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J Virol. Jun 2001; 75(11): 5084–5089.
PMCID: PMC114913

Efficient Infection of Primary Tupaia Hepatocytes with Purified Human and Woolly Monkey Hepatitis B Virus

Abstract

The Asian tree shrew, Tupaia belangeri, has been proposed as a novel animal model for studying hepatitis B virus (HBV) infection. Here, we describe a protocol for efficient and reproducible infection of primary tupaia hepatocytes with HBV. We report that human serum interferes with HBV binding to the hepatocytes, thus limiting the maximum multiplicity of infection. Purification of HBV virions by gradient sedimentation greatly enhances virus binding and infectivity. Covalently closed circular DNA was clearly detectable by Southern blot analysis and newly synthesized single-stranded HBV DNA was visible 2 weeks postinoculation. Primary tupaia hepatocytes are also susceptible to infection with the recently discovered woolly monkey hepatitis B virus (WMHBV) but not to woodchuck hepatitis virus infection. Compared to HBV, WMHBV replicated at a higher rate with single-stranded DNA detectable within the first week postinoculation. Primary tupaia hepatocytes should represent a useful system for studying early steps of HBV and WMHBV infection.

With an estimated 350 million chronically infected people worldwide, hepatitis B virus (HBV) infection represents a major health care problem. Every year nearly 1 million individuals succumb to HBV-associated liver diseases, such as cirrhosis and hepatocellular carcinoma (9, 18). Although an efficient and safe vaccine is available, HBV is spreading, especially in Asia and Africa (10). Treatment of chronic HBV infection is still unsatisfactory. At present, alpha interferon and lamivudine are the only therapeutic options available in clinical practice. However, alpha interferon yields a sustained suppression of viral replication in only about one-third of patients, and lamivudine resistance with mutations in the viral polymerase gene is a frequent event in lamivudine-treated patients (3, 7). Based on transfection studies of hepatoma cell lines, the mechanisms of HBV replication have been elucidated in great detail (11, 13). By contrast, little is known about the early events of the viral life cycle. Unfortunately, permanent cell lines are not permissive to HBV infection, and primary human hepatocytes are not easily available for in vitro infection studies. Furthermore, the quality of liver tissue obtained at surgery for the preparation of primary human hepatocytes is highly variable (5). Therefore, alternative experimental systems for studying HBV infection are urgently needed.

Two reports have described transient HBV infection of the Asian tree shrew, Tupaia belangeri, in vivo (17, 20). Furthermore, successful infection of tupaias with human herpes simplex virus and hepatitis C virus has been described (2, 19). Tupaias are squirrel-like animals that are closely related to primates and are endemic to subtropical areas of southeast Asia (12). The animals are easily bred in captivity. In addition, cultures of primary tupaia hepatocytes (PTH) can be prepared using well-established liver perfusion protocols.

We previously described HBV infection of PTH (17); infection efficiency was too low, however, to allow a detailed analysis of viral replicative intermediates. Here, we report that human serum inhibits binding of HBV virions to PTH, thus limiting the maximum multiplicity of infection. Purification of viral particles by gradient centrifugation strongly enhances HBV binding to PTH and increases the efficiency of infection. We further show that PTH are also susceptible to infection with the recently discovered woolly monkey hepatitis B virus (WMHBV) (8) and that WMHBV replicates at higher levels in PTH than HBV.

MATERIALS AND METHODS

Animals and preparation of primary hepatocytes.

Asian tree shrews (T. belangeri) were originally obtained from the German Primate Center in Göttingen, Germany. The animals were maintained in the animal facility of the University of Freiburg. Details of breeding conditions are available on request. Primary hepatocytes were prepared by two-step collagenase perfusion as described previously (17) with the following modifications: the liver was perfused for 5 min via the portal vein with Hanks solution containing 5 mM EGTA, followed by perfusion for 10 min with Hanks solution containing 5 mM CaCl2 and 0.5 mg of collagenase (HepPlus; Serva, Heidelberg, Germany)/ml. The flow rate was 20 ml per min. The cells were seeded onto collagen-coated six-well plates (1 million viable cells per 9.5 cm2) and kept in Hepato-STIM Hepatocyte Defined Medium (Becton Dickinson, Bedford, Mass.). Hepato-STIM is a serum-free, fully defined medium that was optimized for maintaining primary hepatocytes for up to 3 weeks without loss of cellular function. Primary rat hepatocytes were prepared and cultivated by the identical procedure described for tupaia hepatocytes.

