Generation of Chicken IgY against SARS-COV-2 Spike Protein and Epitope Mapping

Lu, Yan; Wang, Yajun; Zhang, Zhen; Huang, Jingliang; Yao, Meicun; Huang, Guobin; Ge, Yuanyuan; Zhang, Peichun; Huang, Huaxin; Wang, Yong; Li, Huiliang; Wang, Wen

doi:https://doi.org/10.1155/2020/9465398

Journal of Immunology Research

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Abstract Introduction Materials and Methods Results Discussion Conclusions Data Availability Conflicts of Interest Authors’ Contributions Acknowledgments References Copyright Related Articles

Research Article | Open Access

Volume 2020 | Article ID 9465398 | https://doi.org/10.1155/2020/9465398

Generation of Chicken IgY against SARS-COV-2 Spike Protein and Epitope Mapping

Yan Lu,¹Yajun Wang,²Zhen Zhang,³Jingliang Huang,⁴Meicun Yao,⁵Guobin Huang,⁶Yuanyuan Ge,⁶Peichun Zhang,¹Huaxin Huang,¹Yong Wang,⁷Huiliang Li,²and Wen Wang¹

Academic Editor: Juraj Ivanyi

Received19 Jun 2020

Revised16 Sept 2020

Accepted25 Sept 2020

Published17 Oct 2020

Abstract

This new decade has started with a global pandemic of COVID-19 caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), precipitating a worldwide health crisis and economic downturn. Scientists and clinicians have been racing against time to find therapies for COVID-19. Repurposing approved drugs, developing vaccines and employing passive immunization are three major therapeutic approaches to fighting COVID-19. Chicken immunoglobulin Y (IgY) has the potential to be used as neutralizing antibody against respiratory infections, and its advantages include high avidity, low risk of adverse immune responses, and easy local delivery by intranasal administration. In this study, we raised antibody against the spike (S) protein of SARS-CoV-2 in chickens and extracted IgY (called IgY-S) from egg yolk. IgY-S exhibited high immunoreactivity against SARS-CoV-2 S, and by epitope mapping, we found five linear epitopes of IgY-S in SARS-CoV-2 S, two of which are cross-reactive with SARS-CoV S. Notably, epitope SIIAYTMSL, one of the identified epitopes, partially overlaps the S1/S2 cleavage region in SARS-CoV-2 S and is located on the surface of S trimer in 3D structure, close to the S1/S2 cleavage site. Thus, antibody binding at this location could physically block the access of proteolytic enzymes to S1/S2 cleavage site and thereby impede S1/S2 proteolytic cleavage, which is crucial to subsequent virus-cell membrane fusion and viral cell entry. Therefore, the feasibility of using IgY-S or epitope SIIAYTMS-specific IgY as neutralizing antibody for preventing or treating SARS-CoV-2 infection is worth exploring.

1. Introduction

Following the first reported cases of unexplained pneumonia in December 2019 in Wuhan, China [1, 2], severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has since been confirmed to be the pathogen of a novel infectious respiratory disease, namely, coronavirus disease 2019 (COVID-19) [3–5]. In March 2020, the World Health Organization (WHO) declared COVID-19 a global pandemic [6]. At present, the counts of COVID-19 stand at above 37 million confirmed cases including over 1 million recorded deaths worldwide. As COVID-19 continues to rage in some parts of the world and threatens new waves of infection in others with devastating consequences for people’s lives and livelihoods as well as global economy [7], all-round scientific effort towards effective disease management and treatment is urgently needed. Repurposing approved drugs and developing specific vaccines are two main strategies to combat SARS-CoV-2 infection. So far, several repurposed drugs such as remdesivir, an adenosine nucleoside triphosphate analog previously tested for treating Ebola virus disease [8, 9], and chloroquine/hydroxychloroquine, a commonly used antimalaria drug, have produced unsatisfactory results in several COVID-19 clinical trials [10–12]. Despite the fast progress on developing vaccines for SARS-CoV-2 [13–15], we are still faced with uncertainty about the effectiveness and mass production of COVID-19 vaccines [16]. Passive immunization by introducing pregenerated antibodies/immunoglobulins is another old-fashioned treatment being eyed with renewed interest for fighting COVID-19, particularly for patients with immunodeficient conditions [17]. For example, convalescent plasma transfusion has been shown to help improve the clinical outcome of severe COVID-19 [18, 19], but issues regarding supply, safety, and clinical efficacy need to be further addressed in randomized controlled trials [20]. Moreover, several human monoclonal antibodies could neutralize SARS-CoV-2 and inhibit its infectious ability in cultured systems [21–24]. Apart from human antibodies, chicken immunoglobulin Y (IgY) from egg yolk has proved able to neutralize pathogens in the respiratory tract of mice [25–27]. Because of its high specificity and avidity, low risk of adverse immune responses, low manufacture cost, and ease of storage, chicken IgY raised against SARS-CoV-2 is waiting to be tapped into for potential therapeutic application in treating COVID-19 [28, 29].

