We investigated ChAdOx1 nCoV-19 (AZD1222) vaccine efficacy against SARS-CoV-2 variants of concern (VOCs) B.1.1.7 and B.1.351 in Syrian hamsters. We previously showed protection against SARS-CoV-2 disease and pneumonia in hamsters vaccinated with a single dose of ChAdOx1 nCoV-19. Here, we observe a 9.5-fold reduction of virus neutralizing antibody titer in vaccinated hamster sera against B.1.351 compared to B.1.1.7. Vaccinated hamsters challenged with B.1.1.7 or B.1.351 do not lose weight compared to control animals. In contrast to control animals, the lungs of vaccinated animals do not show any gross lesions. Minimal to no viral subgenomic RNA (sgRNA) and no infectious virus can be detected in lungs of vaccinated animals. Histopathological evaluation shows extensive pulmonary pathology caused by B.1.1.7 or B.1.351 replication in the control animals, but none in the vaccinated animals. These data demonstrate the effectiveness of the ChAdOx1 nCoV-19 vaccine against clinical disease caused by B.1.1.7 or B.1.351 VOCs.
The COVID-19 pandemic produced an unprecedented development of SARS-CoV-2 vaccines, and just over a year after the beginning of the outbreak a total of 12 vaccines have been authorized or approved globally. As the pandemic progressed, several variants of concern (VOCs) have been detected. These include the B.1.1.7 and B.1.351 VOCs. The B.1.1.7 VOC was first detected in the United Kingdom and has seven amino acid (AA) substitutions and two deletions in the spike protein1,2 compared to the original Wuhan isolate, Wuhan-Hu-1. The B.1.351 VOC was first detected in South Africa and has eight AA substitutions and one deletion in the spike protein3 (Table 1). All currently licensed vaccines are based on the spike protein of Wuhan-Hu-1, thus, concerns have been raised that the presence of these changes may affect vaccine efficacy. The goal of this study was to evaluate ChAdOx1 nCoV-19 (AZD1222) vaccine efficacy in Syrian hamsters when challenged using naturally occurring isolates of the VOCs B.1.1.7 and B.1.351.
Syrian hamsters (N = 10 per group) were vaccinated intramuscularly with either ChAdOx1 nCoV-19 or ChAdOx1 green fluorescent protein (GFP, 2.5 × 108 IU/hamster) 30 days prior to intranasal challenge with SARS-CoV-2. Vaccination with ChAdOx1 nCoV-19 resulted in high titers of binding antibodies against the SARS-CoV-2 full-length spike protein and receptor binding domain (Fig. 1a) at 25 days post vaccination (DPI). We then investigated neutralizing antibody titers in serum against infectious virus. Neutralization of B.1.351 was significantly reduced compared to neutralization of B.1.1.7 (Fig. 1b, mean titer of 15 vs 142, p < 0.0001, Mann-Whitney test).
ChAdOx1 nCoV-19 vaccinated hamsters are protected against lower respiratory tract infection with B.1.1.7
Hamsters were inoculated with B.1.1.7 via the intranasal route. Weight loss was observed in control hamsters whereas vaccinated hamsters continued to gain weight throughout the experiment (Fig. 2a). A significant difference in weight between vaccinated and control hamsters was observed starting at 4 DPI (Fig. 2a, Student’s t-test corrected for multiple comparisons using the Holm–Šidák method) and continued throughout the remainder of the experiment. Four out of ten hamsters per group were euthanized at 5 DPI and lung tissue was harvested. Lung:body weight ratios on 5 DPI were significantly lower in vaccinated animals compared to control animals (Fig. 2b, p = 0.0286, Mann–Whitney test), indicating no or reduced pulmonary edema in ChAdOx1 nCoV-19-vaccinated animals. Lung tissue of all control animals contained high levels of sgRNA (Fig. 2c, 1010 copies/gram tissue), and was comparable to sgRNA levels previously detected in lung tissue of control animals challenged with SARS-CoV-2 D614G (hCoV-19/USA/MT-RML-7/2020)4. Conversely, no sgRNA was detected in lung tissue obtained from vaccinated hamsters challenged with B.1.1.7 (Fig. 2c, p = 0.0286, Mann–Whitney test). High levels of infectious virus were detected in lung tissue of all control animals, whereas no vaccinated animals had detectable infectious virus in lung tissue (Fig. 2d, p = 0.0286, Mann–Whitney test).
