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Journal of Virology, June 1999, p. 5196-5200, Vol. 73, No. 6
0022-538X/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.

Gamma Interferon (IFN-gamma ) Receptor Null-Mutant Mice Are More Susceptible to Herpes Simplex Virus Type 1 Infection than IFN-gamma Ligand Null-Mutant Mice

Edouard Cantin,1,* Becky Tanamachi,1 Harry Openshaw,1 Jeff Mann,2 and Ken Clarke3

Department of Neurology,1 Division of Biology,2 and Division of Biostatistics,3 Beckman Research Institute, City of Hope National Medical Center, Duarte, California 91010

Received 15 December 1998/Accepted 22 February 1999


    ABSTRACT
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Mouse strains with null mutations in the gamma interferon gene (Ifng) or the gamma interferon receptor gene (Ifngr) have been engineered. The use of these strains as animal models of viral and bacterial infections has enhanced our understanding of the role of gamma interferon (IFN-gamma ) in the host immune response. However, direct comparisons between Ifng-/- (GKO) and Ifngr-/- (RGKO) mice have been problematic because previously available strains of these mice have had different genetic backgrounds (i.e., C57BL/6 and BALB/c for GKO mice and 129/Sv//Ev for RGKO mice). To enable direct comparison of herpes simplex virus type 1 (HSV-1) infections in GKO and RGKO mice, we introduced the IFN-gamma null mutation into the 129/Sv//Ev background. We report that, after HSV-1 inoculation, mortality was significantly greater in RGKO mice than in GKO mice (38 versus 23%, P = 0.0001). Similarly, the mortality from vaccinia virus challenge was significantly greater in RGKO mice than in GKO mice. With differences in genetic background excluded as a confounding issue, these results are consistent with the existence of an alternative ligand(s) for the IFN-gamma receptor that is also capable of mediating protection against viral challenge.


    TEXT
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Gamma interferon (IFN-gamma ) was originally referred to as immune interferon in recognition of its antiviral activity. However, IFN-gamma is currently better known for the remarkable spectrum of pleiotropic effects it elicits in diverse tissues and particularly for its unique immunoregulatory properties which distinguish it from IFN-alpha /beta , other antiviral proteins in the interferon family. The antiviral effects of IFN-gamma are not as well understood, but they appear to be especially important for long-term control of viral infections (4, 38). IFN-gamma also mediates protection against intracellular microbes, including certain viruses, by activating macrophages and other mononuclear phagocytes to produce nitrous oxide (2, 4). IFN-gamma and IFN-alpha /beta bind to distinct receptors, and no cross-reactivity has been observed. IFN-gamma binds to the alpha  chain of the high-affinity IFN-gamma receptor that is ubiquitously expressed on different cell types, and it is the only known ligand for this receptor. A low-affinity IFN-gamma receptor has been identified on human macrophages, but its physiological significance is unknown (1, 13).

Recent studies of null-mutant mice have confirmed the importance of IFN-gamma in the host immune responses to several bacterial and viral pathogens, including herpes simplex virus type 1 (HSV-1), vaccinia virus, measles virus, and Theiler's virus (5, 9, 16, 17, 24). Studies with these IFN-gamma mutant strains have also provided evidence, albeit controversial at times, supporting and refuting the involvement of IFN-gamma in autoimmune diseases such as experimental allergic encephalomyelitis, experimental autoimmune myasthenia gravis, and insulin-dependent diabetes mellitus (2, 15, 25, 40). Controversy has arisen from the fact that different results have been obtained from various studies depending on whether the null mutation is in the IFN-gamma gene (Ifng) (GKO mice) (10) or in the IFN-gamma receptor gene (Ifngr) (RGKO mice) (24). Previously, GKO and RGKO mice have been available only in different genetic backgrounds (i.e., C57BL/6 and BALB/c for GKO and 129/Sv//Ev for RGKO).