SARS-CoV-2 belongs to the coronavirus family, which is a large family of enveloped, single-stranded positive-sense RNA viruses, comprised of alpha, beta, gamma, and delta four subgroups [30]. To date, seven coronaviruses have been identified as being able to infect human and four of them (HCoV-NL63, HCoV-229E, HCoV-OC43, and HCoV-HKU1) have been linked to mild colds, whereas the other three [Middle East respiratory syndrome coronavirus (MERS-CoV), SARS-CoV, and SARS-CoV-2] can lead to severe respiratory infection. MERS-CoV, SARS-CoV, SARS-CoV-2, HCoV-OC43, and HCoV-HKU1 are members of the beta subgroup of coronaviruses. Coronavirus genome encodes four structural proteins, i.e., the spike (S), envelope (E), membrane (M), and nucleocapsid (N) proteins [31]. The highly glycosylated homotrimeric S protein can be cleaved into two subunits, S1 and S2, via host-dependent proteolytic cleavage; the S1 subunit contains a receptor-binding domain (RBD), mediating host receptor recognition, while the S2 subunit anchors the spike in the viral envelope, facilitating virus-cell membrane fusion and viral cell entry [32–34]. Upon interaction between the S1 subunit and its host receptor, conformational changes trigger further cleavage of S2 subunit at the S2 site located immediately upstream of the fusion peptide, the exposure of which leads to membrane fusion and virus invasion [34]. The SARS-CoV S and SARS-CoV-2 S share human angiotensin-converting enzyme 2 (hACE2) as receptor, whereas the MERS S uses dipeptidyl peptidase 4 (DPP4) as receptor. Targeting SARS-CoV-2 S with antibody to block virus-host interaction and thus prevent viral invasion is generally the rationale for vaccine design and for the passive immunization approach [13, 14]. In this study, we immunized chickens with recombinant S protein of SARS-CoV-2 and acquired egg yolk IgY (called IgY-S) with high immunoreactivity. By epitope mapping, we further identified five epitopes of IgY-S in SARS-CoV-2 S, two of which are cross-reactive between SARS-CoV-2 S and SARS-CoV S. Our results lay the foundation for further study on IgY-S as a potential treatment for preventing or combating SARS-CoV-2 infection.

2. Materials and Methods

2.1. IgY-S Generation in Hens

Full-length extracellular domain of SARS-CoV-2 S protein (1-1,213 amino acids; GenBank No. YP_009724390), fused with a polyhistidine tag at the C-terminus, was expressed with the baculovirus-insect cell expression system (Sino Biological, Beijing). 100 μg purified protein was emulsified with an equal volume of Freund’s complete adjuvant (Sigma-Aldrich, MO) and intramuscularly injected into the thigh of laying hens at 5 sites. Two booster injections of 50 μg purified protein mixed with an equal volume of incomplete Freund’s adjuvant were administered at two-week intervals. One week after the final injection, eggs were collected and stored at 4°C. Hens injected with only adjuvant in parallel were used for acquiring control IgY (IgY-C).

2.2. IgY Isolation

The egg yolk was carefully separated from the white, rinsed twice with phosphate-buffered saline (PBS), transferred into an equal volume of 5.33% PEG6000 solution, mixed thoroughly for 15 minutes, and centrifuged at 7,000 × g for 7 minutes at 4°C. The supernatant was carefully transferred, and an equal volume of 40% PEG6000 was slowly added to it. After thorough mixing for 15 minutes, the mixture was centrifuged at 7,000 × g for 7 minutes at 4°C. After removal of the supernatant, the pellet was dissolved into 10 ml PBS with vortexing, followed by centrifugation at 7,000 × g for 7 minutes at 4°C; then, the supernatant was collected and filtered with a 0.22 μm filter. The extracted IgY concentration was determined by the Bradford Reagent (Bio-Rad Laboratories, Shanghai). IgY was freeze-dried for storage at −20°C or stored at 1 mg/ml at −20°C.

2.3. Enzyme-Linked Immunosorbent Assay (ELISA)

MaxiSorb 96-well plates (Thermo Fisher Scientific, Guangzhou) were coated with 100 μl per well of the recombinant extracellular S protein of SARS-CoV-2 at 1.5 μg/ml for 2 hours at 37°C, washed 3 times, and saturated with blocking buffer (5% nonfat dried milk in PBS) for 2 hours at 37°C. IgY stock solution (1 mg/ml) was diluted in blocking buffer to make 1 : 500 dilution, followed by a two-fold serial dilution. The plates were washed, and then 100 μl of serially diluted IgY-S or IgY-C was added in triplicate to the wells and incubated for 1.5 hours at 37°C. The plates were washed and incubated with 100 μl per well of 1 : 2,000 HRP-conjugated goat anti-chicken IgY (Santa Cruz Biotechnology, CA) for 1 hour at 37°C. After washing, 100 μl TMB substrate solution (Hongxiang Biotech, Guangzhou) was added to the wells and incubated for 3 minutes at 37°C; then, the reaction was terminated with 50 μl of 2M H₂SO₄. The plates were scanned on a multiwell spectrophotometer, and optical density was read at 450 nm.

