Staphylococcus aureus biofilm influences the expression of lysozyme, SLPI and gp340 in a human sinonasal explant model / 临床耳鼻咽喉头颈外科杂志
Lin chuang er bi yan hou ke za zhi
; (24): 194-199, 2016.
Article
em Zh
| WPRIM
| ID: wpr-749685
Biblioteca responsável:
WPRO
ABSTRACT
OBJECTIVE@#To investigate the influences of staphylococcus aureus in planktonic and biofilm forms on the expression of lysozyme, SLPI and gp340 in the human sinonasal explant model.@*METHOD@#Mucosa samples from ethmoid sinus were collected from ten patients of cerebrospinal fluid leak and were cultured with and without S. aureus biofilms and planktonic cells. After the infection, the explant model was confirmed by CLSM, and the secretion of lysozyme, SLPI and gp340 was detected by enzyme-linked immunosorbent assay (ELISA) at 8, 16, and 24 h after S. aureus challenge. Expressions of lysozyme, SLPI and gp340 in mRNA and protein levels after 24 h S. aureus challenge were detected using RT-PCR, immunohistochemistry and Western bolt assay respectively.@*RESULT@#The secretion of lysozyme, SLPI and gp340 in the explant model was observed with a trend to increase in a time-dependent manner. At 8 and 16 h after S. aureus challenge, the secretion of lysozyme, SLPI and gp340 in biofilms group was significantly higher than these in planktonic cells group and control group (P 0.05), the biofilms enhanced the expressions of lysozyme, SLPI and gp340 significantly compared with planktonic cells and controls (P < 0.05).@*CONCLUSION@#S. aureus biofilm induced the expressions of lysozyme, SLPI and gp340 to a higher level than planktonic cells, indicating that S. aureus biofilm was an influencing factor on the innate immune system.
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Índice:
WPRIM
Assunto principal:
Infecções Estafilocócicas
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RNA Mensageiro
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Ensaio de Imunoadsorção Enzimática
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Muramidase
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Receptores de Superfície Celular
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Biofilmes
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Técnicas de Cultura de Tecidos
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Seio Etmoidal
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Inibidor Secretado de Peptidases Leucocitárias
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Imunidade Inata
Tipo de estudo:
Prognostic_studies
Limite:
Humans
Idioma:
Zh
Revista:
Lin chuang er bi yan hou ke za zhi
Ano de publicação:
2016
Tipo de documento:
Article