Volume 5 Supplement 4

Abstracts from the 10th Symposium of Experimental Rhinology and Immunology of the Nose (SERIN 2015)

Open Access

Genome wide gene expression analysis of nasal mucosa from patients with chronic rhinosinusitis and nasal polyposis stimulated with staphylococcal enterotoxin B

  • Claudina Perez Novo1,
  • Camilla Rydberg Millrud2,
  • Natalie De Ruyck1,
  • Gabriele Holtappels1,
  • Koen Van Crombruggen1,
  • Lars Olaf Cardell2 and
  • Claus Bachert1
Clinical and Translational Allergy20155(Suppl 4):O7

https://doi.org/10.1186/2045-7022-5-S4-O7

Published: 26 June 2015

Introduction

Colonization of the nasal mucosal with Staphylococcus aureus and the production of superantigenic enterotoxins by the bacteria are crucial amplifying factors of the pro-inflammatory mechanisms operating in chronic upper airways diseases such as chronic rhinosinusitis and nasal polyposis.

Methods

Nasal polyp tissue from 10 patients with chronic rhinosinusitis/nasal polyposis and inferior turbinate from 8 healthy subjects were obtained fragmented and cultured in presence and absence of S. aureus enterotoxin B (0.5µg/ml) for 24 hours. Then total RNA was isolated, transcribed to cDNA and used for microarray analysis using the Affymetrix Human Gene 2.1 ST Array. Data was then corrected and differentially expressed genes were selected according to the corrected P value < 0.05 and a change fold higher than 2. Pathway overrepresentation analysis was then performed in each group of genes.

Results

The number of genes showing differential expression between nasal polyp and control tissues as well as the genes and pathways differentially regulated after stimulation with S. aureus enterotoxin B in each of the groups is described in Table 1.

Conclusions

We demonstrated that S. aureus enterotoxin B may influence important pathways linked to T-cell receptor, interferon signalling and adaptative immune response.

Authors’ Affiliations

(1)
ENT Department, Ghent University
(2)
ENT Department, Karolinska Institute

Copyright

© Perez Novo et al. 2015

This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

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