2.4. Epitope Mapping

IgY-S epitope mapping was performed using the PEPperPRINT peptide microarray system (PEPperPRINT GmbH, Heidelberg). IgY-C was used as mapping control. Microarray assays were conducted using the SARS-CoV-2 Proteome Microarray made up by duplicated spots of 4,883 different peptides, the SARS-CoV Antigen Microarray composed of duplicated spots of 998 different peptides, and the MERS-CoV Proteome Microarray consisting of duplicated spots of 3,818 different peptides. Hemagglutinin (HA) peptides framing the peptide microarrays were used as internal quality control to monitor assay quality and amino acid integrity. Briefly, to investigate background interactions, microarrays were prestained with 0.2 μg/ml DyLight680-conjugated goat anti-chicken IgY (H+L) secondary antibody (Thermo Fisher Scientific) and 0.5 μg/ml DyLight800-conjugated mouse monoclonal anti-HA (12CA5) control antibody (Thermo Fisher Scientific) in incubation buffer at room temperature for 45 minutes. Subsequently, sets of microarrays were incubated with IgY-S and IgY-C at concentrations of 1 μg/ml and 10 μg/ml in incubation buffer for 16 hours at 4°C with shaking at 140 rpm. After washing, the microarrays were incubated with goat anti-chicken secondary antibody and mouse anti-HA control antibody in incubation buffer for 45 minutes at room temperature. Stained microarrays were scanned with the LI-COR Odyssey imaging system (Li-cor Biosciences, Bad Homburg) with parameters set as: scanning offset 0.65 mm, resolution 21 μm and scanning intensities 7/7 (). Microarray image analysis was conducted with PepSlide Analyzer (SICASYS Software, Germersheim). A software algorithm was used to break down the fluorescence intensity of each spot into raw, foreground, and background signals and to calculate average median foreground intensities and spot-to-spot deviations of duplicated spots. Based on average median foreground intensities, intensity maps were generated and incorporated in the peptide maps. Peptide spots related to SARS-CoV-2 S as well as SARS-CoV S were focused on for analysis.

3. Results

3.1. IgY-S Immunoreactivity

IgY-S isolated from egg yolk of immunized chickens was evaluated for reactivity with recombinant S protein of SARS-CoV-2 by ELISA. Compared to IgY-C control, IgY-S displayed significantly elevated ability to bind to the antigen, even at the greatest dilution (1: 32,000)/lowest concentration (0.03125 μg/ml) tested (, Student’s -test) (Figure 1). These data hint at high immunoreactivity of IgY-S against SARS-CoV-2 S.

3.2. IgY-S Epitopes in SARS-CoV-2 S

IgY-S epitope mapping against SARS-CoV-2 S was performed using the SARS-CoV-2 Proteome Microarray made up by 15 amino acid peptides of SARS-CoV-2 with peptide-peptide overlaps of 13 amino acids. The microarrays were incubated with IgY-S at 1 μg/ml and 10 μg/ml. Prestaining of the microarray with the secondary antibody and anti-HA control antibody did not highlight any background interaction with SARS-CoV-2 peptides that could have interfered with the main assay. As standard epitopes are normally shorter than 12 amino acids with the majority of the binding energy typically being derived from around 5 amino acids [35], an epitope should be encompassed by a series of contiguous overlapping peptides and displayed as a distinct signal formation of successive spots (i.e., an “epitope signal pattern”). Six clear such patterns were observed, corresponding to consensus sequence motifs LDPLSET, SIIAYTMSL, QIYKTPP, AIHADQL, DLGDISGIN, and EIL, in order of signal strength from high to low (Figure 2). However, an “epitope signal pattern” was also traced back to sequence motif EIL when IgY-C was used instead of IgY-S (Figure 3), suggesting nonspecific binding of chicken IgY to this motif. In addition, signals from a number of single peptides containing an N-terminal motif TD were detected with IgY-C, but they were rather atypical, not of “epitope signal pattern.” Additional signals were detected in the microarray regions covering other SARS-CoV-2 proteins such as N protein and Orf1ab, but most were weak, possibly caused by nonspecific interaction or noise (data not shown). Taken together, these data reveal five linear motifs, LDPLSET, SIIAYTMSL, QIYKTPP, AIHADQL, and DLGDISGIN 5, as epitopes of IgY-S in SARS-CoV-2 S.

Figure 2

IgY-S epitope mapping against the SARS-CoV-2 Proteome Microarray. Peptide microarrays were performed with IgY-S at 1 μg/ml and 10 μg/ml, and stained microarrays were scanned, and signals were collected. Fluorescence intensities of peptide spots were generated with the PepSlide Analyzer software and plotted against sequential peptides covering SARS-CoV-2 S protein from N- to C-terminus. Fluorescence intensity peaks of peptides containing the consensus motifs LDPLSET, SIIAYTMSL, QIYKTPP, AIHADQL, DLGDISGIN, and EIL are indicated. Weak signal peaks from peptide spots not of “epitope signal pattern” are also shown.

