Dynamics of SARS-CoV-2 Alpha (B.1.1.7) variant spread: The wastewater surveillance approach

• Published in: Environmental research 2022-05, Vol.208, p.112720-112720, Article 112720
• Main Authors: Carcereny, Albert, Garcia-Pedemonte, David, Martínez-Velázquez, Adán, Quer, Josep, Garcia-Cehic, Damir, Gregori, Josep, Antón, Andrés, Andrés, Cristina, Pumarola, Tomàs, Chacón-Villanueva, Carme, Borrego, Carles M., Bosch, Albert, Guix, Susana, Pintó, Rosa M.
• Format: Article
• Language: English
• Subjects: Alpha VOC; COVID-19 - epidemiology; Humans; NGS; Outcompetition rate; SARS-CoV-2 - genetics; Variant of concern; Wastewater; Wastewater-Based Epidemiological Monitoring; Wastewater-based epidemiology
• ISSN: 0013-9351; 1096-0953; 1096-0953
• DOI: 10.1016/j.envres.2022.112720

Wastewater based epidemiology (WBE) offers an overview of the SARS-CoV-2 variants circulating among the population thereby serving as a proper surveillance method. The variant of concern (VOC) Alpha was first identified in September 2020 in the United Kingdom, and rapidly became dominant across Europe. Our objective was to elucidate the Alpha VOC outcompetition rate and identify mutations in the spike glycoprotein (S) gene, indicative of the circulation of the Alpha VOC and/or other variants in the population through wastewater analysis. In the period covered by this study (November 2020–April 2021), forteen wastewater treatment plants (WWTPs) were weekly sampled. The total number of SARS-CoV-2 genome copies per L (GC/L) was determined with a Real-Time qPCR, targeting the N gene. Surveillance of the Alpha VOC circulation was ascertained using a duplex RT-qPCR, targeting and discriminating the S gene. Our results showed that in a period of 6 weeks the Alpha VOC was present in all the studied WWTPs, and became dominant in 11 weeks on average. The outcompetition rates of the Alpha VOC were estimated, and their relationship with different parameters statistically analyzed. The rapid spread of the Alpha VOC was influenced by its initial input and by the previous circulation of SARS-COV-2 in the population. This latter point could be explained by its higher transmissibility, particularly advantadgeous when a certain degree of herd immunity exists. Moreover, the presence of signature mutations of SARS-COV-2 variants were established by deep-sequencing of the complete S gene. The circulation of the Alpha VOC in the area under study was confirmed, and additionally two combinations of mutations in the S glycoprotein (T73A and D253N, and S477N and A522S) that could affect antibody binding were identified. [Display omitted]