Previously we reported a prolonged inflammatory response in the trigeminal ganglion after ocular inoculation with HSV-1 (7). We showed the CD4+ and CD8+ T cells associated with the large amounts of IFN-gamma which were tightly surrounding neurons (some of which were latently infected with HSV-1 as shown by in situ hybridization). These observations led to speculation that IFN-gamma might play a role during HSV-1 infection, and we proposed the use of GKO and RGKO strains to directly test this hypothesis. However, the strain restrictions of these mice were problematic, since it is known that different mouse strains vary in susceptibility to HSV-1, with the C57BL/6 strain being relatively resistant to the virus (26). To circumvent the influence on experimental outcome of the different genetic backgrounds of the mutant mice, the IFN-gamma null mutation was introduced into the 129/Sv//Ev background. This enabled the direct comparison of the outcomes of HSV-1 infections of GKO and RGKO mice, which differed genetically only at the mutant locus.

Isolation of the IFN-gamma null mutation in the 129/Sv//Ev background. The AB-1 embryonic stem (ES) cell clone 97E of the 129/Sv//Ev strain, heterozygous for a mutation in Ifng (9), was obtained from Tim Stewart (Genentech), expanded, and injected into blastocysts of the C57BL/6 strain. Chimeric founder males were mated to 129/Sv//EvTac female mice (Taconic Farms, Inc., Germantown, N.Y.) to generate 129/Sv//Ev mice heterozygous for the IFN-gamma null mutation. Offspring resulting from germ line transmission of the ES cell genome were identified by glucose phosphate isomerase-1 (Gpi-1s) isozyme assay, type A (distinct from type AB) mice (22) were selected, and of these selected mice, those carrying the mutation were identified by PCR. The IFN-gamma mutation was thereby retained in the 129/Sv//Ev genetic background. Ifng+/- heterozygous mice were intercrossed to produce Ifng-/- homozygous, GKO mutant mice which were identified by PCR analysis of DNA extracted from their tails for IFN-gamma and Neor gene sequences. In Fig. 1a, PCR genotyping results for several offspring from matings of heterozygous Ifng+/- mice are presented. GKO mice homozygous for the IFN-gamma null mutation (Ifng-/-) are identified by the exclusive presence of the 375-bp Neor band and the absence of the 220-bp IFN-gamma band (Fig. 1a). The PCR genotyping results were confirmed by probing Southern blots of BamHI-digested tail DNA from the same mice with an Ifng cDNA probe (not shown) (9), and from these latter mice, a breeding colony was derived and maintained. Reverse transcriptase (RT)-PCR analysis of GKO spleen cells stimulated in vitro with concanavalin A (ConA) failed to detect IFN-gamma mRNAs, whereas these transcripts were readily detected in ConA-stimulated spleen cells from RGKO and control 129/Sv//Ev mice, confirming the GKO null-mutant phenotype (Fig. 1b).


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  		FIG. 1.   (a) PCR genotyping of GKO mice. Tail DNA from offspring of matings of heterozygous 129/Sv//Ev mice were analyzed by PCR for IFN-gamma and Neor gene sequences to identify mice homozygous for the IFN-gamma null mutation. The upper band is the Neor gene amplification product, and the lower band is the IFN-gamma gene amplification product. PCR primers for IFN-gamma gene are as follows: forward, 5'-AGAAGTAAGTGGAAGGGCCCAGAAG, and reverse, 5'-AGGGAAACTGGGAGAGGAGAAATAT, giving a 220-bp product. Primers for the Neor gene are as follows: forward, 5'-TCAGCGCAGGGGCGCCCGGTTCTTT, and reverse, 5'-ATCGACAAGACCGGCTTCCATCCGA, giving a 375-bp product. (b) RT-PCR for Ifng mRNA. cDNA preparations from ConA-stimulated spleen cells isolated from 129/Sv//Ev mice (lanes 1 and 2), GKO mice (lanes 3 and 4), and RGKO mice (lanes 5 and 6) were amplified with Ifng-specific primers. M, markers; GAPDH, glyceraldehyde-3-phosphate dehydrogenase.

