期刊论文详细信息
BMC Research Notes
Inhibitory effect of kaolin minerals compound against hepatitis C virus in Huh-7 cell lines
Eyad Hassan Kamel2  Syed Abbas Iqbal2  Amjad Ali3  Irshad Ur Rehman1  Abrar Hussain1  Muhammad Ali1  Muhammad Idrees1  Liaqat Ali1 
[1] Division of Molecular Virology, National Centre of Excellence in Molecular Biology, University of the Punjab, Lahore, 87-West Canal bank Road, Thoker Niaz baig, Lahore 53700, Pakistan;Zainab Memorial Hospital, Lahore, Pakistan;Biotechnology Department, University of Malakand Chakdara Dir (lower), Khyber Pakhtunkhwa, Pakistan
关键词: Kaolinite;    Huh-7 cell line;    HCV genotypes;   
Others  :  1133430
DOI  :  10.1186/1756-0500-7-247
 received in 2013-07-04, accepted in 2014-04-04,  发布年份 2014
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【 摘 要 】

Background

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.

Methods

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.

Results

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.

Conclusions

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.

【 授权许可】

   
2014 Ali et al.; licensee BioMed Central Ltd.

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【 参考文献 】
  • [1]Wasley A, Alter MJ: Epidemiology of hepatitis C: geographic differences and temporal trends. Semin Liver Dis 2000, 20:1-16.
  • [2]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. BioMed Central Full Text
  • [3]Giannini C, Brechot C: Hepatitis C virus biology. Cell Death Differ 2003, 10:S27-38.
  • [4]Shepard CW, Finelli L, Alter MJ: Global epidemiology of hepatitis C virus infection. Lancet Infect Dis 2006, 5:558-567.
  • [5]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.
  • [6]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. BioMed Central Full Text
  • [7]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.
  • [8]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.
  • [9]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]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.
  • [11]Foster GR: Pegylated interferons: Chemical and Clinical Differences. Aliment Pharmacol Ther 2004, 20:825-30.
  • [12]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. BioMed Central Full Text
  • [13]Fried MW, Shiffman ML, Reddy KR, Smith C, Marinos G, Goncales FL Jr, 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.
  • [14]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.
  • [15]Feld JJ, Hoofnagle JH: Mechanism of action of interferon and ribavirin in treatment of hepatitis C. Nature 2005, 436:967-972.
  • [16]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. BioMed Central Full Text
  • [17]Kitamura K, Honda M, Youshizaki H: Baicalin, an inhibitor of HIV-1 production in vitro. Antiviral Res 1998, 37:131-140.
  • [18]Deer WA, Howie RA, Zussman J: An introduction to the rock-forming minerals. 2nd edition. Harlow: Longman; 1992. ISBN 0582300940
  • [19]Yu W, Foster HD, Zhang T: Discovering Chinese Mineral Drugs. J Orthomol Med 1995, 10:31-58.
  • [20]Yang SN: Identification of Chinese Mineral Medicines. Shanghai: Shanghai Scientific Literature Publishing House; 1990.
  • [21]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.
  • [22]Alpert A: Analysis of chlorophyll content in mosses through extraction in DMSO. The Bryologist 1984, 87(4):363-365.
  • [23]Zekri AR, Bahnassy AA, El-Din HM, Salama HM: Consensus siRNA for inhibition of HCV genotype-4 replication. Virol J 2009, 6:13. BioMed Central Full Text
  • [24]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.
  • [25]Hahn JA: Sex, drugs and hepatitis C virus. J Infect Dis 2007, 195:1556-9.
  • [26]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.
  • [27]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. BioMed Central Full Text
  • [28]Stefanie SP, Hubert MM, Eberhard P: Establishment of persistent hepatitis C virus infection and replication in vitro. J Gen Virol 1997, 78:2467-2476.
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