Could a single synthetic molecule outsmart a variety of drug-resistant bacteria?

  16 February 2024

Researchers at Harvard and the University of Illinois at Chicago have developed a new molecule called cresomycin, which effectively vanquished multiple types of bacteria when tested in animals. Cresomycin belongs to a class of enhanced lincosamides and works by targeting a bacterium’s ribosome, the tiny protein factory tucked in every living cell. It is not yet a drug or close to being ready for clinical trials in humans. A nonprofit dedicated to fighting superbugs gave its Harvard creator $1.2 million this week to develop cresomycin and similar substances into new oral antibiotics. Cresomycin belongs to a class of antibiotics known as enhanced lincosamides and works by binding so tightly to the ribosome that it essentially negates the effect of the methyl group. This new molecule represents a promising step toward new treatments, as it represents a promising step toward new treatments for the growing number of antibiotic-resistant superbugs in the US.

Further reading: Los Angeles Times
Author(s): Corinne Purtill
Smart Innovations  
Back

OUR UNDERWRITERS

Unrestricted financial support by:

Antimicrobial Resistance Fighter Coalition

Bangalore Bioinnovation Centre

INTERNATIONAL FEDERATION PHARMACEUTICAL MANUFACTURERS & ASSOCIATIONS

BD





AMR NEWS

Your Biweekly Source for Global AMR Insights!

Stay informed with the essential newsletter that brings together all the latest One Health news on antimicrobial resistance. Delivered straight to your inbox every two weeks, AMR NEWS provides a curated selection of international insights, key publications, and the latest updates in the fight against AMR.

Don’t miss out on staying ahead in the global AMR movement—subscribe now!

Subscribe

What is going on with AMR?
Stay tuned with remarkable global AMR news and developments!

Keep me informed