In vitro infection of PTH.

HBV infection was performed 1 day after PTH preparation. After the medium was changed, the HBV inoculum was added. HBV-positive serum was obtained from an asymptomatic chronic HBeAg-positive individual. The viral titer was about 109 virus genome equivalents (VGE) per ml, as estimated by comparing the Southern blot hybridization signal of purified serum DNA with known amounts of cloned HBV DNA. Woolly monkey serum was obtained from a colony kept in a European zoo, in which several animals were recently found to be HBsAg positive. The viral sequence is closely related to that reported by Lanford et al. (8) (V. Weich, A. Wahl-Feuerstein, and M. Nassal, unpublished data). The WMHBV titer was about 108 VGE per ml. The WHV DNA-positive woodchuck serum used in control experiments was kindly provided by Mengij Lu (University of Essen, Essen, Germany). It contained about 108 WHV VGE per ml. Serum aliquots were stored at −20°C for up to 9 months. To assess viral binding, the cells were incubated for 6 h at 37°C, washed four times with culture medium, and harvested. To study viral infection, the cells were incubated overnight (about 16 h) with the respective viral inoculum, and culture medium was changed daily until harvesting of the cells.

Nycodenz gradient purification of HBV particles.

In all experiments described here, the iodinated bencoic acid derivate Nycodenz (batch 10032780; Nycomed Pharma AS, Oslo, Norway) was dissolved in phosphate-buffered saline (137 mM NaCl, 2.7 mM KCl, 10 mM phosphate [pH 7.4]). HBV DNA-positive serum (200 μl) was loaded onto a preformed Nycodenz gradient ranging from 8 to 50% in 11- by 34-mm polycarbonate centrifuge tubes (Beckman Instruments, Palo Alto, Calif.). Samples were centrifuged in a TLS55 swing-out rotor (Beckman Instruments) for 40 min at 200,000 × g at 20°C. Subsequently, 155-μl aliquots were removed from the top of the gradient and added to the hepatocyte culture (fraction 1, top of the gradient; fraction 8, bottom of the gradient). More recently we found that occasionally a precipitate entrapping most HBV virions forms in the gradient, resulting in greatly reduced infectivity. This effect can be avoided by dissolving Nycodenz in Hepato-STIM Hepatocyte Defined Medium (Becton Dickinson).

Protein analysis.

Samples from the Nycodenz gradient were mixed with Laemmli loading buffer and separated according to the Laemmli sodium dodecyl sulfate-polyacrylamide gel electrophoresis system on a 13% polyacrylamide gel. The proteins were either stained with Coomassie blue or transferred onto a polyvinyldifluoride membrane (Schleicher & Schuell, Keene, N.H.) and probed with a pre-S2/S antigen (Ag)-specific polyclonal mouse serum generated by DNA-based immunization (kindly provided by Michael Geissler, University Hospital of Freiburg, Freiburg, Germany). Bound anti-HBs was visualized by chemiluminescence using the ECLPlus system (Amersham Pharmacia Biotech, Buckinghamshire, England).

Analysis of viral DNA.

After the culture medium was removed, cells were lysed with 400 μl of ATL buffer (QIAamp DNA Mini Kit; Qiagen, Hilden, Germany). The lysate was transferred to an Eppendorf tube and digested with proteinase K (final concentration, 0.1 mg/ml) for 1 h at 56°C. Subsequently, RNase A (final concentration, 0.02 mg/ml) was added, and DNA was purified by absorption onto silica columns according to the protocol of the manufacturer (Qiagen). DNA was eluted, concentrated by ethanol precipitation, and separated on a 1.3% agarose gel that did not contain ethidium bromide. Circular plasmid DNA (0.5-kbp EcoRI/BamHI fragment of HBV in 2.7 kbp of pUC19 vector) was used as a size marker for covalently closed circular DNA (cccDNA). DNA purified from HBV-positive serum served as a marker for relaxed circular viral DNA. Heat-denatured DNA (5 min, 95°C) from HBV DNA-positive serum was used to identify the position of single-stranded DNA (ssDNA). After electrophoresis, the gel was soaked for 10 min in 0.25 M HCl and for 20 min in 0.5 M NaOH–1.5 M NaCl. Nucleic acids were blotted by capillary transfer with 0.5 M NaOH–1.5 M NaCl onto nylon membranes (Amersham Pharmacia Biotech) and visualized by hybridization with a 32P-labeled probe containing the complete HBV genome. This HBV probe was used to detect all mammalian hepadnaviruses analyzed in this study. The stringency of the final washes was 0.1% sodium dodecyl sulfate–40 mM NaCl–4 mM sodium citrate at 60°C. Dot blot analysis was performed by spotting 3-μl aliquots of Nycodenz gradient fractions or serum samples onto nylon membranes. The membrane was soaked in 0.5 M NaOH–1.5 M NaCl and 0.5 M Tris-HCl (pH 7.5)–1.5 M NaCl for 10 min each before hybridization, as described above.

