Glycomic analysis of host response reveals high mannose as a key mediator of influenza severity
Copyright © 2020 the Author(s). Published by PNAS..
Influenza virus infections cause a wide variety of outcomes, from mild disease to 3 to 5 million cases of severe illness and ∼290,000 to 645,000 deaths annually worldwide. The molecular mechanisms underlying these disparate outcomes are currently unknown. Glycosylation within the human host plays a critical role in influenza virus biology. However, the impact these modifications have on the severity of influenza disease has not been examined. Herein, we profile the glycomic host responses to influenza virus infection as a function of disease severity using a ferret model and our lectin microarray technology. We identify the glycan epitope high mannose as a marker of influenza virus-induced pathogenesis and severity of disease outcome. Induction of high mannose is dependent upon the unfolded protein response (UPR) pathway, a pathway previously shown to associate with lung damage and severity of influenza virus infection. Also, the mannan-binding lectin (MBL2), an innate immune lectin that negatively impacts influenza outcomes, recognizes influenza virus-infected cells in a high mannose-dependent manner. Together, our data argue that the high mannose motif is an infection-associated molecular pattern on host cells that may guide immune responses leading to the concomitant damage associated with severity.
Medienart: |
E-Artikel |
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Erscheinungsjahr: |
2020 |
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Erschienen: |
2020 |
Enthalten in: |
Zur Gesamtaufnahme - volume:117 |
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Enthalten in: |
Proceedings of the National Academy of Sciences of the United States of America - 117(2020), 43 vom: 27. Okt., Seite 26926-26935 |
Sprache: |
Englisch |
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Beteiligte Personen: |
Heindel, Daniel W [VerfasserIn] |
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Links: |
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Anmerkungen: |
Date Completed 17.12.2020 Date Revised 17.12.2020 published: Print-Electronic Citation Status MEDLINE |
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doi: |
10.1073/pnas.2008203117 |
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funding: |
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Förderinstitution / Projekttitel: |
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PPN (Katalog-ID): |
NLM316164178 |
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245 | 1 | 0 | |a Glycomic analysis of host response reveals high mannose as a key mediator of influenza severity |
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520 | |a Copyright © 2020 the Author(s). Published by PNAS. | ||
520 | |a Influenza virus infections cause a wide variety of outcomes, from mild disease to 3 to 5 million cases of severe illness and ∼290,000 to 645,000 deaths annually worldwide. The molecular mechanisms underlying these disparate outcomes are currently unknown. Glycosylation within the human host plays a critical role in influenza virus biology. However, the impact these modifications have on the severity of influenza disease has not been examined. Herein, we profile the glycomic host responses to influenza virus infection as a function of disease severity using a ferret model and our lectin microarray technology. We identify the glycan epitope high mannose as a marker of influenza virus-induced pathogenesis and severity of disease outcome. Induction of high mannose is dependent upon the unfolded protein response (UPR) pathway, a pathway previously shown to associate with lung damage and severity of influenza virus infection. Also, the mannan-binding lectin (MBL2), an innate immune lectin that negatively impacts influenza outcomes, recognizes influenza virus-infected cells in a high mannose-dependent manner. Together, our data argue that the high mannose motif is an infection-associated molecular pattern on host cells that may guide immune responses leading to the concomitant damage associated with severity | ||
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650 | 4 | |a Research Support, Non-U.S. Gov't | |
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700 | 1 | |a Koppolu, Sujeethraj |e verfasserin |4 aut | |
700 | 1 | |a Zhang, Yue |e verfasserin |4 aut | |
700 | 1 | |a Kasper, Brian |e verfasserin |4 aut | |
700 | 1 | |a Meche, Lawrence |e verfasserin |4 aut | |
700 | 1 | |a Vaiana, Christopher A |e verfasserin |4 aut | |
700 | 1 | |a Bissel, Stephanie J |e verfasserin |4 aut | |
700 | 1 | |a Carter, Chalise E |e verfasserin |4 aut | |
700 | 1 | |a Kelvin, Alyson A |e verfasserin |4 aut | |
700 | 1 | |a Elaish, Mohamed |e verfasserin |4 aut | |
700 | 1 | |a Lopez-Orozco, Joaquin |e verfasserin |4 aut | |
700 | 1 | |a Zhang, Bin |e verfasserin |4 aut | |
700 | 1 | |a Zhou, Bin |e verfasserin |4 aut | |
700 | 1 | |a Chou, Tsui-Wen |e verfasserin |4 aut | |
700 | 1 | |a Lashua, Lauren |e verfasserin |4 aut | |
700 | 1 | |a Hobman, Tom C |e verfasserin |4 aut | |
700 | 1 | |a Ross, Ted M |e verfasserin |4 aut | |
700 | 1 | |a Ghedin, Elodie |e verfasserin |4 aut | |
700 | 1 | |a Mahal, Lara K |e verfasserin |4 aut | |
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