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Herpesvirus saimiri (HVS) is a gamma herpesvirus with several properties that make it an amenable gene therapy vector; namely its large packaging capacity, its ability to persist as a nonintegrated episome, and its ability to infect numerous human cell types. We used RecA-mediated recombination to develop an HVS vector with a mutated virion protein. The heparan sulphate-binding region of HVS ORF51 was substituted for a peptide sequence which interacts with somatostatin receptors (SSTRs), overexpressed on hepatocellular carcinoma (HCC) cells. HVS mORF51 showed reduced infectivity in non-HCC human cell lines compared to wild-type virus. Strikingly, HVS mORF51 retained its ability to infect HCC cell lines efficiently. However, neutralisation assays suggest that HVS mORF51 has no enhanced binding to SSTRs. Therefore, mutation of the ORF51 glycoprotein has specifically targeted HVS to HCC cell lines by reducing the infectivity of other cell types; however, the mechanism for this targeting is unknown.
Herpesviruses are large double-stranded DNA viruses with genomes of between 100 and 250kb. They are divided into alpha, beta, and gamma subgroups depending on their genetic and biological properties . The best characterised herpesvirus, Herpes simplex virus (HSV), is also the most developed gene therapy vector of this family, with several recombinant viruses involved in clinical trials [2–4]. However, the disadvantage of vectors based on alphaherpesvirinae, such as HSV, is their inability to persist in a dividing cell population. The use of gamma-herpesvirus vectors is an alternative approach. These viruses have many of the advantages of alphaherpesvirinae but are also able to transfer their genome to both daughter cells upon mitosis, thereby persisting in proliferating cells. We are currently developing gene therapy vectors based on Herpesvirus saimiri (HVS) [5–7]. HVS is the prototype gamma-2 herpesvirus  and was originally isolated from mononuclear blood cells of squirrel monkeys, where it causes an asymptomatic persistent infection . It also infects other New World primates causing acute malignant T-cell lymphomas .
HVS is an attractive candidate for a gene therapy vector as, in addition to its persistence in dividing cell populations, its large genome can accept heterologous DNA of up to 150kb. HVS-based vectors also have no effect on cell growth  and are capable of latently infecting a wide range of cells in vitro and in vivo . HVS exists as a stable episome in infected cells, greatly reducing its potential to disrupt genes and regulatory DNA sequences by recombination with genomic DNA. HVS strains used in gene therapy development are rendered nontransforming by the removal of the oncogenic sequences Stp and Tip .
Genetic engineering of HVS is difficult due to its sizeable genome. Originally HVS recombinant viruses were produced by cotransfecting a linearised plasmid, containing the gene of interest along with HVS homologous sequences, into permissive owl monkey kidney (OMK) cells along with the HVS genome [13, 14]. This technique, although successful was time consuming and required replication-competent viruses. Another strategy was the use of an overlapping cosmid library containing the genome of the HVS C488 strain [15, 16]. This system was quicker than the homologous recombination method above; however, the transfection of multiple cosmid constructs into the OMK cells has a low efficiency.
Manipulation of HVS DNA has become easier and quicker with the advent of F-factor-based bacterial artificial chromosomes (BACs). BACs can be maintained in Escherichia coli as a single copy number construct and can stably maintain DNA fragments up to 300kb in length . The first HVS BAC produced had the BAC elements inserted into the H-DNA (the high G+C content terminal repeat region that flanks the L-DNA coding region) of the viral genome . However, this BAC was unable to establish a latent infection as the H-DNA is required for tethering of the HVS genome to host chromosomes during cell division [19–23]. Therefore, a second HVS BAC was produced by our lab with the BAC element inserted into ORF15 . This ORF was chosen as it encodes a nonessential gene that expresses a viral homolog of CD59, a complement control protein. This HVS BAC contains the F-factor-derived elements essential for growth in E. coli, along with cassettes for hygromycin and chloramphenicol resistance, a GFP reporter gene controlled by the CMV promoter and a unique rare restriction site, I-PpoI, to allow conventional cloning of transgenes into the BAC. This HVS BAC is a valuable tool for creating recombinant viruses to develop for gene therapy applications.
