Copper(II)-Bis(Thiosemicarbazonato) Complexes as Antibacterial Agents: Insights into Their Mode of Action and Potential as Therapeutics

Antimicrob Agents Chemother. 2015 Oct;59(10):6444-53. doi: 10.1128/AAC.01289-15. Epub 2015 Aug 3.

Abstract

There is increasing interest in the use of lipophilic copper (Cu)-containing complexes to combat bacterial infections. In this work, we showed that Cu complexes with bis(thiosemicarbazone) ligands [Cu(btsc)] exert antibacterial activity against a range of medically significant pathogens. Previous work using Neisseria gonorrhoeae showed that Cu(btsc) complexes may act as inhibitors of respiratory dehydrogenases in the electron transport chain. We now show that these complexes are also toxic against pathogens that lack a respiratory chain. Respiration in Escherichia coli was slightly affected by Cu(btsc) complexes, but our results indicate that, in this model bacterium, the complexes act primarily as agents that deliver toxic Cu ions efficiently into the cytoplasm. Although the chemistry of Cu(btsc) complexes may dictate their mechanism of action, their efficacy depends heavily on bacterial physiology. This is linked to the ability of the target bacterium to tolerate Cu and, additionally, the susceptibility of the respiratory chain to direct inhibition by Cu(btsc) complexes. The physiology of N. gonorrhoeae, including multidrug-resistant strains, makes it highly susceptible to damage by Cu ions and Cu(btsc) complexes, highlighting the potential of Cu(btsc) complexes (and Cu-based therapeutics) as a promising treatment against this important bacterial pathogen.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Anti-Bacterial Agents / chemistry
  • Anti-Bacterial Agents / toxicity*
  • Biological Transport
  • Coordination Complexes / chemistry
  • Coordination Complexes / toxicity*
  • Copper / chemistry
  • Copper / toxicity*
  • Cytoplasm / drug effects
  • Cytoplasm / metabolism
  • Drug Resistance, Bacterial / drug effects*
  • Electron Transport / drug effects
  • Escherichia coli / drug effects
  • Escherichia coli / growth & development
  • Escherichia coli / metabolism
  • Haemophilus influenzae / drug effects
  • Haemophilus influenzae / growth & development
  • Haemophilus influenzae / metabolism
  • Lactobacillus acidophilus / drug effects
  • Lactobacillus acidophilus / growth & development
  • Lactobacillus acidophilus / metabolism
  • Microbial Sensitivity Tests
  • Microbial Viability / drug effects
  • Mitochondria / drug effects
  • Mitochondria / metabolism
  • Neisseria gonorrhoeae / drug effects
  • Neisseria gonorrhoeae / growth & development
  • Neisseria gonorrhoeae / metabolism
  • Salmonella typhimurium / drug effects
  • Salmonella typhimurium / growth & development
  • Salmonella typhimurium / metabolism
  • Species Specificity
  • Staphylococcus aureus / drug effects
  • Staphylococcus aureus / growth & development
  • Staphylococcus aureus / metabolism
  • Streptococcus pneumoniae / drug effects
  • Streptococcus pneumoniae / growth & development
  • Streptococcus pneumoniae / metabolism
  • Thiosemicarbazones / chemistry
  • Thiosemicarbazones / toxicity*

Substances

  • Anti-Bacterial Agents
  • Coordination Complexes
  • Thiosemicarbazones
  • Copper