INTRODUCTION

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In recent years, both cellular and viral RNAs have been reported to be packaged in virions of human cytomegalovirus (CMV) (1, 4, 7). The observations are of particular interest for several reasons. Foremost, human CMVs are among the largest viruses infecting cells of higher organisms. In addition, these viruses, members of the Herpesviridae family, incorporate into their virions numerous proteins with multiple functions that effectively assist in the creation of an effective intracellular environment for rapid takeover and redirection of cellular functions to the benefit of the virus. In comparison with other members of Herpesviridae family, the functions encoded in their genomes and the ready-made proteins brought into cells during infection should be more than sufficient to render the infected cell a very pliant client. The presence of the RNAs in virions is therefore an unexpected, novel, intriguing facet of herpesvirus biology.

Following the basic premise that viruses do not perform gratuitous functions, we decided to determine whether herpes simplex virus type 1 (HSV-1) virions also contain RNAs and to determine their function. The advantage of HSV-1 is twofold. First, HSV-1 contains fewer open reading frames (ORFs) and the pattern of transcription of the viral genome has been extensively studied. Second, the major functions of HSV-1 gene products are at least in part understood. Hence, if RNAs were packaged in virions, we would have a basis on which to evaluate the significance of the packaged mRNAs.

The purification of HSV-1 virions has been extensively studied and characterized (5, 10). In this report, RNAs extracted from either intracellular or extracellular purified virions after RNase digestion were reverse transcribed, amplified by PCR, and subjected to two kinds of analyses. We report that a fraction of the HSV RNAs are represented in RNAs extracted from purified preparations and that the RNA transcripts of nine ORFs were detected in all purified preparations tested. We also report the presence of cellular RNAs in purified virions. In this instance, the selectivity of the packaged RNAs is less well apparent.

	MATERIALS AND METHODS

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Cells and viruses. Vero and HEp-2 cell lines (American Type Culture Collection) and a rabbit skin cell line (originally obtained from J. McLaren) were propagated in Dulbecco's modified Eagle's medium supplemented with 5% newborn calf serum. HSV-1(F) is the prototype HSV-1 strain used in this laboratory (2). Isolation of the mutant virus R7023 was described elsewhere (6). R7023 lacks the genes U_S8 through U_S12. Titers of the stocks of HSV-1(F) and R7023 on Vero cells were determined.

Purification of virions. HSV-1 and R7023 virions were purified as described by Spear and Roizman (10). Briefly, Vero or HEp-2 cells grown in roller bottles or in 150-cm² flasks were exposed to 5 PFU of virus per cell. The cells were harvested 22 to 24 h after infection and centrifuged at 2,000 rpm for 10 min in an Allegra 6R centrifuge equipped with a GH-3.8 rotor (Beckman Coulter, Inc., Fullerton, Calif.). The supernatant fluids and the infected-cell pellets were collected and processed separately. Viral particles in the supernatant fluids were recovered by centrifugation at 20,000 rpm for 1 h at 4°C in an Optima LE-80K ultracentrifuge equipped with an SW28 rotor (Beckman Coulter, Inc.). The cell pellet was resuspended in 1 mM phosphate buffer and disrupted in a glass homogenizer with three strokes for Vero cells and two strokes for HEp-2 cells. Extracellular and cytoplasmic fractions were individually layered on 36-ml dextran-10 gradients (1.04 to 1.09 g/cm³) in 1 mM phosphate buffer. The gradients were centrifuged for 1 h at 20,000 rpm at 4°C in an Optima LE-80K ultracentrifuge equipped with an SW28 rotor. After centrifugation, virion-containing bands were collected and diluted in 10 mM phosphate buffer. Purified virions were concentrated by pelleting at 25,000 rpm for 2 h as described above. The pellets were resuspended in 200 to 300 µl of 10 mM phosphate buffer and stored at 20°C before processing.

