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Gammaretroviruses of several different host range subgroups have been isolated from laboratory mice. The ecotropic viruses infect mouse cells and rely on the host CAT-1 receptor. The xenotropic/polytropic viruses, and the related human-derived XMRV, can infect cells of other mammalian species and use the XPR1 receptor for entry. The coevolution of these viruses and their receptors in infected mouse populations provides a good example of how genetic conflicts can drive diversifying selection. Genetic and epigenetic variations in the virus envelope glycoproteins can result in altered host range and pathogenicity, and changes in the virus binding sites of the receptors are responsible for host restrictions that reduce virus entry or block it altogether. These battleground regions are marked by mutational changes that have produced 2 functionally distinct variants of the CAT-1 receptor and 5 variants of the XPR1 receptor in mice, as well as a diverse set of infectious viruses, and several endogenous retroviruses coopted by the host to interfere with entry.
The various inbred strains of laboratory mice and wild mouse species differ in their susceptibility to mouse gammaretrovirus infection and to virus-induced diseases. Host resistance is due to numerous constitutively expressed antiviral factors that target specific stages of the retroviral life cycle. These host restriction factors can block entry, postentry uncoating and reverse transcription, trafficking, integration, assembly, and release . The first step in the replicative cycle is entry, and this process relies on host-encoded receptors. Host cell factors that can interfere with virus entry include genetic variations of the cell receptor as well as other host factors such as envelope (Env) glycoproteins produced by endogenous retroviruses (ERVs).
Infectious mouse leukemia viruses (MLVs) of three subgroups have been isolated from laboratory mice, and these subgroups were initially defined by their species tropisms. The ecotropic MLVs (E-MLVs) infect only mouse or rat cells and use the amino acid transporter CAT-1 as receptor. The xenotropic MLVs (X-MLVs) infect cells of non-rodent species , and polytropic MLVs (P-MLVs) infect both mouse and non-rodent cells [3, 4]. The X-MLVs and P-MLVs together constitute the XP-MLVs and both use the XPR1 receptor [5–8].
Receptor choice is determined by the N-terminal portion of the MLV Env, the receptor-binding domain (RBD) [9–11]. The E-MLVs and XP-MLVs both have Env subtypes that differ in their ability to use polymorphic variants of their cognate receptors, and some of these host-range variants, the “xenotropic” MLVs, are completely restricted in mouse cells . Both receptors for the laboratory mouse MLVs, CAT-1 and XPR1, have naturally occurring variants responsible for specific virus resistance phenotypes. There are 2 functionally distinct variants of the CAT-1 receptor for E-MLVs , and there are 5 known variants of the XPR1 receptor for the XP-MLVs in mice [5, 14–17]. These variants are not only important host factors that can restrict infection, but also they can alter virus-receptor interactions in ways that influence virus-induced pathology. This paper will describe the functional variants of these 2 MLV receptors and describe their coevolution with MLV in virus-infected mouse populations.
The first gammaretrovirus receptor gene to be cloned was the CAT-1 receptor for E-MLVs . This gene (gene symbol Slc7a1) encodes a glycoprotein with 14 putative transmembrane domains, and it functions as a cationic amino acid transporter [19, 20] (Figure 1(a)). Ten additional gammaretrovirus receptors have now been cloned; all of these gammaretrovirus receptors are multi-transmembrane proteins, and the receptors with known functions are all transporters of small solutes (reviewed in [21–26]). The human orthologue of mouse CAT-1 does not function as an E-MLV receptor, and the key sites in the mouse protein critical for virus entry lie in the third extracellular loop along with two consensus recognition sites for N-linked glycosylation [27, 28] (Figures 1(a) and 1(b)). CAT-1 is modified posttranslationally by glycosylation, and N-glycans are added to both of the CAT-1 loop 3 glycosylation sites . All E-MLVs rely on the CAT-1 receptor for entry, although initial binding and the efficiency of entry may be influenced by other factors at the cell surface, such as heparin [30, 31].
