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Haemophilus influenzae persists in biofilm communities in a smoke-exposed ferret model of COPD

RATIONALE: Non-typeable Haemophilus influenzae (NTHi) is a common inhabitant of the human nasopharynx and upper airways that can cause opportunistic infections of the airway mucosa including bronchopulmonary infections in patients with chronic obstructive pulmonary disease (COPD). It is clear that o...

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Autores principales: Hunt, Benjamin C., Stanford, Denise, Xu, Xin, Li, Jindong, Gaggar, Amit, Rowe, Steven M., Raju, S. Vamsee, Swords, W. Edward
Formato: Online Artículo Texto
Lenguaje:English
Publicado: European Respiratory Society 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7418822/
https://www.ncbi.nlm.nih.gov/pubmed/32802827
http://dx.doi.org/10.1183/23120541.00200-2020
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author Hunt, Benjamin C.
Stanford, Denise
Xu, Xin
Li, Jindong
Gaggar, Amit
Rowe, Steven M.
Raju, S. Vamsee
Swords, W. Edward
author_facet Hunt, Benjamin C.
Stanford, Denise
Xu, Xin
Li, Jindong
Gaggar, Amit
Rowe, Steven M.
Raju, S. Vamsee
Swords, W. Edward
author_sort Hunt, Benjamin C.
collection PubMed
description RATIONALE: Non-typeable Haemophilus influenzae (NTHi) is a common inhabitant of the human nasopharynx and upper airways that can cause opportunistic infections of the airway mucosa including bronchopulmonary infections in patients with chronic obstructive pulmonary disease (COPD). It is clear that opportunistic infections contribute significantly to inflammatory exacerbations of COPD; however, there remains much to be learned regarding specific host and microbial determinants of persistence and/or clearance in this context. METHODS: In this study, we used a recently described ferret model for COPD, in which animals undergo chronic long-term exposure to cigarette smoke, to define host–pathogen interactions during COPD-related NTHi infections. RESULTS: NTHi bacteria colonised the lungs of smoke-exposed animals to a greater extent than controls, and elicited acute host inflammation and neutrophilic influx and activation, along with a significant increase in airway resistance and a decrease in inspiratory capacity consistent with inflammatory exacerbation; notably, these findings were not observed in air-exposed control animals. NTHi bacteria persisted within multicellular biofilm communities within the airway lumen, as evidenced by immunofluorescent detection of bacterial aggregates encased within a sialylated matrix as is typical of NTHi biofilms and differential bacterial gene expression consistent with the biofilm mode of growth. CONCLUSIONS: Based on these results, we conclude that acute infection with NTHi initiates inflammatory exacerbation of COPD disease. The data also support the widely held hypothesis that NTHi bacteria persist within multicellular biofilm communities in the lungs of patients with COPD.
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spelling pubmed-74188222020-08-14 Haemophilus influenzae persists in biofilm communities in a smoke-exposed ferret model of COPD Hunt, Benjamin C. Stanford, Denise Xu, Xin Li, Jindong Gaggar, Amit Rowe, Steven M. Raju, S. Vamsee Swords, W. Edward ERJ Open Res Original Articles RATIONALE: Non-typeable Haemophilus influenzae (NTHi) is a common inhabitant of the human nasopharynx and upper airways that can cause opportunistic infections of the airway mucosa including bronchopulmonary infections in patients with chronic obstructive pulmonary disease (COPD). It is clear that opportunistic infections contribute significantly to inflammatory exacerbations of COPD; however, there remains much to be learned regarding specific host and microbial determinants of persistence and/or clearance in this context. METHODS: In this study, we used a recently described ferret model for COPD, in which animals undergo chronic long-term exposure to cigarette smoke, to define host–pathogen interactions during COPD-related NTHi infections. RESULTS: NTHi bacteria colonised the lungs of smoke-exposed animals to a greater extent than controls, and elicited acute host inflammation and neutrophilic influx and activation, along with a significant increase in airway resistance and a decrease in inspiratory capacity consistent with inflammatory exacerbation; notably, these findings were not observed in air-exposed control animals. NTHi bacteria persisted within multicellular biofilm communities within the airway lumen, as evidenced by immunofluorescent detection of bacterial aggregates encased within a sialylated matrix as is typical of NTHi biofilms and differential bacterial gene expression consistent with the biofilm mode of growth. CONCLUSIONS: Based on these results, we conclude that acute infection with NTHi initiates inflammatory exacerbation of COPD disease. The data also support the widely held hypothesis that NTHi bacteria persist within multicellular biofilm communities in the lungs of patients with COPD. European Respiratory Society 2020-08-11 /pmc/articles/PMC7418822/ /pubmed/32802827 http://dx.doi.org/10.1183/23120541.00200-2020 Text en Copyright ©ERS 2020 http://creativecommons.org/licenses/by-nc/4.0/This article is open access and distributed under the terms of the Creative Commons Attribution Non-Commercial Licence 4.0.
spellingShingle Original Articles
Hunt, Benjamin C.
Stanford, Denise
Xu, Xin
Li, Jindong
Gaggar, Amit
Rowe, Steven M.
Raju, S. Vamsee
Swords, W. Edward
Haemophilus influenzae persists in biofilm communities in a smoke-exposed ferret model of COPD
title Haemophilus influenzae persists in biofilm communities in a smoke-exposed ferret model of COPD
title_full Haemophilus influenzae persists in biofilm communities in a smoke-exposed ferret model of COPD
title_fullStr Haemophilus influenzae persists in biofilm communities in a smoke-exposed ferret model of COPD
title_full_unstemmed Haemophilus influenzae persists in biofilm communities in a smoke-exposed ferret model of COPD
title_short Haemophilus influenzae persists in biofilm communities in a smoke-exposed ferret model of COPD
title_sort haemophilus influenzae persists in biofilm communities in a smoke-exposed ferret model of copd
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7418822/
https://www.ncbi.nlm.nih.gov/pubmed/32802827
http://dx.doi.org/10.1183/23120541.00200-2020
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