Chlamydia trachomatis infection alters host cell transcription in diverse cellular pathways

被引:66
|
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
来源
JOURNAL OF INFECTIOUS DISEASES | 2003年 / 187卷 / 03期
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 50 条
  • [31] Selection of mutant cell lines resistant to infection by Chlamydia trachomatis and Chlamydia pneumoniae
    Fudyk, T
    Olinger, L
    Stephens, RS
    INFECTION AND IMMUNITY, 2002, 70 (11) : 6444 - 6447
  • [32] Comparative DNA microarray analysis of host cell transcriptional responses to infection by Coxiella burnetii or Chlamydia trachomatis
    Ren, Q
    Robertson, SJ
    Howe, D
    Barrows, LF
    Heinzen, RA
    RICKETTSIOLOGY: PRESENT AND FUTURE DIRECTIONS, 2003, 990 : 701 - 713
  • [33] Human Fallopian Tube Epithelial Cell Culture Model To Study Host Responses to Chlamydia trachomatis Infection
    McQueen, Bryan E.
    Kiatthanapaiboon, Amy
    Fulcher, M. Leslie
    Lam, Mariam
    Patton, Kate
    Powell, Emily
    Kollipara, Avinash
    Madden, Victoria
    Suchland, Robert J.
    Wyrick, Priscilla
    O'Connell, Catherine M.
    Reidel, Boris
    Kesimer, Mehmet
    Randell, Scott H.
    Darville, Toni
    Nagarajan, Uma M.
    INFECTION AND IMMUNITY, 2020, 88 (09)
  • [34] Chlamydia trachomatis infection alters the development of memory CD8+ T cells
    Loomis, Wendy P.
    Starnbach, Michael N.
    JOURNAL OF IMMUNOLOGY, 2006, 176 : S111 - S112
  • [35] Chlamydia trachomatis infection of human mesothelial cells alters proinflammatory, procoagulant, and fibrinolytic responses
    van Westreenen, M
    Pronk, A
    Diepersloot, RJA
    de Groot, PG
    Leguit, P
    INFECTION AND IMMUNITY, 1998, 66 (05) : 2352 - 2355
  • [36] Assessing a Potential Role of Host Pannexin 1 during Chlamydia trachomatis Infection
    McKuen, Mary J.
    Dahl, Gerhard
    Fields, Kenneth A.
    PLOS ONE, 2013, 8 (06):
  • [37] In-Silico Functional Metabolic Pathways Associated to Chlamydia trachomatis Genital Infection
    Filardo, Simone
    Di Pietro, Marisa
    De Angelis, Marta
    Brandolino, Gabriella
    Porpora, Maria Grazia
    Sessa, Rosa
    INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2022, 23 (24)
  • [38] Haploid genetic screen identifies host factors important in Chlamydia trachomatis infection
    Rosmarin, D.
    Carette, J.
    Brummelkamp, T.
    Ploegh, H. L.
    JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2011, 131 : S110 - S110
  • [39] Autophagy-related cellular factors are differentially involved in Chlamydia trachomatis infection
    Braun, P. R.
    Al-Younes, H.
    Meyer, T. F.
    EUROPEAN JOURNAL OF CELL BIOLOGY, 2007, 86 : 32 - 32
  • [40] The dual role of cytokine responses to Chlamydia trachomatis infection in host pathogen crosstalk
    Min, Shuling
    He, Ping
    Zhou, Qianting
    Chen, Hongliang
    MICROBIAL PATHOGENESIS, 2022, 173