agr Expression precedes escape of internalized Staphylococcus aureus from the host endosome

被引:143
|
作者
Qazi, SNA
Counil, E
Morrissey, J
Rees, CED
Cockayne, A
Winzer, K
Chan, WC
Williams, P
Hill, PJ
机构
[1] Univ Nottingham, Sch Biosci, Loughborough LE12 5RD, Leics, England
[2] Univ Nottingham, Queens Med Ctr, Inst Infect & Immun, Nottingham NG7 2UH, England
[3] Univ Nottingham, Sch Pharmaceut Sci, Nottingham NG7 2RD, England
[4] Inst Natl Agron Paris Grignon, Paris, France
关键词
D O I
10.1128/IAI.69.11.7074-7082.2001
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Staphylococcus aureus is a versatile pathogen capable of causing life-threatening infections. Many of its cell wall and exoproduct virulence determinants are controlled via the accessory gene regulator (agr). Although considered primarily as an extracellular pathogen, it is now recognized that S. aureus can be internalized by epithelial and endothelial cells. Traditional experimental approaches to investigate bacterial internalization are extremely time-consuming and notoriously irreproducible. We present here a new reporter gene method to assess intracellular growth of S. aureus in MAC-T cells that utilizes a gfp-luxABCDE, reporter operon under the control of the Bacillus megaterium xylA promoter, which in S. aureus is expressed in a growth-dependent manner. This facilitates assessment of the growth of internalized bacteria in a nondestructive assay. The dual gfp-lux reporter cassette was also evaluated as a reporter of agr expression and used to monitor the temporal induction of agr during the MAC-T internalization process. The data obtained suggest that agr induction occurs prior to endosomal lysis and that agr-regulated exoproteins appear to be required prior to the release and replication of S. aureus within the infected MAC-T cells.
引用
收藏
页码:7074 / 7082
页数:9
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