Lacticaseibacillus casei AMBR2 modulates the epithelial barrier function and immune response in a donor-derived nasal microbiota manner

Live biotherapeutic products (LBP) are emerging as alternative treatment strategies for chronic rhinosinusitis. The selection of interesting candidate LBPs often involves model systems that do not include the polymicrobial background (i.e. the host microbiota) in which they will be introduced. Here, we performed a screening in a simplified model system of upper respiratory epithelium to assess the effect of nasal microbiota composition on the ability to attach and grow of a potential LBP, Lacticaseibacillus casei AMBR2, in this polymicrobial background. After selecting the most permissive and least permissive donor, L. casei AMBR2 colonisation in their respective polymicrobial backgrounds was assessed in more physiologically relevant model systems. We examined cytotoxicity, epithelial barrier function, and cytokine secretion, as well as bacterial cell density and phenotypic diversity in differentiated airway epithelium based models, with or without macrophage-like cells. L. casei AMBR2 could colonize in the presence of both selected donor microbiota and increased epithelial barrier resistance in presence of donor-derived nasal bacteria, as well as anti-inflammatory cytokine secretion in the presence of macrophage-like cells. This study highlights the potential of L. casei AMBR2 as LBP and the necessity to employ physiologically relevant model systems to investigate host–microbe interaction in LBP research.

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Main Authors: De Rudder, C., Garcia-Tímermans, C., De Boeck, I., Lebeer, S., Van de Wiele, T., Calatayud Arroyo, Marta
Format: artículo biblioteca
Language:English
Published: Springer Nature 2020-10-09
Subjects:Experimental models of disease, Microbiome, Mucosal immunology,
Online Access:http://hdl.handle.net/10261/221460
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spelling dig-iata-es-10261-2214602021-12-28T15:40:00Z Lacticaseibacillus casei AMBR2 modulates the epithelial barrier function and immune response in a donor-derived nasal microbiota manner De Rudder, C. Garcia-Tímermans, C. De Boeck, I. Lebeer, S. Van de Wiele, T. Calatayud Arroyo, Marta Experimental models of disease Microbiome Mucosal immunology Live biotherapeutic products (LBP) are emerging as alternative treatment strategies for chronic rhinosinusitis. The selection of interesting candidate LBPs often involves model systems that do not include the polymicrobial background (i.e. the host microbiota) in which they will be introduced. Here, we performed a screening in a simplified model system of upper respiratory epithelium to assess the effect of nasal microbiota composition on the ability to attach and grow of a potential LBP, Lacticaseibacillus casei AMBR2, in this polymicrobial background. After selecting the most permissive and least permissive donor, L. casei AMBR2 colonisation in their respective polymicrobial backgrounds was assessed in more physiologically relevant model systems. We examined cytotoxicity, epithelial barrier function, and cytokine secretion, as well as bacterial cell density and phenotypic diversity in differentiated airway epithelium based models, with or without macrophage-like cells. L. casei AMBR2 could colonize in the presence of both selected donor microbiota and increased epithelial barrier resistance in presence of donor-derived nasal bacteria, as well as anti-inflammatory cytokine secretion in the presence of macrophage-like cells. This study highlights the potential of L. casei AMBR2 as LBP and the necessity to employ physiologically relevant model systems to investigate host–microbe interaction in LBP research. C.D.R., I. D. B., and S.L. were supported by an SBO grant (ProCure: project 150052), and M.C.A. benefited from an FWO postdoctoral fellowship (Research Foundation–Flanders; 118499/12R2717N LV). C.G.-T. was funded by FWO grant G020119N. Peer reviewed 2020-10-21T05:48:01Z 2020-10-21T05:48:01Z 2020-10-09 artículo http://purl.org/coar/resource_type/c_6501 Scientific Reports 10(1): 16939 (2020) http://hdl.handle.net/10261/221460 10.1038/s41598-020-73857-9 2045-2322 33037304 en Publisher's version https://doi.org/10.1038/s41598-020-73857-9 Sí open Springer Nature
institution IATA ES
collection DSpace
country España
countrycode ES
component Bibliográfico
access En linea
databasecode dig-iata-es
tag biblioteca
region Europa del Sur
libraryname Biblioteca del IATA España
language English
topic Experimental models of disease
Microbiome
Mucosal immunology
Experimental models of disease
Microbiome
Mucosal immunology
spellingShingle Experimental models of disease
Microbiome
Mucosal immunology
Experimental models of disease
Microbiome
Mucosal immunology
De Rudder, C.
Garcia-Tímermans, C.
De Boeck, I.
Lebeer, S.
Van de Wiele, T.
Calatayud Arroyo, Marta
Lacticaseibacillus casei AMBR2 modulates the epithelial barrier function and immune response in a donor-derived nasal microbiota manner
description Live biotherapeutic products (LBP) are emerging as alternative treatment strategies for chronic rhinosinusitis. The selection of interesting candidate LBPs often involves model systems that do not include the polymicrobial background (i.e. the host microbiota) in which they will be introduced. Here, we performed a screening in a simplified model system of upper respiratory epithelium to assess the effect of nasal microbiota composition on the ability to attach and grow of a potential LBP, Lacticaseibacillus casei AMBR2, in this polymicrobial background. After selecting the most permissive and least permissive donor, L. casei AMBR2 colonisation in their respective polymicrobial backgrounds was assessed in more physiologically relevant model systems. We examined cytotoxicity, epithelial barrier function, and cytokine secretion, as well as bacterial cell density and phenotypic diversity in differentiated airway epithelium based models, with or without macrophage-like cells. L. casei AMBR2 could colonize in the presence of both selected donor microbiota and increased epithelial barrier resistance in presence of donor-derived nasal bacteria, as well as anti-inflammatory cytokine secretion in the presence of macrophage-like cells. This study highlights the potential of L. casei AMBR2 as LBP and the necessity to employ physiologically relevant model systems to investigate host–microbe interaction in LBP research.
format artículo
topic_facet Experimental models of disease
Microbiome
Mucosal immunology
author De Rudder, C.
Garcia-Tímermans, C.
De Boeck, I.
Lebeer, S.
Van de Wiele, T.
Calatayud Arroyo, Marta
author_facet De Rudder, C.
Garcia-Tímermans, C.
De Boeck, I.
Lebeer, S.
Van de Wiele, T.
Calatayud Arroyo, Marta
author_sort De Rudder, C.
title Lacticaseibacillus casei AMBR2 modulates the epithelial barrier function and immune response in a donor-derived nasal microbiota manner
title_short Lacticaseibacillus casei AMBR2 modulates the epithelial barrier function and immune response in a donor-derived nasal microbiota manner
title_full Lacticaseibacillus casei AMBR2 modulates the epithelial barrier function and immune response in a donor-derived nasal microbiota manner
title_fullStr Lacticaseibacillus casei AMBR2 modulates the epithelial barrier function and immune response in a donor-derived nasal microbiota manner
title_full_unstemmed Lacticaseibacillus casei AMBR2 modulates the epithelial barrier function and immune response in a donor-derived nasal microbiota manner
title_sort lacticaseibacillus casei ambr2 modulates the epithelial barrier function and immune response in a donor-derived nasal microbiota manner
publisher Springer Nature
publishDate 2020-10-09
url http://hdl.handle.net/10261/221460
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