INTRODUCTION

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Mousepox is a devastating disease of laboratory mice that continues to cause major disruption to biomedical research via outbreaks in animal facilities (14; N. S. Lipman, H. Nguyen, and S. Perkins, Letter, Science 284:1123, 1999). This infection is caused by Ectromelia virus (EV), an orthopoxvirus (OPV) that is closely related to Vaccinia virus (VV), Cowpox virus (CPV), and Variola virus (smallpox virus) (31). Like variola virus, EV has a restricted host range, causes a severe disease with a high mortality rate, and produces skin lesions in the later stages of a natural infection (18). These analogies with smallpox led to mousepox being extensively studied as an experimental model of OPV pathogenesis before the eradication of smallpox (17). However, in comparison with VV and CPV, EV has been poorly characterized at the molecular level.

The OPVs are complex cytoplasmic viruses with large, double-stranded DNA genomes that can encode more than 100 gene products. In recent years, it has been recognized that several of these gene products inhibit host cytokine responses in a number of different ways (23, 33, 42, 44). Among these immunomodulatory factors are several soluble, secreted proteins which downregulate inflammatory responses by sequestering cytokines and preventing their interaction with cellular receptors. OPV receptors and binding proteins for interleukin-1 (IL-1) (vIL-1R), tumor necrosis factor (TNF) (vTNFR), alpha/beta interferon (IFN-/) (vIFN-/R), IFN-, IL-18, and CC chemokines (vCKBP) are expressed by VV and CPV. Analysis of genomic sequence information suggests that several of these are also expressed by variola virus (37, 39).

Since EV may well be a natural mouse pathogen and the pathogenesis of mousepox has been extensively characterized in the past, it is clearly a preferred model for studying the role of OPV immunomodulatory factors, such as soluble cytokine receptors, in viral pathogenesis. However, to date, information regarding the expression and in vitro or in vivo characterization of such gene products for EV is scarce. In vitro characterizations of EV receptors and binding proteins for IFN- (32), TNF (25), and IL-18 (10, 43) have been published, and secreted vIFN-/R has been detected in EV-infected cell supernatants (13); however, there is no information concerning EV homologs of vIL-1R or vCKBP. In addition, there has been no study of the differential expression of such gene products by EVs isolated from geographically and temporally distinct outbreaks in laboratory mouse colonies. Such studies have proved useful in the identification of novel VV gene products not expressed by the most commonly used strains (1, 5). Additionally, since soluble cytokine receptors have important effects on the pathogenesis of VV infection in mice (2, 45, 46), knowledge of their expression by EV is relevant to the choice of strain to be used in in vivo studies with this virus. Finally, it is possible that EV immunomodulatory genes have undergone recent evolutionary adaptations which influence the specific disease phenotype produced by this highly virulent pathogen.

We have characterized the expression, binding properties and, where necessary, gene sequences of EV homologs of vCKBP, vTNFR, and vIL-1R in 12 distinct strains and isolates of EV. Our main findings were (i) that functional forms of vCKBP, vIL-1R, and vTNFR are expressed by EV; (ii) that there is very little variability between different isolates with regard to their expression of these (glyco)proteins; and (iii) that the EV vIL-1R has undergone significant adaptation to function in the mouse system, distinguishing it clearly from the homologous proteins of VV and CPV.

	MATERIALS AND METHODS

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Cells and viruses. BSC-1 (African green monkey kidney) cells were cultured in Glasgow minimum essential medium supplemented with 10% fetal calf serum (FCS). Human U937 cells and mouse EL4 6.1 C10 cells, which express a large number of IL-1 binding sites (26), were cultured in RPMI 1640 medium supplemented with 10% FCS. Spodoptera frugiperda (Sf-21) insect cells and Autographa californica nuclear polyhedrosis virus were cultured in TC-100 medium (Sigma) containing 10% FCS.

Reagents. Recombinant human ¹²⁵I-macrophage inflammatory protein 1 (MIP-1), ¹²⁵I-RANTES (regulated upon activation, normal T-cell expressed, and secreted), and ¹²⁵I-IL-8 (all at 2,000 Ci/mmol) were obtained from Amersham (Little Chalfont, United Kingdom). Recombinant human ¹²⁵I-TNF alpha (TNF-) (58.3 µCi/µg), ¹²⁵I-fractalkine (soluble form, 2,200 Ci/mmol), and ¹²⁵I-IL-1 (107 µCi/µg) were obtained from DuPont-New England Nuclear. Recombinant mouse IL-1 was obtained from R & D systems and radioiodinated to a specific activity of 2.2 × 10⁸ cpm/µg using the Iodogen method (28). The following cytokines used in competition experiments were all obtained from Peprotech EC: recombinant human RANTES, MIP-1, IL-8, growth-related oncogene alpha (GRO-), lymphotactin, fractalkine (soluble form), TNF-, TNF- (lymphotoxin alpha [LT-]), and IL-1; recombinant mouse RANTES, MIP-1, KC (also known as N51 or the mouse homolog of GRO-), and IL-1; and recombinant rat TNF-.

