Spatial and temporal localization of cell wall associated pili in Enterococcus faecalis
Enterococcus faecalis virulence requires cell wall-associated proteins, including the sortase-assembled endocarditis and biofilm associated pilus (Ebp), important for biofilm formation in vitro and in vivo. The current paradigm for sortase-assembled pilus biogenesis in Gram-positive bacteria is that...
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sg-ntu-dr.10356-1645602023-02-04T23:34:40Z Spatial and temporal localization of cell wall associated pili in Enterococcus faecalis Choo, Pei Yi Wang, Charles Y. VanNieuwenhze, Michael S. Kline, Kimberly A. School of Biological Sciences Singapore Centre for Environmental Life Sciences and Engineering (SCELSE) Science::Biological sciences Enterococcus Faecalis Spatiotemporal Localization Enterococcus faecalis virulence requires cell wall-associated proteins, including the sortase-assembled endocarditis and biofilm associated pilus (Ebp), important for biofilm formation in vitro and in vivo. The current paradigm for sortase-assembled pilus biogenesis in Gram-positive bacteria is that sortases attach substrates to lipid II peptidoglycan (PG) precursors, prior to their incorporation into the growing cell wall. Contrary to prevailing dogma, by following the distribution of Ebp and PG throughout the E. faecalis cell cycle, we found that cell surface Ebp do not co-localize with newly synthesized PG. Instead, surface-exposed Ebp are localized to the older cell hemisphere and excluded from sites of new PG synthesis at the septum. Moreover, Ebp deposition on the younger hemisphere of the E. faecalis diplococcus appear as foci adjacent to the nascent septum. We propose a new model whereby sortase substrate deposition can occur on older PG rather than at sites of new cell wall synthesis. Consistent with this model, we demonstrate that sequestering lipid II to block PG synthesis via ramoplanin, does not impact new Ebp deposition at the cell surface. These data support an alternative paradigm for sortase substrate deposition in E. faecalis, in which Ebp are anchored directly onto uncrosslinked cell wall, independent of new PG synthesis. Ministry of Education (MOE) National Research Foundation (NRF) Published version This work was supported by National Research Foundation and Ministry of Education Singapore under its Research Centre of Excellence Programme, as well as the National Research Foundation under its Singapore NRF Fellowship programme (NRF-NRFF2011-11). This work was also supported by a Tier 1 grant sponsored by the Singapore Ministry of Education (MOE2017-T1- 001-269). Work in the VanNieuwenhze laboratory was supported by the National Institutes of Health (R35 GM136365). 2023-02-01T03:26:52Z 2023-02-01T03:26:52Z 2023 Journal Article Choo, P. Y., Wang, C. Y., VanNieuwenhze, M. S. & Kline, K. A. (2023). Spatial and temporal localization of cell wall associated pili in Enterococcus faecalis. Molecular Microbiology, 119(1), 1-18. https://dx.doi.org/10.1111/mmi.15008 0950-382X https://hdl.handle.net/10356/164560 10.1111/mmi.15008 36420961 2-s2.0-85143983419 1 119 1 18 en NRF-NRFF2011-11 MOE2017-T1- 001-269 Molecular Microbiology © 2022 The Authors. Molecular Microbiology published by John Wiley & Sons Ltd. This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. application/pdf |
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Science::Biological sciences Enterococcus Faecalis Spatiotemporal Localization Choo, Pei Yi Wang, Charles Y. VanNieuwenhze, Michael S. Kline, Kimberly A. Spatial and temporal localization of cell wall associated pili in Enterococcus faecalis |
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Enterococcus faecalis virulence requires cell wall-associated proteins, including the sortase-assembled endocarditis and biofilm associated pilus (Ebp), important for biofilm formation in vitro and in vivo. The current paradigm for sortase-assembled pilus biogenesis in Gram-positive bacteria is that sortases attach substrates to lipid II peptidoglycan (PG) precursors, prior to their incorporation into the growing cell wall. Contrary to prevailing dogma, by following the distribution of Ebp and PG throughout the E. faecalis cell cycle, we found that cell surface Ebp do not co-localize with newly synthesized PG. Instead, surface-exposed Ebp are localized to the older cell hemisphere and excluded from sites of new PG synthesis at the septum. Moreover, Ebp deposition on the younger hemisphere of the E. faecalis diplococcus appear as foci adjacent to the nascent septum. We propose a new model whereby sortase substrate deposition can occur on older PG rather than at sites of new cell wall synthesis. Consistent with this model, we demonstrate that sequestering lipid II to block PG synthesis via ramoplanin, does not impact new Ebp deposition at the cell surface. These data support an alternative paradigm for sortase substrate deposition in E. faecalis, in which Ebp are anchored directly onto uncrosslinked cell wall, independent of new PG synthesis. |
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School of Biological Sciences |
author_facet |
School of Biological Sciences Choo, Pei Yi Wang, Charles Y. VanNieuwenhze, Michael S. Kline, Kimberly A. |
format |
Article |
author |
Choo, Pei Yi Wang, Charles Y. VanNieuwenhze, Michael S. Kline, Kimberly A. |
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Choo, Pei Yi |
title |
Spatial and temporal localization of cell wall associated pili in Enterococcus faecalis |
title_short |
Spatial and temporal localization of cell wall associated pili in Enterococcus faecalis |
title_full |
Spatial and temporal localization of cell wall associated pili in Enterococcus faecalis |
title_fullStr |
Spatial and temporal localization of cell wall associated pili in Enterococcus faecalis |
title_full_unstemmed |
Spatial and temporal localization of cell wall associated pili in Enterococcus faecalis |
title_sort |
spatial and temporal localization of cell wall associated pili in enterococcus faecalis |
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2023 |
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https://hdl.handle.net/10356/164560 |
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1757048202239934464 |