Systematic surveillance of SARS-CoV-2 reveals dynamics of variant mutagenesis and transmission in a large urban population

M.-M. Aynaud, L. Caldwell, K. Al-Zahrani, S. Barutcu, K. Chan, A. Obersterescu, A. Ogunjimi, M. jin, K.-R. Zakoor, S. Patel, R. padilla, M. Jen, P. Mae, N. Dewsi, F. Yonathan, L. Zhang, A. Ayson-Fortunato, A. Aquino, P. Krzyzanowski, J. T. Simpson, J. Bartlett, I. Lungu, S. Poutanen, B. Wouters, M. Gekas, J. Rini, L. Pelletier, T. Mazzulli, J. L. Wrana
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Abstract

Highly mutable pathogens generate viral diversity that impacts virulence, transmissibility, treatment, and thwarts acquired immunity. We previously described C19-SPAR-Seq, a high-throughput, next-generation sequencing platform to detect SARS-CoV-2 that we deployed to systematically profile variant dynamics of SARS-CoV-2 for over 3 years in a large, North American urban environment (Toronto, Canada). Sequencing of the ACE2 receptor binding motif and polybasic furin cleavage site of Spike in over 70,000 patients revealed that population sweeps of canonical variants of concern (VOCs) occurred in repeating wavelets. Furthermore, we found that subvariants and putative quasi-species with alterations characteristic of future VOCs and/or predicted to be functionally important arose frequently, but always extinguished. Systematic screening of functionally relevant domains in pathogens could thus provide a powerful tool for monitoring spread and mutational trajectories, particularly those with zoonotic potential.
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对 SARS-CoV-2 的系统监控揭示了变异诱变和在大型城市人群中传播的动态过程
高度变异的病原体会产生病毒多样性,从而影响病毒的毒性、传播性、治疗和后天免疫。我们曾介绍过 C19-SPAR-Seq,这是一种用于检测 SARS-CoV-2 的高通量新一代测序平台,我们利用该平台在北美大型城市环境(加拿大多伦多)中对 SARS-CoV-2 的变异动态进行了 3 年多的系统分析。对 7 万多名患者中 Spike 的 ACE2 受体结合基序和多碱性呋喃裂解位点进行测序后发现,相关典型变异体 (VOC) 在人群中以重复小波的形式出现。此外,我们还发现,具有未来 VOCs 特征改变和/或预测具有重要功能改变的亚变异体和准变异体经常出现,但总是消失。因此,对病原体中的功能相关域进行系统筛选可为监测传播和变异轨迹,尤其是那些具有人畜共患病潜能的病原体提供有力的工具。
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