Subject: | |
From: | |
Reply To: | |
Date: | Tue, 25 Oct 2011 09:51:22 -0400 |
Content-Type: | multipart/alternative |
Parts/Attachments: |
|
|
Dissertation Defense Announcement
To: The George Mason University Community
Candidate: Bryan A. Millis
Program: PhD Biosciences*
*
Date: Thursday November 3, 2011
Time: 10:00 a.m.
Place: George Mason University
Occoquan Bldg., Room 203
Prince William campus <http://www.gmu.edu/resources/visitors/findex.html>*
*Dissertation Chair: Dr. Serguei Popov
Committee members: Dr. Charles L. Bailey, Dr. Raymond Weinstein, Dr. Taissia Popova
*
*Title: "Induction of Host Extracellular Protein Dysfunction by /Bacillus anthracis/
Hemolytic Factors"
*
*The dissertation is on reserve in the Johnson Center Library, Fairfax campus.
The doctoral project will not be read at the meeting, but should be read in advance.
/**/
All members of the George Mason University community are invited to attend.
ABSTRACT:* *
Barrier dysfunction represents one of the most predominant
manifestations of an anthrax infection. Massive pleural edema, which is
classic of inhalational anthrax, is perhaps one of the only consistent
symptoms among victims of this pathogen. However, despite much research
into how the pathogen escapes the initial immune response, there remains
little treatment option at later symptomatic stages of infection. This
work demonstrates that a group of molecules having functions in barrier
organization, including Syndecan-1, are either shed from the cell
surface, or dysfunctional in this role. This dysfunction is co-incident
with manifestations of hemodynamic imbalance, resulting in both
accumulation within the liver and induction of disseminated
intravascular coagulopathy. Further, we suggest specific secreted
virulence factors that contribute to this dysfunction through
acceleration of host cell shedding processes regulated by MAP kinase
cascades. The mechanism of action of these virulence factors points
toward signaling disturbances which result not only in loss of these
cell surface molecules, but also cytoskeletal disorganization and
decoupling from adhesion processes.
###
|
|
|