Team:USP-UNESP-Brazil/Associative Memory/Modeling

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<h1 id="Associative Memory">Associative Memory</h1>
<h1 id="Associative Memory">Associative Memory</h1>
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<h1 id="objective">Introduction</h1>
 
<p>We introduced a mathematical model for two populations of bacteria that interact via quorum sensing. Each population  
<p>We introduced a mathematical model for two populations of bacteria that interact via quorum sensing. Each population  
produces its own quorum sensing molecule (QSM) and the QSM of one population can be repressive or excitatory to the other  
produces its own quorum sensing molecule (QSM) and the QSM of one population can be repressive or excitatory to the other  
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examination of the growth curve. </p>
examination of the growth curve. </p>
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{{:Team:USP-UNESP-Brazil/Templates/RImage | image=Circularization.jpeg | caption=Fig. 1. Excision recombination reaction steps for CRE and FLP. All reactions are reversible and the arrows represent the forward and backward reactions. | size=600px }}
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{{:Team:USP-UNESP-Brazil/Templates/RImage | image=KxRphis_alpha.jpg | caption=Fig. 1. The fraction of the up-regulated population as a function of the carrying capacity ($K$) and the ratio $\frac{\phi_A}{\phi_B}$ for the case $\phi_B = \alpha$, at equilibrium. Initial conditions: $N_{Au} = N_{Bu} = A = B = 0$. | size=620px}}
In our model, there are two different types of population of bacteria and each type has his own QSM, represented by $A$ and
In our model, there are two different types of population of bacteria and each type has his own QSM, represented by $A$ and
$B$. In order to evaluate an interaction between the two type of bacteria we introduced a term in the model proposed by  
$B$. In order to evaluate an interaction between the two type of bacteria we introduced a term in the model proposed by  
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Ward et al *********ref***********. We assumed that type A up-regulated cells becomes down-regulated by B with the rate
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Ward et al [1]. We assumed that type A up-regulated cells becomes down-regulated by B with the rate
$\phi_B$ and vice-versa.  
$\phi_B$ and vice-versa.  
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\begin{align}
\begin{align}
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We first evaluated the fraction of cells up-regulated as a function of carrying capacity and of the ratio $\frac{\phi_A}{\phi_B}$,
We first evaluated the fraction of cells up-regulated as a function of carrying capacity and of the ratio $\frac{\phi_A}{\phi_B}$,
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{{:Team:USP-UNESP-Brazil/Templates/RImage | image=Circularization.jpeg | caption=Fig. 1. Excision recombination reaction steps for CRE and FLP. All reactions are reversible and the arrows represent the forward and backward reactions. | size=600px }}
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{{:Team:USP-UNESP-Brazil/Templates/RImage | image=TableMatModelQS.jpeg | caption=Fig. 2. Parameter values obtained by Ward et al. | size=350px}}
The carrying capacity is an important parameter of the model. For values up to $10^8$, in the equilibrium, no population can reach
The carrying capacity is an important parameter of the model. For values up to $10^8$, in the equilibrium, no population can reach
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quorum since the density of cells is too low, figure *****xis*****. On the other hand, for values higher than $10^8$ the population
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quorum since the density of cells is too low, Figure 1. On the other hand, for values higher than $10^8$ the population
that has a higher repressive rate, represented by $\phi$, reachs quorum and represses the other population.  
that has a higher repressive rate, represented by $\phi$, reachs quorum and represses the other population.  
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\end{align}
\end{align}
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These equations can be reduced to two expressions involving $x = N_{Au}/K$ and $y = N_{Bu}/K$:
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\begin{align}
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& \frac{y(\kappa_{Bu} - \kappa_{Bd}) + \kappa_{Bd}}{\alpha_B (1-y) + \lambda^*_B + y\phi_B} &= \frac{\Big[x(\kappa_{Au} - \kappa_{Ad}) + \kappa_{Ad}\Big]\alpha_A (1-x)} {\Big[\alpha_A (1-x) + \lambda^*_A + y\phi_A\Big]x\phi_B} - \frac{\beta_A}{\phi_B} \\
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& \frac{x(\kappa_{Au} - \kappa_{Ad}) + \kappa_{Ad}}{\alpha_A (1-x) + \lambda^*_A + x\phi_A} &= \frac{\Big[y(\kappa_{Bu} - \kappa_{Bd}) + \kappa_{Bd}\Big]\alpha_B (1-y)} {\Big[\alpha_B (1-y) + \lambda^*_B + x\phi_B\Big]y\phi_A} - \frac{\beta_B}{\phi_A}
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\end{align}
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where $\lambda^* = \lambda/K$, and $x$ and $y$ range from 0 up to 1. These expressions are similar, since exchanging $A$ and $B$ turns one equation into the other.
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Thus, the equilibrium points $(x,y)$ are placed in the intersection between the solutions for the relations above. Depending on the set of parameters, one can find two to four equilibria - the first one close to $(0,0)$, representing the repression of both populations, and the second one close to $(1,1)$, representing the activation of both populations, as presented below:
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{{:Team:USP-UNESP-Brazil/Templates/RImage | image=TableMatModelQS.jpeg | caption=Fig. 3. Each curve represents the solution of one equation, their intersections being the equilibrium points. There is one close to $(0,0)$ and another close to $(1,1)$.} | size=350px}}
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A third equilibrium point emerges when $\frac{\phi_A}{\phi_B} \gg 1$ - which means the repression of population A over population B is much greater than its counterpart. In this case, the system reaches an equilibrium close to $(1,0)$: population A activated, population B repressed. The behavior is analogous if $\frac{\phi_A}{\phi_B} \ll 1$.
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{{:Team:USP-UNESP-Brazil/Templates/RImage | image=TableMatModelQS.jpeg | caption=Fig. 4. When $\frac{\phi_A}{\phi_B} \gg 1$, besides the equilibria close to $(0,0)$ and $(1,1)$, there is also a point close to to $(1,0)$$.} | size=350px}}
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Finally, when both $\phi_A$ and $\phi_B$ are big when compared to $\alpha_A$ and $\alpha_B$, both populations A and B are able to
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repress each other, depending on the initial conditions: there are equilibria both close to $(1,0)$ and to $(0,1)$ - with repression
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of one population and activation of the other.
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{{:Team:USP-UNESP-Brazil/Templates/RImage | image=TableMatModelQS.jpeg | caption=Fig. 4. When $\frac{\phi_A}{\alpha_A} \gg 1$ and $\frac{\phi_B}{\alpha_B} \gg 1$, there are four equilibria, close to $(0,0)$, $(1,1)$, $(1,0)$ and $(0,1)$.} | size=350px}}
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{{:Team:USP-UNESP-Brazil/Templates/RImage | image=KxRphis_alpha.jpg | caption=Fig 2.  | size=620px}}
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<h1 id="discussion">Discussion</h1>
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{{:Team:USP-UNESP-Brazil/Templates/RImage | image=TableMatModelQS.jpeg | caption=Fig 2 | size=350px}}
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<h1 id="references">References</h1>
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[1] J. P. Ward, J.R. King, A. J. Koerber, P. Williams, J. M. Croft and R. E. Sockett
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<p>[1] J. P. Ward, J.R. King, A. J. Koerber, P. Williams, J. M. Croft and R. E. Sockett
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''Mathematical modelling of quorum sensing in bacteria''.
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''Mathematical modelling of quorum sensing in bacteria''. </p>
Math Med Biol (2001) 18(3)
Math Med Biol (2001) 18(3)
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[2] http://partsregistry.org/
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<p>[2] http://partsregistry.org/ </p>
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Revision as of 20:57, 26 September 2012