0022-538X/07/$08.00⫹0 doi:10.1128/JVI.01442-07
Copyright © 2007, American Society for Microbiology. All Rights Reserved.
A Recombinant Herpes Simplex Virus Type 1 Expressing Two Additional
Copies of gK Is More Pathogenic than Wild-Type Virus
in Two Different Strains of Mice
䌤
Kevin R. Mott,
1Guey-Chuen Perng,
2Yanira Osorio,
1Konstantin G. Kousoulas,
3and Homayon Ghiasi
1*
Center for Neurobiology and Vaccine Development, Ophthalmology Research, Department of Surgery, Cedars-Sinai Burns &
Allen Research Institute, CSMC-D2024, 8700 Beverly Blvd., Los Angeles, California 900481; Department of
Pathology and Laboratory Medicine, Emory Vaccine Center, Emory University School of Medicine,
Atlanta, Georgia 303222; and Division of Biotechnology and Molecular Medicine, School of
Veterinary Medicine, Louisiana State University, Baton Rouge, Louisiana 708033
Received 2 July 2007/Accepted 19 September 2007
The effect of glycoprotein K (gK) overexpression on herpes simplex virus type 1 (HSV-1) infection in two different strains of mice was evaluated using a recombinant HSV-1 virus that expresses two additional copies of the gK gene in place of the latency-associated transcript (LAT). This mutant virus (HSV-gK3
) expressed higher levels of gK than either the wild-type McKrae virus or the parental dLAT2903 virus both in vitro (in cultured cells) and in vivo (in infected mouse corneas and trigeminal ganglia [TG] of BALB/c and C57BL/6 mice). gK transcripts were detected in the TG of both HSV-gK3
-infected mouse strains on day 30 postinfection (p.i.), while gB transcripts were detected only in the TG of the HSV-gK3
-infected C57BL/6 mice, a finding that suggests that increased gK levels promote chronic infection. C57BL/6 mice infected with HSV-gK3
also contained free virus in their TG on day 30 p.i. Both HSV-gK3
-infected mouse strains had significantly higher corneal scarring (CS) than did McKrae-infected mice. T-cell depletion studies in C57BL/6 mice suggested that this CS enhancement in the HSV-gK3
-infected mice was mediated by a CD8ⴙ T-cell response. Taken together, these results strongly suggest that increased gK levels promote eye disease and chronic infection in infected mice.
Glycoprotein K (gK) is one of 11 known herpes simplex virus type 1 (HSV-1) glycoproteins (21, 28, 37). gK is thought to be an important determinant of virus-induced cell fusion, since single-amino-acid changes within gK cause extensive virus-in-duced cell fusion (3, 6, 34, 47). gK is also an important deter-minant of cytoplasmic virion envelopment, since viruses lack-ing gK fail to efficiently acquire a cytoplasmic envelope, which leads to a drastic defect in virion egress and spread (11, 29, 30). Similar to HSV-1 gK, the gKs of pseudorabies virus and vari-cella-zoster virus also play important roles in virion morpho-genesis and egress (7, 32, 39).
We have previously demonstrated that the immunization of mice with gK, but not with any of the 10 other HSV-1 glycopro-teins, results in an exacerbation of corneal scarring (CS) and herpetic dermatitis following ocular HSV-1 infection (13, 18). This exacerbated CS and facial dermatitis was due to the presence of CD8⫹ T cells in the cornea of ocularly infected mice (44). Furthermore, we have shown that the overexpression of gK in gK-transformed cells causes a collapse of the Golgi apparatus into the endoplasmic reticulum, which inhibits virion egress, glycop-rotein transport, and virus-induced cell fusion (10).
To examine the pleiotropic effects associated with gK immuni-zation or gK overexpression, we inserted the complete open read-ing frame (ORF) of the gK gene into both copies of the latency-associated transcript (LAT) gene (one in each viral long repeat).
These ORFs were placed at the 5⬘end of the LAT gene and are under the control of the LAT promoter. The LAT promoter was chosen for the overexpression of gK since it is the only viral promoter that sustains high levels of transcription during latent as well as primary infection (54). We designed this strategy to over-come the problems inherent in the temporary expression of var-ious genes provided by immediate-early or human cytomegalovi-rus immediate-early promoter. This vicytomegalovi-rus, named HSV-gK3,
expressed elevated levels of gK transcripts both in vitro and in vivo compared with parental controls. Therefore, it can be used to examine the effect(s) of overexpression of gK on HSV-1 patho-genicity in mice.
In the present report, we describe several significant effects of elevated gK expression on HSV infection. First, despite displaying replication similar to that of wild-type (wt) virus in tissue culture, trigeminal ganglia (TG), and mouse tears and having a similar 50% lethal dose, HSV-gK3infection resulted in more severe CS
than wt virus infection. Second, the HSV-gK3 virus induced a
chronic infection in the TG. Third, the level of CD8ⴙT cells in the corneas and TG was higher in HSV-gK3-infected mice than in
wt virus-infected mice, while the level of CD4ⴙT cells was similar. Finally, in mice depleted of CD8ⴙT cells, infection with either HSV-gK3or wt virus led to similar CS, suggesting that a CD8ⴙ T-cell response is involved in the exacerbated CS detected in HSV-gK3-infected mice.
MATERIALS AND METHODS
Viruses, cells, and mice.Triple-plaque-purified wt McKrae, dLAT2903,
HSV-gK3, and HSV-gK3R viruses were used in this study. Rabbit skin (RS) cells (used
for the preparation of virus stocks, the culturing of mouse tear films, and the determination of growth kinetics) were grown in Eagle’s minimal essential
me-* Corresponding author. Mailing address: Center for Neurobiology and Vaccine Development-D2024, Cedars-Sinai Burns and Allen Re-search Institute, 8700 Beverly Blvd., Los Angeles, CA 90048. Phone: (310) 423-0593. Fax: (310) 423-0302. E-mail: [email protected].
䌤Published ahead of print on 26 September 2007.
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dium supplemented with 5% fetal calf serum. The mice used were female 6-week-old inbred BALB/c and C57BL/6 mice (The Jackson Laboratory, Bar Harbor, ME).
