Background
Hepatitis C virus (HCV) is a major etiological agent of chronic liver disease. An estimated 180 million humans are infected with HCV worldwide. Due to similar routes of transmission, co-infection with HCV and human immunodeficiency virus-1 (HIV-1) is common, with the prevalence of co-infection ranging from 4 to 5 million patients [
1]. HCV-related liver diseases have become a major source of morbidity and mortality in HIV-1-infected patients [
2]. Once chronic infection is established, patients with HIV-1/HCV co-infection have a higher rate of viral persistence, faster progression, and earlier development of end-stage liver disease, compared to HCV mono-infected patients [
3,
4]. Infection with HIV-1 is associated with higher HCV viral levels in sera compared to infection with HCV alone [
5]. However, the mechanisms that accelerate progression of HCV/HIV-1 co-infected patients are not fully understood.
HIV-1 infection enhances HCV replication, thus changing the course of HCV-related disease in co-infected patients [
6,
7]. HCV was originally thought to be strictly hepatotropic, while the main cell targets for HIV-1 infection are mononuclear leukocytes bearing CD4 and the chemokine receptors C-C chemokine receptor type 5 (CCR5) and chemokine (C-X-C motif) receptor 4 (CXCR4). However, HCV can also replicate in peripheral blood mononuclear cells (PBMCs), particularly in patients with HIV-1 [
8,
9]. The effect of HIV-1 on PBMC cultures of HCV mono-infected patients
in vitro has previously been investigated. The production of HCV post-HIV infection increases by 1 to 2 logs, compared to uninfected controls [
10]. Also, HIV-1 facilitates replication of HCV in native human macrophages
in vitro [
11].
The interferon γ-inducible protein 10 (IP-10 or CXCL10) is a chemotactic C-X-C chemokine that attracts activated T-lymphocytes and monocytes [
12‐
14]. IP-10 is produced by a variety of cells, including astrocytes and hepatocytes [
15,
16]. Increased levels of IP-10 have been detected in the serum and liver of HCV-infected individuals compared to controls [
17,
18]. Elevated IP-10 is correlated with increased liver damage [
19] and HCV viral loads [
20], as well as enhanced IP-10 levels in HIV-1 mono-infected patients compared to controls [
21]. Increased IP-10 production during HIV-1 infection has been partially attributed to HIV-1 proteins, including HIV-1 accessory protein transactivator of transcription (Tat), in a number of cells such as astrocytes and macrophages [
22,
23]. Serum IP-10 levels are higher in HIV-1/HCV co-infected patients than in HCV mono-infected patients [
24].
HIV-1 Tat is a transactivating protein that contributes to the transactivation of viral and cellular genes [
25]. Extracellular Tat, released from virus-infected cells, can enter neighboring infected or uninfected cells and induce its biological effects, including cytokine expression [
26,
27]. For example, extracellular Tat stimulates IL-10 expression in human monocytes in a time- and dose-dependent manner [
28]. Also, Tat upregulates the expression of specific chemokine receptors, such as CCR5 and CXCR4, which are important for HIV-1 infection [
29]. In addition to its regulatory role in HIV-1 infection, Tat may activate [
30,
31] and facilitate the invasion of viruses [
32].
IP-10 mRNA levels in PBMCs from HIV-1/HCV co-infected and HCV mono-infected patients showed that HIV-1/HCV co-infection was associated with increased expression of IP-10 mRNA and in the replication of HCV RNA. Furthermore, we used two different infectious HCV models to examine the effects of HIV-1 Tat and IP-10 on HCV replication, which demonstrated that both HIV-1 Tat and IP-10 activate HCV replication. Also, HIV-1 Tat activates HCV replication by upregulating IP-10 production. The mechanism involved in the regulation of HCV replication mediated by HIV-1 during co-infection is discussed.
