Inhibitory effect of kaolin minerals compound against hepatitis C virus in Huh-7 cell lines
© Ali et al.; licensee BioMed Central Ltd. 2014
Received: 4 July 2013
Accepted: 4 April 2014
Published: 17 April 2014
Hepatitis C virus (HCV) is estimated to infect 200 million individuals in the globe, including approximately 10 million in Pakistan causing both acute and chronic hepatitis. The standard treatment against HCV is pegylated interferon therapy in combination with a nucleoside analogue ribavirin. In addition, several herbal extracts and phytochemicals derivatives are used traditionally in the treatment of liver diseases as well as HCV infection. The present study determines the inhibitory effect of kaolin minerals compound against hepatitis C virus in Huh-7 cell lines.
Huh-7 cell lines were used for the in vitro HCV replication by using HCV positive sera from different patients with known HCV genotypes and viral titer/load. Total RNA was extracted from these infected cells and was quantified by real-time polymerase chain reaction (Real-time PCR). The viral titer was compared with the control samples to determine the anti-HCV activity of kaolin derived compounds. Kaolin is a group of clay minerals, with the chemical composition Al2 Si2O5 (OH)4.
The results showed promising effectiveness of local kaolin derived anti-HCV compounds by causing 28% to 77% decrease in the HCV titer, when applied to infected Huh-7 cell lines. This study provides the basis for future work on these compounds especially to determine the specific pathway and mechanism for inhibitory action in the replicon systems of viral hepatitis.
Kaolin mineral derivatives show promising inhibitory effects against HCV genotypes 3a and 1a infection, which suggests its possible use as complementary and alternative medicine for HCV viral infection.
Hepatitis C virus (HCV) is contributing increasing disease burden on global healthcare services and nearly 200 million people are infected worldwide by this virus [1, 2]. Most of these infections cause chronic hepatitis and leading to progressive liver disease including cirrhosis, fibrosis and finally hepatocellular carcinoma (HCC) [3–5]. Fibrosis and cirrhosis is caused in up to 30% infected patients. It is estimated that 1-4% of the cirrhotic patients develop HCC [6–9]. Significant correlation of chronic HCV infection and HCC has been reported with genotype 3a in Pakistani population .
The current most effective therapy for HCV consists of pegylated interferon-α (IFN-α), administered once weekly plus daily oral ribavirin (RBV) for 24 to 48 weeks [11, 12]. This combination therapy is quite successful in patients with HCV genotype 3 or 2 infection, leading to sustained virological response (SVR) in about 80-90% of patients treated. However, in patients infected with HCV genotype 1 or 4, only about a half of treated individuals achieve SVR [13, 14]. Further, the treatment is often linked with severe side effects and high expenses. The HCV RNA level before therapy also effect treatment outcome in patients with genotype-1 infection. Patients with low baseline viral loads (e.g., <8 × 105 IU/mL), have a better chance of SVR .
Beside the standard interferon plus ribavirin therapy, several plants, herb species and their derivatives have also been in use as potential anti-viral agents . A number of active phytochemicals including the polyines, flavonoids, alkaloids, thiophenes, terpenoids and proteins have been identified to possess antiviral activity . Most of these compounds have overlapping mechanisms of actions. Many medicinal plants are waiting to be exploited and evaluated for antiviral applications.
Kaolin is a group of clay minerals, with the chemical composition Al2 Si2O5(OH)4. It is a layered silicate mineral with one tetrahedral sheet linked through oxygen atoms to one octahedral sheet of alumina octahedral. It is also known as china clay or white clay. Mostly, white, brownish and grayish white in colour, also waxy and dull and contain common impurities like:Fe, Mg, Na, K,Ti, Ca, H2O . Up to 350 mineral drugs have been identified and reported with medicinal value. Nearly 60 of these are still commonly used but prescribed alone rarely. However, they are usually given in combination with other components [19, 20]. Now a days Selenium and its derivatives are favourable choice of complimentary alternative medicine (CAM) for liver diseases like HCV .
The main objective of the present study was to evaluated local kaolin mineral derivatives for their anti-HCV activity in the human hepatoma cell lines infected with HCV sera of different patients with known viral loads and genotypes.
Serum sample collection
Sera from more than 32 patients (12 and 20 samples of genotype 1a and 3a respectively) chronically infected with HCV infections was obtained from the molecular diagnostics facility, Centre for Applied Molecular Biology (CAMB), Lahore, Pakistan. The average serum viral loads of the samples were in the range of 227 × 103 to 925 × 106 IU/mL. All patients were negative for HBsAg. Informed written consent was obtained from the patients and the study was approved by the institutional ethics committee of National Centre of Excellence in Molecular Biology, Lahore.
