INTRODUCTION

Top Abstract Introduction Materials and Methods Results Discussion References

The early steps of virus entry into cells involve attachment to the cell surface, followed by penetration of the virion or its components into the cytoplasm through the plasma membrane or the membrane of an endocytic vesicle. For many enveloped and nonenveloped viruses such as influenza virus, Semliki Forest virus, vesicular stomatitis virus, adenovirus, and reovirus, endocytic uptake is required for infection (36, 54, 57, 79). Other viruses such as herpesviruses, rotavirus, poliovirus, and some retroviruses may enter the cytoplasm by penetrating or fusing directly to the plasma membrane after binding their appropriate receptors (41, 50, 61, 75).

The general endocytic mechanisms by which ligands including viruses can be taken into the cell are clathrin-mediated endocytosis, uptake via caveolae, macropinocytosis, a poorly characterized caveolin- and clathrin-independent pathway, and phagocytosis (55). Electron microscopic studies show that many viruses bind to coated regions of the plasma membrane and are found in coated vesicles, indicating that they are taken into cells by clathrin-mediated endocytosis, e.g., adenovirus, minute virus of mice (MVM), and influenza virus (46, 53, 60). In contrast, entry and infection of cells by simian virus 40 (SV40) has been shown to occur via caveolae (2).

Canine parvovirus (CPV) is a variant of a feline parvovirus which gained the ability to infect dog cells and dogs through a small number of sequence changes in its capsid coat protein (76). CPV most likely enters and infects cells by an endocytic route as agents which prevent endosome trafficking or acidification block virus infection or replication (8, 81). The uptake of CPV from the plasma membrane has been suggested to occur via a non-clathrin-dependent endocytic pathway on the basis of electron microscopic examination of cells after 15 min of incubation at 37°C (8). However, coated pits and vesicles are short lived, and coated vesicles containing viral particles may rapidly lose their coats. A study of adenovirus entry found the majority of particles within noncoated vesicles, with only a minority of virions bound to coated pits (60). In addition, uptake of the autonomous parvovirus MVM from the plasma membrane occurs within coated vesicles (46). Therefore, it remains possible that CPV infects cells by clathrin-mediated endocytosis.

To initiate infection, CPV must bind to the cells, pass through an endocytic pathway, and eventually deliver its single-stranded DNA genome to the nucleus for replication. CPV has been reported to bind to the basolateral surface of polarized MDCK epithelial cells to a sixfold-greater degree than to the apical surface (7). However, as those cells were not permissive to CPV, the role of that binding in infection is unknown. About 10⁵ high-affinity receptors are reported to be present on the surface of canine A72 cells, and maximal binding of CPV is reached after approximately 1 h of incubation at 4°C (7, 8).

The receptor used for CPV infection has not yet been defined. CPV binds sialic acid, and although sialidase treatment of cells reduces virus binding by ~30%, that does not prevent CPV infection, and a non-sialic acid binding mutant of CPV is highly infectious for cells (5). CPV binds 42- and 116-kDa proteins when cellular protein blots are probed with virus, and it also binds to a glycophosphotidylinositol-linked protein on feline lymphoid cells, although none of these molecules have been confirmed as the receptor used during infection (6, 9). Among other parvoviruses, sialidase treatment of cells blocks infection by MVM, and the receptor for human B19 parvovirus on erythroid cells is globoside, the erythrocyte P antigen (12, 19). Aleutian mink disease parvovirus binds a 67-kDa protein on the surface of Crandell feline kidney cells, and a polyclonal serum against this protein inhibits infection (31). Adeno-associated virus type 2 binds to heparan sulfate, and it also binds to a 150-kDa cell membrane-associated glycoprotein in overlay blots (56, 73), while human fibroblast growth factor and/or the V5 integrin are coreceptors for adeno-associated virus type 2 entry and infection (65, 72).

Ligands that are taken into cells by receptor-mediated endocytosis are trafficked to early sorting endosomes where the low-pH environment causes many ligands to dissociate from their receptors. Receptor-dissociated ligands are rapidly trafficked to late endosomes and then to lysosomes, where they are degraded (55, 68). Specific signals on the cytoplasmic tail of some receptors may cause them to be sorted and returned to the plasma membrane for reuse, while in other cases both the receptor and ligand are targeted to the late endosome/lysosome for degradation (55). The fate of internalized ligands and receptors is complex, and other pathways exist which target receptors and receptor-bound ligands to a perinuclear recycling endosomal compartment and in some cases to the Golgi network (34, 49).

