Cargando…

Transcriptional profiling of the mutualistic bacterium Vibrio fischeri and an hfq mutant under modeled microgravity

For long-duration space missions, it is critical to maintain health-associated homeostasis between astronauts and their microbiome. To achieve this goal it is important to more fully understand the host–symbiont relationship under the physiological stress conditions of spaceflight. To address this i...

Descripción completa

Detalles Bibliográficos
Autores principales: Duscher, Alexandrea A., Conesa, Ana, Bishop, Mary, Vroom, Madeline M., Zubizarreta, Sergio D., Foster, Jamie S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6299092/
https://www.ncbi.nlm.nih.gov/pubmed/30588486
http://dx.doi.org/10.1038/s41526-018-0060-1
_version_ 1783381415835992064
author Duscher, Alexandrea A.
Conesa, Ana
Bishop, Mary
Vroom, Madeline M.
Zubizarreta, Sergio D.
Foster, Jamie S.
author_facet Duscher, Alexandrea A.
Conesa, Ana
Bishop, Mary
Vroom, Madeline M.
Zubizarreta, Sergio D.
Foster, Jamie S.
author_sort Duscher, Alexandrea A.
collection PubMed
description For long-duration space missions, it is critical to maintain health-associated homeostasis between astronauts and their microbiome. To achieve this goal it is important to more fully understand the host–symbiont relationship under the physiological stress conditions of spaceflight. To address this issue we examined the impact of a spaceflight analog, low-shear-modeled microgravity (LSMMG), on the transcriptome of the mutualistic bacterium Vibrio fischeri. Cultures of V. fischeri and a mutant defective in the global regulator Hfq (∆hfq) were exposed to either LSMMG or gravity conditions for 12 h (exponential growth) and 24 h (stationary phase growth). Comparative transcriptomic analysis revealed few to no significant differentially expressed genes between gravity and the LSMMG conditions in the wild type or mutant V. fischeri at exponential or stationary phase. There was, however, a pronounced change in transcriptomic profiles during the transition between exponential and stationary phase growth in both V. fischeri cultures including an overall decrease in gene expression associated with translational activity and an increase in stress response. There were also several upregulated stress genes specific to the LSMMG condition during the transition to stationary phase growth. The ∆hfq mutants exhibited a distinctive transcriptome profile with a significant increase in transcripts associated with flagellar synthesis and transcriptional regulators under LSMMG conditions compared to gravity controls. These results indicate the loss of Hfq significantly influences gene expression under LSMMG conditions in a bacterial symbiont. Together, these results improve our understanding of the mechanisms by which microgravity alters the physiology of beneficial host-associated microbes.
format Online
Article
Text
id pubmed-6299092
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-62990922018-12-26 Transcriptional profiling of the mutualistic bacterium Vibrio fischeri and an hfq mutant under modeled microgravity Duscher, Alexandrea A. Conesa, Ana Bishop, Mary Vroom, Madeline M. Zubizarreta, Sergio D. Foster, Jamie S. NPJ Microgravity Article For long-duration space missions, it is critical to maintain health-associated homeostasis between astronauts and their microbiome. To achieve this goal it is important to more fully understand the host–symbiont relationship under the physiological stress conditions of spaceflight. To address this issue we examined the impact of a spaceflight analog, low-shear-modeled microgravity (LSMMG), on the transcriptome of the mutualistic bacterium Vibrio fischeri. Cultures of V. fischeri and a mutant defective in the global regulator Hfq (∆hfq) were exposed to either LSMMG or gravity conditions for 12 h (exponential growth) and 24 h (stationary phase growth). Comparative transcriptomic analysis revealed few to no significant differentially expressed genes between gravity and the LSMMG conditions in the wild type or mutant V. fischeri at exponential or stationary phase. There was, however, a pronounced change in transcriptomic profiles during the transition between exponential and stationary phase growth in both V. fischeri cultures including an overall decrease in gene expression associated with translational activity and an increase in stress response. There were also several upregulated stress genes specific to the LSMMG condition during the transition to stationary phase growth. The ∆hfq mutants exhibited a distinctive transcriptome profile with a significant increase in transcripts associated with flagellar synthesis and transcriptional regulators under LSMMG conditions compared to gravity controls. These results indicate the loss of Hfq significantly influences gene expression under LSMMG conditions in a bacterial symbiont. Together, these results improve our understanding of the mechanisms by which microgravity alters the physiology of beneficial host-associated microbes. Nature Publishing Group UK 2018-12-18 /pmc/articles/PMC6299092/ /pubmed/30588486 http://dx.doi.org/10.1038/s41526-018-0060-1 Text en © The Author(s) 2018 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Duscher, Alexandrea A.
Conesa, Ana
Bishop, Mary
Vroom, Madeline M.
Zubizarreta, Sergio D.
Foster, Jamie S.
Transcriptional profiling of the mutualistic bacterium Vibrio fischeri and an hfq mutant under modeled microgravity
title Transcriptional profiling of the mutualistic bacterium Vibrio fischeri and an hfq mutant under modeled microgravity
title_full Transcriptional profiling of the mutualistic bacterium Vibrio fischeri and an hfq mutant under modeled microgravity
title_fullStr Transcriptional profiling of the mutualistic bacterium Vibrio fischeri and an hfq mutant under modeled microgravity
title_full_unstemmed Transcriptional profiling of the mutualistic bacterium Vibrio fischeri and an hfq mutant under modeled microgravity
title_short Transcriptional profiling of the mutualistic bacterium Vibrio fischeri and an hfq mutant under modeled microgravity
title_sort transcriptional profiling of the mutualistic bacterium vibrio fischeri and an hfq mutant under modeled microgravity
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6299092/
https://www.ncbi.nlm.nih.gov/pubmed/30588486
http://dx.doi.org/10.1038/s41526-018-0060-1
work_keys_str_mv AT duscheralexandreaa transcriptionalprofilingofthemutualisticbacteriumvibriofischeriandanhfqmutantundermodeledmicrogravity
AT conesaana transcriptionalprofilingofthemutualisticbacteriumvibriofischeriandanhfqmutantundermodeledmicrogravity
AT bishopmary transcriptionalprofilingofthemutualisticbacteriumvibriofischeriandanhfqmutantundermodeledmicrogravity
AT vroommadelinem transcriptionalprofilingofthemutualisticbacteriumvibriofischeriandanhfqmutantundermodeledmicrogravity
AT zubizarretasergiod transcriptionalprofilingofthemutualisticbacteriumvibriofischeriandanhfqmutantundermodeledmicrogravity
AT fosterjamies transcriptionalprofilingofthemutualisticbacteriumvibriofischeriandanhfqmutantundermodeledmicrogravity