AUTHOR=Fornari Gheniffer , Gomes Renata Rodrigues , Degenhardt-Goldbach Juliana , Santos Suelen Silvana dos , Almeida Sandro Rogério de , Santos Germana Davila dos , Muro Marisol Dominguez , Bona Cleusa , Scola Rosana Herminia , Trindade Edvaldo S. , Bini Israel Henrique , Ferreira-Maba Lisandra Santos , Kestring Daiane Rigoni , Nascimento Mariana Machado Fidelis do , Lima Bruna Jacomel Favoreto de Souza , Voidaleski Morgana F. , Steinmacher Douglas André , Soley Bruna da Silva , Deng Shuwen , Bocca Anamelia Lorenzetti , da Silva Moises B. , Salgado Claudio G. , de Azevedo Conceição Maria Pedroso e Silva , Vicente Vania Aparecida , de Hoog Sybren TITLE=A Model for Trans-Kingdom Pathogenicity in Fonsecaea Agents of Human Chromoblastomycosis JOURNAL=Frontiers in Microbiology VOLUME=9 YEAR=2018 URL=https://www.frontiersin.org/journals/microbiology/articles/10.3389/fmicb.2018.02211 DOI=10.3389/fmicb.2018.02211 ISSN=1664-302X ABSTRACT=

The fungal genus Fonsecaea comprises etiological agents of human chromoblastomycosis, a chronic implantation skin disease. The current hypothesis is that patients acquire the infection through an injury from plant material. The present study aimed to evaluate a model of infection in plant and animal hosts to understand the parameters of trans-kingdom pathogenicity. Clinical strains of causative agents of chromoblastomycosis (Fonsecaea pedrosoi and Fonsecaea monophora) were compared with a strain of Fonsecaea erecta isolated from a living plant. The clinical strains of F. monophora and F. pedrosoi remained concentrated near the epidermis, whereas F. erecta colonized deeper plant tissues, resembling an endophytic behavior. In an invertebrate infection model with larvae of a beetle, Tenebrio molitor, F. erecta exhibited the lowest survival rates. However, F. pedrosoi produced dark, spherical to ovoidal cells that resembled muriform cells, the invasive form of human chromoblastomycosis confirming the role of muriform cells as a pathogenic adaptation in animal tissues. An immunologic assay in BALB/c mice demonstrated the high virulence of saprobic species in animal models was subsequently controlled via host higher immune response.