- Open Access
Porcine reproductive and respiratory syndrome virus (PRRSV) infection spreads by cell-to-cell transfer in cultured MARC-145 cells, is dependent on an intact cytoskeleton, and is suppressed by drug-targeting of cell permissiveness to virus infection
© Cafruny et al; licensee BioMed Central Ltd. 2006
- Received: 15 June 2006
- Accepted: 02 November 2006
- Published: 02 November 2006
Porcine reproductive and respiratory syndrome virus (PRRSV) is the etiologic agent of PRRS, causing widespread chronic infections which are largely uncontrolled by currently available vaccines or other antiviral measures. Cultured monkey kidney (MARC-145) cells provide an important tool for the study of PRRSV replication. For the present study, flow cytometric and fluorescence antibody (FA) analyses of PRRSV infection of cultured MARC-145 cells were carried out in experiments designed to clarify viral dynamics and the mechanism of viral spread. The roles of viral permissiveness and the cytoskeleton in PRRSV infection and transmission were examined in conjunction with antiviral and cytotoxic drugs.
Flow cytometric and FA analyses of PRRSV antigen expression revealed distinct primary and secondary phases of MARC-145 cell infection. PRRSV antigen was randomly expressed in a few percent of cells during the primary phase of infection (up to about 20–22 h p.i.), but the logarithmic infection phase (days 2–3 p.i.), was characterized by secondary spread to clusters of infected cells. The formation of secondary clusters of PRRSV-infected cells preceded the development of CPE in MARC-145 cells, and both primary and secondary PRRSV infection were inhibited by colchicine and cytochalasin D, demonstrating a critical role of the cytoskeleton in viral permissiveness as well as cell-to-cell transmission from a subpopulation of cells permissive for free virus to secondary targets. Cellular expression of actin also appeared to correlate with PRRSV resistance, suggesting a second role of the actin cytoskeleton as a potential barrier to cell-to-cell transmission. PRRSV infection and cell-to-cell transmission were efficiently suppressed by interferon-γ (IFN-γ), as well as the more-potent experimental antiviral agent AK-2.
The results demonstrate two distinct mechanisms of PRRSV infection: primary infection of a relatively small subpopulation of innately PRRSV-permissive cells, and secondary cell-to-cell transmission to contiguous cells which appear non-permissive to free virus. The results also indicate that an intact cytoskeleton is critical for PRRSV infection, and that viral permissiveness is a highly efficient drug target to control PRRSV infection. The data from this experimental system have important implications for the mechanisms of PRRSV persistence and pathology, as well as for a better understanding of arterivirus regulation.
- Actin Expression
- Intact Cytoskeleton
- Viral Permissiveness
- Fluorescence Antibody Analysis
Porcine reproductive and respiratory syndrome virus (PRRSV) is an arterivirus which is the etiologic agent of PRRS, a disease of epidemic proportions in swine [1–3]. PRRSV is macrophage-tropic in vivo, where it establishes a chronic infection, and the virus replicates in primary pig macrophages in vitro [4–6]. PRRSV infection has been extensively studied in MARC-145 cells, a PRRSV-permissive monkey kidney cell line [7, 8]. Previous studies have established that PRRSV replication in cultured MARC-145 cells follows a complex time-course, with PRRSV antigens becoming detectable by immunofluorescence analysis between about 10–20 h p.i., and emergence of foci of damage (cytopathic effect; CPE) usually over the next 3–4 days [7, 8].
The fate of PRRSV-infected MARC-145 cell cultures may include death of some cells by modified apoptosis  or necrosis , as well as establishment of chronic PRRSV infection (Cafruny & Rowland, unpublished). Thus, clarifying the behavior of PRRSV in MARC-145 cells is significant to progress in developing anti-viral strategies.
