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Spa33 a Cell Surface-Associated Subunit of the Mxi-Spa Type III Secretory Pathway of Shigella flexneri Regulates Ipa Protein Traffic

机译:Spa33弗氏志贺氏菌的Mxi-Spa III型分泌途径的细胞表面相关亚基调节Ipa蛋白的运输。

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摘要

The Mxi-Spa type III secretion system of Shigella flexneri directs the host cell contact-induced secretion of a set of invasins, referred to as Ipas. In this study, we examined the role of Spa33 in Ipa secretion. A spa33-null mutant was both noninvasive and unable to translocate the Ipas from inner membrane to outer membrane (OM) positions of the Mxi-Spa transmembrane channel. Spa33 was found to be a Mxi-Spa substrate that is translocated to the bacterial cell surface upon the induction of Ipa secretion. This mobility may serve to drive Ipa translocation within Mxi-Spa toward OM positions. Consistent with a second distinct role in regulating Ipa traffic, the overexpression of Spa33 also blocked Ipa secretion and resulted in Ipa accumulation at the OM. Co-overexpression of Spa33 and another OM-associated element, Spa32, did not disrupt Ipa secretion, suggesting an interaction between the two proteins and an effect on the mechanism which serves to regulate Ipa release from the OM. These findings indicate that Spa33 is a mobile element within Mxi-Spa, which is required to control Ipa translocation into and out of OM positions of the secretory structure.
机译:弗氏志贺氏菌的Mxi-Spa III型分泌系统指导宿主细胞接触诱导的一组入侵素的分泌,称为Ipas。在这项研究中,我们检查了Spa33在Ipa分泌中的作用。 spa33-null突变体既无创又无法将Ipas从Mxi-Spa跨膜通道的内膜位置转移到外膜(OM)位置。发现Spa33是Mxi-Spa底物,在诱导Ipa分泌后可转移到细菌细胞表面。这种流动性可能有助于将Mxi-Spa中的Ipa转运推向OM位置。与调节Ipa流量的第二个独特作用一致,Spa33的过表达也阻断了Ipa的分泌,并导致OM处的Ipa积累。 Spa33和另一个与OM相关的元件Spa32的共过量表达并没有破坏Ipa的分泌,这表明这两种蛋白之间存在相互作用,并且对调节Ipa从OM中释放的机制产生了影响。这些发现表明,Spa33是Mxi-Spa中的一种可移动元件,它是控制Ipa进入分泌结构的OM位置和从中分泌出的必需元素。

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