Cargando…

Fitness of Outer Membrane Vesicles From Komagataeibacter intermedius Is Altered Under the Impact of Simulated Mars-like Stressors Outside the International Space Station

Outer membrane vesicles (OMVs), produced by nonpathogenic Gram-negative bacteria, have potentially useful biotechnological applications in extraterrestrial extreme environments. However, their biological effects under the impact of various stressors have to be elucidated for safety reasons. In the s...

Descripción completa

Detalles Bibliográficos
Autores principales: Podolich, Olga, Kukharenko, Olga, Zaets, Iryna, Orlovska, Iryna, Palchykovska, Larysa, Zaika, Leonid, Sysoliatin, Serhii, Zubova, Ganna, Reva, Oleg, Galkin, Maxym, Horid’ko, Tetyana, Kosiakova, Halyna, Borisova, Tatiana, Kravchenko, Volodymyr, Skoryk, Mykola, Kremenskoy, Maxym, Ghosh, Preetam, Barh, Debmalya, Góes-Neto, Aristóteles, Azevedo, Vasco, de Vera, Jean-Pierre, Kozyrovska, Natalia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7333525/
https://www.ncbi.nlm.nih.gov/pubmed/32676055
http://dx.doi.org/10.3389/fmicb.2020.01268
_version_ 1783553771733778432
author Podolich, Olga
Kukharenko, Olga
Zaets, Iryna
Orlovska, Iryna
Palchykovska, Larysa
Zaika, Leonid
Sysoliatin, Serhii
Zubova, Ganna
Reva, Oleg
Galkin, Maxym
Horid’ko, Tetyana
Kosiakova, Halyna
Borisova, Tatiana
Kravchenko, Volodymyr
Skoryk, Mykola
Kremenskoy, Maxym
Ghosh, Preetam
Barh, Debmalya
Góes-Neto, Aristóteles
Azevedo, Vasco
de Vera, Jean-Pierre
Kozyrovska, Natalia
author_facet Podolich, Olga
Kukharenko, Olga
Zaets, Iryna
Orlovska, Iryna
Palchykovska, Larysa
Zaika, Leonid
Sysoliatin, Serhii
Zubova, Ganna
Reva, Oleg
Galkin, Maxym
Horid’ko, Tetyana
Kosiakova, Halyna
Borisova, Tatiana
Kravchenko, Volodymyr
Skoryk, Mykola
Kremenskoy, Maxym
Ghosh, Preetam
Barh, Debmalya
Góes-Neto, Aristóteles
Azevedo, Vasco
de Vera, Jean-Pierre
Kozyrovska, Natalia
author_sort Podolich, Olga
collection PubMed
description Outer membrane vesicles (OMVs), produced by nonpathogenic Gram-negative bacteria, have potentially useful biotechnological applications in extraterrestrial extreme environments. However, their biological effects under the impact of various stressors have to be elucidated for safety reasons. In the spaceflight experiment, model biofilm kombucha microbial community (KMC) samples, in which Komagataeibacter intermedius was a dominant community-member, were exposed under simulated Martian factors (i.e., pressure, atmosphere, and UV-illumination) outside the International Space Station (ISS) for 1.5 years. In this study, we have determined that OMVs from post-flight K. intermedius displayed changes in membrane composition, depending on the location of the samples and some other factors. Membrane lipids such as sterols, fatty acids (FAs), and phospholipids (PLs) were modulated under the Mars-like stressors, and saturated FAs, as well as both short-chain saturated and trans FAs, appeared in the membranes of OMVs shed by both post-UV-illuminated and “dark” bacteria. The relative content of zwitterionic and anionic PLs changed, producing a change in surface properties of outer membranes, thereby resulting in a loss of interaction capability with polynucleotides. The changed composition of membranes promoted a bigger OMV size, which correlated with changes of OMV fitness. Biochemical characterization of the membrane-associated enzymes revealed an increase in their activity (DNAse, dehydrogenase) compared to wild type. Other functional membrane-associated capabilities of OMVs (e.g., proton accumulation, interaction with linear DNA, or synaptosomes) were also altered after exposure to the spaceflight stressors. Despite alterations in membranes, vesicles did not acquire endotoxicity, cytotoxicity, and neurotoxicity. Altogether, our results show that OMVs, originating from rationally selected nonpathogenic Gram-negative bacteria, can be considered as candidates in the design of postbiotics or edible mucosal vaccines for in situ production in extreme environment. Furthermore, these OMVs could also be used as promising delivery vectors for applications in Astromedicine.
