SARS-associated viral hepatitis caused by a novel coronavirus: Report of three cases
Article first published online: 30 JAN 2004
Copyright © 2004 American Association for the Study of Liver Diseases
Volume 39, Issue 2, pages 302–310, February 2004
How to Cite
Chau, T.-N., Lee, K.-C., Yao, H., Tsang, T.-Y., Chow, T.-C., Yeung, Y.-C., Choi, K.-W., Tso, Y.-K., Lau, T., Lai, S.-T. and Lai, C.-L. (2004), SARS-associated viral hepatitis caused by a novel coronavirus: Report of three cases. Hepatology, 39: 302–310. doi: 10.1002/hep.20111
- Issue published online: 30 JAN 2004
- Article first published online: 30 JAN 2004
- Manuscript Accepted: 19 NOV 2003
- Manuscript Received: 20 JUL 2003
Liver impairment is commonly reported in up to 60% of patients who suffer from severe acute respiratory syndrome (SARS). Here we report the clinical course and liver pathology in three SARS patients with liver impairment. Three patients who fulfilled the World Health Organization case definition of probable SARS and developed marked elevation of alanine aminotransferase were included. Percutaneous liver biopsies were performed. Liver specimens were examined by light and electron microscopy, and immunohistochemistry. Reverse-transcriptase polymerase chain reaction (RT-PCR) using enhanced real-time PCR was applied to look for evidence of SARS-associated coronavirus infection. Marked accumulation of cells in mitosis was observed in two patients and apoptosis was observed in all three patients. Other common pathologic features included ballooning of hepatocytes and mild to moderate lobular lymphocytic infiltration. No eosinophilic infiltration, granuloma, cholestasis, fibrosis, or fibrin deposition was noted. Immunohistochemical studies revealed 0.5% to 11.4% of nuclei were positive for proliferative antigen Ki-67. RT-PCR showed evidence of SARS-associated coronavirus in the liver tissues, but not in the sera of all 3 patients. However, electron microscopy could not identify viral particles. No giant mitochondria, micro- or macro-vesicular steatosis was observed. In conclusion, hepatic impairment in patients with SARS is due to SARS-associated coronavirus infection of the liver. The prominence of mitotic activity of hepatocytes is unique and may be due to a hyperproliferative state with or without disruption of cell cycle by the coronavirus. With better knowledge of pathogenesis, specific therapy may be targeted to reduce viral replication and modify the disease course. (HEPATOLOGY 2004;39:302–310.)
Coronaviruses are enveloped viruses with single-stranded, positive-sense RNA that is 5′ capped and 3′polyadenylated and replicates in the cytoplasm of infected cells.1 They include a large number of viruses that infect different animal species. The predominant diseases associated with these viruses are respiratory and enteric infections, although hepatic and neurologic diseases also occur. Severe acute respiratory syndrome–associated coronavirus (SARS-CoV) is a novel virus that has been found to be a causative agent of a recently described atypical pneumonia.2, 3 The disease may progress rapidly, resulting in acute respiratory distress syndrome. At the time of writing, more than 8,221 individuals were affected worldwide and 735 patients had succumbed to the illness, which the World Health Organization (WHO) has termed severe acute respiratory syndrome (SARS).
Liver impairment is common and has been reported in up to 60% of patients suffering from SARS.2, 4, 5 The majority of these patients have been treated with antibiotics, antiviral medications, and steroids, which are potentially hepatotoxic. Hence, whether or not SARS-CoV infection can lead to liver damage per se remains unknown. Here we report the clinical course and liver pathology in three SARS patients with liver impairment.
