Feline calicivirus (FCV) has a worldwide distribution and is a major pathogen of domestic cats, belonging to the Vesivirus genus within the Caliciviridae (reviewed in [1, 2]). It causes a variety of clinical manifestations, such as upper respiratory tract disease, stomatitis and lameness. Highly virulent strains (VS-FCV), causing virulent systemic disease (VSD) leading to high mortality (40–60%), have been reported in North America and Europe [3].
The FCV genome is a positive-sense single stranded RNA (~7.6 kb) that contains three open reading frames (ORFs). ORF1 is located at the 5′ end of the genome and encodes the viral nonstructural proteins. ORF2 encodes the major capsid protein, VP1. ORF3 encodes a putative minor structural protein, VP2. A distinguishing feature unique to vesiviruses, in contrast to other caliciviruses, is the expression of the major capsid protein from ORF2 as a precursor protein (73–78 kDa), which is post-translationally cleaved into the leader capsid protein (LC) and the mature capsid protein of 60 kDa, VP1 (Figure 1A). On the basis of amino acid sequence alignment and antigenic analysis, the capsid precursor protein has been divided into six distinct regions, denoted as regions A–F, [4] (Figure 1A). Region A corresponds to the LC protein. Regions B, D, and F are relatively conserved among FCV isolates, whereas regions C and E are highly variable. Region E is considered immunodominant and has been further divided into 5′ and 3′ hypervariable regions (E5′HVR and E3′HVR), separated by a conserved central region (Econsv) [4, 5].
Caliciviruses are nonenveloped, icosahedral viruses sharing a common architectural framework. The capsid (~40 nm diameter) comprises 180 copies, organized as 90 dimers, of the single capsid subunit, VP1, arranged on a T = 3 icosahedral lattice [6,7,8]. The VP1 monomer has three structural domains (Figure 1B): An internally located N-terminal arm (NTA), a shell domain (S) forming a continuous scaffold, and a flexible protruding domain (P) at the capsid surface, which contains determinants for virus-host receptor interactions and antigenic diversity [5, 9, 10]. The P domain can be further divided into P1 and P2 subdomains, with P2 subdomain located at the outermost surface-exposed region of the viral capsid.
FCV is one of the few caliciviruses for which a protein receptor has been identified. Attachment and entry of FCV is mediated by feline junctional adhesion molecule A (fJAM-A), which binds to the outer face of the P2 subdomain of VP1 [8, 11,12,13].
Monoclonal antibodies (MAbs) are useful tools for analyzing antigenic properties of viruses. Panels of MAbs have been generated against FCV capsid protein, including neutralizing and non-neutralizing antibodies [14,15,16,17]. So far, epitopes recognized by MAbs to the FCV capsid have not been identified, although previous studies mapped the binding sites of linear neutralizing MAbs between amino acids 381 to 458 [14, 18] involving E5′HVR region. In addition, sequence analysis of MAb neutralization-resistant variants clustered point mutations disrupting linear neutralizing epitopes to the E5′HVR region and conformational neutralizing epitopes to the E3′HVR region [15], both within P2 subdomain.
Here we report the generation and characterization of a panel of MAbs against VP1. Most of the MAbs recognized antigenic region E. Two close linear epitopes were identified located within the 35 amino acid long E5′HVR region, one recognized by non-neutralizing and the other recognized by neutralizing MAbs.
We used virus like particles (VLPs) as immunogen for the generation of FCV-specific MAbs, following an approach we had successfully used before to raise MAbs directed against the capsid protein of other caliciviruses, such as swine norovirus [19] and rabbit hemorrhagic disease virus (RHDV) [9]. Briefly, we generated a recombinant baculovirus (BacPAK baculovirus expression system, Clontech) harbouring the coding sequences of mature proteins VP1 and VP2, and the 3′ untranslated region of FCV (Urbana strain GenBank accession no. L40021), following procedures described before [20, 21]. Cultures of H5 insect cells were infected with the recombinant baculovirus to analyze the expression of the recombinant FCV capsid protein. A major polypeptide band with the expected molecular mass of ~60 kDa was identified after analysis by SDS-10% PAGE (Figure 1C, asterisk). Electron microscopy analysis of negatively stained preparations of purified recombinant FCV capsid protein revealed virus-like particles (VLPs) with similar size and morphology to authentic FCV virions (Figure 1D). These FCV VLPs were subsequently used to immunize BALB/c mice in order to obtain FCV VP1-specific MAbs, following previously described procedures [19]. After screening of the hybridoma cell lines, 26 positive clones derived from four different immunized mice were selected.
