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Rapid Detection of Urinary Tract Infections via Bacterial Nuclease Activity

Authors :
Flenker, Katie S.
Burghardt, Elliot L.
Dutta, Nirmal
Burns, William J.
Grover, Julia M.
Kenkel, Elizabeth J.
Weaver, Tyler M.
Mills, James
Kim, Hyeon
Huang, Lingyan
Owczarzy, Richard
Musselman, Catherine A.
Behlke, Mark A.
Ford, Bradley
McNamara, James O.
Source :
Molecular Therapy; June 2017, Vol. 25 Issue: 6 p1353-1362, 10p
Publication Year :
2017

Abstract

Rapid and accurate bacterial detection methods are needed for clinical diagnostic, water, and food testing applications. The wide diversity of bacterial nucleases provides a rich source of enzymes that could be exploited as signal amplifying biomarkers to enable rapid, selective detection of bacterial species. With the exception of the use of micrococcal nuclease activity to detect Staphylococcus aureus, rapid methods that detect bacterial pathogens via their nuclease activities have not been developed. Here, we identify endonuclease I as a robust biomarker for E. coliand develop a rapid ultrasensitive assay that detects its activity. Comparison of nuclease activities of wild-type and nuclease-knockout E. coliclones revealed that endonuclease I is the predominant DNase in E. colilysates. Endonuclease I is detectable by immunoblot and activity assays in uropathogenic E. colistrains. A rapid assay that detects endonuclease I activity in patient urine with an oligonucleotide probe exhibited substantially higher sensitivity for urinary tract infections than that reported for rapid urinalysis methods. The 3 hr turnaround time is much shorter than that of culture-based methods, thereby providing a means for expedited administration of appropriate antimicrobial therapy. We suggest this approach could address various unmet needs for rapid detection of E. coli.

Details

Language :
English
ISSN :
15250016 and 15250024
Volume :
25
Issue :
6
Database :
Supplemental Index
Journal :
Molecular Therapy
Publication Type :
Periodical
Accession number :
ejs41632179
Full Text :
https://doi.org/10.1016/j.ymthe.2017.03.015