Discussion
Co-infection of HCV with HIV-1 is prevalent and causes increased HCV viral loads, as well as increased morbidity in co-infected individuals [
39,
40]. The precise molecular mechanism by which HIV-1 increases HCV persistence and accelerates liver fibrosis is unknown. Chemokines play an important role in the pathogenesis of both HCV and HIV-1 infections. Also, HIV-1 Tat protein is known to activate HCV replication by upregulating IP-10 production.
Elevated IP-10 levels have been detected in HCV-infected patients compared to healthy controls [
17,
18]. This association is supported by the positive correlation between IP-10 levels and HCV viral load, as well as the significant decrease in IP-10 levels after clearance of HCV infection [
17]. Elevated IP-10 mRNA levels were detected in HCV mono-infected patients compared to healthy controls. Also, increased IP-10 mRNA levels were associated with increased HCV RNA levels in HCV-infected patients. This indicates that IP-10 plays an important role in the natural pathogenesis of HCV-induced liver damage. Furthermore, IP-10 promotes HIV-1 replication in monocyte-derived macrophages and peripheral blood lymphocytes [
41]. However, the effect of IP-10 on HCV replication is not well understood. IP-10 upregulates HCV replication in hepatocytes in a time-dependent manner. Treatment with an IP-10-specific monoclonal antibody reduces HCV replication in Huh7.5.1 cells, demonstrating that endogenous IP-10 stimulates HCV replication.
Previous studies have reported that IP-10 levels are elevated in HIV-1 mono-infected patients compared to healthy control subjects [
42], and that IP-10 stimulates HIV-1 replication [
41]. Significantly higher serum IP-10 levels have been reported in HIV-1/HCV co-infected patients than in mono-infected and uninfected control groups [
24]. This suggests that IP-10 plays an important role in the pathogenesis of HIV-1/HCV co-infection. However, no reports are available on the role of IP-10 in the regulation of HIV-1/HCV co-infection. Initially, we measured the IP-10 mRNA levels in PBMCs from a healthy, HCV mono-infected, and HIV-1/HCV co-infected group. HIV-1/HCV co-infection was associated with significantly increased IP-10 mRNA expression in PBMCs compared to HCV mono-infection, suggesting that HIV-1 enhances IP-10 expression in HCV/HIV-1 co-infected patients.
The transactivating effects of Tat are not limited to HIV-1-infected cells because extracellular Tat is secreted into the plasma of HIV-1-infected patients where it can exert its effects on uninfected cells [
43]. Extracellular Tat non-specifically binds to cell membranes and is internalized, which may induce intracellular signals that ultimately change cellular gene expression. For example, Tat upregulates the expression of a number of cytokines (TNF-α, IL-10) [
44,
45] and chemokines (IL-8, IP-10) [
22]. HIV-1 Tat also induces IP-10 in astrocytes [
22,
46]. Our results corroborate these findings because IP-10 expression was increased in Huh7.5.1 cells in the presence of HIV-1 Tat. Also, HCV infection upregulates IP-10 expression in Huh7.5.1 cells. This is consistent with
in vivo findings that demonstrated that IP-10 mRNA levels were higher in HCV-infected patients than in healthy controls. We found that Tat activates IP-10 expression and HCV replication, and that IP-10 upregulates HCV replication in two infectious HCV models. Treatment with an anti-IP-10 monoclonal antibody reduced Tat-activated HCV replication, demonstrating that Tat enhancement of HCV replication is dependent on IP-10. Tat has been implicated in the activation of cytokine transforming growth factor (TGF)-β in HIV-1-infected cells and in the stimulation of JC virus (JCV) gene transcription and DNA replication in oligodendroglia, the primary central nervous system cell type infected by JCV in progressive multifocal leukoencephalopathy [
47]. Tat also activates Kaposi sarcoma-associated herpesvirus (KSHV) lytic cycle replication from latency, in part by modulating janus kinase/signal transducer and activator of transcription (JAK/STAT) pathways, and promotes KS progression [
48]. HIV-1 transactivator protein Tat, produced by HIV-1-infected cells, is secreted into the extracellular matrix where it activates a complex cascade of signaling pathways and alters the intrahepatic chemokine environment, particularly chemokine IP-10. This contributes to the activation of HCV replication and accelerates liver fibrosis observed in patients co-infected with HIV-1 and HCV. The increased level of IP-10 induction in PBMCs from HIV-1-infected individuals may allow for the establishment of more aggressive HCV infection. The downregulation of anti-HCV responses allow for increased HCV replication and higher HCV viral loads. Tat activation of IP-10 may promote HIV-1 immunosuppression and stimulate HCV gene transcription. Elevated IP-10 levels in HCV mono-infected patients are correlated with increased liver disease. The increased IP-10 levels in HCV/HIV-coinfected patients may explain the accelerated progression to liver disease in these individuals. IP-10 expression is also associated with immunological treatment failure following HAART [
21]. Therefore, reducing IP-10 expression and function may enhance the effectiveness of current anti-retroviral treatments.