Isolation of RNA from virions. A 100-µl volume of purified virions was digested with 5 µl of RNase I (100 U/µl) for 3 h at 37°C. After RNase I digestion, RNA was extracted from virions with the aid of RNAquose-4PCR Kit (Ambion, Austin, Tex.) according to the manufacturer's instructions. The purified RNA samples were resuspended in 200 µl of elution buffer (1 mM EDTA; Ambion) and treated with 10 U of DNase I (Life Technologies, Rockville, Md.) for 3 h at 37°C. Fragmented DNA contamination was removed by phenol-chloroform extraction (Fisher Scientific, Huntsville, Ala.), followed by ethanol precipitation. Each sample was dissolved in 20 µl of diethyl pyrocarbonate-treated water.

Preparation of DNA probes from virion RNAs for cDNA arrays. Ten microliters of RNA purified from viral particles was used to generate radioactively labeled cDNA with the aid of an avian myeloblastosis virus (AMV) reverse transcriptase (RT) system (Promega, Madison, Wis.). The reverse transcription was primed with a mixture of oligo(dT)₁₅ primer and random hexanucleotides and performed in the presence of 1 mM dATP, dGTP, and dTTP (Pharmacia, Piscataway, N.J.) and 10 µl of [³²P]dCTP (Amerham Pharmacia; concentration, 10 mCi/ml; specific activity, 3,000 Ci/mmol) in a total reaction volume of 35 µl. The mixture was incubated at 42°C for 45 min, shifted to 52°C for 45 min, and then heat inactivated at 95°C for 5 min. The labeled cDNAs were purified by passage through a Micro BioSpin-6 chromatography column (Bio-Rad, Hercules, Calif.). The efficiency of [³²P]dCTP incorporation was determined in a liquid -spectrometer (Beckman Coulter, Inc.).

Isolation and reverse transcription of RNA extracted from infected cells. HEp-2 and rabbit skin cell lines were infected with HSV-1(F) and harvested 22 and 18 h postinfection (p.i.), respectively. Total RNA was extracted with the aid of TRIZOL reagent according to the manufacturer's instructions (Life Technologies). Poly(A)⁺ RNAs were purified from total RNA with the aid of an Oligotex mRNA Midi Kit (Qiagen). One microgram of poly(A)⁺ RNA was used to generate labeled cDNA by reverse transcription in the presence of [³²P]dCTP. The reverse transcription was done as described above.

Preparation of HSV cDNA arrays. The HSV-1 arrays were made by printing cDNA probes on nylon membranes (VP-Scientific, Inc., San Diego, Calif.). Briefly, primer pairs were designed to amplify approximately 300- to 400-bp fragments of all the known expressed HSV-1 ORFs. Two rounds of PCR amplifications were done. In the first round, a complete set of HSV-1(F) ORFs was amplified from a set of plasmids and cosmids (Table 1). In the second round, the PCR products obtained in the first round were purified and reamplified with the same pairs of primers. The conditions used were as follows: 1 min at 94°C, 1 min at 60°C, 90 s at 72°C for 35 cycles. The final PCR products were diluted to 100 to 200 ng/ml and denatured in 0.8 M NaOH-20 mM EDTA (pH 8.0) at 94°C for 10 min. The arrays were printed with either 10 or 20 ng of amplified DNA per spot onto nylon membranes with the aid of a 380-pin replicator treated with VP110 surfactant (VP-Scientific). The DNA was cross-linked to the membranes with UV light. To test for the reproducibility of delivery, a second set of spots was printed slightly offset relative to the first one.

Hybridization of labeled cDNA to HSV-1 and human cDNA arrays. The membranes imprinted with the HSV-1 cDNA array were preincubated for 4 h at 42°C in 5 ml of MicroHyb prehybridization solution (Research Genetics, Huntsville, Ala.). The prehybridization solution contained 5 µl of poly(dA) (1 µg/µl; Research Genetics) and 5 µl of human Cot-1 DNA (1 µg/µl; Life Technologies). Pure labeled DNAs, derived from viral purified RNAs, were diluted in 5 ml of MicroHyb solution and incubated separately overnight at 42°C. The membranes were then rinsed first with 2× SSC + 1% sodium dodecyl sulfate (SDS) and successively with 0.1× SSC + 1% SDS solutions (1× SSC is 0.15 M NaCl plus 0.015 M sodium citrate). The same membrane was also hybridized with labeled DNAs derived from total RNA extracted from rabbit skin or HEp-2 infected cell lines under the same conditions described above.

