The DOI matches its Crossref record; 35 of the 37 references it cites were found in a registry or an index.
The N501Y spike substitution enhances SARS-CoV-2 transmission
Open accessAbstract
Summary: Beginning in the summer of 2020, a variant of SARS-CoV-2, the cause of the COVID-19 pandemic, emerged in the United Kingdom (UK). This B.1.1.7 variant increased rapidly in prevalence among sequenced strains, attributed to an increase in infection and/or transmission efficiency. The UK variant has 19 nonsynonymous mutations across its viral genome including 8 substitutions or deletions in the spike protein, which interacts with cellular receptors to mediate infection and tropism. Here, using a reverse genetics approach, we show that, of the 8 individual spike protein substitutions, only N501Y exhibited consistent fitness gains for replication in the upper airway in the hamster model as well as primary human airway epithelial cells. The N501Y substitution recapitulated the phenotype of enhanced viral transmission seen with the combined 8 UK spike mutations, suggesting it is a major determinant responsible for increased transmission of this variant. Mechanistically, the N501Y substitution improved the affinity of the viral spike protein for cellular receptors. As suggested by its convergent evolution in Brazil and South Africa, our results indicate that N501Y substitution is a major adaptive spike mutation of major concern.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“N501Y increases ACE2 affinity 128,146,147 and increases virus replication in human upper-airway cells and in the upper respiratory tracts of hamsters 127”
From The biological and clinical significance of emerging SARS-CoV-2 variants (2021) · cites this paper as [127]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
A pneumonia outbreak associated with a new coronavirus of probable bat origin
Zhou, P., Yang, X.-L., Wang, X.-G., Hu, B., Zhang, L., Zhang, W., Si, H.-R., Zhu, Y., Li, B., Huang, C.-L., et al. (2020) · Nature · doi:10.1038/s41586-020-2012-7 · Cited by 21,969
Wan, Y., Shang, J., Graham, R., Baric, R. S., & Li, F. (2020) · Journal of Virology · doi:10.1128/jvi.00127-20 · Cited by 4,341
The New Statistics: Why and How
Cumming, G. (2014) · Psychological Science · doi:10.1177/0956797613504966 · Cited by 3,200 · cited 1×
“Thus, competition assays have been used for many studies of microbial fitness 19-22 including SARS-CoV-2 8 , due to their precision and reproducibility 23 .”
Huang, Y., Yang, C., Xu, X.-F., Xü, W., & Liu, S. (2020) · Acta Pharmacologica Sinica · doi:10.1038/s41401-020-0485-4 · Cited by 2,288
Starr, T. N., Greaney, A. J., Hilton, S. K., Ellis, D., Crawford, K. H. D., Dingens, A. S., Navarro, M. J., Bowen, J. E., Tortorici, M. A., Walls, A. C., et al. (2020) · Cell · doi:10.1016/j.cell.2020.08.012 · Cited by 1,956
Assessing transmissibility of SARS-CoV-2 lineage B.1.1.7 in England
The COVID-19 Genomics UK (COG-UK) consortium, Volz, E., Mishra, S., Chand, M., Barrett, J. C., Johnson, R., Geidelberg, L., Hinsley, W. R., Laydon, D. J., Dabrera, G., et al. (2021) · Nature · doi:10.1038/s41586-021-03470-x · Cited by 1,611
Spike mutation D614G alters SARS-CoV-2 fitness
Plante, J. A., Liu, Y., Liu, J., Xia, H., Johnson, B. A., Lokugamage, K. G., Zhang, X., Muruato, A. E., Zou, J., Fontes-Garfias, C. R., et al. (2021) · Nature · doi:10.1038/s41586-020-2895-3 · Cited by 1,558
Self-citationChan, J. F., Zhang, J., Yuan, S., Poon, V. K., Chan, C. C., Lee, A. C.-Y., Chan, W.-M., Fan, Z., Tsoi, H.-W., Wen, L., et al. (2020) · Clinical Infectious Diseases · doi:10.1093/cid/ciaa325 · Cited by 1,048
SARS-CoV-2 D614G variant exhibits efficient replication ex vivo and transmission in vivo
