Abstract

Paracoccidioides brasiliensis yeast was reported to express paracoccin, a GlcNAc-binding protein that displays N-acetyl-β-d-glucosaminidase (NAGase) activity. Highly specific anti-paracoccin antibodies have been previously used to examine the localization of paracoccin in yeast and inhibit its growth in vitro. In the present study, anti-paracoccin antibodies were used to characterize, by scanning confocal microscopy, the distribution of paracoccin in P. brasiliensis hyphae, transition forms from hyphae to yeast, and mature yeast. In the mycelial phase, paracoccin was detected mainly in the hyphae tips, where it demonstrated a punctate distribution, and was associated with the cell wall. During the first 48 hours after a temperature shift from 26°C to 37°C, paracoccin expression in the differentiating hyphae was mainly detected in the budding regions, i.e. lateral protrusions, and inside the new daughter cells. There was an increased number of chlamydoconidia that expressed a high concentration of paracoccin on their surfaces and/or in their interiors 72–96 hours after the temperature shift. After 120 hours, yeast cells were the predominant form and their cytoplasm stained extensively for paracoccin, whereas Wheat Germ Agglutinin (WGA) staining was predominant on their exterior walls. After 10 days at 37°C, the interior of both mother and daughter yeast cells, as well as the budding regions, stained intensely for paracoccin. The comparison of mRNA-expression in the different fungal forms showed that PCN transcripts, although detected in all evaluated morphological forms, were higher in hypha and yeast-to-hypha transition forms. In conclusion, the pattern of paracoccin distribution in all P. brasiliensis morphotypes supports prevalent beliefs that it plays important roles in fungal growth and dimorphic transformation.

Highlights

  • IntroductionDuring P. brasiliensis infection, the transition from mycelium to yeast cells represents an essential part of the overall virulence strategy of the fungus and is required for the establishment of PCM

  • Paracoccidioides brasiliensis is a dimorphic fungus that causes paracoccidioidomycosis (PCM), the most prevalent systemic mycosis in Latin America, and has a broad geographic distribution that runs from Mexico to Argentina [1, 2].During P. brasiliensis infection, the transition from mycelium to yeast cells represents an essential part of the overall virulence strategy of the fungus and is required for the establishment of PCM

  • We have previously shown that the cell wall of P. brasiliensis yeast contains an N-acetyl-glucosamine- and chitin-binding lectin, named paracoccin (PCN), which has N-acetyl-β-Dglucosaminidase (NAGase) activity [19] and stimulates TNF-α production by macrophages [20]

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Summary

Introduction

During P. brasiliensis infection, the transition from mycelium to yeast cells represents an essential part of the overall virulence strategy of the fungus and is required for the establishment of PCM. The transition is stimulated by the rise in temperature that occurs when the inhaled mycelia or conidia contact the host lungs [3, 4]. This dimorphic fungal transition may be induced in vitro by shifting the incubation temperature from 26 ̊C to 36 ̊C (mycelia to yeast) or from 36 ̊C to 26 ̊C (yeast to mycelia) [5]. The plasticity of gene expression during the morphological transition and the resultant fungal persistence and survival has been demonstrated [8]

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