Reverse transcription and PCR amplification of RNA extracted from virions. RNAs extracted from purified viral particles derived from HSV-1 and R7023 was reverse transcribed to yield single-stranded cDNA using 60 U of AMV RT (Promega) in a total reaction volume of 20 µl. The reverse transcription was primed with oligo(dT)₁₅ primer and performed using a pool of nucleotides consisted of 1 mM concentrations (each) of dGTP, dATP, dTTP, and dCTP (Promega). Forty units of RNasin (Promega) were added to each reaction mixture. The mixture containing only the RNA template, and the oligo(dT)₁₅ was first heated at 70°C for 10 min, chilled on ice, and after the addition of the other components, incubated at 42°C for 45 min, shifted at 52°C for 45 min, and then heat inactivated at 95°C for 5 min.

View larger version (94K): [in this window] [in a new window]   FIG. 1.   Primer sequences.

In vitro translation of purified virion RNAs and immunoprecipitation of U_L48 protein. RNAs extracted from extracellular virions purified from HSV-1(F)-infected HEp-2 cell cultures were translated in vitro in the presence of [³⁵S]methionine with the aid of a rabbit reticulocyte lysate system according to the manufacturer's instructions (Promega). Briefly, 10 µl of RNAs were incubated for 90 min at 30°C in the presence of 40 µCi of [³⁵S]methionine (1,200 Ci/mmol; Amersham) and 35 µl (70% concentration) of the Promega rabbit reticulocyte lysate in a total volume of 50 µl. The labeled translation products were mixed with 250 µl of phosphate-buffered saline buffer containing 1% NP-40 and a cocktail of protease inhibitors (Sigma) and then precleared with preimmune rabbit serum and 50% (vol/vol) protein A (Sigma) for 2 h at 4°C. The U_L48 protein were immunoprecipitated from the total translation mixture with a monoclonal antibody specific for U_L48 (a kind gift of T. Minson, Cambridge, United Kingdom) and protein A (50%) overnight at 4°C. The immune complexes were rinsed three times in phosphate-buffered saline and disrupted by addition of 40 µl of 1× SDS gel loading buffer (2% SDS; 5% -mercaptoethanol; 50 mM Tris, pH 6.8; 2.75% sucrose). Samples were heated at 95°C for 4 min, resolved by 10% polyacrylamide gel electrophoresis, and transferred to a nitrocellulose sheet for autoradiography.

	RESULTS

Top Abstract Introduction Materials and Methods Results Discussion References

Experimental design. The studies described in this report were done on four virion preparations, which were as follows: (i) HSV-1(F) virions derived from intracellular extracts of Vero cells, (ii) HSV-1(F) virions derived from intracellular extracts of HEp-2 cells, (iii) HSV-1(F) virions derived from extracellular medium of infected HEp-2 cells, and (iv) R7023 virions derived from extracellular medium of infected HEp-2 cells. In order to cover the entire transcribed domain of HSV-1, a set of 90 pairs of primers was designed to amplify all 84 expressed ORFs of HSV (Fig. 1). The analyses were done as described in Materials and Methods.

Detection of viral cDNA derived from DNA-free purified virions by HSV-1 cDNA array. The objectives of this series of experiments were twofold. The first was to determine what subset of total viral RNAs accumulating in infected cells could be detected by labeled product of reverse transcription of RNA extracted from infected cells under the conditions described in Materials and Methods. The second objective was to verify the presence and identity of RNAs extracted from purified virions by an additional method. Two series of experiments were done.

