Cargando…

Transcriptomic changes in an animal-bacterial symbiosis under modeled microgravity conditions

Spaceflight imposes numerous adaptive challenges for terrestrial life. The reduction in gravity, or microgravity, represents a novel environment that can disrupt homeostasis of many physiological processes. Additionally, it is becoming increasingly clear that an organism’s microbiome is critical for...

Descripción completa

Detalles Bibliográficos
Autores principales: Casaburi, Giorgio, Goncharenko-Foster, Irina, Duscher, Alexandrea A., Foster, Jamie S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5385879/
https://www.ncbi.nlm.nih.gov/pubmed/28393904
http://dx.doi.org/10.1038/srep46318
_version_ 1782520668416376832
author Casaburi, Giorgio
Goncharenko-Foster, Irina
Duscher, Alexandrea A.
Foster, Jamie S.
author_facet Casaburi, Giorgio
Goncharenko-Foster, Irina
Duscher, Alexandrea A.
Foster, Jamie S.
author_sort Casaburi, Giorgio
collection PubMed
description Spaceflight imposes numerous adaptive challenges for terrestrial life. The reduction in gravity, or microgravity, represents a novel environment that can disrupt homeostasis of many physiological processes. Additionally, it is becoming increasingly clear that an organism’s microbiome is critical for host health and examining its resiliency in microgravity represents a new frontier for space biology research. In this study, we examine the impact of microgravity on the interactions between the squid Euprymna scolopes and its beneficial symbiont Vibrio fischeri, which form a highly specific binary mutualism. First, animals inoculated with V. fischeri aboard the space shuttle showed effective colonization of the host light organ, the site of the symbiosis, during space flight. Second, RNA-Seq analysis of squid exposed to modeled microgravity conditions exhibited extensive differential gene expression in the presence and absence of the symbiotic partner. Transcriptomic analyses revealed in the absence of the symbiont during modeled microgravity there was an enrichment of genes and pathways associated with the innate immune and oxidative stress response. The results suggest that V. fischeri may help modulate the host stress responses under modeled microgravity. This study provides a window into the adaptive responses that the host animal and its symbiont use during modeled microgravity.
format Online
Article
Text
id pubmed-5385879
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher Nature Publishing Group
record_format MEDLINE/PubMed
spelling pubmed-53858792017-04-12 Transcriptomic changes in an animal-bacterial symbiosis under modeled microgravity conditions Casaburi, Giorgio Goncharenko-Foster, Irina Duscher, Alexandrea A. Foster, Jamie S. Sci Rep Article Spaceflight imposes numerous adaptive challenges for terrestrial life. The reduction in gravity, or microgravity, represents a novel environment that can disrupt homeostasis of many physiological processes. Additionally, it is becoming increasingly clear that an organism’s microbiome is critical for host health and examining its resiliency in microgravity represents a new frontier for space biology research. In this study, we examine the impact of microgravity on the interactions between the squid Euprymna scolopes and its beneficial symbiont Vibrio fischeri, which form a highly specific binary mutualism. First, animals inoculated with V. fischeri aboard the space shuttle showed effective colonization of the host light organ, the site of the symbiosis, during space flight. Second, RNA-Seq analysis of squid exposed to modeled microgravity conditions exhibited extensive differential gene expression in the presence and absence of the symbiotic partner. Transcriptomic analyses revealed in the absence of the symbiont during modeled microgravity there was an enrichment of genes and pathways associated with the innate immune and oxidative stress response. The results suggest that V. fischeri may help modulate the host stress responses under modeled microgravity. This study provides a window into the adaptive responses that the host animal and its symbiont use during modeled microgravity. Nature Publishing Group 2017-04-10 /pmc/articles/PMC5385879/ /pubmed/28393904 http://dx.doi.org/10.1038/srep46318 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Casaburi, Giorgio
Goncharenko-Foster, Irina
Duscher, Alexandrea A.
Foster, Jamie S.
Transcriptomic changes in an animal-bacterial symbiosis under modeled microgravity conditions
title Transcriptomic changes in an animal-bacterial symbiosis under modeled microgravity conditions
title_full Transcriptomic changes in an animal-bacterial symbiosis under modeled microgravity conditions
title_fullStr Transcriptomic changes in an animal-bacterial symbiosis under modeled microgravity conditions
title_full_unstemmed Transcriptomic changes in an animal-bacterial symbiosis under modeled microgravity conditions
title_short Transcriptomic changes in an animal-bacterial symbiosis under modeled microgravity conditions
title_sort transcriptomic changes in an animal-bacterial symbiosis under modeled microgravity conditions
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5385879/
https://www.ncbi.nlm.nih.gov/pubmed/28393904
http://dx.doi.org/10.1038/srep46318
work_keys_str_mv AT casaburigiorgio transcriptomicchangesinananimalbacterialsymbiosisundermodeledmicrogravityconditions
AT goncharenkofosteririna transcriptomicchangesinananimalbacterialsymbiosisundermodeledmicrogravityconditions
AT duscheralexandreaa transcriptomicchangesinananimalbacterialsymbiosisundermodeledmicrogravityconditions
AT fosterjamies transcriptomicchangesinananimalbacterialsymbiosisundermodeledmicrogravityconditions