Characteristics of Extracellular Vesicles Released by the Pathogenic Yeast-Like Fungi <i>Candida glabrata</i>, <i>Candida parapsilosis</i> and <i>Candida tropicalis</i>

• Main Authors: Justyna Karkowska-Kuleta, Kamila Kulig, Elzbieta Karnas, Ewa Zuba-Surma, Olga Woznicka, Elzbieta Pyza, Patryk Kuleta, Artur Osyczka, Maria Rapala-Kozik, Andrzej Kozik
• Format: Article
• Language: English
• Published: MDPI AG 2020-07-01
• Series: Cells
• Subjects: extracellular vesicles; pathogenic fungi; candidiasis; moonlighting proteins; non-classical secretion
• Online Access: https://www.mdpi.com/2073-4409/9/7/1722

<i>Candida</i> spp. yeast-like fungi are opportunistic pathogens in humans and have been recently found to release extracellular vesicles (EVs) that are involved in many vital biological processes in fungal cells. These include communication between microorganisms and host–pathogen interactions during infection. The production of EVs and their content have been significantly characterized in the most common candidal species <i>Candida albicans</i>, including the identification of numerous virulence factors and cytoplasmic proteins in the EV cargo. We have here conducted the isolation and proteomic characterization of EVs produced by the clinically important non-albicans <i>Candida</i> species <i>C. glabrata</i>, <i>C. tropicalis</i> and <i>C. parapsilosis</i>. With the use of ultracentrifugation of the cell-free culture supernatant, the candidal EVs were collected and found to be a heterogeneous population of particles for each species with sizes ranging from 60–280 nm. The proteinaceous contents of these vesicles were analyzed using LC-MS/MS, with particular attention paid to surface-expressed proteins that would come into immediate and direct contact with host cells. We thereby identified 42 extracellular and surface-connected proteins from <i>C. glabrata</i>, 33 from <i>C. parapsilosis</i>, and 34 from <i>C. tropicalis,</i> including membrane-associated transporters, glycoproteins and enzymes involved in the organization of the fungal cell wall, as well as several cytoplasmic proteins, including alcohol dehydrogenase, enolase, glyceraldehyde-3-phosphate dehydrogenase, phosphoglycerate kinase and pyruvate kinase, for which the vesicular transport is a possible mechanism underlying their non-classical secretion.