Virginia Tech/infection model

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<h3>Lysogenic and Lytic Infection:</h3>
<h3>Lysogenic and Lytic Infection:</h3>
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When E. coli is infected with lambda phage, the virus can stay dormant in the cell or explode releasing approximately a hundred progeny phage viruses.  If the virus stays dormant, the cell is lysogenic.  If the virus decides to multiply within the cell and explode, the cell is lytic.  In order to model the infection of E. coli, the lytic and lysogenic response needs to be accounted for.
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When ''E. coli'' is infected with λ phage, the virus can stay dormant in the cell or explode releasing approximately a hundred progeny phage viruses.  If the virus stays dormant, the cell is lysogenic.  If the virus decides to multiply within the cell and explode, the cell is lytic.  In order to model the infection of E. coli, the lytic and lysogenic response needs to be accounted for.
<h3>The Cells Decision Circuit for Lysogenic and Lytic Infection</h3>
<h3>The Cells Decision Circuit for Lysogenic and Lytic Infection</h3>

Revision as of 00:06, 25 October 2007

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2nd Scale: Infection of a Single Population

Contents

Lysogenic and Lytic Infection:

When E. coli is infected with λ phage, the virus can stay dormant in the cell or explode releasing approximately a hundred progeny phage viruses. If the virus stays dormant, the cell is lysogenic. If the virus decides to multiply within the cell and explode, the cell is lytic. In order to model the infection of E. coli, the lytic and lysogenic response needs to be accounted for.

The Cells Decision Circuit for Lysogenic and Lytic Infection

The probability of whether the cell becomes lytic or lysogenic is dependent on the ratio of phage to uninfected cells and environmental factors. If there are a small number of phage viruses relative to the number of bacteria, the infected cells will have a greater probability of becoming lytic. If there are a large number of phage viruses relative to the number of bacteria, the cells will have a greater probability of becoming lysogenic. This decision circuit is decided by the multiplicity of infection (MOI) for a cell. If a single cell is infected with multiple phage viruses, this would indicate to the cell that there is an abundance of phage in its surrounding environment and the creation of more phage would be superfluous. The cell therefore becomes lysogenic upon infection. If the cell is infected with a single phage virus, the cell has a greater probability of becoming lytic so that more phage can be introduced to the environment. Occasionally, a lysogenic cell can become lytic. If a lysogenic cell experiences stresses from the surrounding environment, it can turn lytic and release progeny phage before the cell dies.

Infection Match

Explanation of the Simulated Infection

The figure on the left shows an experimental infection curve in blue and a simulation in red. The infection occurs at .25 MOI, which means that there is one phage for every four bacteria. Since there are a significantly lower number of phage viruses in relation to uninfected bacteria, the majority of infected cells become lytic. At 200 minutes into infection, the lytic cells begin to burst releasing phage into the environment. At 400 minutes, the lytic cells have died off and a few lysogenic cells remain. Since the lysogenic cells are immune to further infection, they rapidly grow back and fill the environment.

Reaction Equations







Explanation of the Reaction Equations Model

The table shows the reaction equations that create the infection simulation curve. Space is used as a limiting substrate to inhibit the growth of bacteria. When the simulation begins, there is an initial concentration of space that is steadily depleted by the bacterial growth. As lytic cells burst, the space is returned to the environment so that it is available for lysogenic growth. The lysogenic cells grow much like the uninfected cells. Monad’s derived reaction equations are used to grow the lysogenic cells as well as the uninfected cells.

The reaction equations can be run with stochastic simulation; however, the simulation will not create a large variance in data. The initial concentrations for bacteria are in the thousands and at these high levels, the randomness from the stochastic simulation will not create a significant impact on the shape of the curve.