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Inflammatory immune response in rabbits with Staphylococcus aureus biofilm–associated sinusitis
BACKGROUND: Staphylococcus aureus is the most commonly isolated bacterium from patients with surgically recalcitrant chronic rhinosinusitis (CRS). Understanding the immune responses to S aureus biofilms will provide insights into how the host response may be manipulated by therapeutic agents to impr...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6282565/ https://www.ncbi.nlm.nih.gov/pubmed/29979838 http://dx.doi.org/10.1002/alr.22175 |
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author | Wu, Xianmin Zhang, Yue Chen, Xiaoyun Chen, Jun Jia, Minghui |
author_facet | Wu, Xianmin Zhang, Yue Chen, Xiaoyun Chen, Jun Jia, Minghui |
author_sort | Wu, Xianmin |
collection | PubMed |
description | BACKGROUND: Staphylococcus aureus is the most commonly isolated bacterium from patients with surgically recalcitrant chronic rhinosinusitis (CRS). Understanding the immune responses to S aureus biofilms will provide insights into how the host response may be manipulated by therapeutic agents to improve the chances of successfully preventing and treating these infections. In this study, we investigated the inflammatory immune response in a rabbit model of S aureus biofilm–related sinusitis by analyzing the levels of some major inflammatory cytokines. METHODS: Eighteen New Zealand white rabbits were randomly divided into 3 groups: a blank‐control group; a negative‐control group; and a model group. Four weeks after the biofilm‐associated sinusitis models were established, the sinus mucosa was harvested and examined using hematoxylin‐eosin (H&E) staining, scanning electron microscopy (SEM), reverse transcription polymerase chain reaction (RT‐PCR), and western blotting. The expression levels of inflammatory cytokines were analyzed statistically. RESULTS: Interleukin (IL)‐1β, IL‐8, and tumor necrosis factor (TNF)‐α expression levels were significantly higher in the model group than in the blank‐control group (p < 0.05); mRNA levels were increased by 1600%, 230%, and 130%, respectively, and the protein levels were increased by 180%, 100%, and 100%, respectively. In contrast, IL‐4 and IL‐5 mRNA levels were reduced by 44% and 70%, respectively, compared with the blank‐control group (p < 0.05). CONCLUSION: S aureus biofilms in the rabbit maxillary sinus mucosa were associated with increased IL‐1β, IL‐8, and TNF‐α expression, and decreased IL‐4 and IL‐5 expression. |
format | Online Article Text |
id | pubmed-6282565 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-62825652018-12-11 Inflammatory immune response in rabbits with Staphylococcus aureus biofilm–associated sinusitis Wu, Xianmin Zhang, Yue Chen, Xiaoyun Chen, Jun Jia, Minghui Int Forum Allergy Rhinol Original Articles BACKGROUND: Staphylococcus aureus is the most commonly isolated bacterium from patients with surgically recalcitrant chronic rhinosinusitis (CRS). Understanding the immune responses to S aureus biofilms will provide insights into how the host response may be manipulated by therapeutic agents to improve the chances of successfully preventing and treating these infections. In this study, we investigated the inflammatory immune response in a rabbit model of S aureus biofilm–related sinusitis by analyzing the levels of some major inflammatory cytokines. METHODS: Eighteen New Zealand white rabbits were randomly divided into 3 groups: a blank‐control group; a negative‐control group; and a model group. Four weeks after the biofilm‐associated sinusitis models were established, the sinus mucosa was harvested and examined using hematoxylin‐eosin (H&E) staining, scanning electron microscopy (SEM), reverse transcription polymerase chain reaction (RT‐PCR), and western blotting. The expression levels of inflammatory cytokines were analyzed statistically. RESULTS: Interleukin (IL)‐1β, IL‐8, and tumor necrosis factor (TNF)‐α expression levels were significantly higher in the model group than in the blank‐control group (p < 0.05); mRNA levels were increased by 1600%, 230%, and 130%, respectively, and the protein levels were increased by 180%, 100%, and 100%, respectively. In contrast, IL‐4 and IL‐5 mRNA levels were reduced by 44% and 70%, respectively, compared with the blank‐control group (p < 0.05). CONCLUSION: S aureus biofilms in the rabbit maxillary sinus mucosa were associated with increased IL‐1β, IL‐8, and TNF‐α expression, and decreased IL‐4 and IL‐5 expression. John Wiley and Sons Inc. 2018-07-06 2018-11 /pmc/articles/PMC6282565/ /pubmed/29979838 http://dx.doi.org/10.1002/alr.22175 Text en © 2018 The Authors International Forum of Allergy & Rhinology, published by ARSAAOA, LLC This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Original Articles Wu, Xianmin Zhang, Yue Chen, Xiaoyun Chen, Jun Jia, Minghui Inflammatory immune response in rabbits with Staphylococcus aureus biofilm–associated sinusitis |
title | Inflammatory immune response in rabbits with Staphylococcus aureus biofilm–associated sinusitis |
title_full | Inflammatory immune response in rabbits with Staphylococcus aureus biofilm–associated sinusitis |
title_fullStr | Inflammatory immune response in rabbits with Staphylococcus aureus biofilm–associated sinusitis |
title_full_unstemmed | Inflammatory immune response in rabbits with Staphylococcus aureus biofilm–associated sinusitis |
title_short | Inflammatory immune response in rabbits with Staphylococcus aureus biofilm–associated sinusitis |
title_sort | inflammatory immune response in rabbits with staphylococcus aureus biofilm–associated sinusitis |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6282565/ https://www.ncbi.nlm.nih.gov/pubmed/29979838 http://dx.doi.org/10.1002/alr.22175 |
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