Previous studies have suggested that initial defenses against PRRSV are comprised of innate lung and alveolar macrophage responses ; subsequently, both Th1 and Th2 responses are induced in the respiratory tracts of PRRSV-infected pigs . PRRSV infection of pigs is associated with activation of several cytokines including interferon-γ [IFN-γ; [12, 13]], which has PRRSV-inhibitory activity in vitro . However, the IFN-γ response to PRRSV may be inhibited or delayed by some unknown factors during PRRSV infection or vaccination [15, 16], and ultimately a poorly-neutralizing Th2-dependent response seems to result in many pigs. Combined, the characteristics of these host responses may facilitate viral persistence [15, 16].
The interaction of PRRSV with host cytokines is not well understood, but this area of study is a potential key to understanding host mechanisms during infection. Cytokines have not yet been exploited to control PRRSV infection in vivo, but their potential to regulate PRRSV infection in certain experimental systems provides a rationale for PRRSV discovery research, and anti-PRRSV agents may be important tools for future drug development.
The viral dynamics of another arterivirus, lactate dehydrogenase-elevating virus (LDV), are dominated by regulation of the LDV-permissive state; only a small fraction of mouse macrophages are susceptible to LDV infection, leading to an avirulent chronic infection in most mice which is maintained through development of newly-permissive cells . Viral permissiveness is a logical but poorly exploited target for antiviral drugs [18–20], and the present study utilized two antiviral agents which target permissiveness (IFN-γ and an experimental antiviral known as AK-2), as well as cytoskeleton disruptors, to probe checkpoints in PRRSV replication.
Initially, our goal was to better characterize the dynamics of PRRSV replication in MARC-145 cells. Using flow cytometry and fluorescence microscopy, we demonstrated logarithmic growth of PRRSV in MARC-145 cells, culminating over a period of 3–4 days in the death of most cells. Secondary spread of PRRSV infection was observed to be via cell-to-cell transmission, as demonstrated by emergence of clusters of PRRSV-infected cells in confluent monolayers of MARC-145 cells, which preceded PRRSV-induced CPE, were inhibited by colchicine and cytochalasin D, and correlated with reduced actin expression. PRRSV replication was sensitive to IFN-γ as well as AK-2, which was a relatively more potent PRRSV inhibitor and capable of suppressing both primary and secondary PRRSV infection. The results of this study demonstrate cell-to-cell spread of PRRSV in cultured MARC-145 cells, the dependence of PRRSV infection and transmission on an intact cytoskeleton, and highlight the role of the PRRSV-permissive state as a critical drug target, with important implications for future therapeutic and preventive strategies.
PRRSV replication dynamics in MARC-145 cells
Formation of PRRSV-infected cell clusters (secondary infection)
Role of the cytoskeleton in PRRSV infection
Treatment of cells with 10 μM colchicine simultaneously with PRRSV inoculation, resulted in about 75% inhibition of secondary PRRSV infection (e.g. 70% in control vs. 18% in colchicine-treated culture; counting >1000 total cells at 46 h p.i.) and data representative of numerous experiments are shown in Figure 5E to illustrate the inhibitory effect of colchicine on formation of PRRSV-infected secondary clusters, which are seen spreading throughout the controls (Figure 5C,D). Similarly, exposure of cells to cytochalasin D under several experimental conditions (1 or 2 μM; administered either simultaneously with virus infection or 2 h pre-infection) inhibited PRRSV-positive cells by up to 87% (illustrated in Figure 8A between 13–22 h p.i.; 2 h pre-treatment with 1 μM). These drug effects were confirmed by flow cytometric analyses (about 50–90% inhibition of PRRSV-positive cells; data not shown).
The confluent cultures used in our experiments generally had mean cell-to-cell distances of < 2 μm, and the cells were usually in contact or too close to measure meaningful distances. Due to the wide dynamic range of the fluorescence signals, this is not always apparent in the figures, but some figures, such as 3A, 7A &7B, serve to illustrate the background of cultured cells. By seeding plates with different numbers of cells and then infecting these cultures containing different cell densities, it was possible to measure cell-to-cell distances in hundreds of cells per culture from the captured images, and then correlate the mean with the number of PRRSV-positive clusters (Figure 8B). The results show that formation of PRRSV-positive secondary clusters was density-dependent, with a direct correlation between the cell-to-cell mean distance and the number of clusters (Figure 8B).