The specific role of endocytosis in CPV infection and the details of the pathways used are still not well understood. CPV particles taken into cells appear to be trafficked to a perinuclear vesicular compartment, and capsid proteins are largely intact for several hours after uptake (81, 83). CPV infection of A72 cells can be inhibited with the microtubule-depolymerizing agent nocodazole or by incubation at 18°C (81). Trafficking between the early endosome and the late endosome or recycling endosome is microtubule dependent and inhibited by incubation at <20°C (33, 66), which may indicate that CPV infection requires that the capsid be trafficked beyond the early endosome. It is also possible that microtubules are required to transport the capsid within the cytoplasm, similar to what has been shown for herpesvirus and adenovirus (70, 74).

Many viruses require exposure to an acidic pH during infectious entry into cells (51). For example, influenza virus and Semliki Forest virus require exposure to pH of less than 6.0 in the endosome to cause their glycoprotein spike complexes to undergo conformational changes needed for fusion of the viral envelope with cellular membranes (13, 28, 44), and treating cells with agents which disrupt endosomal acidification processes blocks infection (43, 53). Nonenveloped viruses affected by drug treatments which prevent endosomal acidification include adenovirus type 2 (79), rhinoviruses (63), reovirus (52, 57), and CPV (8), while SV40 (42), poliovirus (61), and hepatitis B virus (68) are not affected by such treatments. However, as well as their direct effects on pH, treatments that prevent acidification of endosomes can also inhibit endosomal trafficking within the cell. Infection by some pH-dependent viruses may therefore be inhibited by these agents because of indirect effects of the treatments on endosomal protease activation or on endosomal trafficking of the viral particle (4, 10, 17).

CPV infection is blocked in cells treated with NH₄Cl or chloroquine, indicating that acidification of endosomes may be required (8). However, the capsid appears not to be directly affected by exposure to low pH. The structures of CPV and feline parvovirus empty capsids at pH 5.5 or 6.2 determined by X-ray crystallography show relatively small changes compared to the structures determined at pH 7.5 (A. Simpson, C. R. Parrish, and M. G. Rossmann, unpublished data), and there is little difference in susceptibility of the capsid to proteases at pH 5.5 and 7.5 (83).

Overexpression of mutants of dynamin I defective in GTP binding in a variety of different cells and organisms leads to inhibition of clathrin-mediated endocytosis (16, 18, 23-25, 78). Expression of the dynamin K44A mutant in HeLa cells reduced or prevented the infectious entry of adenovirus, Semliki Forest virus, Sindbis virus, or human rhinovirus 14, indicating that uptake of these viruses requires an active clathrin-mediated endocytic pathway (27, 82). Dynamin is a large 100-kDa GTPase required for scission of clathrin-coated vesicles budding from the plasma membrane and the Golgi apparatus. At least three unique dynamin gene products have been described that vary in their tissue expression. Dynamin I is expressed predominantly in neurons, while dynamin II is ubiquitously expressed and dynamin III is expressed in the testis, lung, and brain. In addition, each form of dynamin has a variety of alternatively spliced forms, although the specific functions and expression patterns of these isoforms have not all been determined (14, 77).

Here we use a variety of approaches to further define the uptake and infection pathway of CPV into cells. CPV capsids concentrated within electron-dense coated pits on the cell surface and then entered mink lung cells by clathrin-mediated endocytosis. CPV did not significantly permeabilize cells to allow the coentry of the toxin -sarcin. CPV particles became colocalized with transferrin (Tfn) in endosomes but not with dextran, suggesting that viral particles are delivered to a recycling endosomal compartment after endocytic uptake.

	MATERIALS AND METHODS

Top Abstract Introduction Materials and Methods Results Discussion References

Viruses and cells. CPV type 2 (CPV-d) was grown in NLFK cells, and aliquots were frozen and stored at 70°C (59). Virus titers were determined on NLFK cells by 50% tissue culture infective dose assay in 96-well plates as described previously (58). Full CPV particles were purified and quantified as previously described (47) and stored in phosphate-buffered saline (PBS) at 4°C. Canine adenovirus type 1 (CAV-1) grown in MDCK cells was purified by banding on CsCl gradients as described by Cotten et al. (20) and then dialyzed against PBS (pH 7.4). CAV-1 particle concentration was determined spectrophotometrically, using a conversion factor of 1.1 × 10¹² viral particles per 1 unit of optical density at 260 nm (48). Canine A72 cells and NLFK cells were grown and maintained in a 1:1 mixture of McCoy's 5A and Leibovitz L15 medium with 5% fetal bovine serum (FBS), and tTA-Mv1Lu, Mv1Lu-TR, Mv1-WT, and Mv1-K44A cells were grown in Dulbecco modified Eagle medium (DMEM) containing 10% FBS.