Lung tissue was then evaluated for histology. The percentage of lung tissue that showed pathology and the percentage of lung tissue that was positive for SARS-CoV-2 antigen was determined by a veterinary pathologist blinded to the study group allocations. Whereas no pathology nor SARS-CoV-2 antigen was found in lung tissue of vaccinated animals, this was abundantly present in lung tissue of control animals (Fig. 2e, f). Finally, oropharyngeal swabs were collected on 1 to 5 DPI, evaluated for sgRNA, and an area under the curve was calculated per animal to determine the total amount of virus shed. We observed a significant decrease in the total amount of virus found in oropharyngeal swabs from vaccinated animals compared to control animals (Fig. 2g, Mann–Whitney test).
Lung tissue was then evaluated for histology. Microscopically, pulmonary lesions of control animals consisted of a moderate to marked bronchointerstitial pneumonia extending into the adjacent alveoli previously observed in hamsters inoculated with SARS-CoV-2 WA1 or a D614G isolate4,5. Bronchi and bronchioles had multifocal necrotic epithelial cells and moderate numbers of infiltrating neutrophils and macrophages. Alveolar septa were expanded by edema fluid and leucocytes. In contrast, vaccinated animals did not show any evidence of SARS-CoV-2 pathology (Fig. 3a–d). Immunohistochemistry using a monoclonal antibody against SARS-CoV-2 demonstrated viral antigen in bronchial and bronchiolar epithelium, type I and II pneumocytes as well as pulmonary macrophages within the control animals, but not in vaccinated animals (Fig. 3e, f).
ChAdOx1 nCoV-19 vaccinated hamsters are protected against lower respiratory tract infection with B.1.351
This experiment was repeated using B.1.351 (isolate hCoV-19/South Africa/KRISP-K005325/2020) instead of B.1.1.7 as an inoculation virus. Two AA substitutions were found in the spike protein of the B.1.351 virus stock; Q677H (present at 88%) and R682W (present at 89%). A lack of weight gain was observed in control hamsters, but not vaccinated hamsters, which was significant starting at 6 DPI (Fig. 4a, Student’s t-test corrected for multiple comparisons using the Holm–Šidák method). Four out of ten hamsters per group were euthanized at 5 DPI and lung tissue was harvested. Lung:body weight ratios were significantly lower in vaccinated animals compared to control animals (Fig. 4b, p = 0.0286, Mann–Whitney test). Lung tissue of all control animals contained high levels of sgRNA, but only one vaccinated animal had relatively low levels of sgRNA in lungs (Fig. 4c, p = 0.0286, Mann–Whitney test). Likewise, high levels of infectious virus were detected in the lungs of control animals, but not in lungs of vaccinated animals (Fig. 4d, p = 0.0286, Mann–Whitney test). As in the previous experiment, no pathology nor SARS-CoV-2 antigen was found in lung tissue of vaccinated animals compared to control animals (Fig. 4e, f, p = 0.0286, Mann–Whitney test). No decrease in the total amount of virus found in oropharyngeal swabs from vaccinated animals compared to control animals was found (Fig. 4g, Mann–Whitney test).
We investigated the presence of the AA substitutions Q677H and R682W observed in 88–89% of the spike protein of our B.1.351 stock in swabs and lung tissue obtained from control animals challenged. Whereas we did find these substitutions in swabs obtained at 1 DPI, they were not present in swabs obtained at 5 DPI. Likewise, the substitutions were only found in the lung tissue of one out of four control hamsters (Table 2).
Lung tissue was then evaluated for histology. Microscopically, pulmonary lesions of control animals were comparable to results obtained from previous SARS-CoV-2 infections of hamsters. In contrast, vaccinated animals did not show any evidence of SARS-CoV-2 pathology (Fig. 5a–d). Likewise, immunohistochemistry demonstrated viral antigen present in bronchial and bronchiolar epithelium, type I and II pneumocytes as well as pulmonary macrophages within the control animals, but not in vaccinated animals (Fig. 5e, f).
