ORCID Profile
0000-0001-5196-4932
Current Organisation
UiT The Arctic University of Norway
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Publisher: Springer Science and Business Media LLC
Date: 29-02-2016
DOI: 10.1038/SREP22134
Abstract: Staphylococcus aureus is known as a frequent colonizer of the skin and mucosa. Among bacterial factors involved in colonization are adhesins such as the microbial surface components recognizing adhesive matrix molecules (MSCRAMMs). Serine aspartate repeat containing protein D (SdrD) is involved in adhesion to human squamous cells isolated from the nose. Here, we identify Desmoglein 1 (Dsg1) as a novel interaction partner for SdrD. Genetic deletion of sdrD in S. aureus NCTC8325-4 through allelic replacement resulted in decreased bacterial adherence to Dsg1- expressing HaCaT cells in vitro . Complementary gain-of-function was demonstrated by heterologous expression of SdrD in Lactococcus lactis , which increased adherence to HaCaT cells. Also ectopic expression of Dsg1 in HEK293 cells resulted in increased adherence of S. aureus NCTC8325-4 in vitro . Increased adherence of NCTC8325-4, compared to NCTC8325-4Δ sdrD, to the recombinant immobilized Dsg1 demonstrated direct interaction between SdrD and Dsg1. Specificity of SdrD interaction with Dsg1 was further verified using flow cytometry and confirmed binding of recombinant SdrD to HaCaT cells expressing Dsg1 on their surface. These data demonstrate that Dsg1 is a host ligand for SdrD.
Publisher: Oxford University Press (OUP)
Date: 17-07-2014
DOI: 10.1093/JAC/DKU271
Publisher: S. Karger AG
Date: 2014
DOI: 10.1159/000357618
Abstract: Signaling through Toll-like receptors (TLRs), crucial molecules in the induction of host defense responses, requires adaptor proteins that contain a Toll/interleukin-1 receptor (TIR) domain. The pathogen i Staphylococcus aureus /i produces several innate immune-evasion molecules that interfere with the host's innate immune response. A database search analysis suggested the presence of a gene encoding a homologue of the human TIR domain in i S. aureus /i MSSA476 which was named staphylococcal TIR domain protein (TirS). Ectopic expression of TirS in human embryonic kidney, macrophage and keratinocyte cell lines interfered with signaling through TLR2, including MyD88 and TIRAP, NF-& #954 B and/or mitogen-activated protein kinase pathways. Moreover, the presence of TirS reduced the levels of cytokines MCP-1 and G-CSF secreted in response to i S. aureus /i . The effects on NF-& #954 B pathway were confirmed using i S. aureus /i MSSA476 wild type, an isogenic mutant MSSA476& #x0394 i tirS /i , and complemented MSSA476& #x0394 i tirS + /i TirS in a Transwell system where bacteria and host cells were physically separated. Finally, in a systematic mouse infection model, TirS promoted bacterial accumulation in several organs 4 days postinfection. The results of this study reveal a new i S. aureus /i virulence factor that can interfere with PAMP-induced innate immune signaling in vitro and bacterial survival in vivo.
Publisher: American Society for Microbiology
Date: 2017
DOI: 10.1128/IAI.00559-16
Abstract: Staphylococcus aureus expresses a panel of cell wall-anchored adhesins, including proteins belonging to the microbial surface components recognizing adhesive matrix molecule (MSCRAMM) family, exemplified by the serine-aspartate repeat protein D (SdrD), which serve key roles in colonization and infection. Deletion of sdrD from S. aureus subsp. aureus strain NCTC8325-4 attenuated bacterial survival in human whole blood ex vivo , which was associated with increased killing by human neutrophils. Remarkably, SdrD was able to inhibit innate immune-mediated bacterial killing independently of other S. aureus proteins, since addition of recombinant SdrD protein and heterologous expression of SdrD in Lactococcus lactis promoted bacterial survival in human blood. SdrD contributes to bacterial virulence in vivo , since fewer S. aureus subsp. aureus NCTC8325-4 Δ sdrD bacteria than bacteria of the parent strain were recovered from blood and several organs using a murine intravenous infection model. Collectively, our findings reveal a new property of SdrD as an important key contributor to S. aureus survival and the ability to escape the innate immune system in blood.
No related grants have been discovered for Johanna Ulrica Ericson.