Fungal toxin triggers traps: Revealing the clever defence of white blood cells

Umeå University researchers unveil how the most common white blood cells, neutrophils, counter Candida albicanstoxin stopping its tracks. The results have been published in EMBO Reports.

“We found that when exposed to the toxin of the fungal pathogen, neutrophils trigger processes to release a chromatin meshwork which entangles and restrains Candida albicans hyphae, says Constantin Urban, Professor of Immunology at the Department of Clinical Microbiology at Umeå university, Sweden, and supervising investigator of the study.

Systemic infections caused by bacterial and fungal organisms frequently result in a clinical condition termed sepsis which is a leading cause of death of critically ill patients and hence, is considered a global threat. According to the World Health Organization, sepsis is estimated to affect more than 30 million people worldwide every year, leading to an estimated number of six million fatal cases. C. albicans is the most frequent human fungal pathogen and a common cause of invasive candidiasis which may result in sepsis.

A hallmark of C. albicansvirulence is the ability to reversible switch from yeast forms to filamentous forms, hyphae. The organism uses the yeast form to rapidly increase biomass and the hyphae to invade and damage tissue.

While a large proportion of the world population is colonized by C. albicans since birth, those with a weakened immune system due to disease or medical intervention are at risk to develop severe or even life-threatening infections, including sepsis, caused by this fungal organism. Particularly neutrophils, the most abundant white blood cell, are an essential part in the defence against fungal microbes.

The newly published study sheds light on how neutrophils, respond to C. albicans hyphae, which release a peptide toxin called candidalysin. Notably, candidalysin is exclusively secreted when C. albicans grows as hyphae and hence during invasive growth.

The researchers observed that neutrophils triggered cellular pathways which cumulated in the release of neutrophil extracellular traps (NETs). These chromatin fibres are formidable weapons against hyphae. NETs can entrap and inhibit the fungus with the help of large amounts of sticky and antimicrobial proteins located within the structures. The sticky nature of NET proteins efficiently binds microbes, such as fungal cells. The entangled fungus subsequently is attacked by the associated antimicrobial NET proteins.

“We were very surprised to see that neutrophils remained functional in the presence of candidalysin for such a long time. The immune cells continued to produce antimicrobial oxidants and continued to engulf fungal cells,” says Constantin Urban.

In contrast, when neutrophils were infected with engineered strains of C. albicans lacking candidalysin, NET formation was virtually absent.

“Interestingly, candidalysin alone was not a sufficient stimulus to induce NET formation. It resulted in a more compact, less fibrous chromatin meshwork released by neutrophils, so-called NET-like structures, whereas only the combination of candidalysin exposure to and pattern recognition of C. albicans cells by neutrophils resulted in release of fibrous NETs,” says Lucas Unger, research assistant at the Department of Clinical Microbiology at Umeå University at the time of the study, lead experimental researcher of the study.

The study unravels that candidalysin mainly contributes to chromatin swelling – an early step in the release of extracellular DNA structures – via calcium-dependent activation. Through effects upon neutrophil membranes calcium ions are allowed to enter the cells to start these activation processes. The recognition of fungal cells via neutrophil receptor molecules triggers kinase activation and production of antimicrobial oxidants. Calcium influx, kinase activation and oxidant production in combination eventually induce the release of large amounts of NETs.

This work was only possible with engaged international collaborators located in Gothenburg in Sweden, Bristol and London in the United Kingdom, and Jena and Berlin in Germany.

“We are particularly grateful to clinicians from the Charité hospital in Berlin that allowed us access to neutrophils from patients with chronic granulomatous disease. The immunodeficiency renders neutrophils unable to produce antimicrobial oxidants and with the help of these we could thoroughly address the involvement of oxidants in candidalysin-triggered processes,” says Constantin Urban.

About the scientific article:
Candida albicans induces neutrophil extracellular traps and leucotoxic hypercitrullination via candidalysin
Lucas Unger, Samuel Skoluda, Emelie Backman, Borko Amulic, Fernando M Ponce-Garcia, Chinelo NC Etiaba, Sujan Yellagunda, Renate Krüger, Horst von Bernuth, Johan Bylund, Bernhard Hube, Julian R Naglik, Constantin F Urban
EMBO Reports
https://www.embopress.org/doi/10.15252/embr.202357571

Press photos
https://mediabank-umu.qbank-mediaportal.se/selection/aca4acaaffaaf6a937e92fbf539acba8

About Umeå Centre for Microbial Research, UCMR
UCMR is a Centre of Excellence promoting interdisciplinary cutting-edge molecular and translational microbial infection research at Umeå University. UCMR was founded in 2004 and today the science environment comprises 67 research groups with outstanding track records in the fields of microbial pathogenesis, molecular and cell biology, chemistry, clinical microbiology, structural biology, immunology, epidemiology, microbial ecology, physics, mathematics, and data-driven science.

For more information please contact:
Constantin Urban, Department of Clinical Microbiology, Umeå University
Email: constantin.urban@umu.se

Lucas Unger, Aston University, Birmingham, UK
Email: l.unger@aston.ac.uk