The E-MLV Env glycoprotein consists of surface (SU) and transmembrane (TM) subunits that are proteolytically cleaved from the same precursor protein and are linked by disulfide bonds. The SU protein has a 236 residue RBD at its N-terminal end that has 3 variable regions, and this is followed by a proline-rich hinge region and a C-terminal domain (Figure 2(a)). Entry is initiated by virus-receptor binding which precipitates a conformational change in Env that allows for subsequent fusion of viral and cellular membranes, a process that may involve cellular proteases . The CAT-1 receptor recognition site is within the first variable domain (VRA) of the RBD. Three residues within the RBD VRA of the Friend E-MLV, FrMLV, have been identified as critical for entry (S84, D86, and W102) [33–35]. The crystal structure and functional analysis of the FrMLV RBD showed that these residues form a binding pocket on the structure's surface [35, 36] (Figure 2(b)). Several additional Env residues outside the binding pocket affect postbinding entry. Thus, the H8 residue in a conserved SPHQV motif near the SU N-terminus is necessary for fusion [37, 38] although residues at the other end of the MoMLV RBD, at positions 227 and 243 (equivalent to FrMLV sites 229 and 245), can substitute for H8 . The proline-rich region is also involved in mediating postbinding conformational changes and fusion , and residues in two segments of the C-terminus of Env also have roles in fusion [41–43] (Figure 2(a)).
There has been no systematic attempt to screen for CAT-1 receptor variation in mice, but 3 sequence variants have been identified in Mus (Figure 1(b)). The prototype receptor, mCAT-1, was cloned from NIH 3T3 cells . Two sequence variants have been identified in the wild mouse species M. dunni and M. minutoides [13, 44]. Limited testing suggests that the M. minutoides CAT-1 functions like the laboratory mouse mCAT-1 receptor, but the receptor of M. dunni, dCAT-1, differs from mCAT-1. M. dunni cells are relatively resistant to infection by Moloney E-MLV (MoMLV), although these cells are fully susceptible to other E-MLV isolates . dCAT-1 differs from mCAT-1 by 4 residues, two of which are in the receptor determining third extracellular loop; one, I214V, is a substitution, and the second is a glycine insertion within the NVKYGE virus binding site  (Figure 1(b)).
Two mutational changes in the MoMLV RBD VRA independently produce viruses that efficiently infect M. dunni cells: a replacement mutation, S82F, and introduction of two serine residues that are present in other E-MLV VRAs but absent in MoMLV (S76, S77 in FrMLV) (Figure 2(a)) . The MoMLV S82F mutation site corresponds to S84 in Friend MLV, one of the 3 residues critical for virus binding and entry. The importance of this residue for virus tropism is underscored by the fact that MoMLV-S82F is poorly infectious in cells that carry mCAT-1  (Figure 1(b)).
E-MLVs can infect rodent species in addition to Mus, and CAT-1 receptor variants have been described in hamsters and rats (Figure 1(b)). Hamster cells are generally resistant to infection by E-MLVs, but some variants of FrMLV can infect these cells . Infectivity of one such variant, PVC-211, was attributed to Env substitutions E116G and E129K  (Figure 2). Another FrMLV variant, F-S MLV, also inefficiently but reproducibly infects hamster cells; it was suggested that this tropism was influenced by two substitutions: S84A and S79N . Restriction of some E-MLVs can result from complementary changes in the interacting sites of virus Env and the CAT-1 receptor; however, the MoMLV restriction associated with dCAT-1 is reproduced in human cells expressing this receptor , but not in ferret cells , suggesting that other cellular factors may also influence receptor function.
Polymorphisms that alter virus-receptor interactions can affect pathogenesis as well as entry. Cytopathic variants are common among the retroviruses that induce disease in their hosts, including HIV-1 as well as avian leukosis viruses and some pathogenic bovine and feline leukemia viruses [50–52]. These viruses can produce large multinucleated syncytia in cultures of susceptible cells. In contrast, mouse gammaretroviruses rarely produce syncytia although there are three exceptional cytopathic E-MLVs. The MoMLV variant, Spl574 and a FrMLV variant, F-S MLV, both induce syncytia and cell death in M. dunni cells [45, 48]. The third cytopathic virus, TR1.3, is a neuropathic FrMLV variant that also induces syncytia in SC-1 cells .