Tetracycline-regulated expression of wild-type and mutant dynamin. tTA-Mv1Lu cells that stably express the tetracycline-responsive transactivator were obtained from Joan Massague (67). Plasmids pUHD10-3 HA-wt and pUHD10-3 HA-ele1 express wild-type dynamin I and a dominant interfering mutant of dynamin I with lysine 44 changed to alanine (K44A), respectively, from a minimal cytomegalovirus promoter under the control of a tetracycline-responsive enhancer element. The genes are fused to a hemagglutinin (HA) epitope tag at the N terminus and were provided by Sandra Schmid (25, 26). tTA-Mv1Lu cells were transfected with 20 µg of either plasmid pUHD10-3 HA-ele1 or plasmid pUHD10-3 HA-wt together with 1 µg of the puromycin resistance plasmid pBSpac, using a Bio-Rad Gene Pulser II with radiofrequency module at 400 V, 85% modulation, 40-kHz radio frequency, and 5 bursts of 4.0-ms duration with a burst interval of 1 ms. Cells were grown in medium containing puromycin (600 ng/ml) and tetracycline (2 µg/ml), and clones were picked after 7 to 10 days. Clones showing strong inducible expression of wild-type and mutant dynamin were further subcloned and designated Mv1-WT and Mv1-K44A, respectively.

Flow cytometry assay of infection. Mv1-K44A or Mv1-WT cells were cultured for 48 h in DMEM with 10% FBS with or without 2 µg of tetracycline per ml. As the growth rate of cells expressing mutant dynamin was slower than that of cells grown in the presence of tetracycline, the Mv1-K44A cells when grown without tetracycline were seeded at a higher density so that all cells were at the same density 48 h later. Cells were incubated with CPV at a multiplicity of infection of 0.3 for 1 h at 37°C; then fresh medium containing tetracycline (2 µg/ml) was added, and the incubation continued for 15 h at 37°C. Cells were then washed in PBS, trypsinized and resuspended in DMEM-10% FBS, rinsed in PBS, and fixed in 2.5% paraformaldehyde in PBS at 20°C for 10 min. Cells were washed in PBS with 0.5% bovine serum albumin (BSA), then permeabilized in PBS-BSA with 0.1% Triton-X100, and incubated with mouse monoclonal antibody (MAb) CE-10 against the C terminus of the MVM nonstructural protein NS1 (obtained from Caroline Astell [85]) for 1 h at room temperature. The antibody was detected with a fluorescein-conjugated goat anti-mouse antibody; then 20,000 cells assayed in a FACScalibur flow cytometer (Becton Dickinson, San Jose, Calif.).

Cell cycle analysis. Mv1-K44A or Mv1-WT cells were cultured for 48 h in DMEM-10% FBS with or without tetracycline (2 µg/ml), isolated in suspension as described above, and then incubated for 20 min at 20°C in 100% methanol. After washing with PBS, the cells were treated with RNase A (1 mg/ml in PBS) for 30 min at 37°C and then incubated with propidium iodide (0.01 mg/ml in PBS) and 0.02% Triton X-100 at 4°C for 30 min. Cell DNA content was assayed by flow cytometry (45). The data from four independent experiments were modeled, and the percentage of cells in each phase of the cell cycle was estimated with ModFit LT cell cycle analysis software (Verity Software, Topsham, Maine).

Electron microscopy. Cells grown for 24 h on Thermanox 13-mm-diameter coverslips (Nunc Inc., Naperville, Ill.) were washed once in ice-cold DMEM and CPV-d full particles (35 µg/ml) were incubated on the cells for 1 h at 0°C (1 µg of CPV-d full particles is equivalent to ~10¹¹ particles). Immediately after incubation at 0°C or at 5 and 15 min after warming to 37°C, the cells were fixed in 1% glutaraldehyde-0.1 M sodium cacodylate (pH 7.4) for 30 min at room temperature and then for 1.5 h on ice in 2.5% glutaraldehyde in 0.1 M sodium cacodylate (pH 7.5). After being rinsed three times in ice-cold cacodylate buffer, cells were postfixed in 4% osmium tetroxide for 1 h at room temperature, stained for 20 min with a 2% aqueous solution of uranyl acetate, and then dehydrated with ethanol. The cells were embedded in Epon-Araldite plastic; thin sections were cut and further stained for 20 min in 2% aqueous uranyl acetate, rinsed, stained with lead citrate for 7 min, and then examined in a Philips 201 electron microscope. The numbers of particles associated with coated and noncoated regions of the plasma membrane at the 0-min time point were counted.