Construction of the gK plasmid.The parental virus for this construct was dLAT2903, a mutant of the HSV-1 strain McKrae in which the region of both
LAT copies from⫺161 to⫹1667 relative to the LAT transcription start site
(EcoRV-HpaI) was deleted (46). This LAT-null mutant is thus missing
approx-imately 0.2 kb of the LAT promoter and 1.6 kb of the 5⬘end of the primary 8.3-kb
LAT transcript. To make the gK plasmid (pLAT-gK), the BamHI B fragment of McKrae was digested with SwaI-BamHI to produce a 5.5-kb DNA fragment
including the region from⫺1041 to⫹4656 of HSV-1 LAT (46). A PacI linker
was added to this 5.5-kb fragment, and the resulting construct was then ligated into the PacI site of a modified plasmid, pNEB193 (New England Biolabs), that lacks its internal BamHI site. The resulting plasmid was digested with StyI-HpaI
to remove the 1.6-kb LAT fragment that corresponds to LAT nucleotides⫹76 to
⫹1667. A BamHI linker was added, and the resulting plasmid was designated
pLAT. This plasmid contains 880 bp upstream of the BamHI site and 2,989 bp downstream of the BamHI site. A plasmid containing the gK gene from the KOS HSV-1 strain was inserted into the BamHI site of pLAT (21). This gK insert contains the complete 338-amino-acid coding region of the gK gene plus 7 and
15 bp of noncoding 5⬘and 3⬘sequence, respectively. This plasmid, which contains
the 1,036-bp gK gene bounded by 880- and 2,989-bp LAT fragments, was des-ignated pLAT-gK.
Construction of HSV-gK3.HSV-gK3was generated by homologous
recombi-nation as previously described (46). Briefly, pLAT-gK was cotransfected with infectious dLAT2903 DNA by the calcium phosphate method. Viruses from the cotransfection were plated, and isolated plaques were picked and screened for the gK gene insertion using restriction digestion and Southern blot analysis. Selected plaques that contained the gK gene were plaque purified eight times and reanalyzed by restriction digestion and Southern blot analysis to verify that the gK gene was present in the LAT region. A single plaque was chosen for
purification and was designated HSV-gK3. This virus contains the gK gene that
is in the normal LAT location in the viral genome and is under control of the LAT promoter. Thus, in addition to the endogenous HSV-1 gK gene, this virus contains two additional copies of the gK gene under the LAT promoter (one in each viral long repeat).
HSV-gK3R, a rescued virus in which the inserted gK gene was removed and
the original deletion of the LAT gene was restored, was generated by
cotrans-fection and homologous recombination using infectious HSV-gK3DNA and the
pLAT plasmid. This virus behaves similarly to dLAT2903 and wt McKrae in terms of virus replication, survival, and eye diseases in most of the experiments performed in this study. Therefore, the wt McKrae virus was used as the negative control virus for these studies.
Southern analyses.Briefly, viral DNA was digested with EcoRV/MluI; the restriction fragments were separated in a 0.9% agarose gel, transferred to Zeta
paper, rinsed in 2⫻SSC (1⫻SSC is 0.15 M NaCl plus 0.015 M sodium citrate)
for 5 min, and cross-linked to the membrane by UV light; and DNA-DNA
hybridization was performed with32P-labeled gK as previously described (21).
Virus replication in tissue culture.RS cell monolayers at 70 to 80% conflu-ence were infected with 10, 1, or 0.1 PFU/cell. Virus was harvested at various times by subjecting the cell monolayers to two freeze-thawing cycles. Virus titers were determined using standard plaque assays on RS cells as described previ-ously (18).
Ocular infection.Mice were infected ocularly with 2l of tissue culture media
containing 2⫻105
, 2⫻104
, 2⫻103
, or 2⫻102
PFU/eye of the HSV-1 strains
McKrae, dLAT2903, HSV-gK3, or HSV-gK3R (18). In the surviving mice, the
severity of blepharitis (on day 7 postinfection [p.i.]) and CS (on day 30 p.i.) was scored in a masked fashion using a scale from 0 to 4 as described previously (13, 17). Tear films were collected from 40 eyes on days 1 to 5 and 20 eyes on days 6 to 10 for each group as described previously (13). Each swab was placed in 1 ml of tissue culture medium, and the amount of virus in the medium was determined using a standard plaque assay on RS cells.
Detection of infectious virus in TG.BALB/c or C57BL/6 mice were infected
ocularly with 2⫻105
PFU/eye of HSV-gK3
, dLAT2903, or McKrae. On day 3, 5, or 6 p.i. for BALB/c mice or day 30 p.i. for C57BL/6 mice, the infected mice were euthanized, and the TG from each mouse were combined. The TG from each mouse were homogenized, and the debris was removed by centrifugation at 3,000 rpm for 10 min in a Beckman TA10 rotor. The viral titers in the superna-tants of the TG from day 3, 5, or 6 p.i. and appearance of virus-induced cyto-pathic effects (CPE) in the supernatants of the TG from day 30 p.i. were measured on RS cells as described previously (20).
Depletion of T cells.Each C57BL/6 mouse received intraperitoneal injections
of 100 g of purified GK1.5 (anti-CD4ⴙ) or 2.43 (anti-CD8ⴙ) antibodies
(NCCC, Minneapolis, MN) in 100l of phosphate-buffered saline on days⫺4,
⫺1,⫹2, and⫹5 relative to HSV-1 ocular infection. The efficiency of CD4⫹and
CD8ⴙT-cell depletion was monitored by fluorescence-activated cell sorter
anal-ysis. After the second depletion, more than 93% of CD4ⴙor CD8ⴙT cells were
depleted from the spleens of the mice. Isotype-controlled mice were treated with
anti-HLA-DR5 (clone SFR3-DR5) monoclonal antibody in 100l of PBS as
described above, and this group was designated as the mock control. Due to the lack of survival of BALB/c mice following this procedure, the depletion studies were performed only in C57BL/6 mice.
RNA extraction and cDNA preparation.Corneas and TG from ocularly in-fected BALB/c and C57BL/6 mice were collected on days 5 and 30 p.i. The tissues were immersed in the RNAlater RNA stabilization reagent and stored at
⫺80°C until processing. The frozen tissue from each animal was processed for
RNA extraction using TRI reagent (Molecular Research Center, Inc., Cincin-nati, OH) and RNeasy column cleanup (QIAGEN, Inc., Valencia, CA). In the case of RNA extraction from virus-infected RS cells, the cells growing in six-well plates were infected with 10, 1, or 0.1 PFU/cell of the HSV-gK3, dLAT2903, or McKrae strain. The cells were harvested and washed 8 or 16 h p.i. For RNA preparation, frozen tissue or washed RS cells were resuspended in TRI reagent and homogenized, followed by the addition of chloroform and subsequent nu-cleic acid precipitation using isopropanol. The RNA was then treated with DNase I to degrade any contaminating genomic DNA followed by purification using a QIAGEN RNeasy column as described in the manufacturer’s instruc-tions. RNA yield was determined by spectroscopy (NanoDrop ND-1000; Nano-Drop Technologies, Inc., Wilmington, DE). On average, the RNA yields from
each mouse cornea and TG sample were 1.8 to 3.75g and 2.7 to 7.5g,
respectively. Finally, 1,000 ng of total RNA was reverse transcribed using random hexamer primers and murine leukemia virus reverse transcriptase from the high-capacity cDNA reverse transcription (RT) kit from Applied Biosystems, Foster City, CA, in accordance with the manufacturer’s recommendations.