Preparation of medium for binding assays. FCS-free medium from OPV-infected BSC-1 or baculovirus-infected Sf-21 cell cultures was collected at 2 (OPV) or 3 (baculovirus) days postinfection. BSC-1 cell supernatants were adjusted to 20 mM HEPES (pH 7.4), and any infectious VV, EV, or CPV present in them was inactivated with 4,5',8-trimethypsoralen and exposure to UV light (47). The binding medium was RPMI 1640 containing 20 mM HEPES (pH 7.4) and 0.1% (wt/vol) bovine serum albumin. In some instances, supernatants were concentrated and dialyzed against phosphate-buffered saline as described previously (4, 5).

Binding assays. In cross-linking experiments with ¹²⁵I-chemokine and ¹²⁵I-IL-1, supernatants from 10⁴ OPV-infected BSC-1 cells or baculovirus-infected Sf-21 cells were incubated with radioiodinated cytokine or chemokine in a volume of 25 µl for 2 h at room temperature. Viral proteins were cross-linked to labeled cytokines or chemokines with 1-ethyl-3-(3-dimethylaminopropyl)-carbodiimide (EDC; 40 mM) or ethylene glycol-bis-succinamidyl succinate (EGS; 1 mg/ml) (5). Samples were then analyzed by denaturing sodium dodecyl sulfate (SDS)-12.5% polyacrylamide gel electrophoresis (PAGE) and autoradiography. In competition assays with U937 cells, supernatants were incubated in a final volume of 100 µl with 67 pM ¹²⁵I-chemokine, 400 pM mouse ¹²⁵I-IL-1, or 190 pM human ¹²⁵I-IL-1 for 1 h at 4°C. Subsequently, 2.5 × 10⁶ U937 or EL4 6.1 C10 cells were added in 50 µl of binding medium before 2 h of incubation at 4°C. The amount of bound ¹²⁵I-chemokine was determined by phthalate oil centrifugation as previously described (4, 5). Binding assays with human ¹²⁵I-TNF- and human and mouse ¹²⁵I-IL-1 were performed by precipitation of receptor-ligand complexes with polyethylene glycol and filtration as described previously (1, 4).

Extraction of viral DNA and sequencing of viral genes. Viral DNA was prepared from BSC-1 cells infected with EV by extraction from viral cores (15). The vCKBP genes from EV strains Mill Hill and Hampstead were PCR amplified with Taq DNA polymerase using the upstream oligonucleotide EVCKBP-3 (5'-TTATAGTAAGTTTTTTACCC-3'), based on the sequence in EV strain Moscow of the neighboring TNFR II homolog pseudogene (accession no. U86380), and the downstream oligonucleotide EVCKBP-4 (5'-TTTGTGAATGTAGTTAAGAAC-3'), based on the sequence of the 35-kDa vCKBP gene in VV strain Lister (36). The EV Hampstead homolog of the OPV vIL-1R gene was amplified by PCR with Taq DNA polymerase using two oligonucleotides based on the sequence of VV WR (41). The upstream oligonucleotide was B15R-8 (5'-GAGTTGTACATCTTGAC-3'), and the downstream oligonucleotide, based on the sequence of the neighboring B16L gene, was EVB16L-1 (5'-CAATATAGAATTAGTTAGGGC-3'). DNA sequencing was carried out by the DNA sequencing service of the Department of Biochemistry, University of Cambridge, and the sequence data were analyzed using the GCG software package.

Expression in the baculovirus system. The EV Hampstead vIL-1R gene was produced as a recombinant protein fused to a C-terminal His₆ tag in the baculovirus system. The EV vIL-1R was amplified by PCR with Pfu DNA polymerase using viral DNA as a template. The two oligonucleotides used, EVB15RH (5'-CCGAAGCTTATGAGTGCATTATTGACTATTC-3') and EVB15RN (5'-CGCGCGGCCGCCTTTATGCTAATAGTAAGTG-3'), provided HindIII and NotI restriction enzyme sites at the 5' and 3' ends of the open reading frame (ORF), respectively. The DNA fragment was cloned into HindIII- and NotI-digested pBAC-1 to produce pVS1. The DNA sequence of the insert was confirmed not to contain mutations by sequencing. The recombinant baculovirus AcEVIL1R (AcVS1) was produced as described previously (5). The recombinant baculoviruses AcB15R, AcA53R, and Ac35K have been described before (1, 4, 5).