Figure 3

Signal analysis of IgY-C against the SARS-CoV-2 Proteome Microarray. A peptide microarray was performed with IgY-C (10 μg/ml), and the resulting fluorescence intensities were plotted against sequential peptides covering SARS-CoV-2 S protein from N- to C-terminus. The fluorescence intensity plot of IgY-S (10 μg/ml) was incorporated for comparison. Weak signal peaks from peptide spots not of “epitope signal pattern” can be seen, and some of these peptides contain an N-terminal TD motif. Signal peaks corresponding to motif EIL are present for both IgY-S and IgY-C.

3.3. IgY-S Cross-Reactivity with SARS-CoV S

IgY-S epitope mapping against SARS-CoV S protein was performed using the SARS-CoV Antigen Microarray. Three relatively weak but clear “epitope signal patterns” were observed, two of them corresponding to consensus sequence motifs IVAYTMSLG and VDLGDISGI (Figure 4). These two epitopes in SARS-CoV S, IVAYTMSLG and VDLGDISGI, share high sequence homology with epitopes SIIAYTMSL and DLGDISGIN in SARS-CoV-2 S, respectively (identical/similar amino acids underlined). The other sequence motif recognized by IgY-S was an EIL-like epitope, but again the recognition was repeated when IgY-C was used (data not shown) pointing to nonspecific interaction.

Figure 4

IgY-S epitope mapping against the SARS-CoV Antigen Microarray. Peptide microarrays were performed with IgY-S at 1 μg/ml and 10 μg/ml, and the resulting fluorescence intensities were plotted in relation to sequential peptides covering SARS-CoV-2 S protein from N- to C-terminus. Fluorescence intensity peaks corresponding to the consensus motifs IVAYTMSLG and VDLGDISGI as well as an EIL-like motif are indicated. Weak signal peaks from peptide spots not of “epitope signal pattern” are also shown.

Taken all, the above data demonstrate that IgY-S can cross-react with SARS-CoV S via two cross-reactive epitopes between SARS-CoV-2 S and SARS-CoV S, but its epitopes QIYKTPP and AIHADQL appear specific to SARS-CoV-2 S. In addition, IgY-S did not show cross-reactivity with MERS S in a peptide microarray assay using the MERS-CoV Proteome Microarray (data not shown).

3.4. IgY-S Epitope Locations in SARS-CoV-2 S

Similar to SARS-CoV S, the extracellular region of SARS-CoV-2 S contains from N- to C-terminus, signal sequence (SS), N-terminal domain (NTD), RBD, subdomains 1 and 2 (SD1 and SD2), S1/S2 cleavage region, S2 cleavage region, fusion peptide (FP), heptad repeat 1 (HR1), central helix (CH), connector domain (CD), and heptad repeat 2 (HR2) (Figure 5) [36, 37]. Epitope LDPLSET is located at the C-terminus of NTD; SIIAYTMSL partially overlaps S1/S2 cleavage region; QIYKTPP is located between S1/S2 cleavage region and S2 cleavage region; AIHADQL lies within SD2; and DLGDISGIN resides between CD and HR2. In epitope SIIAYTMSL, the SI residues overlapping the S1/S2 cleavage region are thought to be conserved for SARS-CoV-2 and SARS-CoV and may have a bearing on S1/S2 cleavage [37]. In addition, it is possible that antibody binding at this location could interfere with S1/S2 proteolytic cleavage, thereby inhibiting membrane fusion and viral entry into the host cell [38].

(a)

(b)

Figure 5

Schematic illustrations of SARS-Cov-2 S protein. (a) Locations of IgY-S epitopes in SARS-Cov-2 S. Locations of the five identified IgY-S epitopes are indicated by arrows. SS: signal sequence; NTD: N-terminal domain; RBD: receptor-binding domain; SD1: subdomain 1; SD2: subdomain 2; S1/S2: S1/S2 cleavage region; S2: S2 cleavage region; FP: fusion peptide; HR1: heptad repeat 1; CH: central helix; CD: connector domain; HR2: heptad repeat 2. (b) 3D view of SARS-CoV-2 S trimer based on PDB 6VXX [37], constructed by UCSF Chimera. The S1/S2 cleavage site is indicated by an arrowhead. The yellow strand represents a peptide containing epitope SIIAYTMSL.

4. Discussion

Passive immunization is an important approach to tackling SARS-CoV-2 infection [39]. In this study, we raised antibody in chickens against recombinant extracellular S protein of SARS-CoV-2 and obtained egg yolk IgY-S with high immunoreactivity. By epitope mapping, we identified five linear epitopes of IgY-S in SARS-CoV-2 S protein (Figures 2 and 3), two of which are cross-reactive with SARS-CoV S (Figure 4).