Hamsters vaccinated with ChAdOx1 nCoV-19 via the intranasal route are protected against lower respiratory tract infection with B.1.351
Intranasal vaccination of hamsters with ChAdOx1 nCoV-19 resulted in a reduction of shedding of SARS-CoV D614G4. We hypothesized that a similar reduction in shedding would be found upon inoculation with B.1.351. Animals were vaccinated with 2.5 × 108 IU ChAdOx1 nCoV-19/animal, either via the intranasal route or via the intramuscular route. New stock of B.1.351 was obtained, and next-gen sequencing revealed no SNPs in the spike protein (isolate hCoV-19/USA/MD-HP01542/2021) from here on referred to as B.1.351-2. Sixty days post vaccination, animals were challenged with 104 TCID50 of B.1.351-2. As a control group, naïve animals were inoculated. Weight loss was minimal in control animals and absent in vaccinated animals (Fig. 6a). At 5 DPI, four animals per group were euthanized. Compared to control animals, lung:BW ratio of vaccinated animals was significantly reduced, and there was no difference between the two vaccine groups (Fig. 6b). No viral sgRNA or infectious virus was detected in lung tissue of vaccinated animals, whereas it was abundantly present in lung tissue of control animals (Fig. 6c, d). As shown in the previous experiment, no difference in the amount of virus shed was found when animals were vaccinated via the IM route. In contrast, a significant reduction was found in animals vaccinated via the IN route (Fig. 6g).
Histopathology of the lungs collected 5 DPI show pulmonary lesions of control animals with a moderate to marked bronchointerstitial pneumonia extending into the adjacent alveoli. Bronchi and bronchioles had multifocal necrotic epithelial cells and scattered to numerous infiltrating neutrophils and macrophages. Alveolar septa were expanded by edema fluid and leucocytes(Fig. 7c, f). IN vaccinated animals did not show any evidence of SARS-CoV-2 pathology (Fig. 7a, d). IM vaccinated animals had rare foci of interstitial pneumonia (Fig. 7b, e). Immunohistochemistry using a monoclonal antibody against SARS-CoV-2 demonstrated moderate to numerous viral antigens in the bronchial and bronchiolar epithelium, scattered to numerous type I and II pneumocytes as well as rare pulmonary macrophages within the control animals. The IM vaccinated animals had none to rare instances of type I and II pneumocytes and pulmonary macrophages while the IN vaccinated animals showed no evidence of viral antigen in the lungs (Fig. 7g–i).
This study demonstrates efficacy of the ChAdOx1 nCoV-19 vaccine against circulating variants of concern in the SARS-CoV-2 Syrian hamster model. The Syrian hamster SARS-CoV-2 infection model is characterized by natural susceptibility to SARS-CoV-2 and development of a robust upper and lower respiratory tract infection6. The hamster model has been successfully used for the preclinical development of several vaccines including the Ad26 and mRNA-1273 vaccines by Janssen7 and Moderna8, respectively. Several groups have reported the effect of spike protein substitutions observed in B.1.1.7 and B.1.351 VOCs on the virus neutralizing capacity of serum obtained from vaccinated or convalescent individuals. In general, these studies conclude that the substitutions found in the B.1.1.7 spike protein have limited to no effect on virus neutralization titres9,10,11,12,13,14,15. Data from a UK phase III trial taken from a time when B.1.1.7 predominated, showed minimal impact on ChAdOx1 nCoV-19 vaccine efficacy15. Likewise, in an observational study of vaccine effectiveness in adults aged over 70 years in the UK, a single dose of either ChAdOx1 nCoV-19 or the Pfizer/BioNTech vaccine BNT162b2 reduced hospitalization in elderly adults with co-morbidities by 80%16. In contrast, the substitutions found in the B.1.351 spike protein (Table 1) result in a significant reduction of virus neutralizing capacity with pseudotype or infectious virus neutralization assays9,10,11,12,13,14,15,17,18. The ChAdOx1 nCoV-19 vaccine showed a nine times reduction in neutralizing antibody titer against B.1.351 than against an earlier variant circulating in South Africa10,19. In a phase II study of ChAdOx1 nCoV-19 in South Africa, in 2000 adults with a median age of 31 years, vaccine efficacy against mild to moderate disease was reduced when the virus recovered after infection was B.1.351 (19 cases in the vaccinated group and 20 in the placebo group)19. Vaccine efficacy against severe disease could not be determined as no severe cases occurred in this young cohort. The South African arm of the