Nucleotide sequence accession numbers. The GenBank accession numbers for the sequences reported in this paper are AJ277111, AJ277112, and AJ277110.

	RESULTS

Top Abstract Introduction Materials and Methods Results Discussion References

EV isolates. We wanted to assess the degree of variation in the expression of immunomodulatory gene products by different EVs, whether occurring naturally or induced by passage in the laboratory. Therefore, we assembled a collection of EV isolates from temporally and geographically diverse laboratory mousepox outbreaks as well as several strains derived from them. These included EV Hampstead (1930), the first EV to be isolated (27); the highly virulent EV Moscow isolate (1947) (7); several isolates from German and Austrian outbreaks (EVs MP-1, MP-2, MP-3, MP-4, and MP-5) (34); and two recent isolates from the United States, EVs Naval (1995) and Cornell (1998) (14; Lipman et al., Letter). We also obtained two plaque-purified viruses, EV Mos-3-P2 (12), which is derived from EV Moscow, and EV Ishibashi I-111 (22), as well as two egg-passaged derivatives of the Hampstead isolate, EVs Hampstead Egg (16) and Mill Hill. Both EV Hampstead Egg and EV Ishibashi I-111 have been reported to show substantially lower virulence than other isolates after footpad inoculation of mice (18, 19). The results obtained here were identical for EV Mos-3-P2 strain and its parental Moscow isolate; therefore, only those for the latter are shown.

Expression and binding specificity of the EV homolog of vCKBP. While it is known that several strains of VV (including VV Lister) and CPV (including CPV BR) express a secreted vCKBP with specificity for CC chemokines (5, 20, 40), no data are currently available concerning the expression, activity, or gene sequence of any EV homolog of this protein. Supernatants from BSC-1 cells that were uninfected (mock) or infected with VV, WR, VV Lister, VV Lister 35K, CPV BR, or one of the EVs described above were screened for the presence of secreted vCKBP by cross-linking to human ¹²⁵I-MIP-1 (Fig. 1a, upper panel). As reported previously (5), a ¹²⁵I-MIP-1-vCKBP complex was observed with VV Lister and CPV BR but not with mock, VV WR, or VV Lister 35K. VV WR expresses a truncated 7.5-kDa protein from the vCKBP gene that has no chemokine binding activity, and VV Lister 35K is an insertion mutant with an inactivated vCKBP gene (36, 48). Inclusion of an excess of unlabeled MIP-1 inhibited the formation of a cross-linked ¹²⁵I-chemokine-vCKBP complex in the VV Lister supernatant, demonstrating the specificity of chemokine binding. Complexes between the labeled chemokine and secreted vCKBP were formed in all of the EV supernatants except that of EV Mill Hill. The EV complexes were the same size as the chemokine-vCKBP complex from CPV BR (35 kDa) and slightly smaller than the VV Lister complex. A similar experiment was performed with human ¹²⁵I- RANTES (Fig. 1a, lower panel), and a ¹²⁵I-RANTES-vCKBP complex was observed with all 10 of the EV isolates tested (EVs Cornell and Mill Hill were not included).

View larger version (54K): [in this window] [in a new window]   FIG. 1.   Expression and binding specificity of the EV vCKBP. (a) Media from BSC-1 cell cultures uninfected (mock) or infected with the indicated viruses were incubated with 400 pM human 125I-MIP-1 (upper panel) or human 125I-RANTES (lower panel) and treated with the cross-linker EDC before SDS-PAGE and autoradiography. Positions of the 125I-chemokine (upper panel only) and 125I-chemokine-vCKBP complexes and molecular size markers are indicated. Hamp., Hampstead. VVL, VV Lister; Cold CK, 1,000-fold molar excess of unlabeled homologous chemokine was included. (b) Cross-linking of 125I-RANTES to media from EV- and VV-infected BSC-1 cell cultures in the absence (NC) or presence of a 50-, 250-, 1,000-, or 2,000-fold molar excess of the indicated human (h) or mouse (m) chemokine; Lptn, lymphotactin. (c) Cross-linking of human 125I-RANTES to media from BSC-1 cell cultures infected with the indicated viruses in the absence or presence of a 50-, 250-, 1,000-, 2,000-, or 5,000-fold molar excess of soluble human (h) fractalkine.