The differences in expression levels of gK and gB in infected cells were evaluated using custom-made TaqMan gene expression primers described below for the in vivo studies. Relative copy numbers for the gK and gB genes were calculated using similar standard curves generated from the plasmids pGEM-gK1040 and pAc-gB1, respectively. Although glyceraldehyde-3-phosphate dehy-drogenase (GAPDH) is typically used as an internal loading control to normalize signal during quantitative real-time processing, variable GAPDH signals were detected in tissue culture cells infected with different PFU of each virus as was reported previously (43). Therefore, expression of the 18S rRNA gene was used for in vitro normalization. However, no variations in expression of GADPH were detected in the tissues collected from the infected animals. Thus, in all in vivo experiments we used GADPH for normalization of gB, gK, CD4, and CD8 transcripts.
TaqMan real-time PCR.The expression levels of the CD4 and CD8 genes, along with the expression of the GAPDH and 18S rRNA genes (used as an endogenous loading controls), were evaluated using commercially available Taq-Man gene expression assays (Applied Biosystems, Foster City, CA) with opti-mized primer and probe concentrations. Primer probe sets consisted of two unlabeled PCR primers and the 6-carboxyfluorescein (FAM) dye-labeled Taq-Man MGB probe formulated into a single mixture. Additionally, all amplicons included an intron-exon junction to eliminate signal from genomic DNA con-tamination. The following assays were used: (i) CD4 ABI assay Mm00442754_m1 (amplicon length, 72 bp), (ii) CD8 (alpha chain) ABI assay Mn01182108_m1 (amplicon length, 67 bp), (iii) GAPDH ABI assay Mm999999.15_G1 (amplicon length, 107 bp), and (iv) 18S rRNA ABI assay Hs99999901_s1 (amplicon length, 187 bp).
Expression levels of HSV-1 gB and gK were also evaluated using custom-made TaqMan gene expression assays (Applied Biosystems, Foster City, CA). The gB
primers and probe used were as follows: forward primer, 5⬘-AACGCGACGCA
CATCAAG-3⬘; reverse primer, 5⬘-CTGGTACGCGATCAGAAAGC-3⬘; and
probe, 5⬘-FAM-CAGCCGCAGTACTACC-3⬘. The gK primers and probe used
were as follows: forward primer, 5⬘-GGCCACCTACCTCTTGAACTAC-3⬘;
re-verse primer, 5⬘-CAGGCGGGTAATTTTCGTGTAG-3⬘; and probe, 5⬘
-FAM-CAGGCCGCATCGTATC-3⬘. The amplicon lengths for gB and gK were 72 and
82 bp, respectively.
Quantitative real-time PCR was performed using an ABI Prism 7900HT se-quence detection system (Applied Biosystems, Foster City, CA) in 384-well
plates. Briefly, each 20-l reaction mixture contained 2l of cDNA template, 1⫻
TaqMan universal PCR master mix (Applied Biosystems), and 1⫻TaqMan gene
expression assay (CD4, CD8, gB, gK, 18S rRNA, or GAPDH). The universal thermal cycling conditions used were as follows. After an initial 2 min at 50°C to induce AmpErase-UNG activity and 10 min at 95°C, the samples were cycled 40 times at 95°C for 15 s and 60°C for 1 min. Relative gene expression levels were
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normalized to the expression of the housekeeping gene coding for GAPDH (endogenous loading control). Real-time PCR was performed in triplicate for a given tissue sample from each animal in the group. The threshold cycle values, which represents the PCR cycle at which there is a noticeable increase in the reporter fluorescence above baseline, were determined using SDS 2.2 software. In each experiment, an estimated relative copy number of each target gene was calculated using standard curves generated from plasmids containing the gene of interest: pORF-9-mCD8-a (InvivoGen, San Diego, CA), pCMV-Sport1-CD4 (Open Biosystems, Huntsville, AL), pGem-gK (21), and pAc-gB1 (19). Briefly,
each plasmid DNA template was serially diluted 10-fold such that 5l contained
from 103to 1011copies of the desired gene and then was subjected to TaqMan
PCR with the same set of primers as the test samples. By comparing the nor-malized threshold cycle of each sample to the threshold cycle of the standards, the copy number for each reaction was determined.
Statistical analysis.Protective parameters were analyzed with the Student’st
test and Fisher’s exact test using Instat (GraphPad, San Diego, CA). Results
were considered to be statistically significant if thePvalue was⬍0.05.
RESULTS
Structure of the HSV-gK3
virus. We constructed a mutant derivative of HSV-1 strain McKrae that expresses two additional copies of the gK gene to examine the effects of extra doses of gK on HSV-1 pathogenesis. McKrae was used as the original paren-tal virus. The genomic structure of the wt HSV-1 strain McKrae is shown schematically in Fig. 1A. The HSV-1 genome contains a unique long region (UL) and a unique short (US) region, both of
which are flanked by inverted repeats (Fig. 1A; terminal and internal repeats long [TRLand IRL] and terminal and internal
repeats short [TRSand IRS]). The location of the TATA box of
[image:3.594.79.501.65.410.2]the LAT promoter is indicated. The transcription start site of the primary 8.3-kb LAT RNA transcript is 28 nt downstream of the
FIG. 1. Construction and structure of the HSV-gK3mutant virus. (A) The top schematic diagram shows the HSV-1 McKrae genome in the
prototypic orientation. TRLand IRLrepresent the terminal and internal (or inverted) long repeats, respectively, and TRSand IRSrepresent the
terminal and internal (or inverted) short repeats, respectively. ULand USrepresent the long and short unique regions, respectively. The solid
rectangle represents the very stable 2-kb LAT. The start site for LAT transcription is indicated by the arrow at⫹1. “TATA” designates the relative location of the LAT promoter TATA box 28 nt upstream of the start of transcription. (B) dLAT2903 has a deletion from LAT nt⫺161 to⫹1667 in both copies of LAT and makes no LAT RNA. (C) HSV-gK3was constructed from dLAT2903 by homologous recombination between dLAT2903
DNA and a plasmid containing the complete LAT promoter and the entire structural gK gene [including its 3⬘poly(A) signal] as described in Materials and Methods. (D) HSV-gK3Southern blot. Subconfluent RS cell monolayers were infected with 10 PFU/cell of HSV-gK3or McKrae
for 16 h. Viral DNAs were isolated, and 5g of DNA from each virus was digested with EcoRI/EcoRV and hybridized to32P-labeled HSV-1 gK
(HSV-1 nt 112170 to 113193). As expected, only one fragment is seen in the McKrae lane. This band also is observed in HSV-gK3and corresponds
to HSV-1 nt 110094 to 118640 surrounding the naturally occurring gK (HSV-1 nt 112170 to 113193). In contrast to the McKrae lane, in the HSV-gK3lane, in addition to the natural gK, there are two additional bands corresponding to two extra copies of the gK gene inserted within IR
L
(HSV-1 nt 110094 to 118640) and TRL(HSV-1 nt 13 to 7727) regions of dLAT2903. Both regions within the IRLand TRLhave a deletion of
approximately 1,600 bp of LAT.