The MAbs were characterized by analyzing the reactivity of the corresponding hybridoma supernatants in ELISA, Western blot and immunofluorescence assays. All the MAbs reacted positively with purified FCV VLPs in indirect ELISA assays (data not shown). The 26 MAbs also reacted positively in immunofluorescence assays with FCV-infected feline CRFK cells (Figure 2A), demonstrating that the MAbs raised against recombinant VP1 protein (VLPs), recognized the FCV capsid protein expressed in the context of a FCV virus infection. 22 of the 26 MAbs reacted positively in Western blot assays both, against purified FCV VLPs and VP1 protein present in FCV-infected CRFK cell-extracts ([22] and data not shown), suggesting these MAbs recognized linear epitopes. Accordingly, the same 22 MAbs recognized the FCV capsid protein in indirect ELISA assays in which the antigen had been previously denatured by treatment with 7 M urea, before adsorption to the plates. In contrast, the remaining four MAbs did not react in Western blot or in indirect ELISA assays using urea-treated FCV capsid protein, indicating that these MAbs recognized conformational epitopes.
Subsequently, the panel of MAbs was analyzed for neutralizing activity using a plaque-reduction assay specific for FCV virus, as previously described [22]. 12 MAbs exhibited significant levels of anti-FCV neutralizing activity (>90% plaque reduction) while the rest of the MAbs was shown to be non-neutralizing (Figure 2B; in row +MAb, compare 2nd and 5th plates with 1st, 3rd and 4th plates).
As a next step in the characterization of the MAbs, we performed an epitope mapping analysis, which was carried out in subsequent steps, by analyzing MAb reactivities with sets of truncated FCV capsid polypeptides and synthetic peptides (Figure 3). First, truncated polypeptides corresponding to the FCV capsid protein antigenic regions: B, CD, E and F were expressed in E. coli as recombinant glutathione S-transferase (GST) fusion proteins (Figure 3A). Next, the amino acid sequences of antigenic region E: E5′HVR, Econsv and E3′HVR were incorporated as foreign antigens and displayed by chimeric RHDV VLPs, using procedures previously described [22, 23] (Figure 3B). Finally, a set of overlapping synthetic peptides encompassing truncated sequences within E5′HVR region was designed (Figure 3C). The different sets of truncated capsid polypeptides and synthetic peptides prepared were used as antigens in indirect ELISA assays to analyze their reactivity with the panel of FCV MAbs. The results obtained are summarized in Figure 3. Based on the epitope mapping and neutralizing activity analyses performed, the MAbs could be classified into five different groups, G1-G5 (Figures 2 and 3). Group G1, represented by MAb 52H10 in Figure 2, included three non-neutralizing conformational MAbs. Group G2 consisted of conformational MAb 51C9, exhibiting neutralizing activity. The conformational MAbs did not react with any of the truncated polypeptides. Thus, the location of their epitopes could not be determined. Group G3, represented by 81C2 in Figure 2, included three non-neutralizing MAbs recognizing epitopes within region F (Figure 3A). The epitopes recognized by the remaining 19 MAbs, including non-neutralizing ones like 82H9 and neutralizing MAbs like 51B10 (Figure 2), were all mapped to the 35 amino acid region E5′HVR (aa 426 to 460) (Figure 3B). Subsequently, screening of the overlapping peptide set enabled the identification of two close but distinct linear epitopes: an epitope spanning amino acids 431–435 (PAGDY), recognized by 8 non-neutralizing MAbs (group G4), and an epitope spanning amino acids 445-451 (ITTANQY), recognized by 11 neutralizing MAbs (Figure 3C).
Finally, in order to analyze the degree of conservation of the newly identified epitopes, we aligned 181 different full length FCV capsid sequences (using Virus Pathogen Resource database). The non-neutralizing epitope was found to be highly conserved (Figure 4A). The sequence PAGDY (aa 431-435) was strictly conserved in 136 out of 181 sequences analyzed (75%). Residues P431, G433 and Y435 were 100% conserved, while A432 and D434 were 89% and 83% conserved, respectively. In contrast, the sequence corresponding to the neutralizing epitope ITTANQY (aa 445-451) was unique to the FCV Urbana strain used in this study (Figure 4A). Residues I445, T447 and Y451 were highly conserved (99%, 94% and 87%, respectively), while residues T446 and A448 were less conserved (58% and 50%, respectively) and residues N449 and Q450 were very variable (7% and 22%, respectively).
Both epitopes were localized within surface exposed loops of P2 subdomain (Figure 4B). The neutralizing epitope (ITTANQY) lies at the margins of the P2 domain dimer, while the non-neutralizing epitope (PAGDY) locates close to the P2 domain dimer interface (Figures 4C and D).
