Skip to main content
Log in

Bayesian Modeling of Enteric Virus Density in Wastewater Using Left-Censored Data

  • Original Paper
  • Published:
Food and Environmental Virology Aims and scope Submit manuscript

Abstract

Stochastic models are used to express pathogen density in environmental samples for performing microbial risk assessment with quantitative uncertainty. However, enteric virus density in water often falls below the quantification limit (non-detect) of the analytical methods employed, and it is always difficult to apply stochastic models to a dataset with a substantially high number of non-detects, i.e., left-censored data. We applied a Bayesian model that is able to model both the detected data (detects) and non-detects to simulated left-censored datasets of enteric virus density in wastewater. One hundred paired datasets were generated for each of the 39 combinations of a sample size and the number of detects, in which three sample sizes (12, 24, and 48) and the number of detects from 1 to 12, 24 and 48 were employed. The simulated observation data were assigned to one of two groups, i.e., detects and non-detects, by setting values on the limit of quantification to obtain the assumed number of detects for creating censored datasets. Then, the Bayesian model was applied to the censored datasets, and the estimated mean and standard deviation were compared to the true values by root mean square deviation. The difference between the true distribution and posterior predictive distribution was evaluated by Kullback–Leibler (KL) divergence, and it was found that the estimation accuracy was strongly affected by the number of detects. It is difficult to describe universal criteria to decide which level of accuracy is enough, but eight or more detects are required to accurately estimate the posterior predictive distributions when the sample size is 12, 24, or 48. The posterior predictive distribution of virus removal efficiency with a wastewater treatment unit process was obtained as the log ratio posterior distributions between the posterior predictive distributions of enteric viruses in untreated wastewater and treated wastewater. The KL divergence between the true distribution and posterior predictive distribution of virus removal efficiency also depends on the number of detects, and eight or more detects in a dataset of treated wastewater are required for its accurate estimation.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3
Fig. 4

Similar content being viewed by others

References

  • Bosch, A., Guix, S., Sano, D., & Pinto, R. M. (2008). New tools for the study and direct surveillance of viral pathogens in water. Current Opinion in Biotechnology, 19(3), 295–301.

    Article  PubMed  CAS  Google Scholar 

  • Crainiceanu, C. M., Stedinger, J. R., Ruppert, D., & Behr, C. T. (2003). Modeling the U.S. national distribution of waterborne pathogen concentrations with application to Cryptosporidium parvum. Water Resources Research, 39(9), 1235–1249.

    Article  Google Scholar 

  • da Silva, A. K., Le Guyader, F. S., Le Saux, J.-C., Pommepuy, M., Montgomery, M. A., & Elimelech, M. (2008). Norovirus removal and particle association in a waste stabilization pond. Environmental Science and Technology, 42(24), 9151–9157.

    Article  PubMed  Google Scholar 

  • Dorevitch, S., Pratap, P., Wroblewski, M., Hryhorczuk, D. O., Li, H., Liu, L. C., et al. (2012). Health risks of limited-contact water recreation. Environmental Health Perspectives, 120(2), 192–197.

    Article  PubMed  Google Scholar 

  • Emelko, M. B., Schmidt, P. J., & Reilly, P. M. (2010). Particle and microorganism enumeration data: Enabling quantitative rigor and judicious interpretation. Environmental Science and Technology, 44(5), 1720–1727.

    Article  PubMed  CAS  Google Scholar 

  • European Food Safety Authority (2010). Management of left-censored data in dietary exposure assessment of chemical substances. EFSA Journal, 8(3), 1557.

    Google Scholar 

  • Haas, C. N., Rose, J. B., & Gerba, C. P. (1999). Quantitative microbial risk assessment. New York: Wiley.

    Google Scholar 

  • Haramoto, E., Katayama, H., Oguma, K., & Ohgaki, S. (2007). Quantitative analysis of human enteric adenoviruses in aquatic environments. Journal of Applied Microbiology, 103(6), 2153–2159.

    Article  PubMed  CAS  Google Scholar 

  • Helsel, D. R. (2006). Fabricating data: How substituting values for nondetects can ruin results, and what can be done about it. Chemosphere, 65, 2434–2439.

    Article  PubMed  CAS  Google Scholar 

  • Kennedy, M. C. (2010). Bayesian modeling of long-term dietary intakes from multiple sources. Food and Chemical Toxicology, 48, 250–263.

    Article  PubMed  CAS  Google Scholar 

  • Kennedy, M., & Hart, A. (2009). Bayesian modeling of measurement errors and pesticide concentration in dietary risk assessments. Risk Analysis, 29(10), 1427–1442.

    Article  PubMed  Google Scholar 

  • Morales-Morales, H. A., Vidal, G., Olszewski, J., Rock, C. M., Dasgupta, D., Oshima, K. H., et al. (2003). Optimization of a reusable hollow-fiber ultrafilter for simultaneous concentration of enteric bacteria, protozoa, and viruses from water. Applied and Environmental Microbiology, 69(7), 4098–4102.