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TATA box (54). The previously described LAT null mutant, dLAT2903 (Fig. 1B), was derived from the McKrae strain (46). It contains a 1.8-kb deletion in both copies of the LAT gene (one in each of the long repeats). This deletion encompasses 0.2 kb of the LAT promoter and the portion of the LAT gene that encodes the first 1.6 kb of the 8.3-kb primary LAT. The deleted region, des-ignated “XXXXXX” (Fig. 1B), extends to LAT nt position ⫹1667.
HSV-gK3 was derived from the dLAT2903 strain by the
insertion of the gK gene and restoration of the LAT promoter so that the inserted gK genes are under control of the endog-enous LAT promoter (Fig. 1C [described in Materials and Methods]). The genomic structure of HSV-gK3was confirmed
by restriction enzyme analysis, Southern blotting (Fig. 1D), and partial sequencing (not shown). HSV-gK3 contains the
entire sequence of the gK gene, including its polyadenylation signal, under the control of the LAT promoter. There is a noncoding region of 7 nt upstream of the first ATG. This is followed by the complete coding region of 1,014 nt and a 15-nt noncoding region downstream of the gK termination codon. Therefore, HSV-gK3 contains, in addition to its endogenous
gK gene, two additional complete copies of gK, one in each viral long repeat. HSV-gK3is identical to its LAT null mutant
parent, dLAT2903, except that the LAT promoter has been restored to drive the expression of the inserted gK genes. dLAT2903 is identical to its wt parent, McKrae, in all param-eters examined, and the HSV-gK3rescued virus, HSV-gK3R, is
identical to dLAT2903 in all parameters examined. HSV-gK3
virus expresses higher levels of gK transcripts both in vitro and in vivo.To investigate the relative expression of the gK gene in HSV-gK3 as compared to its parental
dLAT2903 virus, confluent monolayers of RS cells were in-fected with HSV-gK3 or dLAT2903 at a multiplicity of 10
PFU/cell. Infected cells were collected 8 or 16 h p.i., and total
RNA was isolated as described in Materials and Methods. TaqMan RT-PCR was performed on the isolated RNA to detect the levels of gK and gB transcripts relative to the levels of 18S rRNA transcripts. As expected, our results suggest that the level of gK transcripts in HSV-gK3-infected RS cells is
significantly higher than in dLAT2903-infected RS cells at both 8 and 16 h p.i. (Fig. 2;P ⬍0.01). However, the levels of gB transcripts were similar between the two viruses (Fig. 2;P⬎
0.05). Similar results were obtained following infection with McKrae virus (data not shown). These results indicate that the two extra copies of gK in HSV-gK3lead to increased
expres-sion of gK.
We next wanted to determine if the HSV-gK3virus expressed
higher levels of gK in vivo (in mouse TG or corneas) using ocular infection in the mouse. Six-week-old female BALB/c or C57BL/6 mice were infected with 2⫻105PFU/eye of HSV-gK3or McKrae
virus. It should be noted that C57BL/6 mice are less sensitive than BALB/c mice to infection with McKrae virus (44), but they can be sensitized to infection by immunization with gK (44). Corneas and TG from each infected mouse were collected 5 days post-ocular infection, and the total RNA was isolated as described in Materials and Methods. TaqMan RT-PCR was performed on the total RNA from the corneas and TG of individual mice to mea-sure the levels of gK and gB mRNA per mouse cornea or TG. GAPDH mRNA levels in each samples were used as internal controls. In both BALB/c and C57BL/6 mice, TG from HSV-gK3
-infected mice had more gK transcripts than the TG from wt McKrae-infected mice (Fig. 3A). In contrast, the levels of gB transcripts were similar in the TG of both BALB/c and C57BL/6 mice infected with either HSV-gK3or McKrae (Fig. 3A). The
corneas of BALB/c and C57BL/6 mice infected with HSV-gK3
[image:4.594.133.452.71.288.2]also had more gK transcripts than the corneas of mice infected with McKrae, while the levels of gB mRNA were similar for both viruses (Fig. 3B). These results suggest that presence of the three
FIG. 2. gK and gB transcriptions in infected RS cells. Subconfluent RS cell monolayers in quadruplicate were infected with 10 PFU/cell of HSV-gK3
or dLAT2903 for 8 and 16 h. Total RNA was isolated from these infected RS cells, and TaqMan RT-PCR was performed as described in Materials and Methods using gB- and gK-specific primers. The 18S rRNA expression was used to normalize the relative expression of gK and gB mRNAs in HSV-gK3
-and dLAT2903-infected RS cells. PI, postinfection. Each point represents the mean⫾standard error of the mean (n⫽4).
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copies of gK in HSV-gK3virus results in higher gK transcription
in HSV-gK3-infected cells both in vitro and in vivo.
Replication of HSV-gK3
in tissue culture.To determine if elevated gK levels affect viral replication, we measured viral yield following the infection of RS cells with 10 PFU/cell of HSV-gK3, dLAT2903, McKrae, or HSV-gK3R. The
replica-tions of each of these four viruses appeared to be similar (Fig. 4A). Additionally, no differences were detected in RS cells infected with HSV-gK3, dLAT2903, or McKrae at 1 or 0.1
PFU/cell (data not shown). Thus, the overexpression of gK in HSV-gK3does not have a detectable effect on virus replication
in tissue culture.