One feature of HVS that makes it amenable to gene therapy vector development is its broad cell tropism. HVS has been shown to infect several human haematopoietic cell lines [6, 14, 16]. Moreover, the virus has been used to infect totipotent mouse ES cells, and GFP transgene expression was maintained throughout differentiation of those cells into mature haematopoietic cells . HVS also has potential as a cancer gene therapy vector. The vector can efficiently infect a number of carcinoma cell lines [26, 27], and studies have shown that it can efficiently penetrate three-dimensional spheroid cell cultures similar to tumours in vitro and can persist as a stable episome in tumour xenografts after direct intratumoral injections in vivo . A separate in vivo study has shown that HVS-GFP-infected tumour xenografts had sustained transgene expression over 3 months in various organs without any spread of the vector .
Although a wide tropism is suitable in some applications, a more targeted approach is preferable to increase vector uptake in diseased cell types. One way to establish a more cell-selective infection is to retarget the virus by altering how it enters cells. Hepesvirus cell entry is a multi-step process mediated by interactions between several glycoproteins at the virion surface and cognate receptors expressed at the cell membrane. Virus binding is followed by membrane fusion (the viral envelope either fuses with the membrane at the cell surface or within an endosome), allowing the viral capsid to enter the cytoplasm, where it is transported to the nuclear periphery. Here, the capsid is degraded and the viral DNA enters the nucleus via the nuclear pore.
Little is known about the mechanisms of HVS cell entry. Initial binding is thought to be mediated via an interaction between the viral glycoprotein ORF51 and cellular glycosaminoglycans (GAGs), such as heparan sulphate . This is suggested to enable further specific interactions between other viral glycoproteins such as gB and gH/gL with as yet unknown receptors, facilitating membrane fusion and viral entry.
HVS ORF51 is not well studied but has a homolog in Kaposi's Sarcoma-associated Herpesvirus (KSHV), glycoprotein K8.1. There is some ambiguity as to the extent that K8.1 affects cell entry, as it has been shown that blocking this receptor inhibits entry whereas other observations see no apparent effect [30, 31]. A research article by Means  investigated the function of HVS ORF51 and showed that the protein contains a putative heparin-binding domain. Moreover, ORF51 was shown to bind to heparin-conjugated beads, and HVS infectivity could be neutralised by incubation with soluble heparin. ORF51 is therefore an ideal candidate to mutate for cellular retargeting, as it does not appear to be intrinsically involved in fusion of the cell membrane and viral envelope. Disruption of the gene will not adversely affect cell-virus fusion, but a gain of function mutation may cause an alteration to the viral tropism.
Although in a natural infection, HVS is found in T-lymphocytes, when administered intravenously in mice several organs are latently infected with HVS. Transgene expression was mainly localised to the liver, with expression also detected in the spleen, lung, and kidneys . This suggests that this vector is suited to gene therapy of liver diseases. We therefore set out to enhance this natural tropism by targeting HVS to neoplastic liver cells.
Hepatocellular carcinoma (HCC) is the 5th most common cancer worldwide  and is caused by sustained liver damage, for example, from chronic hepatic infection or alcohol abuse [34, 35]. One feature of this cancer that could be exploited for gene therapy applications is the overexpression of somatostatin receptors (SSTRs) on the surface of HCC cells . Somatostatin or its analogues octreotide and vapreotide have been used in the treatment of HCC and other cancers; however, their effectiveness has been subject to debate [37, 38]. It has been shown that all 5 types of SSTR are present on the majority of HCCs . Therefore a gene therapy vector that effectively binds to SSTRs could be a valuable tool against hepatocellular carcinoma. We have previously demonstrated that HVS naturally displays a tropism for the liver when administered intravenously in mice . However, it may be possible to further increase this targeting to preferentially infect cancerous liver tissue by incorporating SSTR-binding properties in HVS-based vectors.
We have therefore produced a recombinant virus, HVS mORF51, by RecA-mediated recombination. The HVS mORF51 virus was constructed, so that the heparan sulphate-binding region of HVS ORF51 was substituted for an SSTR binding motif. This mutation was designed to alter the tropism of the glycoprotein, so that it preferentially binds SSTRs, thus increasing the affinity of the mutant virus for HCC cells.
