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Characterization of an engineered mucus microenvironment for in vitro modeling of host–microbe interactions

The human mucus layer plays a vital role in maintaining health by providing a physical barrier to pathogens. This biological hydrogel also provides the microenvironment for commensal bacteria. Common models used to study host–microbe interactions include gnotobiotic animals or mammalian–microbial co...

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Autores principales: Huang, Andy J., O’Brien, Courtney L., Dawe, Nicholas, Tahir, Anas, Scott, Alison J., Leung, Brendan M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8975841/
https://www.ncbi.nlm.nih.gov/pubmed/35365684
http://dx.doi.org/10.1038/s41598-022-09198-6
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author Huang, Andy J.
O’Brien, Courtney L.
Dawe, Nicholas
Tahir, Anas
Scott, Alison J.
Leung, Brendan M.
author_facet Huang, Andy J.
O’Brien, Courtney L.
Dawe, Nicholas
Tahir, Anas
Scott, Alison J.
Leung, Brendan M.
author_sort Huang, Andy J.
collection PubMed
description The human mucus layer plays a vital role in maintaining health by providing a physical barrier to pathogens. This biological hydrogel also provides the microenvironment for commensal bacteria. Common models used to study host–microbe interactions include gnotobiotic animals or mammalian–microbial co-culture platforms. Many of the current in vitro models lack a sufficient mucus layer to host these interactions. In this study, we engineered a mucus-like hydrogel Consisting of a mixed alginate-mucin (ALG-MUC) hydrogel network by using low concentration calcium chloride (CaCl(2)) as crosslinker. We demonstrated that the incorporation of ALG-MUC hydrogels into an aqueous two-phase system (ATPS) co-culture platform can support the growth of a mammalian monolayer and pathogenic bacteria. The ALG-MUC hydrogels displayed selective diffusivity against macromolecules and stability with ATPS microbial patterning. Additionally, we showed that the presence of mucin within hydrogels contributed to an increase in antimicrobial resistance in ATPS patterned microbial colonies. By using common laboratory chemicals to generate a mammalian–microbial co-culture system containing a representative mucus microenvironment, this model can be readily adopted by typical life science laboratories to study host–microbe interaction and drug discovery.
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spelling pubmed-89758412022-04-05 Characterization of an engineered mucus microenvironment for in vitro modeling of host–microbe interactions Huang, Andy J. O’Brien, Courtney L. Dawe, Nicholas Tahir, Anas Scott, Alison J. Leung, Brendan M. Sci Rep Article The human mucus layer plays a vital role in maintaining health by providing a physical barrier to pathogens. This biological hydrogel also provides the microenvironment for commensal bacteria. Common models used to study host–microbe interactions include gnotobiotic animals or mammalian–microbial co-culture platforms. Many of the current in vitro models lack a sufficient mucus layer to host these interactions. In this study, we engineered a mucus-like hydrogel Consisting of a mixed alginate-mucin (ALG-MUC) hydrogel network by using low concentration calcium chloride (CaCl(2)) as crosslinker. We demonstrated that the incorporation of ALG-MUC hydrogels into an aqueous two-phase system (ATPS) co-culture platform can support the growth of a mammalian monolayer and pathogenic bacteria. The ALG-MUC hydrogels displayed selective diffusivity against macromolecules and stability with ATPS microbial patterning. Additionally, we showed that the presence of mucin within hydrogels contributed to an increase in antimicrobial resistance in ATPS patterned microbial colonies. By using common laboratory chemicals to generate a mammalian–microbial co-culture system containing a representative mucus microenvironment, this model can be readily adopted by typical life science laboratories to study host–microbe interaction and drug discovery. Nature Publishing Group UK 2022-04-01 /pmc/articles/PMC8975841/ /pubmed/35365684 http://dx.doi.org/10.1038/s41598-022-09198-6 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Huang, Andy J.
O’Brien, Courtney L.
Dawe, Nicholas
Tahir, Anas
Scott, Alison J.
Leung, Brendan M.
Characterization of an engineered mucus microenvironment for in vitro modeling of host–microbe interactions
title Characterization of an engineered mucus microenvironment for in vitro modeling of host–microbe interactions
title_full Characterization of an engineered mucus microenvironment for in vitro modeling of host–microbe interactions
title_fullStr Characterization of an engineered mucus microenvironment for in vitro modeling of host–microbe interactions
title_full_unstemmed Characterization of an engineered mucus microenvironment for in vitro modeling of host–microbe interactions
title_short Characterization of an engineered mucus microenvironment for in vitro modeling of host–microbe interactions
title_sort characterization of an engineered mucus microenvironment for in vitro modeling of host–microbe interactions
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8975841/
https://www.ncbi.nlm.nih.gov/pubmed/35365684
http://dx.doi.org/10.1038/s41598-022-09198-6
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