Title:
SPATIOTEMPORAL IMPACT OF PHAGE EXPOSURE ON BIOFILM SYSTEMS

dc.contributor.advisor Curtis, Jennifer E.
dc.contributor.advisor Weitz, Joshua S.
dc.contributor.author Selvakumar, Hemaa
dc.contributor.committeeMember Gumbart, James C.
dc.contributor.committeeMember Diggle, Stephen
dc.contributor.committeeMember Yunker, Peter
dc.contributor.department Physics
dc.date.accessioned 2022-01-14T16:13:14Z
dc.date.available 2022-01-14T16:13:14Z
dc.date.created 2021-12
dc.date.issued 2021-12-14
dc.date.submitted December 2021
dc.date.updated 2022-01-14T16:13:14Z
dc.description.abstract When single-celled prokaryotic organisms, one of the simplest forms of life, develop the ability to exhibit complex emergent properties such as social cooperation, resource capture, and enhanced survivability, the individual limitations of existence can be overcome which would otherwise be unlikely. Emergent properties of biofilms such as matrix production, quorum sensing, and coordinated lifecycle offers structural and functional advantages which makes them highly successful at evading destruction by antimicrobials and immune defenses. With few, if any, novel antibiotics in the clinical pipeline, there is a resurgence of interest in alternatives such as phage therapy, the practice of bacterial viruses known as bacteriophages that infect and lyse bacteria to treat infections. In this thesis, we explore the understudied impact of phage titer on biofilm dynamics and outcomes. We determined that the biofilm developmental stage at the time of phage addition modulates its response. These responses vary as a function of the phage dose and can be broadly organized into four distinct classes. In each of these classes, we observe that high phage doses restrain the biofilm from transitioning into the next stage of their developmental cycle. A paradoxical aspect of this result is that mature biofilms exposed to high phage titers are enhanced by phage treatment. Despite this apparently unwanted outcome, the inhibition of biofilm dispersion in phage-treated samples could potentially minimize the further spread of infections to other locations. These results comprehensively demonstrate predictable biofilm outcomes versus phage dosage and biofilm age, and will provide guidance in advancing phage-based personalized medicine when generalized treatments fail. Collectively, this dissertation derives insights on the advantages and limitations of phages to inhibit, control, and eliminate biofilms.
dc.description.degree Ph.D.
dc.format.mimetype application/pdf
dc.identifier.uri http://hdl.handle.net/1853/66168
dc.publisher Georgia Institute of Technology
dc.subject Biophysics
dc.subject Phage therapy
dc.subject Immunophage therapy
dc.subject MIcrobial dynamics
dc.subject Spatiotemporal evolution
dc.title SPATIOTEMPORAL IMPACT OF PHAGE EXPOSURE ON BIOFILM SYSTEMS
dc.type Text
dc.type.genre Dissertation
dspace.entity.type Publication
local.contributor.advisor Curtis, Jennifer E.
local.contributor.advisor Weitz, Joshua S.
local.contributor.corporatename College of Sciences
local.contributor.corporatename School of Physics
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relation.isAdvisorOfPublication b2526611-2493-4ea6-b2d5-bc0a48b76769
relation.isOrgUnitOfPublication 85042be6-2d68-4e07-b384-e1f908fae48a
relation.isOrgUnitOfPublication 2ba39017-11f1-40f4-9bc5-66f17b8f1539
thesis.degree.level Doctoral
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