In contrast to the ability of PRRSV to spread via cell-to-cell transmission, LDV did not exhibit this property, nor was there any dissociation of actin expression by primary cultured mouse macrophages from LDV permissiveness (probed during the replication peak, Figure 7D &7E). Also in contrast to the response of PRRSV in MARC-145 cells, treatment of mouse macrophages with the same concentrations of colchicine had little effect on LDV replication (+17%, -26%, and -21% LDV-positive cells relative to control in three separate experiments), although LDV infection was completely suppressed by cytochalsin D (no LDV-positive cells detected in three separate experiments).
Combined, these data show that after primary acute PRRSV infection of a small subpopulation of PRRSV-permissive MARC-145 cells, the virus spreads secondarily over the next 2–3 days to surrounding cells by cell-to-cell transmission. These virus mechanisms are both actin- and tubulin-dependent, demonstrating the critical role of the cytoskeleton in the processes of PRRSV infection and spread. In contrast, the related arterivirus LDV displays no cell-to-cell transmission in primary culture mouse macrophages and primary LDV replication is not tubulin-dependent as revealed by absence of colchicine sensitivity.
Suppression of PRRSV infection by targeting viral permissivness with AK-2 and IFN-γ
A higher-magnification image of AK-2-treated (single-cell infection only) is shown in Figure 5F, which also illustrates the often-observed appearance of actin fibrils surrounding a PRRSV-positive cell, as if to separate it from other uninfected cells as indicated above for Figure 6G. The data also show the absence of a detectable effect of AK-2 on actin expression.
In other studies, AK-2 pretreatment inhibited PRRSV antigen expression at 20–22 h p.i. by about 90% in primary pig macrophages, in each of two experiments. Similarly, pretreatment of primary mouse macrophages with recombinant murine AK-2 inhibited LDV replication by 86% in a single experiment. Thus, the anti-arterivirus effects of AK-2 are expressed over a broad host cell range.
Observations were also made for the anti-PRRSV effect of IFN-γ pretreatment, which was demonstrated in previous studies to inhibit PRRSV replication . PRRSV inhibition by IFN-γ was less effective than that of AK-2 under the same experimental conditions, as seen for example in the primary response to pretreatment measured by flow cytometry (Figure 2C,I); the effect of IFN-γ pretreatment also waned by 40 h p.i. (Figure 2J). FA analyses confirmed the reduced efficacy of IFN-γ relative to AK-2, since IFN-γ pretreatment did not completely inhibit formation of secondary PRRSV antigen-positive clusters (Figure 4A,D) and there were higher numbers of PRRSV antigen-positive cells in IFN-γ-pretreated cultures (data not shown). Consistent with these data, flow cytometry demonstrated that IFN-γ added at 18 h p.i. had a reduced effect on secondary PRRSV infection (Figure 2G), relative to AK-2 (Figure 2F) or the combination of AK2 and IFN-γ (Figure 2H); the inhibitory effect of post-treatment with both drugs is also shown in Figure 2H, although little if any synergy was observed. Thus, while IFN-γ mediated significant inhibition of PRRSV infection, AK-2 appears to be a more potent anti-PRRSV agent.
The results of this study show that PRRSV replication in an experimental MARC-145 cell system is composed of two discrete phases: primary infection of a relatively small subpopulation of PRRSV-permissive cells during about the first 22 h p.i, followed by secondary cell-to-cell spread over the next several days to contiguous cells, resulting in formation of infected cell clusters and ultimately cell death/CPE by days 3–4 p.i. Flow cytometry of PRRSV infection of pig macrophages has previously been reported , but for the present study we developed a flow technique to quantitatively measure PRRSV antigen expression in MARC-145 cells, a standard cell line for the study of PRRSV infection. Combined with FA analyses by microscopy, this methodology provides evidence that permissiveness to PRRSV infection is dependent on the mechanism of virus presentation, since the majority of cells appear non-permissive to free virus, but become readily infected by exposure to productively-infected cells.