Hou, Y. J., Chiba, S., Halfmann, P., Ehre, C., Kuroda, M., Dinnon, K. H., Leist, S. R., Schäfer, A., Nakajima, N., Takahashi, K., et al. (2020) · Science · doi:10.1126/science.abe8499 · Cited by 900
Chen, R. E., Zhang, X., Case, J. B., Winkler, E. S., Liu, Y., VanBlargan, L. A., Liu, J., Errico, J. M., Xie, X., Suryadevara, N., et al. (2021) · Nature Medicine · doi:10.1038/s41591-021-01294-w · Cited by 881
Self-citation
Cited by
Sorted by citations
SARS-CoV-2 variant biology: immune escape, transmission and fitness
Carabelli, A. M., Peacock, T. P., Thorne, L., Harvey, W. T., Hughes, J., de Silva, T. I., Peacock, S. J., Barclay, W., de Silva, T. I., Towers, G. J., et al. (2023) · Nature Reviews Microbiology · doi:10.1038/s41579-022-00841-7 · Cited by 1,386
The biological and clinical significance of emerging SARS-CoV-2 variants
Tao, K., Tzou, P. L., Nouhin, J., Gupta, R. K., de Oliveira, T., Kosakovsky Pond, S. L., Fera, D., & Shafer, R. W. (2021) · Nature Reviews Genetics · doi:10.1038/s41576-021-00408-x · Cited by 1,009
Lamers, M. M., & Haagmans, B. L. (2022) · Nature Reviews Microbiology · doi:10.1038/s41579-022-00713-0 · Cited by 1,066
Attenuated fusogenicity and pathogenicity of SARS-CoV-2 Omicron variant
Suzuki, R., Yamasoba, D., Kimura, I., Wang, L., Kishimoto, M., Ito, J., Morioka, Y., Nao, N., Nasser, H., Uriu, K., et al. (2022) · Nature · doi:10.1038/s41586-022-04462-1 · Cited by 662
The origins of SARS-CoV-2: A critical review
Holmes, E. C., Goldstein, S. A., Rasmussen, A. L., Robertson, D. L., Crits‐Christoph, A., Wertheim, J. O., Anthony, S. J., Barclay, W., Boni, M. F., Doherty, P. C., et al. (2021) · Cell · doi:10.1016/j.cell.2021.08.017 · Cited by 553
Kurhade, C., Zou, J., Xia, H., Liu, M., Chang, H. C., Ren, P., Xie, X., & Shi, P. (2022) · Nature Medicine · doi:10.1038/s41591-022-02162-x · Cited by 409
Self-citationDelta spike P681R mutation enhances SARS-CoV-2 fitness over Alpha variant
Liu, Y., Liu, J., Johnson, B. A., Xia, H., Ku, Z., Schindewolf, C., Widen, S. G., An, Z., Weaver, S. C., Menachery, V. D., et al. (2022) · Cell Reports · doi:10.1016/j.celrep.2022.110829 · Cited by 409
Self-citationRecurrent emergence of SARS-CoV-2 spike deletion H69/V70 and its role in the Alpha variant B.1.1.7
Meng, B., Kemp, S. A., Papa, G., Datir, R. P., Ferreira, I. A. T. M., Marelli, S., Harvey, W. T., Lytras, S., Mohamed, A., Gallo, G., et al. (2021) · Cell Reports · doi:10.1016/j.celrep.2021.109292 · Cited by 407
BNT162b2-elicited neutralization of B.1.617 and other SARS-CoV-2 variants
Liu, J., Liu, Y., Xia, H., Zou, J., Weaver, S. C., Swanson, K. A., Cai, H., Cutler, M., Cooper, D., Muik, A., et al. (2021) · Nature · doi:10.1038/s41586-021-03693-y · Cited by 342
Self-citationRapid assessment of SARS-CoV-2–evolved variants using virus-like particles
Syed, A. M., Taha, T. Y., Tabata, T., Chen, I. P., Ciling, A., Khalid, M. M., Sreekumar, B. K. N., Chen, P., Hayashi, J. M., Soczek, K. M., et al. (2021) · Science · doi:10.1126/science.abl6184 · Cited by 324
Shifting mutational constraints in the SARS-CoV-2 receptor-binding domain during viral evolution
Starr, T. N., Greaney, A. J., Hannon, W. W., Loes, A. N., Hauser, K., Dillen, J. R., Ferri, E., Farrell, A. G., Dadonaite, B., McCallum, M., et al. (2022) · Science · doi:10.1126/science.abo7896 · Cited by 298
Characterization and antiviral susceptibility of SARS-CoV-2 Omicron BA.2
Uraki, R., Kiso, M., Iida, S., Imai, M., Takashita, E., Kuroda, M., Halfmann, P., Loeber, S. J., Maemura, T., Yamayoshi, S., et al. (2022) · Nature · doi:10.1038/s41586-022-04856-1 · Cited by 281
Self-citationNucleocapsid mutations R203K/G204R increase the infectivity, fitness, and virulence of SARS-CoV-2
