Cargando…

Candida auris Cell Wall Mannosylation Contributes to Neutrophil Evasion through Pathways Divergent from Candida albicans and Candida glabrata

Candida auris, a recently emergent fungal pathogen, has caused invasive infections in health care settings worldwide. Mortality rates approach 60% and hospital spread poses a public health threat. Compared to other Candida spp., C. auris avoids triggering the antifungal activity of neutrophils, inna...

Descripción completa

Detalles Bibliográficos
Autores principales: Horton, Mark V., Johnson, Chad J., Zarnowski, Robert, Andes, Brody D., Schoen, Taylor J., Kernien, John F., Lowman, Douglas, Kruppa, Michael D., Ma, Zuchao, Williams, David L., Huttenlocher, Anna, Nett, Jeniel E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8265655/
https://www.ncbi.nlm.nih.gov/pubmed/34160238
http://dx.doi.org/10.1128/mSphere.00406-21
_version_ 1783719781561532416
author Horton, Mark V.
Johnson, Chad J.
Zarnowski, Robert
Andes, Brody D.
Schoen, Taylor J.
Kernien, John F.
Lowman, Douglas
Kruppa, Michael D.
Ma, Zuchao
Williams, David L.
Huttenlocher, Anna
Nett, Jeniel E.
author_facet Horton, Mark V.
Johnson, Chad J.
Zarnowski, Robert
Andes, Brody D.
Schoen, Taylor J.
Kernien, John F.
Lowman, Douglas
Kruppa, Michael D.
Ma, Zuchao
Williams, David L.
Huttenlocher, Anna
Nett, Jeniel E.
author_sort Horton, Mark V.
collection PubMed
description Candida auris, a recently emergent fungal pathogen, has caused invasive infections in health care settings worldwide. Mortality rates approach 60% and hospital spread poses a public health threat. Compared to other Candida spp., C. auris avoids triggering the antifungal activity of neutrophils, innate immune cells that are critical for responding to many invasive fungal infections, including candidiasis. However, the mechanism underpinning this immune evasion has been largely unknown. Here, we show that C. auris cell wall mannosylation contributes to the evasion of neutrophils ex vivo and in a zebrafish infection model. Genetic disruption of mannosylation pathways (PMR1 and VAN1) diminishes the outer cell wall mannan, unmasks immunostimulatory components, and promotes neutrophil engagement, phagocytosis, and killing. Upon examination of these pathways in other Candida spp. (Candida albicans and Candida glabrata), we did not find an impact on neutrophil interactions. These studies show how C. auris mannosylation contributes to neutrophil evasion though pathways distinct from other common Candida spp. The findings shed light on innate immune evasion for this emerging pathogen. IMPORTANCE The emerging fungal pathogen Candida auris presents a global public health threat. Therapeutic options are often limited for this frequently drug-resistant pathogen, and mortality rates for invasive disease are high. Previous study has demonstrated that neutrophils, leukocytes critical for the antifungal host defense, do not efficiently recognize and kill C. auris. Here, we show how the outer cell wall of C. auris promotes immune evasion. Disruption of this mannan polysaccharide layer renders C. auris susceptible to neutrophil killing ex vivo and in a zebrafish model of invasive candidiasis. The role of these mannosylation pathways for neutrophil evasion appears divergent from other common Candida species.
format Online
Article
Text
id pubmed-8265655
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher American Society for Microbiology
record_format MEDLINE/PubMed
spelling pubmed-82656552021-07-23 Candida auris Cell Wall Mannosylation Contributes to Neutrophil Evasion through Pathways Divergent from Candida albicans and Candida glabrata Horton, Mark V. Johnson, Chad J. Zarnowski, Robert Andes, Brody D. Schoen, Taylor J. Kernien, John F. Lowman, Douglas Kruppa, Michael D. Ma, Zuchao Williams, David L. Huttenlocher, Anna Nett, Jeniel E. mSphere Research Article Candida auris, a recently emergent fungal pathogen, has caused invasive infections in health care settings worldwide. Mortality rates approach 60% and hospital spread poses a public health threat. Compared to other Candida spp., C. auris avoids triggering the antifungal activity of neutrophils, innate immune cells that are critical for responding to many invasive fungal infections, including candidiasis. However, the mechanism underpinning this immune evasion has been largely unknown. Here, we show that C. auris cell wall mannosylation contributes to the evasion of neutrophils ex vivo and in a zebrafish infection model. Genetic disruption of mannosylation pathways (PMR1 and VAN1) diminishes the