View larger version (101K): [in this window] [in a new window]   FIG. 2.   Photographs of autoradiographic images of HSV-1(F) cDNA array. The HSV-1 cDNA arrays representing the known ORFs were constructed as described in Materials and Methods. A total of 75 cDNA arrays were imprinted in duplicate as described, and the identity of each spot is listed in Table 2. (A and B) The arrays were hybridized with 32P-labeled cDNAs derived from poly(A)+ RNA extracted from infected HEp-2 or rabbit skin cells, respectively. (C) The same cDNA array was hybridized with 32P-labeled cDNA derived from RNA extracted from virions purified from extracellular medium of infected HEp-2 cells.

Identification of viral RNA species by reverse PCR of DNA-free RNA extracted from purified virions. The procedure involved in this series of experiments consisted of two steps. In the first round of analyses, we reverse transcribed RNAs extracted from purified virions and amplified the cDNAs by PCR. In the second step, all RNAs found to be positive were retested both by reverse PCR and by PCR without reverse transcription to eliminate the possibility that the positive results were due to contaminating DNA. A photograph of the bands obtained after reverse transcription and PCR amplification of the nine RNAs reproducibly detected in all three experiments are shown in Fig. 3. In each instance, we detected an amplified DNA band with the correct size only after reverse transcription followed by PCR amplification, indicating that the detected material was RNA and not contaminating DNA.

View larger version (76K): [in this window] [in a new window]   FIG. 3.   Photographs of DNA bands derived by reverse transcription and PCR amplification of RNAs extracted from HSV-1(F) virions using primers of selected ORFs. RNAs derived from HSV-1(F) virions was reverse transcribed as described in Materials and Methods. The PCR was performed with primers specific for the HSV-1 ORFs indicated. The selected ORFs were those of RNAs detected in all virion preparations. Vero/I and HEp-2/I, virions purified from homogenized infected cells; HEp-2/E, virions purified from extracellular medium. Lanes RT+, presence of RT in the RT mixture; lanes RT, control reactions in which RT was omitted; lanes CTR+, plasmid DNA containing the sequence of the indicated ORF was used as template; lanes CTR, no template was added to the PCR mixture; lanes MW, 1-kb DNA ladder used as a size marker.

Analyses of virion mRNA in deletion mutant R7023 lacking genes U_S8 though U_S12. A major component of the virion capable of binding RNA is the U_S11 protein. This protein was shown earlier to bind RNA in a conformation- and sequence-specific manner. The only RNAs previously shown to bind U_S11 protein included U_L34 mRNA and an RNA mapping antisense to the U_S11 and U_S12 ORFs. To test the role of this protein in the packaging of RNA in virions, we analyzed the RNAs extracted from purified extracellular virions of HEp-2 cells infected with the mutant virus R7023. The results of this experiment are included in Table 2. As expected, we did not detect cDNA representing U_S8 through U_S12. With these exceptions, all of the RNAs reproducibly detected in wild-type virions were also detected in purified R7023 virions (Fig. 4).

View larger version (70K): [in this window] [in a new window]   FIG. 4.   Photographs of DNA bands derived by reverse transcription and PCR amplification of RNAs extracted from R7023 mutant virions using primers of selected ORFs. The selected ORFs were those of RNAs detected in all virion preparations. Note that the R7023 mutant lacks the genes US8 through US12. The procedures were the same as those described in the legend to Fig. 3. Lanes RT+, presence of RT in the RT mixture; lanes RT, control reactions in which RT was omitted; lanes CTR+, plasmid DNA containing the sequence of the indicated ORF was used as template; lanes CTR, no template was added to the PCR mixture; lanes MW, 1-kb DNA ladder used as a size marker.