Virus binding to cells. Mv1-WT and Mv1-K44A cells cultured with or without tetracycline for 48 h were washed with PBS and then treated with a nonenzymatic cell dissociation solution (Sigma, St. Louis, Mo.) for 15 min at 37°C. Cells were washed in DMEM-10% FBS and then incubated in cold DMEM-1% BSA on ice for 10 min. The cells were pelleted at 4°C and then resuspended in DMEM-1% BSA or in DMEM-1% BSA containing 40 µg of full CPV per ml. After incubation on ice for 1 h, the cells were washed three times with ice-cold PBS, fixed in 2% paraformaldehyde and PBS for 10 min on ice, and then immunostained with a MAb 8 against the intact capsid protein (71). The cells were then washed with PBS, permeabilized with 0.1% Triton X-100 in PBS, and immunostained for the HA epitope tag with a rabbit polyclonal antiserum (Santa Cruz Biotechnology, Inc., Santa Cruz, Calif.). Primary antibodies were detected with fluorescein isothiocyanate (FITC)-conjugated goat anti-rabbit and R-phycoerythrin-conjugated goat anti-mouse secondary antibodies (Jackson Immunoresearch, West Grove, Pa.). Viral binding and HA epitope tag expression were assessed by flow cytometry.

Kinetics of CPV infectious entry. tTA-Mv1Lu cells grown on 60-mm-diameter dishes were incubated with CPV at an multiplicity of infection of 0.3 for 2 h on ice, washed once in cold DMEM to remove unbound virions, and then warmed to 37°C by the addition of prewarmed DMEM-10% FBS. After various times of incubation, a rabbit anti-CPV neutralizing antiserum was added and mixed with the medium. Mock-inoculated cells were also treated with antibody. The cells were then incubated for 24 h at 37°C, fixed, and assayed for infection by staining for NS1 expression as described above.

Control markers of endocytosis. Human Tfn (HuTfn) did not bind Mv1-K44A cells, so we used a cDNA for the HuTfn receptor (HuTfnR) to express the human receptor in those cells. Cells transfected by electroporation were seeded onto glass coverslips in the presence or absence of tetracycline. After 48 h, cells were washed and incubated in DMEM-1% BSA for 45 min at 37°C and then incubated for 10 minutes at 37°C with Texas red-labeled HuTfn (50 µg/ml; Molecular Probes, Eugene, Oreg.) in DMEM-1% BSA. After washing with PBS, the cells were fixed for 10 min in 2.5% paraformaldehyde in PBS, rinsed three times in PBS, then mounted on slides with Prolong (Molecular Probes), and examined by confocal microscopy (25).

Immunofluorescence microscopy. Mv1-K44A cells were seeded onto glass coverslips at a cell density of 1.2 × 10⁴ or 2 × 10⁴/cm² with or without tetracycline (2 µg/ml), respectively. After 48 h, the cells were cooled on ice and incubated with purified CPV full particles (20 µg/ml in DMEM) for 1 h, and then unbound virus was removed by washing with ice-cold DMEM. After warming to 37°C, the cells were incubated for 10, 30, or 90 min, washed three times in ice-cold PBS, and then fixed with 2.5% paraformaldehyde in PBS. Cells were permeabilized with 0.1% Triton X-100 in PBS-BSA, and the capsids were detected either with MAb 8 followed by a Cy3-labeled donkey anti-mouse secondary conjugate (Jackson Immunoresearch) or with a rabbit polyclonal anticapsid serum followed by goat anti-rabbit antibody-FITC conjugate. Confocal optical sections through the center of the cells were collected using a Bio-Rad MR600 confocal system. Single optical sections of approximately 2.2-µm thickness are shown.

Detection of CPV together with HuTfn and dextran in tTA-Mv1Lu cells. tTA-Mv1-Lu cells were transfected with 20 µg of plasmid pCB6 HuTfnR together with 1 µg of pBSPac by electroporation as described above and then seeded into 100-mm-diameter dishes. Stable clones were selected with puromycin (600 ng/ml) as described above. A clone of cells which bound and endocytosed HuTfn was chosen for further use and designated Mv1Lu-TR.

Effect of BFLA1. In initial studies, we determined that 10 nM bafilomycin A1 (BFLA1) inhibited viral infection by 98% when added 30 min prior to virus inoculation. To further examine the effect of BFLA1 on infection, the drug was therefore added to cells either 30 min before or 90 min after virus incubation. tTA-Mv1Lu cells seeded at 2 × 10⁴/cm² in 60-mm-diameter dishes were cultured overnight, preincubated with DMEM alone or DMEM containing 20 nM BFLA1 for 30 min at 37°C, and then incubated with CPV with or without 20 nM BFLA1 for 1 h at 37°C. The cells were washed in DMEM and then in DMEM-10% FBS or DMEM-10% FBS with 20 nM BFLA1 added. In some cases, 20 nM BFLA1 was added to the medium 30 min after removal of virus inoculum. Controls were mock-inoculated cells or cells inoculated without BFLA1. Cells were harvested by trypsinization, and then virus infection was assayed by staining the cells for NS1 expression as described above.

