Breakthrough Antibiotic D22 Shows Promise Against Drug-Resistant Bacteria in Animal Trials

November 21, 2024
Breakthrough Antibiotic D22 Shows Promise Against Drug-Resistant Bacteria in Animal Trials
  • Mice trials indicated that D22 injections were more effective than oral administration, significantly reducing P. aeruginosa growth, although they did not completely clear the infection.

  • This research was published during the World Health Organization's World Antimicrobial Resistance Awareness Week, highlighting the urgency of developing new antibacterial therapies.

  • Researchers have identified a modified darobactin, known as D22, as a promising new antibacterial treatment effective against drug-resistant bacteria, particularly E. coli.

  • In recent animal trials, D22 was shown to effectively clear A. baumannii infections in zebrafish embryos, performing comparably to the antibiotic ciprofloxacin.

  • The study received funding from the Helmholtz Impuls- und Vernetzungsfonds, and some authors are affiliated with Evotec, a drug discovery and development company.

  • Earlier in 2024, the WHO updated its list of concerning bacterial pathogens to include Acinetobacter baumannii, Pseudomonas aeruginosa, and E. coli, underscoring the need for new treatments.

  • In a severe peritonitis model, D22 cleared E. coli infections after four doses within 25 hours, demonstrating its potential for treating critical infections.

  • Darobactin, the basis for D22, is a naturally occurring antibiotic that binds to essential proteins in bacterial cells, leading to their death.

  • Bacterial resistance to antibiotics has created an urgent need for new treatments, as many current antibiotics are becoming less effective.

  • Previous studies led by researchers Rolf Müller and Jennifer Herrmann demonstrated that engineered darobactins, specifically D22, possess antibacterial activity against A. baumannii in laboratory tests.

  • The findings suggest that D22 has strong potential as a new treatment against critical infections and could lead to future clinical trials to combat antimicrobial resistance.

Summary based on 3 sources


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