Microarray analysis of a Chlamydia pneumoniae-infected human epithelial cell line by use of gene ontology hierarchy

被引:18
作者
Alvesalo, Joni [1 ,2 ]
Greco, Dario [3 ]
Leinonen, Maija [4 ]
Raitila, Tuomas [3 ]
Vuorela, Pia [1 ,5 ]
Auvinen, Petri [3 ]
机构
[1] Univ Helsinki, Drug Discovery & Technol Dev Ctr, Fac Pharm, FIN-00014 Helsinki, Finland
[2] Univ Helsinki, Div Pharmaceut Biol, Fac Pharm, FIN-00014 Helsinki, Finland
[3] Univ Helsinki, Inst Biotechnol, FIN-00014 Helsinki, Finland
[4] Natl Publ Hlth Inst, Oulu, Finland
[5] Abo Akad Univ, Dept Biochem & Pharm, SF-20500 Turku, Finland
关键词
D O I
10.1086/524142
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 [免疫学];
摘要
Chlamydia pneumoniae, a gram-negative obligate intracellular bacterium, is a common cause of upper and lower respiratory tract infections worldwide. Persistent C. pneumoniae infections have been linked to chronic disease processes, such as atherosclerosis. In the present study, we examined gene expression changes in the human epithelial cell line at different stages of acute C. pneumoniae infection and used gene ontology annotation, along with single-gene analysis, to select a small group of target genes that could possibly play a key role in C. pneumoniae infection. Selected genes were silenced using small interfering RNA, and the effect of silencing on the number of C. pneumoniae inclusions was measured by time-resolved fluorometric immunoassay. The greatest reduction in the number of C. pneumoniae inclusions was due to the silencing of the gene coding for the transcription factor early growth response 1, which decreased the number of inclusions by 38.6%.
引用
收藏
页码:156 / 162
页数:7
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