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

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.

[1]  Michiel J W Jansen,et al.  Risk assessment of dietary exposure to pesticides using a Bayesian method. , 2005, Pest management science.

[2]  J. Rose,et al.  Quantitative Microbial Risk Assessment , 1999 .

[3]  Marc C Kennedy,et al.  Bayesian modelling of long-term dietary intakes from multiple sources. , 2010, Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association.

[4]  Mark W. LeChevallier,et al.  Enteric virus infection risk from intrusion of sewage into a drinking water distribution network. , 2010, Environmental science & technology.

[5]  D. Hryhorczuk,et al.  Health Risks of Limited-Contact Water Recreation , 2011, Environmental health perspectives.

[6]  D. Sano,et al.  New tools for the study and direct surveillance of viral pathogens in water , 2008, Current Opinion in Biotechnology.

[7]  D. Sano,et al.  Quantification and Genotyping of Human Sapoviruses in the Llobregat River Catchment, Spain , 2010, Applied and Environmental Microbiology.

[8]  S. Rutjes,et al.  Real-Time Detection of Noroviruses in Surface Water by Use of a Broadly Reactive Nucleic Acid Sequence-Based Amplification Assay , 2006, Applied and Environmental Microbiology.

[9]  Jery R. Stedinger,et al.  Modeling the U.S. national distribution of waterborne pathogen concentrations with application to Cryptosporidium parvum , 2003 .

[10]  Dennis R Helsel,et al.  Fabricating data: how substituting values for nondetects can ruin results, and what can be done about it. , 2006, Chemosphere.

[11]  P. Reilly,et al.  Quantification of analytical recovery in particle and microorganism enumeration methods. , 2010, Environmental science & technology.

[12]  L C Rietveld,et al.  How can the UK statutory Cryptosporidium monitoring be used for Quantitative Risk Assessment of Cryptosporidium in drinking water? , 2007, Journal of water and health.

[13]  Timothy Bartrand,et al.  Estimated human health risks from exposure to recreational waters impacted by human and non-human sources of faecal contamination. , 2010, Water research.

[14]  J. R.,et al.  Quantitative analysis , 1892, Nature.

[15]  Hiroaki Tanaka,et al.  Estimating the safety of wastewater reclamation and reuse using enteric virus monitoring data , 1998 .

[16]  Channah M. Rock,et al.  Optimization of a Reusable Hollow-Fiber Ultrafilter for Simultaneous Concentration of Enteric Bacteria, Protozoa, and Viruses from Water , 2003, Applied and Environmental Microbiology.

[17]  Andy Hart,et al.  Bayesian Modeling of Measurement Errors and Pesticide Concentration in Dietary Risk Assessments , 2009, Risk analysis : an official publication of the Society for Risk Analysis.

[18]  P. van Gelder,et al.  Improved methods for modelling drinking water treatment in quantitative microbial risk assessment; a case study of Campylobacter reduction by filtration and ozonation. , 2008, Journal of water and health.

[19]  Nicholas J Ashbolt,et al.  Incorporating method recovery uncertainties in stochastic estimates of raw water protozoan concentrations for QMRA. , 2007, Journal of water and health.

[20]  G. Ozolins,et al.  WHO guidelines for drinking-water quality. , 1984, WHO chronicle.

[21]  K. Oguma,et al.  Quantitative analysis of human enteric adenoviruses in aquatic environments , 2007, Journal of applied microbiology.

[22]  Jack F Schijven,et al.  QMRAspot: a tool for Quantitative Microbial Risk Assessment from surface water to potable water. , 2011, Water research.

[23]  M. Elimelech,et al.  Norovirus removal and particle association in a waste stabilization pond. , 2008, Environmental science & technology.

[24]  Monica B. Emelko,et al.  Particle and microorganism enumeration data: enabling quantitative rigor and judicious interpretation. , 2010, Environmental science & technology.

[25]  D. Sano,et al.  Human norovirus occurrence and diversity in the Llobregat river catchment, Spain. , 2012, Environmental microbiology.

[26]  Hillel Shuval,et al.  Estimating the global burden of thalassogenic diseases: human infectious diseases caused by wastewater pollution of the marine environment. , 2003, Journal of water and health.