key: cord-1038233-rbtyu4cu
authors: LIN, Ying; SHEN, Xu; YANG, Rui Fu; LI, Yi Xue; JI, Yong Yong; HE, You Yu; SHI, Mu De; LU, Wei; SHI, Tie Liu; WANG, Jin; WANG, Hong Xia; JIANG, Hua Liang; SHEN, Jian Hua; XIE, You Hua; WANG, Yuan; PEI, Gang; SHEN, Bei Fen; WU, Jia Rui; SUN, Bing
title: Identification of an epitope of SARS-coronavirus nucleocapsid protein
date: 2003-06-03
journal: Cell Res
DOI: 10.1038/sj.cr.7290158
sha: 09231c006e8603fe345d309934c0f81fd2e51398
doc_id: 1038233
cord_uid: rbtyu4cu

The nucleocapsid (N) protein of severe acute respiratory syndrome-coronavirus (SARS-CoV) is a major virion structural protein. In this study, two epitopes (N1 and N2) of the N protein of SARS-CoV were predicted by bioinformatics analysis. After immunization with two peptides, the peptides-specific antibodies were isolated from the immunized rabbits. The further experiments demonstrated that N1 peptide-induced polyclonal antibodies had a high affinity to bind to E. coli expressed N protein of SARS-CoV. Furthermore, it was confirmed that N1 peptide-specific IgG antibodies were detectable in the sera of severe acute respiratory syndrome (SARS) patients. The results indicated that an epitope of the N protein has been identified and N protein specific Abs were produced by peptide immunization, which will be useful for the study of SARS-CoV.

An outbreak of atypical pneumonia, referred to as SARS and first identified in Guangdong Province, China, has spread to several countries [1] . The mortality of this disease is higher and therefore few hundreds of people have died from the disease. In the absence of effective vaccines and drugs, infectious diseases such as SARS that is spread by the respiratory route must be taken very seriously. It is very important that public health officials are able to identify people infected with SARS at early stages of the disease and isolate them for an appropriate time, thus the cycle of transmission can be broken. Voluntary isolation and quarantine are of great inconvenience for a lot of people, but they are currently our best tools to save lives [2] . An accurate diagnosis method for SARS is urgent needed and it will be great helpful for people against SARS [3] [4] [5] .

A novel coronavirus has been identified in the patients of SARS. SARS-CoV is enveloped, positive-sense, ssRNA virus. The genome of SARS-CoV is 29,727 nucleotides in length, has 11 open reading frames, and the genome organization is similar to that of other coronaviruses. The structural proteins of SARS-CoV contain four proteins including the surface spike (S) glycoprotein, the small membrane (M) protein, the envelope (E) glycoprotein and the nucleocapsid (N) protein [6] [7] .

Based on available information of other coronaviruses, nucleocapsid (N) protein has multiple functions that are involved in providing nuclearimport signal, interfering cell process, virus replication and RNA package. In addition, N protein in many coronaviruses is highly conserved, immunogenic, and abundantly expressed during infection [8] [9] [10] [11] [12] . These features make it to be a suitable candidate for raising neutralizing antibodies and diagnostic applications.

In order to identify the epitopes of the N protein and to be able to quickly make specific antibodies against the N protein of SARS, in this study, two peptides were synthesized according to the sequences of the N protein, and the polyclonal antibodies were raised in the peptide-immunized rabbits. Our data showed that the antibodies were capable of binding to the N protein of SARS-CoV. It was interesting to observe that N1 peptide was also able to bind to IgG antibody from the sera of SARS patients. Our work was the first time to identify an epitope of the N protein of SARS-CoV, the antibodies induced by the peptide will be useful for the SARS diagnosis or analysis of N protein functions.

New Zealand rabbits were purchased from Shanghai Laboratory Animal Center, Chinese Academy of Sciences. Animals were kept in conventional conditions and were handled in compliance with Institute of Biochemistry and Cell Biology, Shanghai Institutes for Biological Sciences Chinese Academy of Sciences (Shanghai, China) guidelines for animal care and use.

