Team:GeorgiaTech/Project

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You <strong>MUST</strong> have a team description page, a project abstract, a complete project description, a lab notebook, and a safety page.  PLEASE keep all of your pages within your teams namespace. 
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{|align="justify"
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|You can write a background of your team here.  Give us a background of your team, the members, etc.  Or tell us more about something of your choosing.
 
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|[[Image:GeorgiaTech_logo.png|200px|right|frame]]
 
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''Tell us more about your project.  Give us background.  Use this is the abstract of your project. Be descriptive but concise (1-2 paragraphs)''
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;Purpose
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|[[Image:GeorgiaTech_team.png|right|frame|Your team picture]]
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:As a research team, our goals are two fold: to mobilize the crispr/cas bacterial immune system on a plasmid, and subsequently utilize this system as an intelligent gene targeting method capable of eliminating antibiotic resistance.
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|align="center"|[[Team:GeorgiaTech | Team Example]]
 
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<!--- The Mission, Experiments --->
 
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== '''Overall project''' ==
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!align="center"|[[Team:GeorgiaTech|Home]]
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!align="center"|[[Team:GeorgiaTech/Team|Team]]
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!align="center"|[https://igem.org/Team.cgi?year=2010&team_name=GeorgiaTech Official Team Profile]
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!align="center"|[[Team:GeorgiaTech/Project|Project]]
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!align="center"|[[Team:GeorgiaTech/Parts|Parts Submitted to the Registry]]
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!align="center"|[[Team:GeorgiaTech/Modeling|Modeling]]
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!align="center"|[[Team:GeorgiaTech/Notebook|Notebook]]
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* Overuse of antibiotics in medical settings has created the problem of multidrug resistant bacteria, also called “super bugs,” which result from exchange of antibiotic resistance genes between bacteria by the process of horizontal gene transfer of plasmids. The experiment outlined in this proposal intends to engineer a unique method of “reverse” vaccination in which a plasmid (foreign DNA) containing an antibiotic resistance gene is specifically targeted and destroyed, rendering the bacteria susceptible to antibiotic treatment. The novel method we are developing utilizes a recently discover bacterial immune system called the CRISPR system (Clustered Regularly Interspaced Short Palindromic Repeats) which we intend to engineer onto a separate plasmid to inactivate the foreign DNA[1].
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* The CRISPR system is a type of immunity predicted to be present in 40% of bacteria and about 90% of archaea [3]. It consists of a series of proteins, called Cas proteins, which are associated with a series of “spacers” separated by short palindromic sequences, that recognize foreign DNA (either plasmid or viral). '''''If foreign DNA is recognized, the cell proceeses the invading DNA. If the DNA is not recognized and the cell survives the infection, it then “saves” pieces of the foreign DNA in subsequent spacers, to be used in future recognition of an attack.'''
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* We will be creating a shuttle vector carrying the CRISPR system and use this plasmid-encoded CRISPR system to deliver this engineered immune system into bacteria. Our research aims to demonstrate that antibiotic resistance genes can be targeted with our engineered CRISPR plasmid in diverse bacterial species, rendering the bacteria more susceptible to antibiotic treatment. Specifically, a kanamycin (kanR) resistant plasmid will be targeted by our CRISPR plasmid that has been engineered to carry a kanR plasmid spacer. In addition, we intend to develop computer modeling approaches to be used for understanding CRISPR spacer uptake. Ultimately, new ways for targeting antibiotic resistance will be realized, helping to spark further research and innovation in this subject and CRISPR systems with real world applications.
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== '''Overall project''' ==
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References:
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Overuse of antibiotics in medical settings has created the problem of extremely antibiotic resistant bacteria, also called “super bugs,” which develop through the process of horizontal gene transfer of plasmids. The experiment outlined in this proposal intends to engineer a unique method of “reverse” vaccination in which the plasmid containing antibiotic resistance genes is specifically targeted and destroyed, rendering the bacteria vulnerable to antibiotic treatment. The novel method we are developing utilizes a CRISPR system (Clustered Regularly Interspaced Short Palindromic Repeats) contained on a separate plasmid to inactivate the foreign DNA.
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[1] Babu, M., N. Beloglazova, et al. A dual function of the CRISPR–Cas system in bacterial antivirus immunity and DNA repair (2011). Molecular Microbiology 79(2): 484-502.
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The CRISPR system is a type of immunity used by about 40% of Bacteria and about 90% of Archaea. It consists of a series of proteins, called cas proteins, which are associated with series “spacers” separated by short palindromic sequences, that recognize foreign DNA (either plasmid or viral). If foreign DNA is recognized, the cell chops up the invading DNA. If the DNA is not recognized and the cell survives the infection, it then ‘saves’ pieces of the foreign DNA in subsequent spacers, to be used in future recognition of an attack (Figure 1)
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[[File:741px-Crispr.png]]
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[2] Horvath P., Barrangou R., CRISPR/Cas, the immune system of bacteria and archaea (2010). Science, 327(5962), 167-170.
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[3] Barrangou, R., C. Fremaux, et al. CRISPR provides acquired resistance against viruses in prokaryotes (2007). Science, 315 (5819), 1709-1712
== Project Details==
== Project Details==
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=== The Experiments ===
=== The Experiments ===
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Using a modified CRISPR system that is delivered via a viral or plasmid vector, our research aims to demonstrate that antibiotic resistance genes can be targeted with the CRISPR system in multiple bacterial species, rendering the bacteria more susceptible to treatment. More specifically, artificial kanamycin resistance in a non-pathogenic S. thermophilus  DGCC7710  strain will be targeted by using a CRISPR system that has a kanamycin resistance plasmid spacer. In addition, our hope is to develop computer modeling approaches to be used for understanding CRISPR spacer uptake, which is not currently well known.  It is hoped with this research that new ways for targeting antibiotic resistance will be realized, helping to spark further research and innovation in this subject and CRISPR systems with real world applications.
 
