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
Cited by
5 articles.
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