The adaptation of Escherichia coli cells grown in simulated microgravity for an extended period is both phenotypic and genomic

Evolution: Bacteria gain advantageous mutations under simulated microgravity Bacteria grown for an extended period of time under simulated microgravity adopt growth advantages. George Fox and colleagues from the University of Houston, Texas, USA, cultured Escherichia coli bacteria for 1000 generatio...

Descripción completa

Guardado en:
Detalles Bibliográficos
Autores principales: Madhan R. Tirumalai, Fathi Karouia, Quyen Tran, Victor G. Stepanov, Rebekah J. Bruce, C. Mark Ott, Duane L. Pierson, George E. Fox
Formato: article
Lenguaje:EN
Publicado: Nature Portfolio 2017
Materias:
Acceso en línea:https://doaj.org/article/00446c7756a24031b3ea4ce32713b3c5
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
id oai:doaj.org-article:00446c7756a24031b3ea4ce32713b3c5
record_format dspace
spelling oai:doaj.org-article:00446c7756a24031b3ea4ce32713b3c52021-12-02T11:51:09ZThe adaptation of Escherichia coli cells grown in simulated microgravity for an extended period is both phenotypic and genomic10.1038/s41526-017-0020-12373-8065https://doaj.org/article/00446c7756a24031b3ea4ce32713b3c52017-05-01T00:00:00Zhttps://doi.org/10.1038/s41526-017-0020-1https://doaj.org/toc/2373-8065Evolution: Bacteria gain advantageous mutations under simulated microgravity Bacteria grown for an extended period of time under simulated microgravity adopt growth advantages. George Fox and colleagues from the University of Houston, Texas, USA, cultured Escherichia coli bacteria for 1000 generations in a high aspect rotating vessel to simulate the low fluid shear microgravity environment encountered during spaceflight. They then performed growth competition assays and found that the 1000-generation adapted bacteria outcompeted control bacteria grown without simulated microgravity. Genomic sequencing of the adapted bacteria revealed 16 mutations, five of which altered protein sequences. These DNA changes likely explain the growth advantage of the bacteria grown for multiple generations in simulated microgravity. Similar adaptations during prolonged space missions could result in nastier pathogens that might threaten the health of astronauts. Fortunately, the microbes did not appear to acquire antibiotic resistance over the 1000 generation in the modeled microgravity culture.Madhan R. TirumalaiFathi KarouiaQuyen TranVictor G. StepanovRebekah J. BruceC. Mark OttDuane L. PiersonGeorge E. FoxNature PortfolioarticleBiotechnologyTP248.13-248.65PhysiologyQP1-981ENnpj Microgravity, Vol 3, Iss 1, Pp 1-9 (2017)
institution DOAJ
collection DOAJ
language EN
topic Biotechnology
TP248.13-248.65
Physiology
QP1-981
spellingShingle Biotechnology
TP248.13-248.65
Physiology
QP1-981
Madhan R. Tirumalai
Fathi Karouia
Quyen Tran
Victor G. Stepanov
Rebekah J. Bruce
C. Mark Ott
Duane L. Pierson
George E. Fox
The adaptation of Escherichia coli cells grown in simulated microgravity for an extended period is both phenotypic and genomic
description Evolution: Bacteria gain advantageous mutations under simulated microgravity Bacteria grown for an extended period of time under simulated microgravity adopt growth advantages. George Fox and colleagues from the University of Houston, Texas, USA, cultured Escherichia coli bacteria for 1000 generations in a high aspect rotating vessel to simulate the low fluid shear microgravity environment encountered during spaceflight. They then performed growth competition assays and found that the 1000-generation adapted bacteria outcompeted control bacteria grown without simulated microgravity. Genomic sequencing of the adapted bacteria revealed 16 mutations, five of which altered protein sequences. These DNA changes likely explain the growth advantage of the bacteria grown for multiple generations in simulated microgravity. Similar adaptations during prolonged space missions could result in nastier pathogens that might threaten the health of astronauts. Fortunately, the microbes did not appear to acquire antibiotic resistance over the 1000 generation in the modeled microgravity culture.
