Host–Virus Interactions during Malaria Infection in Hepatitis B Virus Transgenic Mice

Mice.

HBV transgenic mouse lineages 1.3.32 and 1.3.46 used in this study have been described previously 35. Both lineages of mice replicate HBV at high levels in the liver and kidney without any evidence of cytopathology. Lineage 1.3.32 was derived from an outbred founder. It was expanded by repetitive backcrossing for more than 10 generations against C57BL/6, and then bred 1 generation against BALB/c mice to produce F₁ hybrids that were used in this study. Lineage 1.3.46 was derived from an inbred B10D2 founder and has been continually expanded on that background. In the current study, lineage 1.3.46 was backcrossed against a panel of mice whose IFN-γ (IFN-γ^−/−) 36, IFN-α/β receptor (IFN-α/βR^−/−) 37, TNF-αp55 receptor (TNF-αR^−/−) 38, or inducible nitric oxide synthase (iNOS) (iNOS^−/−) 39 alleles had been knocked out, exactly as described 2 5. The IFN-γ^−/− and IFN-α/βR^−/− mice were provided, respectively, by Timothy Stewart and Michel Aguet (Genentech, Inc., South San Francisco, CA). The TNF-αR^−/− mice were provided by Tak Mak (University of Toronto, Ontario, Canada). The iNOS^−/− mice were provided by John Mudgett (Merck Research Laboratories, Rahway, NJ) and John MacMicking and Carl Nathan (Cornell University Medical College, New York, NY). The genetic background of the original knockout animals was 129/Sv/Ev/ × C57BL/6. Before mating with the HBV transgenic mice, the IFN-γ^−/− mice had been backcrossed four to five generations against BALB/c and the IFN-α/βR^−/−, and the TNF-αR^−/− and iNOS^−/− mice had been backcrossed more than five generations against C57BL/6. The serum from the 1.3.46 × knockout F₁ progeny was tested for hepatitis B e antigen (HBeAg)-positive using a commercially available kit (Abbott Laboratories). HBeAg-positive F₁ mice were backcrossed to the corresponding parental knockout lineage to produce HBeAg-positive F₂ progeny that were either homozygous or heterozygous for the null allele that was distinguishable by allele-specific PCR reactions, as described previously 36 37 38 39. Thus, the HBV × knockout animals were genetically heterogeneous with variable contributions from BALB/c, B10D2, and C57BL/6 parental strains. In all experiments, the mice were matched for age (8 wk), sex (male), and serum HBeAg levels before experimental manipulation. All animals were housed in pathogen-free rooms under strict barrier conditions.

P. yoelii Infection.

The P. yoelii yoelii (17X NL nonlethal strain) was maintained by alternating passage of the parasites in Anopheles stephensi mosquitoes and in B10.D2 mice, as described previously 40 41. Sporozoites were collected 14 d after an infectious blood meal by hand dissection of P. yoelii 17 XNL–infected mosquito salivary glands in M199 medium containing 1% normal mouse serum (Rockland, Inc.) as described previously 42. Erythrocytic stage parasites were obtained from heparinized blood of a previously sporozoite-infected mouse, and maintained by cyclic passages of the parasites in congenic mice, as described previously 43. The parasitized RBCs were collected in equal volume of HBSS (GIBCO BRL) plus 20% glycerol (Sigma-Aldrich) plus 100 U/ml heparin (Sigma-Aldrich), and kept in liquid nitrogen. Mice were injected either intravenously with 10⁶ sporozoites or intraperitoneally with 10⁷ parasitized RBCs. Control mice were injected either with an extract of uninfected salivary glands or with uninfected RBCs, respectively. Animals were killed at multiple time points after infection, and their livers were harvested for histological, immunohistochemical, and histochemical analyses (see below), or they were snap frozen in liquid nitrogen and stored at –80°C for subsequent DNA and RNA analyses. Parasitemia was determined by microscopic examination of Giemsa-stained thin blood smears, obtained from days 1–30 after inoculation.

Tissue DNA and RNA Analyses.