Breeding pairs of mice homozygous for the null mutation in Ifngr (129/Sv//Ev, RGKO) were obtained from Michel Aguet (Institute of Molecular Biology, University of Zurich) (23). RGKO and GKO mice were bred under specific-pathogen-free conditions in a vivarium at the City of Hope National Medical Center. 129/Sv//EvTac control mice (referred to herein as 129/Sv//Ev mice) were purchased from Taconic Farms, Inc. Experiments were conducted in strict compliance with the Guidelines on the Care and Use of Laboratory Animals in facilities accredited by the American Association for Accreditation of Laboratory Animal Care. All experiments with mice were approved by the Institutional Research and Animal Care Committee, and ocular experimental procedures were conducted according to the Association for Research in Vision and Ophthalmology resolution on the use and care of laboratory animals.

Mortality of vaccinia virus-infected GKO, RGKO, and control mice. Prior studies with normal mice and mice unresponsive to IFN-gamma due to a null mutation in Ifng or Ifngr have established that interferon is crucial for survival after inoculation with poxviruses such as vaccinia virus (31). To confirm the susceptibility of GKO mice with the 129/Sv//Ev background to vaccinia virus and to directly compare the response of the GKO and RGKO strains, mutant and control male mice were challenged with vaccinia virus by tail vein inoculation. The results presented in Fig. 2 confirm that the control 129/Sv//Ev mice were completely resistant to vaccinia virus infection as expected (9, 31, 39). Compared to the mortality rates of control mice, the mortality rates in vaccinia virus-infected GKO mice were high (56%) (P = 0.002) and even higher (92%) in RGKO mice (P = 0.0001). The difference in mortality rates between RGKO and GKO mice was significant (P = 0.03) and corresponded to a 3.3-fold increase in the relative risk of death for RGKO mice inoculated with HSV-1 compared to similarly inoculated GKO mice (95% confidence limit).


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  		FIG. 2.   Survival of vaccinia virus-infected 129/Sv//Ev, GKO, and RGKO mice. Deeply anesthetized, 6- to 8-week-old male mice were inoculated intravenously with 107 PFU of vaccinia virus. There were 12 mice in each group, except that the GKO group had 9 mice. Mice were monitored daily over a 20-day period, and mice with symptoms of life-threatening disease were euthanatized.

Mortality of HSV-1 Infected GKO, RGKO, and control mice. To determine the role of IFN-gamma during the acute stage of HSV-1 infection, deeply anesthetized, 6- to 8-week-old male GKO, RGKO, and 129/Sv//Ev mice were inoculated with HSV-1 F strain (American Type Culture Collection, Rockville, Md.) by gently massaging a 4-µl drop containing 105 to 107 PFU of virus into the scarified cornea of the right eye (7). Mice were monitored twice daily for signs of morbidity and development of encephalitis, and mice with symptoms indicative of imminent death due to encephalitis were euthanatized. Clinical signs of HSV-1 infection, including corneal clouding (an early sign of herpes stromal keratitis), eyelid disease, ruffled coat, and signs of encephalitis, such as circling behavior and impaired coordination and movement, were first seen in the IFN-gamma mutant mice and were generally more severe and prolonged in the IFN-gamma mutant mice than in the 129/Sv//Ev mice. The most noticeable sign of HSV-1 infection in these mice (and particularly in the RGKO strain) was periocular skin disease characterized, in its most severe stage, by the complete loss of facial hair around the inoculated eye and extending down the snout and up to, and including, the forehead and often accompanied by bleeding and skin lacerations. Whereas most of the GKO and control mice recovered, most of the RGKO mice showed progressive deterioration.

The survival data for GKO, RGKO, and 129/Sv//Ev mice inoculated with HSV-1 are presented in Fig. 3. Mortality rates were calculated based on the total number of deaths occurring after inoculation with HSV-1. Figure 3 summarizes mortality data accrued from multiple experiments involving HSV-1 infection of large numbers of mice (150 129/Sv//Ev, 244 GKO, and 380 RGKO) used in the course of studying the role of IFN-gamma during acute and latent infection, and therefore, the statistical significance of the data is very high. Univariate Cox regression (8) was performed to identify the risk factors that increased rates of mouse mortality. Possible risk factors evaluated included gender, mouse strain, and inoculum dose. All significance testing was performed at the 0.05 level (two sided).


