Melioidosis: New target to combat a dangerous bacterial infection

Study identifies an enzyme central to infection

Schematic representation of the molecular structure
Active centre of the enzyme BurG, which forms a highly reactive chemical compound that plays a crucial role in melioidosis. Source: Michael Groll/Felix Trottmann

Researchers at the Leibniz-HKI have identified an enzyme that is a promising new therapeutic target to combat the dangerous bacterial disease melioidosis. It helps the pathogenic bacterium Burkholderia pseudomallei construct a toxic molecule that is critical in the infection process. The results were published in Nature Chemistry.

Melioidosis is a life-threatening disease caused by the bacterium Burkholderia pseudomallei. "Without treatment, the disease is usually fatal," Christian Hertweck, head of the Biomolecular Chemistry Department at Leibniz-HKI and professor of Natural Product Chemistry at Friedrich Schiller University in Jena, explains. "And even antibiotic treatment often drags on for many months and is not always successful because common drugs do not work well against these pathogens."

His research group therefore wanted to understand the bacterium's infection mechanisms and has come across a possible new starting point for combating the disease. "We have found an enzyme that synthesises a molecular structure central to the infection," explains Felix Trottmann, first author of the study.

The discovered enzyme BurG forms a cyclopropanol ring, a highly reactive chemical functional group, from a precursor molecule. In previous studies, Trottmann was able to demonstrate that this structure is also produced by other pathogenic bacteria in the genus Burkholderia and apparently has an important role in infection. If the biosynthetic pathway for this molecule is switched off by mutations, the bacteria are far less dangerous.

The research team has also elucidated the 3D structure of the enzyme in cooperation with Michael Groll from TU Munich. "In a next step, we can now try to design active compounds that inhibit the enzyme and thus make the bacteria less virulent," Trottmann explains. According to current knowledge, the enzyme is only found in bacteria and not in humans. "The hope is therefore to be able to specifically inhibit the bacteria," says Hertweck. The immune system could then deal with them more easily.

In the front there's a piece of laboratory equipment out of focus, in the background is Felix Trottmann in lab coat and gloves.
First author Felix Trottmann at a mass spectrometer. Source: Anna Schroll/Leibniz-HKI

To understand the biosynthesis of the molecular structure central to infection, the researchers investigated the gene cluster that contains the DNA instructions for making it. They conducted the laboratory experiments using Burkholderia thailandensis, which is very similar to Burkholderia pseudomallei but is much safer to work with.

Melioidosis mainly occurs in Southeast Asia and Australia. However, experts warn that the disease could spread further. For example, the US Centers for Disease Control and Prevention (CDC) were able to trace the cause of four cases of melioidosis last year, two of which were fatal, to an aromatherapy spray. A closely related species, B. mallei, which also produces the cyclopropanol ring, was used as a biological weapon in both World War I and World War II. And B. pseudomallei was also researched as such in some countries.

The study was supported by the German Research Foundation within the framework of the Collaborative Research Centres 1127 (ChemBioSys) and 1309. In addition, the researchers were supported by the European Regional Development Fund, the Daimler and Benz Foundation and the Chemical Industry Fund. Christian Hertweck used funds from the Gottfried Wilhelm Leibniz Prize for the project, which he was awarded in 2015.

Original publication

Trottmann F, Ishida K, Ishida-Ito M, Kries H, Groll M, Hertweck C (2022). Pathogenic bacteria remodel central metabolic enzyme to build a cyclopropanol warhead. Nature Chemistry. Doi: 10.1038/s41557-022-01005-z


Christian Hertweck
Keishi Ishida
Mie Ishida-Ito
Hajo Kries
Felix Trottmann

Science communication & accreditation

Friederike Gawlik
Charlotte Fuchs


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