Peptides (N1 and N2) derived from the sequences of SARS p utative nucleocapsid protein (NC-004718, Genbank) were synth esized using conventional solid-phase chemistry as described pr eviously [13] and purified by GL Biochem (Shanghai) Ltd. Thes e sequences (amino acid residues 21-44, PTDSTDNNQNGGRN GARPKQRRPQ, N1 peptide, and amino acid residues 138-160, GALNTPKDHIGTRNPNNNAATVL, N2 peptide) were chosen as highly antigenic sites by computer prediction with DNAstar (http://www.dnastar.com/). The synthetic peptides were covalen tly conjugated to bovine serum albumin (BSA, Sigma) by N-(3-Dimethylaminopropyl)-N'-ethylcarbodiimide hydrochloride (ED AC) (Sigma).

Rabbits were immunized s.c. with 200 μg of peptide-BSA in 0. 4 ml emulsion 1/1 v/v with complete Freund's adjuvant (CFA) that had been supplemented with Mycobacterium tuberculosis to the final concentration of 1 mg/ml and were injected subcutaneously at multiple sites on the back of rabbits. Three weeks later, booster injection was done with freshly prepared emulsion of the conjugate and Freund's incomplete adjuvant. Blood was drawn from the rabbits at five weeks following immunization, the blood was allowed to clot at 4 o C, and the antiserum was recovered by centrifugation [14] .

The full length of SARS nucleocapsid gene (1266bp) was subcloned into pQE30 His-tag expression vector (the detailed description will be published elsewhere). The 6XHis residues at the N terminus of the vector facilitated the purification of the expressed SARS N protein using Immobilized Metal Affinity Chromatography (IMAC). The recombinant plasmid was transformed into M15 E. coli cells for expression of the N protein. A freshly isolated colony was chosen and incubated overnight in liquid LB medium containing ampicillin (50 mg/ml) and kanamycin (25 μg/ ml) at 37oC. The overnight culture was diluted 1:10 in the same LB medium and grown at 37oC until A600 reached 0.6-0.8 absorbance units. The expression was then induced at 30oC for about 4 h by the addition of 0.5 mM isopropyl-b-Dthiogalactopyranoside (IPTG). The recombinant N protein was purified using Ni-NTA agarose (Qiagen) according to the procedure provided by the manufacturer. The purified N protein was then subjected to SDS-PAGE.

Purified N protein was loaded in SDS-sample buffer [50 mM Tris-HCl (pH 6.8), 2% w/v SDS, 10% glycerol, 100 mM DTT and 0. 1% w/v bromophenol blue], then subjected to electrophoresis on a 12% polyacrylamide gel followed by electrotransfer to PVDF membranes(Bio-rad). After blocking with 3% gelatin solution, the membrane was incubated with anti-peptide rabbit serum (1/1000 dilution) for one hour and the bound antibodies were detected by the use of HRP-conjugated goat anti-rabbit IgG (H+L) antibodies (Southern Biotech) and ECL detection reagents (Amersham Pharmacia Biotech) were used to develop the film.

The titers of the antisera from rabbits were determined by ELISA as described previously [15] . In brief, 96-well microtiter plates (Corning Costar) were coated with the tested BSA-peptide conjungates in 0.1M carbonate buffer (pH 9.6) (5μg/ml, 50μl/well) at 4 o C overnight. After blocking with PBS containing 3% gelatin/ 0.1% Tween 20, and the plates were incubated with diluted rabbit antisera at various concentrations at 37 o C for 2 h. Bound antibodies were determined with HRP-coupled goat anti-rabbit IgG (Bio-rad) and the OD values were measure by microplate autoreader (Bio-tek) at 450 nm. Nine SARS patients (clinical diagnosed) and 4 health controls were selected and their sera were collected. All the sera from patients were confirmed IgG positive by an ELISA with whole virus lysate as coating antigen and immunoflurorences assay (IFA). The reactivities of the peptides (N1 and N2) to the sera were measured by ELISA. The protocol was similar as mentioned above. The sera dilution was 1:10 and HRP-coupled goat anti-human IgG (Bio-rad) was used to detect IgG antibodies in the sera. All the experiments that were in volved in using the patients' sera were carried on in Bio-safety Level 3 laboratory.

