Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/104884
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dc.contributor.authorVajjala, Anuradhaen
dc.contributor.authorBiswas, Debabrataen
dc.contributor.authorTay, Wei Hongen
dc.contributor.authorHanski, Emanuelen
dc.contributor.authorKline, Kimberly Annen
dc.date.accessioned2019-05-08T09:02:25Zen
dc.date.accessioned2019-12-06T21:41:57Z-
dc.date.available2019-05-08T09:02:25Zen
dc.date.available2019-12-06T21:41:57Z-
dc.date.issued2018en
dc.identifier.citationVajjala, A., Biswas, D., Tay, W. H., Hanski, E., & Kline, K. A. (2018). Streptolysin‐induced endoplasmic reticulum stress promotes Group A Streptococcal host‐associated biofilm formation and necrotising fasciitis. Cellular Microbiology, 21(1), e12956-. doi:10.1111/cmi.12956en
dc.identifier.issn1462-5814en
dc.identifier.urihttps://hdl.handle.net/10356/104884-
dc.identifier.urihttp://hdl.handle.net/10220/48125en
dc.description.abstractGroup A Streptococcus (GAS) is a human pathogen that causes infections ranging from mild to fulminant and life‐threatening. Biofilms have been implicated in acute GAS soft‐tissue infections such as necrotising fasciitis (NF). However, most in vitro models used to study GAS biofilms have been designed to mimic chronic infections and insufficiently recapitulate in vivo conditions along with the host-pathogen interactions that might influence biofilm formation. Here, we establish and characterise an in vitro model of GAS biofilm development on mammalian cells that simulates microcolony formation observed in a mouse model of human NF. We show that on mammalian cells, GAS forms dense aggregates that display hallmark biofilm characteristics including a 3D architecture and enhanced tolerance to antibiotics. In contrast to abiotic‐grown biofilms, host‐associated biofilms require the expression of secreted GAS streptolysins O and S (SLO, SLS) that induce endoplasmic reticulum (ER) stress in the host. In an in vivo mouse model, the streptolysin null mutant is attenuated in both microcolony formation and bacterial spread, but pretreatment of soft‐tissue with an ER stressor restores the ability of the mutant to form wild‐type‐like microcolonies that disseminate throughout the soft tissue. Taken together, we have identified a new role of streptolysin‐driven ER stress in GAS biofilm formation and NF disease progression.en
dc.description.sponsorshipNRF (Natl Research Foundation, S’pore)en
dc.description.sponsorshipNMRC (Natl Medical Research Council, S’pore)en
dc.format.extent16 p.en
dc.language.isoenen
dc.relation.ispartofseriesCellular Microbiologyen
dc.rights© 2018 John Wiley & Sons Ltd. All rights reserved. This paper was published in Cellular Microbiology and is made available with permission of John Wiley & Sons Ltd.en
dc.subjectBiofilmsen
dc.subjectER Stressen
dc.subjectDRNTU::Science::Biological sciencesen
dc.titleStreptolysin-induced endoplasmic reticulum stress promotes Group A Streptococcal host-associated biofilm formation and necrotising fasciitisen
dc.typeJournal Articleen
dc.contributor.schoolSchool of Biological Sciencesen
dc.contributor.organizationCellular and Molecular Mechanisms of Inflammation, Campus for Research Excellence and Technological Enterprise (CREATE)en
dc.contributor.organizationDepartment of Microbiology and Immunology, National University of Singapore (NUS)-The Hebrew University of Jerusalem (HUJ), Singapore.en
dc.contributor.researchSingapore Centre for Environmental Life Sciences and Engineeringen
dc.identifier.doi10.1111/cmi.12956en
dc.description.versionAccepted versionen
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SCELSE Journal Articles
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