Difference between revisions of "Team:Heidelberg/Model/Lagoon Contamination"

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             Here \(c_{X}(t_{0})\) is introduced, which is the initial concentration of the contamination.
 
             Here \(c_{X}(t_{0})\) is introduced, which is the initial concentration of the contamination.
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            <br>
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            When working with the model it is more practical to calculate relative changes in the concentration:
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            $$\frac{c_{X}(t)}{c{X}(t_{0})}$$
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            That simplifies the above equation to
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            $$
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            c_{X}(t) = \cdot e^{\big(-\Phi_{L} + \frac{\ln{2} }{t_{X} }\big) \cdot t}
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            $$
  
 
             The following statements can be made:
 
             The following statements can be made:
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             c_{X}(t) < 0, \quad if \quad \Phi_{L} < \frac{ln(2)}{t_{X } }
 
             c_{X}(t) < 0, \quad if \quad \Phi_{L} < \frac{ln(2)}{t_{X } }
 
             $$
 
             $$
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            <br>
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                 {{Heidelberg/templateus/Tablebox|
 
                 {{Heidelberg/templateus/Tablebox|

Revision as of 21:27, 27 October 2017

Modeling
Lagoon contamination
Contaminations with bacteria other than the host cells that are part of the experiment, funghi or other microorganisms can survive in the lagoons, it is necessary to take precautions. Since these can be costly (e.g. fungicides) an simulation of contamination growth can save resources. If the constant dilution rate of the lagoons is sufficiently high that the overall change in population size of the contamination is negative, the contamination will wash out and not be a lasting problem.
Note: contamination with viruses such as bacteriophages is not modelled here, because exponential growth of the contamination is assumed. This is plausible for bacteria and funghi since the lagoons are constantly diluted so that there is always fresh medium and space available. The change in concentration of the contamination can be described as $$ \frac{\partial c_{X}(t)}{\partial t} = -\Phi_{L} \cdot c_{X}(t) + \frac{\ln{2} }{T_{X} } \cdot c_{X}(t) $$ The concentration of the contamination \(x_{X}\) is assumed only to depend on the time, since the constant dilution reduces effects such as spent resources or growht inhibition by waste. The growth factor \(\frac{ln(2)}{t_{X} }\) is the factor by which the current concentration and its derivative are proportional. There is the dilution term containing the factor \(\Phi_{L}\) that is the flow rate trough the lagoon in volumes per hour and the growth term of the contamination based on the contaminations generation time \(t_{X}\). Solving this equation yields $$ c_{X}(t) = c_{X}(t_{0}) \cdot e^{\big(-\Phi_{L} + \frac{\ln{2} }{t_{X} }\big) \cdot t} $$ Here \(c_{X}(t_{0})\) is introduced, which is the initial concentration of the contamination.
When working with the model it is more practical to calculate relative changes in the concentration: $$\frac{c_{X}(t)}{c{X}(t_{0})}$$ That simplifies the above equation to $$ c_{X}(t) = \cdot e^{\big(-\Phi_{L} + \frac{\ln{2} }{t_{X} }\big) \cdot t} $$ The following statements can be made:
The contamination expands if the flow rate \(\Phi_{L}\) is greater than the growth factor, $$ c_{X}(t) > 0, \quad if \quad \Phi_{L} > \frac{ln(2)}{t_{X} } $$ it remains constant if the flow rate is exactly the growth factor $$ c_{X}(t) = 0, \quad if \quad \Phi_{L} = \frac{ln(2)}{t_{X} } $$ and it diminishes, when the flow rate is higher than the growth factor. $$ c_{X}(t) < 0, \quad if \quad \Phi_{L} < \frac{ln(2)}{t_{X } } $$

Table 1: Additional Variables and Parameters used for the calculation of the number of mutated sequences List of all additional paramters and variables used in the numeric solution of this model. When possible values are given.

Symbol Value and Unit Explanation
\(t \) [h] Total time in lagoon
\(p_{m} \) [bp/bp] Expected number of mutations per sequence
\(p_{M} \) [bp/sequences] Expected number of mutations in all sequences
\(N_{M} \) [bp] Number of mutated basepairs
\(L_{S} \) [bp] Length of sequence that is considered
\(N_{g} \) [generations] Number of generations
\(r_{M} \) \([\frac{1}{bp \cdot generation}]\)
\(\Phi_{L} \) [Vol/h]
\(N_{S} \) [sequences] Number of sequences
\(p_{(N_{M} > 0)} \) Probability to find at least one mutated sequence in a pool of sequences
\(p_{(N_{M} = 0)} \) Probability to find no mutated sequences in a pool of sequences

References