Skip to Main Content
Frequently Asked Questions
Submit an ETD
Global Search Box
Need Help?
Keyword Search
Participating Institutions
Advanced Search
School Logo
Files
File List
ysu1198694566.pdf (835.6 KB)
ETD Abstract Container
Abstract Header
Development of a Rapid Fluorescence-Based Adenovirus Inactivation Assay
Author Info
Zapka, Carrie A.
Permalink:
http://rave.ohiolink.edu/etdc/view?acc_num=ysu1198694566
Abstract Details
Year and Degree
2007, Master of Science in Chemistry, Youngstown State University, Department of Chemistry.
Abstract
Screening of potential antiviral product prototypes is typically performed using The American Society for Testing and Materials (ASTM) method E1052 “Efficacy of Antimicrobial Agents against Viruses in Suspension.” Adenovirus (ADV) is a recommended test virus and demonstrates intermediate resistance to chemical inactivation. The procedures commonly employed to quantify infectious virus are median cell culture infective dose (CCID50) and the plaque assay (PA). The rate-limiting step in both of these procedures is the time needed to form observable cytopathic effect (CPE) in infected cells, which takes approximately 7 days for ADV. Virus inactivation studies were performed according to ASTM E1052 using the traditional PA method as well as an experimental fluorescence-based method utilizing a recombinant ADV (ADV-GFP) that cconstitutively expresses green fluorescent protein (GFP). Infective units were determined by counting the number of fluorescent green cells or plaques. The log
10
reduction (LR) values of virus inactivation were determined for several different concentrations of ethanol and hypochlorite using the traditional PA method and the ADV-GFP method. The LR values using the ADV-GFP method were similar, within +/- 0.5 log
10
, to the LRvalues obtained using the traditional PA method. The ADV-GFP method was shown to be an acceptable substitute yielding results in 2 days vs. 7 days for the traditional methods. In addition, A549 cells were stably transfected with a plasmid construct containing a GFP gene under control of the ADV early gene E2 promoter for the eventual use in a newly conceived assay for quantitating ADV infection.
Committee
Daryl Mincey (Advisor)
Pages
67 p.
Keywords
adenovirus
;
GFP
;
time-kill
;
antiviral
Recommended Citations
Refworks
EndNote
RIS
Mendeley
Citations
Zapka, C. A. (2007).
Development of a Rapid Fluorescence-Based Adenovirus Inactivation Assay
[Master's thesis, Youngstown State University]. OhioLINK Electronic Theses and Dissertations Center. http://rave.ohiolink.edu/etdc/view?acc_num=ysu1198694566
APA Style (7th edition)
Zapka, Carrie.
Development of a Rapid Fluorescence-Based Adenovirus Inactivation Assay.
2007. Youngstown State University, Master's thesis.
OhioLINK Electronic Theses and Dissertations Center
, http://rave.ohiolink.edu/etdc/view?acc_num=ysu1198694566.
MLA Style (8th edition)
Zapka, Carrie. "Development of a Rapid Fluorescence-Based Adenovirus Inactivation Assay." Master's thesis, Youngstown State University, 2007. http://rave.ohiolink.edu/etdc/view?acc_num=ysu1198694566
Chicago Manual of Style (17th edition)
Abstract Footer
Document number:
ysu1198694566
Download Count:
721
Copyright Info
© 2007, all rights reserved.
This open access ETD is published by Youngstown State University and OhioLINK.