ENSEMBLE study which tested vaccine efficacy after a single dose of Janssen’s COVID-19 vaccine candidate enrolled 6,576 participants in South Africa, out of a total of 43,783 in multiple countries, with 34% of participants across the study aged over 60 years. Vaccine efficacy against moderate to severe disease was 64% (CI 41.2%, 78.7%) in South Africa compared to 72% (CI 58.2%, 81.7%) in the USA at 28 DPI20. Efficacy of the vaccine against severe to critical disease was 81.7% in South Africa, which was similar to the reported 85.9% and 87.6% in the USA and Brazil, respectively20. Vaccine efficacy against mild disease was not reported. These clinical trial results are consistent with the findings of the preclinical study reported here; ChAdOx1 nCoV-19 may be less effective at reducing upper respiratory tract infection caused by B.1.351 than by B.1.1.7, consistent with reduced efficacy against mild disease. However, complete protection against lower respiratory tract disease was observed in this challenge study, consistent with protection against severe disease. Based on our data, we hypothesize that the currently available vaccines will still protect against severe disease and hospitalization caused by VOC B.1.351.
Limited data on the immunological determinants of protection are available, however, recent data from rhesus macaques indicate that relatively low neutralizing antibody titers are sufficient for protection against SARS-CoV-2, and that cellular immune responses may contribute to protection if antibody responses are suboptimal21. Induction of binding and neutralizing antibodies as well as SARS-CoV-2 cellular spike protein-specific T cell responses after vaccination have been reported22,23 and most SARS-CoV-2 specific T cell epitopes in both convalescent and vaccinated individuals are not affected by the AA substitutions found in the spike protein of the B.1.1.7 and B.1.351 variants24. Protection against severe COVID-19 disease might be mediated by T cells and therefore may not be different between the current variants. However, as T cell-mediated protection in the lower respiratory tract can only act after the initial infection has occurred, mild, polymerase chain reaction (PCR)-positive disease may still occur in the upper respiratory tract.
It should be noted that the B.1.351 virus stock used to challenge hamsters contained two additional non-fixed AA substitutions; Q677H and R682W at 88% and 89%, respectively. The relative presence of these two AA substitutions was markedly reduced at 1 DPI and absent on 5 DPI. In addition, they were only present in lung tissue of one control hamster at 5 DPI, suggesting that they are rapidly selected against in the SARS-CoV-2 hamster model over the course of infection. Nonetheless, since the substitutions thought to be important in immune evasion, such as E484K18, are still present in the virus stock, and efficient replication and lung pathology was observed in infected hamsters, we believe that conclusions can still be reached from the data presented in Fig. 3. Additionally, we used a B.1.351 stock without AA mutations in the final experiments. Again, we did not find any disease in vaccinated hamsters inoculated with B.1.351, whether they received an IN or an IM vaccination.
Interestingly, in this same study, a reduction in viral detection in oropharyngeal swabs could be detected in hamsters that received an IN vaccination, in contrast to hamsters that received an IM vaccination. These results are in line with previous studies that were done at a shorter time frame (25 and 28 days between vaccination and challenge)4,25. Our study shows that these differences last for at least 60 DPI in hamsters, even with a VOC that has reduced the neutralizing ability of antibodies in sera.
Based on the current studies and healthcare priorities in real-world settings, we believe it is essential to focus on prevention of moderate to severe disease requiring hospitalization. We show that ChAdOx1 nCoV-19 vaccination resulted in complete protection against disease in hamsters. As implied by the data presented by Janssen20, viral vectored vaccines may provide substantial protection against lower respiratory tract infection caused by the B.1.351 variant and subsequent hospitalization and death. With the ongoing evolution of SARS-CoV-2, the readily available and cost-effective hamster model allows rapid evaluation of the protective efficacy of novel VOCs. In addition, it will allow rapid preclinical benchmarking of existing vaccines against preclinical vaccines with updated antigen designs.