Cell permeabilization assay. The ability of CPV to permeabilize A72 or tTA-Mv1Lu cells to the translation-inhibiting toxin -sarcin was assessed as described by Cuadras et al. (22). In brief, purified full CPV at between 2 × 10¹⁰ and 1 × 10¹³ particles per ml or purified CAV-1 at between 4.4 × 10⁸ and 4.4 × 10¹⁰ particles per ml was added to confluent A72 cells or tTA-Mv1Lu cells seeded in 1-cm² wells. After incubation at 37°C for 90 min with or without -sarcin (100 µg/ml), the cells were washed in PBS, incubated with [³⁵S]methionine for 1 h at 37°C, then washed with PBS, and incubated with 5% trichloroacetic acid for 5 min at room temperature. After washing the cells three times with ethanol they were dried and recovered into 0.1 ml of 0.1% sodium dodecyl sulfate in 0.1 M NaOH, and the incorporated [³⁵S]methionine was measured by liquid scintillation counting.

	RESULTS

Top Abstract Introduction Materials and Methods Results Discussion References

Electron microscopy indicates virus binding to coated pits. Virus cell binding and uptake were examined by transmission electron microscopy. At 0 min, 67% (281 of 419 particles counted) of viral particles seen bound to the plasma membrane were in depressions that had an electron-dense coating resembling clathrin-coated pits; 5 min after warming, most viral particles were found in coated vesicles but some were in noncoated vesicles; by 15 min, most viral particles were seen within noncoated vesicles, some of which appeared to be close to the nuclear membrane (Fig. 1).

View larger version (92K): [in this window] [in a new window]   FIG. 1.   Electron microscopy of CPV bound to uninduced Mv1-K44A cells at 0, 5, and 15 min after warming from 4 to 37°C. The bars represents 100 nm; arrows indicate likely viral particles. The nuclear envelope (NE) is indicated.

CPV particles bound on the cell surface rapidly become resistant to neutralizing antibody upon warming. Assays based on postadsorption neutralization of virus have demonstrated that the infectious entry of SV40 virus is slow and occurs in hours, while adenovirus entry occurs in minutes (2, 79). We used a similar assay to determine the kinetics of CPV removal from the surface of mink lung cells. The virus rapidly became resistant to antibody, and 50% of the infecting virus entered the cell by 5 min after warming (Fig. 2). These results are consistent with our finding that virus bound to coated pits.

View larger version (15K): [in this window] [in a new window]   FIG. 2.   Kinetics of uptake of infectious CPV from the cell surface. Virus was bound to tTA-Mv1Lu cells at 4°C, and then the cells were rapidly warmed to 37°C. At various times after warming, neutralizing anti-CPV antibody was added and mixed with the medium. The percentages of infected cells in each dish were assayed 24 h later by immunostaining and flow cytometry. The average and standard deviations of the percent maximal infection of four separate experiments are shown.

Characterization of tTA-Mv1Lu cells which inducibly express wild-type dynamin or mutant dynamin K44A. Overexpression of dynamin K44A in cells inhibits clathrin-mediated endocytosis (26). We prepared and cloned two tTA-Mv1Lu cell lines which inducibly expressed either wild-type dynamin (Mv1-WT) or dynamin K44A (Mv1-K44A) in response to removal of tetracycline from the growth medium, similar to that described for HeLa cells (26). In Mv1-K44A cells grown without tetracycline, dynamin expression was first detected 6 h later, and the amount detected increased over 48 h (Fig. 3A). Results for Mv1-WT cells were similar (data not shown). Experiments with dynamin-expressing cells were therefore carried out after a 48-h induction period.

View larger version (48K): [in this window] [in a new window]   FIG. 3.   Characterization of Mv1-K44A cells. (A) Western blot analysis of dynamin K44A expression in Mv1-K44A cells at various times after tetracycline removal. The dynamin K44A was detected with MAb 12CA5 against the N-terminally fused HA epitope. (B) Expression of dynamin K44A in Mv1-K44A cells. Cells grown with or without tetracycline for 48 h were harvested for flow cytometry. The HA-tagged dynamin was detected by indirect immunofluorescent staining with MAb 12CA5, and 20,000 cells were analyzed by flow cytometry. (C) Uptake of HuTfn by induced and uninduced Mv1-K44A cells. Mv1-K44A cells transfected with the HuTfnR gene were grown in the presence or absence of tetracycline for 48 h on coverslips. Texas red-labeled HuTfn was incubated with the cells for 10 min at 37°C prior to fixation and examination by fluorescence microscopy.

