- Open Access
The receptors for gibbon ape leukemia virus and amphotropic murine leukemia virus are not downregulated in productively infected cells
© Liu and Eiden; licensee BioMed Central Ltd. 2011
- Received: 28 April 2011
- Accepted: 5 July 2011
- Published: 5 July 2011
Over the last several decades it has been noted, using a variety of different methods, that cells infected by a specific gammaretrovirus are resistant to infection by other retroviruses that employ the same receptor; a phenomenon termed receptor interference. Receptor masking is thought to provide an earlier means of blocking superinfection, whereas receptor down regulation is generally considered to occur in chronically infected cells.
We used replication-competent GFP-expressing viruses containing either an amphotropic murine leukemia virus (A-MLV) or the gibbon ape leukemia virus (GALV) envelope. We also constructed similar viruses containing fluorescence-labeled Gag proteins for the detection of viral particles. Using this repertoire of reagents together with a wide range of antibodies, we were able to determine the presence and availability of viral receptors, and detect viral envelope proteins and particles presence on the cell surface of chronically infected cells.
A-MLV or GALV receptors remain on the surface of chronically infected cells and are detectable by respective antibodies, indicating that these receptors are not downregulated in these infected cells as previously proposed. We were also able to detect viral envelope proteins on the infected cell surface and infected cells are unable to bind soluble A-MLV or GALV envelopes indicating that receptor binding sites are masked by endogenously expressed A-MLV or GALV viral envelope. However, receptor masking does not completely prevent A-MLV or GALV superinfection.
- Infected Cell
- Envelope Protein
- CHOK1 Cell
- Rous Sarcoma Virus
- MDBK Cell
Rubin and co-workers discovered, many years ago, that chicken embryos productively infected with Rous Sarcoma Virus (RSV) were resistant to subsequent RSV challenge . This phenomenon was designated as viral superinfection interference. It was later shown that chicken embryos productively infected by RSV were resistant to avian leukosis virus . It is now well established that resistance to superinfection occurs among many genera of retroviruses . Cells productively infected with gammaretroviruses are resistant to challenge infection. This is thought to occur because primary viral envelope expression prevents superinfection by interfering with the binding of viruses that recognize the same receptor. It remains unclear how access of most gammaretroviruses to their receptors are blocked; in superinfection specifically, it is unclear whether the envelope protein interacts with the receptor and down modulates its expression on the cell surface or whether the receptor is masked at the cell surface by viral envelope proteins. Evidence exists for both mechanisms [4–7].
The gammaretroviruses, amphotropic murine leukemia virus (A-MLV) and gibbon ape leukemia virus (GALV), have divergent host ranges and are not in the same interference class . These viruses were therefore anticipated to employ different receptors to infect target cells. When the receptors for GALV and A-MLV were cloned they were indeed shown to encode distinct but related proteins (~60% residue identity) originally designated GLVR1 and GLVR2 . Later, the GALV and A-MLV receptors were identified to function as type III inorganic phosphate transporters and were renamed PiT1 and PiT2. More recently these mammalian type III sodium dependent phosphate transporters have been reclassified according to the more appropriate gene transporter nomenclature, SLC20A1 and SLC20A2, respectively . SLC20A1 and SLC20A2-related proteins are present in all phyla and function as ubiquitously expressed facilitators of Pi uptake. The SLC20A1/2 transporters permit the efficient transfer of Pi across hydrophobic membrane barriers to provide essential nutrients required in cellular metabolism . Unlike the vast majority of other carrier facilitator proteins, there are no known inhibitors of SLC20A1/2 Pi transport . Thus the effects of blocking Pi transport by these viral receptors/type III transporters have not been directly evaluated. Surprisingly productive infection of human cells by both A-MLV and GALV is not cytotoxic. Several hypotheses could account for the absence of cytotoxic effects on cells infected by A-MLV and GALV. First, if productive infection results in receptor masking, as opposed to receptor down-regulation, the transporters on the cell surface, although their viral binding sites are no longer accessible to incoming virus, may still permit Pi transport function as has been reported for infection with ecotropic MLV that employs the basic amino acid transporter mCAT as a receptor [10, 11]. Alternately, the Pi transporter proteins may not directly bind GALV or A-MLV but instead may function as co-receptors. This hypothesis is supported by the recent observation that GALV resistant hamster BHK cells are not rendered susceptible to GALV following the expression of SLC20A1 . The ability of BHK cells, expressing SLC20A1, to bind GALV but not allow GALV entry made the role of this transporter in GALV entry more ambiguous. Finally, it is possible for cells in a culture, productively infected by both A-MLV and GALV, to remain viable despite the loss of SLC20A1/2 Pi transport function because inorganic phosphate can be brought into infected cells by means of type II Pi transporters or other Pi transporters. Type II transporters normally facilitate maintaining Pi homeostasis in the kidney and small intestine but like other genes that exhibit tissue specific expression in vivo these transporters may be turned on in cell lines in vitro making it possible for cultured cells to maintain cellular homeostasis.
