Welcome to Columbia's iGEM 2018!
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Chlamydia and gonorrhea are the two most common sexually transmitted bacterial infections in the world., They are caused by the bacteria Chlamydia trachomatis and Neisseria gonorrhoeae, respectively, affecting millions of people each year. Current methods of detection require the presence of substantial medical resources, as well as a medical professional with the expertise to administer the test. Our proposed detection system can be used in any location, requires no expertise to read, is easily transportable, can be used at one’s own discretion, and is affordable enough for nonprofessional purchase. This makes it especially appealing for those who travel frequently, live in underserved communities, and live in areas that are far away from medical resources. In order to contribute to the effort against these infections, we set out to develop a novel diagnostic test for C. trachomatis and N. gonorrhoeae based on the CRISPR-Cas system. We selected these two pathogens because they are often diagnosed concurrently. Cas13a1 and Cas12a The cas proteins Cas12a and Cas13a1, also known as Cpf1 and C2c2, respectively, have been characterized in recent years., In their natural state, they work by detecting particular sequences of dsDNA and ssRNA, respectively, using CRISPR-RNA, or crRNA. Once these sequences have been detected, the cas proteins engage in promiscuous collateral cleavage of ssDNA and ssRNA, respectively, which we will detect using various methods. The Zhang Lab at the Broad Institute has developed a system called SHERLOCK (Specific High Sensitivity Enzymatic Reporter UnLOCKing), which detects collateral cleavage of RNA due to CRISPR-Cas13a., Upon recognizing and cleaving target RNA sequences of the invading pathogen, Cas13a collaterally cleaves other RNA sequences including a modified RNA oligonucleotide tagged with a fluorophore and a quencher substructure. Once cleaved, a fluorescent signal is produced, indicating that the target RNA was detected. Our team wanted to harness this CRISPR-Cas system to detect Chlamydia trachomatis and Neisseria gonorrhoeae. For each pathogen, we selected genes that were unique to the pathogen to prevent false positives. For Chlamydia trachomatis we chose the ompA gene, which codes for the major outer membrane protein, a “key antigen” of the organism. According to the NIH application BLAST, the ompA gene contains a unique sequence found exclusively in many, if not all, strains of Chlamydia trachomatis. For Neisseria gonorrhoeae we chose the gene porA, which produces porin protein. WHO Guidelines for the Treatment of Chlamydia Trachomatis. World Health Organization, 2016. WHO Guidelines for the Treatment of Neisseria Gonorrhoeae. World Health Organization, 2016. Zetsche, Bernd, et al. "Cpf1 Is a Single RNA-Guided Endonuclease of a Class 2 CRISPR-Cas System." Cell, vol. 163, no. 3, 22 Oct. 2015, pp. 759-71. makov, Sergey, et al. "Discovery and Functional Characterization of Diverse Class 2 CRISPR-Cas Systems." Molecular Cell, vol. 60, no. 3, 5 Nov. 2015, pp. 385-97. Gootenberg, Jonathan S., et al. “Multiplexed and Portable Nucleic Acid Detection Platform with Cas13, Cas12a, and Csm6.” Science, vol. 360, no. 6387, 2018, pp. 439–444. Gootenberg, Jonathan S., et al. “Nucleic Acid Detection with CRISPR-Cas13a/C2c2.” Science, vol. 356, no. 6336, 2017, pp. 438–442. Sashital, Dipali G. “Pathogen Detection in the CRISPR–Cas Era.” Genome Medicine, vol. 10, no. 1, 2018. Nunes, A., et al. “Evolutionary Dynamics of OmpA, the Gene Encoding the Chlamydia Trachomatis Key Antigen.” Journal of Bacteriology, vol. 191, no. 23, 2009, pp. 7182–7192.
Before you start
Please read the following pages:
Styling your wiki
You may style this page as you like or you can simply leave the style as it is. You can easily keep the styling and edit the content of these default wiki pages with your project information and completely fulfill the requirement to document your project.
While you may not win Best Wiki with this styling, your team is still eligible for all other awards. This default wiki meets the requirements, it improves navigability and ease of use for visitors, and you should not feel it is necessary to style beyond what has been provided.
Uploading pictures and files
You must upload any pictures and files to the iGEM 2018 server. Remember to keep all your pictures and files within your team's namespace or at least include your team's name in the file name.
When you upload, set the "Destination Filename" to T--YourOfficialTeamName--NameOfFile.jpg. (If you don't do this, someone else might upload a different file with the same "Destination Filename", and your file would be erased!)
Wiki template information
We have created these wiki template pages to help you get started and to help you think about how your team will be evaluated. You can find a list of all the pages tied to awards here at the Pages for awards link. You must edit these pages to be evaluated for medals and awards, but ultimately the design, layout, style and all other elements of your team wiki is up to you!
Editing your wiki
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!
Use WikiTools - Edit in the black menu bar to edit this page
This wiki will be your team’s first interaction with the rest of the world, so here are a few tips to help you get started:
- State your accomplishments! Tell people what you have achieved from the start.
- Be clear about what you are doing and how you plan to do this.
- You have a global audience! Consider the different backgrounds that your users come from.
- Make sure information is easy to find; nothing should be more than 3 clicks away.
- Avoid using very small fonts and low contrast colors; information should be easy to read.
- Start documenting your project as early as possible; don’t leave anything to the last minute before the Wiki Freeze. For a complete list of deadlines visit the iGEM 2018 calendar
- Have lots of fun!