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Sorting nexin-1 defines an early phase of Salmonella-containing vacuole-remodeling during Salmonella infection
Author(s) -
Miriam V. Bujny,
Philip Ewels,
Suzanne Humphrey,
Naomi Attar,
Mark A. Jepson,
Peter J. Cullen
Publication year - 2008
Publication title -
journal of cell science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.384
H-Index - 278
eISSN - 1477-9137
pISSN - 0021-9533
DOI - 10.1242/jcs.018432
Subject(s) - sorting nexin , vacuole , biology , endosome , salmonella enterica , endocytic cycle , microbiology and biotechnology , intracellular , salmonella , golgi apparatus , endocytosis , bacteria , biochemistry , cytoplasm , cell , genetics , endoplasmic reticulum
Salmonella enterica serovar Typhimurium replicate within host cells in a specialized membrane-bound compartment, the Salmonella-containing vacuole (SCV). Interaction of SCVs with the host endocytic network is modulated by bacterial effectors, some of which, such as SigD/SopB, manipulate the level of endosomal phosphoinositides. Here, we establish that at early stages of Salmonella infection, sorting nexin-1 (SNX1) - a host phosphoinositide-binding protein that normally associates with early endosomes and regulates transport to the trans-Golgi network (TGN) - undergoes a rapid and transient translocation to bacterial entry sites, an event promoted by SigD/SopB. Recruitment of SNX1 to SCVs results in the formation of extensive, long-range tubules that we have termed ;spacious vacuole-associated tubules'. Formation of these tubules is coupled with size reduction of vacuoles and the removal of TGN-resident cargo. SNX1 suppression perturbs intracellular progress of bacteria, resulting in a delayed replication. We propose that SNX1 is important in tubular-based re-modeling of nascent SCVs and, in doing so, regulates intracellular bacterial progression and replication.

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