Materials Map

Discover the materials research landscape. Find experts, partners, networks.

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The Materials Map is an open tool for improving networking and interdisciplinary exchange within materials research. It enables cross-database search for cooperation and network partners and discovering of the research landscape.

The dashboard provides detailed information about the selected scientist, e.g. publications. The dashboard can be filtered and shows the relationship to co-authors in different diagrams. In addition, a link is provided to find contact information.

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The Materials Map is still under development. In its current state, it is only based on one single data source and, thus, incomplete and contains duplicates. We are working on incorporating new open data sources like ORCID to improve the quality and the timeliness of our data. We will update Materials Map as soon as possible and kindly ask for your patience.

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in Cooperation with on an Cooperation-Score of 37%

Topics

Publications (3/3 displayed)

  • 2022Heterogeneity in the transcriptional response of the human pathogen <i>Aspergillus fumigatus</i> to the antifungal agent caspofungin20citations
  • 2020PDMS-urethanesil hybrid multifunctional materials: Combining CO2 use and sol-gel processing10citations
  • 2018Acidic Dressing Based on Agarose/Cs2.5H0.5PW12O40 Nanocomposite for Infection Control in Wound Care.24citations

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Chart of shared publication
Goldman, Gustavo Henrique
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Reis, Thaila
1 / 1 shared
Jaber, Qais Z.
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Brown, Alec
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Fridman, Micha
1 / 1 shared
Rocha, Marina Campos
1 / 1 shared
Pardeshi, Lakhansing
1 / 1 shared
Costa, Jonas Henrique
1 / 1 shared
Wong, Koon Ho
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Colabardini, Ana Cristina
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Wang, Fang
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Dong, Zhiqiang
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Aguiar, Flavio H. B.
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Schneider, Ricardo
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Ribeiro, Sidney J. L.
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Rischka, Klaus
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Lima, Elton F. S.
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Rossi De Aguiar, Kelen M. F.
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Günther, Florian
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Imasato, Hidetake
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Santos, Marcio L.
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Simões, Mateus B.
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Rocha, Marina C.
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Maria Do, Carmo A. J. Mainardi
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2020
2018

Co-Authors (by relevance)

  • Goldman, Gustavo Henrique
  • Reis, Thaila
  • Jaber, Qais Z.
  • Brown, Alec
  • Fridman, Micha
  • Rocha, Marina Campos
  • Pardeshi, Lakhansing
  • Costa, Jonas Henrique
  • Wong, Koon Ho
  • Colabardini, Ana Cristina
  • Wang, Fang
  • Dong, Zhiqiang
  • Aguiar, Flavio H. B.
  • Schneider, Ricardo
  • Ribeiro, Sidney J. L.
  • Rischka, Klaus
  • Wong Chi Man, Michel
  • Bini, Rafael A.
  • Passeti, Tania A.
  • Pereira, Renata
  • Bearzi, Jefferson R.
  • Lima, Elton F. S.
  • Rodrigues Filho, Ubirajara Pereira
  • Rossi De Aguiar, Kelen M. F.
  • Günther, Florian
  • Imasato, Hidetake
  • Santos, Marcio L.
  • Simões, Mateus B.
  • Rocha, Marina C.
  • Maria Do, Carmo A. J. Mainardi
OrganizationsLocationPeople

article

Heterogeneity in the transcriptional response of the human pathogen <i>Aspergillus fumigatus</i> to the antifungal agent caspofungin

  • Goldman, Gustavo Henrique
  • Reis, Thaila
  • Jaber, Qais Z.
  • Brown, Alec
  • Fridman, Micha
  • Rocha, Marina Campos
  • Pardeshi, Lakhansing
  • Costa, Jonas Henrique
  • Wong, Koon Ho
  • Colabardini, Ana Cristina
  • Wang, Fang
  • Dong, Zhiqiang
  • Malavazi, Iran
Abstract

<jats:title>Abstract</jats:title><jats:p>Aspergillus fumigatus is the main causative agent of invasive pulmonary aspergillosis (IPA), a severe disease that affects immunosuppressed patients worldwide. The fungistatic drug caspofungin (CSP) is the second line of therapy against IPA but has increasingly been used against clinical strains that are resistant to azoles, the first line antifungal therapy. In high concentrations, CSP induces a tolerance phenotype with partial reestablishment of fungal growth called CSP paradoxical effect (CPE), resulting from a change in the composition of the cell wall. An increasing number of studies has shown that different isolates of A. fumigatus exhibit phenotypic heterogeneity, including heterogeneity in their CPE response. To gain insights into the underlying molecular mechanisms of CPE response heterogeneity, we analyzed the transcriptomes of two A. fumigatus reference strains, Af293 and CEA17, exposed to low and high CSP concentrations. We found that there is a core transcriptional response that involves genes related to cell wall remodeling processes, mitochondrial function, transmembrane transport, and amino acid and ergosterol metabolism, and a variable response related to secondary metabolite (SM) biosynthesis and iron homeostasis. Specifically, we show here that the overexpression of a SM pathway that works as an iron chelator extinguishes the CPE in both backgrounds, whereas iron depletion is detrimental for the CPE in Af293 but not in CEA17. We next investigated the function of the transcription factor CrzA, whose deletion was previously shown to result in heterogeneity in the CPE response of the Af293 and CEA17 strains. We found that CrzA constitutively binds to and modulates the expression of several genes related to processes involved in CSP tolerance and that crzA deletion differentially impacts the SM production and growth of Af293 and CEA17. As opposed to the ΔcrzACEA17 mutant, the ΔcrzAAf293 mutant fails to activate cell wall remodeling genes upon CSP exposure, which most likely severely affects its macrostructure and extinguishes its CPE. This study describes how heterogeneity in the response to an antifungal agent between A. fumigatus strains stems from heterogeneity in the function of a transcription factor and its downstream target genes.</jats:p>

Topics
  • impedance spectroscopy
  • iron
  • cloud-point extraction