INTRODUCTION

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All enveloped animal viruses use membrane fusion to cross the barrier of the host cell membrane and deliver the virus genome into the cytoplasm. This critical membrane fusion reaction is mediated by the virus spike protein, which undergoes structural rearrangements that convert the protein into a fusion-active form. The general scheme of the structural rearrangements, although differing mechanistically for different groups of viruses, appears to involve the release of a hydrophobic fusion peptide from a previously hidden or inactive position within the spike protein and its insertion into the target membrane to trigger fusion. A key question is the mechanism of protein refolding from a fusion-inactive form to the fusion-active form that carries out fusion peptide insertion. Molecular understanding of this refolding reaction may lead to the development of novel strategies to block virus fusion and infection. For a group of diverse viruses exemplified by influenza virus, the fusogenic spike protein conformational change involves the formation of an extended -helical coiled-coil domain that appears to be a key feature of the fusion mechanism (17, 36).

The alphavirus Semliki Forest virus (SFV) is a small, highly organized enveloped RNA virus whose fusion activity has been extensively studied (20, 21, 40). The SFV fusion reaction is triggered by low pH (<pH 6.2) during the endocytic uptake of the virus by cells. Fusion and infection are blocked by weak bases such as NH₄Cl or specific inhibitors such as bafilomycin, which act to raise the pH within endocytic vesicles (14, 20). The SFV spike promoter is composed of the E1 and E2 transmembrane subunits, each ~50 kDa and associated as a noncovalent heterodimer, and the E3 subunit, a peripheral polypeptide of ~10 kDa. Each virus particle contains 240 copies of this spike promoter organized as 80 trimeric spikes, [E1-E2-E3]₃. Fusion is mediated by the spike E1 subunit, which binds to target membranes and contains a highly conserved hydrophobic domain from amino acids 79 to 97 that is believed to be the fusion peptide (12, 20, 24, 26).

Studies of the SFV spike protein during fusion indicate that upon exposure to mildly acidic pH, the E1-E2 dimer dissociates. E1 then undergoes conformational changes that result in the exposure of previously masked epitopes for monoclonal antibody (MAb) binding and the formation of a highly stable, trypsin-resistant E1 homotrimer (20, 24). These E1 conformational changes occur with kinetics slightly faster than those of fusion (3, 19) and are enhanced by the presence of target membranes containing cholesterol and sphingolipid, two lipid components that are specifically required for SFV fusion (20, 21, 26, 49). E1 then associates with the target membrane by insertion of the fusion peptide, and membrane fusion is triggered.

Central questions in understanding SFV fusion include the mechanism of formation of the critical E1 homotrimer and the identities of the regions of the E1 protein that are involved in its fusogenic refolding. Structural predictions suggest that, unlike spike proteins of the influenza virus class, SFV E1 does not refold into an extended -helical coiled coil during fusion (26). Thus, the formation of the fusion-active E1 trimer may represent a novel refolding mechanism. One tool in identifying regions of viral spike proteins that become exposed during fusion has been to localize the binding sites for MAbs that are specific for the fusion-active conformation of the spike (48). The fusion-active, low-pH-treated form of SFV E1 is specifically recognized by four MAbs that inefficiently recognize the pH 7 form of E1 (23, 45). Three of these MAbs were isolated and characterized by our laboratory (23) and are termed E1a-1, E1a-2, and E1a-3. The fourth MAb, anti-E1", was originally isolated by Boere et al. (1) and further characterized by Wahlberg and coworkers (3, 44, 45). Extensive evidence indicates that exposure of the epitopes recognized by these acid-specific MAbs is relevant to the fusion activity of SFV. First, the epitopes are exposed with the same pH and temperature dependence as are required for virus fusion (3, 19, 23). Detailed kinetic studies demonstrate that epitope exposure occurs slightly faster than fusion (3, 19). This is in contrast to other SFV MAbs that detect spike epitopes exposed after the fusion reaction is completed (19). SFV fusion is remarkably dependent on cholesterol and sphingolipid as well as low pH, and the conformational changes detected by the antibodies are strikingly dependent on both lipids when either the virus (4, 6) or the spike ectodomain (26) is assayed. The epitopes become exposed during the endocytic entry of the virus into the cell and, like fusion, epitope exposure is blocked by agents such as NH₄Cl or monensin that interfere with endosome acidification (23, 28, 32, 38, 45). Several virus E2 mutants that shift the pH dependence of virus fusion by shifting the pH dependence of E1-E2 dimer dissociation also shift the pH dependence of epitope exposure (13, 33). A number of biochemical experiments demonstrate that the epitopes are not simply exposed as part of a general "loosening" of the tightly packed virus structure at low pH, since detergent solubilization, for example, did not make the epitopes accessible (23). Lastly, the same pool of E1 protein reacts with the antibodies, binds specifically to cholesterol- and sphingolipid-containing target liposomes, and forms the homotrimeric structure believed to be critical for the fusion reaction (26). Thus, the kinetics and properties of epitope exposure argue for the relevance of these conformational changes to fusion.

