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J Virol Methods . Assessment of Two Volumetrically Different Concentration Approaches to Improve Sensitivities for SARS-CoV-2 Detection During Waste

tetano

Editor, Senior Moderator
J Virol Methods


. 2022 Nov 1;311:114645.
doi: 10.1016/j.jviromet.2022.114645. Online ahead of print.
Assessment of Two Volumetrically Different Concentration Approaches to Improve Sensitivities for SARS-CoV-2 Detection During Wastewater Monitoring


Brian R McMinn[SUP] 1 [/SUP], Asja Korajkic[SUP] 2 [/SUP], Adin C Pemberton[SUP] 2 [/SUP], Julie Kelleher[SUP] 2 [/SUP], Warish Ahmed[SUP] 3 [/SUP], Eric N Villegas[SUP] 2 [/SUP], Kevin Oshima[SUP] 2 [/SUP]



Affiliations
Free PMC article

Abstract

Wastewater monitoring for severe acute respiratory syndrome coronavirus type 2 (SARS-CoV-2), the virus responsible for the global coronavirus disease 2019 (COVID-19) pandemic, has highlighted the need for methodologies capable of assessing viral prevalence during periods of low population infection. To address this need, two volumetrically different, methodologically similar concentration approaches were compared for their abilities to detect viral nucleic acid and infectious SARS-CoV-2 signal from primary influent samples. For Method 1, 2L of SARS-CoV-2 seeded wastewater was evaluated using a dead-end hollow fiber ultrafilter (D-HFUF) for primary concentration, followed by the CP Select™ for secondary concentration. For Method 2, 100mL of SARS-CoV-2 seeded wastewater was evaluated using the CP Select™ procedure. Following D-HFUF concentration (Method 1), significantly lower levels of infectious SARS-CoV-2 were lost (P value range: 0.0398 to 0.0027) compared to viral gene copy (GC) levels detected by the US Centers for Disease Control (CDC) N1 and N2 reverse-transcriptase quantitative polymerase chain reaction (RT-qPCR) assays. Subsamples at different steps in the concentration process were also taken to better characterize the losses of SARS-CoV-2 during the concentration process. During the centrifugation step (prior to CP Select™ concentration), significantly higher losses (P value range: 0.0003 to <0.0001) occurred for SARS-CoV-2 GC levels compared to infectious virus for Method 1, while between the methods, significantly higher infectious viral losses were observed for Method 2 (P = 0.0002). When analyzing overall recovery of endogenous SARS-CoV-2 in wastewater samples, application of Method 1 improved assay sensitivities (P= <0.0001) compared with Method 2; this was especially evident during periods of lower COVID-19 case rates within the sewershed. This study describes a method which can successfully concentrate infectious SARS-CoV-2 and viral RNA from wastewater. Moreover, we demonstrated that large volume wastewater concentration provides additional sensitivity needed to improve SARS-CoV-2 detection, especially during low levels of community disease prevalence.

Keywords: Environmental Sampling; Large Volume; SARS-CoV-2; Ultrafiltration; Wastewater; qPCR.
 
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