To resolve the role of SLC20A1 in GALV entry and assess the effects of productive infection on SLC20A1/2, we used replication-competent A-MLV and GALV containing enhanced green fluorescence protein (eGFP) as a reporter. We also constructed GALV viruses containing fluorescence-labeled Gag proteins to observe virus-cell membrane association. These reagents, along with epitope-tagged viral receptors, allowed us to determine that both viral receptor and envelope proteins can be detected on the cell surface of productively infected cells. Finally, we showed that under receptor masking conditions, superinfection of cells productively infected with GALV can occur suggesting a mechanism of GALV entry that circumvents the SLC20A1 virus binding site.
Superinfection resistance mediated by GALV or A-MLV
Since there are no antibodies available to recognize GALV envelope proteins, we further modified the GALV-GFP plasmid so that it contains an epitope tag, C11D8. The C11D8 epitope  was introduced in-frame after (the proline rich region) (PRR) of the envelope surface subunit of GALV-GFP and the C11D8 epitope tagged GALV-GFP is hereafter referred to as GALV-GFP-C11D8 (Figure 1). The inclusion of a GFP reporter downstream of an IRES element in these viruses allows us to use GFP as a read out monitor for initial A-MLV or GALV enveloped virus replication and spread.
Superinfection resistance in cells infected with GALV or A-MLV
Infection by challenge virus (no. of blue foci)a
2.1 × 106
1.9 × 106
4.2 × 102
1.6 × 106
3.1 × 102
3.4 × 106
5.3 × 102
3.9 × 102
1.1 × 105
3.6 × 105
3.2 × 105
To assess the specific affects of A-MLV infection on challenge infection by A-MLV vectors, CHOK1 cells were used. CHOK1 cells are non-permissive to A-MLV. CHOK1 cells expressing SLC20A2, exposed to A-MLV-GFP and wild type A-MLV 4070 at one week post-infection, were challenged with A-MLV envelope vectors expressing βgal. Challenge infection was significantly reduced in A-MLV-GFP and A-MLV 4070 infected cells (Table 1). Cells productively infected with A-MLV showed resistance to challenge infection by vectors bearing A-MLV envelope similar to that observed with GALV in cells productively infected by GALV (Table 1).
Finally, to demonstrate the specificity of receptor masking, we infected bovine MDBK cells expressing SLC20A2-HA with A-MLV-GFP. MDBK cells are susceptible to GALV but not A-MLV. MDBK cells expressing SLC20A2 are susceptible to A-MLV. MDBK cells expressing SLC20A2-HA were exposed to A-MLV-GFP and one month later exposed to either A-MLV/βgal or GALV/βgal vectors. As reported in Table 1, A-MLV infection renders MDTF/SLC20A2-HA cells resistant to A-MLV/βgal but not GALV/βgal vectors.