We set out to determine the functional effects of E1 binding by these four MAbs, to characterize the similarities and differences in their binding site(s), and in particular to localize the epitope(s) with which they interact. Our studies showed that the presence of the MAbs did not affect fusion and that all four MAbs bound to a spatially related site(s) on E1. The region of the spike protein recognized by three of the MAbs appears distinct from the fusion peptide and from the epitope recognized by anti-E1". Our results thus indicate a region of E1 other than the virus fusion peptide that becomes exposed during the SFV fusion reaction at acidic pH.

	MATERIALS AND METHODS

Top Abstract Introduction Materials and Methods Results Discussion References

Viruses and antibodies. The wild-type (wt) virus used in these studies was a well-characterized plaque-purified stock virus (13, 42), and the SFV fus-1 mutant was previously isolated and characterized as a pH shift fusion mutant (13, 25). All virus stocks were prepared by propagation in BHK cells at low multiplicity in minimal essential medium plus 0.2% bovine serum albumin (BSA) and 10 mM HEPES (pH 7.4) and stored at 70°C (25). [³⁵S]methionine-[³⁵S]cysteine-labeled virus was prepared in BHK cells, purified by banding on a discontinuous sucrose gradient (25), and stored at 70°C in ~45% (wt/wt) sucrose in TN buffer (50 mM Tris [pH 7.4], 100 mM NaCl). Unlabeled virus was prepared in BHK cells, purified on tartrate gradients, and stored at 70°C in TN buffer (25).

Functional effects of antibodies on virus fusion. Liposome binding studies measured the cofloatation of radiolabeled SFV with liposomes on sucrose gradients as previously described (24), with pH treatment performed in the presence of the indicated concentrations of antibodies. Virus-liposome fusion was assayed by monitoring the decrease in the eximer peak of pyrene-labeled SFV upon fusion with unlabeled liposomes prepared by extrusion (7, 24). Pyrene-labeled wt SFV was prepared by propagation in one roller bottle of BHK cells in which the phospholipids were prelabeled by growth in the presence of 10 µg of pyrene (Molecular Probes, Eugene, Oreg.) per ml (3, 44). Labeled virus was purified by banding on a discontinuous sucrose gradient (25). Fusion assays were performed with pyrene-labeled virus at concentrations of 0.6 µM virus lipid, liposomes at concentrations of 200 µM lipid, and the indicated concentrations of antibodies; HNE buffer (5 mM HEPES [pH 7.0], 150 mM NaCl, 0.1 mM EDTA) was used at 37°C in a stirred cuvette with a Perkin-Elmer LS5 fluorometer (3, 44). Fusion was triggered by the addition of a pretitrated volume of 0.3 M morpholinoethanesulfonic acid (MES) (pH 4.8), to give a final pH of 5.5.

