, Colleen E.
Kasschau, Kristin D.
Varga, Zoltan M.
Kent, Michael L.
Sharpton, Thomas J.
Disentangling the link between zebrafish diet, gut microbiome succession, and Mycobacterium chelonae infection
title Disentangling the link between zebrafish diet, gut microbiome succession, and Mycobacterium chelonae infection
title_full Disentangling the link between zebrafish diet, gut microbiome succession, and Mycobacterium chelonae infection
title_fullStr Disentangling the link between zebrafish diet, gut microbiome succession, and Mycobacterium chelonae infection
title_full_unstemmed Disentangling the link between zebrafish diet, gut microbiome succession, and Mycobacterium chelonae infection
title_short Disentangling the link between zebrafish diet, gut microbiome succession, and Mycobacterium chelonae infection
title_sort disentangling the link between zebrafish diet, gut microbiome succession, and mycobacterium chelonae infection
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10413624/
https://www.ncbi.nlm.nih.gov/pubmed/37563644
http://dx.doi.org/10.1186/s42523-023-00254-8
work_keys_str_mv AT sielermichaelj disentanglingthelinkbetweenzebrafishdietgutmicrobiomesuccessionandmycobacteriumchelonaeinfection
AT alsamarriecolleene disentanglingthelinkbetweenzebrafishdietgutmicrobiomesuccessionandmycobacteriumchelonaeinfection
AT kasschaukristind disentanglingthelinkbetweenzebrafishdietgutmicrobiomesuccessionandmycobacteriumchelonaeinfection
AT vargazoltanm disentanglingthelinkbetweenzebrafishdietgutmicrobiomesuccessionandmycobacteriumchelonaeinfection
AT kentmichaell disentanglingthelinkbetweenzebrafishdietgutmicrobiomesuccessionandmycobacteriumchelonaeinfection
AT sharptonthomasj disentanglingthelinkbetweenzebrafishdietgutmicrobiomesuccessionandmycobacteriumchelonaeinfection