Replication of Wild-Type and Mutant Human Cytomegalovirus in Life-Extended Human Diploid Fibroblasts

Defining the molecular mechanisms that control human cytomegalovirus (HCMV) replication in vitro has been difficult in part due to the virus's limited host range. HCMV is typically propagated in primary cultures of human fibroblasts that yield relatively high titer stocks and produce plaques when infected with HCMV. However, primary human fibroblasts have a finite life span that limits their usefulness in studying HCMV replication. For example, it is difficult to generate stable fibroblast cell lines to complement defective HCMV strains. HCMV has been shown to replicate in a number of different cell types including human umbilical vein endothelial cells (4, 12, 13), macrophages and monocytes (5, 14), an astrocytoma cell line (3, 6), and a teratocarcinoma cell line (8). However, none of these cell lines produce high-titer stocks or plaques when infected with HCMV. Therefore, a life-extended fibroblast cell line capable of generating high-titer HCMV stocks and producing viral plaques would be a valuable tool to better understand the mechanisms of HCMV replication. It has recently been shown that constitutive expression of the catalytic subunit of human telomerase extends the life span of a number of somatic cells including human fibroblasts (2). We report here the generation of life-extended fibroblast clones that are fully permissive for HCMV replication and plaque formation. These life-extended fibroblasts have been used to generate a cell line that complements an HCMV mutant lacking the UL82 gene.

To generate life-extended human diploid foreskin fibroblasts (HFF cells), HFF-R2 cells at passage 6 were transfected with plasmid pGRN145 (2), which expresses the catalytic subunit of telomerase and a puromycin resistance marker. Stable clones were selected in puromycin (1 μg/ml) and analyzed for telomerase activity using the telomeric repeat amplification protocol (TRAP) assay (2, 7). We obtained 22 puromycin-resistant clones; 14 were negative and 8 were positive for telomerase activity (data not shown). We chose three positive and three negative clones for a more detailed analysis. Figure1 shows that clones 12, 16, and 18 were positive and clones 9, 10, and 13 were negative for telomerase activity in the TRAP assay. The parental cells (HFF-R2) were negative for telomerase activity. As a negative control, equivalent cell lysates from all samples were incubated at 85°C for 10 min to inactivate telomerase activity (2, 7). After heat inactivation, none of the samples expressed telomerase activity.

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Fig. 1.

Telomerase activity in stable HFF clones. Stable HFF clones obtained by transfection with pGRN145 expressing the catalytic subunit of telomerase (Tel) were analyzed for telomerase activity by the TRAP assay using a TRAPEZE kit (Intergen) according to the manufacturer's instructions. Two thousand cells were analyzed in all samples. TRAP products were separated by gel electrophoresis (11.25% polyacrylamide) and detected by autoradiography. As a negative control, cell lysates were incubated at 85°C for 10 min (ΔH) to inactivate telomerase. TSR8, positive control for the PCR; IC, internal control for all reactions.

We compared the proliferative life spans of the telomerase-positive and -negative clones. Once clones were expanded to a 10-cm-diameter dish, the population doubling was set at 40. Cells were counted and passed every 5 to 7 days, and new population doublings were calculated. As shown in Fig. 2, the three telomerase-negative clones underwent senescence, i.e., failed to double within 2 weeks, between population doublings 45 and 55. All 14 telomerase-negative clones senesced after 49.4 (±3.0) population doublings (data not shown). In contrast, the three telomerase-positive clones have exceeded 135 population doublings and continue to divide like early-passage HFF cells.

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Fig. 2.

Replicative life span of telomerase-positive and -negative clones. Cells were counted and passaged every 5 to 7 days, and new population doublings were calculated. Cultures were considered senescent (*) if they had undergone less than one population doubling in 2 weeks.

To determine if expression of telomerase affected the ability of HCMV to replicate and produce high-titer stocks, three telomerase-negative and three telomerase-positive clones were infected with HCMV (strain AD169) at a multiplicity of infection (MOI) of 5 PFU/cell, and virus titers were compared to those in HCMV-infected parental HFF cells. Telomerase negative clones 9, 10, and 13 were tested at population doublings 47 to 48.5, prior to undergoing senescence. HCMV replication in telomerase-positive clones 12, 16, and 18 were tested at both lower (46.5 to 51) and higher (65 to 75) population doublings, to determine if there was a difference in viral titers at different passage levels. As shown in Table 1, telomerase-positive and -negative cells were equally permissive for HCMV replication, and the three telomerase-positive clones yielded similar titers at lower or higher population doublings. There was no difference in the yield of HCMV in the parental HFF cells, telomerase-negative clones, or telomerase-positive clones.