format Online
Article
Text
id pubmed-7333525
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-73335252020-07-15 Fitness of Outer Membrane Vesicles From Komagataeibacter intermedius Is Altered Under the Impact of Simulated Mars-like Stressors Outside the International Space Station Podolich, Olga Kukharenko, Olga Zaets, Iryna Orlovska, Iryna Palchykovska, Larysa Zaika, Leonid Sysoliatin, Serhii Zubova, Ganna Reva, Oleg Galkin, Maxym Horid’ko, Tetyana Kosiakova, Halyna Borisova, Tatiana Kravchenko, Volodymyr Skoryk, Mykola Kremenskoy, Maxym Ghosh, Preetam Barh, Debmalya Góes-Neto, Aristóteles Azevedo, Vasco de Vera, Jean-Pierre Kozyrovska, Natalia Front Microbiol Microbiology Outer membrane vesicles (OMVs), produced by nonpathogenic Gram-negative bacteria, have potentially useful biotechnological applications in extraterrestrial extreme environments. However, their biological effects under the impact of various stressors have to be elucidated for safety reasons. In the spaceflight experiment, model biofilm kombucha microbial community (KMC) samples, in which Komagataeibacter intermedius was a dominant community-member, were exposed under simulated Martian factors (i.e., pressure, atmosphere, and UV-illumination) outside the International Space Station (ISS) for 1.5 years. In this study, we have determined that OMVs from post-flight K. intermedius displayed changes in membrane composition, depending on the location of the samples and some other factors. Membrane lipids such as sterols, fatty acids (FAs), and phospholipids (PLs) were modulated under the Mars-like stressors, and saturated FAs, as well as both short-chain saturated and trans FAs, appeared in the membranes of OMVs shed by both post-UV-illuminated and “dark” bacteria. The relative content of zwitterionic and anionic PLs changed, producing a change in surface properties of outer membranes, thereby resulting in a loss of interaction capability with polynucleotides. The changed composition of membranes promoted a bigger OMV size, which correlated with changes of OMV fitness. Biochemical characterization of the membrane-associated enzymes revealed an increase in their activity (DNAse, dehydrogenase) compared to wild type. Other functional membrane-associated capabilities of OMVs (e.g., proton accumulation, interaction with linear DNA, or synaptosomes) were also altered after exposure to the spaceflight stressors. Despite alterations in membranes, vesicles did not acquire endotoxicity, cytotoxicity, and neurotoxicity. Altogether, our results show that OMVs, originating from rationally selected nonpathogenic Gram-negative bacteria, can be considered as candidates in the design of postbiotics or edible mucosal vaccines for in situ production in extreme environment. Furthermore, these OMVs could also be used as promising delivery vectors for applications in Astromedicine. Frontiers Media S.A. 2020-06-26 /pmc/articles/PMC7333525/ /pubmed/32676055 http://dx.doi.org/10.3389/fmicb.2020.01268 Text en Copyright © 2020 Podolich, Kukharenko, Zaets, Orlovska, Palchykovska, Zaika, Sysoliatin, Zubova, Reva, Galkin, Horid’ko, Kosiakova, Borisova, Kravchenko, Skoryk, Kremenskoy, Ghosh, Barh, Góes-Neto, Azevedo, de Vera and Kozyrovska. 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) and the copyright owner(s) 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
Podolich, Olga
Kukharenko, Olga
Zaets, Iryna
Orlovska, Iryna
Palchykovska, Larysa
Zaika, Leonid
Sysoliatin, Serhii
Zubova, Ganna
Reva, Oleg
Galkin, Maxym
Horid’ko, Tetyana
Kosiakova, Halyna
Borisova, Tatiana
Kravchenko, Volodymyr
Skoryk, Mykola
Kremenskoy, Maxym
Ghosh, Preetam
Barh, Debmalya
Góes-Neto, Aristóteles
Azevedo, Vasco
de Vera, Jean-Pierre
Kozyrovska, Natalia
Fitness of Outer Membrane Vesicles From Komagataeibacter intermedius Is Altered Under the Impact of Simulated Mars-like Stressors Outside the International Space Station
title Fitness of Outer Membrane Vesicles From Komagataeibacter intermedius Is Altered Under the Impact of Simulated Mars-like Stressors Outside the International Space Station
title_full Fitness of Outer Membrane Vesicles From Komagataeibacter intermedius Is Altered Under the Impact of Simulated Mars-like Stressors Outside the International Space Station
title_fullStr Fitness of Outer Membrane Vesicles From Komagataeibacter intermedius Is Altered Under the Impact of Simulated Mars-like Stressors Outside the International Space Station