format article
author Madhan R. Tirumalai
Fathi Karouia
Quyen Tran
Victor G. Stepanov
Rebekah J. Bruce
C. Mark Ott
Duane L. Pierson
George E. Fox
author_facet Madhan R. Tirumalai
Fathi Karouia
Quyen Tran
Victor G. Stepanov
Rebekah J. Bruce
C. Mark Ott
Duane L. Pierson
George E. Fox
author_sort Madhan R. Tirumalai
title The adaptation of Escherichia coli cells grown in simulated microgravity for an extended period is both phenotypic and genomic
title_short The adaptation of Escherichia coli cells grown in simulated microgravity for an extended period is both phenotypic and genomic
title_full The adaptation of Escherichia coli cells grown in simulated microgravity for an extended period is both phenotypic and genomic
title_fullStr The adaptation of Escherichia coli cells grown in simulated microgravity for an extended period is both phenotypic and genomic
title_full_unstemmed The adaptation of Escherichia coli cells grown in simulated microgravity for an extended period is both phenotypic and genomic
title_sort adaptation of escherichia coli cells grown in simulated microgravity for an extended period is both phenotypic and genomic
publisher Nature Portfolio
publishDate 2017
url https://doaj.org/article/00446c7756a24031b3ea4ce32713b3c5
work_keys_str_mv AT madhanrtirumalai theadaptationofescherichiacolicellsgrowninsimulatedmicrogravityforanextendedperiodisbothphenotypicandgenomic
AT fathikarouia theadaptationofescherichiacolicellsgrowninsimulatedmicrogravityforanextendedperiodisbothphenotypicandgenomic
AT quyentran theadaptationofescherichiacolicellsgrowninsimulatedmicrogravityforanextendedperiodisbothphenotypicandgenomic
AT victorgstepanov theadaptationofescherichiacolicellsgrowninsimulatedmicrogravityforanextendedperiodisbothphenotypicandgenomic
AT rebekahjbruce theadaptationofescherichiacolicellsgrowninsimulatedmicrogravityforanextendedperiodisbothphenotypicandgenomic
AT cmarkott theadaptationofescherichiacolicellsgrowninsimulatedmicrogravityforanextendedperiodisbothphenotypicandgenomic
AT duanelpierson theadaptationofescherichiacolicellsgrowninsimulatedmicrogravityforanextendedperiodisbothphenotypicandgenomic
AT georgeefox theadaptationofescherichiacolicellsgrowninsimulatedmicrogravityforanextendedperiodisbothphenotypicandgenomic
AT madhanrtirumalai adaptationofescherichiacolicellsgrowninsimulatedmicrogravityforanextendedperiodisbothphenotypicandgenomic
AT fathikarouia adaptationofescherichiacolicellsgrowninsimulatedmicrogravityforanextendedperiodisbothphenotypicandgenomic
AT quyentran adaptationofescherichiacolicellsgrowninsimulatedmicrogravityforanextendedperiodisbothphenotypicandgenomic
AT victorgstepanov adaptationofescherichiacolicellsgrowninsimulatedmicrogravityforanextendedperiodisbothphenotypicandgenomic
AT rebekahjbruce adaptationofescherichiacolicellsgrowninsimulatedmicrogravityforanextendedperiodisbothphenotypicandgenomic
AT cmarkott adaptationofescherichiacolicellsgrowninsimulatedmicrogravityforanextendedperiodisbothphenotypicandgenomic
AT duanelpierson adaptationofescherichiacolicellsgrowninsimulatedmicrogravityforanextendedperiodisbothphenotypicandgenomic
AT georgeefox adaptationofescherichiacolicellsgrowninsimulatedmicrogravityforanextendedperiodisbothphenotypicandgenomic
_version_ 1718395143745175552