Center for Biofilm Engineering
Thesis Abstract:
"A 3D computer model investigation of biofilm detachment and
protection mechanisms"
A biofilm is a dense aggregation of
microorganisms attached to each other and a supporting surface. Biofilms are
ubiquitous in industrial environments and are also recognized as the source
of persistent infections. Biofilm invasions and biofilm-induced infections
are often difficult or impossible to remedy. This dissertation defense
presents the results of a 3D hybrid computer model, BacLAB, which was used
to simulate detachment and protection mechanisms of biofilms in a cellular
automata framework.
We investigated levels of protection
against antimicrobials afforded by each of four hypothesized protective
mechanisms in order to examine population survival versus antimicrobial
exposure time, and the spatial patterns of chemical species and cell types.
When compared to each other, the behaviors of the four different mechanisms
produced distinct shapes of killing curves, non-uniform spatial patterns of
survival and cell type distribution, and anticipated susceptibility patterns
of dispersed biofilm cells.
Detachment is an important process
that allows an organism the possibility of traveling to and colonizing a new
location. Detachment also balances growth and so determines the net
accumulation of biomass on the surface. Three hypothetical mechanisms
representing various physical and biological influences of detachment were
incorporated into BacLAB. The results showed that varying the detachment
mechanism is a critical determinant of biofilm structure and of the dynamics
of biofilm accumulation and loss.
Phenotypic variants, in the form of
dormant cells, can often survive an antimicrobial treatment. The existence
of these cells, termed persisters, is one hypothetical explanation for
biofilm recalcitrance. Four different combinations of random and
substrate-dependant persister mechanisms were simulated through the use of
the BacLAB model. The purpose of this study was to determine and compare the
effects of differing formation and resuscitation strategies on persister-related
protection of biofilms. Analysis of the simulations showed that extended
periods of dormancy, without regard to the mechanism, were directly
responsible for more tolerant biofilms.
A 3D computer model investigation of biofilm detachment and protection
mechanisms, Thesis Defense
by Jason D. Chambless, PhD Candidate in Chemical and Biological
Engineering, Montana State University, February 2008
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