Conclusions
HIV-1/HCV co-infection is associated with a significant increase in the expression of IP-10 mRNA in PBMCs. HCV RNA levels were higher in PBMCs of patients with HIV-1/HCV co-infection than in those with HCV mono-infection. HIV-1 Tat or IP-10 activates HCV replication in a time-dependent manner. Also, HIV-1 Tat induces IP-10 production. In addition, the effect of HIV-1 Tat on HCV replication was blocked by anti-IP-10 monoclonal antibody, demonstrating that the effect of HIV-1 Tat on HCV replication depends on IP-10. Taken together, these results suggest that HIV-1 Tat protein activates HCV replication by upregulating the production of the chemokine IP-10. Thus, IP-10 may be a potential therapeutic target for the treatment of patients with HIV-1/HCV co-infection. Further work is necessary to determine the intermediary pathways responsible for the effects on HCV replication. Our study increases the understanding of the mechanisms involved in the co-infection of two deadly viruses, HIV-1 and HCV.
Methods
Patient samples
PBMCs from 20 HCV mono-infected and 17 HIV-1/HCV co-infected patients were obtained from local AIDS clinics and hospitals. Patients were excluded if they were positive for hepatitis B virus (HBV) surface antigens or had any of the following: renal failure, hepatocellular carcinoma, decompensated liver disease, or any cause of liver disease other than HCV infection. The demographic information on these patients is summarized in Table
1. PBMCs isolated from the blood of 24 age-matched healthy persons collected at a local blood donation center were used as controls. Informed consent was obtained from all patients. Collection of blood samples for research was approved by the Institutional Review Board of the College of Life Sciences, Wuhan University, China, in accordance with the guidelines for the protection of human subjects.
Reagents
Recombinant HIV-1 Tat (ab83353) was purchased from Abcam. Recombinant human IP-10 (266-IP-010) and mouse immunoglobulin G (MSIgG) were purchased from R&D Systems. Antibody against the HCV core protein (sc-52804) and IP-10 (sc-28877) were purchased from Santa Cruz, and antibody against β-actin (cw-0096A) was purchased from CWBio.
Cells and virus stocks
Huh7.5.1 cells were cultured in Dulbecco's modified eagle medium (DMEM) (Gibco BRL, USA) supplemented with 10% fetal calf serum (Gibco BRL, USA), 100 U/ml penicillin, and 100 μg/ml streptomycin sulfate. The cells were maintained at 37°C in a 5% CO2 incubator.
The genotype 2a HCV virus, JFH1, was prepared and used to infect Huh7.5.1 cells, as previously reported [
37]. FL-J6/JFH-5'C19Rluc2AUbi plasmid was kindly provided by Dr. Charles M. Rice, from Rockefeller University and FL-J6/JFH-5'C19Rluc2AUbi virus was prepared as described previously [
49]. Virus titration was measured using a commercial kit (HCV RNA qPCR Diagnostic Kit, KHB).