The SIIAYTMSL epitope, which showed the second highest fluorescence intensity in peptide microarray analysis, is a conserved sequence between SARS-CoV S and SARS-CoV-2 S and overlaps the S1/S2 cleavage region in both S proteins. With the help of the published 3D structure of SARS-CoV-2 S [37], we found that this epitope is located on the surface of S homotrimer, close to the S1/S2 cleavage site (Figure 5), hinting that antibody binding at this location could physically block the access of proteolytic enzymes to the cleavage site. Given the importance of S1/S2 proteolytic cleavage to subsequent membrane fusion and viral cell invasion, it is possible that IgY-S binding to epitope SIIAYTMSL could prevent virus infection [38]. The spatial locations of the other four epitopes are either inside S trimer or difficult to identify with current resolution for the 3D structure. Nevertheless, neutralizing experiments in cultured human cells have been planned to evaluate whether to use IgY-S as a whole or to acquire epitope-specific IgY by affinity purification with each epitope.

As egg yolk IgY can be produced quickly (5 weeks of immunization period) with high yield (40-80 mg per egg) [40], neutralizing IgY has unique advantages as a potential passive immunization therapy for infections by new pathogens, e.g., SARS-CoV-2 with a new mutated form of S protein, which is possible because RNA viruses are known for their high mutation rates [41]. An easy and noninvasive way to deliver agents locally for respiratory tract infection is by intranasal or oral administration. In animal models, egg yolk IgY isolated from immunized chickens has been tested for treating viral respiratory infections by influenza A subtypes H1N1, H3N2, and H5N1 [25–27] and influenza B [42] via intranasal delivery. As chicken eggs are a dietary staple for human, IgY is well tolerated in human [28]. Moreover, because purified IgY does not contain the allergenic egg albumin, it can also be safely used by patients with egg allergy [28]. In a double-blind, randomized, placebo-controlled trial, a specific IgY antibody was effective in treating patients with acute and chronic pharyngitis when administered by oral spray [43], suggesting that IgY could be a safe and effective agent against respiratory infection. Therefore, our IgY-S has the potential to be safely used as a nasal or oral spray to prevent/treat SARS-CoV-2 infection [44]. If our planned in vitro neutralizing assays produce positive results, we will be encouraged to conduct an early-phase clinical trial with IgY-S. In addition, IgY does not interact with mammalian Fc receptors or activate the mammalian complement system, so it can avoid triggering antibody-dependent enhancement (ADE) of disease and complement-mediated adverse inflammatory responses [45]. Therefore, it could be beneficial to administer neutralizing IgY intravascularly to treat SARS-CoV-2 infection, especially to patients with severe symptoms.

Although the great potential of chicken IgY for COVID-19 treatment has been proposed by several labs [29, 44, 46], so far, no follow-up data or epitopes of SARS-CoV-2 targeted by IgY have been published. A previous study on chicken IgY produced against SARS-CoV implied that a dominant epitope existed in the “Se-e” fragment located between amino acid residues 456–650 of SARS-CoV S [47]. The AIHADQL epitope identified in our study is located in the counterpart of “Se-e” fragment in SARS-CoV-2 S. Although AIHADQL is found in “Se-e” fragment of SARS-CoV, it was not recognized by IgY-S in the SARS-CoV peptide microarray assay. The reason could lie in the neighbouring amino acids, which are dissimilar between SARS-CoV and SARS-CoV-2 and may play a role in antibody-epitope binding. In addition, continued search for neutralizing epitopes/antibodies has been conducted using convalescent sera of COVID-19 patients, with the focus on RBD of SARS-CoV-2 S protein [23, 24, 48–52]. Neutralizing epitopes in other domains of S1 subunit such as NTD, as well as domains of S2 subunit, have also been reported [53–56]. However, none of these epitopes are identical to epitopes identified by IgY-S. Interestingly, peptides/epitopes in RBD were found to have less interaction with convalescent sera in a SARS-CoV-2 peptide screening study [57]. The reason behind this could be that RBD epitopes are conformational epitopes or glycosylated, and this is a common limitation to most epitope mapping analyses, ours included.

5. Conclusions

In this study, chicken IgY-S was generated with high immunoreactivity against SARS-CoV-2 S protein and five epitopes of IgY-S were identified. Our work provides a new potential therapeutic tool for COVID-19 treatment. Our study is the first to explore using chicken egg IgY for neutralizing SARS-CoV-2.

Data Availability

The epitope microarray data used to support the findings of this study are available from the corresponding author upon request.

Conflicts of Interest

All authors declare no conflict of interest.

Authors’ Contributions

Yan Lu and Yajun Wang contributed equally.

Acknowledgments

We thank Dr. Ling Zhang and Dr. Cheng Yang for their kind help and discussion. Li’s Lab is supported by BBSRC (BB/S000844/1 and BB/S008934/1) and Shenzhen Sanming Project of Medicine (SZSM201911003); Yajun Wang is a Newton International Fellow (NIF003/1003).

