TY - JOUR
T1 - Rise and fall of SARS-CoV-2 variants in Rotterdam
T2 - Comparison of wastewater and clinical surveillance
AU - Izquierdo-Lara, Ray W.
AU - Heijnen, Leo
AU - Oude Munnink, Bas B.
AU - Schapendonk, Claudia M.E.
AU - Elsinga, Goffe
AU - Langeveld, Jeroen
AU - Post, Johan
AU - Prasad, Divyae K.
AU - Carrizosa, Christian
AU - Been, Frederic
AU - van Beek, Janko
AU - Schilperoort, Remy
AU - Vriend, Rianne
AU - Fanoy, Ewout
AU - de Schepper, Evelien I.T.
AU - Sikkema, Reina S.
AU - Molenkamp, Richard
AU - Aarestrup, Frank M.
AU - Medema, Gertjan
AU - Koopmans, Marion P.G.
AU - de Graaf, Miranda
N1 - This work was supported by the European Union's H2020 grants VEO (grant no. 874735) and METASTAVA (grant no. 773830), the Dutch Research Council (NWO) under the 2018 Stevin award (Koopmans), the Erasmus MC Foundation and the Adessium Foundation.
PY - 2023
Y1 - 2023
N2 - Monitoring of SARS-CoV-2 in wastewater (WW) is a promising tool for epidemiological surveillance, correlating not only viral RNA levels with the infection dynamics within the population, but also to viral diversity. However, the complex mixture of viral lineages in WW samples makes tracking of specific variants or lineages circulating in the population a challenging task. We sequenced sewage samples of 9 WW-catchment areas within the city of Rotterdam, used specific signature mutations from individual SARS-CoV-2 lineages to estimate their relative abundances in WW and compared them against those observed in clinical genomic surveillance of infected individuals between September 2020 and December 2021. We showed that especially for dominant lineages, the median of the frequencies of signature mutations coincides with the occurrence of those lineages in Rotterdam's clinical genomic surveillance. This, along with digital droplet RT-PCR targeting signature mutations of specific variants of concern (VOCs), showed that several VOCs emerged, became dominant and were replaced by the next VOC in Rotterdam at different time points during the study. In addition, single nucleotide variant (SNV) analysis provided evidence that spatio-temporal clusters can also be discerned from WW samples. We were able to detect specific SNVs in sewage, including one resulting in the Q183H amino acid change in the Spike gene, that was not captured by clinical genomic surveillance. Our results highlight the potential use of WW samples for genomic surveillance, increasing the set of epidemiological tools to monitor SARS-CoV-2 diversity.
AB - Monitoring of SARS-CoV-2 in wastewater (WW) is a promising tool for epidemiological surveillance, correlating not only viral RNA levels with the infection dynamics within the population, but also to viral diversity. However, the complex mixture of viral lineages in WW samples makes tracking of specific variants or lineages circulating in the population a challenging task. We sequenced sewage samples of 9 WW-catchment areas within the city of Rotterdam, used specific signature mutations from individual SARS-CoV-2 lineages to estimate their relative abundances in WW and compared them against those observed in clinical genomic surveillance of infected individuals between September 2020 and December 2021. We showed that especially for dominant lineages, the median of the frequencies of signature mutations coincides with the occurrence of those lineages in Rotterdam's clinical genomic surveillance. This, along with digital droplet RT-PCR targeting signature mutations of specific variants of concern (VOCs), showed that several VOCs emerged, became dominant and were replaced by the next VOC in Rotterdam at different time points during the study. In addition, single nucleotide variant (SNV) analysis provided evidence that spatio-temporal clusters can also be discerned from WW samples. We were able to detect specific SNVs in sewage, including one resulting in the Q183H amino acid change in the Spike gene, that was not captured by clinical genomic surveillance. Our results highlight the potential use of WW samples for genomic surveillance, increasing the set of epidemiological tools to monitor SARS-CoV-2 diversity.
KW - SARS-CoV-2
KW - Wastewater genomic surveillance
KW - Next generation sequencing
KW - RT-ddPCR
KW - Single nucleotide variant
KW - Viral diversity
U2 - 10.1016/j.scitotenv.2023.162209
DO - 10.1016/j.scitotenv.2023.162209
M3 - Journal article
C2 - 36796689
SN - 0048-9697
VL - 873
JO - Science of the Total Environment
JF - Science of the Total Environment
M1 - 162209
ER -