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Beating resistance using light and oxygen

26 June 2025
With the help of imaging techniques and by attacking bacteria with light, Wiktor Szymanski hopes to find new ways to fight bacterial infections|Image Sean Sinclair / Unsplash

Since bacteria are becoming increasingly resistant to antimicrobial agents, it is important to use these agents as sparingly as possible. Wiktor Szymanski, Professor of Medicinal Chemistry, Photopharmacology and Imaging, together with his colleagues at the UMCG and the Faculty of Science and Engineering, uses light to localize and attack bacterial infections. ‘This is what I’ll devote the next 20 years to.’

FSE Science Newsroom | Text René Fransen | Images Leoni von Ristok

My aim is to hit the bacteria quickly and in the right location

When a patient undergoes orthopedic surgery, such as getting a new knee implant, it may lead to complications. ‘If the knee doesn’t heal, this could be a reaction to the artificial joint, or it may be a bacterial infection,’ Szymanski says. It takes a few days to find out which bacteria are causing the infection, which is why in current medical practice a broad-spectrum antibiotic is often given initially. However, this contributes to the global problem of resistance in bacteria. Szymanski wants to speed up diagnosis with the help of imaging techniques, but also attack the bacteria using light. ‘My aim is to hit the bacteria quickly and in the right location.’

Bacteria can be roughly divided into two groups: Gram-positive and Gram-negative, each requiring different treatment. To quickly detect which of these two groups is present in the infected area, Szymanski uses an antibiotic called vancomycin that only binds to Gram-positive bacteria. Together with the research group of UMCG Professor Jan Maarten van Dijl, he added a fluorescent substance to this antibiotic, causing it to emit red light when green light is shone on it. This enables the detection of the Gram-positive bacteria. 

Gram-negative and Gram-positive

Bacteria can be divided into two classes: Gram-negative and Gram-positive, based on a dye that makes some bacteria turn purple and others red. The reason for this difference lies in the composition of the cell envelope. Gram-positive cells have a thick layer made up of a molecule called peptidoglycan on the outside of the cell membrane. Gram-negative cells have a second membrane covering the peptidoglycan layer, which causes the discolouration–caused by the dye–to be less pronounced, resulting in a lighter (red) colour. Many antibiotics target the peptidoglycan layer, but these tend to be less effective against Gram-negative bacteria, because the layer in these cells is protected by the second membrane.

Gram-positive bacteria in purple and gram negative in red
Gram-positive bacteria colour purple and Gram-negative bacteria colour red. This is important to determine which kind of antibiotic is needed to fight an infection.|Image Microrao/Wikipedia
Illustration of gram postive and gram negative cell membranes
The composition of the bacteria's outer layer determines how well antibiotics can attack the bacteria. | Image Microbialmatt / Wikipedia

Shining light more easily

PET scans of rats, revealing sites of infetction
Adding a radioactive substance to an antibiotic allows the researchers to detect the source of infection | Image G.B. Spoelstra et al. European Journal of Nuclear Medicine and Molecular Imaging 2024
Again, PET scans of rats revealing sites of infetction
The infection becomes visible through a so-called PET-scan (positron emission tomography), an imaging technique that detects radiation of radioactive decay in a medical scanner | Image G.B. Spoelstra et al. European Journal of Nuclear Medicine and Molecular Imaging 2024

Using light to attack

As far as we know, it seems unlikely that bacteria could become resistant to this type of treatment.

Locating and identifying the infection, however, is only the first step and should be followed by localized treatment. To do this, the Szymanski and Van Dijl research groups modified the light-emitting vancomycin to instead produce a highly reactive type of oxygen that ‘burns’ everything it collides with. ‘This so-called singlet oxygen can kill the bacteria, and, as far as we know, it seems unlikely that bacteria could become resistant to this type of treatment.’ 

Illustration showing how reactive oxygen kills bacteria
The Y-shaped antibody binds to the bacterium and releases a very reactive kind of oxygen when it gets hit with red light, causing the bacterium to die | Image Mafalda Bispo et al. JCI insight 2020

A second approach is to treat the patient with a regular antibiotic equipped with a light-sensitive switch that allows doctors to switch it on at the area of the infection. ‘And it also switches itself off again after a few hours, so the patient’s exposure to this antibiotic is greatly reduced.’ This diminishes the chance that bacteria elsewhere in the body become resistant, and it prevents an active antibiotic from ending up in wastewater after the patient has excreted it.

All this work is being done in research labs, and it will take a lot of time before these methods are ready for use in the clinic. Szymanski: ‘First, we have to demonstrate that these techniques actually work. For example, how can we shine a light deep inside the body? And once it works, we need to prove that it’s safe for patients.’ His ultimate goal is to combine diagnostic imaging and eradication of the infection in one treatment. ‘That’s what I will devote the next twenty years of my career to.’

Last modified:24 June 2025 4.50 p.m.
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