Abstract

We determined the disinfection efficiency of chlorine and chlorine dioxide (ClO 2) using murine norovirus (MNV) and coliphage MS2 as surrogates for human norovirus. Experiments were performed in oxidant demand-free buffer (pH 7.2) at 5 °C and 20 °C. The extent of virus inactivation by a disinfectant was quantified using three different analytical methods: plaque, short template real-time TaqMan reverse transcriptase-polymerase chain reaction (RT-PCR), and long template RT-PCR assays. Rapid inactivation of MNV by both chlorine and chlorine dioxide was observed by the plaque assay. According to the efficiency factor Hom model, Ct values of 0.314 mg/L min and 0.247 mg/L min were required for a 4-log reduction of MNV at 5 °C by chlorine and chlorine dioxide, respectively. Lower Ct values were required at 20 °C. Both long template and short template RT-PCR assays significantly underestimated the virus inactivation compared to the plaque assay. Our study demonstrates that adequate treatment of water with either chlorine or ClO 2 is likely to effectively control the waterborne transmission of human norovirus.

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