The vCKBP of EV blocks the binding of CC chemokines to cellular receptors. We confirmed that vCKBP from EV Hampstead can prevent the specific binding of ¹²⁵I-RANTES to chemokine receptors on human U937 cells (Fig. 2) and is therefore likely to be functional as a chemokine inhibitor in vivo. Preincubation of the ¹²⁵I-chemokine with supernatants from as few as 10,000 EV Hampstead-, VV Lister-, or CPV BR-infected BSC-1 cells reduced its binding to U937 cells to background levels. The dose dependence of this effect was similar for each of the three viruses. Supernatants from VV Lister 35K, a vCKBP insertion mutant, did not significantly reduce the binding of ¹²⁵I-RANTES at any of the doses tested.

View larger version (27K): [in this window] [in a new window]   FIG. 2.   Competitive inhibition of chemokine-receptor binding by the EV vCKBP. U937 cells were incubated with human 125I-RANTES that had been preincubated with various doses of medium equivalent to the indicated numbers of BSC-1 cells infected with different viruses. Cells were then separated from soluble radioactivity by phthalate oil centrifugation, and cell-bound radioactivity was measured with a gamma counter. Data are expressed as the mean and standard deviation of duplicate determinations. In the absence of viral supernatant, total radioactivity bound to the cells was 5,598 ± 341 cpm (n = 8), while in the presence of a 1,000-fold excess of unlabeled human RANTES, it was 159 ± 3 cpm (n = 2), or 2.8% of the total binding.

Sequence of the EV vCKBP gene. We sequenced a segment of the genome of EV Hampstead that contained a predicted vCKBP ORF encoding 247 amino acids (Fig. 3). The amino acid sequence of the EV vCKBP shared between 85.8 and 87.3% identity with predicted vCKBP sequences from VV Lister (36), CPV BR (21), and CPV GRI-90 (38). The EV Hampstead sequence contained a deletion of 10 amino acids corresponding to residues 69 to 78 of the VV Lister sequence. These amino acids were also absent in the CPV BR sequence (21) but were present in the sequence of another CPV strain, GRI-90 (38). This deletion and a stretch of 21 adjacent, variable amino acids in the C-terminal portion were found to align with a 29-amino-acid deletion in the amino acid sequence of the related VV protein encoded by the A41L ORF (41).

View larger version (85K): [in this window] [in a new window]   FIG. 3.   Comparison of the predicted amino acid sequences of OPV vCKBPs. The top five amino acid sequences are from the OPV vCKBP genes (accession numbers D00612, Y15035, J02066, AJ277111, and AJ277112), whereas the bottom sequence is from the related A41L (SalF3L) gene from VV WR (accession number D11079). In this alignment, residues which differ from the corresponding position in the VV Lister sequence are highlighted. Identical amino acids are black on white, nonconservative substitutions are white on black, semiconservative substitutions are white on dark grey, and conservative substitutions are black on pale grey. The predicted sites of N-terminal secretory signal peptide cleavage are indicated by arrowheads. Filled circles indicate the positions of invariant cysteine residues. Dots indicate amino acid deletions, and asterisks indicate stop codons.

Expression of soluble TNFRs by EVs. The Moscow strain of EV expresses a secreted vTNFR (CrmD) that is also present in CPV BR (25) but does not express functional homologs of the other two known OPV vTNFRs, CrmB and CrmC. A full-length, presumably functional CrmD gene has also been sequenced in EVs MP-3, MP-4, and Munich-SF (25). We used a filter-based binding assay (1) to screen EV culture supernatants for the presence of secreted ¹²⁵I-TNF binding proteins and examined their binding specificity by including unlabeled cytokine competitors in the assay. We detected specific binding of human ¹²⁵I-TNF- in all EV supernatants tested (Fig. 4a). In most instances, the signal was of an intensity similar to that obtained with CPV BR supernatants but was lower than that detected with VV Lister supernatants. Expressed as a proportion of the ¹²⁵I-TNF- binding signal observed with VV Lister, the EV Cornell binding signal was slightly more intense than those of the other EVs. Experiments in which molar excesses of unlabeled human, mouse, or rat TNF- were included in binding assays revealed that they bound to vTNFRs from EV Hampstead, but no significant binding of human LT- to soluble receptors could be demonstrated with these assays (Fig. 4b). This EV TNF binding specificity was similar to that found for VV Lister and CPV in such binding assays (Fig. 4b) (1).