These dynamics of PRRSV infection of MARC-145 cells stand in stark contrast to those of the related and relatively benign arterivirus LDV, since primary LDV infection of cultured mouse macrophages peaks at about 8 h p.i. in vitro, and soon thereafter in vivo, but there is little or no secondary virus replication after these events . A likely explanation for this difference is the absence of cell-to-cell (cluster) spread of LDV. The ability of PRRSV to spread secondarily by cell-to-cell transmission may overcome an early block to virus permissiveness, and while it is not yet known whether this mechanism occurs in vivo, it could potentially help PRRSV resist antibody defenses and maintain persistence.
Our studies show that PRRSV transmission to infected cell clusters is dependent upon cytoskeletal function, since the microtubule inhibitor colchine [26–28] as well as the actin inhibitor cytochalasin D [26, 29–31] suppressed secondary virus spread. Consistent with this conclusion, a number of other viruses are dependent on the host cytoskeleton for entry, transport, and/or egress [32–34], and actin polymerization may enhance cell-to-cell virus spread . For example, the actin cytoskeleton is a critical factor for assembly and/or budding of HIV-1 , West Nile virus , respiratory syncytial virus , fowlpox virus , and equine infectious anemia virus . Interestingly, we observed that the pattern of actin expression correlated with PRRSV resistance, since there was often a distinct appearance of actin filaments surrounding PRRSV-negative cells, and a general (but not absolute) negative correlation between viral antigen detection and the level of actin expression. This finding appears to suggest that actin provides a protective barrier to cell-to-cell transmission, and that the actin cytoskeleton may have a dual role in PRRSV infection. This seemingly paradoxical observation may be analogous to that reported for transport of secretory granules, which is both limited and mediated by the actin cortex . Furthermore, the actin cytoskeleton is a potential barrier to exocytosis [41, 42], and the cortical actin network may provide a cellular barrier to SFV  and HIV . PRRSV infection might potentially inhibit the cytoskeleton [44–46], to further promote virus spread in culture. In contrast to the finding with PRRSV, there was no difference between actin expression in LDV-permissive and LDV-non-permissive mouse macrophages. Additional studies of the role of the cytoskeleton should be of interest to PRRSV pathogenesis and the biology of arteriviruses.
Primary infection was dependent on an intact cytoskeleton, and nascent cluster initiation during this time frame was signified by the occasional appearance of infected cell doublets. Formation of secondary PRRSV-infected cell clusters was a function of time p.i. and the cell-to-cell distance, and is thus a physical property of the in vitro system, potentially analogous to tissue sites in vivo. The viral dynamics from our studies are consistent with previous observations demonstrating infection of a small percentage of cells by day 1 p.i., which increases markedly over the next few days, culminating in peak supernant virus titers at about 72–96 h p.i. . The data also suggest that 1 TCID50 contains multiple virions since the number of cells acutely infected can exceed the TCID50 dose and optimal infection is achieved at low M.O.I. (calculated by TCID50) as previously reported (9,14). Future studies to clarify the relationship of M.O.I and TCID50 might help to determine what special characteristics facilitate primary permissiveness to free virus, which could include ability to bind one or more virions as well as biochemical factors regulating virus replication.
Our data show that the logarithmic increase in the percentage of PRRSV infected cells over about 2–4 days p.i. is due to secondary cell-to-cell virus spread, from innately-permissive (reservoir) cells to surrounding uninfected cells. The foci of infection typically observed microscopically, in cultures of PRRSV-infected cells which begin to degenerate by 3–4 days p.i., are thus the outcome of secondary cluster infection and direct virus infection. These data reinforce that secondary spread to clusters in MARC-145 cells provides an important direction for future studies of PRRSV mechanisms, since cell-to-cell virus transmission  might help to explain the resistance of PRRSV to antibody-mediated control as well as PRRS pathology. In a recent study, the replication of PRRSV in transformed pig peripheral blood monocytes was shown to be under genetic control and varied between 23.1–31.4% at 24 h p.i. . Thus, our results suggest the possibility that variations in cell-to-cell PRRSV transmission may underlie differences in PRRSV replication between different cell lines in vitro.
