Regulation of candidalysin underlies Candida albicans persistence in intravascular catheters by modulating NETosis

Kuo Yao Tseng, Yu Tsung Huang, Yu Ting Huang, Yu Ting Su, An Ni Wang, Wen Yen Weng, Cai Ling Ke, Yu Chiao Yeh, Jhih Jie Wang, Shin Hei Du, Zi Qi Gu, Wei Lin Chen, Ching Hsuan Lin, Yu Huan Tsai*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

Abstract

Candida albicans is a leading cause of intravascular catheter-related infections. The capacity for biofilm formation has been proposed to contribute to the persistence of this fungal pathogen on catheter surfaces. While efforts have been devoted to identifying microbial factors that modulate C. albicans biofilm formation in vitro, our understanding of the host factors that may shape C. albicans persistence in intravascular catheters is lacking. Here, we used multiphoton microscopy to characterize biofilms in intravascular catheters removed from candidiasis patients. We demonstrated that, NETosis, a type of neutrophil cell death with antimicrobial activity, was implicated in the interaction of immune cells with C. albicans in the catheters. The catheter isolates exhibited reduced filamentation and candidalysin gene expression, specifically in the total parenteral nutrition culture environment. Furthermore, we showed that the ablation of candidalysin expression in C. albicans reduced NETosis and conferred resistance to neutrophil-mediated fungal biofilm elimination. Our findings illustrate the role of neutrophil NETosis in modulating C. albicans biofilm persistence in an intravascular catheter, highlighting that C. albicans can benefit from reduced virulence expression to promote its persistence in an intravascular catheter.

Original languageEnglish
Article numbere1012319
JournalPLoS Pathogens
Volume20
Issue number6
DOIs
StatePublished - Jun 2024

Fingerprint

Dive into the research topics of 'Regulation of candidalysin underlies Candida albicans persistence in intravascular catheters by modulating NETosis'. Together they form a unique fingerprint.

Cite this