Abstract

P. brasiliensis is a thermally dimorphic fungus belonging to Paracoccidioides complex, causative of a systemic, endemic mycosis limited to Latin American countries. Signal transduction pathways related to important aspects as surviving, proliferation according to the biological niches are linked to the fungal pathogenicity in many species, but its elucidation in P. brasiliensis remains poorly explored. As Drk1, a hybrid histidine kinase, plays regulators functions in other dimorphic fungi species, mainly in dimorphism and virulence, here we investigated its importance in P. brasilensis. We, therefore generated the respective recombinant protein, anti-PbDrk1 polyclonal antibody and a silenced strain. The Drk1 protein shows a random distribution including cell wall location that change its pattern during osmotic stress condition; moreover the P. brasiliensis treatment with anti-PbDrk1 antibody, which does not modify the fungus’s viability, resulted in decreased virulence in G. mellonella model and reduced interaction with pneumocytes. Down-regulating PbDRK1 yielded phenotypic alterations such as yeast cells with more elongated morphology, virulence attenuation in G. mellonella infection model, lower amount of chitin content, increased resistance to osmotic and cell wall stresses, and also caspofungin, and finally increased sensitivity to itraconazole. These observations highlight the importance of PbDrk1 to P. brasiliensis virulence, stress adaptation, morphology, and cell wall organization, and therefore it an interesting target that could help develop new antifungals.

Highlights

  • The morphological changes from the mycelium to the yeast form are essential for the development and establishment of disease in the host. These changes are related to the cell wall, that it can act as a shield to prevent host recognition, and essential to developing a protective immune response [6] that can significantly contribute to infection control [7]

  • P. brasiliensis isolate (Pb18) was maintained on solid Fava-Netto medium before the assays were cultivated in liquid brain-heart-infusion (BHI) medium supplemented with 1%

  • Colony-PCR and double restriction analysis using the target-specific primers and NotI/NdeI enzymes, respectively confirmed the success of transformation with the clones carrying the insert of the size expected for theResults target Drk1 (3879 bp), as well two fragments after digestion: ∼5.4 kb representing the pET28a vector and a ∼3.9 kb fragment representing DRK1 fragment

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Summary

Introduction

Six phylogenetically related ascomycetes genus in the order Onygenales, Blastomyces, Histoplasma, Coccidioides, Sporothrix, Talaromyces, and Paracoccidioides, change their morphologies once spores are inhaled and reach the lungs (or at 37 ◦ C), from mycelia in the environment temperature to pathogenic yeasts form [1]. The morphological changes from the mycelium to the yeast form are essential for the development and establishment of disease in the host. These changes are related to the cell wall, that it can act as a shield to prevent host recognition, and essential to developing a protective immune response [6] that can significantly contribute to infection control [7]

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