References

C. Huang, Y. Wang, X. Li et al., “Clinical features of patients infected with 2019 novel coronavirus in Wuhan, China,” The Lancet, vol. 395, no. 10223, pp. 497–506, 2020.
View at: Publisher Site | Google Scholar
C. Wang, P. W. Horby, F. G. Hayden, and G. F. Gao, “A novel coronavirus outbreak of global health concern,” The Lancet, vol. 395, no. 10223, pp. 470–473, 2020.
View at: Publisher Site | Google Scholar
R. Lu, X. Zhao, J. Li et al., “Genomic characterisation and epidemiology of 2019 novel coronavirus: implications for virus origins and receptor binding,” Lancet, vol. 395, no. 10224, pp. 565–574, 2020.
View at: Publisher Site | Google Scholar
F. Wu, S. Zhao, B. Yu et al., “A new coronavirus associated with human respiratory disease in China,” Nature, vol. 579, no. 7798, pp. 265–269, 2020.
View at: Publisher Site | Google Scholar
P. Zhou, X. L. Yang, X. G. Wang et al., “A pneumonia outbreak associated with a new coronavirus of probable bat origin,” Nature, vol. 579, no. 7798, pp. 270–273, 2020.
View at: Publisher Site | Google Scholar
M. S. Green, “Did the hesitancy in declaring COVID-19 a pandemic reflect a need to redefine the term?” The Lancet, vol. 395, no. 10229, pp. 1034-1035, 2020.
View at: Publisher Site | Google Scholar
The Lancet Infectious Diseases, “COVID-19: endgames,” The Lancet Infectious Diseases, vol. 20, no. 5, 2020.
View at: Publisher Site | Google Scholar
E. Check Hayden, “Experimental drugs poised for use in Ebola outbreak,” Nature, vol. 557, no. 7706, pp. 475-476, 2018.
View at: Publisher Site | Google Scholar
S. Mulangu, L. E. Dodd, Davey RT Jr et al., “A randomized, controlled trial of Ebola virus disease therapeutics,” The New England Journal of Medicine, vol. 381, no. 24, pp. 2293–2303, 2019.
View at: Publisher Site | Google Scholar
J. Geleris, Y. Sun, J. Platt et al., “Observational study of hydroxychloroquine in hospitalized patients with Covid-19,” The New England Journal of Medicine, vol. 382, no. 25, pp. 2411–2418, 2020.
View at: Publisher Site | Google Scholar
W. Tang, Z. Cao, M. Han et al., “Hydroxychloroquine in patients with mainly mild to moderate coronavirus disease 2019: open label, randomised controlled trial,” BMJ, vol. 369, 2020.
View at: Publisher Site | Google Scholar
Y. Wang, D. Zhang, G. du et al., “Remdesivir in adults with severe COVID-19: a randomised, double-blind, placebo-controlled, multicentre trial,” Lancet, vol. 395, no. 10236, pp. 1569–1578, 2020.
View at: Publisher Site | Google Scholar
T. Thanh le, Z. Andreadakis, A. Kumar et al., “The COVID-19 vaccine development landscape,” Nature Reviews. Drug Discovery, vol. 19, no. 5, pp. 305-306, 2020.
View at: Publisher Site | Google Scholar
N. van Doremalen, T. Lambe, A. Spencer et al., “ChAdOx1 nCoV-19 vaccine prevents SARS-CoV-2 pneumonia in rhesus macaques,” Nature, 2020.
View at: Publisher Site | Google Scholar
Q. Gao, L. Bao, H. Mao et al., “development of an inactivated vaccine candidate for SARS-CoV-2,” Science, vol. 369, no. 6499, pp. 77–81, 2020.
View at: Publisher Site | Google Scholar
C. Arnold, “A vaccine is still a long way off,” New Scientist, vol. 246, no. 3280, 2020.
View at: Publisher Site | Google Scholar
L. Hammarström, H. Abolhassani, F. Baldanti, H. Marcotte, and Q. Pan-Hammarström, “Development of passive immunity against SARS-CoV-2 for management of immunodeficient patients - a perspective,” The Journal of Allergy and Clinical Immunology, vol. 146, no. 1, pp. 58–60, 2020.
View at: Publisher Site | Google Scholar
C. Shen, Z. Wang, F. Zhao et al., “Treatment of 5 critically ill patients with COVID-19 with convalescent plasma,” Journal of the American Medical Association, vol. 323, no. 16, pp. 1582–1589, 2020.
View at: Publisher Site | Google Scholar
K. Duan, B. Liu, C. Li et al., “Effectiveness of convalescent plasma therapy in severe COVID-19 patients,” Proceedings of the National Academy of Sciences of the United States of America, vol. 117, no. 17, pp. 9490–9496, 2020.
View at: Publisher Site | Google Scholar
J. D. Roback and J. Guarner, “Convalescent plasma to treat COVID-19,” Journal of the American Medical Association, vol. 323, no. 16, p. 1561, 2020.
View at: Publisher Site | Google Scholar
X. Chen, R. Li, Z. Pan et al., “Human monoclonal antibodies block the binding of SARS-CoV-2 spike protein to angiotensin converting enzyme 2 receptor,” Cellular & Molecular Immunology, vol. 17, no. 6, pp. 647–649, 2020.