Viral receptors are masked but not downregulated on GALV and A-MLV infected cells
Detection of the receptors and viral envelope proteins present on the surface of cells chronically infected with GALV or A-MLV viruses over one month.
Receptor present on the cell surface
Viral envelope present on the cell surface
GALV envelope proteins physically associate with SLC20A1
GALV superinfection occurs in productively infected cells under receptor masking conditions
GALV particles efficiently attach to infected cell surface
Retrovirus superinfection resistance is an important feature of productively infected cells. The inability of chronically infected cells to block superinfection is frequently associated with cytopathic effects that can result in cell death [22–25]. Two envelope-mediated mechanisms have been proposed for superinfection resistance, receptor downregulation and receptor masking [4, 5, 7, 13, 26]. In this report, we investigated one mechanism by which A-MLV and GALV mediate resistance to superinfection. We used replication- competent viruses expressing either GALV or A-MLV envelope proteins together with a GFP reporter gene, GALV-enveloped viruses expressing fluorescence-labeled Gag proteins and antibodies reactive with viral particles, their receptors or soluble envelope proteins. Using this repertoire of reagents, we clearly demonstrated that A-MLV or GALV receptors are masked by viral envelope protein. In cells productively infected with A-MLV or GALV we observed: i: both GALV SLC20A1 and A-MLV SLC20A2 receptors remain present on their respective infected cell surface (Figures 2, 3 and 4); ii: GALV and A-MLV envelope glycoproteins are detected on the surface of infected cells (Figures 2, 3 and 4); iii: infected cells are not able to bind GALV RBD or A-MLV RBD suggesting that the binding sites on these receptors are occupied by viral envelope proteins. We could not, however, rule out that down regulation of receptors also occurs in a small portion of cells chronically infected with GALV or A-MLV.
We have previously reported that A-MLV infection of NIH-3T3 cells overexpressing epsilon-epitope-tagged SLC20A2 results in the redistribution of epsilon-epitope tagged SLC20A2 inside the cell . Confocal microscopy provides representative images of permeabilized infected cells and not quantitative analyses. It has now known that in uninfected cells, PiT2 is detectable in both the cytoplasm and on the cytoplasmic membrane of permeabilized cells based on more recent findings [28, 29]. In this report we have undertaken quantitative comparisons of uninfected and A-MLV infected cells in parallel and demonstrated something not addressed in the prior confocal microscopy studies . The use of FACs analysis allows several advantages over confocal microscopy i) the use of live not fixed nor permeabilized cells for cell surface receptor expression, RBD binding or viral envelope binding analyses ii) dead cells are eliminated from the analyses prior to FACS by propidium iodide staining iii) the employment of GALV or A-MLV expressing GFP in this study allows FACS gating and evaluation of infected cell populations as opposed to uninfected cells and iv) FACs analysis provides quantitative population statistics data.
In Figure 2, we show that GALV infection may be accompanied by a slight down regulation of SLC20A1. However, receptor down regulation is a minor event not a major event accompanying GALV or A-MLV infection. Our conclusions are based on studies on two types of cells lines (MDTF or CHOK1) as well as wild type viruses, GALV (SEATO) and A-MLV (4070) and replication competent modified GALV or A-MLV expressing GFP.
The knock-out of SCL20A1 in mice has been reported to result in embryonic lethality. Furthermore, in vitro depletion of SLC20A1 in cell lines impairs their cellular proliferation . The reasons why deleterious events were not evident in cells infected with GALV may be accounted for in a number of ways. First, receptor masking does not completely abolish transporter function. This is supported by the report that in mouse fibroblasts expressing A-MLV envelope glycoprotein, only a partial reduction of Pi transport is observed . Furthermore, chronic infection with another gammaretrovirus E-MLV that uses a basic amino acid transporter as a receptor causes only a 50-70% loss of transporter function in plasma membranes . Secondly, Bottger et al. have reported that the residues important in sodium phosphate symporter function  are outside of the regions implicated as the receptor binding sites for these proteins [33, 34]. Finally the ability to directly assess SLC20-mediated Pi transport under conditions of productive infection in infected cell lines in culture is compromised by the tendency of cultured cells to express a broader range of genes than those expressed in the tissues they derive from. In the case of MDTF cells, this could extend to the expression of the kidney specific type II Pi transporters.
