Team:EPF Lausanne/Project

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Also Asaia specific biobricks were made. These basics will allow future iGEM teams to use Asaia and manipulate it to fight mosquito-bourne diseases.
Also Asaia specific biobricks were made. These basics will allow future iGEM teams to use Asaia and manipulate it to fight mosquito-bourne diseases.
The expression of the proteins we intended to use to block Plasmodium falciparum was tested in E.coli. We showed that the immunotoxin is expressed and appears in the  supernatant. We could not show expression of the P-proteins. Furthermore we tested the persistance of Asaia in Drosophila to see if we can use it as an alternative host to facilitate research. The results showed that Asaia is not persistant and that the bacterium is very specific to mosquitoes. For the next steps of testing we established a collaboration with the Pasteur institute in Paris that works on mosquitoes.
The expression of the proteins we intended to use to block Plasmodium falciparum was tested in E.coli. We showed that the immunotoxin is expressed and appears in the  supernatant. We could not show expression of the P-proteins. Furthermore we tested the persistance of Asaia in Drosophila to see if we can use it as an alternative host to facilitate research. The results showed that Asaia is not persistant and that the bacterium is very specific to mosquitoes. For the next steps of testing we established a collaboration with the Pasteur institute in Paris that works on mosquitoes.
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= Further improvements =
 
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The next step would be to test Asaia that expresses the immunotoxin in mosquitoes. The efficiency of the immunotoxin could then be measured by counting the number of oocysts outside the mosquito's gut. We are currently collaborating with the Pasteur Institute in Paris to make further test on mosquitoes with our bacteria but unfortunately the results won't be available before this year's jamboree.
 
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Some modeling experiments should also be done to try to measure the impact of introducing our modified bacteria in mosquitoes populations. According to the [http://www.sciencedirect.com/science?_ob=ArticleURL&_udi=B6VRT-4V3K67R-B&_user=164550&_coverDate=12%2F09%2F2008&_rdoc=1&_fmt=high&_orig=search&_origin=search&_sort=d&_docanchor=&view=c&_acct=C000013218&_version=1&_urlVersion=0&_userid=164550&md5=52110befa7e6dce2da04feff33af38dc&searchtype=a literature], Asaia is transmitted from parent to offspring and also from one individual to the other but further measurement should be made to see how quick the spreading would be. Using these values, it might be possible to find out the best way to infect the most mosquitoes without risking an uncontrolled expansion of the bacteria population.
 

Revision as of 22:04, 26 October 2010



Overview

Our project idea

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The aim of our project is to help stopping the propagation of Malaria. To do so, we chose to act on the mosquito. Indeed, if we prevent the mosquito from being infected by malaria, it won't be able to transmit the parasite to healthy humans.

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Our idea is to engineer Asaia, a bacterium that is naturally present in the mosquito's intestinal tract.

Asaia project overview.png

Gut.png


This bacteria would express an immunotoxin and specific proteins to kill the Plasmodium falciparum or prevent its entry into the epithelium.

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The immunotoxin and the proteins then fight the Plasmodium falciparum and thus prevent the mosquito infection.


Asaia is an organism that is not only easy to grow and genetically manipulate but also does not disrupt the ecosystem. We are establishing Asaia as a new chassis so that future iGEM teams can quickly and efficiently engineer new and more potent Asaia strains. This will provide the synthetic biology community with a useful tool in the fight against malaria and other mosquito-borne diseases.



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So... ASAIA is the pink power against malaria.....





For a playful overview of our project, you can watch our great movie iGEM EPFL movie

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Our results

We established Asaia as a new chassis and provided tech-sheets on how to manipulate it. Various biobricks were constructed, with which selected proteins to block malaria infection of mosquitoes can be produced. Also Asaia specific biobricks were made. These basics will allow future iGEM teams to use Asaia and manipulate it to fight mosquito-bourne diseases. The expression of the proteins we intended to use to block Plasmodium falciparum was tested in E.coli. We showed that the immunotoxin is expressed and appears in the supernatant. We could not show expression of the P-proteins. Furthermore we tested the persistance of Asaia in Drosophila to see if we can use it as an alternative host to facilitate research. The results showed that Asaia is not persistant and that the bacterium is very specific to mosquitoes. For the next steps of testing we established a collaboration with the Pasteur institute in Paris that works on mosquitoes.


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