Frozen liver (left lobe) was mechanically pulverized under liquid nitrogen, and total genomic DNA and RNA were isolated for Southern and Northern blot analyses exactly as described previously 35. Nylon membranes were analyzed for HBV DNA, HBV RNA, glyceraldehyde-3-phosphate dehydrogenase (GAPDH), and 2′5′-oligoadenylate synthetase (2′5′-OAS) as described elsewhere 4. Quantification of iNOS, cytokine, T lymphocyte, and macrophage and neutrophil marker mRNAs was performed by RNase Protection assay exactly as described previously 4 8 44. A fragment (nucleotides 124–368) from the mNK1.1 cDNA (Genbank accession number S43141) was subcloned into a PGEM-T Easy vector (Promega) using PCR-assisted cloning 44. The vector was linearized and used for T7 polymerase–directed synthesis of a ³²P-labeled antisense RNA probe. The hybridization reactions, RNase treatments, isolations of protected RNA duplexes, and resolution of protected probes by denaturing PAGE gels were carried out as described 44. Dried gels were placed on film (XAR; Eastman Kodak Co.) with intensifying screens for various periods of time at −70°C.

Biochemical and Histological Analysis.

The extent of hepatocellular injury during malaria infection was monitored histologically and biochemically by measuring serum alanine aminotransferase (sALT) activity at multiple time points after infection. sALT activity was measured in a Paramax chemical analyzer (Baxter Diagnostics, Inc.) exactly as described previously 4. For histological analysis, liver tissue was fixed in 10% zinc-buffered formalin (Anatech), embedded in paraffin, sectioned (3 μm), and stained with hematoxylin and eosin.

P. yoelii Infection: Parasitemia and Liver Disease in HBV Transgenic Mice.

21 age-, sex-, and serum HBeAg-matched transgenic mice from lineage 1.3.32 were infected either intravenously with 10⁶ P. yoelii sporozoites (liver stage), or intraperitoneally with 10⁷ parasitized RBCs (blood stage), and groups of three mice were killed on days 1, 3, 5, 10, 15, and 20 after infection. Control mice were injected with either uninfected salivary glands or uninfected RBCs. The infected animals developed a time-dependent necroinflammatory liver disease that was detectable histologically starting 1 d after infection and lasted for 10–15 d until the parasites were no longer detectable in the blood on day 20 (Fig. 1 A). In keeping with the fact that 10⁶ sporozoites cannot infect more than 10⁶ hepatocytes (1% of the hepatocyte population) and that the blood stage parasites do not infect hepatocytes, very few hepatocytes were destroyed during the infection. This was reflected in the very slight elevation in serum sALT activity that was detectable between days 3 and 10 after liver stage inoculation, and the even smaller sALT elevation between days 1 and 3 after blood stage inoculation (Fig. 1 A). At the peak of parasitemia in both types of infection (day 10), many of the hepatic macrophages (Kupffer cells) were filled with malaria pigment derived from ruptured infected erythrocytes, and at this time a large number of inflammatory foci consisting of Kupffer cells and lymphomononuclear cells were widely distributed throughout the liver (Fig. 1B and Fig. C). Numerous pigment-laden macrophages surrounded by lymphomononuclear cells were present (Fig. 1 C, inset). The histological features of the disease are strikingly similar in both the sporozoite and merozoite infections, suggesting that the inflammatory process in the sporozoite-infected animals was probably due primarily to the blood stage of that infection, although small numbers (∼10⁶ or ∼1% of total) of hepatocytes were destroyed by the sporozoites in the liver stage infection, as suggested by the slightly higher sALT activity in that infection (Fig. 1 A). Finally, the histopathological features of the liver disease during either the liver or the blood stage of infection were not influenced by the genetic background of the animals, since in independent experiments we showed very similar results after malaria infection of C57BL/6, B10.D2, and BALB/c mice (not shown).