Vesicular uptake of CPV particles was delayed in dynamin K44A-expressing cells. The location of viral particles in induced or uninduced Mv1-K44A cells was examined by immunofluorescence. Cells fixed immediately after incubation with virus on ice showed cell surface localization of viral particles in both induced and uninduced cells; after 10 min at 37°C viral particles were found in large, perinuclear vesicles in uninduced cells, while in dynamin K44A-expressing cells the vesicles remained close to the cell surface; after 30 and 90 min at 37°C, the viral particles remained in perinuclear vesicles in the uninduced cells, while the virus-containing vesicles in the dynamin K44A-expressing cells had moved centripetally toward the nucleus (Fig. 4). These results show that expression of dynamin K44A disrupted the normal rapid trafficking of CPV to a perinuclear location within cells. However, the gradual centripetal movement of viral particles may indicate that dynamin K44A expression induced a kinetic block rather than an absolute block to vesicle formation and trafficking.

View larger version (86K): [in this window] [in a new window]   FIG. 4.   CPV uptake into vesicles in uninduced and induced Mv1-K44A cells. Purified CPV full particles were incubated with uninduced or induced Mv1-K44A cells for 1 h at 4°C. The cells were then fixed immediately or after 10, 30, or 90 min of incubation at 37°C. CPV particles were detected by indirect immunofluorescence using a rabbit anticapsid antibody, and confocal images were collected. Because of lower binding of CPV to uninduced cells, images of uninduced cells at time zero were collected using a higher gain than those of the induced cells, and as a result nonspecific nuclear fluorescence is also seen.

Dynamin K44A expression enhances CPV binding but causes cell cycle arrest and reduces infection. By fluorescence microscopy, more CPV particles appeared to bind to induced Mv1-K44A cells than to uninduced cells (Fig. 5A). By flow cytometry, we found that up to 10-fold more viral particles bound to many of the dynamin K44A-expressing Mv1-K44A cells than to uninduced cells (Fig. 5B). The induced Mv1-K44A cells which bound more virus represented approximately 40% of the total population of cells, and this population of cells also expressed more dynamin as indicated by increased HA epitope expression (Fig. 5B, inset). We found no difference in CPV binding to induced or uninduced Mv1-WT cells (data not shown).

View larger version (77K): [in this window] [in a new window]   FIG. 5.   Binding of full CPV particles to uninduced and induced Mv1-K44A cells. (A) Purified CPV full particles were bound to uninduced or induced Mv1-K44A cells for 1 h at 4°C; then the cells were fixed, and capsids were detected by indirect immunofluorescence with MAb 8. Phase-contrast images are shown in the left panels. The two fluorescence images were collected using identical exposures. (B) Mv1-K44A cells grown in the presence or absence of tetracycline were suspended by treatment with EDTA and then incubated for 1 h on ice with or without 40 µg of full CPV particles per ml. After washing, the cells were fixed and immunostained for capsid and then permeabilized, and the dynamin K44A was immunostained using the fused HA epitope tag. Cell-associated fluorescence was determined by flow cytometry for each sample. The histograms shows the binding of CPV to the cell surface. The inset is a dot plot showing the binding of CPV versus expression of the HA tag.

View larger version (41K): [in this window] [in a new window]   FIG. 6.   CPV infection and cell cycle analysis of uninduced and induced Mv1-WT and Mv1-K44A cells. (A) Mv1-WT and Mv1-K44A cells grown with or without tetracycline for 48 h were inoculated with CPV, and the percentage of infected cells was assayed after 16 h by anti-NS1 staining and flow cytometry. The results are expressed as the percentage of cells infected in the induced culture relative to the percentage of cells infected in uninduced cultures. The average and standard deviation of three independent experiments are shown. Each experiment had a minimum of three replicates. (B) Mv1-WT and Mv1-K44A cells grown with or without tetracycline for 48 h were analyzed for DNA content by propidium iodide staining and flow cytometry. The percentage of cells in each phase of the cell cycle was estimated with Modfit LT cell cycle analysis software. Results shown are the average and standard deviation of four independent experiments.

CPV colocalizes with Tfn in a perinuclear vesicular compartment but not with dextran. To examine virus trafficking, we stably transfected tTA-Mv1Lu cells with the HuTfnR (Mv1Lu-TR cells) and examined the localization of virus and Tfn in these cells. After 2 h at 37°C, HuTfn and CPV particles clearly colocalized to perinuclear vesicles in the Mv1Lu-TR cells (Fig. 7A). In contrast, virus and FITC-dextran showed little colocalization in the uninduced Mv1-K44A cells (Fig. 7B). In the induced Mv1-K44A cells the dextran was observed in endosomal vesicles, while the virus remained associated with the plasma membrane (Fig. 7C).

