Chemical interference with iron transport systems to suppress bacterial growth of Streptococcus pneumoniae

PLoS One. 2014 Aug 29;9(8):e105953. doi: 10.1371/journal.pone.0105953. eCollection 2014.

Abstract

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.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • ATP-Binding Cassette Transporters / genetics
  • ATP-Binding Cassette Transporters / metabolism
  • Anti-Bacterial Agents / chemistry
  • Anti-Bacterial Agents / metabolism
  • Anti-Bacterial Agents / pharmacology
  • Bacterial Proteins / genetics
  • Bacterial Proteins / metabolism
  • Biological Transport / drug effects
  • Biological Transport / genetics
  • Cell Line, Tumor
  • Cell Survival / drug effects
  • Coordination Complexes / chemistry
  • Coordination Complexes / metabolism
  • Coordination Complexes / pharmacology
  • Dose-Response Relationship, Drug
  • Ferrichrome / metabolism
  • Humans
  • Iron / metabolism*
  • Microbial Sensitivity Tests
  • Molecular Structure
  • Mutation
  • Organometallic Compounds / chemistry
  • Organometallic Compounds / metabolism
  • Organometallic Compounds / pharmacology*
  • Protein Binding
  • Ruthenium / chemistry*
  • Ruthenium / metabolism
  • Streptococcus pneumoniae / drug effects*
  • Streptococcus pneumoniae / genetics
  • Streptococcus pneumoniae / growth & development

Substances

  • ATP-Binding Cassette Transporters
  • Anti-Bacterial Agents
  • Bacterial Proteins
  • Coordination Complexes
  • Organometallic Compounds
  • R-825 compound
  • Ferrichrome
  • Ruthenium
  • Iron

Grants and funding

This work was supported by the National Natural Science Foundation of China (21271086, to Q.-Y. H.; 31000373, to X. S.), Guangdong Natural Science Research Grant (32213027, to Q.-Y. H.; S2012010008685 to X. S.), the Fundamental Research Funds for the Central Universities (11610101 to Q.-Y. H.; 21611201, to X. S.), and the Pearl River Rising Star of Science and Technology of Guangzhou City (2011J2200003, to X. S.). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.