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  3. A reservoir of Moraxella catarrhalis in human pharyngeal lymphoid tissue
 

A reservoir of Moraxella catarrhalis in human pharyngeal lymphoid tissue

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BORIS DOI
10.7892/boris.23376
Date of Publication
2007
Publication Type
Article
Division/Institute

Institut für Infektio...

Universitätsklinik fü...

Contributor
Heiniger, Nadja
Spaniol, Violeta
Troller, Rolf
Vischer, Mattheus
Universitätsklinik für Hals-, Nasen- und Ohrenkrankheiten (HNO)
Aebi, Christophorcid-logo
Institut für Infektionskrankheiten
Series
Journal of infectious diseases
ISSN or ISBN (if monograph)
0022-1899
Publisher
The University of Chicago Press
Language
English
Publisher DOI
10.1086/521194
PubMed ID
17763332
Description
BACKGROUND: Early exposure of infants and long-term immunity suggest that colonization with Moraxella catarrhalis is more frequent than is determined by routine culture. We characterized a reservoir of M. catarrhalis in pharyngeal lymphoid tissue. METHODS: Tissue from 40 patients (median age, 7.1 years) undergoing elective tonsillectomy and/or adenoidectomy was analyzed for the presence of M. catarrhalis by culture, real-time DNA and RNA polymerase chain reaction (PCR), immunohistochemical analysis (IHC), and fluorescent in situ hybridization (FISH). Histologic sections were double stained for M. catarrhalis and immune cell markers, to characterize the tissue distribution of the organism. Intracellular bacteria were identified using confocal laser scanning microscopy (CLSM). RESULTS: Twenty-nine (91%) of 32 adenoids and 17 (85%) of 20 tonsils were colonized with M. catarrhalis. Detection rates for culture, DNA PCR, RNA PCR, IHC, and FISH were 7 (13%) of 52, 10 (19%) of 52, 21 (41%) of 51, 30 (61%) of 49, and 42 (88%) of 48, respectively (P<.001). Histologic analysis identified M. catarrhalis in crypts, intraepithelially, subepithelially, and (using CLSM) intracellularly. M. catarrhalis colocalized with macrophages and B cells in lymphoid follicles. CONCLUSIONS: Colonization by M. catarrhalis is more frequent than is determined by surface culture, because the organism resides both within and beneath the epithelium and invades host cells.
Handle
https://boris-portal.unibe.ch/handle/20.500.12422/97021
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196-7-1080.pdftextAdobe PDF635.5 KBpublishedOpen
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