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1.
Sci Total Environ ; 851(Pt 2): 158350, 2022 Dec 10.
Article in English | MEDLINE | ID: covidwho-2004490

ABSTRACT

Wastewater-based epidemiology (WBE) has been suggested as a useful tool to predict the emergence and investigate the extent of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). In this study, we screened appropriate population biomarkers for wastewater SARS-CoV-2 normalization and compared the normalized SARS-CoV-2 values across locations with different demographic characteristics in southeastern Michigan. Wastewater samples were collected between December 2020 and October 2021 from nine neighborhood sewersheds in the Detroit Tri-County area. Using reverse transcriptase droplet digital polymerase chain reaction (RT-ddPCR), concentrations of N1 and N2 genes in the studied sites were quantified, with N1 values ranging from 1.92 × 102 genomic copies/L to 6.87 × 103 gc/L and N2 values ranging from 1.91 × 102 gc/L to 6.45 × 103 gc/L. The strongest correlations were observed with between cumulative COVID-19 cases per capita (referred as COVID-19 incidences thereafter), and SARS-CoV-2 concentrations normalized by total Kjeldahl nitrogen (TKN), creatinine, 5-hydroxyindoleacetic acid (5-HIAA) and xanthine when correlating the per capita SARS-CoV-2 and COVID-19 incidences. When SARS-CoV-2 concentrations in wastewater were normalized and compared with COVID-19 incidences, the differences between neighborhoods of varying demographics were reduced as compared to differences observed when comparing non-normalized SARS-CoV-2 with COVID-19 cases. This indicates when studying the disease burden in communities of different demographics, accurate per capita estimation is of great importance. The study suggests that monitoring selected water quality parameters or biomarkers, along with RNA concentrations in wastewater, will allow adequate data normalization for spatial comparisons, especially in areas where detailed sanitary sewage flows and contributing populations in the catchment areas are not available. This opens the possibility of using WBE to assess community infections in rural areas or the developing world where the contributing population of a sample could be unknown.


Subject(s)
COVID-19 , SARS-CoV-2 , Sewage , Humans , COVID-19/epidemiology , Creatinine , Hydroxyindoleacetic Acid , Incidence , Nitrogen , RNA , SARS-CoV-2/isolation & purification , Sewage/virology , United States , Wastewater , Xanthines
2.
Sci Total Environ ; 844: 157040, 2022 Oct 20.
Article in English | MEDLINE | ID: covidwho-1907760

ABSTRACT

Wastewater-based epidemiology (WBE) is useful in predicting temporal fluctuations of COVID-19 incidence in communities and providing early warnings of pending outbreaks. To investigate the relationship between SARS-CoV-2 concentrations in wastewater and COVID-19 incidence in communities, a 12-month study between September 1, 2020, and August 31, 2021, prior to the Omicron surge, was conducted. 407 untreated wastewater samples were collected from the Great Lakes Water Authority (GLWA) in southeastern Michigan. N1 and N2 genes of SARS-CoV-2 were quantified using RT-ddPCR. Daily confirmed COVID-19 cases for the City of Detroit, and Wayne, Macomb, Oakland counties between September 1, 2020, and October 4, 2021, were collected from a public data source. The total concentrations of N1 and N2 genes ranged from 714.85 to 7145.98 gc/L and 820.47 to 6219.05 gc/L, respectively, which were strongly correlated with the 7-day moving average of total daily COVID-19 cases in the associated areas, after 5 weeks of the viral measurement. The results indicate a potential 5-week lag time of wastewater surveillance preceding COVID-19 incidence for the Detroit metropolitan area. Four statistical models were established to analyze the relationship between SARS-CoV-2 concentrations in wastewater and COVID-19 incidence in the study areas. Under a 5-week lag time scenario with both N1 and N2 genes, the autoregression model with seasonal patterns and vector autoregression model were more effective in predicting COVID-19 cases during the study period. To investigate the impact of flow parameters on the correlation, the original N1 and N2 gene concentrations were normalized by wastewater flow parameters. The statistical results indicated the optimum models were consistent for both normalized and non-normalized data. In addition, we discussed parameters that explain the observed lag time. Furthermore, we evaluated the impact of the omicron surge that followed, and the impact of different sampling methods on the estimation of lag time.


Subject(s)
COVID-19 , COVID-19/epidemiology , Humans , Michigan/epidemiology , SARS-CoV-2/genetics , Wastewater , Wastewater-Based Epidemiological Monitoring
4.
Journal of Environmental Engineering ; 147(8), 2021.
Article in English | ProQuest Central | ID: covidwho-1254130

ABSTRACT

This study focuses on using wastewater-based epidemiology to provide early warnings of the second COVID-19 wave in the Detroit metropolitan area of Michigan. SARS-CoV-2 RNA from untreated wastewater samples was compared to reported public health records. Untreated wastewater samples were collected from the Great Lakes Water Authority (GLWA) Water Resource Recovery Facility (WRRF), located in southeast Michigan, between August 6, 2020 and December 14, 2020. The WRRF receives wastewater from its service area via three main interceptors: the Detroit River Interceptor (DRI), the North Interceptor-East Arm (NIEA), and the Oakwood-Northwest-Wayne County Interceptor (ONWI). A total of 144 untreated wastewater samples were collected (45, 48, and 51 for ONWI, NIEA, and DRI, respectively) at the point of intake into the WRRF. Virus-selective sampling was conducted, and viruses were isolated from wastewater using electropositive NanoCeram column filters. For each sample, an average of 33 L of wastewater was passed through NanoCeram electropositive cartridge filters at an average rate of 11  L/min. Viruses were eluted and concentrated, and the SARS-CoV-2 RNA concentrations were quantified with RT-qPCR. SARS-CoV-2 RNA was detected in 98% of the samples, and measured concentrations were in the range of 4.45×104 to 5.30×106 genomic copies/L. Early warnings of COVID-19 peaks were observed approximately 4 weeks prior to reported publicly available clinical data.

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