We also tried to resolve the mechanism by which the rare incidence of superinfection occurs in a chronically infected population of cells. Specifically is the "superinfection event" occurring in a cell that is either not infected, infected but no longer expressing viral envelope proteins (i.e., a situation analogous to viral latency), or productively infected and expressing envelope proteins. We used GALV replication competent viruses containing GFP as a reporter for primary infection and GALV enveloped vectors expressing cherry red to determine superinfection capability. Approximately 95% of the cells were infected by GALV-GFP one month after initial exposure (Figure 6) at which point these cells were demonstrated to be weakly susceptible (1%) to superinfection by vectors expressing cherry red. Superinfection of GALV cherry red vectors is evident in cells expressing both green and red fluorescent proteins (Figure 6 and 7). Superinfected cells also express GALV envelope proteins on their cell surface (Figure 7) suggesting that they are productively infected with GALV and maintain viral envelope expression on the infected cells surface. Therefore, approximately 6.57% or 1.18% superinfection occurs in productively infected cells and not in the 6.50% or 5.23% cells that are not infected by GALV-GFP or in the productively infected cells that retain only GFP gene expression but not viral gene expression (Figure 7). Nonspecific absorption of MLV has been described for a variety of cell types [19–21]. We observed adsorption of infectious Tomato red GALV viral particles on MDTFSLC20A1 cells chronically infected with GALV-GFP (Figure 8). Therefore, it remains possible that superinfection of GALV can occur via "activation in trans" as has been previously described for facilitating the ability of bound, but noninfective virus to enter cells after being exposed to soluble envelope proteins . Alternately, a few unoccupied SLC20A1 on the cell surface could permit GALV superinfection.
In conclusion, resistance to GALV or A-MLV mediated superinfection occurs through receptor masking, not receptor down-regulation. Cells productively infected with either GALV or A-MLV retain the ability to bind viral particles and these bound particles may participate in the rare superinfection event that occurs in infected cells.
Cell lines used in this study include murine Mus dunni tail fibroblasts MDTF , Chinese hamster ovary (CHOK1) cells, CCL61, (ATCC, Manassas, VA), human embryonic kidney 293T cells (Cell Genesys, Foster City CA) Mason-Darby bovine kidney cells (CCL 22, ATCC, Manassas, VA). All cells, with the exception of CHOK1, were maintained in Dulbecco's modified Eagle's medium with Glutamax (DMEM) (Invitrogen, CA), supplemented with 10% fetal bovine serum, 100 units of penicillin/ml, and 100 ug of streptomycin/ml. CHOK1 cells were maintained in alpha minimal essential medium (MEM) supplemented with 10% fetal bovine serum, 100 units of penicillin/ml, and 100 ug of streptomycin/ml. (Invitrogen, CA). Stable cell lines expressing the GALV viral receptor SLC20A1 or A-MLV viral receptor SLC20A2 tagged with HA were made by using vesicular stomatitis virus (VSV) G protein-enveloped vectors with genomes expressing the appropriate receptor cDNA in the retrovirus pLNSX packagable genome and selected for G418 resistance .