Selection of antibody binding mutants. The overall strategy was to pH treat the virus to expose the binding site for MAb E1a-1, remove MAb-reactive virus by immunoprecipitation, and repeat for multiple selections. This strategy is similar to that successfully used to isolate a Sindbis virus MAb-resistant mutant (30). A 150-µl volume of wt virus stock containing ~10⁹ PFU was adjusted to a final pH of ~5.5 by dilution with an equal volume of buffer containing 50 mM succinate (pH 5.0) and 100 mM NaCl, incubated for 5 min on ice, and neutralized by the addition of a precalibrated volume of 0.5 N NaOH. This mild pH treatment did not reduce virus infectivity (3) and induced full reactivity with MAb E1a-1 as tested by enzyme-linked immunosorbent assay (ELISA) of whole virus (data not shown). The virus was then incubated overnight on ice with 3 µg of biotin-conjugated MAb E1a-1. Antibody-virus complexes were removed by gentle rotation for 1 h at 4°C with 100 µl of streptavidin-conjugated magnetic particles (PerSeptive Diagnostics, Inc., Cambridge, Mass.), and bound virus and particles were precipitated with a magnet-containing test tube rack (Dynal, Inc., Lake Success, N.Y.). The specific selection gave a ~10-fold reduction in viral titer, and no reduction resulted when an unrelated biotin-conjugated MAb was substituted. Virus remaining in the supernatant was expanded by growth on four independent plates of BHK cells at a multiplicity of ~1 PFU/cell for 6 to 7 h. The selection of these individual stocks was repeated for a total of nine cycles each, a point at which further selection gave little reduction in the titer of the virus stocks. The selected stocks were plaqued under agarose, and isolated plaques were picked and expanded by growth on BHK cells in 24-well trays until the cells displayed cytopathic effects. Virus isolates were treated at low pH with succinate buffer as above, and screened by the ELISA described below for reactivity with MAbs E2-1 and E1a-1. Isolates showing strong reactivity with the E2 MAb, indicating a high titer of virus, and reduced activity with the selecting MAb were expanded and further tested as described below. Other selections based on neutralization with acid conformation-specific MAb, second antibody, and complement or based on epitope exposure by heat treatment did not produce sufficient specific selection pressure and were not further pursued (data not shown).

ELISA analysis. Antibody competition experiments with intact virus were performed by coating ELISA wells with 1 µg of MAb E2-1 per ml; this MAb was previously shown to bind to intact virus after either acidic or neutral pH treatment (23). The plates were blocked with 1% BSA, purified acidic- or neutral-pH-treated virus was added at a protein concentration of 3 µg/ml, and the mixture incubated overnight at 4°C. The tethered virus was then reacted for 1 to 2 h at 37°C with 60 to 100 ng of biotin-conjugated MAb E1a-1 or anti-E1" per ml, concentrations that were shown to be in the linear range of the assay, in the presence of the indicated concentrations of unlabeled competing MAb. The plate was developed by incubation with saturating concentrations of streptavidin-alkaline phosphatase (Fisher Scientific, Pittsburgh, Pa.) for 1.5 h at 37°C followed by substrate incubation. Antibody competition experiments with purified detergent-solubilized spike proteins were performed by directly coating ELISA wells with 0.5 µg of spike proteins per ml for 1 to 2 h at 37°C, blocking with BSA, and then incubating with biotin-MAb and competitors as above. Spike proteins were purified by Triton X-114 phase separation (2) of gradient-banded wt and mutant viruses.

Virus sequence analysis. RNA was prepared from virus grown at low multiplicity in one 75-cm² flask of BHK cells (13). The sequence of the RNA encoding the structural proteins was determined by reverse-transcription (RT)-PCR amplification with Pfu polymerase (Stratagene, La Jolla, Calif.) and automated sequencing in the Einstein DNA sequencing facility, all as previously described (13, 42). Both strands of the cDNA were sequenced, and sequence changes were confirmed by analysis of an independent RT-PCR product. The sequence of our laboratory wt virus, the parent virus used for mutant selection, was found to contain a lysine (AAA) at position 85 of the capsid protein. This capsid residue is asparagine (AAC) in the wt infectious clone and published wt virus sequence (11).