View larger version (40K): [in this window] [in a new window]   FIG. 4.   Expression and binding specificity of secreted EV vTNFRs. (a) Secretion of vTNFRs by 12 different EVs. Supernatants from 5.4 × 104 BSC-1 cells infected with the indicated viruses were incubated with 300 pM human 125I-TNF- at room temperature for 2 h. Receptor-bound 125I-TNF was separated from free 125I-TNF by filtration through Whatman GF/C glass fiber filters after polyethylene glycol precipitation. Specific 125I-TNF binding was determined by subtraction of background with medium from values obtained with mock-infected cells. Data are expressed as the mean and standard deviation of four separate determinations. Hamp., Hampstead. VVL, VV Lister; Cold hTNF, 500-fold molar excess of unlabeled human TNF- was included. (b) Binding specificity of vTNFRs from EV Hampstead, VV Lister, and CPV BR. Binding assays with human 125I-TNF- and the indicated supernatants were performed as for panel a in the absence or presence of the indicated molar excesses of unlabeled human, mouse, or rat TNF- or human LT-. Data represent the percentage of binding in the absence of a competitor and are expressed as the mean and standard deviation of duplicate (VV Lister and CPV BR) or triplicate (EV Hampstead) determinations after subtraction of background 125I-TNF binding.

Analysis of the secreted vIL-1R expressed by EV. Using a filter-based assay of IL-1 binding in solution similar to that used for TNF, we screened EV supernatants for the presence of a soluble, secreted vIL-1R that bound to human ¹²⁵I-IL-1 (Fig. 5a). As previously described (4), specific binding of this cytokine was observed with medium from BSC-1 cells infected with VV WR but not from cultures infected with a VV which lacks VV vIL-1R gene B15R (vB15R). However, no binding of human ¹²⁵I-IL-1 could be detected in any of the EV supernatants. To examine the possibility that this assay specifically failed to detect an EV vIL-1R-¹²⁵I-IL-1 complex which was nevertheless formed, we developed another assay in which the vIL-1R was cross-linked to ¹²⁵I-IL-1 by use of EGS. Ligand-receptor complexes were then detected by SDS-PAGE and autoradiography. Using this assay, we failed to detect any EV vIL-1R-¹²⁵I-IL-1 complexes under conditions in which specific binding of human ¹²⁵I-IL-1 to the vIL-1R from VV WR (58-kDa complex) or CPV BR (52-kDa complex) was easily detectable (Fig. 5c).

View larger version (50K): [in this window] [in a new window]   FIG. 5.   Expression of vIL-1Rs by EV. (a and b) Detection of the EV vIL-1R with a filter-based binding assay. Supernatants from 5.4 × 104 BSC-1 or 2 × 104 Sf-21 cells infected with the indicated viruses were incubated with 100 pM human 125I-IL-1 (a) or 200 pM mouse 125I-IL-1 (b), and the formation of ligand-receptor complexes was measured as described in the legend to Fig. 4. Data are expressed as the mean and standard deviation of four separate determinations. Hamp., Hampstead. (c and d), Cross-linking assay for vIL-1Rs. Supernatants from 104 BSC-1 or Sf-21 cells infected with the indicated viruses were incubated with either 1.15 nM human 125I-IL-1 (c) or 1.27 nM mouse 125IL-1 (d). Complexes between vIL-1Rs and the labeled cytokine were cross-linked by use of EGS, and the products were analyzed by SDS-PAGE and autoradiography. The positions of 125I-IL-1, 125I-IL-1-vIL-1R complexes, and molecular size markers are indicated. Cold competition of binding to the labeled cytokine was achieved by inclusion of a 500-fold molar excess of homologous human (h) or mouse (m) unlabeled IL-1.

View larger version (32K): [in this window] [in a new window]   FIG. 6.   Binding specificity of the EV vIL-1R and its sequestration of IL-1 in vitro. (a) Filter-based assay of binding to 200 pM mouse 125I-IL-1 by vIL-1R in supernatants from 5.4 × 104 BSC-1 cells infected with VV WR or EV Hampstead. Binding was determined in the absence (NC) or presence of the indicated molar excesses of unlabeled human (h) and mouse (m) cytokines. Results are the mean and standard deviation of duplicate determinations. (b) Inhibition of cellular IL-1R binding by media from EV-infected cells. Binding of 400 pM mouse or 190 pM human 125I-IL-1 to 2.5 × 106 EL4 6.1 C10 cells was determined by phthalate oil centrifugation after preincubation of the cytokine with various doses of medium equivalent to the indicated numbers of BSC-1 cells either uninfected or infected with different viruses. Specific binding of 125I-IL-1 was determined by measuring binding in the presence or absence of a 500-fold molar excess of human IL-1 and subtracting the former value from the latter value. Values for human and mouse cytokines were 1,125 and 1354 cpm, respectively. Data, expressed as the percentage of specific binding, are the mean and standard deviation of duplicate (mouse) and triplicate (human) determinations.