A-MLV-GFP and GALV-GFP (generously provided by Christopher Logg, University of California, Los Angeles, CA,) are replication-competent E-MLVs but contain A-MLV or GALV env protein that replaces E-MLV env gene respectively, as well as an IRES cassette between the env gene and 3' untranslated region. In addition, the GALV-GFP contains an insertion of TCC just upstream of the splice acceptor to allow more efficient replication (Figure 1) . GALV-GFP-C11D8 was constructed by introducing a C11D8 epitope tag at 3' of the PRR within the GALV env gene (Figure 1) . GALV-Gag tomato red was constructed by replacing the IRES-GFP cassette in the GALV-GFP construct with IRES-Gag fused in frame to a fluorescent tomato gene. Briefly, we prepared the following three fragments: an IRES fragment amplified by PCR, cleaved with Mlu and EcoRI sites, a gag fragment obtained from MLV-gag-YFP plasmid (Addgene Inc.)  by double digestion with EcoRI and NheI and tomato red gene fragment amplified by PCR from the CMV-brainbow-1.0-L plasmid (Addgene Inc.) then cleaved with NheI and Not. All three fragments were ligated to GALV-GFP plasmid after digestion with MluI and NotI (Figure 1). The sequences of all plasmids used in these analyses were verified.
Production of replication competent retroviruses and retroviral vectors
293T cells were seeded at a density of 106 per 10 cm dish and the appropriate plasmids were introduced by calcium phosphate transfection (Promega) as previously described . Soluble GALV RBD and A-MLV RBD were generated by transient transfection of 293T cells using plasmids expressing GALV envelope surface unit (SU) or A-MLV envelope SU tagged with V5 as previously described . The GALV-GFP, GALV-GFP-C11D8-, GALV-GagTomato red or A-MLV-GFP plasmids were transfected into 293T cells to make GALV or A-MLV pseudotyped replication-competent viruses. Supernatants containing GALV or A-MLV enveloped retroviral vectors, soluble GALV or A-MLV RBD or replication-competent viruses were harvested 48 to 72 h post-transfection, then passed through a 0.45 mM Millipore (Bedford, Mass.). Supernatant containing GALV-GagTomato viruses was further concentrated using Beckman ultracentrifuge at 25,000 rpm at 4°C for 2 hours through a 25% sucrose cushion.
Stable Cell Lines
Stable cell lines expressing the GALV receptor SLC20A1 or A-MLV receptor SLC20A2, tagged with HA, were made by exposing appropriate target cells to vesicular stomatitis virus (VSV) G protein-enveloped vector particles containing the appropriate receptor cDNA in the pLNSX genome. Transduced cells were selected for G418 resistance as previously described.
Viral infection and titration
Target cells were seeded one day in advance in a 24-well plate at a density of 2 × 104 cells per well. Cells were exposed to supernatant containing respective retroviral vector and then supplemented with 10 mg/ml polybrene. Twenty-four hours later, the medium was changed and cells were cultured for an additional 36 to 48 h before analysis for expression of β-gal by histochemical staining with X-Gal (5-bromo-4 chloro-3-indolyl-b-Dgalactopyranoside), as previously described . Titers were determined by averaging the numbers of blue foci (BFU) obtained with vectors for each cell line tested in three or more independent experiments and expressed as BFU/ml.
Soluble-RBD binding assays and detection of SLC20A1 and SLC20A2 expression as well as viral envelope associated with the cell surface of infected cells
Binding assays using V5-tagged soluble A-MLV or GALV RBD were performed as previously described [29, 37]. 5 × 105 target MDTF or CHOK1 cells expressing SLC20A1 or SLC20A2 receptor fused to an HA epitope tag  were incubated with soluble V5-tagged RBD protein at 37°C for 45 min. The cells were fixed with 1% paraformaldehyde and then analyzed by flow cytometry. HA-tagged receptors were detected on the cell surface by incubation of MDTF cells expressing receptors with monoclonal HA antibody HA.11 (Covance Inc.), followed by incubation with a secondary antibody, R-phyoerythrin-conjugated (Invitrogen, Eugene, Oregon). The detection of GALV or A-MLV envelope protein associated with the surface of cells chronically infected with respective viruses was performed by incubation of the cells with monoclonal antibody C11D8 (Santa Cruz biotechnology, Inc. CA) [14, 15] or rat monoclonal antibody 83A25 (generously provided by Leonard. Evans, National Institute of Allergy and Infectious Diseases, Hamilton, Montana)  at room temperature for 1 hour, followed by incubation with R-phyoerythrin conjugated secondary antibody.