HVS-GFP-BAC is based on the A11 S4 strain as described previously . To produce working stocks of HVS mORF51, the virus was propagated in the permissive owl monkey kidney (OMK) cell line. Viral DNA was transfected into OMK cells in 6 well plates with Lipofectamine 2000 (Invitrogen). Cells were exposed to the lipid-DNA complexes for 4–6h in serum-free DMEM. The media was then exchanged for 5% DMEM to allow viral infection. This virus-containing media was then used to reinfect large quantities of OMKs to produce sufficient amounts of working virus stocks, as previously described. All human cancer cell lines, HEK 293T and OMK cells, were grown and passaged in DMEM with 10% foetal bovine serum and 5units/ml penicillin/streptomycin. Virus propagation was performed in 5% DMEM with pen/strep.
pKOV Kan ΔCm is modified from the pKOV vector described previously . The mutant HVS ORF51 gene was constructed in pCR blunt (Invitrogen). The mutated region of ORF51 (plus homology regions) consisted of nucleotides 72626-73264 of the HVS genome followed by insert sequence AGA TCT CCC ACC GGT GCG TGT CGG TTT TGG AAA ACT TGG TGT GCG AGA TCT and nucleotides 73310-73810. This “mORF51” sequence was then inserted into pKOV Kan ΔCm via NotI/PstI restriction and ligation. pDF25-Tet is based on the pDF25 vector with the CmRgene replaced with a gene conferring tetracycline resistance. This substitution prevented recombination with the HVS-GFP-BAC (which contains a CmR gene) as previously described.
DH10βE. coli cells harbouring the HVS-GFP-BAC episome were made competent with RbCl. Cells were cotransformed with 5μg pDF-Tet and 1μg pKOV Kan mORF51 and then plated onto LB agar containing chloramphenicol (Cm), kanamycin (Kan) and tetracycline (Tet) at 30°C overnight. Positive colonies were picked into 1ml LB, and immediately 200μl was plated onto LB agar plates containing chloramphenicol and kanamycin. These were incubated at 43°C overnight to select for cointegrants. The larger colonies that grew were then analysed by restriction analysis and subsequent pulse field gel electrophoresis.
E. coli containing the cointegrant HVS DNA were made competent as above (but grown at 43°C with Cm and Kan). The cells were transformed with 50ng pDF25-Tet and grown overnight at 30°C on LB agar containing Cm and Tet. Colonies were subsequently picked into 1ml LB containing 5% sucrose (Cm+Tet) and incubated at 30°C. After 4h 100μl of this culture was transferred to 1ml fresh LB with the same selection and again incubated for 4h at 30°C. This was repeated again and the 1ml culture left at 30°C overnight. The overnight culture was streaked onto Cm plates containing 5% sucrose and incubated at 43°C. These colonies were then replica plated onto agar with Cm+Kan, and Cm only plates to screen for colonies with a mutation in the SacB gene of pKOV Kan mORF51. Those colonies that did not grow on the Kan plates were analysed further by PCR, restriction analysis, and DNA sequencing.
1.2% agarose gels were made with pulse field electrophoresis grade agarose (Sigma) and 0.5x TBE buffer. 10μl of DNA loading buffer was mixed with DNA samples prior to loading. Midrange I PFG Marker (New England BioLabs) or PFG Marker II (New England BioLabs) was used along with Lambda DNA HindIII Digest (New England BioLabs) to compare sizes of DNA fragments. The BioRad CHEF-DR II control module was set at 6 volts for 11.5–16.0h depending on the size of expected fragements. The 0.5x TBE buffer in the electrophoresis cell tank was cooled using a Bio-Rad Model 1000 Minichiller set to 15.5°C. Gels were stained using 200ml of 0.1μg/ml ethidium bromide (Sigma) in 0.5x TBE buffer subsequent to running.
All infections were carried out in 6 well plates with media containing 5% FBS. Neutralisation agents (heparin (Sigma), somatostatin (Calbiochem) and SSTR Ab (Diagnostic Biosystems)) were added to the media at the appropriate concentrations, 1h prior to the addition of virus and incubated at 37°C. HVS-infected cells were prepared for FACS analysis 48 hours after infection. 5×106 cells were trypsinised and resuspended in PBS. Data was collected with a BD Facscalibur flow cytometer and data was analysed using Cellquest software.
