ColdZyme Maintains Integrity in SARS-CoV-2-Infected Airway Epithelia

ABSTRACT SARS-CoV-2 infection causing the COVID-19 pandemic calls for immediate interventions to avoid viral transmission, disease progression, and subsequent excessive inflammation and tissue destruction. Primary normal human bronchial epithelial cells are among the first targets of SARS-CoV-2 infe...

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Main Authors: W. Posch, J. Vosper, V. Zaderer, A. Noureen, S. Constant, R. Bellmann-Weiler, C. Lass-Flörl, D. Wilflingseder
Format: Article
Language:English
Published: American Society for Microbiology 2021-04-01
Series:mBio
Subjects:
Online Access:https://journals.asm.org/doi/10.1128/mBio.00904-21
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author W. Posch
J. Vosper
V. Zaderer
A. Noureen
S. Constant
R. Bellmann-Weiler
C. Lass-Flörl
D. Wilflingseder
author_facet W. Posch
J. Vosper
V. Zaderer
A. Noureen
S. Constant
R. Bellmann-Weiler
C. Lass-Flörl
D. Wilflingseder
author_sort W. Posch
collection DOAJ
description ABSTRACT SARS-CoV-2 infection causing the COVID-19 pandemic calls for immediate interventions to avoid viral transmission, disease progression, and subsequent excessive inflammation and tissue destruction. Primary normal human bronchial epithelial cells are among the first targets of SARS-CoV-2 infection. Here, we show that ColdZyme medical device mouth spray efficiently protected against virus entry, excessive inflammation, and tissue damage. Applying ColdZyme to fully differentiated, polarized human epithelium cultured at an air-liquid interphase (ALI) completely blocked binding of SARS-CoV-2 and increased local complement activation mediated by the virus as well as productive infection of the tissue model. While SARS-CoV-2 infection resulted in exaggerated intracellular complement activation immediately following infection and a drop in transepithelial resistance, these parameters were bypassed by single pretreatment of the tissues with ColdZyme mouth spray. Crucially, our study highlights the importance of testing already evaluated and safe drugs such as ColdZyme mouth spray for maintaining epithelial integrity and hindering SARS-CoV-2 entry within standardized three-dimensional (3D) in vitro models mimicking the in vivo human airway epithelium. IMPORTANCE Although our understanding of COVID-19 continuously progresses, essential questions regarding prophylaxis and treatment remain open. A hallmark of severe SARS-CoV-2 infection is a hitherto-undescribed mechanism leading to excessive inflammation and tissue destruction associated with enhanced pathogenicity and mortality. To tackle the problem at the source, transfer of SARS-CoV-2, subsequent binding, infection, and inflammatory responses have to be avoided. In this study, we used fully differentiated, mucus-producing, and ciliated human airway epithelial cultures to test the efficacy of ColdZyme medical device mouth spray in terms of protection from SARS-CoV-2 infection. Importantly, we found that pretreatment of the in vitro airway cultures using ColdZyme mouth spray resulted in significantly shielding the epithelial integrity, hindering virus binding and infection, and blocking excessive intrinsic complement activation within the airway cultures. Our in vitro data suggest that ColdZyme mouth spray may have an impact in prevention of COVID-19.