Wu, H., Xing, N., Meng, K., Fu, B., Xue, W., Dong, P., Tang, W., Xiao, Y., Liu, G., Luo, H., et al. (2021) · Cell Host & Microbe · doi:10.1016/j.chom.2021.11.005 · Cited by 229
Ou, J., Lan, W., Wu, X., Zhao, T., Duan, B., Yang, P., Ren, Y., Quan, L., Zhao, W., Seto, D., et al. (2022) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-022-00992-2 · Cited by 211
Increased immune escape of the new SARS-CoV-2 variant of concern Omicron
Hu, J., Peng, P., Cao, X., Wu, K., Chen, J., Wang, K., Tang, N., & Huang, A.-L. (2022) · Cellular & Molecular Immunology · doi:10.1038/s41423-021-00836-z · Cited by 204
COVID-19: Unmasking Emerging SARS-CoV-2 Variants, Vaccines and Therapeutic Strategies
Raman, R., Patel, K. J., & Ranjan, K. (2021) · Biomolecules · doi:10.3390/biom11070993 · Cited by 194
SARS‐CoV‐2 Alpha, Beta, and Delta variants display enhanced Spike‐mediated syncytia formation
Rajah, M. M., Hubert, M., Bishop, E., Saunders, N., Robinot, R., Grzelak, L., Planas, D., Dufloo, J., Gellenoncourt, S., Bongers, A., et al. (2021) · The EMBO Journal · doi:10.15252/embj.2021108944 · Cited by 192
Mutations in SARS-CoV-2 variants of concern link to increased spike cleavage and virus transmission
Escalera, A., Gonzalez-Reiche, A. S., Aslam, S., Mena, I., Laporte, M., Pearl, R. L., Fossati, A., Rathnasinghe, R., Alshammary, H., van de Guchte, A., et al. (2022) · Cell Host & Microbe · doi:10.1016/j.chom.2022.01.006 · Cited by 173
The Mechanism and Consequences of SARS-CoV-2 Spike-Mediated Fusion and Syncytia Formation
Rajah, M. M., Bernier, A., Buchrieser, J., & Schwartz, O. (2021) · Journal of Molecular Biology · doi:10.1016/j.jmb.2021.167280 · Cited by 188
Defining the risk of SARS-CoV-2 variants on immune protection
DeGrace, M. M., Ghedin, E., Frieman, M. B., Krammer, F., Grifoni, A., Alisoltani, A., Alter, G., Amara, R. R., Baric, R. S., Barouch, D. H., et al. (2022) · Nature · doi:10.1038/s41586-022-04690-5 · Cited by 168
Self-citationNucleocapsid mutations in SARS-CoV-2 augment replication and pathogenesis
Johnson, B. A., Zhou, Y., Lokugamage, K. G., Vu, M. N., Bopp, N. E., Crocquet-Valdes, P. A., Kalveram, B., Schindewolf, C., Liu, Y., Scharton, D., et al. (2022) · PLoS Pathogens · doi:10.1371/journal.ppat.1010627 · Cited by 161
Self-citationSARS-CoV-2 Mutations and Their Impact on Diagnostics, Therapeutics and Vaccines
Thakur, S., Sasi, S., Pillai, S. G., Nag, A., Shukla, D., Singhal, R., Phalke, S., & Velu, G. S. K. (2022) · Frontiers in Medicine · doi:10.3389/fmed.2022.815389 · Cited by 167
The origins and molecular evolution of SARS-CoV-2 lineage B.1.1.7 in the UK
Hill, V., du Plessis, L., Peacock, T. P., Aggarwal, D., Colquhoun, R., Carabelli, A. M., Ellaby, N. A. F., Gallagher, E., Groves, N., Jackson, B., et al. (2022) · Virus Evolution · doi:10.1093/ve/veac080 · Cited by 145
Quantifying the relationship between SARS-CoV-2 viral load and infectiousness
Marc, A., Kerioui, M., Blanquart, F., Bertrand, J., Mitjà, J., Corbacho‐Monné, M., Marks, M., & Guedj, J. (2021) · eLife · doi:10.7554/elife.69302 · Cited by 146
Spike deep mutational scanning helps predict success of SARS-CoV-2 clades
Dadonaite, B., Brown, J. T., McMahon, T. E., Farrell, A. G., Figgins, M. D., Asarnow, D. E., Stewart, C., Lee, J., Logue, J., Bedford, T., et al. (2024) · Nature · doi:10.1038/s41586-024-07636-1 · Cited by 145
Fibrin drives thromboinflammation and neuropathology in COVID-19
Ryu, J. K., Yan, Z., Montano, M., Sozmen, E. G., Dixit, K., Suryawanshi, R. K., Matsui, Y., Helmy, E., Kaushal, P., Makanani, S. K., et al. (2024) · Nature · doi:10.1038/s41586-024-07873-4 · Cited by 116
Self-citationStructural and antigenic variations in the spike protein of emerging SARS-CoV-2 variants
