Respiring to infect: Emerging links between mitochondria, the electron transport chain, and fungal pathogenesis
Critically important activities related to drug susceptibility and resistance are the subject of other recent reviews [2–9]. cAMP, cyclic adenosine monophosphate; ETC, electron transport chain; PKA, protein kinase A; ROS, reactive oxygen species. https://doi.org/10.1371/journal.ppat.1009661.g001 [Fi...
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Published in | PLoS pathogens Vol. 17; no. 7; p. e1009661 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
San Francisco
Public Library of Science
08.07.2021
Public Library of Science (PLoS) |
Subjects | |
Online Access | Get full text |
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Summary: | Critically important activities related to drug susceptibility and resistance are the subject of other recent reviews [2–9]. cAMP, cyclic adenosine monophosphate; ETC, electron transport chain; PKA, protein kinase A; ROS, reactive oxygen species. https://doi.org/10.1371/journal.ppat.1009661.g001 [Figure omitted. ETC, electron transport chain; SHAM, salicylhydroxamic acid; SNP, sodium nitroprusside. https://doi.org/10.1371/journal.ppat.1009661.g002 The electron transport chain is connected to fungal pathogenesis Mitochondrial function is important for fungi to cause disease, particularly in the context of adaptation to challenges in the mammalian environment (e.g., nutrient limitation, the response to stress, and the immune response). The response to iron limitation was dependent on the iron permease, Ftr1, cyclic adenosine monophosphate (cAMP)-dependent protein kinase A (PKA), and the transcription factor Sef1 that activates the expression of iron uptake functions and is required for candidiasis [21]. Furthermore, iron acquisition, cell wall integrity, mitochondrial function, and virulence in C. neoformans are dependent on Vps45, a Sec1/Munc18 (SM) protein that participates in vesicle fusion in the trans-Golgi network-early endosome and the late endosome pathways via interactions with soluble N-ethylmaleimide-sensitive attachment protein receptor (SNARE) proteins [28]. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 ObjectType-Review-3 content type line 23 The authors have declared that no competing interests exist. |
ISSN: | 1553-7374 1553-7366 1553-7374 |
DOI: | 10.1371/journal.ppat.1009661 |