Neutrophil Interactions Stimulate Evasive Hyphal Branching by Aspergillus fumigatus.

Invasive aspergillosis (IA), primarily caused by Aspergillus fumigatus, is an opportunistic fungal infection predominantly affecting immunocompromised and neutropenic patients that is difficult to treat and results in high mortality. Investigations of neutrophil-hypha interaction in vitro and in ani...

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Main Authors: Felix Ellett, Julianne Jorgensen, Galit H Frydman, Caroline N Jones, Daniel Irimia
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2017-01-01
Series:PLoS Pathogens
Online Access:http://europepmc.org/articles/PMC5261818?pdf=render
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spelling doaj-383a7320827441f38027b5da6d7c4cab2020-11-25T00:27:49ZengPublic Library of Science (PLoS)PLoS Pathogens1553-73661553-73742017-01-01131e100615410.1371/journal.ppat.1006154Neutrophil Interactions Stimulate Evasive Hyphal Branching by Aspergillus fumigatus.Felix EllettJulianne JorgensenGalit H FrydmanCaroline N JonesDaniel IrimiaInvasive aspergillosis (IA), primarily caused by Aspergillus fumigatus, is an opportunistic fungal infection predominantly affecting immunocompromised and neutropenic patients that is difficult to treat and results in high mortality. Investigations of neutrophil-hypha interaction in vitro and in animal models of IA are limited by lack of temporal and spatial control over interactions. This study presents a new approach for studying neutrophil-hypha interaction at single cell resolution over time, which revealed an evasive fungal behavior triggered by interaction with neutrophils: Interacting hyphae performed de novo tip formation to generate new hyphal branches, allowing the fungi to avoid the interaction point and continue invasive growth. Induction of this mechanism was independent of neutrophil NADPH oxidase activity and neutrophil extracellular trap (NET) formation, but could be phenocopied by iron chelation and mechanical or physiological stalling of hyphal tip extension. The consequence of branch induction upon interaction outcome depends on the number and activity of neutrophils available: In the presence of sufficient neutrophils branching makes hyphae more vulnerable to destruction, while in the presence of limited neutrophils the interaction increases the number of hyphal tips, potentially making the infection more aggressive. This has direct implications for infections in neutrophil-deficient patients and opens new avenues for treatments targeting fungal branching.http://europepmc.org/articles/PMC5261818?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Felix Ellett
Julianne Jorgensen
Galit H Frydman
Caroline N Jones
Daniel Irimia
spellingShingle Felix Ellett
Julianne Jorgensen
Galit H Frydman
Caroline N Jones
Daniel Irimia
Neutrophil Interactions Stimulate Evasive Hyphal Branching by Aspergillus fumigatus.
PLoS Pathogens
author_facet Felix Ellett
Julianne Jorgensen
Galit H Frydman
Caroline N Jones
Daniel Irimia
author_sort Felix Ellett
title Neutrophil Interactions Stimulate Evasive Hyphal Branching by Aspergillus fumigatus.
title_short Neutrophil Interactions Stimulate Evasive Hyphal Branching by Aspergillus fumigatus.
title_full Neutrophil Interactions Stimulate Evasive Hyphal Branching by Aspergillus fumigatus.
title_fullStr Neutrophil Interactions Stimulate Evasive Hyphal Branching by Aspergillus fumigatus.
title_full_unstemmed Neutrophil Interactions Stimulate Evasive Hyphal Branching by Aspergillus fumigatus.
title_sort neutrophil interactions stimulate evasive hyphal branching by aspergillus fumigatus.
publisher Public Library of Science (PLoS)
series PLoS Pathogens
issn 1553-7366
1553-7374
publishDate 2017-01-01
description Invasive aspergillosis (IA), primarily caused by Aspergillus fumigatus, is an opportunistic fungal infection predominantly affecting immunocompromised and neutropenic patients that is difficult to treat and results in high mortality. Investigations of neutrophil-hypha interaction in vitro and in animal models of IA are limited by lack of temporal and spatial control over interactions. This study presents a new approach for studying neutrophil-hypha interaction at single cell resolution over time, which revealed an evasive fungal behavior triggered by interaction with neutrophils: Interacting hyphae performed de novo tip formation to generate new hyphal branches, allowing the fungi to avoid the interaction point and continue invasive growth. Induction of this mechanism was independent of neutrophil NADPH oxidase activity and neutrophil extracellular trap (NET) formation, but could be phenocopied by iron chelation and mechanical or physiological stalling of hyphal tip extension. The consequence of branch induction upon interaction outcome depends on the number and activity of neutrophils available: In the presence of sufficient neutrophils branching makes hyphae more vulnerable to destruction, while in the presence of limited neutrophils the interaction increases the number of hyphal tips, potentially making the infection more aggressive. This has direct implications for infections in neutrophil-deficient patients and opens new avenues for treatments targeting fungal branching.
url http://europepmc.org/articles/PMC5261818?pdf=render
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