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Vanina Dengler

Researcher at Harvard University

Publications -  9
Citations -  491

Vanina Dengler is an academic researcher from Harvard University. The author has contributed to research in topics: Teichoic acid & Cell wall. The author has an hindex of 7, co-authored 9 publications receiving 423 citations. Previous affiliations of Vanina Dengler include ETH Zurich & University of Zurich.

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An Electrostatic Net Model for the Role of Extracellular DNA in Biofilm Formation by Staphylococcus aureus

TL;DR: It is suggested that eDNA acts as an electrostatic net, interconnecting cells surrounded by positively charged matrix proteins at a low pH, that tethers cells together via the proteinaceous layer of the biofilm matrix.
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Staphylococcus aureus Mutants Lacking the LytR-CpsA-Psr Family of Enzymes Release Cell Wall Teichoic Acids into the Extracellular Medium

TL;DR: A model whereby the S. aureus Δlcp mutant, defective in tethering WTA to the cell wall, cleaves WTA synthesis intermediates, releasing ribitol phosphate into the medium and recycling bactoprenol for peptidoglycan synthesis is proposed.
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Induction kinetics of the Staphylococcus aureus cell wall stress stimulon in response to different cell wall active antibiotics.

TL;DR: Differences observed in optimal induction conditions for specific antibiotics should be determined and taken into account when designing and interpreting CWSS induction studies.
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Mutation in the C-Di-AMP Cyclase dacA Affects Fitness and Resistance of Methicillin Resistant Staphylococcus aureus

TL;DR: Results indicate that c-di-AMP affects cell envelope-related signalling in S. aureus and could be a mechanism by which MRSA strains can increase their fitness levels by reducing their methicillin resistance levels.
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Deletion of hypothetical wall teichoic acid ligases in Staphylococcus aureus activates the cell wall stress response

TL;DR: Intrinsic activation of the CWSS upon LCP deletion and the fact that LCP proteins were essential for WTA-loading of the cell wall, highlight their important role(s) in S. aureus cell envelope biogenesis.