Proton Motive Force Inhibitors Are Detrimental to Methicillin-Resistant Staphylococcus aureus Strains

Sayed Golam Mohiuddin1, Sreyashi Ghosh1, Pouria Kavousi1

  • 1Department of Chemical and Biomolecular Engineering, University of Houstongrid.266436.3, Houston, Texas, USA.

Microbiology Spectrum
|August 9, 2022
PubMed

Insights

Proton motive force (PMF) inhibitors effectively kill antibiotic-tolerant Methicillin-resistant Staphylococcus aureus (MRSA) by disrupting cell membranes. This study identifies new PMF-targeting drugs for combating dangerous MRSA infections.

Area of Science:

  • Microbiology
  • Infectious Diseases
  • Drug Discovery

Background:

  • Methicillin-resistant Staphylococcus aureus (MRSA) is a dangerous pathogen resistant to conventional antibiotics.
  • Antibiotic-tolerant MRSA cells contribute to chronic infections and the development of further resistance.
  • Proton motive force (PMF) inhibitors have shown potential in killing bacterial cells.

Purpose of the Study:

  • To investigate the efficacy of PMF inhibitors as a novel treatment strategy against antibiotic-tolerant MRSA.
  • To identify specific PMF inhibitors that can effectively eliminate MRSA cells.
  • To understand the mechanism by which PMF inhibitors exert their bactericidal effect on MRSA.

Main Methods:

  • Utilized known PMF inhibitors against two MRSA isolates.
  • Screened a chemical library to identify compounds that disrupt MRSA PMF.
  • Assessed the correlation between PMF disruption, membrane permeabilization, and bactericidal activity.

Main Results:

  • PMF inhibitor potency correlated with their ability to disrupt PMF and permeabilize MRSA cell membranes.
  • Identified nordihydroguaiaretic acid, gossypol, trifluoperazine, and amitriptyline as potent PMF disruptors.
  • These identified compounds significantly reduced MRSA cell levels below detection limits.

Conclusions:

  • Cellular PMF is a crucial target for developing new bactericidal therapeutics against pathogens like MRSA.
  • PMF inhibitors that dissipate transmembrane electric potential or proton gradient show robust efficacy.
  • This research offers a promising new avenue for combating antibiotic-tolerant MRSA infections.

Related Concept Videos

Combined Effects of Drugs: Synergism01:27

Combined Effects of Drugs: Synergism

Synergism is a useful mechanism where combining two or more drugs is more effective than each constituent used alone. Such combinations are also called supra-additive interactions. The drugs collectively enhance the final therapeutic effect by acting on different targets. Another advantage is that the low dose of each constituent drug is sufficient to achieve the desired effect. This helps reduce the duration of therapy and lower the adverse effects of these drugs.
Such synergistic combinations...
4.6K
Acid Suppressive Drugs for Peptic Ulcer Disease: Proton Pump Inhibitors01:13

Acid Suppressive Drugs for Peptic Ulcer Disease: Proton Pump Inhibitors

Peptic ulcers, often induced by H. pylori infections or NSAID usage, arise from disruptions in the delicate balance of gastric acid production. Peptic ulcers stem from heightened gastric acid levels due to H. pylori infections or NSAID use. The protective mucus layer diminishes in the presence of these factors, allowing gastric acid to erode the stomach lining and form ulcers.
Gastric acid, a potent cocktail of hydrogen and chloride ions, is produced in specialized parietal cells within the...
520
Antimicrobial Proteins01:23

Antimicrobial Proteins

Antimicrobial proteins are important components of the immune system. They aid the body in combating pathogens by either killing them directly or hindering their replication processes. Four main types of antimicrobial substances are interferons, the complement system, iron-binding proteins, and antimicrobial proteins.
Interferons
Interferons (IFNs) are proteins produced by lymphocytes, macrophages, and fibroblasts infected with viruses. While IFNs cannot prevent viruses from entering and...
3.9K
Development of Antibiotic Resistance01:30

Development of Antibiotic Resistance

Antibiotic resistance is a major public health concern that arises when bacteria evolve mechanisms to withstand the effects of antibiotic treatments. This resistance can be intrinsic, acquired through genetic mutations, or transferred between bacteria via horizontal gene transfer. The development of antibiotic resistance poses significant challenges in treating bacterial infections and necessitates ongoing research to develop new therapeutic strategies.Intrinsic resistance occurs when bacterial...
173
Drugs for Peptic Ulcer Disease: Prostaglandin Analogs as Mucosal Protective Agents01:20

Drugs for Peptic Ulcer Disease: Prostaglandin Analogs as Mucosal Protective Agents

The gastric mucosa produces prostaglandins E2 (PGE2) and prostacyclin (PGI2), crucial in maintaining gastric health. They exert cytoprotective effects, including increasing bicarbonate secretion, releasing protective mucin, reducing gastric acid output, and preventing harmful vasoconstriction. These effects are mediated through various receptors, such as EP1, EP2, EP3, and EP4.
Non-steroidal anti-inflammatory drugs (NSAIDs) can induce peptic ulcers by inhibiting cyclooxygenase, decreasing...
580
The Electron Transport Chain01:30

The Electron Transport Chain

The electron transport chain or oxidative phosphorylation is an exothermic process in which free energy released during electron transfer reactions is coupled to ATP synthesis. This process is a significant source of energy in aerobic cells, and therefore inhibitors of the electron transport chain can be detrimental to the cell's metabolic processes.
Inhibitors of the electron transport chain
Rotenone, a widely used pesticide, prevents electron transfer from Fe-S cluster to ubiquinone or Q...
17.2K