View at: Publisher Site | Google Scholar
C. Wang, W. Li, D. Drabek et al., “A human monoclonal antibody blocking SARS-CoV-2 infection,” Nature Communications, vol. 11, no. 1, p. 2251, 2020.
View at: Publisher Site | Google Scholar
Y. Wu, F. Wang, C. Shen et al., “A noncompeting pair of human neutralizing antibodies block COVID-19 virus binding to its receptor ACE2,” Science, vol. 368, no. 6496, pp. 1274–1278, 2020.
View at: Publisher Site | Google Scholar
Y. Cao, B. Su, X. Guo et al., “Potent neutralizing antibodies against SARS-CoV-2 identified by high-throughput single-cell sequencing of convalescent patients’ B cells,” Cell, vol. 182, no. 1, pp. 73–84.e16, 2020.
View at: Publisher Site | Google Scholar
M. G. Wallach, R. J. Webby, F. Islam et al., “Cross-protection of chicken immunoglobulin Y antibodies against H5N1 and H1N1 viruses passively administered in mice,” Clinical and Vaccine Immunology, vol. 18, no. 7, pp. 1083–1090, 2011.
View at: Publisher Site | Google Scholar
M. Tsukamoto, S. Hiroi, K. Adachi et al., “Antibodies against swine influenza virus neutralize the pandemic influenza virus A/H1N1,” Molecular Medicine Reports, vol. 4, no. 2, pp. 209–214, 2011.
View at: Publisher Site | Google Scholar
Y. E. Yang, J. Wen, S. Zhao, K. Zhang, and Y. Zhou, “Prophylaxis and therapy of pandemic H1N1 virus infection using egg yolk antibody,” Journal of Virological Methods, vol. 206, pp. 19–26, 2014.
View at: Publisher Site | Google Scholar
A. T. Abbas, S. A. el-Kafrawy, S. S. Sohrab, and E. I. A. Azhar, “IgY antibodies for the immunoprophylaxis and therapy of respiratory infections,” Human Vaccines & Immunotherapeutics, vol. 15, no. 1, pp. 264–275, 2019.
View at: Publisher Site | Google Scholar
C. Constantin, M. Neagu, T. Supeanu, V. Chiurciu, and D. Spandidos, “IgY - turning the page toward passive immunization in COVID-19 infection (review),” Experimental and Therapeutic Medicine, vol. 20, no. 1, pp. 151–158, 2020.
View at: Publisher Site | Google Scholar
Coronaviridae Study Group of the International Committee on Taxonomy of Viruses, “The species severe acute respiratory syndrome-related coronavirus: classifying 2019-nCoV and naming it SARS-CoV-2,” Nature Microbiology, vol. 5, no. 4, pp. 536–544, 2020.
View at: Publisher Site | Google Scholar
Y. Chen, Q. Liu, and D. Guo, “Emerging coronaviruses: genome structure, replication, and pathogenesis,” Journal of Medical Virology, vol. 92, no. 4, pp. 418–423, 2020.
View at: Publisher Site | Google Scholar
P. M. Colman and M. C. Lawrence, “The structural biology of type I viral membrane fusion,” Nature Reviews. Molecular Cell Biology, vol. 4, no. 4, pp. 309–319, 2003.
View at: Publisher Site | Google Scholar
B. J. Bosch, R. van der Zee, C. A. de Haan, and P. J. M. Rottier, “The coronavirus spike protein is a class I virus fusion protein: structural and functional characterization of the fusion core complex,” Journal of Virology, vol. 77, no. 16, pp. 8801–8811, 2003.
View at: Publisher Site | Google Scholar
S. Belouzard, V. C. Chu, and G. R. Whittaker, “Activation of the SARS coronavirus spike protein via sequential proteolytic cleavage at two distinct sites,” Proceedings of the National Academy of Sciences of the United States of America, vol. 106, no. 14, pp. 5871–5876, 2009.
View at: Publisher Site | Google Scholar
K. F. Sykes, J. B. Legutki, and P. Stafford, “Immunosignaturing: a critical review,” Trends in Biotechnology, vol. 31, no. 1, pp. 45–51, 2013.
View at: Publisher Site | Google Scholar
D. Wrapp, N. Wang, K. S. Corbett et al., “Cryo-EM structure of the 2019-nCoV spike in the prefusion conformation,” Science, vol. 367, no. 6483, pp. 1260–1263, 2020.
View at: Publisher Site | Google Scholar
A. C. Walls, Y. J. Park, M. A. Tortorici, A. Wall, A. T. McGuire, and D. Veesler, “Structure, function, and antigenicity of the SARS-CoV-2 spike glycoprotein,” Cell, vol. 181, no. 2, pp. 281–292.e6, 2020, e6.
View at: Publisher Site | Google Scholar
M. Hoffmann, H. Kleine-Weber, and S. Pohlmann, “A multibasic cleavage site in the spike protein of SARS-CoV-2 is essential for infection of human lung cells,” Molecular Cell, vol. 78, no. 4, pp. 779–784.e5, 2020.
View at: Publisher Site | Google Scholar
A. Casadevall and L. A. Pirofski, “The convalescent sera option for containing COVID-19,” The Journal of Clinical Investigation, vol. 130, no. 4, pp. 1545–1548, 2020.
View at: Publisher Site | Google Scholar