Three patients who fulfilled the WHO case definition of probable SARS6 and developed liver derangement were included in the study. Briefly, the case definition was: fever of 38° C or higher, cough or difficulty breathing, radiographic evidence of infiltrates consistent with pneumonia or respiratory distress syndrome, and either a history of exposure to a patient with SARS or a lack of response to empirical antimicrobial coverage for typical and atypical pneumonia. After informed consent was obtained from each patient, percutaneous liver biopsy was performed to look for the cause of elevated liver enzymes. Common causes of hepatitis were excluded by serologic tests, including anti–hepatitis A virus IgM antibodies, anti–hepatitis B core IgM, hepatitis B surface antigen, anti–hepatitis C antibody, and cytomegalovirus pp65 antigen. Abdominal ultrasonography was performed to rule out space-occupying lesions and biliary tract diseases. All patients received antimicrobial coverage for community-acquired pneumonia with ceftriaxone and clarithromycin or levofloxacin alone. Combination therapy using oral ribavirin 600 mg twice daily and Kaletra (lopinavir/ritonavir, Abbott Laboratories, North Chicago, IL) 1000 mg daily were commenced when patients did not respond to antibiotics within 48 hours. Kaletra is a co-formulation of two protease inhibitors: lopinavir and ritonavir. It is an experimental drug for coronavirus that depends on protease for cleavage of polypeptides and formation of viral structure. Methylprednisolone, given in three pulses at a dose of 500 mg to 1000 mg daily, was offered to patients who had persistent fever, radiologic progression of lung infiltrates, or signs of respiratory distress despite antiviral therapy.
In addition to the aforementioned tests for viral hepatitis, routine microbiological investigations included blood, urine, and sputum culture for bacterial pathogens. The acute and convalescent sera were tested in parallel for SARS-associated coronavirus immunoglobulin G, with SARS-CoV–infected Vero cells fixed in acetone in an indirect immunofluorescent format.7 Reverse-transcriptase polymerase chain reaction (RT-PCR) for coronavirus was done on nasal and throat swabs, stool specimens, and liver tissues of patients.
Cores of 10- to 15-mm-long liver tissue were sent fresh to the histopathology laboratory for processing. Two 1-mm tissue fragments were fixed in 2.5% glutaraldehyde for transmission electron microscopy examination. A 5-mm-long tissue was immediately kept frozen at −70° C for molecular study. The remaining core of tissue was fixed in 10% neutral buffered formalin. The paraffin-embedded blocks of liver tissues were sectioned at 4 μm for light microscopy. A panel of stains including hematoxylin and eosin, diastase periodic acid-schiff, Perls, Gordon and Sweets' reticulin, and Orcein were performed. The number of mitoses was counted in 1000 hepatocytes in each specimen, and the mitotic index was expressed as the percentage. Immunohistochemical study for Ki-67 antigen (DAKO rabbit antihuman Ki-67 antigen, code no. A047) was performed using the BIOTEK TM500-220 automated immunohistochemical stainer (DAKO, CA, USA). Ki-67 is a human nuclear antigen that is expressed during G1, S, G2, and M phases of the cell cycle but is absent in the quiescent G0 phase.8 Proliferating hepatocytes were identified by immunohistochemical staining of Ki-67. Only hepatocytes with distinct and near-total nuclear staining were considered positive. One thousand hepatocytes were counted in each specimen. The Ki-67 index was expressed as percentage of hepatocyte nuclei that showed positive staining pattern. Immunostaining for cytomegalovirus (CMV) using monoclonal mouse anti-cytomegalovirus antibodies (DAKO-CMV DDG9, CCH2, code no. M854) was also performed to exclude CMV infection.
Enhanced Real-Time PCR
Total RNA from samples was collected using a QIAamp Viral RNA Mini Kit (Qiagen, Hilden, Germany) according to the manufacturer's instructions. RNA was converted to cDNA using SuperScript II RNase H- Reverse Transcriptase (Invitrogen Inc., CA, USA) according to the manufacturer's instructions, except that 300-ng random hexamer primers were used in place of oligo (dT)12–18, and nuclease-free water was used in place of RNaseOUT Recombinant Ribonuclease Inhibitor (Invitrogen Inc., CA, USA). The new assay comprised a first round of conventional PCR followed by Taqman real-time fluorescent PCR (Eurogenetic Group, Belgium).9
First-round conventional PCR was as follows: in a total volume of 25 μL, the following components were mixed: nuclease-free water (19.2 μL), 0.2 mM dNTPs, 1U Platinum Taq DNA polymerase (Invitrogen), 5 mM MgCl2, 1× PCR buffer, primers (10 μM, 0.5 μL each), and cDNA template (≈100 ng, 1 μL). The PCR amplification was performed in a MasterCycler (Eppendorf, Hamburg, Germany) with the following temperature profile: DNA polymerase activation (95° C, 3 minutes); 10 cycles of denaturation (95° C, 10 seconds); annealing (60° C, 10 seconds); 1° C reduction after each cycle and extension (72° C, 20 seconds); 40 cycles of denaturation (95° C, 10 seconds); annealing (56° C, 10 seconds); and extension (72° C, 20 seconds). A variety of primers for conventional PCR were compared; their sequences are listed in Table 1.