P. yoelii Infection: Effect on HBV Gene Expression and Replication.

Northern and Southern blot analyses were performed to compare the levels of HBV RNA and replicative HBV DNA forms in P. yoelii–infected mice and in age- and sex-matched transgenic controls. After extraction, total hepatic RNA and DNA from three mice per group were pooled for analysis. As shown in Fig. 2 (A and B), hepatic HBV RNA and replicative DNA forms were slightly reduced on day 1 after liver stage infection while they were unchanged at this time after blood stage infection. Correspondingly, 2′5′-OAS mRNA, a type 1 IFN-inducible gene, TNF-α mRNA, iNOS mRNA, as well as the macrophage marker F4/80 were slightly induced in the liver stage but not the blood stage infection, and IFN-γ, CD3, CD4, CD8, and NK1.1 mRNAs were not increased (Fig. 2 C). These results indicate that macrophages are the likely source of the IFN-α/β, TNF-α, and iNOS detected on day 1, especially since they are known to produce these factors upon activation 45.

By day 3, hepatic HBV RNA and DNA were strongly reduced in both liver stage and blood stage infected mice. In the liver stage infection, this was accompanied by a strong induction of IFN-γ and iNOS mRNA and a slight further increase in 2′5′-OAS and TNF-α mRNA even though T cell markers were unchanged and NK cell markers were only slightly increased. In contrast, on day 3 of the blood stage infection, IFN-γ and iNOS mRNAs were much less strongly induced than in the liver stage infection, even though the T cell and macrophage markers were more strongly induced. In addition, 2′5′-OAS and NK cell mRNAs were relatively more abundant in these mice than in the liver stage infection. The relatively strong induction of IFN-γ after liver stage infection suggests that the resident and/or recruited intrahepatic population of NK, NKT, and T cells may have become activated to produce the cytokines at this time. The induction of iNOS mRNA suggests that the macrophages were further activated at this time point, presumably due to the increased levels of IFN-γ in the liver.

On day 5 after both infections, HBV replication and HBV gene expression remained suppressed, especially in the liver stage infection where 2′5′-OAS mRNA was very strongly induced, and where NK1.1 mRNA was more prominent and T cell markers were strongly enhanced. Not surprisingly, this was associated with the continued expression of iNOS, IFN-γ, and TNF-α. In both infections, the T cell and macrophage response, as well as IFN-γ and TNF-α gene expression, continued through day 10 when the parasitemia was at its peak (Fig. 1 A) and HBV replication was most profoundly suppressed. By day 15, the parasites were almost completely cleared from the circulation, and cytokine, macrophage, T cell markers, and sALT activity returned toward baseline levels, as did the hepatic content of HBV DNA and HBV RNA. All of these events were completed by day 20.

In summary, while the histological features of the two infections are quite similar, the liver stage infection appeared to trigger an early T cell–independent cytokine response as well as a delayed cytokine response that coincided with the infiltration of T cells. In contrast, the T cell response occurred earlier in the blood stage than in liver stage infection, perhaps because parasitemia was detectable earlier in those animals, and a T cell–independent phase was not observed, perhaps indicating that it was induced primarily by infected hepatocytes. In both cases, however, the induced cytokine responses were associated with a decrease in HBV RNA and DNA in the liver.

