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Bacterial conversion of a host weapon into a nutritional signal
Bacteria engulfed by phagocytic cells must resist oxidation damage and adapt to cellular hypoxia, but the mechanisms involved in this process are not completely elucidated. Recent work by Kim et al. in the Journal of Biological Chemistry investigated how the intracellular pathogen Salmonella enteric...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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American Society for Biochemistry and Molecular Biology
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9637811/ https://www.ncbi.nlm.nih.gov/pubmed/36244456 http://dx.doi.org/10.1016/j.jbc.2022.102600 |
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author | Valvano, Miguel A. |
author_facet | Valvano, Miguel A. |
author_sort | Valvano, Miguel A. |
collection | PubMed |
description | Bacteria engulfed by phagocytic cells must resist oxidation damage and adapt to cellular hypoxia, but the mechanisms involved in this process are not completely elucidated. Recent work by Kim et al. in the Journal of Biological Chemistry investigated how the intracellular pathogen Salmonella enterica activates gene expression required to counteract oxidative damage. The authors show that this bacterium utilizes host oxidative molecules to activate regulatory proteins that enhance the production of effector molecules, counteracting the host weapon NADPH oxidase and inducing a protective response. |
format | Online Article Text |
id | pubmed-9637811 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Society for Biochemistry and Molecular Biology |
record_format | MEDLINE/PubMed |
spelling | pubmed-96378112022-11-14 Bacterial conversion of a host weapon into a nutritional signal Valvano, Miguel A. J Biol Chem Editors' Pick Highlight Bacteria engulfed by phagocytic cells must resist oxidation damage and adapt to cellular hypoxia, but the mechanisms involved in this process are not completely elucidated. Recent work by Kim et al. in the Journal of Biological Chemistry investigated how the intracellular pathogen Salmonella enterica activates gene expression required to counteract oxidative damage. The authors show that this bacterium utilizes host oxidative molecules to activate regulatory proteins that enhance the production of effector molecules, counteracting the host weapon NADPH oxidase and inducing a protective response. American Society for Biochemistry and Molecular Biology 2022-10-14 /pmc/articles/PMC9637811/ /pubmed/36244456 http://dx.doi.org/10.1016/j.jbc.2022.102600 Text en © 2022 The Author https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Editors' Pick Highlight Valvano, Miguel A. Bacterial conversion of a host weapon into a nutritional signal |
title | Bacterial conversion of a host weapon into a nutritional signal |
title_full | Bacterial conversion of a host weapon into a nutritional signal |
title_fullStr | Bacterial conversion of a host weapon into a nutritional signal |
title_full_unstemmed | Bacterial conversion of a host weapon into a nutritional signal |
title_short | Bacterial conversion of a host weapon into a nutritional signal |
title_sort | bacterial conversion of a host weapon into a nutritional signal |
topic | Editors' Pick Highlight |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9637811/ https://www.ncbi.nlm.nih.gov/pubmed/36244456 http://dx.doi.org/10.1016/j.jbc.2022.102600 |
work_keys_str_mv | AT valvanomiguela bacterialconversionofahostweaponintoanutritionalsignal |