Team:Calgary
From 2013.igem.org
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Our Project
Outbreaks of foodborne illnesses are a growing problem in our lives. In 2011, the Centers for Disease Control and Prevention (CDC) in the United States, identified 767 outbreaks of foodborne illnesses affecting nearly 14,000 people. Pathogenic E. coli was a recurring theme in many of these outbreaks. We recently experienced a foodborne disease outbreak here in Alberta in late 2012. This outbreak was the result of pathogenic E. coli serotype O157 and led to significant food recall alongside many hospitalizations, deaths, massive economic losses and an overall loss of consumer confidence in food safety. The current detection methods have long wait times due to the long incubation times needed to amplify E. coli in the sample which are followed by amplification to verify the presence of genes known to be associated with pathogenic E. coli
One of the contributing factors connected with the outbreak in Alberta was the lack of a rapid on-site detection system. Thus, the University of Calgary 2013 iGEM Collegiate team is using synthetic biology to develop a system to rapidly detect the presence of pathogenic E. coli in the beef industry. By using engineered biological nanoparticles and DNA binding proteins we can specifically detect pathogenic DNA sequences. Our biosensor functions at the genomic level to detect the presence or absence of pathogenic E. coli in a sample. This system allows us to pinpoint contamination during meat processing and also provides the ability to prescreen cattle to help prevent outbreaks by limiting potential sources of contamination in the processing chain. Our system provides a powerful new tool for food safety, but also shows promise as a platform for the rapid detection of target organisms that are identified as key targets in a myriad of sectors from health to environment to biosecurity.
Our Sensor
We are using DNA binding proteins called Transcription Activator Like Effectors (TALEs) to detect pathogenic E. coli DNA. The TALEs are modular, stable and bind the DNA of interest with high affinity. To show that TALEs are specific we made proof of concept TALEs ADD LINK. We also designed TALEs for E. coli. For more information about design of TALEs click here
Data Page
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Human Practices
To better inform the design and execution of our system we talked to people who would be using these systems. With lower sensitivity but quicker turnaround times we wanted to find out if our system would add any value to the current methods and where it would fit in the meat processing chain. To accomplish this goal we we met a rancher, a meat factory employee and ???. To find out more click here.
Collaboration
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