Mittal, A., Khattri, A., & Verma, V. (2022) · PLoS Pathogens · doi:10.1371/journal.ppat.1010260 · Cited by 124
Neutralization against Omicron SARS-CoV-2 from previous non-Omicron infection
Zou, J., Xia, H., Xie, X., Kurhade, C., Machado, R. R. G., Weaver, S. C., Ren, P., & Shi, P. (2022) · Nature Communications · doi:10.1038/s41467-022-28544-w · Cited by 114
Self-citationThe Spike of Concern—The Novel Variants of SARS-CoV-2
Winger, A., & Caspari, T. (2021) · Viruses · doi:10.3390/v13061002 · Cited by 122
Guo, Y., Han, J., Zhang, Y., He, J., Yu, W., Zhang, X., Wu, J., Zhang, S., Kong, Y., Guo, Y., et al. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.877101 · Cited by 118
Self-citationDroplet digital RT-PCR to detect SARS-CoV-2 signature mutations of variants of concern in wastewater
Heijnen, L., Elsinga, G., de Graaf, M., Molenkamp, R., Koopmans, M., & Medema, G. J. (2021) · The Science of The Total Environment · doi:10.1016/j.scitotenv.2021.149456 · Cited by 109
Variants with the N501Y mutation extend SARS-CoV-2 host range to mice, with contact transmissionPreprint
Montagutelli, X., Prot, M., Levillayer, L., Baquero, E., Jouvion, G., Conquet, L., Beretta, M., Donati, F., Albert, M., Gámbaro, F., et al. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.03.18.436013 · Cited by 114
Animal models in SARS-CoV-2 research
Chu, H., Chan, J. F.-W., & Yuen, K.-Y. (2022) · Nature Methods · doi:10.1038/s41592-022-01447-w · Cited by 103
SARS-CoV-2, CT-Values, and Infectivity—Conclusions to Be Drawn from Side Observations
Platten, M., Hoffmann, D., Grosser, R., Wisplinghoff, F., Wisplinghoff, H., Wiesmüller, G. A., Schildgen, O., & Schildgen, V. (2021) · Viruses · doi:10.3390/v13081459 · Cited by 109
Transmission of SARS-CoV-2 in free-ranging white-tailed deer in the United States
Feng, A., Bevins, S. N., Chandler, J. C., Deliberto, T. J., Ghai, R. R., Lantz, K., Lenoch, J. B., Retchless, A. C., Shriner, S. A., Tang, C. Y., et al. (2023) · Nature Communications · doi:10.1038/s41467-023-39782-x · Cited by 112
Enhanced fitness of SARS-CoV-2 variant of concern Alpha but not Beta
Ulrich, L., Halwe, N. J., Taddeo, A., Ebert, N., Schön, J., Devisme, C., Trüeb, B. S., Hoffmann, B., Wider, M., Fan, X., et al. (2021) · Nature · doi:10.1038/s41586-021-04342-0 · Cited by 98
COVID-19: Challenges of Viral Variants
Jacobs, J. L., Haidar, G., & Mellors, J. W. (2022) · Annual Review of Medicine · doi:10.1146/annurev-med-042921-020956 · Cited by 105
Cool, K. R., Gaudreault, N. N., Morozov, I., Trujillo, J. D., Meekins, D. A., McDowell, C. D., Carossino, M., Bold, D., Mitzel, D., Kwon, T., et al. (2021) · Emerging Microbes & Infections · doi:10.1080/22221751.2021.2012528 · Cited by 103
Kumar, V., Singh, J., Hasnain, S. E., & Sundar, D. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22179131 · Cited by 96
A live-attenuated SARS-CoV-2 vaccine candidate with accessory protein deletions
Liu, Y., Zhang, X., Liu, J., Xia, H., Zou, J., Muruato, A. E., Periasamy, S., Kurhade, C., Plante, J. A., Bopp, N. E., et al. (2022) · Nature Communications · doi:10.1038/s41467-022-31930-z · Cited by 92
Self-citationContribution of single mutations to selected SARS-CoV-2 emerging variants spike antigenicity
Gong, S. Y., Chatterjee, D., Richard, J., Prévost, J., Tauzin, A., Gasser, R., Bo, Y., Vézina, D., Goyette, G., Gendron‐Lepage, G., et al. (2021) · Virology · doi:10.1016/j.virol.2021.09.001 · Cited by 81
Mouse-adapted SARS-CoV-2 protects animals from lethal SARS-CoV challenge
Muruato, A. E., Vu, M. N., Johnson, B. A., Davis-Gardner, M. E., Vanderheiden, A., Lokugamage, K. G., Schindewolf, C., Crocquet-Valdes, P. A., Langsjoen, R. M., Plante, J. A., et al. (2021) · PLoS Biology · doi:10.1371/journal.pbio.3001284 · Cited by 77
