Chlamydia trachomatis infection alters host cell transcription in diverse cellular pathways

被引:65
作者
Xia, MS
Bumgarner, RE
Lampe, MF
Stamm, WE
机构
[1] Univ Washington, Dept Med, Div Infect Dis, Seattle, WA 98195 USA
[2] Univ Washington, Ctr Express Arrays, Seattle, WA 98195 USA
[3] Univ Washington, Dept Lab Med, Seattle, WA 98195 USA
关键词
D O I
10.1086/367962
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
To study the responses of the host cell to chlamydial infection, differentially transcribed genes of the host cells were examined. Complementary DNA (cDNA) probes were made from messenger RNAs of HeLa cells infected with Chlamydia trachomatis and were hybridized to a high-density human DNA microarray of 15,000 genes and expressed sequence tags. C. trachomatis alters host cell transcription at both the early and middle phases of its developmental cycle. At 2 h after infection, 13 host genes showed mean expression ratios greater than or equal to2-fold. At 16 h after infection, 130 genes were differentially transcribed. These genes encoded factors inhibiting apoptosis and factors regulating cell differentiation, components of the cytoskeleton, transcription factors, and proinflammatory cytokines. This indicates that chlamydial infection, despite its intravacuolar location, alters the transcription of a broad range of host genes in diverse cellular pathways and provides a framework for future studies.
引用
收藏
页码:424 / 434
页数:11
相关论文
共 34 条
  • [1] Serotypes of Chlamydia trachomatis and risk for development of cervical squamous cell carcinoma
    Anttila, T
    Saikku, P
    Koskela, P
    Bloigu, A
    Dillner, J
    Ikäheimo, I
    Jellum, E
    Lehtinen, M
    Lenner, P
    Hakulinen, T
    Närvänen, A
    Pukkala, E
    Thoresen, S
    Youngman, L
    Paavonen, J
    [J]. JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2001, 285 (01): : 47 - 51
  • [2] TRYPTOPHAN DEPLETION AS A MECHANISM OF GAMMA-INTERFERON-MEDIATED CHLAMYDIAL PERSISTENCE
    BEATTY, WL
    BELANGER, TA
    DESAI, AA
    MORRISON, RP
    BYRNE, GI
    [J]. INFECTION AND IMMUNITY, 1994, 62 (09) : 3705 - 3711
  • [3] BRONCHIAL EPITHELIAL-CELLS OF PATIENTS WITH ASTHMA RELEASE CHEMOATTRACTANT FACTORS FOR T-LYMPHOCYTES
    BELLINI, A
    YOSHIMURA, H
    VITTORI, E
    MARINI, M
    MATTOLI, S
    [J]. JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 1993, 92 (03) : 412 - 424
  • [4] ESX: A structurally unique Ets overexpressed early during human breast tumorigenesis
    Chang, CH
    Scott, GK
    Kuo, WL
    Xiong, XH
    Suzdaltseva, Y
    Park, JW
    Sayre, P
    Erny, K
    Collins, C
    Gray, JW
    Benz, CC
    [J]. ONCOGENE, 1997, 14 (13) : 1617 - 1622
  • [5] cDNA array analysis of altered gene expression in human endothelial cells in response to Chlamydia pneumoniae infection
    Coombes, BK
    Mahony, JB
    [J]. INFECTION AND IMMUNITY, 2001, 69 (03) : 1420 - 1427
  • [6] CRUIKSHANK W, 1982, J IMMUNOL, V128, P2569
  • [7] CRUIKSHANK WW, 1987, J IMMUNOL, V138, P3817
  • [8] Chlamydial infection of polarized HeLa cells induces PMN chemotaxis but the cytokine profile varies between disseminating and non-disseminating strains
    Dessus-Babus, S
    Knight, ST
    Wyrick, PB
    [J]. CELLULAR MICROBIOLOGY, 2000, 2 (04) : 317 - 327
  • [9] Expression of intercellular adhesion molecule 3 (CDw50) on endothelial cells in cutaneous lymphomas - A comparative study between nodal and cutaneous lymphomas
    Dommann, SNW
    DommannScherrer, CC
    Ziegler, T
    Meyer, J
    Trueb, RM
    Kundig, T
    Panizzon, R
    Burg, G
    [J]. AMERICAN JOURNAL OF DERMATOPATHOLOGY, 1997, 19 (04) : 391 - 395
  • [10] DUNLOP EMC, 1989, GENITOURIN MED, V65, P22