Jie-Li Hu, P. Peng, K. Wang, Liang Fang, F. Luo, A. Jin, Beizhong Liu, N. Tang, A. Huang
Cellular & molecular immunology, 2021
Coronaviruses are enveloped, positive-stranded RNA viruses that contain the largest known RNA genomes to date. As severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) continues to circulate in the human population, multiple mutations have accumulated over time, which may affect its transmission, virulence and antigenicity. Neutralizing antibodies (NAbs) elicited by natural infection or vaccination are likely to be a key immune correlate for protection against SARS-CoV-2 infection. A decline in the antibody response to SARS-CoV-2 in convalescent individuals and reinfections by different viral variants have been reported. It is therefore important to gain insights into the infectivity and antigenicity of SARS-CoV-2 variants. Spike-specific antibodies contribute the majority of the neutralizing activity in most convalescent human sera. Two SARS-CoV-2 variants, N501Y.V1 (also known as B.1.1.7 lineage or VOC-202012/01) and N501Y.V2 (B.1.351 lineage), reported from the United Kingdom and South Africa, respectively, contain several mutations in the receptor-binding domain (RBD) of Spike and are of particular concern. To address the infectivity and neutralization escape phenotypes potentially caused by these mutations, we used the SARS-CoV-2 pseudovirus system to compare the viral infectivity as well as the neutralization activities of convalescent sera and monoclonal antibodies (mAbs) against SARS-CoV-2 variants. The blood samples (n= 40) of 20 patients with COVID-19 obtained in February and October 2020 in Chongqing were previously described. Eight RBD-specific mAbs with neutralizing capability against SARS-CoV-2 were obtained from the blood samples of COVID-19 convalescent patients. DNA sequences encoding the reference strain wild-type (WT) and mutant Spike proteins of SARS-CoV-2 were codon-optimized and synthesized by Sino Biological Inc. (Beijing, China) and GenScript Inc. (Nanjing, China). Using a luciferase-expressing lentiviral pseudotype system, we expressed WT and N501Y.V1 (variant 1) and N501Y.V2 (variant 2) mutant Spike proteins in enveloped virions. NAbs were measured by pseudovirus-based assays in 293T-ACE2 cells. The inhibitory dose (ID50) was calculated based on the titers of NAbs. First, the infectivity of pseudotyped viral particles was measured by luciferase assay as previously described. As shown in Fig. 1a, the entry efficiencies of Spike pseudotyped viruses bearing the N501Y variant 1 or variant 2 mutant were ~3 to 4.4 times higher than that of the WT pseudovirus when viral input was normalized, suggesting that these spike variants promote the infectivity of SARS-CoV-2. Then, we assessed the neutralizing efficacy of 40 convalescent serum samples from 20 individuals at two time points with a pseudovirus neutralization assay. At follow-up time point 1, corresponding to a median of 25 days (range 5–33 days) post symptom onset, most sera were significantly less effective than the WT pseudovirus in neutralizing the N501Y variant 1 and variant 2 (Fig. 1b). The mean NAb titers were 825 for WT, 343 for variant 1, and 148 for variant 2. The neutralizing activity of two samples against N501Y.V1 was reduced by greater than tenfold. Notably, the NAb titers of six samples (30%) decreased below the threshold against variant 2 (Fig. 1b). At ~8 months post symptom onset (follow-up time point 2), 17 samples of 20 participants (85%) retained titers of ID50 > 40 against WT pseudovirus, whereas the NAb titers of 8 samples (40%) and 18 samples (90%) decreased below the threshold against N501Y variant 1 and variant 2, respectively (Fig. 1c). These data indicate that N501Y variant 1 and variant 2 escape neutralizing antibodies in some COVID-19 convalescent sera. In addition, we assessed the impact of these variants on the neutralizing activity of human mAbs isolated from COVID-19 convalescent patients. All eight antibodies potently neutralized the WT pseudovirus, while two mAbs (CQ016 and CQ045) were only minimally affected by the variants. However, the neutralization activities of the six other mAbs were reduced or abolished by either N501Y variant 1 or variant 2 (Fig. 1d). Among them, three mAbs were threefold or more less effective against N501Y.V1 and five against N501Y.V2 (Fig. 1d). Notably, two mAbs (CQ026 and CQ038) showed no neutralizing activity against N501Y.V2. Moreover, variant 2 reduced the neutralization sensitivity with CQ046 by 26-fold, which showed the most potent activity against WT pseudovirus. The IC50 of the mAb CQ046 increased from 7.4 ng/ml (WT) to 194 ng/ml (variant 2) (Fig. 1e). Overall, both N501Y variant 1 and variant 2 reduced neutralization sensitivity to most mAbs tested, while N501Y.V2 even abrogated the neutralizing activity of two mAbs. Our findings indicated that N501Y variant 1 and variant 2 increase viral infectivity compared to that of the reference strain in vitro. Notably, both N501Y variant 1 and variant 2 contain the D614G and N501Y mutations in the Spike protein. The findings that variant 1 and variant 2 enhanced the infectivity of SARS-CoV2 in vitro are highly consistent with previous studies, which demonstrated that D614G and N501Y mutations enhanced the fitness and transmissibility of the virus, as evidenced by structure
Cited by 14 publications.
Field of study: Medicine