Self-citationNewman, J., Thakur, N., Peacock, T. P., Bialy, D., Elrefaey, A. M. E., Bogaardt, C., Horton, D. L., Ho, S., Kankeyan, T., Carr, C., et al. (2022) · Nature Microbiology · doi:10.1038/s41564-022-01163-3 · Cited by 85
SARS-CoV-2 Causes Lung Infection without Severe Disease in Human ACE2 Knock-In Mice
Winkler, E. S., Chen, R. E., Alam, F., Yildiz, S., Case, J. B., Uccellini, M. B., Holtzman, M. J., García‐Sastre, A., Schotsaert, M., & Diamond, M. (2021) · Journal of Virology · doi:10.1128/jvi.01511-21 · Cited by 78
Accelerated evolution of SARS-CoV-2 in free-ranging white-tailed deer
McBride, D. S., Garushyants, S. K., Franks, J., Magee, A. F., Overend, S. H., Huey, D. D., Williams, A. M., Faith, S. A., Kandeil, A., Trifkovic, S., et al. (2023) · Nature Communications · doi:10.1038/s41467-023-40706-y · Cited by 82
Shastri, J. S., Parikh, S., Aggarwal, V., Agrawal, S. R., Chatterjee, N., Shah, R. J., Devi, P., Mehta, P., & Pandey, R. (2021) · Frontiers in Medicine · doi:10.3389/fmed.2021.737007 · Cited by 78
Melo-González, F., Soto, J. A., González, L. A., Fernández, J. O., Duarte, L. F., Schultz, B. M., Gálvez, N. M. S., Pacheco, G. A., Ríos, M., Vázquez, Y., et al. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.747830 · Cited by 75
An early warning system for emerging SARS-CoV-2 variants
Subissi, L., von Gottberg, A., Thukral, L., Worp, N., Munnink, B. B. O., Rathore, S., Abu-Raddad, L. J., Aguilera, X., Alm, E., Archer, B. N., et al. (2022) · Nature Medicine · doi:10.1038/s41591-022-01836-w · Cited by 79
Zhou, H., Møhlenberg, M., Thakor, J. C., Tuli, H. S., Wang, P., Assaraf, Y. G., Dhama, K., & Jiang, S. (2022) · Clinical Microbiology Reviews · doi:10.1128/cmr.00014-22 · Cited by 78
PCR performance in the SARS-CoV-2 Omicron variant of concern?
Metzger, C., Lienhard, R., Seth-Smith, H. M. B., Roloff, T. C., Wegner, F., Sieber, J., Bel, M., Greub, G., & Egli, A. (2021) · Swiss Medical Weekly · doi:10.4414/smw.2021.w30120 · Cited by 73
Li, M., Ren, Y., Aw, Z. Q., Chen, B., Yang, Z., Lei, Y., Cheng, L., Liang, Q., Hong, J., Yang, Y., et al. (2022) · Nature Communications · doi:10.1038/s41467-022-35642-2 · Cited by 72
Xue, S., Han, Y., Wu, F., & Wang, Q. (2024) · Protein & Cell · doi:10.1093/procel/pwae007 · Cited by 81
Goethem, N. V., Chung, P. Y. J., Meurisse, M., Vandromme, M., Mot, L. D., Brondeel, R., Stouten, V., Klamer, S., Cuypers, L., Braeye, T., et al. (2022) · Viruses · doi:10.3390/v14061297 · Cited by 69
Insights on the mutational landscape of the SARS-CoV-2 Omicron variant receptor-binding domain
Miller, N. L., Clark, T., Raman, R., & Sasisekharan, R. (2022) · Cell Reports Medicine · doi:10.1016/j.xcrm.2022.100527 · Cited by 80
Immune evasion and ACE2 binding affinity contribute to SARS-CoV-2 evolution
Ma, W., Fu, H., Jian, F., Cao, Y., & Li, M. (2023) · Nature Ecology & Evolution · doi:10.1038/s41559-023-02123-8 · Cited by 66
Controversy surrounding the Sputnik V vaccine
Cazzola, M., Rogliani, P., Mazzeo, F., & Matera, M. G. (2021) · Respiratory Medicine · doi:10.1016/j.rmed.2021.106569 · Cited by 66
SARS-CoV-2 variants and effectiveness of vaccines: a review of current evidence
Tatsi, E., Filippatos, F., & Michos, A. G. (2021) · Epidemiology and Infection · doi:10.1017/s0950268821002430 · Cited by 68
Genomic Perspectives on the Emerging SARS-CoV-2 Omicron Variant
Ma, W., Yang, J., Fu, H., Su, C., Yu, C., Wang, Q., de Vasconcelos, A. T. R., Bazykin, G. A., Bào, Y., & Li, M. (2022) · Genomics Proteomics & Bioinformatics · doi:10.1016/j.gpb.2022.01.001 · Cited by 59
Rapid and accurate detection of SARS-CoV-2 mutations using a Cas12a-based sensing platform
He, C., Lin, C., Mo, G., Xi, B., Li, A., Huang, D., Wan, Y., Chen, F., Liang, Y., Zuo, Q., et al. (2021) · Biosensors and Bioelectronics · doi:10.1016/j.bios.2021.113857 · Cited by 61