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spelling doaj.art-5d59a8b61eb8401bb6d831102cd74afd2022-12-21T21:19:35ZengAmerican Society for MicrobiologymBio2150-75112021-04-0112210.1128/mBio.00904-21ColdZyme Maintains Integrity in SARS-CoV-2-Infected Airway EpitheliaW. Posch0J. Vosper1V. Zaderer2A. Noureen3S. Constant4R. Bellmann-Weiler5C. Lass-Flörl6D. Wilflingseder7Institute of Hygiene and Medical Microbiology, Medical University of Innsbruck, Innsbruck, AustriaInstitute of Medical Biochemistry, Geneva, SwitzerlandInstitute of Hygiene and Medical Microbiology, Medical University of Innsbruck, Innsbruck, AustriaInstitute of Hygiene and Medical Microbiology, Medical University of Innsbruck, Innsbruck, AustriaEpithelix Sàrl, Geneva, SwitzerlandUniversity Hospital of Internal Medicine II, Medical University of Innsbruck, Innsbruck, AustriaInstitute of Hygiene and Medical Microbiology, Medical University of Innsbruck, Innsbruck, AustriaInstitute of Hygiene and Medical Microbiology, Medical University of Innsbruck, Innsbruck, AustriaABSTRACT SARS-CoV-2 infection causing the COVID-19 pandemic calls for immediate interventions to avoid viral transmission, disease progression, and subsequent excessive inflammation and tissue destruction. Primary normal human bronchial epithelial cells are among the first targets of SARS-CoV-2 infection. Here, we show that ColdZyme medical device mouth spray efficiently protected against virus entry, excessive inflammation, and tissue damage. Applying ColdZyme to fully differentiated, polarized human epithelium cultured at an air-liquid interphase (ALI) completely blocked binding of SARS-CoV-2 and increased local complement activation mediated by the virus as well as productive infection of the tissue model. While SARS-CoV-2 infection resulted in exaggerated intracellular complement activation immediately following infection and a drop in transepithelial resistance, these parameters were bypassed by single pretreatment of the tissues with ColdZyme mouth spray. Crucially, our study highlights the importance of testing already evaluated and safe drugs such as ColdZyme mouth spray for maintaining epithelial integrity and hindering SARS-CoV-2 entry within standardized three-dimensional (3D) in vitro models mimicking the in vivo human airway epithelium. IMPORTANCE Although our understanding of COVID-19 continuously progresses, essential questions regarding prophylaxis and treatment remain open. A hallmark of severe SARS-CoV-2 infection is a hitherto-undescribed mechanism leading to excessive inflammation and tissue destruction associated with enhanced pathogenicity and mortality. To tackle the problem at the source, transfer of SARS-CoV-2, subsequent binding, infection, and inflammatory responses have to be avoided. In this study, we used fully differentiated, mucus-producing, and ciliated human airway epithelial cultures to test the efficacy of ColdZyme medical device mouth spray in terms of protection from SARS-CoV-2 infection. Importantly, we found that pretreatment of the in vitro airway cultures using ColdZyme mouth spray resulted in significantly shielding the epithelial integrity, hindering virus binding and infection, and blocking excessive intrinsic complement activation within the airway cultures. Our in vitro data suggest that ColdZyme mouth spray may have an impact in prevention of COVID-19.https://journals.asm.org/doi/10.1128/mBio.00904-21ColdZymeSARS-CoV-2airway epitheliaanaphylatoxinsantiviral response
spellingShingle W. Posch
J. Vosper
V. Zaderer
A. Noureen
S. Constant
R. Bellmann-Weiler
C. Lass-Flörl
D. Wilflingseder
ColdZyme Maintains Integrity in SARS-CoV-2-Infected Airway Epithelia
mBio
ColdZyme
SARS-CoV-2
airway epithelia
anaphylatoxins
antiviral response
title ColdZyme Maintains Integrity in SARS-CoV-2-Infected Airway Epithelia
title_full ColdZyme Maintains Integrity in SARS-CoV-2-Infected Airway Epithelia
title_fullStr ColdZyme Maintains Integrity in SARS-CoV-2-Infected Airway Epithelia
title_full_unstemmed ColdZyme Maintains Integrity in SARS-CoV-2-Infected Airway Epithelia
title_short ColdZyme Maintains Integrity in SARS-CoV-2-Infected Airway Epithelia
title_sort coldzyme maintains integrity in sars cov 2 infected airway epithelia
topic ColdZyme
SARS-CoV-2
airway epithelia
anaphylatoxins
antiviral response
url https://journals.asm.org/doi/10.1128/mBio.00904-21
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