The Huh-7 and CHO cell lines were obtained from the Cell Bank of CEMB, University of the Punjab, Lahore.
Total two different kaolin derivatives (kaolin minerals) were obtained in dimethyl sulfoxide (DMSO) as solvent, using modified method described by Alpert in 1984 . The two different silicates minerals were obtained by using different soil from different places. Mineral derivative “A” as obtained from muddy soil while “B” was from sandy soil. Finally, these two compounds were selected for the determination of anti-HCV activity in vitro using Huh-7 cell lines. The mineral derivative of Kaolin was basically obtained from muddy and sandy soil.
Physical properties of the kaolin
Mostly, White,Brownish white, Grayish white, Yellowish white and in color also Waxy, Dull and Pearly. Visible crystals extremely rare. Non fluorescent and Transparent to translucent diaphaneity etc.
Chemical properties of the kaolin
Formula: Al2 Si2O5 (OH)4
Essential Elements: Al, H, O, Si
Common Impurities: Fe, Mg, Na, K, Ti, Ca, H2O
The Huh-7 and Chinese hamster ovary (CHO) cell line were grown in Dulbecco’s modified eagle medium (DMEM) supplemented with 100 μg/ml penicillin, 100 μg/ml streptomycin and 10% fetal bovine serum (FBS) (Wisent INC., Montreal, Canada) incubated at 37°C with 5% CO2. They are highly permissive for the initiation of HCV replication.
Cell splitting and plating
The Huh-7 cell line grown in DMEM supplemented with appropriate antibiotic, 10% FBS and CO2 was split and plated for toxicological analysis of kaolin derivatives.
Anti-HCV analysis of kaolin minerals derivatives in Huh-7 cells
Huh-7 cell line was used for the in vitro HCV replication as described previously [23, 24]. Total RNA was extracted from the Huh-7 cells infected with HCV serum using the Purescript RNA Isolation kit (Life Technologies, USA).
HCV RNA quantitative detection in Huh-7 cells by real time PCR
HCV REAL-TM Quant SC kit (Sacace Biotechnologies, Italy) used in Smart Cycler (Cepheid) was used for Real-Time quantitative assay of HCV RNA in human plasma following procedure given in the kit protocol.
Toxicity analysis of kaolin derivatives in Huh-7 cells
Antiviral analysis of kaolin derivatives in Huh-7 cell line
Viral titer of genotype 3a in infected Huh-7 cell lines was decreased up to 70% by using minerals derivatives “A” and 56% by administration of “B” as compared to the positive control samples. Similarly, reduction in HCV RNA of genotype 1a was observed up to 77% and 28% by administering “A and B” respectively. These results show that kaolin derivatives “A” is relatively more effective against genotype 3a and 1a, which suggests its use as complementary and alternative medicine for the treatment of HCV infection.
Currently, there is no antiviral drug completely effective against HCV infection . The standard treatment against HCV infection is interferon therapy in combination with a nucleoside analogue ribavirin . However, the treatment with pegylated interferon (IFN) plus ribavirin leads to a sustained virologic response in about 50% of patients  and lead to emergence of resistant quasispecies/strains due to increased drug pressure . For rest of 50% non-respondents, supportive therapy with non-traditional compounds such as kaolin mineral obtained from the soil of different sources, which are suggested to have anti-HCV properties.
The present study describes antiviral activity of two conventional derivatives of kaolin mineral compounds against HCV in two different cell lines (i.e. Huh-7 & CHO cell lines). Different solvents such as dimethyl sulfoxide (DMSO), ethanol, methanol, acetone and water were used to determine solubility of the compounds. Huh-7 cell lines are important in studying antiviral activity in vitro as it allows HCV replication due to its expression of LDL-receptor molecules . HCV genotype 3a and 1a were used for evaluation of antiviral responses. Viral titer was considered as an indicator of antiviral response. The concentrations of 50 μg/mL to 50 mg/mL with volume of 10-60 μl of both drugs were used.
Initially, different concentrations of kaolin derivatives “A and B” were analyzed for cytotoxicity in the Huh-7 and CHO cell lines. Both the compounds were found non-toxic up to the administration of 30 μl (50 μg of kaolin derivative/ml). At these concentrations cells did not display any significant cytotoxicity during regular cell passage and trypan blue counting. Cells viability was counted by haemocytometer and trypan blue stain method. The present study provides experimental data of local kaolin derived drugs for clinical treatment of chronic hepatitis C virus infection.