By analysing the amino acid sequence of ORF51, Means  identified motifs which could encode some of the structural features of the protein, including a putative heparan sulphate-binding sequence, comprising residues 214–228. Figure 1 outlines the alteration made to the ORF51 sequence by replacing amino acids 214–228 (peptide sequence SKHTNKLKPFKHKLQ) with a sequence determined by phage library selection to have a nanomolar affinity for all 5 SSTRs (CRFWKTWC) . This peptide contains a disulphide bridge between the flanking cysteine residues which is essential for ligand binding. Restriction endonuclease sites were also added in order to clone the this peptide sequence into a vector prior to RecA mediated recombination; BglII at either end of the sequence to allow insertion into the gene, and AgeI as an analytical tool (AgeI cuts infrequently in the HVS genome, so this added restriction site could be used for identifying positive clones). Alanines were used between the SSTR binding sequence and the restriction sites to exchange a similar number of residues with the original sequence. The final peptide sequence that replaced the heparan sulphate-binding motif is therefore RSPTGACRFWKTWCKRS. The recombination method used, consisting of a cointegration step and a second step where mutant clones are resolved, is outlined in Figure 2.
Competent E. coli cells harbouring HVS-GFP-BAC episomal DNA were cotransformed with the pKOV Kan mORF51 integrating vector and the pDF25-Tet vector which expresses RecA. This promoted the insertion of pKOV Kan mORF51 into HVS-GFP-BAC via a recombination event at one of the two homology regions flanking mORF51. Depending on the site of recombination, the plasmid could be inserted in 2 different orientations (shown in Figure 3(b)). It is preferable to obtain cointegrants in both orientations as one may be more dynamically favourable for the subsequent recombination step (being more likely to produce a mutant clone rather than revertant, due to steric hindrance). Both orientations can be identified by AgeI restriction digest analysis of purified HVS DNA (Figure 3(a)).
12 possible cointegrant clones were investigated using AgeI restriction analysis and then separated on a pulse field electrophoresis gel. These were compared to the “wild-type” HVS-GFP-BAC. All 12 had a restriction pattern consistent with pKOV Kan mORF51 insertion. Figure 4 shows four of these clones 3, 4, 8, and 9 with the HVS-GFP-BAC digest. As predicted, the 130kb band present in the HVS-GFP-BAC lane has been digested into two smaller bands in the cointegrant clones, indicating that pKOV Kan mORF51 has successfully inserted into the genome at the correct location. These clones also clearly show the two different expected restriction patterns consistent with both possible orientations of pKOV Kan mORF51. Clones 3 and 4 have the pKOV Kan mORF51 vector in orientation 1, whereas clones 8 and 9 are in orientation 2 (as predicted in Figure 3). Interestingly, the largest fragments in clones 8 and 9 are different sizes due to the variable terminal repeat region in the H-DNA of the genome. After sequence analysis to assess for any unwanted mutation, these four clones were used for further recombination.
Clones 3, 4, 8, and 9 were made chemically competent and then transformed with pDF25-Tet to induce a second recombination event. This could result in either a revertant or a mutant clone as shown in Figure 5. After the appropriate selection, BAC DNA from resulting clones was purified by miniprep, digested with AgeI, and analysed by pulse field electrophoresis. Colonies were formed after recombination of cointegrants 3 and 9. Figure 6(a) shows the restriction analysis of 6 colonies from each of these cointegrants (representative of 12 screened). HVS-GFP-BAC was also digested as a negative control. All of the colonies originating from cointegrant 3 have reverted back to “wild type,” showing the same restriction pattern as the HVS-GFP-BAC lane. The loss of the AgeI restriction site at ~80kb on the restriction map (Figure 3) restores the ~130kb band seen with “wild-type” viral DNA. Clones 9A, 9B, and 9F are also revertants. The restriction pattern of 9C is not consistent with either a revertant or mutant genotype, with a band at approximately 95kb. This may have been due to the genome undergoing a deletion. 9E seems to have a dual population of genomes, some of which have reverted and some of which have retained the mutant copy of the gene. However, 9D shows the correct restriction pattern and therefore has the pKOV Kan plasmid removed while retaining the mutation.
As seen in Figure 6(b), the revertant restriction pattern is identical to the “wild type,” however, the bands for the mutant clone 9D are slightly different in size to its parental cointegrant 9. This is due to the removal of the 7kb plasmid, shortening the 52kb band seen with cointegrant 9 to 45kb. Sequence analysis confirmed the presence of the mutant gene in the HVS mORF51 genome, and working stocks of the recombinant virus were then produced by transfection into permissive OMK cells.