All animal experiments were conducted in an AAALAC International-accredited facility and were approved by the Rocky Mountain Laboratories Institutional Care and Use Committee following the guidelines put forth in the Guide for the Care and Use of Laboratory Animals 8th edition, the Animal Welfare Act, United States Department of Agriculture and the United States Public Health Service Policy on the Humane Care and Use of Laboratory Animals.
The Institutional Biosafety Committee (IBC) approved work with infectious SARS-CoV-2 virus strains under BSL3 conditions. Virus inactivation of all samples was performed according to IBC-approved standard operating procedures for the removal of specimens from high containment areas.
Cells and virus
SARS-CoV-2 variant B.1.351-1 (hCoV-19/South African/KRISP-K005325/2020, EPI_ISL_678615) was obtained from Dr. Tulio de Oliveira and Dr. Alex Sigal at the Nelson R Mandela School of Medicine, UKZN. SARS-CoV-2 variant B.1.1.7 (hCoV-19/England/204820464/2020, EPI_ISL_683466) was obtained from Public Health England via BEI. SARS-CoV-2 variant B.1.351-2 (USA/MD-HP01542/2021, EPI_ISL_890360) was obtained from Andrew Pekosz at John Hopkins Bloomberg School of Public Health. Virus propagation was performed in VeroE6 cells in DMEM supplemented with 2% fetal bovine serum, 1 mM L-glutamine, 50 U/ml penicillin, and 50 μg/ml streptomycin (DMEM2). VeroE6 cells were maintained in DMEM supplemented with 10% fetal bovine serum, 1 mM L-glutamine, 50 U/ml penicillin, and 50 μg/ml streptomycin. Mycoplasma testing is performed at regular intervals and no mycoplasma was detected.
ChAdOx1 nCoV-19 was formulated as previously described26. Four groups of 10, 4–6-week-old female Syrian hamsters (Envigo Indianapolis, IN) were vaccinated with 2.5 × 108 infectious units of ChAdOx1 nCoV-19 vaccine or ChAdOx1-GFP delivered intramuscularly in two 50 µL doses into the posterior thighs 30 days prior to the challenge. Five days prior to challenge a blood sample was collected via the retro-orbital plexus under isoflurane anesthesia and spun at 2000 g for 10 min to obtain serum. Two groups (10 ChAdOx1 nCoV-19 vaccinated and 10 ChAdOx1 GFP vaccinated hamsters) were challenged with 104 TCID50/mL B.1.1.7 diluted in sterile Dulbecco’s Modified Eagle’s media (DMEM), in a 40 µL bolus delivered intranasally, one-half into each nostril. Two other groups (10 ChAdOx1 nCoV-19 vaccinated and 10 ChAdOx1 GFP vaccinated hamsters) were similarly challenged with B.1.351-1 also diluted in sterile DMEM. Weights were recorded daily until 14 DPI. Oropharyngeal swabs were collected daily in 1 mL of DMEM2 up until 5 DPI. On 5 DPI four animals from each group were euthanized. The lungs were excised, weighed, and photographed, and samples were taken for qRT-PCR analysis, virus titrations, and histopathology. The remaining six animals in each group were monitored daily for signs of disease and weighed until 14 DPI.
Two groups of 12 female Syrian hamsters (Envigo Indianapolis, IN) were vaccinated with 2.5 × 108 infectious units of ChAdOx1 nCoV-19 vaccine or ChAdOx1-GFP delivered intramuscularly (IM group) in two 50 µL doses into the posterior thighs or delivered intranasally (IN group) in one 40 µL dose delivered equally split between each nostril 60 days prior to challenge. One group of 10 naïve female hamsters was used as a control. All three groups were challenged with 104 TCID50/mL B.1.351-2 diluted in sterile Dulbecco’s Modified Eagle’s media (DMEM), in a 40 µL bolus delivered intranasally, equally split between each nostril. Weights were recorded daily until 14 DPI. Oropharyngeal swabs were collected daily in 1 mL of DMEM2 up until 5 DPI. On 5 DPI four animals from each group were euthanized. The lungs were excised, weighed, and samples were taken for qRT-PCR analysis, virus titrations, and histopathology. The remaining animals in each group were monitored daily for signs of disease and weighed until 14 DPI.
