Team:Aachen/Safety

From 2014.igem.org

(Difference between revisions)
(Biosafety)
Line 4: Line 4:
= Biosafety =
= Biosafety =
-
DRAFT: ''The Aachen team is committed to consider all aspects of the entire project, including biosafety.''
+
Our iGEM team is committed to consider all aspects of the entire project, including biosafety. For this project, two biosafety aspects have to be consider. On the one hand, we are using ''E.coli'' as genetically modified organism, and on the other hand, we are detecting ''Pseudomonas aeruginosa'', a human pathogen. While using ''P. aeruginoas'', we should prevent proliferation. For ''E.coli'', we have to look after the non-release of genetically modified organisms. In general, we developed and designed the measurement device as closed system for a better safety handling. This way, neither the sampled pathogens nor the genetically modified sensor cells can escape our biosensor unit. Moreover, the electronic components are in a separate compartment and inaccessible for the user, preventing electric shock or other injuries. For the detection, we are using one-time usage sampling and sensor chips which can be disposed of after autoclaving or irradation with strong UV light.
-
For our project two biosafety aspects have to be consider. On the one hand we are using E.coli as genetically modified organism and on the other hand we are detecting Pseudomonas aeruginosa a human pathogen. While using Pseudomonas we have the problem of non-proliferation. For E.coli we have to look after the non-release of genetically modified organisms. In general we developed and designed the measurenment device as closed system for a better safety handling. In  this way neither the sampled pathogens nor the genetically modified sensor cells can escape out of our biosensor unit. Also the electronic components are inaccessible so that no one could get an electric shock. For the detection we are using one way sampling and sensor chips which can be disposed after autoclaving or irradate them with a strong UV light.
+
To detect ''P. aeruginosa'' cells, an sampling agar chip is slightly pressed against the solid surface to be tested. Afterwards, the sampling chip is immediately introduced into our measurement device and will not be removed until the detection is finished and the chips have be doused with disinfectant. The sensor chips must be handled in S1 environments only since they contain genetically modified ''E. coli''. However, once introduced into the measurement device, the sensor chips, too, will not be removed before disinfection.  
-
Pseudomonas aeruginosa
+
The living cells inside the measurement device are effectively killed after a detection by using desinfectants such as Bacillol. For this procedure, the drawer of the measurement device is opened and Bacillol is poured over the sampling and sensor chips. Afterwards, both chips can be autoclaved and be disposed of. The whole lining of the measurement device is build from plastic so that it can be disinfected easily.
-
* get the pure agar chip on a solid surface to improve contamination with Pseudomonas
+
To simulate the worst case scenario, we did replica plating of some sensor chips. In three experiments, we got an arithmetic mean of five colonies which were picked up. We concluded that the risk of infection is still really low even if the measurement device and chips are not handled properly.
-
* put the sampling chip into the measurement device for detection
+
-
* don't get this sampling chip out of the device until you finished detection
+
-
E.coli
 
-
* build a sensor chip including E.coli cells which have to be handled in S1 laboratories
 
-
* that is the reason why it's only allowed to use the measurement device in S1 labs
 
-
* put the sensor chip into the device like the sampling chip before
 
-
* don't get the sensor chip out of the device until you finished detection
 
-
 
-
The living cells inside the measurement device are ensured to be killed after detection at first by using desinfectant like bacillol. For this procedure open the drawer of the measurement device and pour bacillol on the sampling and also on the sensor chip. After this measures both chips can be autoclaved and later disposed. The whole lining of the measurement device is build on plastic so it could be desinfected completly.
 
-
For the worst case scenario we made a stamp pront of the used sensor chip. In three experiments we got an arithmetic mean of five colonies which could get out of these chip. To conclude the infection risk is really low if you are not using the measurement device as descripted.
 
{{Team:Aachen/Footer}}
{{Team:Aachen/Footer}}

Revision as of 16:07, 8 October 2014

Biosafety

Our iGEM team is committed to consider all aspects of the entire project, including biosafety. For this project, two biosafety aspects have to be consider. On the one hand, we are using E.coli as genetically modified organism, and on the other hand, we are detecting Pseudomonas aeruginosa, a human pathogen. While using P. aeruginoas, we should prevent proliferation. For E.coli, we have to look after the non-release of genetically modified organisms. In general, we developed and designed the measurement device as closed system for a better safety handling. This way, neither the sampled pathogens nor the genetically modified sensor cells can escape our biosensor unit. Moreover, the electronic components are in a separate compartment and inaccessible for the user, preventing electric shock or other injuries. For the detection, we are using one-time usage sampling and sensor chips which can be disposed of after autoclaving or irradation with strong UV light.

To detect P. aeruginosa cells, an sampling agar chip is slightly pressed against the solid surface to be tested. Afterwards, the sampling chip is immediately introduced into our measurement device and will not be removed until the detection is finished and the chips have be doused with disinfectant. The sensor chips must be handled in S1 environments only since they contain genetically modified E. coli. However, once introduced into the measurement device, the sensor chips, too, will not be removed before disinfection.

The living cells inside the measurement device are effectively killed after a detection by using desinfectants such as Bacillol. For this procedure, the drawer of the measurement device is opened and Bacillol is poured over the sampling and sensor chips. Afterwards, both chips can be autoclaved and be disposed of. The whole lining of the measurement device is build from plastic so that it can be disinfected easily. To simulate the worst case scenario, we did replica plating of some sensor chips. In three experiments, we got an arithmetic mean of five colonies which were picked up. We concluded that the risk of infection is still really low even if the measurement device and chips are not handled properly.