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Quantification of the capacity of vibrio fischeri to establish symbiosis with Euprymna scolopes

Most animals establish long-term symbiotic associations with bacteria that are critical for normal host physiology. The symbiosis that forms between the Hawaiian squid Euprymna scolopes and the bioluminescent bacterium Vibrio fischeri serves as an important model system for investigating the molecul...

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Autores principales: Donnelly, Aidan R., Giacobe, Elizabeth J., Cook, Rachel A., Francis, Gareth M., Buddle, Grace K., Beaubrun, Christina L., Cecere, Andrew G., Miyashiro, Tim I.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10343157/
https://www.ncbi.nlm.nih.gov/pubmed/37440554
http://dx.doi.org/10.1371/journal.pone.0287519
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author Donnelly, Aidan R.
Giacobe, Elizabeth J.
Cook, Rachel A.
Francis, Gareth M.
Buddle, Grace K.
Beaubrun, Christina L.
Cecere, Andrew G.
Miyashiro, Tim I.
author_facet Donnelly, Aidan R.
Giacobe, Elizabeth J.
Cook, Rachel A.
Francis, Gareth M.
Buddle, Grace K.
Beaubrun, Christina L.
Cecere, Andrew G.
Miyashiro, Tim I.
author_sort Donnelly, Aidan R.
collection PubMed
description Most animals establish long-term symbiotic associations with bacteria that are critical for normal host physiology. The symbiosis that forms between the Hawaiian squid Euprymna scolopes and the bioluminescent bacterium Vibrio fischeri serves as an important model system for investigating the molecular mechanisms that promote animal-bacterial symbioses. E. scolopes hatch from their eggs uncolonized, which has led to the development of squid-colonization assays that are based on introducing culture-grown V. fischeri cells to freshly hatched juvenile squid. Recent studies have revealed that strains often exhibit large differences in how they establish symbiosis. Therefore, we sought to develop a simplified and reproducible protocol that permits researchers to determine appropriate inoculum levels and provides a platform to standardize the assay across different laboratories. In our protocol, we adapt a method commonly used for evaluating the infectivity of pathogens to quantify the symbiotic capacity of V. fischeri strains. The resulting metric, the symbiotic dose-50 (SD(50)), estimates the inoculum level that is necessary for a specific V. fischeri strain to establish a light-emitting symbiosis. Relative to other protocols, our method requires 2–5-fold fewer animals. Furthermore, the power analysis presented here suggests that the protocol can detect up to a 3-fold change in the SD(50) between different strains.
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spelling pubmed-103431572023-07-14 Quantification of the capacity of vibrio fischeri to establish symbiosis with Euprymna scolopes Donnelly, Aidan R. Giacobe, Elizabeth J. Cook, Rachel A. Francis, Gareth M. Buddle, Grace K. Beaubrun, Christina L. Cecere, Andrew G. Miyashiro, Tim I. PLoS One Lab Protocol Most animals establish long-term symbiotic associations with bacteria that are critical for normal host physiology. The symbiosis that forms between the Hawaiian squid Euprymna scolopes and the bioluminescent bacterium Vibrio fischeri serves as an important model system for investigating the molecular mechanisms that promote animal-bacterial symbioses. E. scolopes hatch from their eggs uncolonized, which has led to the development of squid-colonization assays that are based on introducing culture-grown V. fischeri cells to freshly hatched juvenile squid. Recent studies have revealed that strains often exhibit large differences in how they establish symbiosis. Therefore, we sought to develop a simplified and reproducible protocol that permits researchers to determine appropriate inoculum levels and provides a platform to standardize the assay across different laboratories. In our protocol, we adapt a method commonly used for evaluating the infectivity of pathogens to quantify the symbiotic capacity of V. fischeri strains. The resulting metric, the symbiotic dose-50 (SD(50)), estimates the inoculum level that is necessary for a specific V. fischeri strain to establish a light-emitting symbiosis. Relative to other protocols, our method requires 2–5-fold fewer animals. Furthermore, the power analysis presented here suggests that the protocol can detect up to a 3-fold change in the SD(50) between different strains. Public Library of Science 2023-07-13 /pmc/articles/PMC10343157/ /pubmed/37440554 http://dx.doi.org/10.1371/journal.pone.0287519 Text en © 2023 Donnelly et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Lab Protocol
Donnelly, Aidan R.
Giacobe, Elizabeth J.
Cook, Rachel A.
Francis, Gareth M.
Buddle, Grace K.
Beaubrun, Christina L.
Cecere, Andrew G.
Miyashiro, Tim I.
Quantification of the capacity of vibrio fischeri to establish symbiosis with Euprymna scolopes
title Quantification of the capacity of vibrio fischeri to establish symbiosis with Euprymna scolopes
title_full Quantification of the capacity of vibrio fischeri to establish symbiosis with Euprymna scolopes
title_fullStr Quantification of the capacity of vibrio fischeri to establish symbiosis with Euprymna scolopes
title_full_unstemmed Quantification of the capacity of vibrio fischeri to establish symbiosis with Euprymna scolopes
title_short Quantification of the capacity of vibrio fischeri to establish symbiosis with Euprymna scolopes
title_sort quantification of the capacity of vibrio fischeri to establish symbiosis with euprymna scolopes
topic Lab Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10343157/
https://www.ncbi.nlm.nih.gov/pubmed/37440554
http://dx.doi.org/10.1371/journal.pone.0287519
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