|Name||Origin||Assay, Orientation||Sequence (5′–3′)||Coordinates*|
|Primer C||This study||Real-time PCR, antisense||AGT TGC ATG ACA GCC CTC TAC A||18260-18245|
|Primer D||This study||Real-time PCR, sense||CCC GCG AAG AAG CTA TTC G||18193-18211|
|Probe E||This study||Real-time PCR, flurogenic probe||CGT TCG TGC GTG GAT TGG CTT TG||18215-18237|
|SAR1S||CDC†||Conventional PCR, sense||CCT CTC TTG TTC TTG CTC GCA||15291-15271|
|SAR1As||CDC†||Conventional PCR, antisense||TAT AGT GAG CCG CCA CAC ATG||15371-15391|
|COR1||GVU‡||Conventional PCR, sense||CAC CGT TTC TAC AGG TTA GCT AAC GA||15318-15343|
|COR2||GVU‡||Conventional PCR, antisense||AAA TGT TTA CGC AGG TAA GCG TAA AA||15628-15603|
|BNIoutS2||BNI§||Conventional PCR, sense||ATG AAT TAC CAA GTC AAT GGT TAC||18153-18176|
|BNIoutAs||BNI§||Conventional PCR, antisense||CAT AAC CAG TCG GTA CAG CTA C||18342-18321|
Taqman real-time fluorescent PCR consisted of the following: in a total volume of 25 μL, the following components were mixed: nuclease-free water (9.9 μL), PCR mastermix (dNTPs, dUTP, HotStart Taq DNA polymerase, MgCl2, uracil-N-glycosylase, and passive reference; 12.5 μL), primer C (5 μM, 1.0 μL), primer D (5 μM, 1.0 μL), probe E (10 μM, 2.6 μL), and amplified DNA template (≈100 ng, 1 μL). The 40 cycles of amplification were performed in an ABI Prism 7700 Sequence Detector (Applied Biosystems, CA, USA) with the following temperature profile: initial incubation (50° C, 2 minutes); DNA polymerase activation (95° C, 10 minutes); denaturation (95° C, 15 seconds), and annealing/extension (58°C, 1 minutes).
A 45-year-old woman who had enjoyed good health before her illness presented with a fever that had begun 4 days prior to admission. Initial investigations showed left upper zone consolidation (chest radiograph) and lymphopenia (peripheral blood examination). The patient failed to respond to levofloxacin with subsequent radiographs, showing progressive involvement of both lower zones. Oral ribavirin and Kaletra were initiated on day 8 after onset of symptoms. In view of persistent fever and increased oxygen demand, pulse methylprednisolone 1 g daily was prescribed for 3 days on day 14. By day 17, the patient's alanine aminotransferase (ALT) level became elevated to 196 IU/L and her albumin level dropped to 27 g/L; bilirubin and coagulation profiles were normal. She did not have a rash, abdominal pain, or jaundice. Her renal function tests and amylase and creatine phosphokinase levels were normal. Lactic acidosis was absent. Despite withdrawal of antivirals on day 22, ALT peaked on day 28 at 493 IU/L (Fig. 1A).
Liver biopsy on day 31 showed mild lobular activities with occasional acidophilic bodies and prominent Kupffer cells. The portal tract was mildly inflamed with lymphocytic infiltration (Fig. 2A). Hepatocytes showed focal balloon degeneration (Fig. 2B). The mitotic activities were brisk; the mitotic index was 2.1% (Fig. 3). There was no piecemeal necrosis, eosinophilic infiltration, granuloma, cholestasis, fibrosis, steatosis, or fibrin deposition. Immunostaining for CMV was negative. Immunohistochemical study using Ki-67 stain showed numerous hepatocytes in the replicative phase, and the Ki-67 proliferative index was 11.4% (Fig. 4). No abnormal mitosis was noted. Electron microscopy showed a few laminated myelin bodies in the cytoplasm of hepatocytes and Kupffer cells. Microvesicular or macrovesiclar fat was minimal. Neither viral particles nor giant mitochondria were seen. RT-PCR for SARS-CoV was positive in liver tissue (Fig. 5A) but not in the serum (Fig. 5B).