Sequence of the EV vIL-1R and its expression in the baculovirus system. Sequencing of the EV homolog of the VV vIL-1R gene revealed that the EV gene encodes a 328-amino-acid polypeptide whose sequence is distinct from those of its VV and CPV homologs. The EV sequence differs from the vIL-1R consensus sequence at 51 amino acid residues, compared to only 14 and 9 residues for the VV and CPV sequences, respectively (Fig. 7). The EV vIL-1R amino acid sequence is 81.8% identical to that of VV WR and 83.4% identical to that of CPV BR, while the VV WR and CPV BR sequences share 93.4% identical amino acids. Thirty of the 51 mutated EV amino acid residues are concentrated in three discrete regions which together constitute only 27% of the total EV vIL-1R sequence. These regions are amino acids 3 to 32, before the first immunoglobulin (Ig) domain (10 mutations); amino acids 152 to 178, in the second Ig domain (11 mutations); and amino acids 253 to 285, in the third Ig domain (9 mutations).

View larger version (67K): [in this window] [in a new window]   FIG. 7.   Amino acid sequence comparison of OPV vIL-1Rs. Identical residues are white on black, conservative substitutions are white on dark grey, semiconservative substitutions are black on pale grey, and nonconservative substitutions are black on white. The Ig domains (1, 2, and 3) are indicated by an unbroken line above the sequences, and their characteristic cysteine and tryptophan residues are indicated by filled circles. Predicted sites of N-terminal signal peptide cleavage in the three vIL-1Rs are marked by labeled arrowheads. Dots indicate amino acid deletions, and asterisks indicate stop codons. The accession numbers of the sequences shown are as follows: VV WR, D11079; CPV BR, M95202; and EV Hampstead, AJ277110.

	DISCUSSION

Top Abstract Introduction Materials and Methods Results Discussion References

The immunomodulatory factors expressed by OPVs have a major influence on the pathogenesis of the acute infections produced by these complex viruses. For example, deletion of the vIL-1R and vIFN-/R genes from VV has marked effects on the infections produced by this virus in mice (2, 4, 45, 46). However, to date, there have been few in vivo studies of the function of the products of such genes in the presence of the immune system encountered by an OPV in its natural host (10). Such studies can be performed using the mousepox model, since all available evidence suggests that EV is likely to be a natural mouse pathogen (18). Here we have taken steps toward exploiting the full potential of this model by characterizing the expression and properties of three major EV immunomodulatory activities.

Several general observations about EV cytokine inhibitors can be made on the basis of data presented here and elsewhere (13, 25, 26, 32, 43). First, EV expresses soluble cytokine inhibitors belonging to all of the classes which have thus far been identified in OPVs, including proteins that bind to and inhibit IL-1, TNF, CC chemokines, IFN-, IFN-/, and IL-18 (10, 13, 25, 32, 43). Second, the expression of all of these receptors is now known to be uniformly conserved in EVs isolated from laboratory outbreaks that occurred at different times and in widespread geographic locations (43) (V. Smith and A. Alcami, unpublished data). Finally, whereas particular cytokine receptors expressed by different OPVs tend to be virtually identical in terms of their amino acid sequences and binding specificities, there is an example of an EV receptor, the vIFN-R (32), which has an amino acid sequence and binding properties distinct from those of other OPV receptors. These differences may have resulted from a prolonged period of viral coevolution with the mouse immune system. Here we present evidence that the sequence of the EV vIL-1R has also diverged from those of its OPV homologs. This sequence divergence may have resulted in quantitative, if not qualitative, differences in its inhibition of IL-1 activity.

