Structure and antiviral activity of a pectic polysaccharide from the root of Sanguisorba officinalis against enterovirus 71 in vitro/vivo

被引:35
作者
Kim, Minyeong [1 ,2 ]
Kim, Seong-Ryeol [3 ]
Park, Jiye [1 ,2 ]
Mun, Seo-Hyeon [3 ]
Kwak, Myounghai [4 ]
Ko, Hyun-Jeong [3 ]
Baek, Seung-Hoon [1 ,2 ]
机构
[1] Ajou Univ, Coll Pharm, 206 Worldcup Ro, Suwon 16499, South Korea
[2] Ajou Univ, Res Inst Pharmaceut Sci & Technol RIPST, Suwon 16499, South Korea
[3] Kangwon Natl Univ, Dept Pharm, 1 Gangwondaehakgil, Chuncheon Si 24341, Gangwon Do, South Korea
[4] Natl Inst Biol Resources, Plant Resources Div, 42 Hwangyeong Ro, Incheon 22689, South Korea
基金
新加坡国家研究基金会;
关键词
Sanguisorba officinalis; Pectin; Glucan; Arabinogalactan; Enterovirus; 71; Antiviral activity; CHEMICAL-CONSTITUENTS; BIOLOGICAL-ACTIVITIES; INFECTION; METHYLATION; RHINOVIRUS; EXTRACTS; INHIBIT;
D O I
10.1016/j.carbpol.2021.119057
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
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-alpha-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.
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页数:11
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