P. yoelii–induced Suppression of HBV Replication Is Mediated by IFNs.

Since IFN-γ, TNF-α, 2′5′-OAS, and iNOS gene expression coincided with HBV downregulation in the foregoing experiment, and since we have previously shown that the corresponding cytokines and NO inhibit HBV replication under other experimental conditions 2 3 4 5 6 7, we monitored the ability of P. yoelii merozoites to inhibit HBV replication in HBV transgenic mice whose ability to produce IFN-γ or iNOS, or to respond to TNF-α or IFN-α/β had been knocked out. Groups of four age-, sex-, and HBeAg-matched transgenic mice that were either homozygous or heterozygous for each of these null alleles were injected intraperitoneally with 10⁷ merozoite-infected RBCs to initiate a blood stage infection. 10 d after infection, their livers were harvested and total hepatic DNA and RNA were extracted and subjected to Southern blot analysis for HBV DNA, Northern blot analysis for 2′5′-OAS mRNA, and RNase Protection assays for cytokine, F4/80, and T cell mRNA content. Since each mouse in each group of four mice showed identical results, two representative mice per group are shown in Fig. 3. As expected, HBV replication was abolished in all of the heterozygous control mice (represented by the IFN-α/β^+/− heterozygous animals in Fig. 3 A), coinciding with induction of 2′5′-OAS, TNF-α, IFN-γ, and T cell mRNAs (Fig. 3 B). Importantly, HBV replication was not suppressed in the IFN-γ knockout mice, despite the induction of 2′5′-OAS; it was only slightly suppressed in the absence of the IFN-α/β receptor, despite the induction of IFN-γ. These results suggest that IFN-γ and IFN-α/β act independently to inhibit HBV replication after P. yoelii infection. Surprisingly, HBV replication was inhibited in the absence of both iNOS and the TNFp55 receptor, indicating that neither NO nor TNF-α receptor–mediated signaling contributes substantially to the antiviral effect of the merozoites as long as IFN-α/β and IFN-γ are expressed in the liver. The surprising apparent irrelevance of TNF-α might be explained by the fact that 2′5′-OAS (i.e., IFN-α/β) and IFN-γ are hyperinduced in these animals, suggesting that, at these levels, the IFNs might compensate for the absence of TNF-α and be sufficient to downregulate HBV independently. The fact that the IFN-γ–associated antiviral effect was not seen in the iNOS knockout mice (Fig. 3) was also surprising, since the IFN-γ–dependent inhibition of HBV replication by CTLs is mediated by NO 4. This is compatible with two interpretations. First, the antiviral effect in those animals could be mediated by IFN-α/β since the 2′5′-OAS mRNA was strongly induced, and we have shown that the antiviral effect of IFN-α/β is NO independent. Alternatively, the IFN-γ–dependent antiviral effect triggered by P. yoelii might not be mediated by NO. This would be consistent with reports that certain IFN-γ–dependent effects are mediated by NO-independent mechanisms 46 47. This putative activity could be enhanced by the fact that IFN-γ and TNF-α appear to be hyperinduced in these mice.

In summary, we report that HBV replication and gene expression are inhibited during P. yoelii infection which ultimately clears HBV virions from the liver by triggering an inflammatory response and the induction of IFN-γ, IFN-α/β, TNF-α, and iNOS in the liver. While all of these cytokines probably function collectively to inhibit HBV replication, it appears that IFN-γ and IFN-α/β are essential, and that TNF-α and iNOS are dispensable for the antiviral effect to occur. Since merozoite infection is sufficient to inhibit HBV replication in these mice, and since hepatocytes are not infected by the blood stages of the parasite, the antiviral effect of malaria is likely to be triggered principally by phagocytosis of infected erythrocytes by Kupffer cells, leading to their activation and production of chemokines that recruit NK cells, NKT cells, and malaria-specific T cells, all of which probably produce inflammatory cytokines that eliminate HBV from the hepatocytes.

These results suggest that similar antiviral events may limit HBV infection during human malaria infection, especially in endemic areas where both pathogens coexist at high frequency. Indeed, in a study investigating the interactions between malaria and hepatitis B in Papua New Guinea, it has been shown that patients with the highest rates of malaria infection had the lowest prevalence of hepatitis B infection 48. It is also noteworthy that viremia in chronic hepatitis B infection appears to fluctuate in concert with Plasmodium falciparum infection 49, suggesting that the amount and type of intrahepatic inflammatory cytokines induced by malaria infection may influence the course of HBV infection in man. Furthermore, mice infected with nonlethal strains of P. yoelii and Plasmodium chabaudi have been shown to produce a stronger IFN-γ response to infection than mice infected with the respective lethal strains 23, suggesting that the amount and quality of the inflammatory cytokines induced in the liver might control those infections.

In conclusion, these results suggest that the inflammatory cytokines induced and/or secreted by activated macrophages and the inflammatory cells they recruit into the liver during malaria infection may play a pivotal role in the outcome of coexisting HBV infection. These results not only provide insight into the possible impact of malaria on HBV replication in coinfected humans, they also suggest that pharmacological strategies designed to activate the intrahepatic macrophage may have therapeutic merit during chronic HBV infection.