Assays of the mutant phenotype. The NH₄Cl sensitivity of wt and mutant virus infection was assayed as previously described by infecting BHK cells in 24-well trays for 90 min with virus at a multiplicity of ~1 PFU/cell in the presence of the indicated concentrations of NH₄Cl and quantitating virus-specific RNA synthesis by labeling with [³H]uridine for 3.5 h (13). Low-pH-dependent conformational changes in the virus spike proteins were assayed by treating [³⁵S]methionine-[³⁵S]cysteine-labeled virus at the indicated pH for 10 min at 37°C in the presence of 1 mM liposomes prepared by extrusion as indicated. Formation of the E1 homotrimer in these samples was investigated by incubating samples in sodium dodecyl sulfate (SDS) gel sample buffer for 3 min at 30°C and analyzing them by SDS-PAGE (24, 45). E1 conversion to trypsin resistance was assayed by digestion of samples for 10 min at 37°C with 200 µg of tolysulfonyl phenylalanyl chloromethyl ketone (TPCK)-trypsin per ml in 1% Triton X-100 in phosphate-buffered saline (PBS) containing calcium and magnesium (24, 35), and the presence of acid conformation-specific epitopes was determined by immunoprecipitation with the indicated MAbs (23) followed by SDS-PAGE analysis. The pH dependence of E1-E2 dimer dissociation was assayed by coimmunoprecipitation (8, 43). Fluorograms of SDS-gels were quantitated by PhosphorImager analysis (ImageQuant version 1.2; Molecular Dynamics, Inc., Sunnyvale, Calif.).

	RESULTS

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Functional effects of acid-specific MAbs on virus fusion. We wished to compare the functional properties of our three acid conformation-specific MAbs with those of MAb anti-E1". Previous studies suggested that the presence of anti-E1" inhibited low-pH-induced fusion of SFV with cell plasma membranes (45) or liposomes (44) and low-pH-induced virus-liposome attachment (44). If the acid conformation-specific MAbs inhibit virus-cell fusion, this could be the basis of a selection for MAb-resistant virus mutants. To test for inhibition of SFV-plasma membrane fusion, virus was bound to BHK cells on ice and treated for 1 min at pH 5.5 to induce fusion, and the infected cells resulting from virus fusion were quantitated by immunofluorescence with a polyclonal antibody to the virus spike protein. Under these conditions, no virus infected the cells during a 1-min treatment at pH 7 and between 209 and 256 cells were infected by virus at pH 5.5 (Table 1). When the pH treatment was performed in the presence of either MAb anti-E1" or E2-1, a nonneutralizing MAb to the E2 subunit, little inhibition resulted from the presence of either MAb at ~300 µg/ml (Table 1, experiment I), from MAb anti-E1" at higher concentrations (500 or 900 µg/ml) (experiment II), or from MAb anti-E1" when the conformational changes and fusion were slowed by incubation at either 20 or 4°C (data not shown). The previous results reported inhibition of virus-cell membrane fusion by anti-E1" at concentrations ranging from a 1:10 dilution of ascities fluid to 350 µg of MAb/ml (45). Our acid-specific MAbs E1a-1, E1a-2, and E1a-3 also had no effect on virus-cell fusion (experiment III). In contrast, a polyclonal rabbit antibody to the SFV spike specifically inhibited virus-cell fusion when used under conditions previously shown to neutralize virus infectivity (23) (experiment IV). Thus, the lack of inhibition by the acid conformation-specific MAbs is not due to an inherent inability to detect inhibition in this assay. Control ELISA experiments also demonstrated that all four acid-specific MAbs were fully active in spike protein binding even when maintained at pH 5.5 (data not shown) and thus were capable of binding the virus under low-pH conditions.