View larger version (30K): [in this window] [in a new window]   FIG. 7.   Confocal images showing co-uptake of CPV and Texas red HuTfn in Mv1Lu-TR cells or of CPV and FITC-dextran in uninduced and induced Mv1-K44A cells. (A) Mv1Lu-TR cells stably expressing the HuTfnR were incubated with full CPV particles and Texas red-labeled HuTfn for 2 h at 37°C. Capsids were detected with MAb 8. The upper panels show a 630× magnification; the lower panels show a 1500× magnification of a single cell. The arrows indicate individual vesicles containing virus and Tfn. Mv1-K44A cells grown for 48 h with (B) or without (C) 2 µg of tetracycline per ml were incubated with full CPV particles for 1 h at 4°C and then warmed to 37°C by the addition of warm DMEM-1% BSA containing 2 mg of lysine-fixable FITC-dextran per ml. After incubation at 37°C for 15 min, the cells were fixed and permeabilized, and capsids were detected with MAb 8.

BFLA1 inhibited CPV infection. Previous studies of CPV entry have shown that treatment of cells with ammonium chloride or chloroquine prevents viral infection (8). BFLA1 at micromolar concentrations specifically inhibits the vacuolar proton ATPase, preventing acidification of endosomes (11), and it also inhibits transport from early to late endosomes in HeLa cells (10). However, Bayer et al. found only a small increase (0.2 pH units) in the intravesicular pH of HeLa cells treated with 20 nM BFLA1 (10). We found that addition of 10 nM BFLA1 to NLFK and A72 cells 30 min before inoculation with virus reduced the 50% tissue culture infective dose titer measured 48 h later by 95% in NLFK cells and 98% in A72 cells (data not shown). There was a 96% reduction in the infection rate of tTA-Mv1Lu cells treated with 20 nM BFLA1 30 min prior to incubation with virus and a 71% reduction when BFLA1 was added 90 min after virus inoculation (Fig. 8A). The cell cycle distribution of tTA-Mv1Lu cells treated with 100 nM BFLA1 for 16 h was no different from that of untreated cells (data not shown). From these data, we conclude that 20 nM BFLA1 inhibits CPV infection of tTA-Mv1Lu cells and that this inhibition was not due to an indirect effect of BFLA1 on the cell cycle.

View larger version (43K): [in this window] [in a new window]   FIG. 8.   Effect of BFLA1 on CPV infection and the distribution of virus-containing vesicles in tTA-Mv1Lu cells. (A) BFLA1 (20 nM) was added to tTA-Mv1Lu cells either 30 before virus incubation or 90 min after inoculation and then maintained with the cells for a further 16 h. Control cells were inoculated but not treated with BFLA1. Cells were trypsinized, fixed, and immunostained for flow cytometry. Results shown are the average and standard deviations from three replicates. (B) tTA-Mv1Lu cells grown on coverslips were treated for 30 min with 20 or 200 nM BFLA1 at 37°C, and then full CPV particles (20 µg/ml) were bound to the cells for 1 h on ice in the presence of the drug. After washing in cold PBS, the cells were warmed to 37°C for 10 min. Similarly, 10 mg of FITC-dextran per ml was added for 20 min to cells treated with 20 or 200 nM BFLA1 for 30 min at 37°C. After washing in cold PBS, the cells were fixed and capsids detected with MAb 8. Confocal images are shown.

CAV-1 but not CPV particles permeabilized cells to -sarcin. Human adenovirus type 2, poliovirus, and rotavirus are nonenveloped viruses that are known to permeabilize host cells and permit the entry of certain proteins or toxins (29, 30). Coincubation of A72 cells with 10¹³ particles of CPV per ml and 100 µg of -sarcin per ml resulted in an insignificant decrease in [³⁵S]methionine incorporation, while adding 2.5 × 10¹⁰ particles of CAV-1 per ml with 100 µg of -sarcin per ml resulted in a 89% decrease in incorporation of [³⁵S]methionine (Fig. 9). Results were similar when the experiment was carried out in tTA-Mv1Lu cells (Fig. 9). In both cell lines, the degree of permeabilization to -sarcin by CAV-1 particles increased with increasing amounts of virus, but no change was seen with increasing amounts of CPV.

View larger version (35K): [in this window] [in a new window]   FIG. 9.   Effect of CAV-1 or CPV capsids on the permeability of cells to the protein synthesis inhibitor -sarcin. CPV full capsids or CAV-1 particles at the concentrations shown (particles per milliliter) were incubated with A72 or tTA-Mv1Lu cells with or without 100 µg of -sarcin per ml for 90 min at 37°C and then incubated with [35S]methionine for an additional 1 h. Incorporated [35S]methionine was measured by scintillation counting. Results are expressed as the mean and standard deviation of three separate dishes.

