Systematic detection of co-infection and intra-host recombination in more than 2 million global SARS-CoV-2 samples

被引:18
作者
Pipek, Orsolya Anna [1 ]
Medgyes-Horvath, Anna [1 ]
Steger, Jozsef [1 ]
Papp, Krisztian [1 ]
Visontai, David [1 ]
Koopmans, Marion [2 ]
Nieuwenhuijse, David [2 ]
Munnink, Bas B. Oude [2 ]
Csabai, Istvan
机构
[1] Eotvos Lorand Univ, Dept Phys Complex Syst, Pazmany Ps 1A, H-1117 Budapest, Hungary
[2] Erasmus MC, Dept Virosci, Rotterdam, Netherlands
基金
欧盟地平线“2020”;
关键词
CORONAVIRUS; GENERATION; RNA;
D O I
10.1038/s41467-023-43391-z
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Systematic monitoring of SARS-CoV-2 co-infections between different lineages and assessing the risk of intra-host recombinant emergence are crucial for forecasting viral evolution. Here we present a comprehensive analysis of more than 2 million SARS-CoV-2 raw read datasets submitted to the European COVID-19 Data Portal to identify co-infections and intra-host recombination. Co-infection was observed in 0.35% of the investigated cases. Two independent procedures were implemented to detect intra-host recombination. We show that sensitivity is predominantly determined by the density of lineage-defining mutations along the genome, thus we used an expanded list of mutually exclusive defining mutations of specific variant combinations to increase statistical power. We call attention to multiple challenges rendering recombinant detection difficult and provide guidelines for the reduction of false positives arising from chimeric sequences produced during PCR amplification. Additionally, we identify three recombination hotspots of Delta - Omicron BA.1 intra-host recombinants.
引用
收藏
页数:13
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