Lung sections were weighed and homogenized in 1 mL of DMEM. Virus titrations were performed by end-point titration of 10-fold dilutions of virus swab media or tissue homogenates on VeroE6 cells in 96-well plates. When titrating tissue homogenate, the top 2 rows of cells were washed two times with PBS prior to the addition of a final 100 µl of DMEM2. Cells were incubated at 37 °C and 5% CO2. Cytopathic effect was read 6 days later.
Sera were heat-inactivated (30 min, 56 °C). After an initial 1:10 dilution of the sera, two-fold serial dilutions were prepared in DMEM2. 100 TCID50 of SARS-CoV-2 variant B.1.1.7 or B.1.351 was added to the diluted sera. After a 1 hr incubation at 37 °C and 5% CO2, the virus-serum mixture was added to VeroE6 cells. The cells were incubated for 6 days at 37 °C and 5% CO2 at which time they were evaluated for CPE. The virus neutralization titer was expressed as the reciprocal value of the highest dilution of the serum that still inhibited virus replication.
RNA extraction and quantitative reverse-transcription polymerase chain reaction
RNA was extracted from oropharyngeal swabs using the QiaAmp Viral RNA kit (Qiagen) according to the manufacturer’s instructions and following high containment laboratory protocols. Lung samples were homogenized and extracted using the RNeasy kit (Qiagen) according to the manufacturer’s instructions and following high containment laboratory protocols. A viral sgRNA27 specific assay was used for the detection of viral RNA. Five microliters of extracted RNA was tested with the Quantstudio 3 system (Thermo Fisher) according to instructions from the manufacturer. A standard curve was generated during each run using SARS-CoV-2 standards containing a known number of genome copies. Primer sequences can be found in table S1.
Viral RNA sequencing
For sequencing from viral stocks, sequencing libraries were prepared using Stranded Total RNA Prep Ligation with Ribo-Zero Plus kit per manufacturer’s protocol (Illumina) and sequenced on an Illumina MiSeq at 2 × 150 base pair reads. For sequencing from swab and lung tissue, total RNA was depleted of ribosomal RNA using the Ribo-Zero Gold rRNA Removal Kit (Illumina). Sequencing libraries were constructed using the KAPA RNA HyperPrep kit following the manufacturer’s protocol (Roche Sequencing Solutions). To enrich for SARS-CoV-2 sequence, libraries were hybridized to myBaits Expert Virus biotinylated oligonucleotide baits following the manufacturer’s manual, version 4.01 (Arbor Biosciences, Ann Arbor, MI). Enriched libraries were sequenced on the Illumina MiSeq instrument as paired-end 2 × 151 base pair reads. Raw FASTQ reads were trimmed of Illumina adapter sequences using cutadapt version 1.1228 and then trimmed and filtered for quality using the FASTX-Toolkit (version 0.0.14, Hannon Lab, CSHL). Remaining reads were mapped to the SARS-CoV-2 2019-nCoV/USA-WA1/2020 genome (MN985325.1) or hCoV-19/England/204820464/2020 (EPI_ISL_683466) or hCoV-19/SouthAfrica/KRISP-K005325/2020 (EPI_ISL_678615) using Bowtie2 version 2.2.929 with parameters --local --no-mixed -X 1500. PCR duplicates were removed using Picard MarkDuplicates (version 2.18.7, Broad Institute) and variants were called using GATK HaplotypeCaller version 4.1.2.030 with parameter -ploidy 2. Variants were filtered for QUAL > 500 and DP > 20 using bcftools (version 1.10.2).
