scholarly journals Development of a Quantitative PCR Method to Differentiate Between Viable and Non-Viable Bacteria in Environmental Water Samples

2007 ◽  
Vol 2007 (13) ◽  
pp. 5064-5078
Author(s):  
Phillip B. Gedalanga ◽  
Betty H. Olson
2018 ◽  
Vol 33 (3) ◽  
pp. 309-316 ◽  
Author(s):  
Rajani Ghaju Shrestha ◽  
Yasuhiro Tanaka ◽  
Bikash Malla ◽  
Sarmila Tandukar ◽  
Dinesh Bhandari ◽  
...  

2015 ◽  
Vol 81 (9) ◽  
pp. 3077-3085 ◽  
Author(s):  
Rupert Bliem ◽  
Sonja Schauer ◽  
Helga Plicka ◽  
Adelheid Obwaller ◽  
Regina Sommer ◽  
...  

ABSTRACTVibrio choleraeis a severe human pathogen and a frequent member of aquatic ecosystems. Quantification ofV. choleraein environmental water samples is therefore fundamental for ecological studies and health risk assessment. Beside time-consuming cultivation techniques, quantitative PCR (qPCR) has the potential to provide reliable quantitative data and offers the opportunity to quantify multiple targets simultaneously. A novel triplex qPCR strategy was developed in order to simultaneously quantify toxigenic and nontoxigenicV. choleraein environmental water samples. To obtain quality-controlled PCR results, an internal amplification control was included. The qPCR assay was specific, highly sensitive, and quantitative across the tested 5-log dynamic range down to a method detection limit of 5 copies per reaction. Repeatability and reproducibility were high for all three tested target genes. For environmental application, global DNA recovery (GR) rates were assessed for drinking water, river water, and water from different lakes. GR rates ranged from 1.6% to 76.4% and were dependent on the environmental background. Uncorrected and GR-correctedV. choleraeabundances were determined in two lakes with extremely high turbidity. Uncorrected abundances ranged from 4.6 × 102to 2.3 × 104cell equivalents liter−1, whereas GR-corrected abundances ranged from 4.7 × 103to 1.6 × 106cell equivalents liter−1. GR-corrected qPCR results were in good agreement with an independent cell-based direct detection method but were up to 1.6 log higher than cultivation-based abundances. We recommend the newly developed triplex qPCR strategy as a powerful tool to simultaneously quantify toxigenic and nontoxigenicV. choleraein various aquatic environments for ecological studies as well as for risk assessment programs.


2014 ◽  
Vol 80 (24) ◽  
pp. 7505-7511 ◽  
Author(s):  
Satoshi Ishii ◽  
Gaku Kitamura ◽  
Takahiro Segawa ◽  
Ayano Kobayashi ◽  
Takayuki Miura ◽  
...  

ABSTRACTTo secure food and water safety, quantitative information on multiple pathogens is important. In this study, we developed a microfluidic quantitative PCR (MFQPCR) system to simultaneously quantify 11 major human viral pathogens, including adenovirus, Aichi virus, astrovirus, enterovirus, human norovirus, rotavirus, sapovirus, and hepatitis A and E viruses. Murine norovirus and mengovirus were also quantified in our MFQPCR system as a sample processing control and an internal amplification control, respectively. River water contaminated with effluents from a wastewater treatment plant in Sapporo, Japan, was collected and used to validate our MFQPCR system for multiple viruses. High-throughput quantitative information was obtained with a quantification limit of 2 copies/μl of cDNA/DNA. Using this MFQPCR system, we could simultaneously quantify multiple viral pathogens in environmental water samples. The viral quantities obtained using MFQPCR were similar to those determined by conventional quantitative PCR. Thus, the MFQPCR system developed in this study can provide direct and quantitative information for viral pathogens, which is essential for risk assessments.


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