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Histidine-Rich Glycoprotein Protects from Systemic Candida Infection
Fungi, such as Candida spp., are commonly found on the skin and at mucosal surfaces. Yet, they rarely cause invasive infections in immunocompetent individuals, an observation reflecting the ability of our innate immune system to control potentially invasive microbes found at biological boundaries. A...
Autores principales: | , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Public Library of Science
2008
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2537934/ https://www.ncbi.nlm.nih.gov/pubmed/18797515 http://dx.doi.org/10.1371/journal.ppat.1000116 |
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author | Rydengård, Victoria Shannon, Oonagh Lundqvist, Katarina Kacprzyk, Lukasz Chalupka, Anna Olsson, Anna-Karin Mörgelin, Matthias Jahnen-Dechent, Willi Malmsten, Martin Schmidtchen, Artur |
author_facet | Rydengård, Victoria Shannon, Oonagh Lundqvist, Katarina Kacprzyk, Lukasz Chalupka, Anna Olsson, Anna-Karin Mörgelin, Matthias Jahnen-Dechent, Willi Malmsten, Martin Schmidtchen, Artur |
author_sort | Rydengård, Victoria |
collection | PubMed |
description | Fungi, such as Candida spp., are commonly found on the skin and at mucosal surfaces. Yet, they rarely cause invasive infections in immunocompetent individuals, an observation reflecting the ability of our innate immune system to control potentially invasive microbes found at biological boundaries. Antimicrobial proteins and peptides are becoming increasingly recognized as important effectors of innate immunity. This is illustrated further by the present investigation, demonstrating a novel antifungal role of histidine-rich glycoprotein (HRG), an abundant and multimodular plasma protein. HRG bound to Candida cells, and induced breaks in the cell walls of the organisms. Correspondingly, HRG preferentially lysed ergosterol-containing liposomes but not cholesterol-containing ones, indicating a specificity for fungal versus other types of eukaryotic membranes. Both antifungal and membrane-rupturing activities of HRG were enhanced at low pH, and mapped to the histidine-rich region of the protein. Ex vivo, HRG-containing plasma as well as fibrin clots exerted antifungal effects. In vivo, Hrg(−/−) mice were susceptible to infection by C. albicans, in contrast to wild-type mice, which were highly resistant to infection. The results demonstrate a key and previously unknown antifungal role of HRG in innate immunity. |
format | Text |
id | pubmed-2537934 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-25379342008-09-17 Histidine-Rich Glycoprotein Protects from Systemic Candida Infection Rydengård, Victoria Shannon, Oonagh Lundqvist, Katarina Kacprzyk, Lukasz Chalupka, Anna Olsson, Anna-Karin Mörgelin, Matthias Jahnen-Dechent, Willi Malmsten, Martin Schmidtchen, Artur PLoS Pathog Research Article Fungi, such as Candida spp., are commonly found on the skin and at mucosal surfaces. Yet, they rarely cause invasive infections in immunocompetent individuals, an observation reflecting the ability of our innate immune system to control potentially invasive microbes found at biological boundaries. Antimicrobial proteins and peptides are becoming increasingly recognized as important effectors of innate immunity. This is illustrated further by the present investigation, demonstrating a novel antifungal role of histidine-rich glycoprotein (HRG), an abundant and multimodular plasma protein. HRG bound to Candida cells, and induced breaks in the cell walls of the organisms. Correspondingly, HRG preferentially lysed ergosterol-containing liposomes but not cholesterol-containing ones, indicating a specificity for fungal versus other types of eukaryotic membranes. Both antifungal and membrane-rupturing activities of HRG were enhanced at low pH, and mapped to the histidine-rich region of the protein. Ex vivo, HRG-containing plasma as well as fibrin clots exerted antifungal effects. In vivo, Hrg(−/−) mice were susceptible to infection by C. albicans, in contrast to wild-type mice, which were highly resistant to infection. The results demonstrate a key and previously unknown antifungal role of HRG in innate immunity. Public Library of Science 2008-08-01 /pmc/articles/PMC2537934/ /pubmed/18797515 http://dx.doi.org/10.1371/journal.ppat.1000116 Text en Rydengård et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Rydengård, Victoria Shannon, Oonagh Lundqvist, Katarina Kacprzyk, Lukasz Chalupka, Anna Olsson, Anna-Karin Mörgelin, Matthias Jahnen-Dechent, Willi Malmsten, Martin Schmidtchen, Artur Histidine-Rich Glycoprotein Protects from Systemic Candida Infection |
title | Histidine-Rich Glycoprotein Protects from Systemic Candida Infection |
title_full | Histidine-Rich Glycoprotein Protects from Systemic Candida Infection |
title_fullStr | Histidine-Rich Glycoprotein Protects from Systemic Candida Infection |
title_full_unstemmed | Histidine-Rich Glycoprotein Protects from Systemic Candida Infection |
title_short | Histidine-Rich Glycoprotein Protects from Systemic Candida Infection |
title_sort | histidine-rich glycoprotein protects from systemic candida infection |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2537934/ https://www.ncbi.nlm.nih.gov/pubmed/18797515 http://dx.doi.org/10.1371/journal.ppat.1000116 |
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