Global analysis of more than 50,000 SARS-CoV-2 genomes reveals epistasis between eight viral genes

被引:42
作者
Zeng, Hong-Li [1 ,2 ,3 ]
Dichio, Vito [2 ,3 ,4 ,5 ]
Horta, Edwin Rodriguez [6 ]
Thorell, Kaisa [7 ,8 ]
Aurell, Erik [5 ]
机构
[1] Nanjing Univ Posts & Telecommun, Sch Sci, New Energy Technol Engn Lab Jiangsu Prov, Nanjing 210023, Peoples R China
[2] Royal Inst Technol, Nord Inst Theoret Phys, S-10691 Stockholm, Sweden
[3] Stockholm Univ, S-10691 Stockholm, Sweden
[4] Univ Trieste, Dept Phys, I-34151 Trieste, Italy
[5] AlbaNova Univ Ctr, Dept Computat Sci & Technol, S-10691 Stockholm, Sweden
[6] Univ Havana, Phys Fac, Dept Theoret Phys, Grp Complex Syst & Stat Phys, Havana 10400, Cuba
[7] Univ Gothenburg, Sahlgrenska Acad, Inst Biomed, Dept Infect Dis, S-40530 Gothenburg, Sweden
[8] Karolinska Inst, Dept Microbiol Cell & Tumor Biol, Ctr Translat Microbiome Res, S-17177 Stockholm, Sweden
基金
中国国家自然科学基金; 欧盟地平线“2020”;
关键词
SARS-CoV-2; epistasis; recombination; direct coupling analysis; DIRECT-COUPLING ANALYSIS; SEQUENCE ALIGNMENT; PROTEIN; RECOMBINATION; INFORMATION; LINKAGE;
D O I
10.1073/pnas.2012331117
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
Genome-wide epistasis analysis is a powerful tool to infer gene interactions, which can guide drug and vaccine development and lead to deeper understanding of microbial pathogenesis. We have considered all complete severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) genomes deposited in the Global Initiative on Sharing All Influenza Data (GISAID) repository until four different cutoff dates, and used direct coupling analysis together with an assumption of quasi-linkage equilibrium to infer epistatic contributions to fitness from polymorphic loci. We find eight interactions, of which three are between pairs where one locus lies in gene ORF3a, both loci holding nonsynonymous mutations. We also find interactions between two loci in gene nsp13, both holding nonsynonymous mutations, and four interactions involving one locus holding a synonymous mutation. Altogether, we infer interactions between loci in viral genes ORF3a and nsp2, nsp12, and nsp6, between ORF8 and nsp4, and between loci in genes nsp2, nsp13, and nsp14. The paper opens the prospect to use prominent epistatically linked pairs as a starting point to search for combinatorial weaknesses of recombinant viral pathogens.
引用
收藏
页码:31519 / 31526
页数:8
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