Detection of cellular cDNA derived from DNA-free purified virions by a human gene array. The purpose of this series of experiments was to determine whether cellular RNAs were also represented among RNAs extracted from purified virions. Specifically, the labeled cDNA from purified intracellular and extracellular virions were sequentially hybridized to a Research Genetics cDNA array (GF2111) containing probes for >4,000 known human genes (Fig. 5B and C, respectively). The results obtained with labeled cDNA derived from purified virions may be compared with the results of analyses on similar cDNA array of labeled cDNA derived from HSV-1-infected HEp-2 cells (Fig. 5A). The cDNA derived from these cells hybridized to approximately 1,500 probes. A detailed comparison of the hybridization of the labeled DNA derived from virions and that of RNA derived from the infected cells could not be done for two reasons. First, the cDNA derived from the infected cells RNA was labeled with ³³P in contrast to the ³²P-labeled DNA prepared from virion RNAs. The consequences were that the signal derived from virion cDNA arrays was more likely to impinge on signals derived from hybridization to nearby probes. Second, the virion RNA lacked the marker RNAs that would permit precise alignment of the autoradiographic images of the cellular and virion cDNA arrays. Nevertheless, the overall patterns are strikingly similar with respect to both position and relative intensity of the signal. Some of the cellular DNAs were readily identified on that basis (Fig. 5A, B, and C, arrows). The relatively abundant cellular genes identified in Fig. 5 are shown in Table 3.

View larger version (67K): [in this window] [in a new window]   FIG. 5.   Autoradiographic image of a human cDNA array hybridized to labeled cDNAs derived from cellular or virion RNAs. (A) Human cDNA array (GF2111; Research Genetics) membrane was probed with 33P-labeled cDNA generated by reverse transcription of total RNA isolated from HSV-1-infected HEp-2 cells 22 h after infection. The same membrane was probed with 32P-labeled cDNA generated by reverse transcription of RNA isolated from intracellular (B) or extracellular (C) purified HSV-I(F) virions from infected HEp-2 cells. Arrows indicate relatively abundant mRNA species consistently positive in all preparations.

In vitro translation of purified virion RNA and immunoprecipitation of U_L48 protein. This experiment was designed to determine whether the RNA detected in virions was intact or fragmented oligoribonucleotides. As described in Materials and Methods, the RNAs were translated in vitro in the presence of [³⁵S]methionine. The translation mixture was reacted with monoclonal antibody to U_L48 protein, and the immune complexes recovered with protein A were subjected to electrophoresis in denaturing polyacrylamide gels. As shown in Fig. 6, lane 3, the closely migrating labeled doublet had the immune reactivity and electrophoretic mobility of the U_L48 protein, suggesting that at least some of the RNAs whose presence we have detected in virions were intact.

View larger version (80K): [in this window] [in a new window]   FIG. 6.   Autoradiographic images of in vitro translation of purified virions RNAs and subsequent immunoprecipitation with UL48 antibody. Lane 1, autoradiographic image of electrophoretically separated products of in vitro translation of virion RNAs; lane 2, electrophoretic mobility of the in vitro translation mixture to which no exogenous RNA was added (negative control); lane 3, autoradiographic image of the electrophoretically separated immunoprecipitate of the translation products shown in lane 1 obtained with the anti-UL48 antibody; lane 4, the autoradiographic image of electrophoretically separate precipitate obtained from the translation products shown in lane 2 with the anti-UL48 antibody.

	DISCUSSION

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It is convenient to begin the discussion with a summary of the results and their conclusions. In essence, (i) we designed primers for amplification of probes corresponding to HSV-1 ORFs to detect all of the transcripts expressed in infected cells. Labeled DNA derived from poly(A)-selected RNA purified from infected cell hybridized to all but two of the probes in the cDNA array, validating the primer set.

