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228 PCR Analysis of Microorganisms in Chronic Rhinosinusitis with Nasal Polyps

BACKGROUND: Chronic rhinosinusitis (CRS) with nasal polyps is characterized by tissue eosinophilia, which is speculated to be related to Staphylococcus superantigen and fungus, in European and U.S patients. However, Japanese patients with CRS with nasal polyps showed 2 distinct phenotypes of eosinop...

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Autores principales: Hirotsu, Mikio, Ikeda, Katsuhisa, Ono, Noritsgu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: World Allergy Organization Journal 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3512889/
http://dx.doi.org/10.1097/01.WOX.0000411985.10675.6a
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author Hirotsu, Mikio
Ikeda, Katsuhisa
Ono, Noritsgu
author_facet Hirotsu, Mikio
Ikeda, Katsuhisa
Ono, Noritsgu
author_sort Hirotsu, Mikio
collection PubMed
description BACKGROUND: Chronic rhinosinusitis (CRS) with nasal polyps is characterized by tissue eosinophilia, which is speculated to be related to Staphylococcus superantigen and fungus, in European and U.S patients. However, Japanese patients with CRS with nasal polyps showed 2 distinct phenotypes of eosinophilic and neutrophilic inflammation (Hirotsu et al 2011). We attempted to analyze the microorganisms from nasal polyps of Japanese patients by PCR method. METHODS: Eleven specimens of nasal polyps with CRS were collected for examination by endoscopic sinus surgery. All specimens were treated with 70% ethanol and physiologic saline to eliminate microorganisms outside of the nasal polyps. Bacterial and fungal culture was performed for 2 weeks using 5 different culture media. We detected 16S rRNA bacteria and 18S rDNA-ITS-26S rDNA fungus, and then identified species of microorganisms by direct-sequence. In addition, the number of eosinophils in the nasal polyps was counted. RESULTS: No bacteria or fungus were recovered from any of the nasal polyps by culture medium. By the PCR analysis, DNA for bacteria could not be detected, whereas 7 samples of the nasal polyps showed amplification of fungal DNA such as Candida parapsilosis, Candida glabrata, and Rhodotorula etc. Grocott dyeing for the nasal polyps, however, showed no intracellular presence of fungus. The number of the eosinophils in the nasal poly with the patients with the presence of fungal DNA (240 ± 191) was significantly (P < 0.05) higher than that in the absence (56 ± 40). CONCLUSIONS: The present study suggests the participation of fungus in eosinophilic CRS with nasal polyps.
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spelling pubmed-35128892012-12-21 228 PCR Analysis of Microorganisms in Chronic Rhinosinusitis with Nasal Polyps Hirotsu, Mikio Ikeda, Katsuhisa Ono, Noritsgu World Allergy Organ J Abstracts of the XXII World Allergy Congress BACKGROUND: Chronic rhinosinusitis (CRS) with nasal polyps is characterized by tissue eosinophilia, which is speculated to be related to Staphylococcus superantigen and fungus, in European and U.S patients. However, Japanese patients with CRS with nasal polyps showed 2 distinct phenotypes of eosinophilic and neutrophilic inflammation (Hirotsu et al 2011). We attempted to analyze the microorganisms from nasal polyps of Japanese patients by PCR method. METHODS: Eleven specimens of nasal polyps with CRS were collected for examination by endoscopic sinus surgery. All specimens were treated with 70% ethanol and physiologic saline to eliminate microorganisms outside of the nasal polyps. Bacterial and fungal culture was performed for 2 weeks using 5 different culture media. We detected 16S rRNA bacteria and 18S rDNA-ITS-26S rDNA fungus, and then identified species of microorganisms by direct-sequence. In addition, the number of eosinophils in the nasal polyps was counted. RESULTS: No bacteria or fungus were recovered from any of the nasal polyps by culture medium. By the PCR analysis, DNA for bacteria could not be detected, whereas 7 samples of the nasal polyps showed amplification of fungal DNA such as Candida parapsilosis, Candida glabrata, and Rhodotorula etc. Grocott dyeing for the nasal polyps, however, showed no intracellular presence of fungus. The number of the eosinophils in the nasal poly with the patients with the presence of fungal DNA (240 ± 191) was significantly (P < 0.05) higher than that in the absence (56 ± 40). CONCLUSIONS: The present study suggests the participation of fungus in eosinophilic CRS with nasal polyps. World Allergy Organization Journal 2012-02-17 /pmc/articles/PMC3512889/ http://dx.doi.org/10.1097/01.WOX.0000411985.10675.6a Text en Copyright © 2012 by World Allergy Organization
spellingShingle Abstracts of the XXII World Allergy Congress
Hirotsu, Mikio
Ikeda, Katsuhisa
Ono, Noritsgu
228 PCR Analysis of Microorganisms in Chronic Rhinosinusitis with Nasal Polyps
title 228 PCR Analysis of Microorganisms in Chronic Rhinosinusitis with Nasal Polyps
title_full 228 PCR Analysis of Microorganisms in Chronic Rhinosinusitis with Nasal Polyps
title_fullStr 228 PCR Analysis of Microorganisms in Chronic Rhinosinusitis with Nasal Polyps
title_full_unstemmed 228 PCR Analysis of Microorganisms in Chronic Rhinosinusitis with Nasal Polyps
title_short 228 PCR Analysis of Microorganisms in Chronic Rhinosinusitis with Nasal Polyps
title_sort 228 pcr analysis of microorganisms in chronic rhinosinusitis with nasal polyps
topic Abstracts of the XXII World Allergy Congress
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3512889/
http://dx.doi.org/10.1097/01.WOX.0000411985.10675.6a
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