Escape of Intracellular Shigella from Autophagy

Author:

Ogawa Michinaga12345,Yoshimori Tamotsu12345,Suzuki Toshihiko12345,Sagara Hiroshi12345,Mizushima Noboru12345,Sasakawa Chihiro12345

Affiliation:

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.

Abstract

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.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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