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Team:Paris Bettencourt/Project/Sabotage
From 2013.igem.org
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<div class="leftparagraph"> | <div class="leftparagraph"> | ||
<p> | <p> | ||
| - | <b>Design a genetic element that spread in a population</b> | + | <b>Design a genetic element that spread in a population</b><br> |
| - | In nature, non-lytic filamentous bacteriophages are quite good at spreading genetic elements in bacterial populations and we thus imediately thought about them as vectors of choice. However being infected by a phage represent a huge burden for an individual bacteria which we thought would be detrimental for our construct to be able to maintain itself long enough in a population for this system to be clinically relevant. Therefore we choose to use a phagemid/helper system which is composed of two mobile interacting elements. The « heavy » elements of this system is an M13 phage which genome contains an altered packaging signal thus reducing the probability of packaging in a protein capside and escaping from the cell. Its role is to produce capside proteins which will in fact be used by a « light » element called phagemid which is a normal plasmid harboring a packaging signal | + | In nature, non-lytic filamentous bacteriophages are quite good at spreading genetic elements in bacterial populations and we thus imediately thought about them as vectors of choice. However being infected by a phage represent a huge burden for an individual bacteria which we thought would be detrimental for our construct to be able to maintain itself long enough in a population for this system to be clinically relevant. <br>Therefore we choose to use a phagemid/helper system which is composed of two mobile interacting elements. The « heavy » elements of this system is an M13 phage which genome contains an altered packaging signal thus reducing the probability of packaging in a protein capside and escaping from the cell. Its role is to produce capside proteins which will in fact be used by a « light » element called phagemid which is a normal plasmid harboring a packaging signal. |
</p> | </p> | ||
</div> | </div> | ||
<div class="rightparagraph"> | <div class="rightparagraph"> | ||
<p> | <p> | ||
| + | As a result a cell containing both elements will produce and secrete a lot of phagemid encapsulated plus some helper phages from time to time. We expect such a system to infect with light elements the majority of cells in a population and to be able to spread and maintain itself thanks to a small number of coinfected cells harboring both light (phagemid) and heavy (helper phage) elements transforming them into phage-producing cells.<br> | ||
Our silencing device is loaded on the light element in order to spread it efficiently. As the post-transcriptional regulation we are using only rely on RNA and doesn’t require synthesis of any protein, its cost for the cell will be very low. Moreover producing protective proteins against antibiotics is costly for the cell and lower its fitness in an antibiotic free environment, we thus expect our silencing device to be a temporary relief for the infected cell which should avoid early counterselection dynamics | Our silencing device is loaded on the light element in order to spread it efficiently. As the post-transcriptional regulation we are using only rely on RNA and doesn’t require synthesis of any protein, its cost for the cell will be very low. Moreover producing protective proteins against antibiotics is costly for the cell and lower its fitness in an antibiotic free environment, we thus expect our silencing device to be a temporary relief for the infected cell which should avoid early counterselection dynamics | ||
</p> | </p> | ||
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<div class="leftparagraph"> | <div class="leftparagraph"> | ||
<p> | <p> | ||
| - | <b>Design of a sequential killing strategy</b> | + | <b>Design of a sequential killing strategy</b> <br> |
To perform our proof of concept experiments, our targeted genes were different antibiotic resistance genes on commercial plasmids that were transformed in MG1655 cells. | To perform our proof of concept experiments, our targeted genes were different antibiotic resistance genes on commercial plasmids that were transformed in MG1655 cells. | ||
The experimental set up consisted of a seuquential strategy : phage infection followed by a treatment with antibiotics. | The experimental set up consisted of a seuquential strategy : phage infection followed by a treatment with antibiotics. | ||
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<div class="rightparagraph"> | <div class="rightparagraph"> | ||
| - | + | BLABLA | |
</div> | </div> | ||
| + | <div style="clear: both;"></div> | ||
<h2>Characterization of the phagemid system</h2> | <h2>Characterization of the phagemid system</h2> | ||
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<img src="https://static.igem.org/mediawiki/2013/e/e9/PB_TH_Characterizationphagemidhelper.png" width="535px"/> | <img src="https://static.igem.org/mediawiki/2013/e/e9/PB_TH_Characterizationphagemidhelper.png" width="535px"/> | ||
</div> | </div> | ||