The present results show that AK-2 is a potent inhibitor of arterivirus (PRRSV and LDV) replication. This is the first published report of the antiviral effects of AK-2, which suppresses viral permissiveness by activating an antiviral gene program (Wong; unpublished), and which we exploited to supplement our studies of the IFN-γ response. Pretreatment was required for full expression of the drug effects, likely due to a lag phase for activation of the antiviral gene program. Both primary as well as secondary (cluster) PRRSV infection were susceptible to the antiviral actions of AK-2, but required optimal conditions of pretreatment for induction of the PRRSV-resistant state, and secondary PRRSV infection was controlled independently of primary infection by simultaneous or delayed drug exposure. IFN-γ was relatively less effective under our experimental conditions, but our IFN-γ data reinforce the conclusion that the viral-permissive state is an important drug target in PRRSV infection. This is also the case for LDV-mediated fetal infection [49, 50] and neuropathology , since suppression of LDV-permissiveness by IFN-γ reduces these viral phenomena, and the arteriviruses may be good models for the role of permissiveness in antiviral strategies. Despite sensitivity to IFN-α, PRRSV may be a relatively weak inducer of this cytokine , facilitating evasion of host defenses. Thus, development of useful drugs which target viral permissiveness could be a superior strategy to inhibit primary or secondary phases of PRRSV infection, particularly if secondary cell-to-cell spread is resistant to a conventional antibody attack, and might also provide a superior toxicity profile, since the induction of PRRSV resistance is fundamentally a physiological process.
PRRSV infection has been shown to spread by cell-to-cell transmission in a stable MARC-145 cell line. Two stages of viral infection have been identified: primary (innate) permissiveness to free-virus which appears in a relatively small percentage of cells, and secondary permissiveness to cell-to-cell transmission which is highly expressed and culminates in CPE. PRRSV infection of MARC-145 cells requires an intact cytoskeleton, but actin expression may also correlate with cell protection. Drugs such as AK-2 which induce a block in PRRSV permissiveness reveal a potentially important drug target for suppression of primary and secondary PRRSV infection.
A stable and mycoplasma-free MARC-145 cell line was utilized in these experiments. Cells were cultured in DMEM containing10% fetal bovine serum, and for virus infections the medium was switched to MEM containing 2% horse serum. Cells for virus infections were grown to confluency in either T-25 flasks (seeded with about 5 × 105 cells/culture) or 8-well glass slide chambers (seeded with about 10,000 cells/culture; Lab-Tek II; Nalge Nunc International), and for the cell density studies, serial two-fold dilutions of the cells were used. Cells were inoculated with PRRSV at about 1–2 days after seeding (time to approximate doubling of the population).
Primary pig macrophages
Pig cells were collected from 4–8 week old pigs by lung lavage with PBS [21–23]. Cells were cultured in DMEM containing 10% FBS. After 18–24 h, non-adherent cells were removed by washing. The remaining adherent cells were cultured for an additional 24 h in RPMI containing 2% horse serum, and then inoculated with PRRSV (M.O.I. approximately 0.1 TCID50).
PRRSV isolate SD-23983 was passaged on MARC-145 cells, preparing high-titer (~ 105 TCID50 per ml) virus stocks from culture supernatants at 48–96 h p.i. PRRSV stocks were sequentially filtered through 0.45, 0.22, and 0.10 um filters and confirmed to be mycoplasma-free by testing on PPLO medium. As reported previously (9,14), maximum efficiency of PRRSV infection of MARC-145 cells occurs with low M.O.I as determined by TCID50, probably due to the presence of multiple virions per TCID50. For the present studies, M.O.I. of about 0.01 TCID50 (slide cultures) and 0.001 TCID50 (T-flask cultures) were found to result in near-optimal efficiency of infection, and were thus used for our studies unless otherwise noted in Results.
