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dc.contributor.advisorHefty, P. Scott
dc.contributor.authorSpedding, Lindsey
dc.date.accessioned2009-08-31T03:06:41Z
dc.date.available2009-08-31T03:06:41Z
dc.date.issued2009-04-29
dc.date.submitted2009
dc.identifier.otherhttp://dissertations.umi.com/ku:10361
dc.identifier.urihttp://hdl.handle.net/1808/5457
dc.description.abstractChlamydia trachomatis is an obligate intracellular bacterial pathogen with a significant public health impact. A unifying characteristic of Chlamydia is the biphasic developmental cycle that is intimately linked to pathogenesis. Due to its intracellular lifestyle within a membrane bound vacuole, Chlamydia requires a mechanism to interact with and manipulate the host. To facilitate this interaction, C. trachomatis encodes a Type III Secretion System (T3SS) that is likely requisite for chlamydial growth and integral to the developmental cycle. Additionally, little is known about the mechanisms that regulate the developmental cycle, and the T3SS. This thesis is focused on a translocated T3SS effector protein, CT667, that may serve in manipulation of the host, and the role of a transcriptional factor, ChxR, involved in regulating T3SS expression.
dc.format.extent116 pages
dc.language.isoEN
dc.publisherUniversity of Kansas
dc.rightsThis item is protected by copyright and unless otherwise specified the copyright of this thesis/dissertation is held by the author.
dc.subjectBiology
dc.subjectMicrobiology
dc.titleNovel Effector Protein Secretion and Transcriptional Regulation of the Type Three Secretion System in Chlamydia trachomatis.
dc.typeThesis
dc.contributor.cmtememberEgan, Susan
dc.contributor.cmtememberPicking, William
dc.thesis.degreeDisciplineMolecular Biosciences
dc.thesis.degreeLevelM.A.
kusw.oastatusna
kusw.oapolicyThis item does not meet KU Open Access policy criteria.
dc.rights.accessrightsopenAccess


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