We suggest that there could be excellent therapeutic agents in kaolin mineral compounds for the treatment of HCV infections. However, further studies are required to identify the specific active ingredients by using various techniques. This study also provides basis for future work on these compounds especially minerals derivatives A to determine its mechanism of action in the replicon systems and clinical trials for the treatment of the hepatitis C. Moreover, this study will be helpful to explore the new horizons of the discoveries of the kaolin derivatives, which shows promising inhibitory effects against HCV.
This work was partially supported by the Higher Education Commission (HEC) of Pakistan.
- Wasley A, Alter MJ: Epidemiology of hepatitis C: geographic differences and temporal trends. Semin Liver Dis. 2000, 20: 1-16. 10.1055/s-2000-9506.PubMedView ArticleGoogle Scholar
- Rehman I, Idrees M, Ali M, Ali L, Butt S, Hussain A, Akbar H, Afzal S: Hepatitis C virus genotype 3a with phylogenetically distinct origin is circulating in Pakistan. Genet Vaccines Ther. 2011, 9: 2-10.1186/1479-0556-9-2.PubMedPubMed CentralView ArticleGoogle Scholar
- Giannini C, Brechot C: Hepatitis C virus biology. Cell Death Differ. 2003, 10: S27-38. 10.1038/sj.cdd.4401121.PubMedView ArticleGoogle Scholar
- Shepard CW, Finelli L, Alter MJ: Global epidemiology of hepatitis C virus infection. Lancet Infect Dis. 2006, 5: 558-567.View ArticleGoogle Scholar
- Akbar H, Idrees M, Manzoor S, Rehman IU, Butt S, Yousaf MZ, Rafique S, Awan Z, Khubaib B, Akram M, Aftab M: Hepatitis C virus infection: A review of the current and future aspects and concerns in Pakistan. JGMV. 2009, 1: 012-018.Google Scholar
- Lederer SL, Walters KA, Proll S, Paeper B, Robinzon S, Boix L, Fausto N: Distinct cellular responses differentiating alcohol- and hepatitis C virus-induced liver cirrhosis. Virol J. 2006, 3: 98-10.1186/1743-422X-3-98.PubMedPubMed CentralView ArticleGoogle Scholar
- Miura K, Taura K, Kodama Y, Schnabl B, Brenner DA: Hepatitis C virus-induced oxidative stress suppresses hepcidin expression through increased histone deacetylase activity. Viral Hepatitis. 2008, 48: 1420-1429.Google Scholar
- Joyce MA, Walters KA, Lamb SE, Yeh MM, Zhu LF, Kneteman N, Doyle JS, Katze MG, Tyrrell DL: HCV Induces Oxidative and ER Stress, and Sensitizes Infected Cells to Apoptosis in SCID/Alb-uPA Mice. PLoS Pathog. 2009, 5 (2): e1000291-10.1371/journal.ppat.1000291.PubMedPubMed CentralView ArticleGoogle Scholar
- Walters KA, Syder AJ, Lederer SL, Diamond DL, Paeper B, Rice CM, Katze MG: Genomic analysis revealsb a potential role for cell cycle perturbation in HCV mediated apoptosis of cultured hepatocytes. Plos pathogens. 2009, 5: e1000269-10.1371/journal.ppat.1000269.PubMedPubMed CentralView ArticleGoogle Scholar
- Idrees M, Rafique S, Rehman I, Akbar H, Yousaf MZ, Butt S, Awan Z, Manzoor S, Akram M, Aftab M, Khubaib B, Riazuddin S: Hepatitis C virus genotype 3a infection and hepatocellular carcinoma: Pakistan experience. World J Gastroenterol. 2009, 15: 5080-5085. 10.3748/wjg.15.5080.PubMedPubMed CentralView ArticleGoogle Scholar
- Foster GR: Pegylated interferons: Chemical and Clinical Differences. Aliment Pharmacol Ther. 2004, 20: 825-30. 10.1111/j.1365-2036.2004.02170.x.PubMedView ArticleGoogle Scholar
- Afzal S, Idrees M, Ali M, Ilyas M, Hussain A, Akram M, Butt S, Rehman I, Ali L, Shahid M: Envelope 2 protein phosphorrylat-ion sites S75 & 277 of hepatitis C virus genotype 1a and interferon resistance: A sequence alignment approach. Virol J. 2011, 8: 71-10.1186/1743-422X-8-71.PubMedPubMed CentralView ArticleGoogle Scholar