Structures of Omicron spike complexes and implications for neutralizing antibody development
Guo, H., Gao, Y., Li, T., Li, T., Lu, Y., Zheng, L., Liu, Y., Yang, T., Luo, F., Song, S., et al. (2022) · Cell Reports · doi:10.1016/j.celrep.2022.110770 · Cited by 61
Self-citationThe ins and outs of SARS-CoV-2 variants of concern (VOCs)
Salehi-Vaziri, ., Fazlalipour, M., Khorrami, S. M. S., Azadmanesh, K., Pouriayevali, M. H., Jalali, T., Shoja, Z., & Maleki, A. (2022) · Archives of Virology · doi:10.1007/s00705-022-05365-2 · Cited by 61
In vitro evaluation of therapeutic antibodies against a SARS-CoV-2 Omicron B.1.1.529 isolate
Touret, F., Baronti, C., Bouzidi, H. S., & de Lamballerie, X. N. (2022) · Scientific Reports · doi:10.1038/s41598-022-08559-5 · Cited by 59
A delicate balance between antibody evasion and ACE2 affinity for Omicron BA.2.75
Huo, J., Dijokaite-Guraliuc, A., Liu, C., Zhou, D., Ginn, H. M., Das, R., Supasa, P., Selvaraj, M., Nutalai, R., Tuekprakhon, A., et al. (2022) · Cell Reports · doi:10.1016/j.celrep.2022.111903 · Cited by 55
SARS-CoV-2 spike N-terminal domain modulates TMPRSS2-dependent viral entry and fusogenicity
Meng, B., Datir, R. P., Choi, J., Baker, S. G., Dougan, G., Hess, C., Kingston, N., Lehner, P. J., Lyons, P., Matheson, N. J., et al. (2022) · Cell Reports · doi:10.1016/j.celrep.2022.111220 · Cited by 58
Understanding Mutations in Human SARS-CoV-2 Spike Glycoprotein: A Systematic Review & Meta-Analysis
Kumar, R., Srivastava, Y., Muthuramalingam, P., Singh, S. K., Verma, G., Tiwari, S., Tandel, N., Beura, S. K., Panigrahi, A. R., Maji, S., et al. (2023) · Viruses · doi:10.3390/v15040856 · Cited by 57
Molecular Mechanism of Porcine Epidemic Diarrhea Virus Cell Tropism
Li, Z., Ma, Z., Dong, L., Yang, T., Li, Y., Jiao, D., Han, W., Zheng, H., & Xiao, S. (2022) · mBio · doi:10.1128/mbio.03739-21 · Cited by 52
Differential Pathogenesis of SARS-CoV-2 Variants of Concern in Human ACE2-Expressing Mice
Natekar, J. P., Pathak, H., Stone, S., Kumari, P., Sharma, S., Auroni, T. T., Arora, K., Rothan, H. A., & Kumar, M. (2022) · Viruses · doi:10.3390/v14061139 · Cited by 57
Shuai, H., Chan, J. F., Hu, B., Chai, Y., Yoon, C., Liu, H., Liu, Y., Shi, J., Zhu, T., Hu, J., et al. (2023) · EBioMedicine · doi:10.1016/j.ebiom.2023.104753 · Cited by 51
Self-citationSARS-CoV-2 spike protein: structure, viral entry and variants
Chen, B., Farzan, M., & Choe, H. (2025) · Nature Reviews Microbiology · doi:10.1038/s41579-025-01185-8 · Cited by 57
Variations within the Glycan Shield of SARS-CoV-2 Impact Viral Spike Dynamics
Newby, M. L., Fogarty, C. A., Allen, J. D., Butler, J., Fadda, E., & Crispin, M. (2022) · Journal of Molecular Biology · doi:10.1016/j.jmb.2022.167928 · Cited by 49
SARS-CoV-2 Uses Nonstructural Protein 16 To Evade Restriction by IFIT1 and IFIT3
Schindewolf, C., Lokugamage, K. G., Vu, M. N., Johnson, B. A., Scharton, D., Plante, J. A., Kalveram, B., Crocquet-Valdes, P. A., Sotcheff, S. L., Jaworski, E. A., et al. (2023) · Journal of Virology · doi:10.1128/jvi.01532-22 · Cited by 52
Self-citationAhmad, L. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.742167 · Cited by 46
Chen, Y., Sun, L., Ullah, I., Beaudoin-Bussières, G., Anand, S. P., Hederman, A. P., Tolbert, W. D., Sherburn, R. T., Nguyen, D. N. P., Marchitto, L., et al. (2022) · Science Advances · doi:10.1126/sciadv.abn4188 · Cited by 49
Molecular Interactions of Tannic Acid with Proteins Associated with SARS-CoV-2 Infectivity
Haddad, M., Gaudreault, R., Sasseville, G., Nguyen, P. T., Wiebe, H., van de Ven, T. G. M., Bourgault, S., Mousseau, N., & Ramassamy, C. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23052643 · Cited by 47