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  		FIG. 3.   Survival of HSV-1-infected 129/Sv//Ev, GKO, and RGKO mice. Male, 6- to 8-week-old mice were inoculated in the right eye by ocular scarification with doses of HSV-1 ranging from 105 to 107 PFU. Mice were monitored daily over a 20-day period for signs of encephalitis, and mice with pronounced symptoms indicative of imminent death were euthanatized. As no statistically significant difference was found between groups given inocula of 105, 106, or 107 PFU, the data from these three groups were pooled and analyzed together.

Two significant findings emerged from the studies that compared HSV-1 infection in GKO and RGKO mice to infection in 129/Sv//Ev mice. The first is that disruption of Ifng did not affect rates of mortality in HSV-1-infected mice compared to the mortality rates in control 129/Sv//Ev mice (Fig. 3). The mortality rate was 23% in both groups. The second, and most interesting, finding in our study was that mice with a disrupted Ifngr gene had a twofold increase in risk of death (at the 95% confidence limit) after HSV-1 inoculation compared to GKO and 129/Sv//Ev mice (Fig. 3). The overall mortality rate was 38% in RGKO mice, compared to 23% in GKO mice (P = 0.0001) and 23% in the 129/Sv//Ev mice (P = 0.0003). The difference in susceptibility of RGKO and GKO mice to HSV-1 essentially confirms the results obtained after vaccinia virus challenge (Fig. 2) and suggests that the difference in viral susceptibility of RGKO and GKO mice might be more general. These results show that IFN-gamma fails to confer protection against mortality induced by HSV-1 infection, while, in contrast, the presence of the IFN-gamma receptor (as in GKO mice) was associated with a significant protective effect.

Time course of HSV-1 infection in RGKO and GKO mice. The increased mortality of RGKO compared to GKO and 129/Sv//Ev mice suggested the possibility of enhanced replication and/or persistence of HSV-1 in the RGKO mice. We have previously reported a statistically significant higher mean titer in the trigeminal ganglia and brain stem cells of RGKO than in 129/Sv//Ev mice 3 to 4 days after HSV-1 inoculation; however, the difference in titer was slight (<0.5 log) (7). More recently, we determined the daily viral titers in trigeminal ganglia and brain stem cells from days 2 to 7 after HSV-1 inoculation. The results showed that, contrary to expectation, there was no significant difference in either the kinetics of HSV-1 replication or clearance in the trigeminal ganglia of RGKO, GKO, and 129/Sv//Ev mice (6). More relevant to the mortality results presented here, Fig. 4 shows a time course of daily brain stem HSV-1 titers in the RGKO, GKO, and 129/Sv//Ev mice. For statistical comparison of HSV-1 titers, the total plaque counts for the three mouse groups were fitted to an overdispersed Poisson model. Statistical analysis of HSV-1 titers in the eye indicated a significantly greater likelihood of HSV-1 persistence in the eyes of GKO and RGKO mice than in 129/Sv//Ev mice (not shown), similar to the study of Bouley et al., which showed persistence of HSV-1 in the tear film of GKO, but not control, mice (5). Persistence of HSV-1 in the eyes of IFN-gamma mutant mice shows that IFN-gamma -dependent mechanisms are crucial for clearance of HSV-1 from the eye, as was previously shown for skin infections (21, 35). However, we found no significant difference in brain stem viral titers over the course of the infection (Fig. 4). All the mice surviving inoculation with HSV-1 were confirmed as being latently infected.


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  		FIG. 4.   Time course of HSV-1 infection in 129/Sv//Ev, GKO, and RGKO mice. The right eyes of 6- to 8-week-old male mice were inoculated with 106 PFU of HSV-1 by ocular scarification. Three mice from each group were sacrificed daily from day 2 through day 7, and HSV-1 titers in brain stem cells were determined. The whole-tissue HSV-1 titers were plotted against day postinoculation for 129/Sv//Ev (strain T), GKO (strain G), and RGKO (strain R) mice. There was no statistically significant difference in HSV-1 titers in the brain stem cells for the three groups of mice.