(ii) We have detected and identified RNA species in extracts of purified intracellular and extracellular virions by two methods: hybridization of labeled DNA strands reverse transcribed from virion-extracted RNA and by PCR-assisted amplification of DNA strands reverse transcribed from virion RNA. The packaged RNA species identified by both methods represented a subset of viral transcripts detected in the population of poly(A)-selected RNA extracted from infected cells. Of this subset, only a small set comprising nine RNAs was reproducibly detected in all preparations tested. In one case, we were able to establish that the RNA was intact and encoded a full-length protein. Several aspects of the data require elaboration since they impinge on the overall conclusions of this report. First, the assays based on RT-PCR yielded unambiguous, i.e., positive or negative, results, but these were not fully reproducible from one preparation to another. Of the 27 RNAs detected at least once, only nine were positive in all preparations. The nine RNAs present in all virion preparations are likely to be a minimal set, defined by an abundance of specific RNAs in either the infected cells or in virions or to as-yet-undefined limitations of the RT-PCR. The cDNA arrays, on the other hand, did not yield discontinuous values. As is the case for all analyses of data derived from microarrays, we set a cutoff threshold based on the intensity of the signal. The 24 mRNAs defined as positive on the basis of this criterion included the seven mRNAs reproducibly detected in virions by RT-PCR. The remaining two were barely detected by hybridization of cDNA derived from total infected-cell DNA and therefore may reflect a defect in the cDNA array rather than an absence from virions. The necessary conclusion, however, is that by both procedures we identified only the most abundant RNAs associated with virions rather than the entire set of mRNAs that may be present. It remains to be determined how the abundance of the mRNAs detected in this study translates into average RNA molecules per virion.

(iii) We could not associate the presence of specific RNAs in the virion with the presence of the U_S11 protein shown earlier to bind RNA.

(iv) Cellular RNAs were also detected in RNA extracted from virions. In this instance, a superficial analysis of the cellular RNAs suggests that virions contain the more abundant species of cellular RNAs.

The key issues that arise from the data are the specificity and significance of the RNAs extracted from purified virions. Relevant to these issues are the following. (i) The presence of viral RNA in virions does not appear to be the result of simple contamination of virions with cellular debris containing RNA. There are three reasons for this conclusion. First, the major contaminating components of purified virions are membranous vesicles that cosediment in dextran-10 gradients. These vesicles arise in part during homogenization and would be expected to be more numerous in preparations of intracellular virus than in virus released into the extracellular medium. We have not found significant differences between the RNAs packaged in extracellular and intracellular virions. Moreover, the nature of the RNAs detected in the virion preparation argues against the hypothesis that the detected RNAs were derived from cosedimenting cellular vesicles. If membranous vesicles were the source of the RNA, we would expect to see a prevalence of RNAs bound to membranes. Only U_L10 (gM), U_S4 (gG), and possibly U_L34 mRNAs were reproducibly found in virions. The failure to find U_S6 (gD) RNA or, more significantly, the U_L44 (gC) RNA expressed late in infection is inconsistent with the hypothesis that membranous vesicles are responsible for the presence of RNA in virion preparations. Second, the results are inconsistent with the hypothesis that the RNA detected in these preparations represents mRNA that is resistant to RNase digestion. Thus, in vitro translation of the RNAs extracted from virions resulted in the synthesis of high-molecular-weight proteins. Analyses of the in vitro translation products revealed the presence of full-length VP16, a finding inconsistent with the hypothesis that the detected RNAs represent incompletely digested RNAs. Lastly, even assuming that all RNAs are present in virions but that the majority are present at an abundance below the level of detection, the nine RNAs reproducibly detected in virion preparations by RT-PCR were not uniformly the most abundant RNAs present in infected cells at the moment of harvest as illustrated in Fig. 2. The firm conclusion is that while the species detected in virions may simply reflect their abundance above the limits of detection, they are not representative of the most abundant viral RNA species accumulating in infected cells.

(ii) The hypothesis that the RNAs represent a selection of RNAs present in infected cells during the process of viral maturation raises the question as to the basis of the selectivity. We can exclude the hypothesis that they represent a single kinetic class: of the nine RNAs reproducibly found in virion preparations by RT-PCR, one is an -RNA (U_S1/1.5), one is a -RNA (U_L42), and the rest are -RNAs. We can also exclude high G+C content that could be responsible for the unusual secondary structures since the conserved RNAs are on the average 63 to 67 G+C mol%, and RNAs of much higher G+C content (e.g., U_L26, U_L43, 0, 4, ORF P, ₁34.5, etc., in the range of 71 to 84 G+C mol%) were not reproducibly detected in virion preparations. If sequence or structure were the basis for the selectivity of the packaged RNAs, they have not been identified. To some extent, the sequence and structural basis for the selectivity of the packaged RNA is compromised by the evidence that a large number of cellular RNAs are also packaged, and in this instance, selectivity is less readily demonstrable.

