This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowReprints and Permissions
Right arrow Copyright Information
Right arrow Books from ASM Press
Right arrow MicrobeWorld
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Shin, G.-A.
Right arrow Articles by Sobsey, M. D.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Shin, G.-A.
Right arrow Articles by Sobsey, M. D.
Agricola
Right arrow Articles by Shin, G.-A.
Right arrow Articles by Sobsey, M. D.

 Previous Article  |  Next Article 

Applied and Environmental Microbiology, July 2003, p. 3975-3978, Vol. 69, No. 7
0099-2240/03/$08.00+0     DOI: 10.1128/AEM.69.7.3975-3978.2003
Copyright © 2003, American Society for Microbiology. All Rights Reserved.

Reduction of Norwalk Virus, Poliovirus 1, and Bacteriophage MS2 by Ozone Disinfection of Water

Gwy-Am Shin* and Mark D. Sobsey

Department of Environmental Sciences and Engineering, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina 27599-7400

Received 2 October 2002/ Accepted 7 April 2003

Norwalk virus and other human caliciviruses (noroviruses) are major agents of gastroenteritis, and water is a major route of their transmission. In an effort to control Norwalk virus in drinking water, Norwalk virus reduction by bench-scale ozone disinfection was determined using quantitative reverse transcription (RT)-PCR for virus assays. Two other enteric viruses, poliovirus 1 and coliphage MS2, were included for comparison, and their reductions were assayed by infectivity assays as well as by RT-PCR. Virus reductions by ozone were determined using a dose of 0.37 mg of ozone/liter at pH 7 and 5°C for up to 5 min. Based on two RT-PCR assays, the reductions of Norwalk virus were >3 log10 within a contact time of 10 s, and these were similar to the reductions of the other two viruses determined by the same assay methods. Also, the virus reductions detected by RT-PCR assays were similar to those detected by infectivity assays, indicating that the RT-PCR assay is a reliable surrogate assay for both culturable and nonculturable viruses disinfected with ozone. Overall, the results of this study indicate that Norwalk virus as well as other enteric viruses can be reduced rapidly and extensively by ozone disinfection and that RT-PCR is a useful surrogate assay for both culturable and nonculturable viruses disinfected with ozone.


* Corresponding author. Mailing address: Department of Environmental Sciences and Engineering, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599-7431. Phone: (919) 966-7316. Fax: (919) 966-4711. E-mail: gwyam{at}isis.unc.edu.


Applied and Environmental Microbiology, July 2003, p. 3975-3978, Vol. 69, No. 7
0099-2240/03/$08.00+0     DOI: 10.1128/AEM.69.7.3975-3978.2003
Copyright © 2003, American Society for Microbiology. All Rights Reserved.




This article has been cited by other articles:

  • Pecson, B. M., Martin, L. V., Kohn, T. (2009). Quantitative PCR for Determining the Infectivity of Bacteriophage MS2 upon Inactivation by Heat, UV-B Radiation, and Singlet Oxygen: Advantages and Limitations of an Enzymatic Treatment To Reduce False-Positive Results. Appl. Environ. Microbiol. 75: 5544-5554 [Abstract] [Full Text]  
  • Aw, T. G., Gin, K. Y.-H., Ean Oon, L. L., Chen, E. X., Woo, C. H. (2009). Prevalence and Genotypes of Human Noroviruses in Tropical Urban Surface Waters and Clinical Samples in Singapore. Appl. Environ. Microbiol. 75: 4984-4992 [Abstract] [Full Text]  
  • Rodriguez, R. A., Pepper, I. L., Gerba, C. P. (2009). Application of PCR-Based Methods To Assess the Infectivity of Enteric Viruses in Environmental Samples. Appl. Environ. Microbiol. 75: 297-307 [Full Text]  
  • Bae, J., Schwab, K. J. (2008). Evaluation of Murine Norovirus, Feline Calicivirus, Poliovirus, and MS2 as Surrogates for Human Norovirus in a Model of Viral Persistence in Surface Water and Groundwater. Appl. Environ. Microbiol. 74: 477-484 [Abstract] [Full Text]  
  • Park, G. W., Boston, D. M., Kase, J. A., Sampson, M. N., Sobsey, M. D. (2007). Evaluation of Liquid- and Fog-Based Application of Sterilox Hypochlorous Acid Solution for Surface Inactivation of Human Norovirus. Appl. Environ. Microbiol. 73: 4463-4468 [Abstract] [Full Text]  
  • BURTON, N. C., GRINSHPUN, S. A., REPONEN, T. (2007). Physical Collection Efficiency of Filter Materials for Bacteria and Viruses. ANN OCCUP HYG 51: 143-151 [Abstract] [Full Text]  
  • Simonet, J., Gantzer, C. (2006). Inactivation of Poliovirus 1 and F-Specific RNA Phages and Degradation of Their Genomes by UV Irradiation at 254 Nanometers. Appl. Environ. Microbiol. 72: 7671-7677 [Abstract] [Full Text]  
  • O'Connell, K. P., Bucher, J. R., Anderson, P. E., Cao, C. J., Khan, A. S., Gostomski, M. V., Valdes, J. J. (2006). Real-Time Fluorogenic Reverse Transcription-PCR Assays for Detection of Bacteriophage MS2. Appl. Environ. Microbiol. 72: 478-483 [Abstract] [Full Text]  
  • Dreier, J., Stormer, M., Kleesiek, K. (2005). Use of Bacteriophage MS2 as an Internal Control in Viral Reverse Transcription-PCR Assays. J. Clin. Microbiol. 43: 4551-4557 [Abstract] [Full Text]