EV is a further example of an OPV which produces a comprehensive repertoire of inhibitors of inflammatory cytokines. Biochemical, biological, or sequence data suggest that certain CPV strains produce an even broader range of soluble cytokine receptors than EV, including a panel of three distinct soluble vTNFRs. Various strains of VV express subsets of all of the above types of cytokine receptors (6, 42) as well as a novel membrane-bound TNF binding factor (1), while sequencing data suggest that variola virus expresses functional forms of all but the vIL-1R (37, 39). Retention of most of these immunomodulators by OPVs may therefore be essential for a productive infection to occur. The loss of one or two activities may in fact be compensated for by redundancy in the anti-inflammatory effects of the remaining gene products. The study of mutant EVs from which multiple immunomodulatory genes have been deleted would be informative in this regard.

The retention of functional vTNFRs, vIL-1Rs, and vCKBPs by all of the EV isolates studied here is interesting, since similar studies with multiple VV strains have revealed considerable interstrain heterogeneity in the expression of these immunomodulators (1, 4, 5). The most obvious explanation for this observation is that all of the EVs were originally isolated from laboratory mousepox outbreaks that were presumably caused by virus transmitted from a natural host reservoir (14, 18; Lipman et al., Letter). In contrast, the natural host of VV is unknown, and this virus has been derived from a range of different hosts and conditions of laboratory passage (3). If different mousepox outbreaks were caused by transmission from discrete natural reservoirs of the virus, then there must be considerable pressure to conserve functional immunomodulatory factors in the wild. It is also interesting to note that the Hampstead Egg strain, which was extensively passaged on chick chorioallantoic membranes to induce attenuation (16), has retained functional copies of all three of the genes studied here, despite the fact that it shows reduced virulence in experimental infections. In contrast, laboratory passage of EV Mill Hill appears to have resulted in the loss of the functional vCKBP expressed by the parental Hampstead isolate.

We report for the first time that EV encodes a vCKBP that effectively sequesters CC chemokines, presumably preventing their induction of multiple proinflammatory effects, such as an increase in the influx of leukocytes into sites of infection (8). The in vitro properties of the EV protein appear to be very similar to those described for its VV and CPV homologs (5, 20, 24, 40) and are likely, on the basis of sequence data, to closely resemble those of the predicted variola virus protein (29). The sequence of the EV protein contains a short deletion of 10 amino acids which are also absent from the sequence of the CPV BR protein (21). This deletion may be responsible for the slightly smaller size of the EV and CPV vCKBP-¹²⁵I-chemokine complexes than of complexes seen with VV Lister in our cross-linking experiments. Interestingly, sequence information shows that this deletion event has not occurred in CPV GRI-90 (38), raising the possibility that it may have occurred independently in both CPV BR and EV. According to the recently reported X-ray crystallographic structure of the vCKBP from CPV BR (11), this region of the protein lies within an extended loop that forms contacts between the two molecules present in the vCKBP homodimer. However, this dimer is unlikely to be formed in solution. In the monomeric form of vCKBP, the loop would be exposed on the surface of the molecule. Nevertheless, the variability of this region between otherwise fully functional vCKBPs suggests that it does not have a major role in chemokine binding. The absence of the domain from the related protein encoded by the VV A41L gene is further evidence that it is not involved in the overall folding or function of this class of molecules.

Until recently, the production of vCKBPs was thought to be a mechanism of immune evasion restricted exclusively to poxviruses (23). However, the identification of an unrelated soluble, secreted vCKBP produced by the murine gamma herpesvirus MHV-68 (35) has extended this strategy to a second major family of large DNA viruses. Here we have demonstrated that vCKBPs from VV, CPV, and EV do not bind the CX₃C chemokine fractalkine and therefore are absolutely specific for CC chemokines. In contrast, the MHV-68 vCKBP, encoded by the M3 gene, can bind to chemokines from all four classes. This difference in binding specificity may reflect the different roles of chemokines in the control of herpesvirus and poxvirus infections, and the study of its structural basis will be highly relevant for the design of therapeutic chemokine inhibitors.

All of the EVs which we tested produced secreted TNF binding activity. This result extends the previous report that EV Moscow and three other EV isolates express functional forms of the vTNFR CrmD, which is also expressed by CPV. Sequence analysis of the EV homologs of the vTNFRs CrmB and CrmC has shown their genes to be truncated (25). Thus far, sequence data therefore provide no evidence for the presence of any vTNFR other than CrmD in this virus. If this is the case, it seems that VV (CrmC), EV (CrmD), CPV (CrmB, CrmC, and CrmD), and variola virus (CrmB) all produce different subsets of the OPV vTNFR family. These differences in interactions with the host TNF system may contribute to the different disease phenotypes produced by these viruses. Competition experiments revealed that EV supernatants contained a factor(s) capable of binding human, mouse, and rat TNF- but not human LT-. This observation is inconsistent with results from previous studies (25) which detected LT- binding in supernatants from EV-infected cells. This discrepancy may be due to the use of different assay methods in the two studies.