The cytopathicity of these 3 viruses is due to single amino acid substitutions at two of the 3 amino acids that form the receptor binding site. The cytopathicity of TR1.3 is due to W102G , and the cytopathicity of the other variants is due to different amino acid substitutions at the same critical Env residue: S82F in Spl574, and S84A in F-S MLV [45, 48]. Syncytium formation by Spl574 and F-S MLV is accompanied by the accumulation of large amounts of unintegrated viral DNA , a phenomenon which is also a hallmark of other cytopathic retroviruses and has been attributed to the absence of superinfection interference . TR1.3 shows significantly reduced receptor binding avidity that correlates with its inability to block superinfection . That cytopathicity is a consequence of altered receptor virus interactions is also supported by the fact, noted above, that MoMLV-S82F shows altered host range (Figure 1(b)) and also by the fact that syncytia formation by Spl574 is observed in cells of heterologous species expressing dCAT-1, but not mCAT-1 . Thus, the cytopathicity of these 3 viruses in cultured cells and the neurovirulence of TR1.3 are governed by sequence differences in the viral env and, for 2 of these viruses, by corresponding differences in the CAT-1 receptor.
Other polymorphisms of the E-MLV env can alter cell tropism and influence disease type. The thymotropism of radiation leukemia virus has been mapped to env , and several E-MLVs have neuropathogenic properties due to env polymorphisms. For example, TRM, a mutant variant of the neuropathic TR1.3, induces a different disease pathology resulting from reversion of the TR1.3 G102W mutation and a new Env mutation, S159P . The most extensively studied neuropathic E-MLV is CasBrE, an isolate from California wild mice. Early studies mapped neurovirulence determinants to the CasBrE Env , and recent data indicate that CasBrE neuropathology is mediated by Env at two levels. First, the CasBrE Env targets the virus to cells within the CNS that express significant levels of CAT-1, and second, disease-associated spongiosis is induced by MLV-receptor-independent toxicity of this Env, determinants of which have not been identified but are presumably shared with other neurovirulent MLVs . Env residues have also been implicated in the targeting of the neuropathic Friend PVC-211 variant to brain capillary endothelial cells . This tropism is due to 2 mutations, E116G in VRA and E129K in VRC, mutations that also alter host range and interference properties [47, 59]. These findings indicate that specific replacement substitutions at different positions in the Env of pathogenic E-MLVs can affect receptor interactions, cell tropism, disease induction, and disease type.
The retroviral Env is glycosylated, as are cellular proteins involved in entry. Many viruses use the glycans on cell surface glycoproteins as attachment factors , but glycosylation of the CAT-1 receptor is not required for virus entry. CAT-1 continues to support virus entry after both loop 3 N-glycan sites have been removed by mutagenesis . However, host cell glycans can modulate entry of some E-MLVs. Thus, resistance of M. dunni cells to MoMLV, resistance of NIH 3T3 cells to Spl574, and resistance of primary rat fibroblasts and hamster cells to E-MLVs are relieved by inhibitors of glycosylation [49, 62–66]. It is not clear whether the responsible glycoprotein is CAT-1 or other host glycoproteins, like the secreted factor associated with resistance to gibbon ape leukemia virus in hamster cells . There is, however, some evidence that the restriction of E-MLV infection in rat cells may be regulated by the glycosylation of rat CAT-1. The CAT-1 of rat XC sarcoma cells lacks one of the glycosylation sites found in the CAT-1 gene of other rat cells (Figure 1(b)), and heterologous cells expressing xcCAT-1 were found to be more susceptible to MoMLV than cells expressing rCAT-1 .
Glycosylation of the viral Env has been associated with altered infectivity of multiple viruses including retroviruses such as HIV-1 . MLV Envs can have up to 9 N-linked glycans (Figure 2(a)), and while glycans are critical for the maturation and transport of Env , functional roles for the individual Env glycans are poorly defined. It has been shown that loss of MoMLV gs2 results in a virus that is temperature sensitive in Rat2 cells, loss of gs4 produces noninfectious virus lacking SU protein, and loss of gs7 alters fusion and infectivity [70–73]. Removal of either of the 2 glycosylation sites in the Env RBD, gs1 and gs2, can produce viruses restricted by M. dunni cells due to altered virus binding to dCAT-1, although E-MLVs differ in their reliance on these glycans [74, 75]. Thus, N-linked glycans on the viral Env are required for proper folding and can influence the entry process, while glycans are not needed for CAT-1 receptor processing or receptor function and have, at best, limited ability to modulate virus entry.
