The Power of a Plant-Derived Toxin

A robust plant-derived toxin with a singular approach of killing dangerous micro organism has been recognized as one of the promising new antibiotics in a long time.

Albicidin, a brand new antibiotic, is produced by the plant pathogen Xanthomonas albilineans, answerable for inflicting sugar cane’s harmful leaf scald illness. The toxin is believed to help the pathogen’s unfold by attacking the plant. Albicidin has been proven to be extremely efficient towards dangerous micro organism, together with drug-resistant superbugs equivalent to E. coli and S. aureus.

Despite its antibiotic potential and low toxicity in pre-clinical experiments, pharmaceutical improvement of albicidin has been hampered as a result of scientists didn’t know exactly the way it interacted with its goal, the bacterial enzyme DNA gyrase (gyrase). This enzyme binds to DNA and, through a series of elegant movements, twists it up, a process known as supercoiling which is vital for cells to function properly.

Now, Dr. Dmitry Ghilarov’s research group at the John Innes Centre, alongside the laboratories of Prof. Roderich Süssmuth at Technische Universität Berlin, Germany, and Prof. Jonathan Heddle at Jagiellonian University, Poland, have exploited advances in cryo-electron microscopy to obtain a first snapshot of albicidin bound to gyrase.

It showed that albicidin forms an L-shape, enabling it to interact with both the gyrase and the DNA in a unique way. In this state, gyrase can no longer move to bring the DNA ends together. The effect of albicidin is akin to a spanner thrown between two gears.

The way albicidin interacts with gyrase is sufficiently different from existing antibiotics that the molecule and its derivatives are likely to be effective against many of the current antibiotic-resistant bacteria.

“It seems by the nature of the interaction, albicidin targets a really essential part of the enzyme and it’s hard for bacteria to evolve resistance to that,” said Dr. Ghilarov. “Now that we have a structural understanding, we can look to further exploit this binding pocket and make more modifications to albicidin to improve its efficacy and pharmacological properties.”

This work has already begun: the team used their observations to chemically synthesize variations of the antibiotic with improved properties. In tests, these variants were effective against some of the most dangerous hospital-acquired bacterial infections including Escherichia coli, Klebsiella pneumoniae, Pseudomonas aeruginosa, and Salmonella typhimurium.

Dr. Ghilarov said: “We believe this is one of the most exciting new antibiotic candidates in many years. It has extremely high effectiveness in small concentrations and is highly potent against pathogenic bacteria – even those resistant to the widely used antibiotics such as fluoroquinolones.”

“This molecule has been around for decades”, continued Dr. Ghilarov, “Now advances in cryo-electron microscopy has made it possible to determine structures of even the most elaborate protein-DNA complexes. To be the first person to see the molecule bound to its target and how it works is a huge privilege, and the best reward one can have as a scientist. But this work is a big team effort, and we would not have done it without our European colleagues.”

The next step for this research is to engage with academic and industrial collaborators and to seek funding to take the research forward to human clinical trials. This could lead to the development of an urgently needed new class of antibiotics in the face of a global threat of antimicrobial resistance, AMR.

Albicidin – how does it work? 

Albicidin targets an enzyme found in both plants and bacteria called DNA gyrase (or simply “gyrase”). This enzyme binds to DNA and, through a series of elegant movements, twists it up (a process known as supercoiling) – a vital process for cells to function properly. However, gyrase has an Achilles heel; to do its job it must momentarily cut the DNA double helix. This is dangerous, as broken DNA is lethal to the cell. Normally, gyrase quickly joints the two pieces of DNA back together again as it works, but albicidin prevents it from happening, resulting in broken DNA and bacterial death. 

Anti-Microbial Resistance (AMR) 

Multi-drug resistant pathogens such as Escherichia coli, Pseudomonas aeruginosa, and Salmonella typhimurium present a dangerous healthcare burden, exacerbated by the COVID-19 pandemic. 

Infections by resistant pathogens are a leading cause of death in hospital intensive care units, with some strains becoming pan-resistant. Gram-negative drug-resistant pathogens were a cause of 50,000 deaths in 2019. 

Despite urgently needed new medicines to combat this threat, drug discovery programs have yielded no new classes of antibiotics for several decades. 

Reference: “Molecular mechanism of topoisomerase poisoning by the peptide antibiotic albicidin” by Elizabeth Michalczyk, Kay Hommernick, Iraj Behroz, Marcel Kulike, Zuzanna Pakosz-Stępień, Lukasz Mazurek, Maria Seidel, Maria Kunert, Karine Santos, Holger von Moeller, Bernhard Loll, John B. Weston, Andi Mainz, Jonathan G. Heddle, Roderich D. Süssmuth and Dmitry Ghilarov, 23 January 2023, Nature Catalysis.
DOI: 10.1038/s41929-022-00904-1