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Multidrug-resistant Acinetobacter pittii is adapting to and exhibiting potential succession aboard the International Space Station

BACKGROUND: Monitoring the adaptation of microorganisms to the extreme environment of the International Space Station (ISS) is crucial to understanding microbial evolution and infection prevention. Acinetobacter pittii is an opportunistic nosocomial pathogen, primarily impacting immunocompromised pa...

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Autores principales: Tierney, Braden T., Singh, Nitin K., Simpson, Anna C., Hujer, Andrea M., Bonomo, Robert A., Mason, Christopher E., Venkateswaran, Kasthuri
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9743659/
https://www.ncbi.nlm.nih.gov/pubmed/36503581
http://dx.doi.org/10.1186/s40168-022-01358-0
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author Tierney, Braden T.
Singh, Nitin K.
Simpson, Anna C.
Hujer, Andrea M.
Bonomo, Robert A.
Mason, Christopher E.
Venkateswaran, Kasthuri
author_facet Tierney, Braden T.
Singh, Nitin K.
Simpson, Anna C.
Hujer, Andrea M.
Bonomo, Robert A.
Mason, Christopher E.
Venkateswaran, Kasthuri
author_sort Tierney, Braden T.
collection PubMed
description BACKGROUND: Monitoring the adaptation of microorganisms to the extreme environment of the International Space Station (ISS) is crucial to understanding microbial evolution and infection prevention. Acinetobacter pittii is an opportunistic nosocomial pathogen, primarily impacting immunocompromised patients, that was recently isolated from two missions aboard the ISS. RESULTS: Here, we report how ISS-associated A. pittii (n = 20 genomes) has formed its own genetically and functionally discrete clade distinct from most Earth-bound isolates (n = 291 genomes). The antimicrobial susceptibility testing of ISS strains and two related clinical isolates demonstrated that ISS strains acquired more resistance, specifically with regard to expanded-spectrum cephalosporins, despite no prediction of increased resistance based on genomic analysis of resistance genes. By investigating 402 longitudinal environmental and host-associated ISS metagenomes, we observed that viable A. pittii is increasing in relative abundance and therefore potentially exhibiting succession, being identified in >2X more metagenomic samples in back-to-back missions. ISS strains additionally contain functions that enable them to survive in harsh environments, including the transcriptional regulator LexA. Via a genome-wide association study, we identified a high level of mutational burden in methionine sulfoxide reductase genes relative to the most closely related Earth strains. CONCLUSIONS: Overall, these results indicated a step forward in understanding how microorganisms might evolve and alter their antibiotic resistance phenotype in extreme, resource-limited, human-built environments. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40168-022-01358-0.
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spelling pubmed-97436592022-12-13 Multidrug-resistant Acinetobacter pittii is adapting to and exhibiting potential succession aboard the International Space Station Tierney, Braden T. Singh, Nitin K. Simpson, Anna C. Hujer, Andrea M. Bonomo, Robert A. Mason, Christopher E. Venkateswaran, Kasthuri Microbiome Research BACKGROUND: Monitoring the adaptation of microorganisms to the extreme environment of the International Space Station (ISS) is crucial to understanding microbial evolution and infection prevention. Acinetobacter pittii is an opportunistic nosocomial pathogen, primarily impacting immunocompromised patients, that was recently isolated from two missions aboard the ISS. RESULTS: Here, we report how ISS-associated A. pittii (n = 20 genomes) has formed its own genetically and functionally discrete clade distinct from most Earth-bound isolates (n = 291 genomes). The antimicrobial susceptibility testing of ISS strains and two related clinical isolates demonstrated that ISS strains acquired more resistance, specifically with regard to expanded-spectrum cephalosporins, despite no prediction of increased resistance based on genomic analysis of resistance genes. By investigating 402 longitudinal environmental and host-associated ISS metagenomes, we observed that viable A. pittii is increasing in relative abundance and therefore potentially exhibiting succession, being identified in >2X more metagenomic samples in back-to-back missions. ISS strains additionally contain functions that enable them to survive in harsh environments, including the transcriptional regulator LexA. Via a genome-wide association study, we identified a high level of mutational burden in methionine sulfoxide reductase genes relative to the most closely related Earth strains. CONCLUSIONS: Overall, these results indicated a step forward in understanding how microorganisms might evolve and alter their antibiotic resistance phenotype in extreme, resource-limited, human-built environments. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40168-022-01358-0. BioMed Central 2022-12-12 /pmc/articles/PMC9743659/ /pubmed/36503581 http://dx.doi.org/10.1186/s40168-022-01358-0 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Tierney, Braden T.
Singh, Nitin K.
Simpson, Anna C.
Hujer, Andrea M.
Bonomo, Robert A.
Mason, Christopher E.
Venkateswaran, Kasthuri
Multidrug-resistant Acinetobacter pittii is adapting to and exhibiting potential succession aboard the International Space Station
title Multidrug-resistant Acinetobacter pittii is adapting to and exhibiting potential succession aboard the International Space Station
title_full Multidrug-resistant Acinetobacter pittii is adapting to and exhibiting potential succession aboard the International Space Station
title_fullStr Multidrug-resistant Acinetobacter pittii is adapting to and exhibiting potential succession aboard the International Space Station
title_full_unstemmed Multidrug-resistant Acinetobacter pittii is adapting to and exhibiting potential succession aboard the International Space Station
title_short Multidrug-resistant Acinetobacter pittii is adapting to and exhibiting potential succession aboard the International Space Station
title_sort multidrug-resistant acinetobacter pittii is adapting to and exhibiting potential succession aboard the international space station
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9743659/
https://www.ncbi.nlm.nih.gov/pubmed/36503581
http://dx.doi.org/10.1186/s40168-022-01358-0
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