Candida albicans uses the surface protein Gpm1 to attach to human endothelial cells and to keratinocytes via the adhesive protein vitronectin

Candida albicans is a major cause of invasive fungal infections worldwide. Upon infection and when in contact with human plasma as well as body fluids the fungus is challenged by the activated complement system a central part of the human innate immune response. C. albicans controls and evades host...

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Bibliographic Details
Main Authors: Lopez, Crisanto M. (Author) , Wallich, Reinhard (Author) , Riesbeck, Kristian (Author) , Skerka, Christine (Author) , Zipfel, Peter F. (Author)
Format: Article (Journal)
Language:English
Published: March 13, 2014
In: PLOS ONE
Year: 2014, Volume: 9, Issue: 3
ISSN:1932-6203
DOI:10.1371/journal.pone.0090796
Online Access:Resolving-System, lizenzpflichtig, Volltext: https://doi.org/10.1371/journal.pone.0090796
Verlag, lizenzpflichtig, Volltext: https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0090796
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Author Notes:Crisanto M. Lopez, Reinhard Wallich, Kristian Riesbeck, Christine Skerka, Peter F. Zipfel
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Summary:Candida albicans is a major cause of invasive fungal infections worldwide. Upon infection and when in contact with human plasma as well as body fluids the fungus is challenged by the activated complement system a central part of the human innate immune response. C. albicans controls and evades host complement attack by binding several human complement regulators like Factor H, Factor H-like protein 1 and C4BP to the surface. Gpm1 (Phosphoglycerate mutase 1) is one fungal Factor H/FHL1 -binding protein. As Gpm1 is surface exposed, we asked whether Gpm1 also contributes to host cell attachment. Here, we show by flow cytometry and by laser scanning microscopy that candida Gpm1 binds to human umbilical vein endothelial cells (HUVEC) to keratinocytes (HaCaT), and also to monocytic U937 cells.
Item Description:Gesehen am 23.09.2020
Physical Description:Online Resource
ISSN:1932-6203
DOI:10.1371/journal.pone.0090796