The antiviral activity of sulfated polysaccharides against dengue virus is dependent on virus serotype and host cell

被引:210
作者
Talarico, LB
Pujol, CA
Zibetti, RGM
Faría, PCS
Noseda, MD
Duarte, MER
Damonte, EB
机构
[1] Univ Buenos Aires, Fac Ciencias Exactas & Nat, Dept Quim Biol, Ciudad Univ,Lab Virol, RA-1428 Buenos Aires, DF, Argentina
[2] Univ Fed Parana, Dept Bioquim & Biol Mol, BR-80060000 Curitiba, Parana, Brazil
关键词
Dengue virus; flaviviruses; antiviral activity; sulfated polysaccharides; viral entry;
D O I
10.1016/j.antiviral.2005.02.001
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Two homogeneous sulfated polysaccharides obtained from the red seaweeds Gymnogongrus griffithsiae and Cryptonemia crenulata, the kappa/iota/nu carrageenan G3d and the DL-galactan hybrid C2S-3, were assayed for their antiviral properties against the four serotypes of dengue virus (DENV) in different host cell types. Both seaweed derivatives were selective inhibitors of DENV-2 multiplication in Vero cells with inhibitory concentration 50% (IC50) values around 1 mu g/ml and selectivity indices > 1000. The Compounds had a lower antiviral effect against DENV-3 (IC50 values in the range 13.9-14.2 mu g/ml), an even lower effect against DENV-4 (IC50 values in the range 29.3 to > 50 mu g/ml) and were totally inactive against DENV-1, With respect to the host cell, the polysulfates were inhibitors of DENV-2 and DENV-3 in the human hepatoma HepG2 and foreskin PH cells, with similar antiviral effectiveness as in Vero cells, but were totally inactive in mosquito C6/36 HT cells. Mechanistic studies demonstrated that G3d and C2S-3 were active DENV-2 inhibitors only when added together with the virus or early after infection, and both initial processes of virus adsorption and internalization are the main targets of these compounds. Therefore, the variations in antiviral activity of the polysaccharides depending on the viral serotype and the host cell may be ascribed to differences in the virus-cell interaction leading to virus entry. (c) 2005 Published by Elsevier B.V.
引用
收藏
页码:103 / 110
页数:8
相关论文
共 40 条
[21]   Heparin inhibits dengue-2 virus infection of five human liver cell lines [J].
Lin, YL ;
Leib, HY ;
Lin, YS ;
Yeh, TM ;
Chen, SH ;
Liu, HS .
ANTIVIRAL RESEARCH, 2002, 56 (01) :93-96
[22]  
Lindenbach B. D., 2001, Fundamental virology, P589
[23]   Dengue 1 virus binding to human hepatoma HepG2 and simian Vero cell surfaces differs [J].
Marianneau, P ;
Megret, F ;
Olivier, R ;
Morens, DM ;
Deubel, V .
JOURNAL OF GENERAL VIROLOGY, 1996, 77 :2547-2554
[24]   Broad-spectrum antiviral activity of the IMP dehydrogenase inhibitor VX-497: a comparison with ribavirin and demonstration of antiviral additivity with alpha interferon [J].
Markland, W ;
McQuaid, TJ ;
Jain, J ;
Kwong, AD .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2000, 44 (04) :859-866
[25]   Probing the interaction of dengue virus envelope protein with heparin:: Assessment of glycosaminoglycan-derived inhibitors [J].
Marks, RM ;
Lu, H ;
Sundaresan, R ;
Toida, T ;
Suzuki, A ;
Imanari, T ;
Hernáiz, MJ ;
Linhardt, RJ .
JOURNAL OF MEDICINAL CHEMISTRY, 2001, 44 (13) :2178-2187
[26]   Identification of a putative coreceptor on vero cells that participates in dengue 4 virus infection [J].
Martínez-Barragán, JD ;
Del Angel, RM .
JOURNAL OF VIROLOGY, 2001, 75 (17) :7818-7827
[27]   Dengue viral infections; pathogenesis and epidemiology [J].
McBride, WJH ;
Bielefeldt-Ohmann, H .
MICROBES AND INFECTION, 2000, 2 (09) :1041-1050
[28]   Genetic characterization of dengue virus type 3 isolates in the State of Rio de Janeiro, 2001 [J].
Miagostovich, MP ;
dos Santos, FB ;
de Simone, TS ;
Costa, EV ;
Filippis, AMB ;
Schatzmayr, HG ;
Nogueira, RMR .
BRAZILIAN JOURNAL OF MEDICAL AND BIOLOGICAL RESEARCH, 2002, 35 (08) :869-872
[29]   Non Fc receptor-mediated infection of human macrophages by dengue virus serotype 2 [J].
Moreno-Altamirano, MMB ;
Sánchez-García, FJ ;
Muñoz, ML .
JOURNAL OF GENERAL VIROLOGY, 2002, 83 :1123-1130
[30]  
Muñoz MD, 1998, FEMS MICROBIOL LETT, V168, P251, DOI 10.1111/j.1574-6968.1998.tb13281.x