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Review
. 2017 Apr 7:7:118.
doi: 10.3389/fcimb.2017.00118. eCollection 2017.

The Cell Biology of the Trichosporon-Host Interaction

Affiliations
Review

The Cell Biology of the Trichosporon-Host Interaction

Cláudio Duarte-Oliveira et al. Front Cell Infect Microbiol. .

Abstract

Fungi of the genus Trichosporon are increasingly recognized as causative agents of superficial and invasive fungal disease in humans. Although most species are considered commensals of the human skin and gastrointestinal tract, these basidiomycetes are an increasing cause of fungal disease among immunocompromised hosts, such as hematological patients and solid organ transplant recipients. The initiation of commensal or pathogenic programs by Trichosporon spp. involves the adaptation to the host microenvironment and its immune system. However, the exact virulence factors activated upon the transition to a pathogenic lifestyle, including the intricate biology of the cell wall, and how these interact with and subvert the host immune responses remain largely unknown. Here, we revisit our current understanding of the virulence attributes of Trichosporon spp., particularly T. asahii, and their interaction with the host immune system, and accommodate this knowledge within novel perspectives on fungal diagnostics and therapeutics.

Keywords: Trichosporon; antifungal immunity; host-pathogen interaction; trichosporonosis; virulence factors.

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Figures

Figure 1
Figure 1
The virulence landscape of Trichosporon species. The ability to evade the host immune system and trigger disease is a polygenic trait in Trichosporon spp., particularly T. asahii, and that involves a dynamic regulation of biochemical, physiological, genetic and morphogenetic characteristics. GXM, glucuronoxylomannan.
Figure 2
Figure 2
The interaction of T. asahii with host immune cells. (A) Blastoconidia and pseudohyphae morphotypes of T. asahii stained with Calcofluor White. (B) Phagocytosis of T. asahii by human macrophages. Fungal structures and macrophages were stained with fluorescein isothiocyanate (FITC) and phycoerythrin (PE)-conjugated anti-CD14 antibody, respectively. Trichosporon cells were incubated overnight at 4°C with FITC (Sigma-Aldrich) at a concentration of 0.1 mg/mL in 0.1M Na2CO3 buffer. (C) Bright-field microscopy visualization of human peripheral blood mononuclear cells aggregated around the different morphotypes of T. asahii.

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