title_full_unstemmed Fitness of Outer Membrane Vesicles From Komagataeibacter intermedius Is Altered Under the Impact of Simulated Mars-like Stressors Outside the International Space Station
title_short Fitness of Outer Membrane Vesicles From Komagataeibacter intermedius Is Altered Under the Impact of Simulated Mars-like Stressors Outside the International Space Station
title_sort fitness of outer membrane vesicles from komagataeibacter intermedius is altered under the impact of simulated mars-like stressors outside the international space station
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7333525/
https://www.ncbi.nlm.nih.gov/pubmed/32676055
http://dx.doi.org/10.3389/fmicb.2020.01268
work_keys_str_mv AT podolicholga fitnessofoutermembranevesiclesfromkomagataeibacterintermediusisalteredundertheimpactofsimulatedmarslikestressorsoutsidetheinternationalspacestation
AT kukharenkoolga fitnessofoutermembranevesiclesfromkomagataeibacterintermediusisalteredundertheimpactofsimulatedmarslikestressorsoutsidetheinternationalspacestation
AT zaetsiryna fitnessofoutermembranevesiclesfromkomagataeibacterintermediusisalteredundertheimpactofsimulatedmarslikestressorsoutsidetheinternationalspacestation
AT orlovskairyna fitnessofoutermembranevesiclesfromkomagataeibacterintermediusisalteredundertheimpactofsimulatedmarslikestressorsoutsidetheinternationalspacestation
AT palchykovskalarysa fitnessofoutermembranevesiclesfromkomagataeibacterintermediusisalteredundertheimpactofsimulatedmarslikestressorsoutsidetheinternationalspacestation
AT zaikaleonid fitnessofoutermembranevesiclesfromkomagataeibacterintermediusisalteredundertheimpactofsimulatedmarslikestressorsoutsidetheinternationalspacestation
AT sysoliatinserhii fitnessofoutermembranevesiclesfromkomagataeibacterintermediusisalteredundertheimpactofsimulatedmarslikestressorsoutsidetheinternationalspacestation
AT zubovaganna fitnessofoutermembranevesiclesfromkomagataeibacterintermediusisalteredundertheimpactofsimulatedmarslikestressorsoutsidetheinternationalspacestation
AT revaoleg fitnessofoutermembranevesiclesfromkomagataeibacterintermediusisalteredundertheimpactofsimulatedmarslikestressorsoutsidetheinternationalspacestation
AT galkinmaxym fitnessofoutermembranevesiclesfromkomagataeibacterintermediusisalteredundertheimpactofsimulatedmarslikestressorsoutsidetheinternationalspacestation
AT horidkotetyana fitnessofoutermembranevesiclesfromkomagataeibacterintermediusisalteredundertheimpactofsimulatedmarslikestressorsoutsidetheinternationalspacestation
AT kosiakovahalyna fitnessofoutermembranevesiclesfromkomagataeibacterintermediusisalteredundertheimpactofsimulatedmarslikestressorsoutsidetheinternationalspacestation
AT borisovatatiana fitnessofoutermembranevesiclesfromkomagataeibacterintermediusisalteredundertheimpactofsimulatedmarslikestressorsoutsidetheinternationalspacestation
AT kravchenkovolodymyr fitnessofoutermembranevesiclesfromkomagataeibacterintermediusisalteredundertheimpactofsimulatedmarslikestressorsoutsidetheinternationalspacestation
AT skorykmykola fitnessofoutermembranevesiclesfromkomagataeibacterintermediusisalteredundertheimpactofsimulatedmarslikestressorsoutsidetheinternationalspacestation
AT kremenskoymaxym fitnessofoutermembranevesiclesfromkomagataeibacterintermediusisalteredundertheimpactofsimulatedmarslikestressorsoutsidetheinternationalspacestation
AT ghoshpreetam fitnessofoutermembranevesiclesfromkomagataeibacterintermediusisalteredundertheimpactofsimulatedmarslikestressorsoutsidetheinternationalspacestation
AT barhdebmalya fitnessofoutermembranevesiclesfromkomagataeibacterintermediusisalteredundertheimpactofsimulatedmarslikestressorsoutsidetheinternationalspacestation
AT goesnetoaristoteles fitnessofoutermembranevesiclesfromkomagataeibacterintermediusisalteredundertheimpactofsimulatedmarslikestressorsoutsidetheinternationalspacestation
AT azevedovasco fitnessofoutermembranevesiclesfromkomagataeibacterintermediusisalteredundertheimpactofsimulatedmarslikestressorsoutsidetheinternationalspacestation
AT deverajeanpierre fitnessofoutermembranevesiclesfromkomagataeibacterintermediusisalteredundertheimpactofsimulatedmarslikestressorsoutsidetheinternationalspacestation
AT kozyrovskanatalia fitnessofoutermembranevesiclesfromkomagataeibacterintermediusisalteredundertheimpactofsimulatedmarslikestressorsoutsidetheinternationalspacestation