Rapid Detection of Urinary Tract Infections via Bacterial Nuclease Activity

被引:20
作者
Flenker, Katie S. [1 ]
Burghardt, Elliot L. [1 ]
Dutta, Nirmal [1 ]
Burns, William J. [1 ]
Grover, Julia M. [1 ]
Kenkel, Elizabeth J. [1 ]
Weaver, Tyler M. [2 ]
Mills, James [3 ]
Kim, Hyeon [4 ]
Huang, Lingyan [5 ]
Owczarzy, Richard
Musselman, Catherine A. [2 ]
Behlke, Mark A. [5 ]
Ford, Bradley [6 ]
McNamara, James O., II [1 ]
机构
[1] Univ Iowa, Dept Internal Med, Roy J & Lucille A Carver Coll Med, 285 Newton Rd,Room 3270C CBRB, Iowa City, IA 52242 USA
[2] Univ Iowa, Dept Biochem, Roy J & Lucille A Carver Coll Med, Iowa City, IA 52242 USA
[3] Univ Iowa, Dept Psychiat, Roy J & Lucille A Carver Coll Med, Iowa City, IA 52242 USA
[4] Univ Iowa, Univ Iowa Res Fdn, Iowa City, IA 52242 USA
[5] IDT, Coralville, IA 52241 USA
[6] Univ Iowa, Dept Pathol, Roy J & Lucille A Carver Coll Med, Iowa City, IA 52242 USA
基金
美国国家科学基金会;
关键词
ESCHERICHIA-COLI; DIAGNOSIS;
D O I
10.1016/j.ymthe.2017.03.015
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
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 bio-markers 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. coli and develop a rapid ultrasensitive assay that detects its activity. Comparison of nuclease activities of wild-type and nuclease-knockout E. coli clones revealed that endonuclease I is the predominant DNase in E. coli lysates. Endonudease I is detectable by immunoblot and activity assays in uropathogenic E. coli strains. 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 prairiding a means for expedited administration of appropriate antimicrobial therapy. We suggest this approach could address various unmet needs for rapid detection of E. coli.
引用
收藏
页码:1353 / 1362
页数:10
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