To investigate the effects of mutating ORF51, a panel of cell lines were infected with HVS-GFP-BAC or HVS mORF51, and the infection rate for each cell line was compared. Due to potential changes in vector tropism, infectivity was compared by analysing dose-dependent rates of infection using increasing viral titres. The resulting fluorescence was measured as an indication of the level of infection using flow cytometry. Examples of the raw dot plots obtained when infecting permissive OMK cells with HVS-GFP-BAC are shown in Figure 7(c). Data confirm previous experiments in our laboratory showing that HVS-GFP-BAC can infect a wide range of human cancer cell lines [6, 28]. Figure 7(a) shows the percentage of HVS-GFP-BAC infected cells (measured by GFP expression) in a range of human cell lines, including lung, colon, and liver. Also shown is infection in the fully permissive OMK cell line as a positive control. HVS-GFP-BAC has a high tropism for the Huh7 and 7.5 cell lines, with an m.o.i of 2 infecting nearly 100% of cells. The HepG2 liver cancer cell line is less efficiently infected, with the same titre infecting only 35% of the cells. Interestingly the infection rate in HCC cell lines is higher than that observed in lung, colorectal, and the human embryonic kidney cell line. As expected, the OMK cells are relatively well infected.
When an equivalent titre of HVS mORF51 virus was used to infect the same cell lines, a distinct infection profile is observed (Figure 7(b)). All three HCC cell lines have similar infection rates to those previously observed with the “wild-type” HVS-GFP-BAC virus, for example, 30% of HepG2 cells are infected compared to a 35% infection with HVS-GFP-BAC. However, the level of infection for all the other cell types decreased dramatically. This effect appears most prominent with the OMK cell line, where HVS-GFP-BAC at an m.o.i of 2 results in an 80% infection rate as measured by fluorescence, whereas the same titre of HVS mORF51 infected on average 17% of cells.
This pattern can be more clearly observed in Figure 8. Here, the HVS mORF51 infection (using an m.o.i of 2) is displayed as a ratio of the infection seen with the equivalent titre of HVS-GFP-BAC. This removes the variability of viral tropism and allows a more relevant comparison of different cell types. Where HVS mORF51 can infect HCC cell lines to a similar extent to HVS-GFP-BAC (over 80%), infection levels of the mutant virus in A549 lung carcinoma cell line, OMK, and HEK 293T are all reduced to only ~20% of “wild-type” infection. The SW480 infection is most attenuated by the mutation, retaining only 4% of “wild-type” infection. These results suggest that mutation of the ORF51 protein affects viral entry in certain cell types. The mutation in HVS mORF51 is designed to ablate the heparan sulphate-binding role of the protein, and this loss of function may be responsible for the decreased infection rates. Alternatively, the insertion of the SSTR binding motif may have provided a gain of function to the protein, allowing higher rates of infection specifically in the HCC cell lines.
Somatostatin is a repressor of gastrointestinal hormone production and also inhibits the release of insulin and glucagon from the pancreas [41, 42]. Therefore, somatostatin receptors are present in healthy pancreatic tissue. It has been documented that during the development of pancreatic cancer the expression of these SSTRs is lost . Consequently, pancreatic cancer cell lines would provide a suitable negative control cell for HVS mORF51. We compared HVS mORF51 infection between these cells and pancreatic cancer cell lines stably transfected with a construct expressing SSTR1 . Figure 9 shows the infection levels observed, measured by GFP expression. In both cell lines, there was no increased infectivity in the SSTR1-positive cells. Surprisingly, the infection rate was slightly higher in the SSTR1 negative cells. This result indicates that the high levels of infection observed in the HCC cell lines may not be due to the presence of SSTR1 on the cell membrane. However, there are 5 types of SSTR, and although the SSTR binding motif used in the HVS mORF51 mutation should bind all 5 of these G- protein coupled receptors, it may have higher affinities for certain receptors than others, especially if it is in a restricted conformation.