	DISCUSSION

Top Abstract Introduction Materials and Methods Results Discussion References

Here we have defined several steps in the capsid uptake and infection pathway of CPV which have not been previously reported. This small and very stable virus enters cells and transports its DNA to the nucleus for replication. The success of cell infection can vary more than 10⁶-fold, depending on the host of origin of the cell and on the presence of single or double amino acid substitutions in the surface of the virus capsid (15, 58, 76). The host range mutations affect infection after virus binding to the cell surface but before DNA replication (38, 58).

Virus and its receptor enters cells via dynamin-mediated endocytosis. We have demonstrated that uptake of viral particles from the plasma membrane occurred rapidly via clathrin-coated vesicles. This was shown by the rapid removal of virus from the cell surface, by the localization and concentration of the particles within coated pits and vesicles, and also by the observation that uptake and transport of virus-containing vesicles were strongly inhibited by overexpression of dynamin K44A mutant in the cells.

Later stages of virus entry and endosomal trafficking are blocked by BFLA1 treatment of cells. Twenty nanomolar BFLA1 inhibited CPV infection by >95% when added to cells prior to virus addition but also resulted in a 70% reduction in infection when added to cells 90 min after the virus (Fig. 8A). In addition, we observed a clear alteration of the distribution of virus-containing vesicles in cells treated with 20 or 200 nM BFLA1 compared to untreated cells (Fig. 8B). This suggests that although viral particles rapidly enter cells within vesicles, the majority of particles remain within endosomal compartments for up to 90 min after uptake. When we examined the effect of 20 or 200 nM BFLA1 on the distribution of FITC-dextran-containing vesicles in tTA-Mv1Lu cells, we saw no difference between treated cells and the untreated control at 20 nM, but there were obvious differences in vesicle distribution in cells treated with 200 nM BFLA1, as has been reported for HeLa cells (10). The difference between the vesicular trafficking of viral particles and FITC-dextran in cells treated with 20 nM BFLA1 is likely to be due to differential effects of BFLA1 on fluid-phase versus receptor-mediated endocytosis. Cell infection by many viruses is inhibited by BFLA1 (10, 35, 52). In micromolar amounts, BFLA1 inhibits the vacuolar proton pump and prevents acidification of endosomes, and it blocks cell infection by adenoviruses, reoviruses, and certain picornaviruses (52, 62, 63). However, treatment of HeLa cells with 20 nM BFLA1 has minimal effects on endosomal pH (10). We do not know what effect 20 nM BFLA1 had on the endosomal pH of tTA-Mv1Lu cells. BFLA1 treatment inhibits early to late endosomal vesicular transport in some cells (10, 17) and affects the recycling of Tfn (39, 64). It is therefore unclear whether the inhibition of CPV infection that we observed was due to an effect of BFLA1 on vesicle pH or on trafficking, or both. Interestingly, the microtubule-destabilizing drug nocodazole inhibits CPV infection when added at 60 min but not at 120 min after virus uptake (81). These results suggest that capsids entering the cell are sequestered in a vesicular compartment and may be only gradually trafficked to another compartment from which they enter the cytoplasm and infect the cell.

Entry of CPV does not result in permeabilization of cells to -sarcin. At some stage in infection, the CPV capsid must penetrate a membrane barrier to deliver its genome into the cytoplasm of the host cell, prior to delivery to the nucleus. It is not known whether the intact CPV particle passes through the endosomal membrane or whether perhaps pores are formed through which the DNA can pass. The toxin -sarcin has been used to examine the effects of virus capsids on cell membrane permeability (22, 29, 52). Even very large amounts of CPV capsids did not significantly increase the permeability of the endosomes of mink or canine cells to -sarcin (Fig. 9), while CAV-1 gave over 90% inhibition of translation, similar to the results reported for the human adenoviruses (30, 62). Adenovirus particles lyse an early endosomal compartment in response to receptor binding and low pH, allowing the entry of other molecules, including -sarcin, or DNA into the cell cytosol (21, 29).

CPV particles colocalize with Tfn in endosomes. CPV particles clearly colocalized with Tfn in perinuclear vesicles of Mv1Lu-TR cells after 2 h at 37°C (Fig. 7A). As Tfn efficiently enters the perinuclear recycling vesicle in nonpolarized cells (84) and more than 80% of the cell TfnR molecules reside in this recycling compartment (34), it appears that CPV is also trafficked to and becomes retained in the perinuclear recycling vesicle. This would be consistent with the observation that CPV particles do not become degraded even after many hours of incubation with cells (83), as proteases are excluded from the perinuclear recycling endosomes, but they would normally be present in late endosomes or lysosomes.