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Phenotypic Changes Exhibited by E. coli Cultured in Space

Bacteria will accompany humans in our exploration of space, making it of importance to study their adaptation to the microgravity environment. To investigate potential phenotypic changes for bacteria grown in space, Escherichia coli was cultured onboard the International Space Station with matched c...

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Autores principales: Zea, Luis, Larsen, Michael, Estante, Frederico, Qvortrup, Klaus, Moeller, Ralf, Dias de Oliveira, Sílvia, Stodieck, Louis, Klaus, David
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5581483/
https://www.ncbi.nlm.nih.gov/pubmed/28894439
http://dx.doi.org/10.3389/fmicb.2017.01598
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author Zea, Luis
Larsen, Michael
Estante, Frederico
Qvortrup, Klaus
Moeller, Ralf
Dias de Oliveira, Sílvia
Stodieck, Louis
Klaus, David
author_facet Zea, Luis
Larsen, Michael
Estante, Frederico
Qvortrup, Klaus
Moeller, Ralf
Dias de Oliveira, Sílvia
Stodieck, Louis
Klaus, David
author_sort Zea, Luis
collection PubMed
description Bacteria will accompany humans in our exploration of space, making it of importance to study their adaptation to the microgravity environment. To investigate potential phenotypic changes for bacteria grown in space, Escherichia coli was cultured onboard the International Space Station with matched controls on Earth. Samples were challenged with different concentrations of gentamicin sulfate to study the role of drug concentration on the dependent variables in the space environment. Analyses included assessments of final cell count, cell size, cell envelope thickness, cell ultrastructure, and culture morphology. A 13-fold increase in final cell count was observed in space with respect to the ground controls and the space flight cells were able to grow in the presence of normally inhibitory levels of gentamicin sulfate. Contrast light microscopy and focused ion beam/scanning electron microscopy showed that, on average, cells in space were 37% of the volume of their matched controls, which may alter the rate of molecule–cell interactions in a diffusion-limited mass transport regime as is expected to occur in microgravity. TEM imagery showed an increase in cell envelope thickness of between 25 and 43% in space with respect to the Earth control group. Outer membrane vesicles were observed on the spaceflight samples, but not on the Earth cultures. While E. coli suspension cultures on Earth were homogenously distributed throughout the liquid medium, in space they tended to form a cluster, leaving the surrounding medium visibly clear of cells. This cell aggregation behavior may be associated with enhanced biofilm formation observed in other spaceflight experiments.
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spelling pubmed-55814832017-09-11 Phenotypic Changes Exhibited by E. coli Cultured in Space Zea, Luis Larsen, Michael Estante, Frederico Qvortrup, Klaus Moeller, Ralf Dias de Oliveira, Sílvia Stodieck, Louis Klaus, David Front Microbiol Microbiology Bacteria will accompany humans in our exploration of space, making it of importance to study their adaptation to the microgravity environment. To investigate potential phenotypic changes for bacteria grown in space, Escherichia coli was cultured onboard the International Space Station with matched controls on Earth. Samples were challenged with different concentrations of gentamicin sulfate to study the role of drug concentration on the dependent variables in the space environment. Analyses included assessments of final cell count, cell size, cell envelope thickness, cell ultrastructure, and culture morphology. A 13-fold increase in final cell count was observed in space with respect to the ground controls and the space flight cells were able to grow in the presence of normally inhibitory levels of gentamicin sulfate. Contrast light microscopy and focused ion beam/scanning electron microscopy showed that, on average, cells in space were 37% of the volume of their matched controls, which may alter the rate of molecule–cell interactions in a diffusion-limited mass transport regime as is expected to occur in microgravity. TEM imagery showed an increase in cell envelope thickness of between 25 and 43% in space with respect to the Earth control group. Outer membrane vesicles were observed on the spaceflight samples, but not on the Earth cultures. While E. coli suspension cultures on Earth were homogenously distributed throughout the liquid medium, in space they tended to form a cluster, leaving the surrounding medium visibly clear of cells. This cell aggregation behavior may be associated with enhanced biofilm formation observed in other spaceflight experiments. Frontiers Media S.A. 2017-08-28 /pmc/articles/PMC5581483/ /pubmed/28894439 http://dx.doi.org/10.3389/fmicb.2017.01598 Text en Copyright © 2017 Zea, Larsen, Estante, Qvortrup, Moeller, Dias de Oliveira, Stodieck and Klaus. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Zea, Luis
Larsen, Michael
Estante, Frederico
Qvortrup, Klaus
Moeller, Ralf
Dias de Oliveira, Sílvia
Stodieck, Louis
Klaus, David
Phenotypic Changes Exhibited by E. coli Cultured in Space
title Phenotypic Changes Exhibited by E. coli Cultured in Space
title_full Phenotypic Changes Exhibited by E. coli Cultured in Space
title_fullStr Phenotypic Changes Exhibited by E. coli Cultured in Space
title_full_unstemmed Phenotypic Changes Exhibited by E. coli Cultured in Space
title_short Phenotypic Changes Exhibited by E. coli Cultured in Space
title_sort phenotypic changes exhibited by e. coli cultured in space
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5581483/
https://www.ncbi.nlm.nih.gov/pubmed/28894439
http://dx.doi.org/10.3389/fmicb.2017.01598
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