The patient's liver function improved gradually, with ALT decreasing to less than 200 IU/L on day 37 upon discharge. She experienced a full recovery, and a liver function test was normal 3 months after discharge. Convalescent serum showed elevation of antibodies to the coronavirus with a titer of 1 in 800.
A 25-year-old woman presented with intermittent fever after contact with a SARS patient in a hospital. Serial chest radiographs were normal. Routine microbiologic and virologic investigations were negative. The patient developed lymphopenia on day 12; on day 14, high-resolution CT of the thorax showed right lower lobe consolidation over posterior retrocardiac segments. RT-PCR for coronavirus was positive in stool specimens on day 16. Ribavirin and Kaletra were started on the same day. On day 21, the patient still had a persistent fever, and high-resolution CT showed increased involvement over both lung fields. Her ALT had elevated to 475 IU/L and her albumin dropped to 27 g/L; liver function subsequently improved (Fig. 1B). Ribavirin and Kaletra were stopped on day 24. Convalescent serum showed elevated antibodies to the coronavirus with a titer of 1 in 400. She was asymptomatic, and her liver function test was normal 3 months after discharge.
Liver biopsy on day 29 showed similar histology to the first patient with mild portal and lobular activity (Fig. 2C) and occasional acidophilic bodies. Prominent mitotic figures were seen in the hepatocytes. The mitotic index was 0.5%. The portal tracts were mildly inflamed. No piecemeal necrosis, steatosis, eosinophilic infiltration, or cholestasis was seen. RT-PCR for coronavirus was positive in the liver tissue (Fig. 5A) but not in the serum (Fig. 5B). The Ki-67 proliferative index was 5.6%. Electron microscopy showed a small number of elongated mitochondria (Fig. 6A) and myelin bodies in hepatocytes. No giant mitochondria, micro- or macro-vesicular steatosis, or viral particles were observed.
A 34-year-old woman presented with fever and cough for 4 days. An initial chest radiograph showed bilateral lower zone consolidation. RT-PCR for coronavirus on nasopharyngeal aspirate was positive. Ribavirin and Kaletra were started on day 7 after onset of symptoms when fever persisted despite antibiotics. On day 10, the patient's ALT rose to 399 IU/L and her bilirubin level increased from 6 mmol/L to 21 mmol/L. Pulse methylprednisolone was given on the same day for persistent fever and increased dyspnea. On day 13, the patient improved clinically with resolution of radiographic abnormalities, but her ALT further increased to 941 IU/L. The antivirals were withdrawn. Liver function tests returned to normal on day 26 (Fig. 1C). Both acute and convalescent sera were negative for SARS-associated coronavirus immunoglobulin G.
Liver biopsy on day 14 showed mild to moderate portal and lobular inflammation with predominant lymphocytic infiltration and scattered neutrophils (Fig. 2D). Some hepatocytes showed focal and mild ballooning. The mitotic index was less than 0.1%. A few acidophilic bodies with prominent Kupffer cells were seen. No piecemeal necrosis, steatosis, eosinophilic infiltration, fibrin deposition, or fibrosis was seen. The Ki-67 proliferative index was 0.5%. RT-PCR for coronavirus was positive in liver tissue (Fig. 5A) but not in the serum (Fig. 5B). A few mitotic figures of hepatocytes were identified in the semi-thin section of the electron microscopy block (Fig. 6B). A few lipid droplets were seen in other hepatocytes, but no macro- or micro- vesicular steatosis was observed. Some mitochondria were elongated, but no giant mitochondria were identified. Some Kupffer cells contained lysosomes.
