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Barbara E. Murray

Researcher at University of Texas at Austin

Publications -  235
Citations -  23158

Barbara E. Murray is an academic researcher from University of Texas at Austin. The author has contributed to research in topics: Enterococcus faecalis & Enterococcus faecium. The author has an hindex of 73, co-authored 232 publications receiving 21704 citations. Previous affiliations of Barbara E. Murray include Emerging Pathogens Institute & University of Texas Health Science Center at Houston.

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Repetitive Sequence-Based PCR versus Pulsed-Field Gel Electrophoresis for Typing of Enterococcus faecalis at the Subspecies Level

TL;DR: Repetitive sequence-based PCR was compared to pulsed-field gel electrophoresis (PFGE) for the ability to discriminateEnterococcus faecalis isolates at the subspecies level and results were more difficult to interpret than PFGE results.
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Evidence that the enterococcal polysaccharide antigen gene (epa) cluster is widespread in Enterococcus faecalis and influences resistance to phagocytic killing of E. faecalis.

TL;DR: The results indicate that the epa gene cluster is widespread among E. faecalis and confers some protection against human host defenses.
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Mechanism for Sortase Localization and the Role of Sortase Localization in Efficient Pilus Assembly in Enterococcus faecalis

TL;DR: It is found that a positively charged domain can act as a localization retention signal for the focal compartmentalization of membrane proteins in E. faecalis and abolished both its retention at single foci and its function in efficient pilus assembly.
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Relative Contributions of Ebp Pili and the Collagen Adhesin Ace to Host Extracellular Matrix Protein Adherence and Experimental Urinary Tract Infection by Enterococcus faecalis OG1RF

TL;DR: Data implicate the Ebp pili as having some role in collagen adherence, albeit less than that of Ace, and a very major role in fibrinogen adherence, which may explain in part the importance of these pili in experimental endocarditis.
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Relapse of Type A β-Lactamase-Producing Staphylococcus aureus Native Valve Endocarditis during Cefazolin Therapy: Revisiting the Issue

TL;DR: Analysis of the infecting strain disclosed a high minimum inhibitory concentration of cefazolin when a large inoculum was used, as well as rapid and complete cefzolin degradation, which was associated with regrowth in a time-kill experiment.