Xylans from Scinaia hatei: Structural features, sulfation and anti-HSV activity
Natural compounds offer interesting pharmacological perspectives for antiviral drug development with regard to broad-spectrum antiviral properties and novel modes of action. In this study, we have analyzed alkali-extracted xylan of Scinaia hatei. Alkali extraction of this red alga yielded a xylan sh...
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Acceso en línea: | https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_01418130_v46_n2_p173_Mandal http://hdl.handle.net/20.500.12110/paper_01418130_v46_n2_p173_Mandal |
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paper:paper_01418130_v46_n2_p173_Mandal2023-06-08T15:11:24Z Xylans from Scinaia hatei: Structural features, sulfation and anti-HSV activity Pujol, Carlos Alberto Damonte, Elsa Beatriz Antiviral activity Herpes simplex virus Liagoraceae Scinaia hatei Sulfation Xylan acetone antivirus agent petroleum ether polysaccharide sulfate xylan animal cell antiviral activity article chemical bond controlled study drug cytotoxicity drug structure gel permeation chromatography glycosidic linkage Herpes simplex virus Herpes simplex virus 1 Herpes simplex virus 2 macromolecule molecular weight nonhuman proton nuclear magnetic resonance Scinaia hatei seaweed solvent extraction Soxhlet extraction structure activity relation sulfation virion virus inactivation Algae, Red Animals Antiviral Agents Cercopithecus aethiops Chromatography, Gel Glycosides Herpesvirus 1, Human Herpesvirus 2, Human Magnetic Resonance Spectroscopy Molecular Weight Sulfur Vero Cells Xylans Liagoraceae Rhodophyta Scinaia Simplexvirus Natural compounds offer interesting pharmacological perspectives for antiviral drug development with regard to broad-spectrum antiviral properties and novel modes of action. In this study, we have analyzed alkali-extracted xylan of Scinaia hatei. Alkali extraction of this red alga yielded a xylan shown to have a molecular mass of 120kDa and a linear structure of (1→4)-linked β-d-xylopyranosyl residues. Derivatives (S1, S2, S3 and S4) generated by chemical sulfation from this macromolecule had degree of sulfation between 0.93 and 1.95, and contained strong anti-HSV activity with inhibitory concentration 50% (IC50) from 0.22 to 1.37μg/ml. Furthermore, they had no direct inactivating effect on virions in a virucidal assay. Sulfate groups account for their in vitro antiviral activity. Interestingly, sulfated xylans already exerted anti-HSV activity when only pre-incubated with the cultured cells prior to infection, thus pointing to a main inhibitory effect on viral entry. © 2009 Elsevier B.V. Fil:Pujol, C.A. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Damonte, E.B. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. 2010 https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_01418130_v46_n2_p173_Mandal http://hdl.handle.net/20.500.12110/paper_01418130_v46_n2_p173_Mandal |
institution |
Universidad de Buenos Aires |
institution_str |
I-28 |
repository_str |
R-134 |
collection |
Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA) |
topic |
Antiviral activity Herpes simplex virus Liagoraceae Scinaia hatei Sulfation Xylan acetone antivirus agent petroleum ether polysaccharide sulfate xylan animal cell antiviral activity article chemical bond controlled study drug cytotoxicity drug structure gel permeation chromatography glycosidic linkage Herpes simplex virus Herpes simplex virus 1 Herpes simplex virus 2 macromolecule molecular weight nonhuman proton nuclear magnetic resonance Scinaia hatei seaweed solvent extraction Soxhlet extraction structure activity relation sulfation virion virus inactivation Algae, Red Animals Antiviral Agents Cercopithecus aethiops Chromatography, Gel Glycosides Herpesvirus 1, Human Herpesvirus 2, Human Magnetic Resonance Spectroscopy Molecular Weight Sulfur Vero Cells Xylans Liagoraceae Rhodophyta Scinaia Simplexvirus |
