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Originally published in Science Express on 2 December 2004
Science 4 February 2005: Vol. 307. no. 5710, pp. 727 - 731
DOI: 10.1126/science.1106036
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Reports
Escape of Intracellular Shigella from Autophagy
Michinaga Ogawa,1
Tamotsu Yoshimori,3,6
Toshihiko Suzuki,1,5
Hiroshi Sagara,2
Noboru Mizushima,4,5
Chihiro Sasakawa1,6*
The degradation of undesirable cellular components or organelles, including invading microbes, by autophagy is crucial for cell survival. Here, Shigella, an invasive bacteria, was found to be able to escape autophagy by secreting IcsB by means of the type III secretion system. Mutant bacteria lacking IcsB were trapped by autophagy during multiplication within the host cells. IcsB did not directly inhibit autophagy. Rather, Shigella VirG, a protein required for intracellular actin-based motility, induced autophagy by binding to the autophagy protein, Atg5. In nonmutant Shigella, this binding is competitively inhibited by IcsB binding to VirG.
1 Department of Microbiology and Immunology, Institute of Medical Science, University of Tokyo, 4-6-1, Shirokanedai, Minato-ku, Tokyo 108-8639, Japan.
2 Department of Fine Morphology, Institute of Medical Science, University of Tokyo, 4-6-1, Shirokanedai, Minato-ku, Tokyo 108-8639, Japan.
3 Department of Cell Genetics, National Institute of Genetics, 1111, Yata, Mishima, Shizuoka 411-8540, Japan.
4 Department of Bioregulation and Metabolism, Tokyo Metropolitan Institute of Medical Science, 3-18-22, Hon-komagome, Bunkyo-ku, Tokyo 113-8613, Japan.
5 Precursory Research for Embryonic Science and Technology (PRESTO), Japan Science and Technology Agency, Kawaguchi 332-0012, Japan.
6 Core Research for Evolutional Science and Technology (CREST), Japan Science and Technology Agency, Kawaguchi 332-0012, Japan.
* To whom correspondence should be addressed. E-mail: sasakawa{at}ims.u-tokyo.ac.jp
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