Analysis of viral RNA.

For RNA preparation, cells were lysed with 350 μl of RLT buffer (RNeasy Mini kit; Qiagen). RNA was purified by adsorption onto silica columns as recommended by the supplier. Samples were treated with DNase to eliminate viral DNA. Successful DNase digestion was verified by PCR amplification of a small aliquot of purified RNA. The RNA was separated on morpholinopropanesulfonic acid-buffered 1% agarose gels containing 1.2% formaldehyde. The gel was soaked in 50 mM NaOH–1.5 M NaCl for 10 min and in 1.5 M NaCl–0.5 M Tris-HCl (pH 7.5) for 20 min. RNA was blotted onto nylon membranes by capillary transfer with 1.5 M NaCl–150 mM sodium citrate. The position of the rRNA was identified by staining the blotting membrane with methylene blue. HBV RNA was visualized by hybridization with the 32P-labeled HBV DNA probe, as described above.

RESULTS

Human serum competes with HBV virions for binding to PTH.

In the previously published study of infection of PTH with HBV, virus entry was demonstrated by the detection of newly synthesized HBV RNA in cells and secreted viral antigens in the culture medium (17). A detailed analysis of viral replicative intermediates, however, was precluded by the low efficiency of infection. Our main intention, therefore, was to improve the in vitro infection protocol. First, the optimal amount of infectious serum that should be added to a given number of PTH was determined in a virus binding assay. PTH were incubated in 1 ml of culture medium supplemented with increasing amounts of HBV-positive serum for 6 h at 37°C. After being extensively washed with culture medium, the cells were harvested and virus attachment was assessed by Southern blot analysis.

A typical experiment is shown in Fig. Fig.1.1. At low doses of serum (2 and 10 μl per ml of culture medium), the amount of particles bound increased with increasing volume of added HBV serum. Surprisingly, however, a higher amount of serum (50 and 200 μl per ml of culture medium) did not result in an increase of cell-associated viral DNA but rather reduced the number of HBV particles attached to the cells. This effect was possibly due to an inhibitory factor present in the serum sample used. In particular, empty HBsAg particles might compete for HBV binding to the cells. To address this point, 10 μl of HBV DNA-positive serum was mixed with 200 μl of anti-HBsAg-negative, HBsAg-negative normal human serum. Virus attachment to PTH was assessed as described above. As shown in Fig. Fig.1,1, lane 6, attachment to PTH was dramatically reduced in this experimental setting. The same effect was observed with serum samples obtained from seven other healthy and nonvaccinated individuals (data not shown). These results suggest that human serum contains one or more components that compete with HBV for cellular binding sites on PTH and that empty viral particles do not account for the observed effects.

FIG. 1
HBV binding to PTH. Cells were incubated for 6 h with increasing volumes of HBV DNA-positive serum (lanes 2 to 5) or a mixture of HBV-positive serum (10 μl) and HBV-negative human serum (200 μl) (lane 6). HBV binding was assessed by Southern ...

Purification of viral particles enhances binding to PTH.

Based on the above results, it was conceivable that purification of HBV virions from human serum might enhance binding to PTH and increase the maximum multiplicity of infection that can be achieved in this system. To test this hypothesis, HBV DNA-positive serum was subjected to gradient centrifugation, and gradient fractions were analyzed by the virus binding assay. The iodinated bencoic acid derivate Nycodenz was chosen as a gradient medium because it is not toxic to cells in culture and is well suited for virus purification (4). As shown in Fig. Fig.2A,2A, the bulk of serum proteins floated on top of the gradient, while HBV virions readily sedimented into the gradient under our experimental conditions. Compared with nonfractionated infectious serum, binding of gradient-purified HBV virions to PTH was greatly enhanced (Fig. (Fig.2B).2B). This was not due to a nonspecific biophysical property of Nycodenz, since mixing Nycodenz with the inoculum without sedimentation did not enhance binding (data not shown). These results suggest that serum components which interfere with HBV binding to PTH can be removed by gradient centrifugation.