View larger version (44K): [in this window] [in a new window]   FIG. 1.   Functional effects of MAbs on SFV membrane attachment and fusion. (A) Virus-liposome attachment. [35S]methionine-[35S]cysteine-labeled wt SFV was mixed with liposomes and the indicated antibodies at final concentrations of 1.2 mM lipid and 50 µg of antibody per ml. The samples were preequilibrated for 3 to 5 min at 37°C, adjusted to pH 5.5 for 10 min at 37°C unless otherwise indicated, and then returned to neutral pH. Virus association with liposomes was quantitated by flotation on sucrose gradients (see Materials and Methods). Data shown are the average of two experiments. (B) Virus-membrane fusion. Pyrene-labeled wt SFV (0.6 µM) was mixed with unlabeled liposomes (200 µM) in the presence of 50 µg of the indicated antibodies per ml, preequilibrated for 3 to 5 min at 37°C, and adjusted to pH 5.5, and the final extent of fusion was measured after ~30 s at 37°C by quantitating the decrease in the pyrene eximer peak by spectrofluorometry (see Materials and Methods). Treatment with the rabbit preimmune and anti-spike antibodies was performed by overnight incubation at 4°C followed by incubation as above. Data shown are the average of two or three experiments.

Competition analysis of MAb binding to virus and spike proteins. To use the acid conformation-specific MAbs as a tool to localize the conformational changes in E1, it is important to know if the MAbs recognize the same site on the SFV E1 polypeptide or identify several independent E1 sites that become accessible as part of overall refolding during fusion. All four MAbs are clearly independent (23), even in one case having been isolated by a different laboratory (1). However, the properties of the epitope(s) recognized by these four MAbs are indistinguishable in all of the assays that have been performed to date. Exposure of the epitope(s) has similar pH dependence (23), comparable kinetics in in vitro assays (3, 19) and in vivo during endocytic uptake of virus by cells (23, 32, 45), and a comparable cholesterol requirement (23, 26). All four MAbs are also nonneutralizing and do not recognize SDS-denatured E1 (1, 23). We therefore used competition analysis to characterize the locations of the MAb binding sites on E1. We first established two types of assay systems. One assay tested the recognition of whole virus particles by the MAbs. Purified virus was pretreated at acidic or neutral pH, returned to neutral pH, and tethered to ELISA plates with E2-1, a MAb to the E2 spike subunit. Tethered virus was reacted with biotin-conjugated MAb, and MAb binding was detected with streptavidin-alkaline phosphatase. Results for MAb E1a-1 are shown in Fig. 2A. The whole virus ELISA faithfully reproduced the increased MAb binding observed in previous assays of the acid-treated virus (23), with binding at nonsaturating MAb concentrations being five- to sixfold higher in the acid-treated samples. A second assay tested the reactivity of purified, detergent-solubilized spike proteins that were adsorbed directly to the ELISA plate. Similar to results from other low pH-dependent virus systems (47), direct adsorption of the spike protein caused sufficient protein unfolding to expose the E1a-1 epitope (Fig. 2B), and no further increase in MAb binding was observed when the spikes were pretreated at acidic pH (data not shown). Binding to isolated spike proteins was somewhat more efficient than binding to intact virus particles, since a comparable MAb concentration gave similar binding levels with about a sixfold-lower level of spike proteins in the isolated preparations. This probably represents steric hindrance in the intact virus, in keeping with the tight packing of the spike proteins. Similar results for both types of assays were obtained with MAb anti-E1" (data not shown).

View larger version (13K): [in this window] [in a new window]   FIG. 2.   MAb E1a-1 binding to whole virus and isolated spike proteins. (A) Binding to whole virus. Gradient-purified wt SFV was pretreated at pH 5.5 or 7.0 for 5 min at 37°C as indicated, returned to neutral pH, and adjusted to 3 µg/ml. Virus was tethered to ELISA plates that were precoated with a MAb to the E2 spike subunit (E2-1). Biotin-conjugated MAb E1a-1 was added at the indicated concentrations and allowed to react with the virus for 1 h at 37°C. Biotinylated MAb binding was detected by incubation with streptavidin conjugated to alkaline phosphatase followed by incubation with substrate, each for 1 h at 37°C. Data shown are a representative example of four experiments. (B) Binding to adsorbed spike proteins. Using gradient-purified wt SFV, spike proteins were prepared by Triton X-114 phase separation and adsorbed directly to ELISA plates at 0.5 µg/ml. Biotin-conjugated MAb E1a-1 was added at the indicated concentrations and allowed to react with immobilized spike proteins for 1 h at 37°C. MAb binding was detected by incubation with streptavidan conjugated to alkaline phosphatase followed by incubation with substrate, each for 1 h at 37°C. The control consists of biotin-conjugated MAb E1a-1 binding in the absence of adsorbed spike proteins. Similar low absorbance was observed for binding of an unrelated MAb to wells containing spike protein. Data shown are a representative example of two experiments.