At face value, the equivalent titers are surprising, since cell culture studies have demonstrated inhibition of HSV-1 by IFN-gamma (11, 14). However, the results from our time course study are in agreement with an earlier study of GKO mice from another group which showed no difference in mean HSV-1 titers in nervous system tissue at set times after HSV-1 inoculation (19). Indeed, other studies using an IFN-gamma -transgenic model showed that IFN-gamma protected against HSV-1-induced mortality without significantly affecting HSV-1 titers in the nervous system of transgenic, compared to nontransgenic, mice (18). Similarly, in studies with murine gamma herpesvirus 68, there was no difference in viral load or rate of virus clearance in the lungs of infected RGKO mice compared to 129/Sv//Ev mice (12). In contrast to the apparent dispensability of IFN-gamma in the control of murine gamma herpesvirus 68 in the lung, severe structural damage and elevated latency loads were seen in the spleens of RGKO, but not 129/Sv//Ev, mice.

Contrasting its role in acute infection, we have recently demonstrated a role for IFN-gamma in the control of reactivated HSV-1 whereby it contributes to the maintenance of biological latency (i.e., the absence of infectious HSV-1 in ganglionic homogenates or HSV-1 antigens in ganglionic sections) (6). Because infectious HSV-1 has never been found in mice not subjected to hyperthermia to induce reactivation, we suggested that IFN-gamma does not maintain molecular latency (i.e., it does not block the reactivation process itself). Considered together, the results of our studies assessing the role of IFN-gamma during acute and latent infection are consistent with the postulated role of IFN-gamma in the long-term control of viral infections (38).

Possible explanations for the phenotypic difference between RGKO and GKO mice. We do not think that minor differences in genetic background can explain the higher mortality rates of RGKO compared to GKO mice (3, 20). This is because the GKO strain used in this study was derived from the same 129/Sv//Ev background as was the RGKO strain. Although the 129/Sv//Ev strain used to derive the GKO strain was Gpi1sc/Gpi1sc, we selected Gpi1sa/Gpi1sa animals for propagation because RGKO mice, also derived with AB-1 ES cells, are Gpi1sa/Gpi1sa (unpublished observation). For the GKO strain, the Gpi1sa allele originated from the AB-1 ES cell clone that carried the targeted mutation of Ifng (24). We typed two independent AB-1 ES clones, including the clone used here, and found that they were both Gpi1sa/Gpi1sa and not Gpi1sc/Gpi1sc, as previously reported for AB-1 ES cells (34). Based on this analysis, we believe the GKO and RGKO strains to be isogenic except for the mutant locus and to differ from the control 129/Sv//Ev strain at Gpi1s. Such minor differences in histocompatibility loci between the IFN-gamma knockout strains (GKO and RGKO mice) and 129/Sv//Ev would not be expected to influence the results reported here. However, prior studies of HSV-1 infection in GKO mice of different genetic backgrounds have produced dramatically different results. Thus, Geiger et al. (19) reported no mortality in C57BL/6 control or C57BL/6 GKO mice inoculated with HSV-1 strain F, while, in contrast, Bouley et al. (5) reported that BALB/c GKO mice died after inoculation with a dose of HSV-1 which was sublethal when routinely used to induce herpes stromal keratitis in control BALB/c mice. Aside from differences in the genetic background of GKO strain studied, differences in HSV-1 strain, route of inoculation, age, and gender of the mice used could all contribute to the discrepant mortality rates of the different GKO strains (3, 34). For example, we found that gender strongly influenced the outcome of HSV-1 infection in both IFN-gamma mutant and control mice, with males being more susceptible than females (20a).