In March 2003, a novel coronavirus, SARS-CoV, was discovered to be the causative agent of SARS. The complete genome of SARS-CoV has been sequenced. Phylogenetic analyses and sequence comparisons show that it is not closely related to other known coronaviruses, including two human coronaviruses, HCoV-OC43 and HCoV-229E.10, 11 Disease spectrum related to this novel coronavirus and its pathogenesis have yet to be explored. Other members of the genus Coronavirus (e.g., mouse hepatitis virus, which is a group 2 coronavirus) can cause liver damage ranging from minimal changes to fulminant hepatitis.12–15 The spike protein found on the virion envelope and on the plasma membrane of infected cells is responsible for attachment to viral receptor and virus–cell fusion during viral entry and for cell-to-cell fusion during the latter stages of the infection.16, 17 Studies of mouse hepatitis virus showed that the spike gene determined the viral load in the liver and that the amount of antigen staining and necrosis in the liver correlated with the viral load. Mutation in the spike gene might abbreviate the severity of hepatitis.18 Pairwise amino acid identity between SARS-coronavirus and other known coronaviruses was less than 30%,11 hence the hepatotropism of this novel coronavirus is unpredictable.
Liver impairment occurs commonly among patients with SARS.2, 4, 5 Our patients have fulfilled the WHO case definition of clinical SARS. The diagnosis was supported by laboratory tests, including (1) a fourfold or greater rise in antibody titer between acute and convalescent phase sera tested in parallel in patients 1 and 2 and (2) PCR positive for SARS-CoV in a stool specimen of patient 2 and nasopharyngeal aspirate of patient 3, respectively. In our three SARS patients with moderate to marked elevation of ALT, prominent mitoses, acidophilic bodies, Kupffer cells, and mild to moderate lobular inflammation were the common histologic features. All of our patients showed positive RT-PCR for SARS-CoV in liver tissue but not in the sera, suggesting that the virus was localized in liver. Indeed, SARS-CoV is detectable in less than 50% of sera of SARS patients beyond 14 days after fever onset.19 Because ribavirin and Kaletra were given to all three patients prior to liver biopsy, viral replication might possibly be suppressed and hence no virus could be identified by electron microscopy. Alternatively, the viral load in liver may be so low that it would be difficult to be observed ultrastructurally. The only report of liver histology in SARS (other than the present study) was an autopsy showing microvesicular fatty change, focal hemorrhages, and hepatocyte necrosis with scattered acidophilic bodies in liver, but no viral inclusions were observed.20 Because that patient developed respiratory failure and multi-organ failure before death, the changes in liver histology might not be solely due to SARS-CoV infection.
The most remarkable finding in our liver histology was the conspicuous mitoses, which were readily seen by both light and electron microscopy. Immunohistochemical study using Ki-67 stain showed that hepatocytes were highly replicative. Ki-67 proliferative index has also been reported as 0.4% to 1% in chronic active hepatitis C,8, 21, 22 but the index for acute viral hepatitis remains unknown. However, hepatocytes in the mitotic phase are uncommonly seen even in acute or chronic hepatitis and liver cirrhosis even when regeneration takes place rapidly.23 The finding of conspicious mitoses in our patients appears out of proportion to the extent of liver cell damage as assessed biochemically or histologically. The possibility of cell cycle disruption caused by coronavirus should be considered. Studies of transmissible gastroenteritis virus (a group 1 coronavirus) and mouse hepatitis virus showed that nucleolar localization of nucleoprotein (N protein) is a common feature of the coronavirus family, and about 30% of Vero cells transfected with the nucleoprotein appear to undergo cell division.24 This observation has also been reported in the avian infectious bronchitis virus (a group 3 coronavirus).25 A delay in mitosis or inhibition of cytokinesis could lead to an accumulation of cells in the M phase of the cell cycle and hence the appearance that a significant number of cells undergo cell division. Unlike patients 1 and 2, patient 3 had negative serology for SARS-CoV despite repeatedly positive RT-PCR results on nasal and throat swabs and liver tissue. The lack of immunoglobulin G seroconversion has been described in up to 7% of patients with SARS.7 The liver biopsy of this patient also showed higher lobular activities and less prominent mitotic figures, which might represent another spectrum of disease as a result of different host response to the virus.