MDTFSLC20A1-HA cell lines uninfected or infected over one month were grown on 35 mm tissue culture dishes with cover glass bottom of 0.17 mm in thickness overnight (World Precision Instruments, Inc.) and then incubated with 1 ml of 20-fold concentrated GALV-Gag tomato virus at 37°C for 45 minutes. After extensive washes, cells were fixed with 2% paraformaldehyde and images were taken with LSM 510 inverted Meta confocal microscope as described below.
Coimmunoprecipitation (Co-IP) and crosslinking Co-IP
All immunoprecipitation procedures were carried out at 4°C. 3 × 106 MDTF cells expressing HA-tagged SLC20A1 protein were incubated with 5 ml of V5 tagged GALVRBD at 37°C for 45 minutes, followed by extensive washes. Crude cell plasma membranes were then prepared as described previously . Crude cell plasma membranes were transferred to tubes and centrifuged at 15,000g for 60 minutes. Subsequently, the membrane pellets were resuspended in 500 μl lysis buffer (150 mM NaCl, 50 mM Tris-HCl, 2.5 mM EDTA, complete proteinase inhibitor tablet and 1% CHAPs) and incubated for 30 minutes, followed by centrifugation. The resultant supernatant was incubated with anti-V5 affinity sepharose beads (Sigma) overnight. Dissociated protein complexes were then separated with 4-20% tris-glycine SDS-PAGE gel (Invitrogen, Inc. CA).
Cross linking co-IP was performed on MDTFSLC20A1-HA cells grown on 10 cm tissue culture dish by incubation with V5 tagged GALV RBD at 37°C for 45 minutes, and then treated with a homobifunctional, water-soluble, non-cleavable and membrane impermeable crosslinker, Bis(sulfosuccinimidyl)suberate (BS3) (Thermo Scientific Pierce) at a concentration of 1 mM in 2.5 ml HBSS buffer, on a shaker for one hour. After extensive washes with HBSS buffer, the cells were scraped off in 1 ml lysis buffer containing 1% NP40 and lysed for 20 minutes, followed by high speed centrifugation for 30 minutes. The resultant supernatant was used for crude cell membrane preparation and Co-IP as described above.
Cells were grown on 35 mm tissue culture dish with glass bottom of 0.17 mm in thickness over night, followed by fixation with 2% paraformadyhyde in PBS and blocked with 5% bovine serum albumin in PBS. Subsequently, cells were probed with monoclonal antibodies (C11D8) and stained with dylight conjugated goat anti-mouse IgG (Thermo scientific Pierce). Images were collected on an LSM510 invert Meta confocal microscope (Carl Zeiss, Thornwood, NY). The 488 and 568 nm lines of a krypton/argon laser were used for fluorescence excitation of GFP and cherry red respectively and 420 nm line for dylight.
Epics XL (Beckman Coulter, Fullerton, CA) and FACScan (Becton Dickinson, Franklin Lakes, NJ) flow cytometers were used for analysis of GFP and cherry red expression in infected and transfected cells using a 525 nm or a 530 nm band pass emission filter. 20,000 cells from each sample were analyzed after trypsinization and suspension in PBS.
We thank Karen B. Farrell for technical advice; Jim Nagle and Debbie Kauffmann at the NINDS Sequencing Facility (National Institutes of Health) for sequencing; Parisa Moghaddam-Taaheri for experimental help; Jon Marsh and Jill Russ for supervising FACS operation and Vincent Schram and Lynne Holtzclaw in the Microscropy & Imaging Core, NICHD, NIH for technical guidance in confocal microscope and Wenqin Xu for her thoughtful comments and editorial assistance. NIMH intramural funding supported this work.
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