Islam, M. A., Haque, M. A., Rahman, M. A., Hossen, F., Reza, M., Barua, A., Marzan, A. A., Das, T., Baral, S. K., He, C., et al. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.837290 · Cited by 50
Molecular insights into the adaptive evolution of SARS-CoV-2 spike protein
Yao, Z., Zhang, L., Duan, Y., Tang, X., & Lü, J. (2024) · Journal of Infection · doi:10.1016/j.jinf.2024.106121 · Cited by 49
Spike protein of SARS-CoV-2 variants: a brief review and practical implications
Candido, K. L., Eich, C. R., de Fariña, L. O., Kadowaki, M. K., Silva, J. L. D. C., Maller, A., & Simão, R. D. C. G. (2022) · Brazilian Journal of Microbiology · doi:10.1007/s42770-022-00743-z · Cited by 46
The Development of SARS-CoV-2 Variants: The Gene Makes the Disease
Pérez-Gómez, R. (2021) · Journal of Developmental Biology · doi:10.3390/jdb9040058 · Cited by 47
Kumar, R., Murugan, N. A., & Srivastava, V. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23063409 · Cited by 45
Yang, Z. L., Zhang, S., Tang, Y., Zhang, S., Xu, D.-Q., Yue, S., & Liu, Q. (2022) · Aging and Disease · doi:10.14336/ad.2021.1210 · Cited by 46
Hawman, D. W., Meade-White, K. D., Clancy, C. S., Archer, J. F., Hinkley, T. C., Leventhal, S. S., Rao, D., Stamper, A., Lewis, M. C., Rosenke, R., et al. (2022) · EBioMedicine · doi:10.1016/j.ebiom.2022.104196 · Cited by 43
A comparative overview of SARS‑CoV‑2 and its variants of concern
Ahmad, A., Fawaz, M. A. M., & Aisha, A. (2022) · Infezioni in Medicina · doi:10.53854/liim-3003-2 · Cited by 50
Saha, A., Roy, S. G., Dwivedi, R., Tripathi, P., Kumar, K., Nambiar, S. M., & Pathak, R. (2025) · Vaccines · doi:10.3390/vaccines13040424 · Cited by 47
Evolution of the SARS-CoV-2 genome and emergence of variants of concern
Safari, I., & Elahi, E. (2021) · Archives of Virology · doi:10.1007/s00705-021-05295-5 · Cited by 41
Hybrid CRISPR/Cas protein for one-pot detection of DNA and RNA
Guk, K., Yi, S., Kim, H., Bae, Y., Yong, D., Kim, S., Lee, K., Lim, E., Kang, T., & Jung, J. (2022) · Biosensors and Bioelectronics · doi:10.1016/j.bios.2022.114819 · Cited by 42
Kane, Y., Wong, G., & Gao, G. F. (2023) · Annual Review of Animal Biosciences · doi:10.1146/annurev-animal-020420-025011 · Cited by 43
SARS-CoV-2 Delta variant induces enhanced pathology and inflammatory responses in K18-hACE2 mice
Lee, K. S., Wong, T. Y., Russ, B. P., Horspool, A. M., Miller, O. A., Rader, N. A., Givi, J. P., Winters, M. T., Wong, Z. Y., Cyphert, H. A., et al. (2022) · PLoS ONE · doi:10.1371/journal.pone.0273430 · Cited by 42
Rapid escape of new SARS-CoV-2 Omicron variants from BA.2-directed antibody responses
Dijokaite-Guraliuc, A., Das, R., Zhou, D., Ginn, H. M., Liu, C., Duyvesteyn, H. M. E., Huo, J., Nutalai, R., Supasa, P., Selvaraj, M., et al. (2023) · Cell Reports · doi:10.1016/j.celrep.2023.112271 · Cited by 46
SARS-CoV-2 variants: biology, pathogenicity, immunity and control
Uraki, R., Korber, B., Diamond, M., & Kawaoka, Y. (2025) · Nature Reviews Microbiology · doi:10.1038/s41579-025-01255-x · Cited by 50
ACE2 N-glycosylation modulates interactions with SARS-CoV-2 spike protein in a site-specific manner
Isobe, A., Arai, Y., Kuroda, D., Okumura, N., Ono, T., Ushiba, S., Nakakita, S., Daidoji, T., Suzuki, Y., Nakaya, T., et al. (2022) · Communications Biology · doi:10.1038/s42003-022-04170-6 · Cited by 40
Wang, Q., Ye, S., Zhou, Z., Song, A., Zhu, X., Peng, J., Liang, R., Yang, C., Yu, X., Huang, X., et al. (2022) · Journal of Medical Virology · doi:10.1002/jmv.28407 · Cited by 37
Antigenic evolution of SARS coronavirus 2
Mykytyn, A. Z., Fouchier, R. A. M., & Haagmans, B. L. (2023) · Current Opinion in Virology · doi:10.1016/j.coviro.2023.101349 · Cited by 36