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<img src="https://static.igem.org/mediawiki/2013/d/d7/PB_TH_Killingatdifferentconcentration%24.png" width="535px" /> | <img src="https://static.igem.org/mediawiki/2013/d/d7/PB_TH_Killingatdifferentconcentration%24.png" width="535px" /> | ||
</div> | </div> | ||
| - | + | <div style="clear: both;"></div> | |
<h2>Origin of resistance </h2> | <h2>Origin of resistance </h2> | ||
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<img src="https://static.igem.org/mediawiki/2013/3/3c/PB_TH_Wheredoresistancecome.png" width="535px" /> | <img src="https://static.igem.org/mediawiki/2013/3/3c/PB_TH_Wheredoresistancecome.png" width="535px" /> | ||
</div> | </div> | ||
| + | <div style="clear: both;"></div> | ||
| + | <h2>Conclusion and perspectives</h2> | ||
| - | |||
| - | |||
<div class="leftparagraph"> | <div class="leftparagraph"> | ||
<p> | <p> | ||
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</div> | </div> | ||
<div class="rightparagraph"> | <div class="rightparagraph"> | ||
| + | <p> | ||
<b>Possible Applications : </b> BLABLABLA | <b>Possible Applications : </b> BLABLABLA | ||
| + | </p> | ||
</div> | </div> | ||
Revision as of 18:45, 4 October 2013
Background
One of the main concern about tuberculosis today is the emergence of antibiotic resistant strain
Results
- Construction and characterization of phagemids coding for small RNA targeting antibiotic resistance proteins
- successful conversion of antibiotic resistant population of E. coli to a sensitive state
BioBricks
Aims
Our objective is to make an antibiotic-resistant bacterial population sensitive again to those same antibiotics.
Introduction
As resistance against antibiotics are growing and pharmaceutical pipelines are drying up, we decided to investigate a new strategy based on specific silencing of the genes responsible for resistance through bioengineered stealth bacteriophages. The silencing of the genes is obtained with a simple and modular system of tailormade small RNAs and the spreading of this construct in a bacterial population is based on an autonomous phagemid/helper phage system. We demonstrated the validity of this trojan horse strategy by converting back to a sensitive state populations of bacteria initially resistant to antibiotics like chloramphenicol or kanamycin.
Design
Design a silencing device
We choose a straight forward strategy to force bacteria to stop producing those proteins by targeting the mRNA coding for those proteins with tailormade small RNAs.In order to design our silencing device (small RNA) we used the protocol described in Na et al 2013 and inserted a 24bp sequence complementary to the RBS area of the target genes inside the scaffold sequence that allow the stabilization of the hybridization. We designed three sRNA respectively targeting Kanamycine resistance gene of Duet Vector pACYc), Chloramphenicol ones ()and lac Z
.
Design a genetic element that spread in a population
In nature, non-lytic filamentous bacteriophages are quite good at spreading genetic elements in bacterial populations and we thus imediately thought about them as vectors of choice. However being infected by a phage represent a huge burden for an individual bacteria which we thought would be detrimental for our construct to be able to maintain itself long enough in a population for this system to be clinically relevant.
Therefore we choose to use a phagemid/helper system which is composed of two mobile interacting elements. The « heavy » elements of this system is an M13 phage which genome contains an altered packaging signal thus reducing the probability of packaging in a protein capside and escaping from the cell. Its role is to produce capside proteins which will in fact be used by a « light » element called phagemid which is a normal plasmid harboring a packaging signal.
As a result a cell containing both elements will produce and secrete a lot of phagemid encapsulated plus some helper phages from time to time. We expect such a system to infect with light elements the majority of cells in a population and to be able to spread and maintain itself thanks to a small number of coinfected cells harboring both light (phagemid) and heavy (helper phage) elements transforming them into phage-producing cells.
Our silencing device is loaded on the light element in order to spread it efficiently. As the post-transcriptional regulation we are using only rely on RNA and doesn’t require synthesis of any protein, its cost for the cell will be very low. Moreover producing protective proteins against antibiotics is costly for the cell and lower its fitness in an antibiotic free environment, we thus expect our silencing device to be a temporary relief for the infected cell which should avoid early counterselection dynamics
Design of a sequential killing strategy
To perform our proof of concept experiments, our targeted genes were different antibiotic resistance genes on commercial plasmids that were transformed in MG1655 cells.
The experimental set up consisted of a seuquential strategy : phage infection followed by a treatment with antibiotics.
Characterization of the phagemid system
Sequential killing
Results, generalization fro Kan
Origin of resistance
Conclusion and perspectives
Several sRNA on the same plasmid : BLABLABLA
Building a library of sRNA : BLABLABLA
Possible Applications : BLABLABLA
+33 1 44 41 25 22/25
team2013@igem-paris.org 
