Cargando…
Host subversion of bacterial metallophore usage drives copper intoxication
Microorganisms can acquire metal ions in metal-limited environments using small molecules called metallophores. While metals and their importers are essential, metals can also be toxic, and metallophores have limited ability to discriminate metals. The impact of the metallophore-mediated non-cognate...
Autores principales: | , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10312489/ https://www.ncbi.nlm.nih.gov/pubmed/37398167 http://dx.doi.org/10.1101/2023.05.30.542972 |
_version_ | 1785066938926366720 |
---|---|
author | Hossain, Saika Morey, Jacqueline R. Neville, Stephanie L. Ganio, Katherine Radin, Jana N. Norambuena, Javiera Boyd, Jeffrey M. McDevitt, Christopher A. Kehl-Fie, Thomas E. |
author_facet | Hossain, Saika Morey, Jacqueline R. Neville, Stephanie L. Ganio, Katherine Radin, Jana N. Norambuena, Javiera Boyd, Jeffrey M. McDevitt, Christopher A. Kehl-Fie, Thomas E. |
author_sort | Hossain, Saika |
collection | PubMed |
description | Microorganisms can acquire metal ions in metal-limited environments using small molecules called metallophores. While metals and their importers are essential, metals can also be toxic, and metallophores have limited ability to discriminate metals. The impact of the metallophore-mediated non-cognate metal uptake on bacterial metal homeostasis and pathogenesis remains to be defined. The globally significant pathogen Staphylococcus aureus uses the Cnt system to secrete the metallophore staphylopine in zinc-limited host niches. Here, we show that staphylopine and the Cnt system facilitate bacterial copper uptake, potentiating the need for copper detoxification. During in vivo infection, staphylopine usage increased S. aureus susceptibility to host-mediated copper stress, indicating that the innate immune response can harness the antimicrobial potential of altered elemental abundances in host niches. Collectively, these observations show that while the broad-spectrum metal-chelating properties of metallophores can be advantageous, the host can exploit these properties to drive metal intoxication and mediate antibacterial control. |
format | Online Article Text |
id | pubmed-10312489 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Cold Spring Harbor Laboratory |
record_format | MEDLINE/PubMed |
spelling | pubmed-103124892023-07-01 Host subversion of bacterial metallophore usage drives copper intoxication Hossain, Saika Morey, Jacqueline R. Neville, Stephanie L. Ganio, Katherine Radin, Jana N. Norambuena, Javiera Boyd, Jeffrey M. McDevitt, Christopher A. Kehl-Fie, Thomas E. bioRxiv Article Microorganisms can acquire metal ions in metal-limited environments using small molecules called metallophores. While metals and their importers are essential, metals can also be toxic, and metallophores have limited ability to discriminate metals. The impact of the metallophore-mediated non-cognate metal uptake on bacterial metal homeostasis and pathogenesis remains to be defined. The globally significant pathogen Staphylococcus aureus uses the Cnt system to secrete the metallophore staphylopine in zinc-limited host niches. Here, we show that staphylopine and the Cnt system facilitate bacterial copper uptake, potentiating the need for copper detoxification. During in vivo infection, staphylopine usage increased S. aureus susceptibility to host-mediated copper stress, indicating that the innate immune response can harness the antimicrobial potential of altered elemental abundances in host niches. Collectively, these observations show that while the broad-spectrum metal-chelating properties of metallophores can be advantageous, the host can exploit these properties to drive metal intoxication and mediate antibacterial control. Cold Spring Harbor Laboratory 2023-05-31 /pmc/articles/PMC10312489/ /pubmed/37398167 http://dx.doi.org/10.1101/2023.05.30.542972 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which allows reusers to copy and distribute the material in any medium or format in unadapted form only, for noncommercial purposes only, and only so long as attribution is given to the creator. |
spellingShingle | Article Hossain, Saika Morey, Jacqueline R. Neville, Stephanie L. Ganio, Katherine Radin, Jana N. Norambuena, Javiera Boyd, Jeffrey M. McDevitt, Christopher A. Kehl-Fie, Thomas E. Host subversion of bacterial metallophore usage drives copper intoxication |
title | Host subversion of bacterial metallophore usage drives copper intoxication |
title_full | Host subversion of bacterial metallophore usage drives copper intoxication |
title_fullStr | Host subversion of bacterial metallophore usage drives copper intoxication |
title_full_unstemmed | Host subversion of bacterial metallophore usage drives copper intoxication |
title_short | Host subversion of bacterial metallophore usage drives copper intoxication |
title_sort | host subversion of bacterial metallophore usage drives copper intoxication |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10312489/ https://www.ncbi.nlm.nih.gov/pubmed/37398167 http://dx.doi.org/10.1101/2023.05.30.542972 |
work_keys_str_mv | AT hossainsaika hostsubversionofbacterialmetallophoreusagedrivescopperintoxication AT moreyjacqueliner hostsubversionofbacterialmetallophoreusagedrivescopperintoxication AT nevillestephaniel hostsubversionofbacterialmetallophoreusagedrivescopperintoxication AT ganiokatherine hostsubversionofbacterialmetallophoreusagedrivescopperintoxication AT radinjanan hostsubversionofbacterialmetallophoreusagedrivescopperintoxication AT norambuenajaviera hostsubversionofbacterialmetallophoreusagedrivescopperintoxication AT boydjeffreym hostsubversionofbacterialmetallophoreusagedrivescopperintoxication AT mcdevittchristophera hostsubversionofbacterialmetallophoreusagedrivescopperintoxication AT kehlfiethomase hostsubversionofbacterialmetallophoreusagedrivescopperintoxication |