- Fried MW, Shiffman ML, Reddy KR, Smith C, Marinos G, Goncales FL, Haussinger D, Diago M, Carosi G, Dhumeaux D, Craxi A, Lin A, Hoffman J, Yu J: Peginterferon alfa-2a plus ribavirin for chronic hepatitis C virus infection. N Engl J Med. 2002, 347: 975-82. 10.1056/NEJMoa020047.PubMedView ArticleGoogle Scholar
- Manns MP, McHutchison JG, Gordon SC, Rustgi VK, Shiffman M, Reindollar R, Goodman ZD, Koury K, Ling M, Albrecht JK: Peg interferon alfa-2b plus ribavirin compared with interferon alfa-2b plus ribavirin for initial treatment of chronic hepatitis C: a randomised trial. Lancet. 2001, 358: 958-65. 10.1016/S0140-6736(01)06102-5.PubMedView ArticleGoogle Scholar
- Feld JJ, Hoofnagle JH: Mechanism of action of interferon and ribavirin in treatment of hepatitis C. Nature. 2005, 436: 967-972. 10.1038/nature04082.PubMedView ArticleGoogle Scholar
- Javed T, Ashfaq UA, Riaz S, Rehman S, Riazuddin S: In-vitro antiviral activity of Solanum nigrum against activity Hepatitis C Virus. Virol J. 2011, 8: 26-10.1186/1743-422X-8-26.PubMedPubMed CentralView ArticleGoogle Scholar
- Kitamura K, Honda M, Youshizaki H: Baicalin, an inhibitor of HIV-1 production in vitro. Antiviral Res. 1998, 37: 131-140. 10.1016/S0166-3542(97)00069-7.PubMedView ArticleGoogle Scholar
- Deer WA, Howie RA, Zussman J: An introduction to the rock-forming minerals. 1992, Harlow: Longman, ISBN 0582300940, 2Google Scholar
- Yu W, Foster HD, Zhang T: Discovering Chinese Mineral Drugs. J Orthomol Med. 1995, 10: 31-58.Google Scholar
- Yang SN: Identification of Chinese Mineral Medicines. 1990, Shanghai: Shanghai Scientific Literature Publishing HouseGoogle Scholar
- Kolachi NF, Kazi TG, Afridi HI, Kazi NG, Mughal MA, Khan S: Effects of selenium and zinc status in biological samples of hepatitis C patient after herbal and pharmaceutical supplements. Biol Trace Elem Res. 2013, 152 (2): 187-94. 10.1007/s12011-013-9617-8.PubMedView ArticleGoogle Scholar
- Alpert A: Analysis of chlorophyll content in mosses through extraction in DMSO. The Bryologist. 1984, 87 (4): 363-365. 10.2307/3242964.View ArticleGoogle Scholar
- Zekri AR, Bahnassy AA, El-Din HM, Salama HM: Consensus siRNA for inhibition of HCV genotype-4 replication. Virol J. 2009, 6: 13-10.1186/1743-422X-6-13.PubMedPubMed CentralView ArticleGoogle Scholar
- El-Awady MK, Tabll AA, El-Abd YS, Bahgat MM, Shoeb HA, Youssef SS, NG B e-D, El RM R, El-Demellawy M, Omran MH, El-Garf WT, Goueli SA: HepG2 cells support viral replication and gene expression of hepatitis C virus genotype 4 in vitro. World J Gastroenterol. 2006, 12: 4836-4842.PubMedPubMed CentralGoogle Scholar
- Hahn JA: Sex, drugs and hepatitis C virus. J Infect Dis. 2007, 195: 1556-9. 10.1086/516792.PubMedView ArticleGoogle Scholar
- Rong L, Perelson AS: Treatment of hepatitis C virus infection with interferon and small molecule direct antivirals: viral kinetics and modeling. Crit Rev Immunol. 2010, 30: 131-148. 10.1615/CritRevImmunol.v30.i2.30.PubMedPubMed CentralView ArticleGoogle Scholar
- Inamullah , Idrees M, Ahmed H, Ghafoor S, Ali M, Ali L, Ahmed A: Hepatitis C virus genotypes circulating in district Swat of Khyber Pakhtoonkhaw, Pakistan. Virol J. 2011, 8: 16-10.1186/1743-422X-8-16.PubMedPubMed CentralView ArticleGoogle Scholar
- Stefanie SP, Hubert MM, Eberhard P: Establishment of persistent hepatitis C virus infection and replication in vitro. J Gen Virol. 1997, 78: 2467-2476.View ArticleGoogle Scholar
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