FIG. 2
Effect of virus purification on viral attachment to PTH. (A) Purification of HBV particles by Nycodenz gradient centrifugation. (Top) Coomassie blue staining of fractionated serum proteins. (Middle) Detection of HBsAg by Western blot analysis. (Bottom) ...

Gradient purification of viral particles enhances the efficiency of infection.

Next, we asked whether enhanced binding of purified HBV virions to PTH results in enhanced infectivity. Cells were incubated overnight either with gradient-purified viral particles or with nonfractionated HBV-positive serum, followed by 6 days in culture. Cells were harvested and analyzed for viral replicative intermediates by Southern blotting. Figure Figure3A3A shows that cccDNA, a hallmark of hepadnavirus infection (15), is clearly visible in cells infected with purified HBV virions, while it is hardly detectable in cells incubated with nonfractionated HBV DNA-positive serum. DNA digestion with the restriction enzyme NcoI generated a linear 3.2-kbp fragment, confirming the circular nature of the respective DNA species (Fig. (Fig.3B,3B, compare lanes 2 and 3). In a control experiment, primary rat hepatocytes were incubated with gradient-purified HBV virions and assayed for cccDNA formation. Figure Figure3B,3B, lane 1, shows that HBV virions bound to rat hepatocytes but no virus entry occurred, based on the lack of cccDNA formation. Thus, purification of HBV virions by Nycodenz gradient centrifugation does not mediate nonspecific viral uptake.

FIG. 3
Infection studies with purified HBV. (A) Infectivity of purified and nonpurified virus. Viral DNA was detected by Southern blot analysis on day 6 postinfection. Note that cccDNA is clearly detectable only in PTH inoculated with purified virus. (B) Inoculation ...

We then performed a time course experiment with longer culture times. As illustrated in Fig. Fig.3C,3C, cccDNA but not ssDNA is detectable by Southern blot analysis at day 7 postincubation. At day 16, an additional fast-migrating DNA species is visible which comigrates with denaturated serum HBV DNA and thus most likely represents newly synthesized ssDNA. The total amount of viral DNA only slightly increased from day 7 to day 16 (Fig. (Fig.3C,3C, compare lanes 6 and 7), indicating that the rate of HBV replication is low in PTH.

PTH are permissive to WMHBV infection.

WMHBV is a recently discovered hepadnavirus that has been isolated from woolly monkeys in captivity (8). We tested whether PTH are susceptible to WMHBV infection. Serum from an infected woolly monkey was processed by gradient centrifugation. PTH were incubated with gradient fractions as described above. In a control experiment, PTH were incubated with purified woodchuck hepatitis virus (WHV) (1, 14). Cells were harvested at the times indicated and assayed for viral replication by Southern blotting. While both viruses bound to PTH, cccDNA and ssDNA formation was only observed in cells inoculated with WMHBV. Thus, PTH are permissive to WMHBV infection (Fig. (Fig.4A)4A) but not to WHV infection (Fig. (Fig.4B).4B). In contrast to HBV (Fig. (Fig.3C),3C), WMHBV ssDNA was detectable as early as 7 days postinfection, and the total amount of replicative intermediates clearly increased by day 13 postinfection, suggesting that WMHBV replicates more efficiently in PTH than does HBV.

FIG. 4
Infection of PTH with WMHBV and WHV. (A) WMHBV-positive serum was processed by gradient centrifugation as described for HBV. Cells were harvested on days 1, 7, and 13 postinfection. Viral DNA was analyzed by Southern blotting. Note that cccDNA and ssDNA ...