We next compared HCMV gene expression in telomerase-positive clones to that in the parental HFF cells. Expression of the immediate-early 1 (IE1) protein and the UL99 (pp28) late protein were examined in HFF and telomerase 18 cells at various times after infection. As shown in Fig.3, the expression level and kinetics for IE1 and pp28 are identical between the two cell lines. Similar results were obtained with telomerase-positive clones 12 and 16 (data not shown). To ensure that all telomerase cells in culture were permissive for HCMV, HFF and telomerase 18 cells were infected at an MOI of 5 PFU/cell and stained 72 h postinfection for expression of the late antigen pp28. Over 95% of HFF and telomerase 18 cells stained positive for pp28 expression (data not shown).

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Fig. 3.

Comparison of immediate-early and late gene expression in HFF and telomerase-positive cells. HFF or telomerase 18 cells were infected with HCMV at an MOI of 5. Cell lysates were prepared at the indicated times postinfection (P.I.), and 50 μg of protein from each sample was analyzed by Western blotting using antibodies against either IE1 (Chemicon 810) or pp28 (9, 11).

To demonstrate that the life-extended fibroblasts could be used to complement a defective HCMV mutant, we generated a derivative clone expressing the HCMV UL82 (pp71) gene product. UL82 was chosen because previous attempts to propagate a UL82 deletion mutant have been unsuccessful in our laboratory, suggesting that UL82 may be required for efficient HCMV replication (data not shown). UL82 was put under the control of the HCMV UL99 promoter to inhibit expression of UL82 in the absence of HCMV infection, thereby ameliorating a potential detrimental effect of UL82 on cell growth. The UL82 (pp71) expression vector was constructed by using oligonucleotides (5′-AGATCTGCGCCGGCGTCTCGCCGGGCATC-3′ and 5′-GCTAGCCACGTTGAGCCGGCCCAGCAGCTC-3′) for PCR amplification of the UL99 promoter from HCMV AD169 viral DNA and cloned into the pGEMT-Easy vector (Promega). A BglII/NheI fragment containing the UL99 promoter was cloned into the pCI-neo vector (Promega) that had been digested withBglII/NheI. The resulting plasmid, pWF28, replaced the HCMV immediate-early enhancer/promoter with the UL99 promoter. The UL82 cDNA containing a hemagglutinin tag was then amplified from pCGN71 (1) using oligonucleotides (5′-CTATGGCTTCTAGCTATCCTTATGAC-3′ and 5′-CTCTAGATGCGGGGTCGACTGCG), cloned into the pGEMT-Easy vector, and sequenced. The tagged cDNA was removed via EcoRI digestion and cloned intoEcoRI-digested pWF28. The resulting plasmid, pWF28-71-HA, was then transfected into telomerase 12 cells via electroporation (260 V, 960 μF) at population doubling 60 and cultured in the presence of 400 μg of G418 per ml. G418-resistant clones were selected and screened for UL82 expression. A UL82 deletion virus (ADsubUL82) was then purified and propagated on one stable clone (WF28-71-HA) expressing UL82. ADsubUL82 was generated by homologous recombination using a previously described insertion cassette (10) containing the green fluorescent protein. This cassette was flanked by sequences corresponding to nucleotides 116666 to 117628 and 119206 to 120278 of the HCMV AD169 genome. This cassette containing the UL82 flanking sequences was then transfected into HFF cells together with infectious AD169 viral DNA. Green fluorescent plaques were picked, purified on WF28-71-HA cells, and screened by Southern blotting and PCR amplification to ensure that we had obtained a pure virus stock and correct recombination.

The mutant virus was then assayed for its ability to replicate on noncomplementing HFF cells compared to complementing WF28-71-HA cells. HFF or WF28-71-HA cells were infected at an MOI of 0.01 PFU/ml with either wild-type AD169 or ADsubUL82, and viral titers were determined at 21 days postinfection. As shown in Table2, the wild-type virus gave rise to similar titers on both HFF and WF28-71-HA cells. In contrast, ADsubUL82 did not grow on the noncomplementing HFF cells but yielded near-wild-type titers on the complementing WF28-71-HA cells (Table 2).

In conclusion, life-extended fibroblasts supported the efficient replication of HCMV and provided the opportunity to generate derivative cell clones expressing viral genes that are useful for the propagation of mutant viruses.

• Copyright © 2000 American Society for Microbiology