View larger version (32K): [in this window] [in a new window]   FIG. 3.   Antibody competition analysis. The ELISAs in Fig. 2 were used to analyze MAb binding to pH 5.5-treated intact wt virus (A and B) or purified wt spike proteins adsorbed to ELISA plates (C and D). The binding of biotin-conjugated MAb E1a-1 (A and C) or biotin-conjugated MAb anti-E1" (B and D) was quantitated at a constant biotin-MAb concentration of 100 ng/ml, in the presence of the indicated concentrations of competing, nonconjugated MAbs. Final binding results (in duplicate) were expressed as a percentage of the reactivity obtained with biotin-MAb in the absence of any competing MAb.

Selection and screening for MAb-resistant SFV mutants. To specifically localize the binding site(s) for the acid conformation-specific MAbs, we wished to select for MAb-resistant virus mutants. The four acid conformation-specific MAbs are nonneutralizing (1, 23), do not inhibit virus-cell fusion (Table 1), and do not recognize linear sequences, precluding the use of synthetic peptides for mapping studies (1, 23). We therefore used an immunodepletion method to enrich for nonreactive viruses. A nonmutagenized virus stock was treated briefly at pH 5.5 on ice. The virus was then incubated with excess biotin-conjugated MAb E1a-1, antibody-reactive viruses were removed with streptavidin-conjugated magnetic particles, and the remaining virus was propagated on independent plates of BHK cells. The conditions of pH treatment were selected to obtain binding to the MAb (which according to all the published data represents an irreversible conformational change) without inactivating infectivity. Under these conditions, only a 10-fold decrease in virus titer resulted from the MAb treatment. The selection was therefore repeated for a total of nine cycles to increase the chances of significantly enriching for MAb-resistant mutants. Isolated plaques were then picked from the selected virus stocks, and the virus was expanded, treated at low pH, and screened by an ELISA for reactivity with both an E2 MAb and the selecting MAb. Two independent isolates, SFV 1-8 and SFV 4-2, were chosen for further study on the basis of their strong reactivity with MAb E2-1 and reduced (SFV 1-8) or negligible (SFV 4-2) reactivity with MAb E1a-1 after acid treatment.

View larger version (14K): [in this window] [in a new window]   FIG. 4.   pH dependence of MAb E1a-1 binding to wt and mutant SFV. wt SFV and the 1-8 and 4-2 mutant virus isolates were diluted to a final titer of 108 PFU/ml in MES-saline-BSA buffer, and adjusted to the indicated pH for 5 min at 37°C. The samples were adjusted to neutral pH and 0.5% Triton X-100 and incubated in ELISA plates that were precoated with saturating concentrations of MAb E1a-1 (1 µg/ml). Bound spike protein was detected by the addition of a rabbit polyclonal antibody to the virus spike and an alkaline phosphatase-conjugated second antibody. Data shown are a representative example of four experiments.

View larger version (51K): [in this window] [in a new window]   FIG. 5.   MAb binding to isolated mutant spike proteins. wt virus, SFV 1-8, and SFV 4-2 were purified by gradient sedimentation, and spike proteins were isolated by Triton X-114 phase separation. Spike proteins were adsorbed directly to ELISA plates at 0.5 µg/ml and reacted with 100 ng of the indicated biotin-conjugated MAbs per ml. This concentration was within the linear range of MAb binding to wt spike proteins (Fig. 2B). MAb binding was detected by reacting with streptavidin conjugated to alkaline phosphatase, and mutant spike protein reactivity was expressed as percentage of wt binding. SFV 4-2 binding is shown as solid bars, and SFV 1-8 binding is shown as hatched bars. Data are a representative example of three experiments.