Of the proteins packaged in the virion, U_S11 is known to bind RNA in a sequence- and conformation-specific fashion (9). Since the repertoire of RNAs packaged in virions of R7023 mutant lacking the genes U_S8 to U_S12 was similar to that of HSV-1(F), the results suggest that the packaging of RNAs in virions is not sequence specific and either does not involve U_S11 protein or involves additional RNA-binding proteins. More recent studies have identified two additional tegument proteins capable of binding RNAs. The specificity of RNAs bound by these proteins is presently under study (M. T. Sciortino and B. Roizman, unpublished data).

(iii) Another criterion for determining the specificity of packaging of the RNAs is functionality. We should point out that the conditions of virus infection and especially spread from cell to cell is vastly different in vivo than it is in cultured cells in vitro. A characteristic of in vivo infection is the establishment after the first round of replication of a microenvironment in which the infected cell releases, in addition to virus particles, a variety of induced cytokines, a large number of cellular products, damaged organelles, and other cell debris. All of these by-products of infection could be expected to influence the cells infected by the progeny of the first infected cell. It is conceivable that, to overcome activated host responses, the virus must bring into cells RNA capable of directing the synthesis of proteins before newly made viral RNA is capable of taking over this process. But, if this is the case, the role of the products of the packaged RNAs in such a process is not readily apparent. In the case of gene-expressing glycoproteins, it could be argued that the protein carried into the cell by the virion may not get to where the virus needs these proteins early in infection. In the case of U_L34, it has been shown that this protein interacts with the intermediate chain of the cytoplasmic neuronal dynein (12). One unproven scenario is that newly synthesized U_L34 protein could initiate the transport of the virus to the nucleus. A similar argument was made by Brensnahan and Shenk (1) to explain the presence of one RNA in CMV virions. Except for this one scenario, no other could presently be envisioned to account for the presence of the remaining viral RNAs found in purified virions.

(iv) The question as to where the RNAs are packaged into virions remains unresolved. Greijer et al. (4) reported that the RNA packaged in CMV virions was contained in capsids. However, these authors prepared capsids by extraction of virion preparations with Triton X-100 only and the purity of the capsids was not determined. In the experience of this laboratory, this procedure does not strip tegument proteins or even fully remove glycoproteins from HSV virions. To fully remove glycoproteins and tegument proteins, it is necessary to treat virions with nonionic detergents and desoxycholate (3). While we cannot exclude the possibility that RNA is packaged in capsids, the more likely site is the tegument.

Currently, two models for maturation and egress prevail. The single envelopment model predicts that capsid envelopment takes place only at the inner nuclear membrane and that the virus is then transported through the Golgi to the extracellular space. The double envelopment model predicts that virus enveloped at the nuclear membrane is de-enveloped in the cytoplasm and then re-enveloped at a cytoplasmic membrane (8). The packaging of RNAs into virions is compatible with both models, but the sources of the RNA would be different. Greijer et al. (4) also reported that whereas both cellular and viral RNAs were associated with intact capsids, only viral RNAs were detected in their capsid preparations. The authors concluded that the RNAs were packaged in capsids and virions in different compartments. The results however are marred by the observation that the amounts of RNA extracted from capsids were far lower than those extracted from virions.

In essence, there is little doubt that, consistent with other herpesviruses, the HSV-1 virions package RNAs. The central question is the role of these RNAs in the course of the infectious process. While Brensnahan and Shenk (1) found a plausible explanation for at least some of the packaged RNAs, Greiger et al. (4) concluded on the basis of less data that they have no function whatsoever. For heuristic reasons if none other, it is appropriate to assume that viruses do not encode vestigial genes or perform useless functions. Both the studies by Brensnahan and Shenk (1) and those reported here suggest a level of selectivity of incorporation of RNAs that must be explored further.