Please use this identifier to cite or link to this item: https://doi.org/10.7554/eLife.45311
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dc.titleSingle cell, super-resolution imaging reveals an acid pH-dependent conformational switch in SsrB regulates SPI-2
dc.contributor.authorLiew, A.T.F.
dc.contributor.authorFoo, Y.H.
dc.contributor.authorGao, Y.
dc.contributor.authorZangoui, P.
dc.contributor.authorSingh, M.K.
dc.contributor.authorGulvady, R.
dc.contributor.authorKenney, L.J.
dc.date.accessioned2021-12-06T04:25:17Z
dc.date.available2021-12-06T04:25:17Z
dc.date.issued2019
dc.identifier.citationLiew, A.T.F., Foo, Y.H., Gao, Y., Zangoui, P., Singh, M.K., Gulvady, R., Kenney, L.J. (2019). Single cell, super-resolution imaging reveals an acid pH-dependent conformational switch in SsrB regulates SPI-2. eLife 8 : e45311. ScholarBank@NUS Repository. https://doi.org/10.7554/eLife.45311
dc.identifier.issn2050-084X
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/209586
dc.description.abstractAfter Salmonella is phagocytosed, it resides in an acidic vacuole. Its cytoplasm acidifies to pH 5.6; acidification activates pathogenicity island 2 (SPI-2). SPI-2 encodes a type three secretion system whose effectors modify the vacuole, driving endosomal tubulation. Using super-resolution imaging in single bacterial cells, we show that low pH induces expression of the SPI-2 SsrA/B signaling system. Single particle tracking, atomic force microscopy, and single molecule unzipping assays identified pH-dependent stimulation of DNA binding by SsrB. A so-called phosphomimetic form (D56E) was unable to bind to DNA in live cells. Acid-dependent DNA binding was not intrinsic to regulators, as PhoP and OmpR binding was not pH-sensitive. The low level of SPI-2 injectisomes observed in single cells is not due to fluctuating SsrB levels. This work highlights the surprising role that acid pH plays in virulence and intracellular lifestyles of Salmonella; modifying acid survival pathways represents a target for inhibiting Salmonella. © Liew et al.
dc.publishereLife Sciences Publications Ltd
dc.rightsAttribution 4.0 International
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.sourceScopus OA2019
dc.typeArticle
dc.contributor.departmentMECHANOBIOLOGY INSTITUTE
dc.description.doi10.7554/eLife.45311
dc.description.sourcetitleeLife
dc.description.volume8
dc.description.pagee45311
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