Sulphated glucuronomannan tetramer and hexamer from Sargassum thunbergii exhibit anti-human cytomegalovirus activity by blocking viral entry

Human cytomegalovirus (HCMV) remains a major public health burden worldwide. The anti-HCMV activity of glucuronomannan oligosaccharides (Gs) and sulphated glucuronomannan oligosaccharides (SGs) was investigated. Among these Gs and SGs, G4S1 and G6S1 (higher sulphated glucuronomannan tetramer and hex...

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Veröffentlicht in:Carbohydrate polymers 2021-12, Vol.273, p.118510-118510, Article 118510
Hauptverfasser: Wang, Sanying, Xu, Xiaogang, Sun, Chuan, Zhang, Jing, He, Xinyue, Zhang, Zhongshan, Huang, Hong, Yan, Jing, Jin, Weihua, Mao, Genxiang
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container_end_page 118510
container_issue
container_start_page 118510
container_title Carbohydrate polymers
container_volume 273
creator Wang, Sanying
Xu, Xiaogang
Sun, Chuan
Zhang, Jing
He, Xinyue
Zhang, Zhongshan
Huang, Hong
Yan, Jing
Jin, Weihua
Mao, Genxiang
description Human cytomegalovirus (HCMV) remains a major public health burden worldwide. The anti-HCMV activity of glucuronomannan oligosaccharides (Gs) and sulphated glucuronomannan oligosaccharides (SGs) was investigated. Among these Gs and SGs, G4S1 and G6S1 (higher sulphated glucuronomannan tetramer and hexamer) showed satisfactory anti-HCMV activity starting at 50 μg/mL and 10 μg/mL, respectively. The results of the morphology, western blotting, qPCR and TCID50 assay showed that they prevented lytic cytopathic changes, inhibited the expression of IE1/2 and UL44, and reduced the UL123 copy number and virus titre significantly. It was interesting to note that degree of sulphation and polymerization was more important for anti-HCMV activity. Moreover, the anti-HCMV activities of G4S1 and G6S1 were stable when stored at 4 °C, −20 °C, and −80 °C for at least three months and mainly occurred in the early stage of HCMV infection through the negative charge of the sulphate groups and the interaction between SGs and the host cells. •Sargassum thunbergii Gs and sulphated Gs showed anti-HCMV activity.•Higher sulphated Gs prevented lytic cytopathic changes in infected cells.•Higher sulphated Gs inhibited IE1/2 and UL44 expression and reduced virus titre.•Anti-HCMV activities were stable and occurred in the early stage of infection.•Interactions with virus particles and host cells responsible for anti-HCMV activity.
doi_str_mv 10.1016/j.carbpol.2021.118510
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The anti-HCMV activity of glucuronomannan oligosaccharides (Gs) and sulphated glucuronomannan oligosaccharides (SGs) was investigated. Among these Gs and SGs, G4S1 and G6S1 (higher sulphated glucuronomannan tetramer and hexamer) showed satisfactory anti-HCMV activity starting at 50 μg/mL and 10 μg/mL, respectively. The results of the morphology, western blotting, qPCR and TCID50 assay showed that they prevented lytic cytopathic changes, inhibited the expression of IE1/2 and UL44, and reduced the UL123 copy number and virus titre significantly. It was interesting to note that degree of sulphation and polymerization was more important for anti-HCMV activity. 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The anti-HCMV activity of glucuronomannan oligosaccharides (Gs) and sulphated glucuronomannan oligosaccharides (SGs) was investigated. Among these Gs and SGs, G4S1 and G6S1 (higher sulphated glucuronomannan tetramer and hexamer) showed satisfactory anti-HCMV activity starting at 50 μg/mL and 10 μg/mL, respectively. The results of the morphology, western blotting, qPCR and TCID50 assay showed that they prevented lytic cytopathic changes, inhibited the expression of IE1/2 and UL44, and reduced the UL123 copy number and virus titre significantly. It was interesting to note that degree of sulphation and polymerization was more important for anti-HCMV activity. Moreover, the anti-HCMV activities of G4S1 and G6S1 were stable when stored at 4 °C, −20 °C, and −80 °C for at least three months and mainly occurred in the early stage of HCMV infection through the negative charge of the sulphate groups and the interaction between SGs and the host cells. •Sargassum thunbergii Gs and sulphated Gs showed anti-HCMV activity.•Higher sulphated Gs prevented lytic cytopathic changes in infected cells.•Higher sulphated Gs inhibited IE1/2 and UL44 expression and reduced virus titre.•Anti-HCMV activities were stable and occurred in the early stage of infection.•Interactions with virus particles and host cells responsible for anti-HCMV activity.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>34560939</pmid><doi>10.1016/j.carbpol.2021.118510</doi><tpages>1</tpages></addata></record>
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subjects Antiviral Agents - pharmacology
Cell Line
Cell Survival - drug effects
Cytomegalovirus - drug effects
Cytomegalovirus Infections - virology
Glucuronates - chemistry
Glucuronates - pharmacology
Human cytomegalovirus
Humans
Mannose - analogs & derivatives
Mannose - chemistry
Mannose - pharmacology
Sargassum - chemistry
Sargassum thunbergii
Sulfates - chemistry
Sulphated glucuronomannan
Viral entry
Virus Internalization - drug effects
Virus Replication - drug effects
title Sulphated glucuronomannan tetramer and hexamer from Sargassum thunbergii exhibit anti-human cytomegalovirus activity by blocking viral entry
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