Replication of HSV-gK3
in mouse tears. Viral replication during ocular infection was measured indirectly by determining the PFU in the tear films of infected mice. BALB/c or C57BL/6 mice were infected ocularly with 2⫻105PFU/eye of HSV-gK3,
dLAT2903, or McKrae (see Materials and Methods). Tear
films were collected, and the amount of virus in those films was determined using plaque assays on RS cells. Throughout the course of the experiment, virus titers were similar in the tear films of C57BL/6 mice infected with HSV-gK3, dLAT2903, or
McKrae (Fig. 4B;P⬎0.1). In BALB/c mice, virus titers were similar in the tear films of mice infected with HSV-gK3,
dLAT2903, or McKrae 1 to 3 days p.i. (Fig. 4C; P ⬎ 0.1). However, 4 to 6 days p.i., the tear films of dLAT2903- or McKrae-infected mice had significantly higher virus titers than did the tear films of HSV-gK3-infected mice (Fig. 4C; P ⬍
0.01). By day 7 p.i., the three viruses produced similar low viral titers in BALB/c mice, and by day 8 p.i., no virus was detected in any eye for either BALB/c- or C57BL/6-infected mice (Fig. 4B and C).
Thus, it appears that the presence of two additional copies of gK significantly decreases the amount of HSV-1 found in the tear films of infected BALB/c mice 4 to 6 days p.i., but it has little effect on the amount of virus present in the tear films of infected C57BL/6 mice.
Virus replication in TG.The results described above suggest that virus replication in the tears of BALB/c mice infected with HSV-gK3was lower 4 to 6 days post-ocular infection than it
was in the tears of mice infected with wt McKrae or parental dLAT2903. To determine if the lower virus titer correlated with virus replication in TG, BALB/c mice were ocularly in-fected with HSV-gK3, dLAT2903, or McKrae (as described in
Materials and Methods). On days 3, 5, and 6 p.i., mice were sacrificed and TG were harvested for analysis of infectious virus as described in Materials and Methods. In contrast to the differences observed in viral titer between the three viruses in the eyes of BALB/c-infected mice, no significant differences were detected in the amount of virus recovered on day 3, 5, or 6 p.i. in the TG extracts of BALB/c mice infected with HSV-gK3, dLAT2903, or McKrae (Fig. 4D). Thus, HSV-gK3
ap-pears to replicate similarly to wt McKrae or dLAT2903 in the TG of infected BALB/c mice during primary infection.
Virulence of HSV-gK3
in BALB/c and C57BL/6 mice. To determine whether there is a difference in the virulence of the HSV-gK3 virus, the parental dLAT2903 virus, the wt McKrae
virus, or the HSV-gK3R rescued virus, the ability of these viruses
to cause a lethal infection in BALB/c mice (that are sensitive to HSV-1 infection) and C57BL/6 mice (that are resistant to HSV-1 infection) was evaluated. Groups of 5 to 50 BALB/c mice from one to four experiments were infected ocularly with 10-fold serial dilutions of HSV-gK3, wt McKrae, dLAT2903, or HSV-gK3R (as
described in Materials and Methods). No significant differences were detected in BALB/c mice infected with different doses of HSV-gK3compared with mice infected with McKrae, dLAT2903,
or HSV-gK3R (Table 1;P⬎0.05).
To determine the effect of HSV-gK3infection on the
mor-tality of C57BL/6 mice, groups of 39 and 30 mice from two separate experiments were infected ocularly with 2⫻105PFU/
eye of HSV-gK3or McKrae, respectively (as described in
Ma-terials and Methods). None of the infected mice died following ocular infection (Table 1;P⫽1). These results suggest that the pattern of neurovirulence in HSV-gK3-infected mice is similar
to that of the dLAT2903, wt McKrae, and HSV-gK3R rescued
viruses.
[image:5.594.47.278.66.409.2]Effect of gK overexpression on eye diseases in infected mice. To determine the effect of gK overexpression on eye disease,
FIG. 3. Quantitation of gK and gB mRNAs in vivo. (A) gK and gB transcriptions in TG. BALB/c or C57BL/6 mice were ocularly infected with 2⫻105PFU/eye of HSV-gK3or McKrae virus. TG from
indi-vidual mice were isolated 5 days p.i. (PI), and TaqMan RT-PCR was performed as described in Materials and Methods. GAPDH expres-sion was used to normalize the relative expresexpres-sion of gK and gB mRNA in HSV-gK3- and McKrae-infected TGs. Each point represents
the mean⫾standard error of the mean from five mice. (B) gK and gB transcription in corneas. Individual mouse corneas infected as de-scribed above were harvested, and TaqMan RT-PCRs for gK and gB transcripts were performed as described above. Each point represents the mean⫾standard error of the mean from 5 mice.
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the severity of blepharitis (inflammation of the eyelid) and CS were evaluated following the ocular infection of BALB/c mice with 2⫻105PFU/eye of either HSV-gK3or wt McKrae virus.
Blepharitis and CS were measured in the surviving mice 7 and
30 days, respectively, post-ocular infection. BALB/c mice in-fected with HSV-gK3developed similar levels of blepharitis to
[image:6.594.49.530.65.426.2]mice infected with the wt McKrae virus, while CS was signifi-cantly higher in the mice infected with HSV-gK3than in those
FIG. 4. Replication of HSV-gK3in vitro and in vivo. (A) Virus replication in RS cells. Subconfluent RS cell monolayers in triplicate from two
separate experiments were infected with 10 PFU/cell of HSV-gK3, dLAT2903, McKrae, or HSV-gK3R as described in Materials and Methods.
Total virus was harvested at the indicated times p.i. by two cycles of freeze-thawing. The amount of virus at each time point was determined by standard plaque assays on RS cells. Each point represents the mean⫾standard error of the mean (n⫽6). (B and C) Virus replication in mouse tears. BALB/c (B) or C57BL/6 (C) mice were ocularly infected with 2⫻105PFU/eye of HSV-gK3, dLAT2903, or McKrae virus. Tear films were
collected from days 1 to 10, and virus titers were determined by standard plaque assays. Each point represents the mean titers of 40 eyes from two separate experiments for days 1 to 5 and 20 eyes from two separate experiments for days 6 to 10. (D) Virus titers in TG. BALB/c mice were ocularly infected with 2⫻105PFU/eye of HSV-gK3, dLAT2903, or McKrae virus as described above. Mice were euthanized on the indicated days, TG from
each mouse were removed, combined, and homogenized, and virus titers were determined for the TG from each mouse. Each bar represents the mean⫾standard error of the mean of the TG from 5, 15, and 5 mice for days 3, 5, and 6 p.i., respectively.