We report for the first time that EV, like VV and CPV (2, 4, 45), expresses a vIL-1R that is capable of binding to both mouse IL-1 and human IL-1 and preventing their interaction with mouse cellular IL-1R. Like other known OPV vIL-1Rs, the EV protein does not bind mouse IL-1 (2). There is a discussion of unpublished data (18) which states that, in contrast to our results, mouse IL-1 binding activity was undetectable in medium from EV-infected cells under conditions in which binding of the VV vIL-1R was observed. This contradiction with our findings is explicable because in our assays, the IL-1 binding signals measured in infected-cell supernatants were lower for EV than for VV or CPV. It is also interesting to note that although we demonstrated, using cold competition experiments, that the EV vIL-1R binds human IL-1, it was not possible to directly detect binding of the viral protein to human ¹²⁵I-IL-1 using two different methods of assay. In the same experiments, the binding of VV and CPV vIL-1Rs to human ¹²⁵I-IL-1 was readily detected.

There are two possible explanations for these unusual binding data. One is that the vIL-1R is secreted at much lower levels by EV than by VV or CPV, with a corresponding reduction in the amounts of labeled cytokine bound in assays. However, natural and recombinant vIL-1Rs from both VV and EV are secreted in sufficient quantities to detect the binding of murine ¹²⁵I-IL-1 in cross-linking and filter-based binding assays. The second explanation is that the difference in binding of human ¹²⁵I-IL-1 and mouse ¹²⁵I-IL-1 by the EV vIL-1R results from amino acid sequence changes that have modified its absolute and relative affinities for the two cytokines, albeit not to the extent that its ability to sequester them has been lost. These possibilities are not mutually exclusive, and examination of the sequence of the EV vIL-1R gene provides circumstantial evidence for both.

The amino acid sequence of the EV vIL-1R has diverged from those of its functional CPV and VV homologs and from that of the presumed product of the functional ancestor of the variola virus vIL-1R gene. Three regions of the protein carry an especially high proportion of unique amino acid residues. The predicted 21-amino-acid N-terminal signal sequence of the EV vIL-1R differs from those of its VV and CPV homologs at six positions. Such mutations may affect the efficiency of secretion of the EV vIL-1R from infected cells. Two other regions that carry a high proportion of mutated residues are in the center of the second and third Ig domains. It is possible that such mutations have an influence on the interaction of the protein with IL-1 either via direct interactions with the ligand or via influence on the overall folding of the protein. Unfortunately, there is no available evidence concerning the contribution of different domains or residues of the vIL-1R to cytokine binding. Interestingly, alignment of the EV vIL-1R amino acid sequence with that of a soluble, extracellular form of the human type I IL-1R which has been structurally characterized in a complex with human IL-1 (49) reveals that several of the unique EV amino acid residues, most notably five between amino acids 152 and 158, align with regions of the human receptor shown to contact IL-1 in the receptor-ligand complex (data not shown).

Previous studies of the effects of the vIL-1R on VV pathogenesis have revealed that this receptor is responsible for the suppression of febrile responses and attenuation of the virus after intranasal inoculation of mice (2, 4). It has been suggested that the expression of this activity is associated with VV virulence in humans, since certain highly reactogenic VV vaccine strains, such as VV Copenhagen and VV Tashkent, are vIL-1R negative, whereas the safer Lister strain is vIL-1R positive. In addition, variola virus, which causes a systemic infection associated with high fever, does not express a functional vIL-1R, while CPV, which produces a milder infection, is vIL-1R positive. EV does not fit with this hypothesis because, although it produces a severe systemic infection in mice, it expresses a functional vIL-1R that is present in all of the isolates which we tested. In light of this finding, it would be interesting to assess the contribution of the EV vIL-1R to mortality and morbidity in the mousepox model.

In conclusion, we have demonstrated that EV, a species-specific, highly virulent OPV, expresses three major types of immunomodulatory cytokine receptors. The expression of these molecules is highly conserved among different virus isolates, suggesting that they have a positive influence on the persistence of this virus in the wild. We have also found evidence that the EV vIL-1R gene has undergone some evolutionary changes which are presumably the result of an extended period of adaptation in a restricted range of natural hosts. The study of the function of these molecules using the laboratory mousepox model should provide further insights into their roles in vivo.