by Juliane Seeber, Friedrich Schiller University of Jena

Drug resistant fungi spreading: Focus on Candida parapsilosis

Timeline and hospital network dynamics of a Candida parapsilosis outbreak in Berlin, Germany. Credit: The Lancet Microbe (2024). DOI: 10.1016/j.lanmic.2024.07.012

Candida parapsilosis is a yeast fungus that can colonize the skin and digestive tract of humans and is usually harmless. However, it can cause severe wound and tissue infections, including life-threatening septicemia, in people who are immunocompromised as a result of cancer or organ transplants or with serious medical conditions requiring prolonged hospitalization.

Just as antibiotics are used to treat bacterial infections, antifungal agents are used to treat fungal infections. In recent years, however, the frequency of strains that are resistant to these drugs has increased dramatically, making these infections much more difficult to treat.

A team led by Dr. Amelia Barber from the Cluster of Excellence "Balance of the Microverse" at Friedrich Schiller University Jena and Dr. Grit Walther from the National Reference Centre for Invasive Fungal Infections (NRZMyk) has investigated an outbreak of a multi-drug resistant, hospital-acquired strain of this fungus. The researchers developed a new molecular detection method that can quickly and cost-effectively differentiate strains of C. parapsilosis.

The results are published in The Lancet Microbe.

A dangerous fungus is spreading

The study provides a detailed genomic analysis of a long-lasting outbreak event caused by antimicrobial-resistant C. parapsilosis in several health care facilities in Berlin. The research team found that a single, genetically indistinguishable strain alone caused 33 invasive infections between 2018 and 2022.

Although the number may sound small at first, invasive infections always require intensive medical care and lead to severe impairment of quality of life. What is particularly worrying is that the pathogen was spread from person to person and also across different facilities. Its resistance to the preferred antifungal drugs makes it a serious threat.

Significantly, the strain from the Berlin hospitals was closely related to strains already found in Canada, the Middle East and East Asia, demonstrating the global spread of drug-resistant fungi.

Development of an innovative typing scheme

In their study, the researchers not only uncovered the genetic relationships and transmission dynamics of the strains of C. parapsilosis associated with the outbreak, but also developed a new identification (typing) strategy for this pathogen. This typing strategy, known as Multilocus Sequence Typing (MLST), involves sequencing multiple short DNA regions to genetically distinguish strains. This offers a cheaper and faster alternative to whole genome sequencing.

"The newly developed MLST scheme enables rapid and cost-effective differentiation and tracking of C. parapsilosis strains. This allows us to react quickly to new outbreaks and effectively contain this often drug-resistant fungus. This is particularly valuable when genome sequencing is simply not possible due to cost or lack of local bioinformatics knowledge," explains Dr. Barber, head of the Fungal Informatics junior research group at University of Jena.

Dr. Walther, co-author of the paper and co-director of the NRZMyk at the Leibniz Institute for Natural Product Research and Infection Biology—Hans Knöll Institute (Leibniz-HKI), adds, "The study highlights the importance of quickly recognizing fungal infections and possible resistance in order to prevent transmission to other patients or other facilities If clinics do not have the facilities to carry out the MLST themselves, they can contact the NRZMyk if an outbreak is suspected."

More information: Phillip J T Brassington et al, Genomic reconstruction of an azole-resistant Candida parapsilosis outbreak and the creation of a multi-locus sequence typing scheme: a retrospective observational and genomic epidemiology study, The Lancet Microbe (2024). DOI: 10.1016/j.lanmic.2024.07.012

Journal information: The Lancet Microbe 

Provided by Friedrich Schiller University of Jena