Paracoccin Overexpression in Paracoccidioides brasiliensis Enhances Fungal Virulence by Remodeling Chitin Properties of the Cell Wall

Author:

Gonçales Relber Aguiar123ORCID,Ricci-Azevedo Rafael1,Vieira Vanessa C S2,Fernandes Fabrício F1,Thomaz Sandra M de O1,Carvalho Agostinho23,Vendruscolo Patrícia E1,Cunha Cristina23,Roque-Barreira Maria Cristina1,Rodrigues Fernando23

Affiliation:

1. Department of Cell and Molecular Biology and Pathogenic Bioagents, Ribeirão Preto Medical School, University of São Paulo, Ribeirão Preto/São Paulo, Brazil

2. Life and Health Sciences Research Institute School of Medicine, University of Minho, Braga, Portugal

3. ICVS/3B’s–PT Government Associate Laboratory, Braga/Guimarães, Portugal

Abstract

Abstract Background The thermodimorphic fungi Paracoccidioides spp. are the etiological agents of paracoccidioidomycosis. Although poorly studied, paracoccin (PCN) from Paracoccidioides brasiliensis has been shown to harbor lectinic, enzymatic, and immunomodulatory properties that affect disease development. Methods Mutants of P. brasiliensis overexpressing PCN (ov-PCN) were constructed by Agrobacterium tumefaciens–mediated transformation. ov-PCN strains were analyzed and inoculated intranasally or intravenously to mice. Fungal burden, lung pathology, and survival were monitored to evaluate virulence. Electron microscopy was used to evaluate the size of chito-oligomer particles released by ov-PCN or wild-type strains to growth media. Results ov-PCN strains revealed no differences in cell growth and viability, although PCN overexpression favored cell separation, chitin processing that results in the release of smaller chito-oligomer particles, and enhanced virulence. Our data show that PCN triggers a critical effect in the cell wall biogenesis through the chitinase activity resulting from overexpression of PCN. As such, PCN overexpression aggravates the disease caused by P. brasiliensis. Conclusions Our data are consistent with a model in which PCN modulates the cell wall architecture via its chitinase activity. These findings highlight the potential for exploiting PCN function in future therapeutic approaches.

Funder

São Paulo Research Foundation

Conselho Nacional de Desenvolvimento Cientifico e Tecnológico

Financiadora de Estudos e Projetos

Coordenação de Aperfeiçoamento de Pessoal de Nível Superior

Fundação para a Ciência e Tecnologia

Northern Portugal Regional Operational Programme

European Regional Development Fund

European Union’s Horizon 2020

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Immunology and Allergy

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