Ishii Satoshi, Kitamura Gaku, Segawa Takahiro, Kobayashi Ayano, Miura Takayuki, Sano Daisuke, Okabe Satoshi
Division of Environmental Engineering, Faculty of Engineering, Hokkaido University, Sapporo, Hokkaido, Japan
Division of Environmental Engineering, Faculty of Engineering, Hokkaido University, Sapporo, Hokkaido, Japan.
Appl Environ Microbiol. 2014 Dec;80(24):7505-11. doi: 10.1128/AEM.02578-14. Epub 2014 Sep 26.
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.
为确保食品和水安全,获取多种病原体的定量信息至关重要。在本研究中,我们开发了一种微流控定量PCR(MFQPCR)系统,用于同时定量11种主要的人类病毒病原体,包括腺病毒、爱知病毒、星状病毒、肠道病毒、人诺如病毒、轮状病毒、札幌病毒以及甲型和戊型肝炎病毒。在我们的MFQPCR系统中,还分别将小鼠诺如病毒和脑心肌炎病毒作为样本处理对照和内部扩增对照进行了定量。收集了受日本札幌市一家污水处理厂废水污染的河水,用于验证我们的MFQPCR系统对多种病毒的检测能力。该系统获得了高通量定量信息,定量限为2拷贝/μl的cDNA/DNA。使用该MFQPCR系统,我们能够同时定量环境水样中的多种病毒病原体。使用MFQPCR获得的病毒量与传统定量PCR测定的结果相似。因此,本研究开发的MFQPCR系统可为病毒病原体提供直接的定量信息,这对风险评估至关重要。