TY - JOUR
T1 - Bioluminescence imaging in Paracoccidioides spp.
T2 - a tool to monitor the infectious processes
AU - Milhomem Cruz-Leite, Vanessa Rafaela
AU - Tomazett, Mariana Vieira
AU - Santana de Curcio, Juliana
AU - Sbaraini, Nicolau
AU - Bailão, Alexandre Melo
AU - Gonçales, Relber Aguiar
AU - Moraes, Dayane
AU - Pereira, Maristela
AU - Vainstein, Marilene Henning
AU - Schrank, Augusto
AU - Peres da Silva, Roberta
AU - Brock, Matthias
AU - Maria de Almeida Soares, Célia
N1 - Copyright © 2022 Institut Pasteur. Published by Elsevier Masson SAS. All rights reserved.
PY - 2022/9
Y1 - 2022/9
N2 - The genus Paracoccidioides comprises the species complex causing paracoccidioidomycoses (PCM). These fungi are a serious public health problem due to the long-term drug therapy, follow-up treatment, and frequent sequelae generated by the infection, such as pulmonary fibrosis. In this sense, the objective of this work was to generate bioluminescent reporter strains of Paracoccidioides spp. harboring a thermostable, red-shifted luciferase gene under the control of different constitutive promoters. The strains were generated by the integration of a species-specific codon-optimized luciferase gene upon actin or enolase promoter's control. The insertion of the constructs in Paracoccidioides brasiliensis and Paracoccidioides lutzii yeast cells were performed through Agrobacterium tumefaciens-mediated transformation. The results demonstrated the presence of several transformants harboring the luciferase gene. These transformants were further confirmed by the expression of luciferase and by the presence of the hygromycin resistance gene. Moreover, the luciferase activity could be detected in in vitro bioluminescence assays and in vivo models of infection. In general, this work presents the methodology for the construction of bioluminescent strains of Paracoccidioides spp., highlighting potential promoters and proposing an in vivo model, in which those strains could be used for the systemic study of PCM.
AB - The genus Paracoccidioides comprises the species complex causing paracoccidioidomycoses (PCM). These fungi are a serious public health problem due to the long-term drug therapy, follow-up treatment, and frequent sequelae generated by the infection, such as pulmonary fibrosis. In this sense, the objective of this work was to generate bioluminescent reporter strains of Paracoccidioides spp. harboring a thermostable, red-shifted luciferase gene under the control of different constitutive promoters. The strains were generated by the integration of a species-specific codon-optimized luciferase gene upon actin or enolase promoter's control. The insertion of the constructs in Paracoccidioides brasiliensis and Paracoccidioides lutzii yeast cells were performed through Agrobacterium tumefaciens-mediated transformation. The results demonstrated the presence of several transformants harboring the luciferase gene. These transformants were further confirmed by the expression of luciferase and by the presence of the hygromycin resistance gene. Moreover, the luciferase activity could be detected in in vitro bioluminescence assays and in vivo models of infection. In general, this work presents the methodology for the construction of bioluminescent strains of Paracoccidioides spp., highlighting potential promoters and proposing an in vivo model, in which those strains could be used for the systemic study of PCM.
KW - Actins
KW - Paracoccidioides/genetics
KW - Paracoccidioidomycosis/microbiology
KW - Phosphopyruvate Hydratase
U2 - 10.1016/j.micinf.2022.104975
DO - 10.1016/j.micinf.2022.104975
M3 - Article
C2 - 35381358
SN - 1286-4579
VL - 24
JO - Microbes and Infection
JF - Microbes and Infection
IS - 6-7
M1 - 104975
ER -