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Structural mechanism reveals how antibiotic resistance to fusidic acid works

New molecular movie reveals how antibiotic resistance to fusidic acid works
Schematic of the fusidic acid resistance "stop-motion" movie. On the left, the protein EF-G (green) is locked to the ribosome (light blue and white) by the antibiotic fusidic acid (dark blue). In the middle, FusB (pink) binds and breaks EF-G off the ribosome, which releases fusidic acid. On the right, the rescued ribosome is ready to resume protein synthesis. Credit: Uppsala University

In an article in Nature Communications, researchers from Uppsala Antibiotic Center, Uppsala University and SciLifeLab describe a fundamental mechanism of antibiotic resistance. What happens in a bacterium that is resistant to the antibiotic fusidic acid?

With a stop-motion movie at the atomic level, they can show that the resistance protein FusB works nearly like a crowbar.

Antibiotic resistance is a global issue that requires action and research at many levels. This study describes the molecular mechanism of the most prevalent type of fusidic acid resistance in the bacterium Staphylococcus aureus.

Antibiotics function in many different ways. Fusidic acid belongs to the large group of antibiotics that target harmful bacteria by blocking their ribosomes, the machineries that translate the into proteins. However, bacteria can develop resistance to antibiotics in several ways, such as by pumping out a drug or deactivating it. Some resistance mechanisms are more advanced and specific.

"The mechanism behind fusidic acid resistance has been a long-standing mystery," says Maria Selmer, professor and researcher.

Morph showing the conformational changes of EF-G from the POST state to the FusB•EF-G•70S complex induced by binding of FusB, with structures aligned by 23S rRNA . Credit: Uppsala University

In the new article, researchers revealed how FusB, a resistance protein found in clinically resistant strains of the common bacterium Staphylococcus aureus, can rescue ribosomes from fusidic acid. Using , they show that FusB works like a molecular crowbar that frees the blocked ribosome. The researchers describe their method as a "stop-motion movie" at the molecular level.

"With traditional methods, we would be too late to the 'crime scene.' Thanks to this methodology, we could catch the resistance protein in the act, right as the 'crowbar' is 'breaking into' the molecular complex," says Adrián González López, Ph.D. student.

More information: Adrián González-López et al, Structural mechanism of FusB-mediated rescue from fusidic acid inhibition of protein synthesis, Nature Communications (2025).

Journal information: Nature Communications

Provided by Uppsala University

Citation: Structural mechanism reveals how antibiotic resistance to fusidic acid works (2025, May 16) retrieved 16 May 2025 from /news/2025-05-mechanism-reveals-antibiotic-resistance-fusidic.html
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