    Article  PubMed  CAS  Google Scholar 

  • Paulo, M. J., van der Voet, H., Jansen, M. J. W., ter Braak, C. J. F., & van Klaveren, J. D. (2005). Risk assessment of dietary exposure to pesticides using a Bayesian method. Pest Management Science, 61, 759–766.

    Article  PubMed  CAS  Google Scholar 

  • Perez-Sautu, U., Sano, D., Guix, S., Georg, K., Pinto, R. M., & Bosch, A. (2012). Human norovirus occurence and diversity in the Llobregat river catchment, Spain. Environmental Microbiology, 14(2), 494–502.

    Article  PubMed  CAS  Google Scholar 

  • Petterson, S. R., Signor, R. S., & Ashbolt, N. J. (2007). Incorporating method recovery uncertainties in stochastic estimates of raw water protozoan concentrations for QMRA. Journal of Water and Health, 5(S1), 51–65.

    Article  PubMed  Google Scholar 

  • Rutjes, S. A., van den Berg, H. H. J. L., Lodder, W. J., & de Roda Husman, A. M. (2006). Real-time detection of noroviruses in surface water by use of a broadly reactive nucleic acid sequence-based amplification assay. Applied and Environmental Microbiology, 72(8), 5349–5358.

    Article  PubMed  CAS  Google Scholar 

  • Sano, D., Perez, U., Guix, S., Pinto, R. M., Miura, T., Okabe, S., et al. (2011). Quantification and genotyping of human sapoviruses in the Llobregat River catchment, Spain. Applied and Environmental Microbiology, 77(3), 1111–1114.

    Article  PubMed  CAS  Google Scholar 

  • Schijven, J. F., Teunis, P. F. M., Rutjes, S. A., Bouwknegt, M., & de Roda Husman, A. M. (2011). QMRAspot: A tool for quantitative microbioal risk assessment from surface water to potable water. Water Research, 45(17), 5564–6676.

    Article  PubMed  CAS  Google Scholar 

  • Schmidt, P. J., Emelko, M. B., & Reilly, P. M. (2010). Quantification of analytical recovery in particle and microorganism enumeration methods. Environmental Science and Technology, 44(5), 1705–1712.

    Article  PubMed  CAS  Google Scholar 

  • Shuval, H. (2003). Estimating the global burden of thalassogenic diseases: Human infectious diseases caused by wastewater pollution of the marine environment. Journal of Water and Health, 1(2), 53–64.

    PubMed  Google Scholar 

  • Smeets, P. W. M. H., Dullemont, Y. J., van Gelder, P. H. A. J. M., van Dijk, J. C., & Medema, G. J. (2008). Improved methods for modelling drinking water treatment in quantitative microbial risk assessment: A case study of Campylobacter reduction by filtration and ozonation. Journal of Water and Health, 6(3), 301–314.

    Article  PubMed  CAS  Google Scholar 

  • Smeets, P. W. M. H., van Dijk, J. C., Stanfield, G., Rietveld, L. C., & Medema, G. J. (2007). How can the UK statutory Cryptosporidium monitoring be used for quantitative risk assessment of Cryptosporidium in drinking water? Journal of Water and Health, 5(S1), 107–118.

    Article  PubMed  Google Scholar 

  • Soller, J. A., Schoen, M. E., Bartrand, T., Ravenscroft, J. E., & Ashbolt, N. J. (2010). Estimated human health risks from exposure to recreational waters impacted by human and non-human sources of faecal contamination. Water Research, 44(16), 4674–4691.

    Article  PubMed  CAS  Google Scholar 

  • Tanaka, H., Asano, T., Schroeder, E. D., & Tchobanoglous, G. (1998). Estimating the safety of wastewater reclamation and reuse enteric virus monitoring data. Water Environment Research, 70(1), 39–51.

    Article  CAS  Google Scholar 

  • Teunis, P. F. M., Xu, M., Freming, K. K., Yang, J., Moe, C. L., & Lechevallier, M. W. (2010). Enteric virus infection risk from intrusion of sewage into a drinking water distribution network. Environmental Science and Technology, 44(22), 8561–8566.

    Article  PubMed  CAS  Google Scholar 

  • World Health Organization. (2011). Guidelines for drinking-water quality. Geneva: World Health Organization.

    Google Scholar 

Download references

Acknowledgments

This study was supported by the Japan Science and Technology Agency through a Grant-in-Aid for Core Research for Evolutionary Science and Technology (CREST), and the Japan Society for the Promotion of Science through Grant-in-Aid for Young Scientist (A) (22686049) and Scientific Research (A) (24246089).

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Daisuke Sano.

Electronic supplementary material

Below is the link to the electronic supplementary material.

Supplementary material 1 (PDF 6345 kb)

Rights and permissions

Reprints and permissions

About this article

Cite this article

Kato, T., Miura, T., Okabe, S. et al. Bayesian Modeling of Enteric Virus Density in Wastewater Using Left-Censored Data. Food Environ Virol 5, 185–193 (2013). https://doi.org/10.1007/s12560-013-9125-1

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s12560-013-9125-1

Keywords

Navigation