D. Pauly, P. A. Chacana, E. G. Calzado, B. Brembs, and R. Schade, “IgY technology: extraction of chicken antibodies from egg yolk by polyethylene glycol (PEG) precipitation,” Journal of Visualized Experiments, no. 51, article e3084, 2011.
View at: Publisher Site | Google Scholar
S. Duffy, “Why are RNA virus mutation rates so damn high?” PLoS Biology, vol. 16, no. 8, article e3000003, 2018.
View at: Publisher Site | Google Scholar
J. Wen, S. Zhao, D. He, Y. Yang, Y. Li, and S. Zhu, “Preparation and characterization of egg yolk immunoglobulin Y specific to influenza B virus,” Antiviral Research, vol. 93, no. 1, pp. 154–159, 2012.
View at: Publisher Site | Google Scholar
M. Q. Xie, Y. X. Meng, Z. H. Li et al., “Effect of specific immunoglobulin Y in the treatment of acute and chronic pharyngitis,” Zhonghua Er Bi Yan Hou Ke Za Zhi, vol. 39, no. 2, pp. 112–115, 2004.
View at: Google Scholar
J. M. Pérez de la Lastra, V. Baca-González, P. Asensio-Calavia, S. González-Acosta, and A. Morales-delaNuez, “Can immunization of hens provide oral-based therapeutics against COVID-19?” Vaccines, vol. 8, no. 3, p. 486, 2020.
View at: Publisher Site | Google Scholar
J. Kovacs-Nolan and Y. Mine, “Egg yolk antibodies for passive immunity,” Annual Review of Food Science and Technology, vol. 3, no. 1, pp. 163–182, 2012.
View at: Publisher Site | Google Scholar
R. Somasundaram, A. Choraria, and M. Antonysamy, “An approach towards development of monoclonal IgY antibodies against SARS CoV-2 spike protein (S) using phage display method: a review,” International Immunopharmacology, vol. 85, article 106654, 2020.
View at: Publisher Site | Google Scholar
Y. C. Lee, S. J. Leu, H. C. Hung et al., “A dominant antigenic epitope on SARS-CoV spike protein identified by an avian single-chain variable fragment (scFv)-expressing phage,” Veterinary Immunology and Immunopathology, vol. 117, no. 1-2, pp. 75–85, 2007.
View at: Publisher Site | Google Scholar
J. Hansen, A. Baum, K. E. Pascal et al., “Studies in humanized mice and convalescent humans yield a SARS-CoV-2 antibody cocktail,” Science, vol. 369, no. 6506, pp. 1010–1014, 2020.
View at: Publisher Site | Google Scholar
D. F. Robbiani, C. Gaebler, F. Muecksch et al., “Convergent antibody responses to SARS-CoV-2 in convalescent individuals,” Nature, vol. 584, no. 7821, pp. 437–442, 2020.
View at: Publisher Site | Google Scholar
D. Zhou, H. M. E. Duyvesteyn, C. P. Chen et al., “Structural basis for the neutralization of SARS-CoV-2 by an antibody from a convalescent patient,” Nature Structural & Molecular Biology, vol. 27, no. 10, pp. 950–958, 2020.
View at: Publisher Site | Google Scholar
M. Yuan, N. C. Wu, X. Zhu et al., “A highly conserved cryptic epitope in the receptor binding domains of SARS-CoV-2 and SARS-CoV,” Science, vol. 368, no. 6491, pp. 630–633, 2020.
View at: Publisher Site | Google Scholar
R. Shi, C. Shan, X. Duan et al., “A human neutralizing antibody targets the receptor-binding site of SARS-CoV-2,” Nature, vol. 584, no. 7819, pp. 120–124, 2020.
View at: Publisher Site | Google Scholar
C. O. Barnes, A. P. West Jr., K. E. Huey-Tubman et al., “Structures of human antibodies bound to SARS-CoV-2 spike reveal common epitopes and recurrent features of antibodies,” Cell, vol. 182, no. 4, pp. 828–842.e16, 2020.
View at: Publisher Site | Google Scholar
X. Chi, R. Yan, J. Zhang et al., “A neutralizing human antibody binds to the N-terminal domain of the spike protein of SARS-CoV-2,” Science, vol. 369, no. 6504, pp. 650–655, 2020.
View at: Publisher Site | Google Scholar
P. J. M. Brouwer, T. G. Caniels, K. van der Straten et al., “Potent neutralizing antibodies from COVID-19 patients define multiple targets of vulnerability,” Science, vol. 369, no. 6504, pp. 643–650, 2020.
View at: Publisher Site | Google Scholar
C. M. Poh, G. Carissimo, B. Wang et al., “Two linear epitopes on the SARS-CoV-2 spike protein that elicit neutralising antibodies in COVID-19 patients,” Nature Communications, vol. 11, no. 1, 2020.
View at: Publisher Site | Google Scholar
Z. Yi, Y. Ling, X. Zhang et al., “Functional mapping of B-cell linear epitopes of SARS-CoV-2 in COVID-19 convalescent population,” Emerging Microbes & Infections, vol. 9, no. 1, pp. 1988–1996, 2020.
View at: Publisher Site | Google Scholar

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Copyright © 2020 Yan Lu et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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