Exposure to E-MLV gammaretroviruses occurred only recently in the evolution of Mus . Although E-MLV ERVs are found in few of the 40 Mus species, wild mice carry three distinctive Env subtypes of E-MLVs (Figure 3). Sequence identity in SUenv among these virus types is 70–77%. The first E-MLV type, the AKV E-MLVs of the laboratory mouse, is found as ERVs in multiple inbred strains . Many of these proviruses are capable of producing infectious virus , and the widely used laboratory virus strains MoMLV, FrMLV, and Rauscher MLV are derived from AKV MLV  (Figure 3). Among the wild mouse species, AKV MLV ERVs are found in the Asian species M. molossinus and in M. musculus of Korea and China but not eastern Europe [76, 80]. A second E-MLV subtype was initially identified in California wild mice [81, 82]. Proviruses with this CasBrE Env type have also been found in the Asian species M. castaneus, and these virus-infected mice were likely introduced to California by passive transport from Asia [76, 80, 83, 84]. A third E-MLV subtype, HoMLV, was isolated from the eastern European species M. spicilegus, but is transmitted only as an exogenous virus .
The evidence indicates that these 3 E-MLV Env variants did not coevolve with receptor polymorphisms. Sequence comparisons indicate that the 3rd extracellular loop of the CAT-1 gene is invariant in wild-derived mice carrying these 3 E-MLVs: M. castaneus, M. molossinus, M. spicilegus, and M. musculus (GenBank Accession nos. JN226407–JN226410). The only known functional variant of this receptor in mice is dCAT-1 of M. dunni, and it is not clear if this variant arose in mice exposed to virus; the single available M. dunni sample is a cell line that does not carry E-MLV ERVs indicative of past infections , and it has not been determined if dCAT-1 is present in natural populations of M. dunni (now termed M. terricolor) or whether it originated by mutation in this cultured cell line. Sequence conservation of the receptor determining region of CAT-1 in Mus is not due to functional constraints as the third extracellular loops of the CAT-1 (SLC7A1) genes of various non-Mus species are quite variable (Figure 1(b)). Although E-MLVs can use CAT-1 receptor variants in non-Mus rodents, the replacement mutations in other mammalian species are incompatible with receptor function, thus limiting E-MLVs to rodents, a type of host range restriction that is not shared by other gammaretroviruses. The absence of polymorphism in the Mus CAT-1 gene, even in virus-infected wild mouse populations, is consistent with the conclusion that exposure to E-MLVs is very recent in Mus  and suggests that these mice rely on alternative survival strategies to limit the deleterious effects of infection, including posttranslational modification of receptor function, receptor interference, or postentry blocks in the retroviral lifecycle.
Two subgroups of nonecotropic MLVs have been isolated from laboratory mice. These viruses were originally described as having distinct host ranges, but they use the same receptor, XPR1. X-MLVs and P-MLVs are both capable of infecting cells of nonrodent species, and although P-MLVs can efficiently infect mouse cells, X-MLVs were initially identified as incapable of infecting their natural hosts [2, 87, 88]. X-MLVs and P-MLVs are closely related viruses, and sequence differences in env and LTR are responsible for their differences in species tropism, for their nonreciprocal interference patterns, and for the pathogenicity of P-MLVs in mice [11, 89–92]. Although it is clear that the RBD VRA region is the major determinant of P-MLV and X-MLV host range , the critical VRA residues involved in XPR1 receptor recognition have not been identified, although 2 residues outside VRA can influence the ability of these viruses to infect cells of other mammalian species (Figure 4) . Viruses in the XP-MLV family are highly variable in the Env segment containing the RBD (Figure 4), and the wild mouse viruses, CasE#1 and Cz524, show atypical host range patterns that distinguish them from prototypical P-MLVs and X-MLVs (Table 1) [16, 89, 94].