View larger version (17K): [in this window] [in a new window]   FIG. 6.   Antibody competition analysis of isolated mutant spike proteins. Purified spike proteins were prepared from SFV 1-8 (A) and SFV 4-2 (B) and adsorbed to ELISA plates, and the binding of biotin-conjugated MAb anti-E1" was quantitated in the presence of the indicated concentrations of competing, nonconjugated MAbs, all as in Fig. 3D. Final binding results (in duplicate) were expressed as a percentage of the reactivity obtained with biotin-MAb in the absence of any competing MAb.

Biochemical and sequence analysis of SFV mutants. Given that our selection involved low-pH treatment of the virus, albeit under noninactivating conditions, we were concerned that our mutants might be low-pH resistant. To determine if the spike proteins of both mutants still mediated entry with a similar pH dependence to that of wt virus, we tested the sensitivity of virus infection to inhibition by the weak base NH₄Cl (Fig. 7). Cells were infected with wt, SFV 1-8, SFV 4-2, or the pH shift SFV mutant fus-1 (13) in the presence of various concentrations of NH₄Cl. Virus infection was quantitated by monitoring the incorporation of [³H]uridine into viral RNA (13). As previously observed (13, 25), both wt and fus-1 infections were inhibited by NH₄Cl and fus-1 was sensitive to lower NH₄Cl concentrations than was wt, in keeping with the relative acid resistance of the fus-1 fusion (pH threshold of ~pH 5.5 for fus-1 compared to ~pH 6.2 for wt). Both SFV 1-8 and SFV 4-2 showed NH₄Cl sensitivities similar to that of wt SFV, indicating that both viruses had pH-dependent entry mechanisms with comparable pH requirements as wt SFV.

View larger version (21K): [in this window] [in a new window]   FIG. 7.   Sensitivity of wt and mutant virus infection to inhibition by NH4Cl. BHK cells in 24-well trays were infected with 1 PFU of wt or mutant SFV per cell in the presence of the indicated concentration of NH4Cl for 90 min. Infection was then quantitated by determining the incorporation of [3H]uridine into viral RNA, in the presence of 20 mM NH4Cl to prevent secondary infection. Data shown are a representative example of two experiments.

View larger version (72K): [in this window] [in a new window]   FIG. 8.   MAb reactivity of isolated E1 homotrimers from wt and mutant SFV. [35S]methionine-[35S]cysteine-labeled wt SFV (A), SFV 1-8 (B), or SFV 4-2 (C) was mixed with liposomes (final concentration, 0.8 mM), adjusted to the indicated pH for 10 min at 37°C, and returned to neutral pH. One set of samples (pH 5 plus trypsin) was then treated with 200 µg of trypsin per ml in 1% Triton X-100 in PBS for 10 min at 37°C to digest E2, capsid, and any nontrimerized E1, and the digestion was terminated by the addition of trypsin inhibitor. All other samples were treated with premixed trypsin and trypsin inhibitor in 1% Triton X-100 in PBS. Antibody reactivity was analyzed by immunoprecipitation with the indicated antibodies followed by SDS-PAGE. rab indicates a rabbit polyclonal antibody against the SFV E1 and E2 subunits.

	DISCUSSION

Top Abstract Introduction Materials and Methods Results Discussion References

Functional effects of the acid-specific MAbs. Our studies showed that the four acid conformation-specific E1 MAbs do not have strong inhibitory effects on SFV-membrane fusion. SFV fusion is extremely rapid and is completed within seconds at 37°C (3). Cryoelectron microscopy studies have shown that spike protein conformational changes can be detected within the first 25 ms of low-pH treatment (10). The lack of effect of the MAbs on fusion thus may be due either to the rapid completion of fusion prior to recognition by MAb or to noninhibitory MAb binding prior to fusion. Our data do not differentiate between these two possibilities, but decreasing the rate of virus fusion with the cell plasma membrane by low pH incubation at either 20 or 4°C did not increase inhibition by added MAbs (see results above).

