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 |
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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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•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.</description><identifier>ISSN: 0144-8617</identifier><identifier>EISSN: 1879-1344</identifier><identifier>DOI: 10.1016/j.carbpol.2021.118510</identifier><identifier>PMID: 34560939</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>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</subject><ispartof>Carbohydrate polymers, 2021-12, Vol.273, p.118510-118510, Article 118510</ispartof><rights>2021 Elsevier Ltd</rights><rights>Copyright © 2021 Elsevier Ltd. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c365t-44d47913759f8ec7444572ff83f15746d1fe8306e10aae077270abce26dab7b23</citedby><cites>FETCH-LOGICAL-c365t-44d47913759f8ec7444572ff83f15746d1fe8306e10aae077270abce26dab7b23</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.carbpol.2021.118510$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,778,782,3539,27907,27908,45978</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34560939$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wang, Sanying</creatorcontrib><creatorcontrib>Xu, Xiaogang</creatorcontrib><creatorcontrib>Sun, Chuan</creatorcontrib><creatorcontrib>Zhang, Jing</creatorcontrib><creatorcontrib>He, Xinyue</creatorcontrib><creatorcontrib>Zhang, Zhongshan</creatorcontrib><creatorcontrib>Huang, Hong</creatorcontrib><creatorcontrib>Yan, Jing</creatorcontrib><creatorcontrib>Jin, Weihua</creatorcontrib><creatorcontrib>Mao, Genxiang</creatorcontrib><title>Sulphated glucuronomannan tetramer and hexamer from Sargassum thunbergii exhibit anti-human cytomegalovirus activity by blocking viral entry</title><title>Carbohydrate polymers</title><addtitle>Carbohydr Polym</addtitle><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.</description><subject>Antiviral Agents - pharmacology</subject><subject>Cell Line</subject><subject>Cell Survival - drug effects</subject><subject>Cytomegalovirus - drug effects</subject><subject>Cytomegalovirus Infections - virology</subject><subject>Glucuronates - chemistry</subject><subject>Glucuronates - pharmacology</subject><subject>Human cytomegalovirus</subject><subject>Humans</subject><subject>Mannose - analogs & derivatives</subject><subject>Mannose - chemistry</subject><subject>Mannose - pharmacology</subject><subject>Sargassum - chemistry</subject><subject>Sargassum thunbergii</subject><subject>Sulfates - chemistry</subject><subject>Sulphated glucuronomannan</subject><subject>Viral entry</subject><subject>Virus Internalization - drug effects</subject><subject>Virus Replication - drug effects</subject><issn>0144-8617</issn><issn>1879-1344</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkc1u1DAQxy1ERZfCI4B85JLFjh07OSFUlQ-pUg8tZ8txJokXx178seq-Aw_dlF24MhppRprfzGjmj9A7SraUUPFxtzU69vvgtjWp6ZbStqHkBdrQVnYVZZy_RBtCOa9aQeUlep3SjqwmKHmFLhlvBOlYt0G_74vbzzrDgCdXTInBh0V7rz3OkKNeIGLtBzzD4598jGHB9zpOOqWy4DwX30OcrMXwONve5pXOtprLOgSbYw4LTNqFg40lYW2yPdh8xP3qLpif1k94LWmHwed4fIMuRu0SvD3HK_Tjy83D9bfq9u7r9-vPt5VhoskV5wOXHWWy6cYWjOScN7Iex5aNtJFcDHSElhEBlGgNRMpaEt0bqMWge9nX7Ap9OM3dx_CrQMpqscmAc9pDKEnVjRSiEYzJFW1OqIkhpQij2ke76HhUlKhnIdROnYVQz0KokxBr3_vzitIvMPzr-vv5Ffh0AmA99GAhqmQseAODjWCyGoL9z4onfUmgLA</recordid><startdate>20211201</startdate><enddate>20211201</enddate><creator>Wang, Sanying</creator><creator>Xu, Xiaogang</creator><creator>Sun, Chuan</creator><creator>Zhang, Jing</creator><creator>He, Xinyue</creator><creator>Zhang, Zhongshan</creator><creator>Huang, Hong</creator><creator>Yan, Jing</creator><creator>Jin, Weihua</creator><creator>Mao, Genxiang</creator><general>Elsevier Ltd</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20211201</creationdate><title>Sulphated glucuronomannan tetramer and hexamer from Sargassum thunbergii exhibit anti-human cytomegalovirus activity by blocking viral entry</title><author>Wang, Sanying ; Xu, Xiaogang ; Sun, Chuan ; Zhang, Jing ; He, Xinyue ; Zhang, Zhongshan ; Huang, Hong ; Yan, Jing ; Jin, Weihua ; Mao, Genxiang</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c365t-44d47913759f8ec7444572ff83f15746d1fe8306e10aae077270abce26dab7b23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Antiviral Agents - pharmacology</topic><topic>Cell Line</topic><topic>Cell Survival - drug effects</topic><topic>Cytomegalovirus - drug effects</topic><topic>Cytomegalovirus Infections - virology</topic><topic>Glucuronates - chemistry</topic><topic>Glucuronates - pharmacology</topic><topic>Human cytomegalovirus</topic><topic>Humans</topic><topic>Mannose - analogs & derivatives</topic><topic>Mannose - chemistry</topic><topic>Mannose - pharmacology</topic><topic>Sargassum - chemistry</topic><topic>Sargassum thunbergii</topic><topic>Sulfates - chemistry</topic><topic>Sulphated glucuronomannan</topic><topic>Viral entry</topic><topic>Virus Internalization - drug effects</topic><topic>Virus Replication - drug effects</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wang, Sanying</creatorcontrib><creatorcontrib>Xu, Xiaogang</creatorcontrib><creatorcontrib>Sun, Chuan</creatorcontrib><creatorcontrib>Zhang, Jing</creatorcontrib><creatorcontrib>He, Xinyue</creatorcontrib><creatorcontrib>Zhang, Zhongshan</creatorcontrib><creatorcontrib>Huang, Hong</creatorcontrib><creatorcontrib>Yan, Jing</creatorcontrib><creatorcontrib>Jin, Weihua</creatorcontrib><creatorcontrib>Mao, Genxiang</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Carbohydrate polymers</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wang, Sanying</au><au>Xu, Xiaogang</au><au>Sun, Chuan</au><au>Zhang, Jing</au><au>He, Xinyue</au><au>Zhang, Zhongshan</au><au>Huang, Hong</au><au>Yan, Jing</au><au>Jin, Weihua</au><au>Mao, Genxiang</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Sulphated glucuronomannan tetramer and hexamer from Sargassum thunbergii exhibit anti-human cytomegalovirus activity by blocking viral entry</atitle><jtitle>Carbohydrate polymers</jtitle><addtitle>Carbohydr Polym</addtitle><date>2021-12-01</date><risdate>2021</risdate><volume>273</volume><spage>118510</spage><epage>118510</epage><pages>118510-118510</pages><artnum>118510</artnum><issn>0144-8617</issn><eissn>1879-1344</eissn><abstract>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.</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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