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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Autores principales: Pujol, Carlos Alberto, Damonte, Elsa Beatriz
Publicado: 2010
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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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spelling 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
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