Detection of viable bacterial pathogens in a drinking water source using propidium monoazide-quantitative PCR
Author:
Affiliation:
1. NSERC Chair in Water Treatment, Department of Civil and Environmental Engineering, University of Waterloo, 200 University Avenue West, Waterloo, Ontario, Canada N2L 3G1
Publisher
IWA Publishing
Subject
Health, Toxicology and Mutagenesis,Water Science and Technology,Environmental Engineering
Link
http://iwaponline.com/aqua/article-pdf/64/2/139/400087/jws0640139.pdf
Reference47 articles.
1. Long-amplicon propidium monoazide-PCR enumeration assay to detect viable Campylobacter and Salmonella;Banihashemi;J. Appl. Microbiol.,2012
2. Kinetics of enzymatic hydrolysis of DNA in sea water;Bazelyan;Oceanology,1979
3. Cryptosporidium propidium monoazide-PCR, a molecular biology-based technique for genotyping of viable Cryptosporidium oocysts;Brescia;Appl. Environ. Microbiol.,2009
4. Development of a multiplex and real time PCR assay for the specific detection of Arcobacter butzleri and Arcobacter cryaerophilus;Brightwell;J. Microbiol. Methods,2007
5. Selective PCR detection of viable Enterobacter sakazakii cells utilizing propidium monoazide or ethidium bromide monoazide;Cawthorn;J. Appl. Microbiol.,2008
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