Sorting nexin-1 defines an early phase of Salmonella-containing vacuole-remodeling during Salmonella infection

被引:82
作者
Bujny, Miriam V. [1 ]
Ewels, Phil A. [1 ]
Humphrey, Suzanne
Attar, Naomi [1 ]
Jepson, Mark A.
Cullen, Peter J. [1 ]
机构
[1] Univ Bristol, Sch Med Sci, Dept Biochem, Henry Wellcome Integrated Signalling Labs, Bristol BS8 1TD, Avon, England
基金
英国生物技术与生命科学研究理事会; 英国医学研究理事会; 英国惠康基金;
关键词
phosphoinositide; Salmonella; SCV; endosome; retromer; SigD; sorting nexin;
D O I
10.1242/jcs.018432
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
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.
引用
收藏
页码:2027 / 2036
页数:10
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