Evidence for mapping of the E1a-1 epitope. Competition studies on isolated wt spike proteins demonstrated that all four independent acid conformation-specific MAbs bound to sites on E1 that were either identical or sufficiently adjacent to produce binding interference. The SFV 4-2 mutation, E1 G157R, decreased the binding of the acid conformation-specific MAbs E1a-1, E1a-2, and E1a-3, while the binding of anti-E1" was essentially unaffected. Thus, while the competition data suggested close proximity of the anti-E1" binding site to those of the other acid conformation-specific MAbs, the SFV 4-2 mutation indicated that these epitopes were nevertheless distinct. It was possible that the SFV 4-2 mutation was acting indirectly to inhibit MAb binding by inducing a conformational change in a distant E1 epitope (31). We have tested the reactivity of E1 after triggering epitope exposure by acid treatment of virus particles and assay of the spike protein dimer (Fig. 4), by direct adsorption and denaturation of purified spike proteins on ELISA plates (Fig. 5 and 6), and by acid treatment of virus followed by isolation of homotrimeric E1 (Fig. 8). The decreased binding to SFV 4-2 E1 under all assay conditions strongly suggests that the 4-2 mutation acts by directly affecting the MAb binding site and therefore that the G157 region of E1 is masked in the neutral-pH structure and becomes accessible during fusion-permissive conditions.

Comparisons with other alphavirus epitopes. Anti-E1" was originally designated UM8.64 and characterized as nonneutralizing and nonprotective in mice but active in hemagglutination inhibition (1). This MAb defined an antigenic determinant termed E1_d in competition analysis. Our competition analysis also places MAbs E1a-1, E1a-2, and E1a-3 in the E1_d group with anti-E1". Thus, to date, all the acid conformation-specific MAbs against SFV E1 fall into this group, and it is not known if additional, noncompeting acid-specific antigenic determinants exist. However, although the competition analysis shows that all four acid conformation-specific MAbs have spatially related binding sites, the SFV 4-2 mutant data indicate that three of the current members of the E1_d group bind an epitope different from that of anti-E1". The exact recognition site of anti-E1" has not been defined, except for its spatial relationship to G157 in competition analysis.

Conclusions. The data presented here suggest that a region of E1 defined by the G157R mutation becomes exposed or more accessible during the low-pH-induced fusion of SFV and can then be recognized by the acid conformation-specific MAbs E1a-1, E1a-2, and E1a-3. The acid-dependent refolding involving the E1 157 region is part of the overall series of conformational changes in the SFV spike protein during fusion. Kinetic studies of fusion (3) and results with SFV mutants with altered E1-E2 dimer dissociation (13, 33) indicate that acid conformation-specific epitope exposure is blocked until the E1-E2 dimer dissociates. Results with an SFV fusion peptide mutant indicate that the acid conformation-specific MAbs recognize a conformational change that can occur in the absence of E1 trimerization (24). Taken together, the results to date suggest a fusion model in which G157 epitope exposure occurs after E1-E2 dimer dissociation but prior to formation of the E1 homotrimer and insertion of the SFV fusion peptide into the target membrane. The kinetics of exposure of the G157 epitope are strongly enhanced by the presence of cholesterol and sphingolipid-containing liposomes (4, 6, 26), suggesting that E1 interacts in some way with the target membrane already during this relatively early stage of the fusion reaction. Future studies will address the role of lipid in the conformational changes that lead to epitope exposure. In addition, advances in cryoelectron microscopy (5, 10) may make it possible to localize the G157 region in the virus particle during exposure to low pH. As our knowledge of the SFV spike protein structure becomes more detailed, it may be possible to design virus mutations that could inhibit the rearrangement of the G157 region (15), thus potentially trapping an intermediate in virus-membrane fusion and permitting detailed characterization of its phenotype.