Iron Deprivation Modulates the Exoproteome in .

Front Cell Infect Microbiol

Laboratório de Biologia Molecular, Instituto de Ciências Biológicas, ICB II, Campus II, Universidade Federal de Goiás, Goiânia, Brazil.

Published: June 2022

Fungi of the genus are the etiological agents of the systemic mycosis paracoccidioidomycosis and, when in the host, they find a challenging environment that is scarce in nutrients and micronutrients, such as Fe, which is indispensable for the survival of the pathogen. Previous studies have shown that fungi of this genus, in response to Fe deprivation, are able to synthesize and capture siderophores (Fe chelators), use Fe-containing host proteins as a source of the metal, and use a non-canonical reductive pathway for Fe assimilation. Despite all of these findings, there are still gaps that need to be filled in the pathogen response to metal deprivation. To contribute to the knowledge related to this subject, we obtained the exoproteome of (18) undergoing Fe deprivation and by nanoUPLC-MS. One hundred forty-one proteins were identified, and out of these, 64 proteins were predicted to be secreted. We also identified the regulation of several virulence factors. Among the results, we highlight Cyb5 as a secreted molecule of in the exoproteome obtained during Fe deprivation. Cyb5 is described as necessary for the Fe deprivation response of and Experimental data and molecular modeling indicated that Cyb5 can bind to Fe ions , suggesting that it can be relevant in the arsenal of molecules related to iron homeostasis in .

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9205457PMC
http://dx.doi.org/10.3389/fcimb.2022.903070DOI Listing

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