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DNA Research Advance Access published online on January 24, 2008

DNA Research, doi:10.1093/dnares/dsm032
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© The Author 2008. Kazusa DNA Research Institute
The online version of this article has been published under an open access model. Users are entitled to use, reproduce, disseminate, or display the open access version of this article for non-commercial purposes provided that: the original authorship is properly and fully attributed; the Journal and Oxford University Press are attributed as the original place of publication with the correct citation details given; if an article is subsequently reproduced or disseminated not in its entirety but only in part or as a derivative work this must be clearly indicated. For commercial re-use, please contact journals.permissions@oxfordjournals.org

Genome-wide Analysis of Chlamydophila pneumoniae Gene Expression at the Late Stage of Infection

Koshiro Miura1 {dagger}, Hidehiro Toh1, Hideki Hirakawa2, Manabu Sugii1, Masayuki Murata1, Kenta Nakai3, Kosuke Tashiro4, Satoru Kuhara4, Yoshinao Azuma1,* and Mutsunori Shirai1

1 Department of Microbiology and Immunology, Yamaguchi University School of Medicine, 1-1-1 Minami-Kogushi, Ube, Yamaguchi 755-8505, Japan
2 Graduate School of Systems Life Sciences, Kyushu University, Hakozaki 6-10-1, Higashi-ku, Fukuoka 812-8581, Japan
3 Laboratory of Functional Analysis in silico, Human Genome Center, The Institute of Medical Science, The University of Tokyo, 4-6-1 Shirokane-dai, Minato-ku, Tokyo 108-8639, Japan
4 Graduate School of Genetic Resources Technology, Kyushu University, 6-10-1 Hakozaki, Higashi-ku, Fukuoka 812-8581, Japan

Received 15 June 2007 ; accepted 12 December 2007.

Chlamydophila pneumoniae, an obligate intracellular eubacterium, changes its form from a vegetative reticulate body into an infectious elementary body during the late stage of its infection cycle. Comprehension of the molecular events in the morphological change is important to understand the switching mechanism between acute and chronic infection, which is deemed to relate to the pathogenesis of atherosclerosis. Herein, we have attempted to screen genes expressed in the late stage with a genome-wide DNA microarray, resulting in nomination of 17 genes as the late-stage genes. Fourteen of the 17 genes and six other genes predicted as late-stage genes were confirmed to be up-regulated in the late stage with a quantitative reverse transcriptase–polymerase chain reaction. These 20 late-stage genes were classified into two groups by clustering analysis: ‘drastically induced’ and ‘moderately induced’ genes. Out of eight drastically induced genes, four contain {sigma}28 promoter-like sequences and the other four contain an upstream common sequence. It suggests that besides {sigma}28, there are certain up-regulatory mechanisms at the late stage, which may be involved in the chlamydial morphological change and thus pathogenesis.

Key words: Chlamydophila pneumoniae; DNA microarray; genome; chlamydia; gene expression


* To whom correspondence should be addressed. Tel. +81 836-22-2227. Fax. +81 836-22-2415. E-mail: yazuma{at}yamaguchi-u.ac.jp

Edited by Katsumi Isono

{dagger} Present address: Department of Veterinary Biosciences, The Ohio State University, 1900 Coffey Rd., Columbus, OH 43210, USA


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