TABLE 1. Mortality of BALB/c and C57BL/6 mice following ocular infection with HSV-gK3
Virus
No. (%) of mice that died/no. infected with titer showna:
BALB/c
C57BL/6 (2⫻105)
2⫻102 2⫻103 2⫻104 2⫻105
HSV-gK3 12/25 (48)b 5/5 (100) 5/5 (100) 39/50 (78)b 0/39 (0)b
dLAT2903 12/25 (48)b 4/5 (80) 5/5 (100) 5/5 (100) ND
McKrae 2/5 (40) 5/5 (100) 5/5 (100) 32/50 (64)b 0/30 (0)b
HSV-gK3Rc 2/5 (40) 5/5 (100) 5/5 (100) 5/5 (100) ND
aBALB/c or C57BL/6 mice were ocularly infected with the specified virus titers (PFU/eye), and mortality was determined 30 days after infection. ND, not done.
bData from four separate experiments.
cHSV-gK3R rescued virus is a control virus with only the endogenous copy of gK (see Materials and Methods for details).
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[image:6.594.40.543.613.699.2]infected with the McKrae virus (Fig. 5; BALB/c). Similar re-sults were obtained following infection with parental dLAT2903 virus (data not shown).
Previously, we have shown that C57BL/6 mice with detect-able levels of preexisting gK antibody titers are more suscep-tible to virus-mediated eye diseases than naive mice (17). In the present study, we examined the effect of HSV-gK3
infec-tion on eye diseases in C57BL/6 mice, which are refractory to HSV-1 infection. C57BL/6 mice were infected ocularly with 2⫻105PFU/eye of HSV-gK3or McKrae virus, and blepharitis
and CS were measured as described above. Mice infected with HSV-gK3displayed higher levels of blepharitis and CS than
mice infected with the wt McKrae virus (Fig. 5; C57BL/6). Furthermore, approximately 50% of HSV-gK3-infected C57BL/6
mice developed severe facial dermatitis, while none of the McKrae-infected mice showed any sign of dermatitis (data not shown). Some of the surviving BALB/c mice infected with HSV-gK3 also showed higher levels of facial dermatitis than those
infected with the wt McKrae virus (data not shown). Thus, the overexpression of gK exacerbates virus-induced CS in HSV-gK3
-infected BALB/c and C57BL/6 mice.
Effect of gK overexpression on CD4 and CD8 transcription in TG and corneas of ocularly infected mice.Both CD4⫹and CD8⫹ T cells have been implicated in HSV-1-induced eye diseases (1, 2, 23, 38, 42, 53). Since the overexpression of gK also induces eye disease in C57BL/6 mice, we next determined whether gK overexpression altered T-cell differentiation in HSV-1-infected TG and corneas. CD4 and CD8 mRNA levels were estimated in the corneas and TG following ocular infec-tion with 2⫻ 105 PFU/eye of either the HSV-gK3or the wt
McKrae virus. The corneas and TG from five mice per group were collected on days 5 and 30 post-ocular infection, and TaqMan RT-PCR for CD4 and CD8 was performed on the total RNA from the corneas or TG of individual mice (as described in Materials and Methods). On day 5 p.i., the level of CD8 transcript in the corneas of BALB/c mice infected with HSV-gK3was higher than that in the corneas of BALB/c mice
infected with the wt McKrae virus (Fig. 6A). Similar results were found using C57BL/6 mice (Fig. 6A). In contrast, in the TG, the patterns of CD4 and CD8 transcript levels on day 5 p.i. were similar for both viruses in both BALB/c mice and C57BL/6 mice (Fig. 6B).
On day 30 p.i., no significant differences were detected for CD4 transcript levels in the corneas (Fig. 6C) or TG (Fig. 6D) of BALB/c or C57BL/6 mice infected with either HSV-gK3or
wt McKrae. However, the levels of CD8 transcripts were sig-nificantly higher in the corneas of mice infected with the HSV-gK3virus than in mice infected with the wt McKrae virus (Fig.
6C). Similarly, the level of CD8 transcript was higher in the TG of HSV-gK3-infected BALB/c and C57BL/6 mice than in mice
infected with McKrae (Fig. 6D), although these differences were not statistically significant. Thus, there is a correlation between higher CD8 transcript levels in the corneas of infected mice (at days 5 and 30 p.i.) and more severe eye disease, especially in HSV-gK3-infected mice.
Effect of CD4ⴙand CD8ⴙT-cell depletion on CS following HSV-gK3
infection. The RT-PCR analyses described above suggest that the level of CD8 transcripts in the corneas of HSV-gK3-infected mice, especially in C57BL/6 mice,
corre-lates with the severity of CS. To examine the potential role CD4⫹and CD8⫹T cells play in HSV-1-induced eye disease, we used antibodies to specifically deplete these subclasses of T cells from C57BL/6 mice (as described in Materials and Meth-ods). Irrespective of the virus that was used for ocular infec-tion, 9 of 10 (90%) CD8⫹-depleted mice, 8 of 10 (80%) CD4⫹ -depleted mice, and 10 of 10 (100%) mock--depleted mice survived the ocular infection (not shown). CS in surviving mice was determined 30 days after ocular infection. As expected, the amount of CS was decreased in the CD8⫹-depleted mice in-fected with HSV-gK3, while it was increased in CD8⫹-depleted mice infected with McKrae (Fig. 7; CD8 depleted). These differences between CD8⫹-depleted mice infected with
HSV-FIG. 5. Eye diseases in mice infected with HSV-gK3. BALB/c and
C57BL/6 mice were ocularly infected with 2⫻105PFU/eye of
HSV-gK3or McKrae virus and were used to determine blepharitis and CS.
Blepharitis and CS in surviving mice were examined on days 7 and 30 p.i. as described in Materials and Methods. In the BALB/c mice, the blepharitis and CS scores represents the average⫾standard error of the mean from 100 and 22 eyes, respectively, from HSV-gK3-infected
mice and 100 and 36 eyes, respectively, from McKrae-infected mice. In C57BL/6 mice, the blepharitis and CS scores represent the average⫾ standard error of the mean from 78 eyes for HSV-gK3-infected mice
and 60 eyes for McKrae-infected mice.
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[image:7.594.40.279.70.465.2]gK3 or McKrae were not statistically significant (Fig. 7;P ⫽
0.8). In contrast, depletion of CD4⫹ T cells significantly in-creased CS in mice infected with HSV-gK3 compared with
mice infected with McKrae (Fig. 7;P ⫽ 0.005), while mock depletion had no effect on CS in infected mice (Fig. 7;P ⫽
0.0009). Thus, these results suggest that, in C57BL/6 mice ocularly infected with HSV-gK3, increased CS is dependent on
the presence of CD8⫹but not CD4⫹T cells.