The natural cellular ligand of ORF51 is purported to be heparan sulphate-containing proteoglycans present on the surface of cells.Means  demonstrated that ORF51 binds heparin and that soluble heparin inhibits HVS infection of OMK cells. To confirm these results, thisexperiment was repeated using a flow cytometry assay measuring GFP-expression as an indicator of viral infection. Soluble heparin was incubated with cells for 1h at 37°C prior to the addition of HVS-GFP-BAC or HVS mORF51. The heparin neutralisation curve for HVS-GFP-BAC is shown in Figure 10. Results demonstrate that as the concentration of soluble heparin was increased from 0.01 to 1mg/ml an initial slight increase in viral infection was observed as previously reported by Means , followed by a sharp decline in GFP expressing cells. The percentage of GFP positive cells drops from 77% in the absence of heparin to 12% at a heparin concentration of 1mg/ml. This result is also consistent with previously published findings and indicates that the assay is appropriate for measuring any change in viral entry. Also shown in Figure 10 is the neutralisation curve for HVS mORF51. A similar pattern is seen for the mutant virus; however, the decrease in GFP positive cells is less marked. The percentage of infected cells falls from 63% to 25%, suggesting that although heparin does interfere with viral entry in HVS mOR51, this virus is less dependent on binding heparin than its “wild-type” counterpart. HVS viral entry involves several glycoproteins and some, including gB, are also capable of binding heparin. Therefore, the only partial neutralisation observed for HVS mORF51 may be due to soluble heparin interacting with gB. Moreover, the decreased neutralisation activity of soluble heparin on HVS mORF51 compared to HVS-GFP-BAC may be due to the removal of the heparan sulphate-binding motif from ORF51 of the virus, making it less sensitive to competitive inhibition.
To further investigate the role of SSTRs in HVS mORF51 infectivity, the heparin neutralisation assay was modified to measure the effects of the 14-amino acid peptide somatostatin on virus entry. Again, concentrations from 0.01 to 1.0mg/ml of soluble somatostatin were initially used; however, incubation with 1mg/ml somatostatin proved to be toxic to the cells (Figures 11(a) and 11(b)). Therefore, the 1.0mg/ml measurement was removed. Figure 10 plots the infection rate of HVS-GFP-BAC and HVS mORF51 against somatostatin concentration. Neither HVS-GFP-BAC nor HVS mORF51 appear to be neutralised by somatostatin. The infection rate at 0.25mg/ml is similar to the rate when no somatostatin was added. The percentage GFP expression does decrease slightly when incubated with 0.5mg/ml somatostatin, but this may be due to such a large amount of the peptide having an adverse effect on cell metabolism. Somatostatin naturally occurs in much lower concentrations in human plasma, typically around 50 pg/ml. These results are consistent with the data obtained using the SSTR1-expressing cell lines and seem to imply that although the mutation has impaired the heparin-binding ability of mORF51, the protein does not bind somatostatin receptors.
The data so far suggests that HVS mORF51 has not gained the ability to bind SSTR expressing cells. However the toxic nature of high concentrations of somatostatin make interpretation of the neutralisation assay difficult. For this reason the assay was repeated, using an antibody raised against all 5 subtypes of somatostatin receptor. An antibody against mouse IgG was used as a negative control. The results of the neutralisation trial are shown in Figure 12. The level of GFP expression is fairly constant in all four assays, suggesting that increasing concentrations of SSTR antibody, as well as the antibody against IgG, fail to neutralise viral entry, irrespective of the mutated ORF51 protein. This result is consistent with the previous data and contradicts the hypothesis that somatostatin receptors are used for HVS mORF51 entry.
Viruses are powerful gene therapy tools as they have evolved to efficiently enter their target cells and manipulate those cells into transcribing and translating their genetic material. To further exploit their gene therapy potential, techniques have been developed to retarget a virus to specifically enter or block entry to a particular cell type. Retargeting involves the modification of proteins on the surface of the virion and can be achieved by several means; molecules such as PEG can be covalently attached to the virus surface (although this is better described as detargeting) [44, 45]. Alternatively, specific viral proteins can be modified to enhance binding to target cells. Bispecific molecules such as bivalent ScFvs or antibodies covalently conjugated to ligands can alter binding [46, 47], or genetic mutation of viral proteins can provide a permanent change in tropism [48, 49].
Genetic modification affects all copies of the protein and would be preferable in conditionally replicating vectors to maintain targeting in the progeny virus. However, recombination is time consuming, and the mutation may impair virus production. Chemical modification is a more flexible system, allowing conjugation of multiple targeting ligands to one viral particle. The ratio of conjugated viral proteins can also be adjusted to suit the application, but production of bispecific peptides and/or antibodies is costly. Both strategies have been successfully applied in preclinical studies, suggesting that vector retargeting could have clinical benefit. We chose to use a genetic approach to ensure that all copies of the target protein contained the new binding motif.
