TY - JOUR
T1 - Microfluidic quantitative PCR for simultaneous quantification of multiple viruses in environmental water samples
AU - Ishii, Satoshi
AU - Kitamura, Gaku
AU - Segawa, Takahiro
AU - Kobayashi, Ayano
AU - Miura, Takayuki
AU - Sano, Daisuke
AU - Okabe, Satoshi
N1 - Publisher Copyright:
© 2014, American Society for Microbiology.
PY - 2014
Y1 - 2014
N2 - To 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.
AB - To 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.
UR - http://www.scopus.com/inward/record.url?scp=84917709066&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84917709066&partnerID=8YFLogxK
U2 - 10.1128/AEM.02578-14
DO - 10.1128/AEM.02578-14
M3 - Article
C2 - 25261510
AN - SCOPUS:84917709066
SN - 0099-2240
VL - 80
SP - 7505
EP - 7511
JO - Applied and environmental microbiology
JF - Applied and environmental microbiology
IS - 24
ER -