Luciferase reporter gene assay
To harvest samples for luciferase assays, cells were washed once with phosphate buffered solution (PBS), and then 100 μl lysis buffer (Promega) was added to each well of a 24-well plate, and a 50 μl sample was mixed with luciferase assay substrate (Promega). Luciferase activity was typically measured for 10 s using a luminometer (Turner Designs TD-20/20). Assays were performed in triplicate and are expressed as the mean ± standard deviation (SD) of luciferase activity.
Real-time RT-PCR
Total RNA was extracted from PBMCs or cells using Trizol reagent (Invitrogen), according to the manufacturer's protocol. DNA was removed from the sample by on-column DNase I treatment. RNA was used as a template to synthesize cDNA using random primers and MMLV-RT (Promega) at 42°C for 60 min, followed by denaturation for 10 min at 70°C. Real-time reverse transcriptase polymerase chain reaction (RT-PCR) was performed using SYBR Green PCR master mix (Roche) in LightCycler 480 (Roche). After an initial incubation at 95°C for 5 min, reaction mixtures were subjected to 40 cycles of amplification under the following conditions: 94°C for 15 s, 55°C for 15 s, and 72°C for 20 s. To examine the quality of detection primers, the fluorescence was measured at this step, followed by a final melting curve step from 50°C to 95°C. Primers for HCV detection were 5'-TCGTATGATACCCGATGCT-3' (forward) and 5'-GTTTGACCCTTGCTGTTGA-3' (reverse). Primers for IP10 detection were 5'-TCTAGAACCGTACGCTGTACCTGC-3' (forward) and 5'-CTGGTTTTAAGGAGATCT-3' (reverse). Primers for internal reference GAPDH detection were 5'-AAGGCTGTGGGCAAGG-3' (forward) and 5'-TGGAGGAGTGGGTGTCG-3' (reverse). Each sample was run in triplicate; threshold cycles (CT) were averaged and normalized to endogenous GAPDH. The relative amount of amplified product was calculated using the comparative CT method (Roche).
Western blotting and ELISA
Protein was resolved on a 12% sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) gel and transferred to nitrocellulose membranes (minipore). Membranes were blocked with PBS containing 5% fat-free milk powder and 0.1% Tween 20 for 1 h, blotted with the appropriate primary antibodies for 2 h, incubated with HRP-conjugated secondary antibody (GE) for 1 h, washed, incubated with HRP substrate luminol reagent (Millipore), and analyzed using a Luminescent Image Analyzer (Fujifilm LAS-4000). IP-10 protein levels in supernatants were measured using a commercially available enzyme-linked immunosorbent assay (ELISA) kit (BD Biosciences).
Statistical Analyses
Data that were Gaussian distributed were analyzed by parametric t-tests for independent samples or by analysis of variance (ANOVA). Correlation coefficients were calculated by linear regression analysis.
Acknowledgements
We would like to thank Dr. Takaji Wakita of Tokyo Metropolitan Institute for Neuroscience for providing infectious HCV virus JFH1 DNA construct, Dr. Francis Chisari of Scripps Research Institute for providing the Huh7.5.1 cell line, and Dr. Charles Rice of Rockefeller University for providing the plasmid FL-J6/JFH-5'C19Rluc2AUbi.
This work was supported by research grants from the Major State Basic Research Development Program (973 Program) (2012CB518900), the National Natural Science Foundation of China (30730001 and 81171525), National Mega Project on Major Infectious Disease Prevention (2012ZX10002006-003 and 2012ZX10004-207), National Mega Project on Major Drug Development (2011ZX09401-302), Fundamental Research Funds for the Central Universities (1102001), and Specialized Research Fund for the Doctoral Program of Higher Education (20090141110033) to J.W.
Authors' contributions
JQ designed and performed the experiments, and drafted the manuscript. QZ performed some of the infection assays. YL, WL and LC participated in recruitment of patient samples. JW and YZ designed and coordinated the study. All authors read and approved the final manuscript.