spellingShingle |
Antiviral activity Herpes simplex virus Liagoraceae Scinaia hatei Sulfation Xylan acetone antivirus agent petroleum ether polysaccharide sulfate xylan animal cell antiviral activity article chemical bond controlled study drug cytotoxicity drug structure gel permeation chromatography glycosidic linkage Herpes simplex virus Herpes simplex virus 1 Herpes simplex virus 2 macromolecule molecular weight nonhuman proton nuclear magnetic resonance Scinaia hatei seaweed solvent extraction Soxhlet extraction structure activity relation sulfation virion virus inactivation Algae, Red Animals Antiviral Agents Cercopithecus aethiops Chromatography, Gel Glycosides Herpesvirus 1, Human Herpesvirus 2, Human Magnetic Resonance Spectroscopy Molecular Weight Sulfur Vero Cells Xylans Liagoraceae Rhodophyta Scinaia Simplexvirus Pujol, Carlos Alberto Damonte, Elsa Beatriz Xylans from Scinaia hatei: Structural features, sulfation and anti-HSV activity |
topic_facet |
Antiviral activity Herpes simplex virus Liagoraceae Scinaia hatei Sulfation Xylan acetone antivirus agent petroleum ether polysaccharide sulfate xylan animal cell antiviral activity article chemical bond controlled study drug cytotoxicity drug structure gel permeation chromatography glycosidic linkage Herpes simplex virus Herpes simplex virus 1 Herpes simplex virus 2 macromolecule molecular weight nonhuman proton nuclear magnetic resonance Scinaia hatei seaweed solvent extraction Soxhlet extraction structure activity relation sulfation virion virus inactivation Algae, Red Animals Antiviral Agents Cercopithecus aethiops Chromatography, Gel Glycosides Herpesvirus 1, Human Herpesvirus 2, Human Magnetic Resonance Spectroscopy Molecular Weight Sulfur Vero Cells Xylans Liagoraceae Rhodophyta Scinaia Simplexvirus |
description |
Natural compounds offer interesting pharmacological perspectives for antiviral drug development with regard to broad-spectrum antiviral properties and novel modes of action. In this study, we have analyzed alkali-extracted xylan of Scinaia hatei. Alkali extraction of this red alga yielded a xylan shown to have a molecular mass of 120kDa and a linear structure of (1→4)-linked β-d-xylopyranosyl residues. Derivatives (S1, S2, S3 and S4) generated by chemical sulfation from this macromolecule had degree of sulfation between 0.93 and 1.95, and contained strong anti-HSV activity with inhibitory concentration 50% (IC50) from 0.22 to 1.37μg/ml. Furthermore, they had no direct inactivating effect on virions in a virucidal assay. Sulfate groups account for their in vitro antiviral activity. Interestingly, sulfated xylans already exerted anti-HSV activity when only pre-incubated with the cultured cells prior to infection, thus pointing to a main inhibitory effect on viral entry. © 2009 Elsevier B.V. |
author |
Pujol, Carlos Alberto Damonte, Elsa Beatriz |
author_facet |
Pujol, Carlos Alberto Damonte, Elsa Beatriz |
author_sort |
Pujol, Carlos Alberto |
title |
Xylans from Scinaia hatei: Structural features, sulfation and anti-HSV activity |
title_short |
Xylans from Scinaia hatei: Structural features, sulfation and anti-HSV activity |
title_full |
Xylans from Scinaia hatei: Structural features, sulfation and anti-HSV activity |
title_fullStr |
Xylans from Scinaia hatei: Structural features, sulfation and anti-HSV activity |
title_full_unstemmed |
Xylans from Scinaia hatei: Structural features, sulfation and anti-HSV activity |
title_sort |
xylans from scinaia hatei: structural features, sulfation and anti-hsv activity |
publishDate |
2010 |
url |
https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_01418130_v46_n2_p173_Mandal http://hdl.handle.net/20.500.12110/paper_01418130_v46_n2_p173_Mandal |
work_keys_str_mv |
AT pujolcarlosalberto xylansfromscinaiahateistructuralfeaturessulfationandantihsvactivity AT damonteelsabeatriz xylansfromscinaiahateistructuralfeaturessulfationandantihsvactivity |
_version_ |
1768545043382009856 |