| Literature DB >> 35303559 |
Elena Radu1, Amandine Masseron2, Fabian Amman3, Anna Schedl3, Benedikt Agerer3, Lukas Endler3, Thomas Penz3, Christoph Bock3, Andreas Bergthaler3, Julia Vierheilig2, Peter Hufnagl4, Irina Korschineck5, Jörg Krampe2, Norbert Kreuzinger6.
Abstract
Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) gave rise to an international public health emergency in 3 months after its emergence in Wuhan, China. Typically for an RNA virus, random mutations occur constantly leading to new lineages, incidental with a higher transmissibility. The highly infective alpha lineage, firstly discovered in the UK, led to elevated mortality and morbidity rates as a consequence of Covid-19, worldwide. Wastewater surveillance proved to be a powerful tool for early detection and subsequent monitoring of the dynamics of SARS-CoV-2 and its variants in a defined catchment. Using a combination of sequencing and RT-qPCR approaches, we investigated the total SARS-CoV-2 concentration and the emergence of the alpha lineage in wastewater samples in Vienna, Austria linking it to clinical data. Based on a non-linear regression model and occurrence of signature mutations, we conclude that the alpha variant was present in Vienna sewage samples already in December 2020, even one month before the first clinical case was officially confirmed and reported by the health authorities. This provides evidence that a well-designed wastewater monitoring approach can provide a fast snapshot and may detect the circulating lineages in wastewater weeks before they are detectable in the clinical samples. Furthermore, declining 14 days prevalence data with simultaneously increasing SARS-CoV-2 total concentration in wastewater indicate a different shedding behavior for the alpha variant. Overall, our results support wastewater surveillance to be a suitable approach to spot early circulating SARS-CoV-2 lineages based on whole genome sequencing and signature mutations analysis.Entities:
Keywords: Alpha lineage; SARS-CoV-2 dynamics; Signature mutations; WBE (Wastewater Based Epidemiology); epidemiological data; whole genome sequencing
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Year: 2022 PMID: 35303559 PMCID: PMC8898540 DOI: 10.1016/j.watres.2022.118257
Source DB: PubMed Journal: Water Res ISSN: 0043-1354 Impact factor: 13.400
Fig. 1Total SARS-CoV-2 concentration per ml per day load calculated to the active cases, in wastewater samples (brown smooth data line); Alpha lineage percentage in wastewater samples (non-linear regression model based on a dynamic fitting curve - Rsqr = 0.9876 - dashed red line and WGS data – red dots) and active clinical cases per 100,000 inhabitants (blue area). Period considered: October 2020 - May 2021.
Fig. 2Schematic representation (smooth data) of the 14 days incidence per 100,000 inhabitants (x-axis) and SARS-CoV-2 GC in wastewater per active case (y-axis) during the study period; lockdowns and openings are marked on the graph. Three important periods are outlined: at the beginning of the study (squares) when the SARS-CoV-2 GC remain rather constant but the 14 days incidence fluctuates; the second period highlighted by the boost of SARS-CoV-2 shedding per person in wastewater (bullets) during the 3rd lockdown and 14 days incidence continues to decline; last part of the study, when the viral shedding per person stays rather constant again but active cases increase (triangles).
Fig. 3Graphical representation of all mutations observed in the wastewater from Vienna until May 2021, which are detected in at least six samples, in at least 3 consecutive timepoints, and with an allele frequency of at least 0.3 in at least one sample. The top annotation bar depicts the assigned pangolin lineage of the consensus sequence of the respective sample. The annotation on the righthand side depicts the observed mutation and a categorization if this mutation is a marker for alpha (if present in at least 90% of all genomes from GISAID as of May 20th, 2021 with the lineage assignment alpha). Mutations which are found to be markers exclusive for alpha are denoted as “specific”. If the marker is also associated with other lineages, it is denoted as “unspecific”.
Fig. 4Percentage of alpha lineage and N501Y mutation in clinical (black line and scatter) and wastewater (gray area) samples retrieved from WGS data and non-linear regression model describing a dynamic fitting curve based on 3-parameter function to estimate the date when the variant emerged in Vienna sewage samples.