To address this issue, the replication rates of WMHBV and HBV in PTH were compared directly. Cells were incubated with purified virions and harvested at day 6 postinfection (Fig. (Fig.5A).5A). Even though the original WMHBV serum contained fewer viral genome equivalents than HBV serum, WMHBV replicated to substantially higher levels than HBV. In particular, WMHBV but not HBV produced significant amounts of ssDNA at this time point. As one of several explanations to account for this observation, HBV and WMHBV might produce different RNA levels in PTH. To test this possibility, HBV- and WMHBV-infected PTH were harvested at day 5 postinfection and analyzed for viral RNA synthesis by Northern blotting. Figure Figure5B5B illustrates that both viruses produced abundant amounts of pre-S/S mRNA (sgRNA), while only low levels of pregenomic RNA (pgRNA) were detected. Notably, however, the ratio of pgRNA to sgRNA was slightly higher for WMHBV than for HBV in this experiment.

FIG. 5
Viral replication and transcription in HBV- and WMHBV-infected PTH. (A) Southern blot analysis of infected PTH on day 6 postinfection (top); dot blot analysis of HBV and WMHBV serum (2 μl each; bottom). Note that only WMHBV produced ssDNA at this ...

DISCUSSION

We have previously reported that primary hepatocytes from T. belangeri can be infected with HBV (17). However, the practical use of this system was limited by the low efficiency of infection. Here, we show that human serum interferes with viral attachment, thereby greatly reducing viral infection. On the other hand, purification of virions by gradient centrifugation strongly enhances both HBV binding and infection. Thus, newly synthesized cccDNA and ssDNA and viral RNA were unambiguously detectable by Southern and Northern blot analysis, respectively. Infection of PTH with Nycodenz gradient-purified HBV particles represents an authentic biological process, because the viral host tropism was preserved in cell culture and Nycodenz itself does not affect binding of HBV to PTH. This is in contrast to polyethylene glycol-based protocols (6, 17), because polyethylene glycol may induce nonphysiological membrane fusion.

The biochemical nature of the inhibitory serum component is unclear at present. Preliminary results indicate that the inhibitory factor cannot be removed by dialysis and that albumin and immunoglobulins, which are the most abundant serum proteins, do not account for the inhibitory effect (J. Köck and F. von Weizsäcker, unpublished data). Interestingly, attachment of duck hepatitis B virus to primary duck hepatocytes is not inhibited by duck serum (J. Köck and F. von Weizsäcker, unpublished). This may explain in part the high efficiency of duck hepatitis B virus infection in vitro (16).

Compared to human hepatocytes, PTH have the principal advantage of being readily available from in-house-bred animals. PTH, therefore, allow the highly reproducible infection with HBV under the experimental conditions described, while the suitability of primary hepatocytes prepared from human liver for infection experiments is very variable (5).

PTH were also infected by WMHBV but not by WHV. This finding substantiates PTH as a useful in vitro model system for studying hepadnavirus infection and rules out the possibility that viral uptake in PTH is promiscuous. The permissiveness of PTH to primate but not rodent hepadnaviruses is in line with the fact that tupaias are phylogenetically closely related to primates but not to rodents (12).

It is important to note that the replication rate of HBV in PTH is low. Newly synthesized HBV ssDNA was not detected until about 2 weeks postinfection. It seems unlikely that the low replication rate of HBV in PTH is due to inadequate cell preparation or culture conditions, since WMHBV ssDNA was visible as early as 6 days postinfection (Fig. (Fig.5A).5A). The precise viral and/or cellular factors determining the replication rate of HBV and WMHBV in PTH remain to be further elucidated. Initial experiments comparing HBV and WMHBV RNA synthesis in PTH revealed an overall low abundance of pgRNA, in HBV- as well as WMHBV-infected cells. The ratio of pgRNA to sgRNA, however, was slightly higher in WMHBV- than in HBV-infected PTH. Since pgRNA is pivotal for replication and capsid formation, subtle changes in pgRNA production might translate into substantial effects on viral replication rates. Compatible with this notion, there are significant differences in the core promoter regions of WMHBV and HBV. We are currently preparing a replication-competent WMHBV construct that would allow us to directly address this question in transfected cells.

ACKNOWLEDGMENTS

This study was supported by grants from the Deutsche Forschungs-gemeinschaft (We 1365/2-2), the Bundesministerium für Bildung und Forschung (01Kl9951), and the Zentrum für Klinische Forschung I (3000 0447 01 B2).

We thank H. Schaller for providing cloned HBV DNA, M. Lu for providing WHV serum, and M. Geissler for providing mouse anti-pre-S2/S antibodies.

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