Other common pathologic features among the three liver specimens were presence of acidophilic bodies, ballooning of hepatocytes, and mild to moderate lobular activities, which are similar to the hepatic pathology of mouse hepatitis virus in mice.26 The findings suggest that the liver damage due to SARS-coronavirus is mainly mediated by apoptosis. Studies show that some coronaviruses exert extensive cytopathic effect through the induction of apoptosis of their host cells by caspase activation.27, 28 Mouse hepatitis virus can also activate the immune coagulation system by the fgl2 gene, which encodes a specific prothrombinase. It induces macrophage procoagulant activity,29 which in turn leads to fibrin deposition on the endothelium of intrahepatic veins and hepatic sinusoids resulting in confluent hepatocellular necrosis. However, our specimens did not show any sinusoidal dilatation or fibrin deposition on the hepatic veins. On the other hand, fibrin thrombi and intimal swelling of pulmonary vessels have been reported among patients with SARS.30
An alternative explanation of the liver impairment in SARS patients is hepatotoxicity due to antiviral treatment. Kaletra has been used for the treatment of SARS in more than 100 patients in Hong Kong. Preliminary results show that 30-day mortality and intubation rates are lower in the Kaletra-treated group compared with patients treated with ribavirin.31 Elevation in ALT greater than fivefold the upper limit of normal has been reported in 3% to 11% of patients taking Kaletra.32 Ribavirin also increases mitochondrial toxicity in HIV-infected patients treated with protease inhibitors.33, 34 However, we do not favor this possibility, because hepatotoxicity usually develops only after long-term use of antiviral agents. Furthermore, our patients had no pancreatitis, myopathy, lactic acidosis, or other clinical features suggestive of mitochondrial toxicity. Occasionally, hepatotoxicity may occur in the first few weeks after initiating antiviral therapy; this is typically related to immune-mediated hypersensitivity and generally occurs in conjunction with allergic reactions such as fever and rash.35 However, our patients had no such clinical features, and their liver biopsies did not show any eosinophilia, giant mitochondria, or microvesicular steatosis suggestive of drug toxicity.36–39 Furthermore, there is no consistent temporal relationship between the antiviral treatment and liver function impairment. In primary human hepatocytes, ribavirin can also inhibit cell proliferation induced by mitogenic factors by way of a delayed progression to the S phase of the cell cycle.40 However, liver histology of patients with chronic hepatitis C does not show any features of cell cycle arrest after ribavirin monotherapy.41, 42 Further studies are warranted to determine whether or not SARS-CoV infection, like chronic hepatitis B and C virus infection,43–45 may increase the hepatotoxicity of the antivirals.
In conclusion, SARS-CoV can infect livers leading to mild to moderate lobular inflammation and apoptosis. The presence of prominent mitoses among hepatocytes possibly due to hyperproliferative state and cell cycle arrest is a cardinal feature of liver pathology in SARS. With a better knowledge of the pathogenesis of SARS-CoV infection, including the possible viral replication in hepatocytes, specific therapy may be targeted to reduce the viral replication and modify the clinical course of the disease.
- 1Coronaviridae and their replication. In: FieldsB, KnipeD, HowleyP, eds. Fields virology. 3rd edition. Philadelphia: Lippincott-Raven, 1996: 1075., .
- 6WHO. Severe acute respiratory syndrome (SARS). Wkly Epidemiol Rec 2003; 78: 81–83.
- 9Enhanced detection of the coronavirus associated with severe acute respiratory syndrome (SARS). Abstract presented at the ASEAN, China, Japan, and ROK (10+3) High-Level Symposium on Severe Acute Respiratory Syndrome (SARS) 2003, June 3–4, Beijing, China, 2003. p 31–32., , .
- 23The liver. In: WrightN, AlisonM, eds. The Biology Epithelial Cell Populations Volume 2. Oxford: University Press, 1984: 880–956., .
- 26Hepatic pathology resulting from mouse hepatitis virus S infection in severe combined immunodeficiency mice. Lab Anim Sci 1996; 42: 167–173., , , , .
- 31Treatment-Kaletra. Abstract Presented at the SARS Clinical Management Workshop. June 13–14, 2003, Hong Kong, China..
- 35Liver disease in HIV: an update. PRN Notebook 2002; 7: 10–15..
- 37Hepatotoxicity associated with ritonavir. Ann Intern Med 1998; 129: 670–671., , .
- 45Severe hepatic cytolysis: incidence and risk factors in patients treated by antiretroviral combinations Aquitaine cohort, France, 1996–1998. AIDS 1999; 13: 115–151., , , , , , , et al.