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Instructions

Student presentations must have a faculty sponsor.

Abstracts must include a title and a description of the research, scholarship, or creative work. The description should be 150-225 words in length and constructed in a format or style appropriate for the presenter’s discipline.

The following points should be addressed within the selected format or style for the abstract:

  • A clear statement of the problem or question you pursued, or the scholarly goal or creative theme achieved in your work.
  • A brief comment about the significance or uniqueness of the work.
  • A clear description of the methods used to achieve the purpose or goals for the work.
  • A statement of the conclusions, results, outcomes, or recommendations, or if the work is still in progress, the results you expect to report at the event.

Presenter photographs should be head and shoulder shots comparable to passport photos.

Additional Information

More information is available at carthage.edu/celebration-scholars/. The following are members of the Research, Scholarship, and Creativity Committee who are eager to listen to ideas and answer questions:

  • Jun Wang
  • Kim Instenes
  • John Kirk
  • Nora Nickels
  • Andrew Pustina
  • James Ripley

#31: Tool Development for Detection of Potato Virus Y

Name: Vanessa Gonzalez
Major: Biology
Hometown: Crystal Lake, IL
Faculty Sponsor:
Other Sponsors:  
Type of research: SURE
Funding: SURE

Abstract

More than a billion people worldwide eat potatoes, and it is the third most important food crop in the world. There are a host of different viruses that affect potatoes. The most prevalent virus affecting potatoes in all regions of the world is potato virus Y (PVY). A potato plant infected with PVY is hard to identify because this cannot be detected through appearance. Current detection methods are time-consuming, and obtaining a high viral load takes a long time. This project worked towards the development of a detection method for PVY infection that would be faster and would enable real-time detection by linking green fluorescent protein (GFP) to viral enzymatic activity. Previous research indicated greater space was needed between GFP and a quenching peptide to allow for cleavage. This research involved generating a construct of a six glycine linker to allow the potential for cleavage. Testing of this construct is ongoing. 


Poster file

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