Expression and purification of SARS-CoV-2 S and receptor binding domain
Protein production was performed as described previously31,32. Expression plasmids encoding the codon optimized SARS-CoV-2 full length S and RBD were obtained from Kizzmekia Corbett and Barney Graham (Vaccine Research Center, Bethesda, USA)33 and Florian Krammer (Icahn School of Medicine at Mt. Sinai, NY, USA)34. Expression was performed in Freestyle 293-F cells (Thermofisher), maintained in Freestyle 293 Expression Medium (Gibco) at 37 °C and 8% CO2 shaking at 130 rpm. Cultures totaling 500 mL were transfected with PEI at a density of one million cells per mL. Supernatant was harvested 7 days post transfection, clarified by centrifugation, and filtered through a 0.22 µM membrane. The protein was purified using Ni-NTA immobilized metal-affinity chromatography (IMAC) using Ni Sepharose 6 Fast Flow Resin (GE Lifesciences) or NiNTA Agarose (QIAGEN) and gravity flow. After elution the protein was buffer exchanged into 10 mM Tris pH8, 150 mM NaCl buffer (S) or PBS (RBD) and stored at − 80 °C.
Maxisorp plates (Nunc) were coated overnight at 4 °C with 50 ng/well S or RBD protein in PBS. Plates were blocked with 100 µl of casein in PBS (Thermo Fisher) for 1 hr at RT. Serum diluted 1:6,400 was further 2-fold serially diluted in casein in PBS was incubated at RT for 1 hr. Antibodies were detected using affinity-purified polyclonal antibody peroxidase-labeled goat-anti-hamster IgG (Seracare, 5220-0371) in casein followed by TMB 2-component peroxidase substrate (Seracare, 5120-0047). The reaction was stopped using a stop solution (Seracare, 5150-0021) and read at 450 nm. All wells were washed 4x with PBST 0.1% tween in between steps. The threshold for positivity was set at 2x OD value of negative control (serum obtained from unvaccinated hamsters prior to the start of the experiment).
Statistical analysis was completed using Graphpad Prism 8.2.1.
Further information on research design is available in the Nature Research Reporting Summary linked to this article.
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We would like to thank Mukul Ranjan, Sujatha Rashid, Kimberly Stemple, Alan Sutherland, Anita Mora, Kizzmekia Corbett, Barney Graham, Florian Krammer, Fatima Amanat, Victoria Avanzato, and the animal caretakers for their assistance during the study. The following reagent was obtained through BEI Resources, NIAID, NIH: SARS-Related Coronavirus 2, Isolate hCoV-19/South Africa/KRISP-K005325/2020, NR-54009, contributed by Alex Sigal and Tulio de Oliveira, and SARS-Related Coronavirus 2, Isolate hCoV-19/England/204820464/2020, NR-54000, contributed by Bassam Hallis. Isolate hCoV-19/USA/MD-HP01542/2021 was obtained from Andrew Pekosz, John Hopkins Bloomberg School of Public Health.
This work was supported by the Intramural Research Program of the National Institute of Allergy and Infectious Diseases (NIAID), National Institutes of Health (NIH) (1ZIAAI001179-01), and the Department of Health and Social Care using UK Aid funding managed by the NIHR.
S.C.G. is a board member of Vaccitech and named as an inventor on a patent covering the use of ChAdOx1-vector-based vaccines and a patent application covering a SARS-CoV-2 (nCoV-19) vaccine (UK patent application no. 2003670.3). T.L. is named as an inventor on a patent application covering a SARS-CoV-2 (nCoV-19) vaccine (UK patent application no. 2003670.3). The University of Oxford and Vaccitech, having joint rights in the vaccine, entered into a partnership with AstraZeneca in April 2020 for further development, large-scale manufacture, and global supply of the vaccine. Equitable access to the vaccine is a key component of the partnership. Neither Oxford University nor Vaccitech will receive any royalties during the pandemic period or from any sales of the vaccine in developing countries. All other authors declare no competing interests.
Peer review information Nature Communications thanks Robbert Boudewijns and the other, anonymous, reviewer(s) for their contribution to the peer review of this work.
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Fischer, R.J., van Doremalen, N., Adney, D.R. et al. ChAdOx1 nCoV-19 (AZD1222) protects Syrian hamsters against SARS-CoV-2 B.1.351 and B.1.1.7. Nat Commun 12, 5868 (2021). https://doi.org/10.1038/s41467-021-26178-y
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