Detection of gK transcript during the latent state of infec-tion. During HSV-1 neuronal latency, only one viral gene is consistently expressed at high levels (8, 48). This viral gene is called the LAT gene (12, 48, 52). The LAT gene has a powerful promoter that is active in most cell types (31, 36), and the two additional copies of gK in the HSV-gK3virus are expressed from
this promoter. We next wanted to determine whether gK was expressed in a latent HSV-gK3 infection. Thus, the surviving
BALB/c or C57BL/6 mice described in Table 1 and ocularly infected with 2⫻ 105 PFU/eye of HSV-gK3 or McKrae were
euthanized and corneas and TG from individual mouse were isolated. TaqMan RT-PCR was performed on the total RNA isolated from these tissues, and the levels of gK and gB transcripts
from each virus were determined. In the BALB/c mice, gK tran-scription was detected in four of the five mice infected with HSV-gK3and in two of the five mice infected with McKrae (Fig. 8).
However, no gB transcript was detected in BALB/c mice infected with either the HSV-gK3or McKrae virus (Fig. 8), an expected
result given that gB is not expressed during latency. C57BL/6 mice infected with HSV-gK3had detectable levels of gK transcripts in
all five of the TG tested, while the mice infected with the wt McKrae virus had detectable levels of gK transcripts in only one of the five TG tested (Fig. 8). In contrast to the absence of the gB transcript in the TG of BALB/c mice infected with HSV-gK3,
100% (five of five) of TG from C57BL/6 mice infected with HSV-gK3expressed gB transcript (Fig. 8). No gB transcript was
detected in the TG of C57BL/6 mice infected with the wt McKrae virus (Fig. 8). Neither gK nor gB transcripts were detected in the corneas nor brains of these mice on day 30 p.i. (data not shown). To summarize, gK transcription is detected in the TG of both BALB/c and C57BL/6 mice infected with HSV-gK3and in
[image:8.594.114.475.67.410.2]20 to 40% of mice infected with the wt McKrae virus. These results indicate that, as expected, gK is being expressed from the LAT promoter during latency. Finally, the presence of gB
FIG. 6. Estimation of CD4 and CD8 copy numbers in corneas and TG of infected mice. BALB/c or C57BL/6 mice were ocularly infected with 2⫻105PFU/eye of HSV-gK3or McKrae virus. Corneas and TG from individual mice were isolated on day 5 or 30 p.i. (PI), and TaqMan RT-PCR
was performed on total RNA isolated from those tissues as described in Materials and Methods. GAPDH was used as an endogenous control to normalize the relative expression of CD4 and CD8 mRNA in HSV-gK3- and McKrae-infected corneas and TG. Each point represents the mean⫾
standard error of the mean from 5 mice. (A) CD4 and CD8 mRNAs in mouse corneas on day 5 p.i. (B) CD4 and CD8 mRNAs in mouse TG on day 5 p.i. (C) CD4 and CD8 mRNAs in mouse corneas on day 30 p.i. (D) CD4 and CD8 mRNAs in mouse TG on day 30 p.i.
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transcripts in the TG of C57BL/6 mice may suggest a chronic infection in addition to possible latent infection.
HSV-gK3
induces a chronic infection in the TG of infected mice.The analyses described above revealed the presence of gB mRNA in the TG of HSV-gK3-infected mice but not in the TG of
wt McKrae-infected C57BL/6 mice. During HSV neuronal la-tency, there is an absence of viral proteins and infectious virus and LAT is the only gene product consistently detected in abundance (51). The detection of the gK mRNA was not unexpected since the two additional copies of gK are under the control of the LAT promoter. However, the detection of gB mRNA in the TG of infected mice 30 days p.i. suggests that HSV-gK3may have
es-tablished a chronic infection in addition to a possible latent in-fection. To determine if presence of gB mRNA in the TG of HSV-gK3-infected C57BL/6 mice was a result of the lack of viral
clearance, C57BL/6 mice were infected ocularly with 2⫻ 105
PFU/eye of either HSV-gK3or McKrae and their TG were
ana-lyzed for the presence of infection virus. Thirty days post-ocular infection, a time at which latency has been established in wt mice and no infectious virus can be detected in the TG (5, 15), the surviving mice were euthanized. TG from individual mice were homogenized, and the extracts were plated on indicator (RS) cells to look for the presence of infectious virus (as described in Ma-terials and Methods). All TG (10/10 [100%]) from the C57BL/6 mice infected with the HSV-gK3 virus contained infectious
HSV-1 particles. In contrast, no infectious virus (0/10 [0%]) was detected in the TG of C57BL/6 mice infected with the wt McKrae virus (P⬍0.0001). Thus, when infected with virus carrying two additional copies of gK, the mouse immune system is unable to efficiently clear infectious HSV-1 virus from the TGs.
DISCUSSION
We demonstrated previously that the immunization of mice with gK, but not with any of the other known HSV-1
glyco-proteins, results in an exacerbation of CS and facial dermatitis following ocular HSV-1 infection (13, 18). The exacerbated CS is independent of mouse or virus strains (17). Vaccination with gK also appears to block viral clearance from the trigeminal ganglia, which results in a chronic, productive infection (15). We also found that the exacerbation of CS in the gK-immu-nized mice was due to the presence of CD8⫹ T cells in the cornea of ocularly infected mice (44). The depletion of CD8⫹ T cells, but not the depletion of CD4⫹T cells or macrophages, reduced the severity of the eye disease to the level detected in mock-immunized or ocularly infected mice. Of many different protein antigens tested in conjunction with Freund’s adjuvant, gK was the only antigen that induced a CD8⫹T-cell response in the cornea of ocularly infected mice (44). To help define the effect of gK on HSV-1 pathogenesis, we constructed a recom-binant HSV-1 virus that expresses two additional copies of the HSV-1 gK gene, each under the control of the LAT promoter. This virus provided a useful tool for studying how the overex-pression of gK affects HSV-1-induced eye disease.
The viral titers of HSV-gK3in RS cells, BALB/c TG, and
C57BL/6 tears as well as the 50% lethal doses and duration of virus clearance were similar to those of the parental and con-trol viruses. Despite having lower virus titers in the tears of BALB/c mice, HSV-gK3-infected mice had more severe CS
than mice infected with the wt McKrae virus. These results demonstrate that the exacerbated CS in HSV-gK3-infected
BALB/c or C57BL/6 mice was independent of virus titers in the eyes or TG.