Kazybay, B., Ahmad, A., Mu, C., Mengdesh, D., & Xie, Y. (2021) · Travel Medicine and Infectious Disease · doi:10.1016/j.tmaid.2021.102242 · Cited by 35
Shi, Y., Huang, J., Liu, Y., Liu, J., Guo, X., Li, J., Gong, L., Zhou, X., Cheng, G., Qiu, Y., et al. (2022) · Science Advances · doi:10.1126/sciadv.abo1827 · Cited by 36
Self-citationUmair, M., Ikram, A., Salman, M., Haider, S. A., Badar, N., Rehman, Z., Ammar, M., Rana, M. S., & Ali, Q. (2021) · Journal of Medical Virology · doi:10.1002/jmv.27429 · Cited by 44
Villa, A. M., Brunialti, E., Dellavedova, J., Meda, C., Rebecchi, M., Conti, M., Donnici, L., Francesco, R. D., Reggiani, A. M., Lionetti, V., et al. (2021) · Pharmacological Research · doi:10.1016/j.phrs.2021.105982 · Cited by 35
da Silva, S. J. R., de Lima, S. C., da Silva, R. C., Kohl, A., & Pena, L. (2022) · Frontiers in Medicine · doi:10.3389/fmed.2021.836826 · Cited by 35
Tracking SARS-CoV-2 variants through pandemic waves using RT-PCR testing in low-resource settings
Nasir, A., Aamir, U. B., Kanji, A., Bukhari, A. R., Ansar, Z., Ghanchi, N. K., Masood, K. I., Samreen, A., Islam, N., Ghani, S., et al. (2023) · PLOS Global Public Health · doi:10.1371/journal.pgph.0001896 · Cited by 35
Insights on the mutational landscape of the SARS-CoV-2 Omicron variantPreprint
Miller, N. L., Clark, T., Raman, R., & Sasisekharan, R. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.12.06.471499 · Cited by 35
Beesley, L. J., Moran, K. R., Wagh, K., Castro, L. A., Theiler, J. P., Yoon, H., Fischer, W., Hengartner, N., Korber, B., & Valle, S. Y. D. (2023) · EBioMedicine · doi:10.1016/j.ebiom.2023.104534 · Cited by 34
Metadata
- Authors
- Liu, Y., Liu, J., Plante, K. S., Plante, J. A., Xie, X., Zhang, X., Ku, Z., An, Z., Scharton, D., Schindewolf, C., Menachery, V. D., Shi, P.-Y., & Weaver, S. C.
- Affiliations
- The University of Texas Medical Branch at Galveston (US)
- Brown Foundation Institute of Molecular Medicine for the Prevention of Human Diseases (US)
- Corresponding author
- Shi, Pei-Yong
- Weaver, Scott C.
- ORCID
- Venue
- Nature
- Publisher
- openRxiv
- Published
- 2021-03-09
- Volume
- 602
- Issue
- 7896
- Pages
- 294-299
- ISSN
- 0028-0836 (ISSN-L)
- PMC
- PMC8900207
- OpenAlex
- W3216019834
- Cited by
- 574
- References
- 37
- Citations by year
- 2026: 25 · 2025: 71 · 2024: 84 · 2023: 125 · 2022: 181 · 2021: 87
- FWCI
- 37.77
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Nature (publishedVersion)
- bioRxiv (Cold Spring Harbor Laboratory) (acceptedVersion, cc-by-nc-nd)
- Research Square (acceptedVersion, cc-by)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- PubMed Central (submittedVersion, cc-by-nc-nd)
- RePEc: Research Papers in Economics (submittedVersion)
- Funders
- Cancer Prevention and Research Institute of Texas (RP150551, RP150551 and RP190561, RP190561, AI153602)
- University of Texas System
- National Institutes of Health (AG049042, UL1TR001439)
- National Institute on Aging (AG049042)
- National Institute of Allergy and Infectious Diseases (R24AI120942, R01AI134907, R01AI153602, AI153602, AG049042, AI134907, T32AI007526)
- National Center for Advancing Translational Sciences
- Topics
- Health Sciences › Medicine › Infectious Diseases › SARS-CoV-2 and COVID-19 Research
- Health Sciences › Medicine › Infectious Diseases › COVID-19 Clinical Research Studies
- Physical Sciences › Mathematics › Modeling and Simulation › COVID-19 epidemiological studies
- Keywords
- SARS-CoV-2, N501Y mutation, spike protein, B.1.1.7 Alpha variant, virus transmission, viral fitness, receptor binding affinity, airway epithelial cells, hamster model, convergent evolution, COVID-19 pandemic
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review