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Structure and antiviral activity of a pectic polysaccharide from the root of Sanguisorba officinalis against enterovirus 71 in vitro/vivo
  • Kim, Minyeong ;
  • Kim, Seong Ryeol ;
  • Park, Jiye ;
  • Mun, Seo Hyeon ;
  • Kwak, Myounghai ;
  • Ko, Hyun Jeong ;
  • Baek, Seung Hoon
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Publication Year
2022-04-01
Publisher
Elsevier Ltd
Citation
Carbohydrate Polymers, Vol.281
Keyword
Antiviral activityArabinogalactanEnterovirus 71GlucanPectinSanguisorba officinalis
Mesh Keyword
Antiviral activitiesArabinogalactanEnterovirus 71GlucansIn-vitroPectic polysaccharidesPectinSanguisorba officinaliStructure activityViral diseaseAnimalsAntiviral AgentsChlorocebus aethiopsEnterovirusEnterovirus A, HumanMicePolysaccharidesSanguisorbaVero CellsVirus Replication
All Science Classification Codes (ASJC)
Organic ChemistryPolymers and PlasticsMaterials Chemistry
Abstract
The increasing prevalence and pandemic risk of viral diseases warrant the development of safe and effective treatments. In this study, we aimed to elucidate the structure and anti-enterovirus 71 (EV71) effects of polysaccharides isolated from the roots of Sanguisorba officinalis (SO), traditionally used for infectious diseases. The purified polysaccharide (S-a3) was a homogenous macromolecule (260.4 kDa) with a concave and porous surface. Linkage and NMR analyses confirmed that S-a3 is a polysaccharide interlinked with homogalacturonan, rhamnogalacturonan-I, 1,4-α-glucan, and arabinogalactan. S-a3 significantly inhibited cell death and viral gene expression in EV71-infected Vero cells, and alleviated EV71-induced body weight loss, death, and paralysis in the hSCARB2-transgenic mouse model. The effective dose of S-a3 was non-toxic to cells and mice. The antiviral mechanism of S-a3 was associated with the disruption of EV71 attachment to host cells. Our findings demonstrate that polysaccharides from SO can be a safe and effective treatment for EV71 infection.
ISSN
0144-8617
Language
eng
URI
https://dspace.ajou.ac.kr/dev/handle/2018.oak/32470
DOI
https://doi.org/10.1016/j.carbpol.2021.119057
Fulltext

Type
Article
Funding
Confocal imaging was performed at the Central Laboratory of the Kangwon National University. This work was supported by the National Research Foundation of Korea (NRF) grant funded by the Korean government (MSIT) ( 2020R1A2B5B02001552 ; 2021R1A2C2013628 ).Confocal imaging was performed at the Central Laboratory of the Kangwon National University. This work was supported by the National Research Foundation of Korea (NRF) grant funded by the Korean government (MSIT) (2020R1A2B5B02001552; 2021R1A2C2013628).
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