Fluorescence (FA) detection of viral and cellular target molecules
PRRSV replication was detected using FITC-labeled IgG anti-PRRSV nucleocapsid monoclonal antibody (SDOW17; ). MARC-145 cells were cultured and inoculated with PRRSV in glass-bottom slide chambers, fixed in 80% acetone, and incubated for 1 h at 37°C with a 1:100 dilution of FITC-conjugated SDOW17 antibody made in PBS containing 5% fetal bovine serum. Then the cells were washed three times with cold PBS prior to examination under a fluorescence microscope, screening about 30–40,000 total cells to obtain the incidence of antigen-positive cells. Confocal fluorescence microscopy was performed using an Olympus BX61 microscope and Fluoview software. Images shown in Figures 3 and 4 display the yellow scale bar captured with the original image, along with a higher-contrast white scale line. For flow cytometry, MARC-145 cells were cultured and PRRSV-inoculated in T-flasks, the cells were suspended in trypsin-versene, pelleted at 1000 rpm, resuspended in DMEM with 2% horse serum, fixed in cold 80% acetone for 10 min, washed twice in PBS, and resuspended in 1 ml PBS containing 60 ul of fetal bovine serum. FITC-conjugated SDOW17 antibody was then added to the cells (2.5 ul/ml), incubation was carried out at 37°C for 60 min, the cells were washed with PBS, examined under a fluorescence microscope, and flow cytometry was performed with a FACSVantage SE (Becton Dickenson) equipped with a 488 Enterprise II coherent laser. Twenty thousand events per sample were analyzed with CellQuest software. Cell cycle analyses were also performed on the same samples, by staining with propidium iodide for 20 minutes at room temperature and analyzing the flow cytometric results with ModFit LT 2.0 software. PRRSV replication in primary pig alveolar macrophages [22, 23] was assessed by FA under a fluorescent microscope. Cellular expression of actin was determined by incubating acetone-fixed cells with AlexaFluor 594 phalloidin (Invitrogen) according to the manufacturer's instructions, with the modification of simultaneous PRRSV detection as above, such that combined labels were applied for 60 min at 37°C, permitting two-color fluorescence detection by confocal microscopy. Data shown are representative of at least 2 replicate experiments for each type of experiment described in the Results.
LDV infection of primary mouse macrophages
Peritoneal macrophages were collected from outbred ICR mice, seeded onto glass coverslips, and inoculated with a standard dose of LDV-P as described previously . LDV replication was assessed in cells fixed in acetone at 8 h p.i by IFA assay as described previously .
Purified recombinant human interferon-γ (IFN-γ; 100 ug/ml) and actokine-2 (AK-2; 50 ug/ml) were provided by Actokine Therapeutics. AK-2 is a cytokine-based experimental antiviral being developed by Actokine Therapeutics, which consists of recombinant normal human proteins comprising part of the mammalian cell response to virus infection (Wong; unpublished). Soluble stocks of these agents were stored at 4°C in fetal bovine serum, which also served as the drug-vehicle control for the experiments, and were diluted 1:50 or 1:100 in medium to yield concentrations in cell cultures of about 1–2 ug/ml. As noted for individual experiments, cells were exposed to the drug or control treatments prior to PRRSV infection (pretreatment), during the course of PRRSV infection (delayed or post-treatment), or simultaneously with PRRSV infection. Based on previous studies of in vitro efficacy, the microtubule inhibitor colchicine which binds to tubulin (Sigma; 5 or 10 μM; 26–28) or the microfilament disruptor cytochalasin D which depolymerizes actin (Sigma; 1 or 2 μM; [26, 29–31]) were added to cell cultures at the times indicated.
This research was supported by a grant from the Center for Infectious Disease Research and Vaccinology (WAC) and an internal summer medical student research stipend (PWD). We thank Dr. Fran Day for assistance with microscopy, and Debdutta Mukherjee and Megan Hora for microscopic analyses.
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