outer cell wall mannan, unmasks immunostimulatory components, and promotes neutrophil engagement, phagocytosis, and killing. Upon examination of these pathways in other Candida spp. (Candida albicans and Candida glabrata), we did not find an impact on neutrophil interactions. These studies show how C. auris mannosylation contributes to neutrophil evasion though pathways distinct from other common Candida spp. The findings shed light on innate immune evasion for this emerging pathogen. IMPORTANCE The emerging fungal pathogen Candida auris presents a global public health threat. Therapeutic options are often limited for this frequently drug-resistant pathogen, and mortality rates for invasive disease are high. Previous study has demonstrated that neutrophils, leukocytes critical for the antifungal host defense, do not efficiently recognize and kill C. auris. Here, we show how the outer cell wall of C. auris promotes immune evasion. Disruption of this mannan polysaccharide layer renders C. auris susceptible to neutrophil killing ex vivo and in a zebrafish model of invasive candidiasis. The role of these mannosylation pathways for neutrophil evasion appears divergent from other common Candida species. American Society for Microbiology 2021-06-23 /pmc/articles/PMC8265655/ /pubmed/34160238 http://dx.doi.org/10.1128/mSphere.00406-21 Text en Copyright © 2021 Horton et al. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research Article
Horton, Mark V.
Johnson, Chad J.
Zarnowski, Robert
Andes, Brody D.
Schoen, Taylor J.
Kernien, John F.
Lowman, Douglas
Kruppa, Michael D.
Ma, Zuchao
Williams, David L.
Huttenlocher, Anna
Nett, Jeniel E.
Candida auris Cell Wall Mannosylation Contributes to Neutrophil Evasion through Pathways Divergent from Candida albicans and Candida glabrata
title Candida auris Cell Wall Mannosylation Contributes to Neutrophil Evasion through Pathways Divergent from Candida albicans and Candida glabrata
title_full Candida auris Cell Wall Mannosylation Contributes to Neutrophil Evasion through Pathways Divergent from Candida albicans and Candida glabrata
title_fullStr Candida auris Cell Wall Mannosylation Contributes to Neutrophil Evasion through Pathways Divergent from Candida albicans and Candida glabrata
title_full_unstemmed Candida auris Cell Wall Mannosylation Contributes to Neutrophil Evasion through Pathways Divergent from Candida albicans and Candida glabrata
title_short Candida auris Cell Wall Mannosylation Contributes to Neutrophil Evasion through Pathways Divergent from Candida albicans and Candida glabrata
title_sort candida auris cell wall mannosylation contributes to neutrophil evasion through pathways divergent from candida albicans and candida glabrata
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8265655/
https://www.ncbi.nlm.nih.gov/pubmed/34160238
http://dx.doi.org/10.1128/mSphere.00406-21
work_keys_str_mv AT hortonmarkv candidaauriscellwallmannosylationcontributestoneutrophilevasionthroughpathwaysdivergentfromcandidaalbicansandcandidaglabrata
AT johnsonchadj candidaauriscellwallmannosylationcontributestoneutrophilevasionthroughpathwaysdivergentfromcandidaalbicansandcandidaglabrata
AT zarnowskirobert candidaauriscellwallmannosylationcontributestoneutrophilevasionthroughpathwaysdivergentfromcandidaalbicansandcandidaglabrata
AT andesbrodyd candidaauriscellwallmannosylationcontributestoneutrophilevasionthroughpathwaysdivergentfromcandidaalbicansandcandidaglabrata
AT schoentaylorj candidaauriscellwallmannosylationcontributestoneutrophilevasionthroughpathwaysdivergentfromcandidaalbicansandcandidaglabrata
AT kernienjohnf candidaauriscellwallmannosylationcontributestoneutrophilevasionthroughpathwaysdivergentfromcandidaalbicansandcandidaglabrata
AT lowmandouglas candidaauriscellwallmannosylationcontributestoneutrophilevasionthroughpathwaysdivergentfromcandidaalbicansandcandidaglabrata
AT kruppamichaeld candidaauriscellwallmannosylationcontributestoneutrophilevasionthroughpathwaysdivergentfromcandidaalbicansandcandidaglabrata
AT mazuchao candidaauriscellwallmannosylationcontributestoneutrophilevasionthroughpathwaysdivergentfromcandidaalbicansandcandidaglabrata
AT williamsdavidl candidaauriscellwallmannosylationcontributestoneutrophilevasionthroughpathwaysdivergentfromcandidaalbicansandcandidaglabrata
AT huttenlocheranna candidaauriscellwallmannosylationcontributestoneutrophilevasionthroughpathwaysdivergentfromcandidaalbicansandcandidaglabrata
AT nettjeniele candidaauriscellwallmannosylationcontributestoneutrophilevasionthroughpathwaysdivergentfromcandidaalbicansandcandidaglabrata