4.7 Article

Refining detection methods for emerging SARS-CoV-2 mutants in wastewater: A case study on the Omicron variants

Journal

SCIENCE OF THE TOTAL ENVIRONMENT
Volume 904, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.scitotenv.2023.166215

Keywords

SARS-CoV-2; Mutations; RT-qPCR; Wastewater surveillance; Omicron variants; Sequencing

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COVID-19 is a global public health threat caused by SARS-CoV-2. Wastewater surveillance is a useful tool in controlling the pandemic. With the emergence of new variants, modifications in primer/probe sequences are needed to improve detection methods in wastewater.
COVID-19 is an ongoing public health threat worldwide driven by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). Wastewater surveillance has emerged as a complementary tool to clinical surveillance to control the COVID-19 pandemic. With the emergence of new variants of SARS-CoV-2, accumulated mutations that occurred in the SARS-CoV-2 genome raise new challenges for RT-qPCR diagnosis used in wastewater surveillance. There is a pressing need to develop refined methods for modifying primer/probes to better detect these emerging variants in wastewater. Here, we exemplified this process by focusing on the Omicron variants, for which we have developed and validated a modified detection method. We first modified the primers/probe mismatches of three assays commonly used in wastewater surveillance according to in silico analysis results for the mutations of 882 sequences collected during the fifth-wave outbreak in Hong Kong, and then evaluated them alongside the seven original assays. The results showed that five of seven original assays had better sensitivity for detecting Omicron variants, with the limits of detection (LoDs) ranging from 1.53 to 2.76 copies/& mu;L. UCDC-N1 and Charite & PRIME;-E sets had poor performances, having LoDs higher than 10 copies/& mu;L and false-positive/false-negative results in wastewater testing, probably due to the mismatch and demonstrating the need for modification of primer/probe sequences. The modified assays exhibited higher sensitivity and specificity, along with better reproducibility in detecting 81 wastewater samples. In addition, the sequencing results of six wastewater samples by Illumina also validated the presence of mismatches in the primer/probe binding sites of the three assays. This study highlights the importance of re-configuration of the primer-probe sets and refinements for the sequences to ensure the diagnostic effectiveness of RT-qPCR detection.

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