The XPR1 receptor was originally described in laboratory mice as a P-MLV susceptibility gene . Subsequent studies demonstrated that wild-mouse-derived cell lines, SC-1 and M. dunni, are susceptible to X-MLVs as well as P-MLVs [86, 96], while cells of the Asian species M. castaneus are resistant to P-MLVs . That a single gene controls susceptibility to these two viruses was supported by the equivalent chromosome map locations of the genes controlling wild mouse susceptibility to X-MLVs and P-MLVs and by their cross-interference [5, 15, 89, 97]. The human and mouse Xpr1 genes were cloned [6–8] and shown to encode a protein with 8 putative transmembrane domains (Figure 5). While a cellular function has not been assigned to XPR1, XPR1 is upregulated following activation of the NF-κB RANKL-RANK signaling pathway  and its closest homologues in yeast (SYG1) and plants (PHO1) function in signal transduction and phosphate sensing and transport, respectively .
The genus Mus includes about 40 species, and all available species have been screened for sequence and functional variants of Xpr1 (Figures (Figures55 and and6).6). Of the 5 sequence variants found in wild mice, 4 show unique receptor phenotypes based on their ability to support entry of different virus isolates that rely on this receptor (Table 1). The most common receptor variant among wild mouse species was originally termed Sxv (susceptibility to xenotropic virus) . This variant is found in many Asian species as well as western European house mice [17, 99], and mice with Sxv were introduced into the Americas by European immigrants and explorers (Figure 7). Sxv is also carried by several of the common inbred strains of laboratory mice . Sxv is the most permissive of the Xpr1 alleles and supports entry of all XP-MLV host range variants (Table 1). The second most geographically widespread Xpr1 allele, Xpr1m, is found in two house mouse species, M. musculus, which ranges from central Europe to the Pacific, and M. molossinus, found in Japan . This variant is highly restrictive, allowing inefficient entry of X-MLVs, while restricting all other XP-MLVs. A third allele, Xpr1c, is found in the southeast Asian mouse, M. castaneus, and is responsible for resistance to infection by P-MLVs [15, 99]. A fourth wild mouse Xpr1 allele is restricted to the Asian species M. pahari; these mice are susceptible to X-MLVs and to CasE#1  (Table 1).
There is a fifth mouse Xpr1 variant, Xpr1n. The first of the receptor alleles to be identified, Xpr1n, was cloned from NIH 3T3 laboratory mouse cells [6–8]. This variant is responsible for the restrictive phenotype originally used to define the “xenotropic” host range subgroup, that is, viruses unable to infect cells of their home species . Xpr1n is unusable by X-MLVs or by the 2 wild mouse virus isolates, although it supports entry by P-MLVs (Table 1). The origin of this laboratory mouse variant is unclear. Although Xpr1n is carried by the majority of common inbred mouse strains, it has not been found in any wild-trapped mouse [17, 95] (Figure 6). The common strains of laboratory mice were derived from colonies of fancy mice maintained by hobbyists, and they represent a mosaic of wild mouse species [100, 101]. Genomic analysis of multiple strains indicates that the predominant contributor to the laboratory mouse is M. domesticus, the western European mouse, with smaller contributions from M. musculus and M. castaneus . Although this would suggest an M. domesticus origin for the laboratory mouse receptor allele, M. domesticus mice trapped in disparate locations in Europe and the Americans all carry the permissive allele  suggesting that Xpr1n arose and/or was selected in the fancy mice (Figure 7).
Initial studies on Xpr1 receptor function focused on sequence differences between the phenotypic variants identified in NIH 3T3 cells (Xpr1n) and M. dunni (Xpr1sxv) . Two critical amino acids were identified for X-MLV entry that lie in different putative extracellular loops (Figure 5). The restrictive Xpr1n carries a substitution, K500E, in its third extracellular loop (ECL3), and a deletion, T582Δ, in the fourth loop (ECL4). Corrective mutations at either of these sites produce functional receptors for X-MLVs without compromising P-MLV receptor function . Subsequent studies on the mouse receptor showed that these 2 critical residues are not equivalently used by the XP-MLVs, as CasE#1 can use Xpr1n-Δ582T but not Xpr1n-E500K . Mutational analysis of other polymorphic sites in the various Mus Xpr1s identified residues at additional sites that modulate virus entry: ECL3 positions 500, 507, and 508 and ECL4 positions 579 and 583 (Figure 5) [17, 94].
