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An Initial Step of GAS-Containing Autophagosome-Like Vacuoles Formation Requires Rab7
Author(s) -
Hitomi Yamaguchi,
Ichirô Nakagawa,
Akitsugu Yamamoto,
Atsuo Amano,
Takeshi Noda,
Tamotsu Yoshimori
Publication year - 2009
Publication title -
plos pathogens
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.719
H-Index - 206
eISSN - 1553-7374
pISSN - 1553-7366
DOI - 10.1371/journal.ppat.1000670
Subject(s) - autophagosome , vacuole , autophagy , endocytic cycle , microbiology and biotechnology , cytoplasm , phagosome , endocytosis , biology , streptococcus pyogenes , internalization , gene knockdown , chemistry , cell , biochemistry , intracellular , gene , apoptosis , genetics , bacteria , staphylococcus aureus
Group A streptococcus (GAS; Streptococcus pyogenes ) is a common pathogen that invades non-phagocytic human cells via endocytosis. Once taken up by cells, it escapes from the endocytic pathway to the cytoplasm, but here it is contained within a membrane-bound structure termed GAS-containing autophagosome-like vacuoles (GcAVs). The autophagosome marker GFP-LC3 associates with GcAVs, and other components of the autophagosomal pathway are involved in GcAV formation. However, the mechanistic relationship between GcAV and canonical autophagy is largely unknown. Here, we morphologically analyzed GcAV formation in detail. Initially, a small, GFP-LC3-positive GcAV sequesters each streptococcal chain, and these then coalesce into a single, large GcAV. Expression of a dominant-negative form of Rab7 or RNAi-mediated knockdown of Rab7 prevented the initial formation of small GcAV structures. Our results demonstrate that mechanisms of GcAV formation includes not only the common machinery of autophagy, but also Rab7 as an additional component, which is dispensable in canonical autophagosome formation.

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