=== Part 3 ===
=== Part 3 ===

Latest revision as of 08:11, 15 August 2011

Purpose
As a research team, our goals are two fold: to mobilize the crispr/cas bacterial immune system on a plasmid, and subsequently utilize this system as an intelligent gene targeting method capable of eliminating antibiotic resistance.


Contents

Overall project

  • Overuse of antibiotics in medical settings has created the problem of multidrug resistant bacteria, also called “super bugs,” which result from exchange of antibiotic resistance genes between bacteria by the process of horizontal gene transfer of plasmids. The experiment outlined in this proposal intends to engineer a unique method of “reverse” vaccination in which a plasmid (foreign DNA) containing an antibiotic resistance gene is specifically targeted and destroyed, rendering the bacteria susceptible to antibiotic treatment. The novel method we are developing utilizes a recently discover bacterial immune system called the CRISPR system (Clustered Regularly Interspaced Short Palindromic Repeats) which we intend to engineer onto a separate plasmid to inactivate the foreign DNA[1].
  • The CRISPR system is a type of immunity predicted to be present in 40% of bacteria and about 90% of archaea [3]. It consists of a series of proteins, called Cas proteins, which are associated with a series of “spacers” separated by short palindromic sequences, that recognize foreign DNA (either plasmid or viral). If foreign DNA is recognized, the cell proceeses the invading DNA. If the DNA is not recognized and the cell survives the infection, it then “saves” pieces of the foreign DNA in subsequent spacers, to be used in future recognition of an attack.

  • We will be creating a shuttle vector carrying the CRISPR system and use this plasmid-encoded CRISPR system to deliver this engineered immune system into bacteria. Our research aims to demonstrate that antibiotic resistance genes can be targeted with our engineered CRISPR plasmid in diverse bacterial species, rendering the bacteria more susceptible to antibiotic treatment. Specifically, a kanamycin (kanR) resistant plasmid will be targeted by our CRISPR plasmid that has been engineered to carry a kanR plasmid spacer. In addition, we intend to develop computer modeling approaches to be used for understanding CRISPR spacer uptake. Ultimately, new ways for targeting antibiotic resistance will be realized, helping to spark further research and innovation in this subject and CRISPR systems with real world applications.


References:

[1] Babu, M., N. Beloglazova, et al. A dual function of the CRISPR–Cas system in bacterial antivirus immunity and DNA repair (2011). Molecular Microbiology 79(2): 484-502.

[2] Horvath P., Barrangou R., CRISPR/Cas, the immune system of bacteria and archaea (2010). Science, 327(5962), 167-170.

[3] Barrangou, R., C. Fremaux, et al. CRISPR provides acquired resistance against viruses in prokaryotes (2007). Science, 315 (5819), 1709-1712

Project Details

Part 2

The Experiments

Part 3

Results