Different mouse strains have differential susceptibilities to HSV-1 infection. C57BL/6 (H-2b) mice are more resistant to
[image:9.594.308.529.67.239.2]HSV-1 infection, and even the highly virulent wt McKrae strain does not produce CS in these mice (16). In contrast, BALB/c (H-2d) mice are very susceptible to ocular infection with the FIG. 7. CS in C57BL/6 mice is CD8⫹T-cell dependent. Ten C57BL/6
mice were depleted of their CD4ⴙ or CD8ⴙ T cells prior to ocular infection with HSV-gK3or McKrae virus as described in Materials and
Methods. Mock control mice were depleted with irrelevant monoclonal antibody. CS was measured 30 days after ocular infection in surviving mice. For each bar, CS (yaxis) represents the average of the scarring from 16 eyes (CD4ⴙdepleted), 18 eyes (CD8ⴙdepleted), or 20 eyes (mock depleted). The error bars indicate the standard error of the mean.
FIG. 8. Detection of gK and gB transcripts in the TG during la-tency. BALB/c or C57BL/6 mice were ocularly infected with 2⫻105
PFU/eye of HSV-gK3or McKrae virus. TG from individual mice were
isolated 30 days p.i. (PI), and TaqMan RT-PCR was performed as described in Materials and Methods. GAPDH was used as an endog-enous control to normalize the relative expression of gK and gB mRNAs in HSV-gK3-and McKrae-infected TG. Each point represents
the mean⫾standard error of the mean from 5 mice. The numbers in parentheses on top of each bar indicate the number of positive mouse TG per total mouse TG tested for each transcript.
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McKrae strain. Exacerbation of CS in the C57BL/6 mice infected with HSV-gK3was surprising, but the result was consistent with
our previous finding that immunization with gK followed by in-fection with McKrae (or with the avirulent HSV-1 KOS virus) leads to CS in both BALB/c and C57BL/6 mice (17).
The immune response leading to HSV-1-induced CS is cell mediated (14, 24, 42), and macrophages, CD4ⴙT cells, and CD8ⴙT cells have been implicated in this response (1, 2, 23, 38, 42, 53). The results presented here show that, following ocular infection, CD8ⴙT-cell transcripts in the eyes and TG of HSV-gK3-infected mice were higher than in McKrae-infected
mice. In addition, the depletion of CD8ⴙT cells, but not the depletion of CD4ⴙ T cells, eliminated the exacerbated CS observed in HSV-gK3-infected mice. These results suggest that
CD8ⴙT cells are involved in the exacerbation of CS in these mice, a result consistent with the finding that CD8ⴙT cells play a major role in HSV-1-mediated corneal pathogenesis (1, 25, 26, 49). Furthermore, we have previously shown that the CS exacerbation in gK-immunized mice correlates with CD8ⴙT cells, but not with CD4ⴙ T cells or macrophages (44). Re-cently, it was shown that CD8⫹ T cells mediate transient herpes stromal keratitis in CD4-deficient mice (33), and that CD8⫹ T cells are also actively involved in autoimmune dis-eases (27, 41, 45, 50). However, our results contradict previous reports that CD4⫹T cells play a major role in HSV-1-induced eye disease (4). Although it is unlikely, the possible effect of CD4⫹T-cell depletion on CD25⫹regulatory T cells cannot be ruled out as reason for our observed contradiction. However, our preliminary results have shown that these regulatory T cells are not detectable in the corneas of infected mice (data not shown). Previously, we have shown that the overexpression of gK in gK-transformed cells collapses the Golgi apparatus into the endoplasmic reticulum (10). Thus, the disruption of the Golgi structure by the overexpression of gK in the HSV-gK3 virus may also damage cellular structure of the eye that
may result in the exacerbation of CS in infected mice. During HSV neuronal latency, there is an absence of viral proteins and infectious virus, and LAT is the only gene product consistently detected in abundance (51). Detection of the gK transcript in the TG of HSV-gK3latently infected mice is not
unexpected, given that the two additional copies of gK are under control of the LAT promoter. However, gK transcripts were also detected in some mice infected with the wt McKrae virus. These results suggest that gK is transcribed in the TG of latently infected mice. The low level of expression of gK in some of the infected mice could explain our recently published data showing that individuals with a history of ocular HSV-1 infection had higher anti-gK antibody titers than did HSV-1-seropositive individuals with no history of ocular infection (40). In support of this idea, analysis of latently infected TG sections revealed abundant expression of viral transcripts, viral protein, and viral DNA replication in about 1 neuron per 10 TG tested (9). However, no infectious virus was detected in any of these TG.
In this study, we also detected gB transcripts 30 days p.i. in the TG of C57BL/6 mice, indicating that a chronic infection can be established by HSV-gK3(but not in BALB/c mice, an
effect that may be due to differential responses of these two mouse strains to virus infection). The TG, specifically the nuclei of neuron bodies, are known to be the site of latent, not
chronic, infection following the HSV-1 ocular challenge of mice (5, 51). When mouse TG are removed at autopsy and the explant is cocultivated in tissue culture media with indicator cells, latent viruses reactivate and can be observed via CPE on the indicator cell monolayer (15, 22). In contrast, when cell-free lysates of latently infected TG are plated on indicator cells, CPE is not observed (15). This indicates that there is no infectious virus present in the TG and confirms that reactiva-tion from latency by cocultivareactiva-tion requires that explant of intact neurons (5, 15, 22). However, in this study we have shown that the HSV-gK3-mediated ocular infection of mice
resulted in a chronic infection in the TG. Although we repeat-edly found infectious virus in the TG of gK3“latently” infected
mice, we did not detect infectious virus in the brains or cornea of the same mice. The reason for this is currently not under-stood, but it suggests that this virus in the TG does not effi-ciently spread to and/or replicate in the brain or the cornea at this time. Similar to HSV-gK3virus, we have previously shown
that ocular infection of AO/Omice immunized with
baculo-virus-expressed gK also resulted in a chronic HSV-1 infection in those mice (15). Finally, during latency, the levels of CD8⫹ T-cell transcripts in the TG of mice infected with HSV-gK3or
McKrae were higher than the levels of CD4⫹T-cell transcripts, especially in HSV-gK3-infected mice. Previously, it was shown
that CD8⫹T cells could block HSV-1 reactivation from latency in sensory neurons without destroying the infected neurons (35). However, in HSV-gK3-infected C57BL/6 mice, the
pres-ence of high levels of CD8⫹T-cell transcripts in the TG did not correlate with the quiescence of virus during the latent stage of HSV-1 infection.
In summary, the results presented here support the hypoth-esis that overexpression of gK from the LAT promoter in-creases CS in mice.
The pathogenic role of gK in HSV-1-induced CS appears to be mediated by CD8ⴙT cells. However, the effect of similar overexpression of a different HSV-1 glycoprotein on CS in mice remains to be determined. Finally, these results suggest that viral gK may play a role in immune evasion.
ACKNOWLEDGMENTS
This work was supported by NIH grant EY13615 and the Skirball Program in Molecular Ophthalmology to H.G.
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