The interpretation that we favor for these results is that some novel ligand induced by viral infection elicits a protective response against HSV-1 and vaccinia virus infections in GKO mice by virtue of its interaction with the IFN-gamma receptor which is functional in GKO, but not in RGKO, mice (9, 24). Although not formally excluded, the notion that the mere presence of the receptor, independent of ligand binding, can somehow protect against viral challenge is much less attractive, because it is difficult to envisage how such a mechanism could affect virus infection. We considered potential developmental effects of the Ifng-/- and Ifngr-/- mutations but could not conceive an explanation that could account for our results without the presence of an alternative ligand for the receptor. As an explanation for our results, we also considered the possibility that IFN-gamma signaling through the low-affinity IFN-gamma receptor (1, 13) somehow enhances susceptibility to viral infections in RGKO mice. But, even if this mechanism exists, it would not explain the relative resistance to viral infection that we observed in GKO mice. We even considered the possibility that a prior, inapparent, bacterial or viral infection in our IFN-gamma mutant colonies could, through effects on the host immune response, have altered the outcome of a subsequent virus infection, as was recently shown for selected virus pairs (33). Since both colonies of mice were housed together, it is likely that both would have been infected with the unknown agent (if such an infection had occurred), and hence, it is difficult to explain the relative resistance of GKO mice compared to RGKO mice on this basis. Finally, our hypothesis is consistent with the conclusions drawn in other systems where similar phenotypic discrepancies between ligand and receptor null mutants have been found. Invariably, the proposed, and in some instances verified, explanation for the discrepancy has been that the receptor was indeed being utilized by another, closely related but previously unrecognized, ligand(s) (10, 28, 29).

A candidate for the novel ligand in the GKO mice is the neuronal IFN-gamma immunoreactive molecule (N-IFN-gamma ), which has recently been purified from rat trigeminal ganglia by using two monoclonal antibodies (DB1 and DB16) that recognize distinct epitopes in rat IFN-gamma (30). Although distinct from authentic IFN-gamma , N-IFN-gamma shares many of its biological properties, including induction of major histocompatibility complex class I and II antigens on macrophages and cultured skeletal muscle cells, direct antiviral activity, and growth-stimulatory activity for Trypanosoma brucei. The proposed existence of N-IFN-gamma is controversial, though, because no other reports confirming the isolation of this protein have been made. However, a recent independent study, combining whole-cell patch-clamp electrophysiology with single-cell RT-PCR and confocal laser immunocytochemistry, has demonstrated the expression of IFN-gamma in cultured, fetal-rat, dorsal root ganglion neurons (27). Because the same DB1 antibody was used for immunostaining, this neuron-expressed IFN-gamma may be identical to N-IFN-gamma (30). The putative N-IFN-gamma is an attractive candidate as the novel ligand for the IFN-gamma receptor, since it is thought to be expressed in sensory ganglionic neurons, the primary site of HSV-1 replication and latency (32, 36). After ocular inoculation, HSV-1 spreads by retrograde axonal transport to sensory ganglionic and central nervous system neurons, where compensatory upregulation of inducible N-IFN-gamma expression may occur, conferring resistance to infection to GKO mice. The validity of this hypothesis can be tested once the putative N-IFN-gamma gene is isolated, as detailed characterization and elucidation of the pattern of expression of the protein will then be possible. Derivation of the IFN-gamma null mutation in the same 129/Sv//Ev background as the IFN-gamma receptor null mutation should prove useful for examining the diverse biological roles of IFN-gamma . In particular, these strains can be used to determine the mechanisms underlying the differences in susceptibilities to autoimmune diseases and infections previously reported for IFN-gamma null mutant mice (15, 25, 37, 41).


    ACKNOWLEDGMENTS

We thank Michel Aguet for supplying the RGKO mouse strain and Tim Stewart for supplying the ES cell clone carrying the null mutation for Ifng.

This work was supported by Public Health Service grant MH55784 from the National Institute of Mental Health.


    FOOTNOTES

* Corresponding author. Mailing address: City of Hope Medical Center, Department of Neurology, 1500 E. Duarte Rd., Duarte, CA 91010. Phone: (626) 301-8480. Fax: (626) 301-8852. E-mail: ecantin{at}coh.org.


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Journal of Virology, June 1999, p. 5196-5200, Vol. 73, No. 6
0022-538X/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.


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