Although it is possible that the XPR1 protein carries two separate receptor determinants on ECL3 and ECL4 , it is more likely that the key residues in ECL3 and ECL4 form a single virus attachment site. The various viruses that use XPR1 for entry are sensitive to mutational changes in both ECL3 and ECL4 [16, 17, 94] (Figure 8). Thus, P-MLVs and the wild mouse viruses CasE#1 and Cz524 show different patterns of infectivity for Xpr1p mutants that have substitutions in ECL3 but identical ECL4 sequences. These same viruses also differ in their infectivity for cells with Xpr1m, Xpr1c, and Xpr1sxv, which have identical ECL3 sequences but different deletions in ECL4. The involvement of residues in multiple receptor domains is also characteristic of other retrovirus receptors . While the different domains required for these other retroviral receptors can have distinctive roles in virus attachment and entry [104, 105], this division of labor has not yet been shown to be the case for the XPR1 ECL3 and ECL4 domains.
Although it is clear that MLV entry is typically mediated by specific cell surface receptors, some MLVs are capable of bypassing the need for their cognate receptors and can infect cells that lack receptors and may also be able to infect cells in which those receptors are downregulated by superinfection [106, 107]. Such alternative entry mechanisms seem to be particularly important for P-MLVs, viruses that are less able to establish effective superinfection immunity against further infection [99, 108] either because they may have lower binding affinity for the XPR1 receptor than the X-MLVs or because Env-bound receptors may recycle rapidly into acidic compartments where the Env-receptor complex is disrupted allowing the freed receptor to recycle back to the plasma membrane. This ineffective or delayed establishment of interference to exogenous infection has been linked to the massive accumulation of viral DNA in P-MLV-infected mice  and to the ability of P-MLVs to induce cytopathic responses in mink lung cells in which superinfection induces an ER stress response and apoptosis [4, 110, 111].
Infectious P-MLVs arise in preleukemic tissues of mice with high levels of E-MLVs. P-MLVs have recombinant genomes in which env sequences are derived from endogenous polytropic or modified polytropic sequences, the Pmvs or Mpmvs . The Pmv and Mpmv proviruses that give rise to these recombinants have not been shown to be capable of producing infectious virus directly , but transmission of these ERVs and recombinant infectious P-MLVs can be accomplished through several mechanisms that are independent of XPR1. First, P-MLVs are generally transmitted in viremic mice as pseudotypes of E-MLVs and thus use mCAT-1 for entry [114, 115]. Also, homodimers representing the transcribed products of Mpmv and Pmv proviruses can be packaged into E-MLV virions, and these “mobilized” proviruses can infect cells, replicate in those new cells, and spread to other cells as pseudotyped virus . Another transmission mechanism allows infectious, recombinant P-MLVs to use alternative receptors in the presence of the soluble RBD glycoprotein for that receptor. P-MLVs and entry defective E-MLVs, but not X-MLVs, can be “transactivated” in this way by E-MLV RBD [38, 108]. This transactivation process is controlled, at least in part, by the conserved Env residue H8 and has also been described for other viruses such as feline leukemia viruses . While these mechanisms provide alternative routes for P-MLV transmission that are independent of the receptor, it should be noted that interference with the XPR1 receptor protects mice from P-MLV-induced disease  highlighting the crucial role of XPR1-mediated entry in the disease process.