We have mutated the HVS glycoprotein ORF51 in order to increase binding to hepatocellular carcinoma cells. The putative heparan sulphate-binding region of this protein was replaced with a motif designed to bind somatostatin receptors, which are overexpressed in this form of cancer. RecA-mediated recombination was used to introduce this specific mutation into the large HVS genome, as this powerful technique can mutate a single base in the context of the 170kb virus. The desired mutation resulted in the exchange of just 17 amino acids, swapping residues 214–228 of ORF51 (SKHTNKLKPFKHKLQ) with the sequence (RSPTGACRFWKTWCKRS). The underlined SSTR binding sequence was flanked by codons that contain restriction sites required for cloning and analysis.
The engineered HVS mORF51 virus was then used to infect a range of cancer cell lines to investigate any difference in tropism compared to wild type HVS. The mutant virus demonstrated a striking affinity for HCC cells while showing a reduced infectivity in other cell types, including the permissive owl monkey kidney line. Surprisingly, further investigation revealed that HVS mORF51 did not bind SSTRs, and that this change in tropism was due to another as yet unidentified mechanism. As the introduced mutation disrupts native ORF51 function, these results suggest that ORF51 is not required for HCC entry but does play a role in cell entry in a number of human cells.
ORF51 may act in a similar manner to EBV gp42, which is required for B-cell entry, but not for epithelial cell infection . Other HVS glycoproteins such as gM and gN may facilitate initial binding of HCC cells or be involved in membrane fusion. To determine the essential glycoproteins required for entry in particular cell types, a series of mutant viruses with deleted glycoproteins could be constructed and characterised for infectivity. Although time consuming, this collection of viruses would provide a wealth of data regarding HVS infection and could aid in identification of corresponding cellular receptors for these glycoproteins. Alternatively, to locate possible HVS ligands on HCC cells, a cDNA library of HCC genes could be produced in OMK cells and virus-binding assays performed.
We cannot conclude that functional ORF51 is expressed in the HVS mORF51 virus therefore, the nature of the mutant protein can at present only be speculated. It is possible that the mutation caused such a dramatic change in structure that the protein cannot attain its native conformation, causing degradation. Alternatively, oligomerisation may have been affected, preventing ligand binding. Similarly, the SSTR binding region may be obscured, or in the wrong orientation to allow ligand interaction. The SSTR binding sequence itself contains an essential disulphide bridge between the flanking cysteine residues. Disruption of this bond would prevent the mORF51 protein-binding SSTRs on HCC cells. Investigation into the structural status of wild-type and mutant ORF51 could provide valuable data about its function. In addition, further studies with purified mORF51 protein could be carried out to assess its binding capabilities to SSTRs compared to wild-type ORF51. Expression would have to be performed in a eukaryotic system to ensure that the protein is appropriately glycosylated. Moreover, it would be interesting to determine the cell infectivity profile of a HVS ΔORF51 virus, to assess if ORF51 is required for HCC cell entry, in contrast to other cell lines.
ORF51 shares genomic colinearity with EBV gp220/350, which binds complement receptor 2 (CR2) on host B cells . This induces a signalling cascade which results in upregulated proliferation. It is possible that HVS ORF51 has a separate ligand in addition to heparan sulphate, and that interaction with this receptor induces beneficial changes to the intracellular environment for the virus. Many viruses have evolved to bind receptors that stimulate specific signalling pathways, which “prime” the cell for viral infection in this manner. Therefore, mutation of these viral proteins, and subsequent disruption of signalling may affect viral fitness and transgene expression by reducing the ability of the virus to control the cellular environment. This may contribute to the reduced infectivity of HVS mORF51. This phenomenon should be taken into account when designing retargeted vectors. One way to tackle this problem is to retain a wild-type copy of the mutant gene in the viral genome; however, this may mask the effects of the mutated protein.
HVS infection is a complex process, involving a variety of viral glycoproteins that act in concert to facilitate entry in HCC cells. Little research has been conducted into how these glycoproteins interact with cellular receptors and each other during this process. The data described here illustrates that ORF51 contributes to efficient cell entry in a number of human cell lines but does not appear to be involved in HCC cell entry. From these findings, it is clear that mutation of ORF51 has practical implications for HVS in gene therapy. Therefore, this research highlights the potential of a retargeted HVS-based vector in redirecting cell tropism.
The authors wish to thank Dr. Li Min of the Baylor College of Medicine, Houston, Texas for the kind donation of the pancreatic cancer cell lines stably expressing SSTR1. Thanks also go to Dr. Robert White of Imperial College London, for his guidance and expertise with the RecA-mediated recombination system, and to Gareth Howell of the University of Leeds for his technical assistance with the FACS data. This work was supported by the BBSRC.