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Differential inhibition of dengue virus infection in mammalian and mosquito cells by iota-carrageenan.
J Gen Virol. 2011 Jun; 92(Pt 6):1332-1342.JG

Abstract

The antiviral activity against dengue virus-2 (DENV-2) of carrageenans reported here has shown a differential susceptibility of C6/36 HT and Vero cells, taken as models of mosquito and mammalian cells, depending on the structural class of polysaccharides: all polysaccharides blocked DENV-2 infection in monkey Vero cells, but only iota-carrageenans were virus inhibitors in mosquito cells. However, iota-carrageenans were less effective in mosquito cells in comparison with mammalian cells with effective concentration 50 % (EC(50)) values in C6/36 HT cells 4.9-17.5-fold higher than in Vero cells, as determined by virus yield reduction assay. The mode of action of iota-carrageenan in both cell types was strikingly different: in Vero cells the inhibitory activity was exerted only at the initiation of the cycle, affecting virion binding, whereas in mosquito cells DENV-2 adsorption was not affected and comparable levels of inhibition were obtained if the compound was added to cells together with the virus, after 8 h of infection or by cell pre-treatment before infection. Furthermore, iota-carrageenans induced a subtle alteration in mosquito cells, detected by cell proliferation and protein synthesis analyses, suggesting that a probable cellular target may be responsible for the refractory state of mosquito cells to DENV-2 infection produced by this class of polysulfates. The failure of iota-carrageenan to block DENV-2 adsorption to mosquito cells appeared to be related to the low presence of adequate heparan sulfate (HS) in C6/36 HT cell surface and is indicative of a differential participation of HS residues for DENV-2 entry in both types of cells.

Authors+Show Affiliations

Laboratorio de Virología, Departamento de Química Biológica, Facultad de Ciencias Exactas y Naturales, Universidad de Buenos Aires, 1428 Buenos Aires, Argentina.Departamento de Bioquímica e Biologia Molecular, Universidade Federal do Paraná, PO Box 19046, Curitiba, Paraná, Brazil.Departamento de Bioquímica e Biologia Molecular, Universidade Federal do Paraná, PO Box 19046, Curitiba, Paraná, Brazil.Departamento de Bioquímica e Biologia Molecular, Universidade Federal do Paraná, PO Box 19046, Curitiba, Paraná, Brazil.Laboratorio de Virología, Departamento de Química Biológica, Facultad de Ciencias Exactas y Naturales, Universidad de Buenos Aires, 1428 Buenos Aires, Argentina.

Pub Type(s)

Comparative Study
Journal Article
Research Support, Non-U.S. Gov't

Language

eng

PubMed ID

21325483

Citation

Talarico, Laura B., et al. "Differential Inhibition of Dengue Virus Infection in Mammalian and Mosquito Cells By Iota-carrageenan." The Journal of General Virology, vol. 92, no. Pt 6, 2011, pp. 1332-1342.
Talarico LB, Noseda MD, Ducatti DRB, et al. Differential inhibition of dengue virus infection in mammalian and mosquito cells by iota-carrageenan. J Gen Virol. 2011;92(Pt 6):1332-1342.
Talarico, L. B., Noseda, M. D., Ducatti, D. R. B., Duarte, M. E. R., & Damonte, E. B. (2011). Differential inhibition of dengue virus infection in mammalian and mosquito cells by iota-carrageenan. The Journal of General Virology, 92(Pt 6), 1332-1342. https://doi.org/10.1099/vir.0.028522-0
Talarico LB, et al. Differential Inhibition of Dengue Virus Infection in Mammalian and Mosquito Cells By Iota-carrageenan. J Gen Virol. 2011;92(Pt 6):1332-1342. PubMed PMID: 21325483.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Differential inhibition of dengue virus infection in mammalian and mosquito cells by iota-carrageenan. AU - Talarico,Laura B, AU - Noseda,Miguel D, AU - Ducatti,Diogo R B, AU - Duarte,Maria E R, AU - Damonte,Elsa B, Y1 - 2011/02/16/ PY - 2011/2/18/entrez PY - 2011/2/18/pubmed PY - 2011/7/13/medline SP - 1332 EP - 1342 JF - The Journal of general virology JO - J Gen Virol VL - 92 IS - Pt 6 N2 - The antiviral activity against dengue virus-2 (DENV-2) of carrageenans reported here has shown a differential susceptibility of C6/36 HT and Vero cells, taken as models of mosquito and mammalian cells, depending on the structural class of polysaccharides: all polysaccharides blocked DENV-2 infection in monkey Vero cells, but only iota-carrageenans were virus inhibitors in mosquito cells. However, iota-carrageenans were less effective in mosquito cells in comparison with mammalian cells with effective concentration 50 % (EC(50)) values in C6/36 HT cells 4.9-17.5-fold higher than in Vero cells, as determined by virus yield reduction assay. The mode of action of iota-carrageenan in both cell types was strikingly different: in Vero cells the inhibitory activity was exerted only at the initiation of the cycle, affecting virion binding, whereas in mosquito cells DENV-2 adsorption was not affected and comparable levels of inhibition were obtained if the compound was added to cells together with the virus, after 8 h of infection or by cell pre-treatment before infection. Furthermore, iota-carrageenans induced a subtle alteration in mosquito cells, detected by cell proliferation and protein synthesis analyses, suggesting that a probable cellular target may be responsible for the refractory state of mosquito cells to DENV-2 infection produced by this class of polysulfates. The failure of iota-carrageenan to block DENV-2 adsorption to mosquito cells appeared to be related to the low presence of adequate heparan sulfate (HS) in C6/36 HT cell surface and is indicative of a differential participation of HS residues for DENV-2 entry in both types of cells. SN - 1465-2099 UR - https://www.unboundmedicine.com/medline/citation/21325483/Differential_inhibition_of_dengue_virus_infection_in_mammalian_and_mosquito_cells_by_iota_carrageenan_ L2 - http://jgv.microbiologyresearch.org/pubmed/content/journal/jgv/10.1099/vir.0.028522-0 DB - PRIME DP - Unbound Medicine ER -