Team:UMayor-Chile/Project

From 2014.igem.org

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<h3>References </h3>
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<p>http://redsalud.uc.cl/ucchristus/vidasaludable/glosario/F/fibrosis_quistica.act</p>
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iGEM teams are encouraged to record references you use during the course of your research. They should be posted somewhere on your wiki so that judges and other visitors can see how you though about your project and what works inspired you. </p>  
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<p>http://www.fibrosisquisticadelpancreas.cl/noticias/10-generales/16-ministro-de-salud-inauguro-congreso-de-actualizacion-en-fibrosis-quistica-.html</p>
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<p>http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0370-41062014000300003</p>
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<p>http://www.cff.org/</p>
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<p>Taylor Sitarik Cohen & Alice Prince. Cystic fibrosis: a mucosal immunodeficiency syndrome (doi:10.1038/nm.2715)</p>
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Revision as of 06:34, 17 October 2014



WELCOME TO iGEM 2014!

Your team has been approved and you are ready to start the iGEM season!
On this page you can document your project, introduce your team members, document your progress
and share your iGEM experience with the rest of the world!


Click here to edit this page!

Home Team Official Team Profile Project Parts Modeling Notebook Safety Attributions

Cystic fibrosis (CF)

Our troyhorse warriors have a plan!!!

70,000 people with CF worldwide, a lifespan depending of the resources (in USA the lifespan it’s about 40 years old, while in Chile the average lifespan it’s about 18 years old).


It’s a disease caused by the expression of a deficient transmembrane protein called CFTR. This affects different kind of cells, mainly the epithelial cells from the airway and pancreas, causing the production of a defective mucus.


In the lungs, this defective mucus leads that several opportunistic pathogens enter to the lower airway and initiate an infection, with a consecutively progressive lung dysfunction.


One of the main pathogens found in an infection of the lungs are the Pseudomonas aeruginosa. When it colonize the airway, initiates the production of biofilm, a barrier that protect it of a lot of antimicrobial substances and gave best environment for it develop.


The actual treatments for controlling the symptoms consist in maintain controlled the pathogens, clear the airway of the sticky mucus, administrate complementary enzymes and regulate the function of the CFTR channel.


References

http://redsalud.uc.cl/ucchristus/vidasaludable/glosario/F/fibrosis_quistica.act

http://www.fibrosisquisticadelpancreas.cl/noticias/10-generales/16-ministro-de-salud-inauguro-congreso-de-actualizacion-en-fibrosis-quistica-.html

http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0370-41062014000300003

http://www.cff.org/

Taylor Sitarik Cohen & Alice Prince. Cystic fibrosis: a mucosal immunodeficiency syndrome (doi:10.1038/nm.2715)

We propose smart warriors E. coli for the battle against the P. aeruginosa. We are training them now, teaching the action plan!!! Pay attention:


1. The first part of the plan is simple: looking for the Biofilm fortress.

We have to find our enemy. Our warriors will to enter to the fortress been guide by the clues left by our enemies, the Pseudomonas aeruguinosa.


2. Well, here we are… it’s time to start the part II:

Our E. coli tryhorse now know they are in the zone. It’s time to start the attack. Our enemy are protected by his thick barrier and our warriors know his weak point.


3. They are under attack!!! Pseudomonas are communicating themselves for rebuild the biofilm:

We have to cut the communications between the Pseudomonas as an intelligent strategy. The biofilm it’s a community work. If they can´t send signals, they won’t work in community.


4. Say goodbye everybody, the antibiotics are now available:

There’s no protection of the biofilm. Both P. aeruginosa and our E. coli Troyhorse are exposed to the final cut… a massive antibiotic attack!!!