Based on the computer software analysis, the Antigenic Index (AI) was similar between N1 and N2 peptides. So it was expected that both of them were capable of inducing Abs. When sera were analyzed by ELISA, the anti-serum titers were similar between two peptides-immunized rabbits (Tab 1). The data showed that both of N1 and N2 peptides were antigenic and induced the peptide-specific antibodies in the rabbits.

In order to determine whether N1 and N2 peptide-induced polyclonal Abs bind to N protein of SARS-CoV, the expressed full length N protein (422 amino acids) was served as target protein and the binding activity of N protein to antibodies was measured with western blot analysis. Our data demonstrated that the purified E.coli expressed N protein (47 kD) was clearly observed in SDS-PAGE electro-phoresis analysis (Fig 1) . The E.coli expressed glutathion-S-transferase (GST) protein was selected as unrelated protein control (Fig 1) and the binding activity of both N protein and GST protein (26 kD) to the anti-sera was analyzed by western blotting (Fig 2) . The results showed that N1 peptide-induced antiserum had a strong binding signal to the N protein and the anti-N2 serum revealed relatively low signal. Whereas there are no signal in GST controls and normal rabbit serum control. The results suggested that N1-peptide was a good epitope of the N protein of SARS-CoV. The N1-peptide induced Ab was capable of binding to the expressed N protein of SARS-CoV. The peptide-induced antibodies were capable of binding to N protein of SARS-CoV measured by western blot analysis. Lanes 1, 3 and 5 with loading of the purified N protein of SARS-CoV. Lanes 2, 4, 6 with loading of GST control protein. Lanes 1-2 were blotted with N1-peptide immunized rabbit serum. Lane 3-4 with N2-peptide immunized rabbit serum and Lane 5-6 with normal rabbit serum. The N protein and control GST protein were subjected to SDS-PAGE, then were transferred to PVDF membrane. The blot was probed with the antiserum (1:1000), and the immunological complex was detected with HRP-conjugated goat-anti rabbits IgG (Southern Biotech).

Since N1 peptide was a good epitope of the N protein of SARS-CoV, it was reasonable to ask whether N1 peptide has a capacity to binding to human IgG from SARS patients. To address our question, N1 and N2 peptides served as an antigen were used to screen the sera of nine SARS patients (clinical diagnosed) and four health people by ELISA. It was interested to observe that three of nine (33%) SARS patients had positive response to N1 peptide, whereas N2 peptide showed negative response to all tested sera (Tab 2). At mean time, four health controls also had a negative response to both Tab 2. N1-and N2-peptide specific antibodies (total IgG) were detected in the sera from SARS patients and normal health controls by ELISA.

peptides.

In this study, we were the first time to identify an epitope (N1) of the N protein of SARS-CoV, which will be helpful to study the functions of the N protein.

First, two peptides (N1 and N2) were selected from the sequences of N protein of SARS-CoV by computer software analysis. Theoretically, both of peptides were good antigens based on AI. When antisera were analyzed, the peptide-specific antibodies were detectable in N1 and N2 peptide-immunized rabbit and the titers of Abs were at similar levels.

Secondly, whether that synthetic peptide closely mimics the native structure of target protein is critical for peptide application. Our data showed that only N1 peptide-induced antibodies had a high affinity with the N protein, indicating N1 peptide was a good epitope of the N protein. In addition, N1 peptideinduced antibodies will be useful for the study of the N protein. The data also suggested that only limited synthetic peptides might induce good antibodies that will bind to native protein.

To further confirm whether the differences of the two peptides antibodies to bind to the expressed N protein reflected really the difference of their antigenicities in vivo, two peptides in responding to the IgG from the sera of SARS patients were measured by ELISA. It is obviously observed that the N1 peptide (20 amino acids in length) from SARS-CoV was the good epitope to induce antibodies in SARS patients. Although only 33% (3/9) of the patients were positive, it was reasonable rate. We have also observed that when the N protein of SARS-CoV (422 amino acids in length) was used as an antigen to determine the specific-antibodies of sera from SARS patients, only 40% positive response could be detected in SARS patients who had been confirmed by the clinical diagnosis (Rui-Fu Yang, unpublished data). Our work was the first time to identify an epitope of the N protein of SARS-CoV, the antibodies induced by the peptide will be useful for the SARS diagnosis or analysis of N protein functions.

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