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Chemical Interference with Iron Transport Systems to Suppress Bacterial Growth of Streptococcus pneumoniae
Iron is an essential nutrient for the growth of most bacteria. To obtain iron, bacteria have developed specific iron-transport systems located on the membrane surface to uptake iron and iron complexes such as ferrichrome. Interference with the iron-acquisition systems should be therefore an efficien...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4149436/ https://www.ncbi.nlm.nih.gov/pubmed/25170896 http://dx.doi.org/10.1371/journal.pone.0105953 |
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author | Yang, Xiao-Yan Sun, Bin Zhang, Liang Li, Nan Han, Junlong Zhang, Jing Sun, Xuesong He, Qing-Yu |
author_facet | Yang, Xiao-Yan Sun, Bin Zhang, Liang Li, Nan Han, Junlong Zhang, Jing Sun, Xuesong He, Qing-Yu |
author_sort | Yang, Xiao-Yan |
collection | PubMed |
description | Iron is an essential nutrient for the growth of most bacteria. To obtain iron, bacteria have developed specific iron-transport systems located on the membrane surface to uptake iron and iron complexes such as ferrichrome. Interference with the iron-acquisition systems should be therefore an efficient strategy to suppress bacterial growth and infection. Based on the chemical similarity of iron and ruthenium, we used a Ru(II) complex R-825 to compete with ferrichrome for the ferrichrome-transport pathway in Streptococcus pneumoniae. R-825 inhibited the bacterial growth of S. pneumoniae and stimulated the expression of PiuA, the iron-binding protein in the ferrichrome-uptake system on the cell surface. R-825 treatment decreased the cellular content of iron, accompanying with the increase of Ru(II) level in the bacterium. When the piuA gene (SPD_0915) was deleted in the bacterium, the mutant strain became resistant to R-825 treatment, with decreased content of Ru(II). Addition of ferrichrome can rescue the bacterial growth that was suppressed by R-825. Fluorescence spectral quenching showed that R-825 can bind with PiuA in a similar pattern to the ferrichrome-PiuA interaction in vitro. These observations demonstrated that Ru(II) complex R-825 can compete with ferrichrome for the ferrichrome-transport system to enter S. pneumoniae, reduce the cellular iron supply, and thus suppress the bacterial growth. This finding suggests a novel antimicrobial approach by interfering with iron-uptake pathways, which is different from the mechanisms used by current antibiotics. |
format | Online Article Text |
id | pubmed-4149436 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-41494362014-09-03 Chemical Interference with Iron Transport Systems to Suppress Bacterial Growth of Streptococcus pneumoniae Yang, Xiao-Yan Sun, Bin Zhang, Liang Li, Nan Han, Junlong Zhang, Jing Sun, Xuesong He, Qing-Yu PLoS One Research Article Iron is an essential nutrient for the growth of most bacteria. To obtain iron, bacteria have developed specific iron-transport systems located on the membrane surface to uptake iron and iron complexes such as ferrichrome. Interference with the iron-acquisition systems should be therefore an efficient strategy to suppress bacterial growth and infection. Based on the chemical similarity of iron and ruthenium, we used a Ru(II) complex R-825 to compete with ferrichrome for the ferrichrome-transport pathway in Streptococcus pneumoniae. R-825 inhibited the bacterial growth of S. pneumoniae and stimulated the expression of PiuA, the iron-binding protein in the ferrichrome-uptake system on the cell surface. R-825 treatment decreased the cellular content of iron, accompanying with the increase of Ru(II) level in the bacterium. When the piuA gene (SPD_0915) was deleted in the bacterium, the mutant strain became resistant to R-825 treatment, with decreased content of Ru(II). Addition of ferrichrome can rescue the bacterial growth that was suppressed by R-825. Fluorescence spectral quenching showed that R-825 can bind with PiuA in a similar pattern to the ferrichrome-PiuA interaction in vitro. These observations demonstrated that Ru(II) complex R-825 can compete with ferrichrome for the ferrichrome-transport system to enter S. pneumoniae, reduce the cellular iron supply, and thus suppress the bacterial growth. This finding suggests a novel antimicrobial approach by interfering with iron-uptake pathways, which is different from the mechanisms used by current antibiotics. Public Library of Science 2014-08-29 /pmc/articles/PMC4149436/ /pubmed/25170896 http://dx.doi.org/10.1371/journal.pone.0105953 Text en © 2014 Yang et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Yang, Xiao-Yan Sun, Bin Zhang, Liang Li, Nan Han, Junlong Zhang, Jing Sun, Xuesong He, Qing-Yu Chemical Interference with Iron Transport Systems to Suppress Bacterial Growth of Streptococcus pneumoniae |
title | Chemical Interference with Iron Transport Systems to Suppress Bacterial Growth of Streptococcus pneumoniae
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title_full | Chemical Interference with Iron Transport Systems to Suppress Bacterial Growth of Streptococcus pneumoniae
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title_fullStr | Chemical Interference with Iron Transport Systems to Suppress Bacterial Growth of Streptococcus pneumoniae
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title_full_unstemmed | Chemical Interference with Iron Transport Systems to Suppress Bacterial Growth of Streptococcus pneumoniae
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title_short | Chemical Interference with Iron Transport Systems to Suppress Bacterial Growth of Streptococcus pneumoniae
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title_sort | chemical interference with iron transport systems to suppress bacterial growth of streptococcus pneumoniae |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4149436/ https://www.ncbi.nlm.nih.gov/pubmed/25170896 http://dx.doi.org/10.1371/journal.pone.0105953 |
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