The species distribution of the Mus XPR1 variants indicates that polymorphic, virus-restrictive receptors appeared when mice were exposed to XP-MLVs, especially X-MLVs (Figure 6). For most of the 8 million years of Mus evolution, species carried the permissive Xpr1sxv allele. Mice were subjected to XP-MLV infection about 0.5MYA, and this exposure is marked by the acquisition of MLV ERVs in the 4 house mouse species [76, 119, 120]. M. domesticus carries P-MLV ERVs, whereas M. castaneus, M. musculus, and M. molossinus carry predominantly X-MLVs . The common laboratory mouse strains, which are mosaics of these wild mouse species, generally carry multiple copies of X-MLVs and P-MLVs [121, 122]. The acquisition of these germline ERVs, and specifically X-MLVs, roughly coincides with the appearance of restrictive Xpr1 alleles: Xpr1c in M. castaneus, Xpr1m in M. molossinus and M. musculus, and Xpr1n in laboratory mice (Figure 6). Each of these restrictive receptors carries a unique deletion in the XPR1 ECL4 (Figure 5) . M. domesticus, the species carrying only inactive P-MLV ERVs, maintains the full-length, permissive Xpr1sxv receptor common to ancestral species of Mus. The fact that restrictive receptors have evolved in X-MLV infected mice suggests that this host pathogen interface has been an important evolutionary battleground. This also suggests that X-MLV infection is deleterious for mice, although the consequences of X-MLV infection have not yet been described because mouse gammaretroviruses have been studied largely in X-MLV-resistant laboratory mice. The discovery of mouse species and strains with XPR1 variants that efficiently support X-MLV entry now provides the basis for studies on pathogenesis of these viruses, and such studies have now been initiated .
Virus entry can be inhibited by receptor mutants but can also be blocked by members of a second set of genes found in E-MLV- or X-MLV-infected wild mice. This family of resistance genes governs production of MLV Env glycoproteins that are thought to restrict virus through receptor interference. These genes include Fv4, which blocks E-MLVs , and the genes Rmcf and Rmcf2 which restrict XP-MLVs and, in the case of Rmcf, inhibit P-MLV-induced disease [118, 124–126]. There is also evidence suggesting that additional Rmcf-like XPR1 receptor blocking genes are present in M. castaneus . Specific ERVs have been mapped to 3 of these resistance genes, all of which are defective for virus production but have intact env genes. Fv4 is a truncated provirus, Rmcf has a major deletion spanning gag-pol [124, 128], and Rmcf2 has a stop codon that prematurely terminates integrase . It has been proposed that the products of Fv4, Rcmf, and Rcmf2 reduce or downregulate activity of their cognate receptors, and Fv4 also has a defect in the fusion peptide of TMenv, so incorporation of this Env into virions in virus-infected cells results in their reduced infectivity .
Interference genes that target both host range types are found in the Asian species M. castaneus, mice that are infected with X-MLVs as well as with E-MLVs that are related to the leukemogenic and neuropathic CasBrE E-MLV [76, 80, 130]. These mice rely on several survival strategies to mitigate the consequences of infection. In addition to their restrictive Xpr1c receptor, these mice carry Fv4 as well as Rmcf-type XP-MLV interference genes. These interference genes likely arose in this species [80, 125]; CasBrE and Fv4 have related Env genes (Figure 3) . Transmission into other gene pools can proceed quickly for invasive genes like retrotransposons and for virus restriction genes that provide an immediate survival advantage. While the number and geographic distribution of Rmcf-type genes in Asian mice is not known, Fv4 is found in AKV MLV-infected mice trapped in Japan (M. molossinus) and in Korea . CasBrE and Fv4 are both found in California mice, where Asian mice were likely introduced by the shipping trade [76, 82, 131]. The discovery of multiple interfering loci in infected mouse species and their geographic spread suggests that these coopted Env genes represent an effective survival mechanism. The general importance of this form of innate immunity is also illustrated by the fact that Env genes with similar antiviral functions have also been identified in chickens, sheep, and cats [132–134].
The XP-MLVs are capable of infecting cells of other species, including humans (Figure 9). Cells of nearly all mammals are permissive to infection by X-MLVs, whereas a subset of these species is also susceptible to P-MLVs. This suggests that X-MLVs have less stringent receptor requirements than P-MLVs [17, 87, 88]. Some mammalian species show distinctive patterns of virus susceptibility not found in mice, for example, the restriction of P-MLVs and both wild mouse XP-MLVs by dog and buffalo cells (Figure 9) . Analysis of mammalian XPR1 genes reveals significant sequence variability especially in the receptor determining ECL4, although this 13 residue segment contains 3 nonvariant residues, S578, T580, and G589. These conserved residues do not contribute to the receptor attachment site . Further analysis of these functionally distinctive XPR1 genes may provide insight into the factors that facilitate transspecies transmission.
