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More and more bacterial pathogens are developing resistance. There is an increasing risk that common drugs will no longer be effective against infectious diseases. Researchers from the University of Bonn, the German Center for Infection Research (DZIF), Utrecht University (Netherlands), Northeastern University in Boston (USA) and the company NovoBiotic Pharmaceuticals in Cambridge (USA) now have discovered and deciphered the mode of action of a new antibiotic. Clovibactin is derived from a soil bacterium. This antibiotic is highly effective at attacking the cell wall of bacteria, including many multi-resistant “superbugs.” The results have now been published in the renowned journal “Cell.”
“We urgently need new antibiotics to stay ahead in the race against bacteria that have become resistant,” says Prof. Dr. Tanja Schneider of the Institute for Pharmaceutical Microbiology at the University of Bonn and the University Hospital Bonn. She adds that in recent decades, not many new substances to combat bacterial pathogens have come onto the market. “Clovibactin is novel compared to current antibiotics in use,” says the co-spokesperson of the Transregional Collaborative Research Center “Antibiotic CellMAP,” who is also a member of the Transdisciplinary Research Area “Life & Health” and the Cluster of Excellence “ImmunoSensation2.” The Institute for Pharmaceutical Microbiology, together with the German Center for Infection Research, specializes in deciphering the mode of action of antibiotic candidates.
The soil bacterium Eleftheria terrae subspecies carolina carries its place of origin in its name: It was isolated from a soil sample in the US state of North Carolina and produces the new antibiotic compound clovibactin to protect itself from competing bacteria. “The new antibiotic simultaneously attacks the bacterial cell wall at several sites by blocking essential building blocks,” explains Tanja Schneider. It specifically binds to these building blocks with unusual intensity and kills the bacteria by destroying their cell envelope.
Clovibactin surrounds the target structure like a cage
Research groups from different disciplines and countries worked together to unravel exactly how this works. The team led by Prof. Kim Lewis of the Antimicrobial Discovery Center at Northeastern University in Boston (USA) and the company NovoBiotic Pharmaceuticals in Cambridge (USA) discovered clovibactin using the iCHip device. This allows bacteria to be grown in the laboratory that were previously considered unculturable and were not available for the development of new antibiotics.
“Our discovery of this exciting new antibiotic further validates the iCHip culturing technology for finding new therapeutic compounds from previously uncultivated microorganisms,” says Dallas Hughes, Ph.D., president of NovoBiotic Pharmaceuticals, LLC. The company has demonstrated that clovibactin has very good activity against a broad spectrum of bacterial pathogens and has successfully treated mice in preclinical studies.
The mode of action of the new antibiotic was elucidated by researchers led by Tanja Schneider. The researchers from Bonn were able to show that clovibactin binds very selectively and with high specificity to pyrophosphate groups of bacterial cell wall components. Prof. Markus Weingarth’s group from the Department of Chemistry at Utrecht University in the Netherlands uncovered exactly what this interaction looks like. Using solid-state NMR spectroscopy, the researchers deciphered the structure of the complex of clovibactin and the bacterial target structure lipid II - under conditions similar to those found in the bacterial cell. These studies showed that clovibactin grips around the pyrophosphate group. This is where the name “Clovibactin” comes from, derived from the Greek “Klouvi” (cage), because it encloses the target structure like a cage.
Combined attack minimizes resistance development
Clovibactin acts primarily on gram-positive bacteria. These include “hospital pathogens,” such as MRSA bacteria but also the pathogens of the widespread tuberculosis, which affects many millions of people worldwide. “We are very confident that the bacteria will not develop resistance to clovibactin so quickly,” Tanja Schneider says. This is because the pathogens cannot change the cell wall building blocks so easily to undermine the antibiotic - their Achilles’ heel therefore remains.
But clovibactin can do even more. After docking to the target structures, clovibactin forms supramolecular filamentous structures that tightly enclose and further damage the target structures of the bacteria. Bacteria that encounter clovibactin are also stimulated to release certain enzymes, known as autolysins, which then uncontrollably dissolve their own cell envelope. “The combination of these different mechanisms is the reason for the exceptional resilience to resistance,” says Tanja Schneider. This shows the potential that still exists in the natural diversity of bacteria that are candidates for new antibiotics.
“Without the interdisciplinary cooperation between the partners, this important step in the fight against resistance would not have succeeded,” says Prof. Markus Weingarth. The research team now plans to use its findings to further increase the effectiveness of clovibactin. “But there is still a long way to go before a new antibiotic hits the market,” says Tanja Schneider.
Participating institutions and funding:
In addition to the Institute for Pharmaceutical Microbiology and the Clausius Institute for Physical and Theoretical Chemistry at the University of Bonn, participants in this study included Utrecht University (Netherlands), NovoBiotic Pharmaceutical in Cambridge (USA), the Rijksuniversiteit Groningen (Netherlands), the University of Tübingen, the German Center for Infection Research, Tianjin Medical University (China), the Novartis Institutes for Biomedical Research in Cambridge (USA), the University of Florence (Italy), the Consorzio Interuniversitario Risonanze Magnetiche di Metallo Proteine in Sesto Fiorentino (Italy) and Northeastern University in Boston (USA). The German Center for Infection Research and the Transregional Collaborative Research Center “Antibiotic CellMAP” of the German Research Foundation funded the project on the Bonn and Tübingen side.
Prof. Dr. Tanja Schneider
Institute for Pharmaceutical Microbiology
University of Bonn
University Hospital Bonn
Tel. +49 (0)228 735688
Email: tschneider@uni-bonn.de
Prof. Dr. Markus Weingarth
Department of Chemistry
Utrecht University
Tel. +31 (0)640828581
Email: m.h.weingarth@uu.nl
Rhythm Shukla, Aaron J. Peoples, Kevin C. Ludwig, Sourav Maity, Maik G.N. Derks, Stefania De Benedetti, Annika M Krueger, Bram J.A. Vermeulen, Theresa Harbig, Francesca Lavore, Raj Kumar, Rodrigo V. Honorato, Fabian Grein, Kay Nieselt, Yangping Liu, Alexandre Bonvin, Marc Baldus, Ulrich Kubitscheck, Eefjan Breukink, Catherine Achorn, Anthony Nitti, Christopher J. Schwalen, Amy L. Spoering, Losee Lucy Ling, Dallas Hughes, Moreno Lelli, Wouter H. Roos, Kim Lewis, Tanja Schneider, Markus Weingarth: A new antibiotic from an uncultured bacterium binds to an immutable target, Cell, DOI: 10.1016/j.cell.2023.07.038
The team at the Institute of Pharmaceutical Microbiology: (from left) Annika Krüger, Prof. Dr. Tanja ...
Photo: Gregor Hübl/University of Bonn
Reflection in the protective screen: Prof. Dr. Tanja Schneider and her team from the Institute of Ph ...
Photo: Gregor Hübl/University of Bonn
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