Mice are important vectors of diseases that infect humans and their livestock , and MLV-infected house mouse species have a worldwide geographic distribution . The horizontal transfer of infectious MLVs between individuals has been documented in wild mouse populations and in laboratory mice [82, 137], and MLV-related viral sequences, proteins, and antibodies have been reported in human blood donors and patients with prostate cancer and chronic fatigue syndrome [138–140]. An infectious virus first identified in prostate cancer patients, termed XMRV (xenotropic murine leukemia virus-related virus), shows close sequence homology with XP-MLVs , uses the XPR1 receptor , and has xenotropic host range . Although XMRV origin by transspecies transmission is consistent with the evidence of MLV transmission between mice and evidence of transmission of mouse C-type viruses to other species [142–144], several recent studies on XMRV have implicated laboratory contamination [145–148]. Additional studies aiming to resolve the origins issue are focused on patient samples and the characterization of mice for XMRV-related sequences .
It is clear that XMRV differs from MLVs isolated from mice in several biological properties, including host range and receptor usage. The two critical residues for X-MLV entry in Mus XPR1, K500 and T582 , independently produce equivalent receptor determinants for X-MLV but not for XMRV  or for the wild mouse isolate CasE#1 . While T582 but not K500 is required for CasE#1, XMRV preferentially relies on K500 [16, 17]. XMRV also differs from XP-MLVs in its ability to infect cells of different mammalian species. Although X-MLVs are able to infect all mammals, XMRV is uniquely restricted by cells of 3 species: Chinese hamster, Syrian hamster, and gerbil (Figure 9). For gerbil, this difference is likely attributable to XPR1 receptor polymorphism, as expression of the gerbil XPR1 receptor in heterologous cells reproduced the gerbil susceptibility pattern . The restriction of XMRV in Syrian hamster BHK cells may involve other host factors. Expression of human Xpr1 in these cells resulted in susceptibility to X-MLV but not XMRV, and analysis of interspecies somatic cell hybrids suggested that BHK cells lack a secondary factor needed for XMRV infection . These results suggest that XMRV differs from other X-MLVs in its interaction with XPR1 receptor determinants and also suggest that XMRV may be uniquely dependent on an as yet unidentified receptor cofactor. Further studies with this virus may provide additional insight into xenotropism and the interactions and identity of viral and host proteins that direct entry.
Retrovirus entry is dependent on the presence and accessibility of specific cell surface receptors. Mutational changes in these receptors and in the receptor attachment sites in the virus Env can alter the very first step in the virus life cycle and can thus have profound consequences for virus replication. Inhibition of virus entry has been a particularly effective antiviral tactic in mice infected with MLVs as well as with other gammaretroviruses . Entry is also the target of host restrictions in other species subject to retrovirus infection as shown by the discovery of interfering ERV Envs in multiple species [132–134] and by the discovery of inhibitory mutations in other receptors, such as the HIV-1 CCR5 coreceptor .
For the laboratory mouse MLVs, alterations in host receptors and/or virus Env can result in virus restriction, can alter the type and tempo of infection-induced pathology, and may also influence postentry events . The interacting sites of these receptors and Env are highly polymorphic, as expected for coevolving entities in an “arms race” driven by sequential reciprocal adaptations. For the XP-MLVs and XMRV, the battleground at the cell surface has produced 5 functionally distinct receptors in mice and more than a half dozen distinctive host range virus variants, variants that interact with different but overlapping sets of determinants on the XPR1 receptor or rely on alternative mechanisms of transmission independent of XPR1. For the E-MLVs, CAT-1 shows more limited variation although multiple viral Env subtypes have evolved. The interacting interfaces of virus and host proteins are targeted not just by mutational changes but also by epigenetic modifications resulting from glycosylation and by a host defensive strategy that relies on co-option of germline env genes to interfere with virus infection. There is also evidence of additional host factors or co-factors that influence entry of the mouse gammaretroviruses, some of which are affected by glycosylation [150, 154]. Future studies on the mouse gammaretroviruses should identify other host factors involved in entry and trans-species transmission, should describe the consequences of X-MLV infection in mice permissive to the “xenotropic” viruses, and should further illuminate the coevolutionary paths of these pathogens and their hosts.
This work was supported by the Intramural Research Program of the NIAID, NIH. The author would like to thank Reza Sadjapour, Carrie Martin, and Michael Dolan for assistance with figure preparation.