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Title 

Both α2,3- and α2,6-linked sialic acids on O-linked glycoproteins act as functional receptors for porcine sapovirus

Authors 

D S KimM HosmilloM M AlfajaroJ Y KimJ G ParkK Y SonE H RyuF SorgeloosKwon Hyung JunSu-Jin ParkWoo Song LeeD ChoJ KwonJ S ChoiM I KangI GoodfellowK O Cho

Publisher 

Public Library of Science

Issue Date 

2014

Citation 

Plos Pathogens, vol. 10, no. 6, pp. 1004172-1004172

Abstract 

Sapovirus, a member of the Caliciviridae family, is an important cause of acute gastroenteritis in humans and pigs. Currently, the porcine sapovirus (PSaV) Cowden strain remains the only cultivable member of the Sapovirus genus. While some caliciviruses are known to utilize carbohydrate receptors for entry and infection, a functional receptor for sapovirus is unknown. To characterize the functional receptor of the Cowden strain of PSaV, we undertook a comprehensive series of protein-ligand biochemical assays in mock and PSaV-infected cell culture and/or piglet intestinal tissue sections. PSaV revealed neither hemagglutination activity with red blood cells from any species nor binding activity to synthetic histo-blood group antigens, indicating that PSaV does not use histo-blood group antigens as receptors. Attachment and infection of PSaV were markedly blocked by sialic acid and Vibrio cholerae neuraminidase (NA), suggesting a role for α2,3-linked, α2,6-linked or α2,8-linked sialic acid in virus attachment. However, viral attachment and infection were only partially inhibited by treatment of cells with sialidase S (SS) or Maackia amurensis lectin (MAL), both specific for α2,3-linked sialic acid, or Sambucus nigra lectin (SNL), specific for α2,6-linked sialic acid. These results indicated that PSaV recognizes both α2,3- and α2,6-linked sialic acids for viral attachment and infection. Treatment of cells with proteases or with benzyl 4-O-β-D-galactopyranosyl-β-D-glucopyranoside (benzylGalNAc), which inhibits O-linked glycosylation, also reduced virus binding and infection, whereas inhibition of glycolipd synthesis or N-linked glycosylation had no such effect on virus binding or infection. These data suggest PSaV binds to cellular receptors that consist of α2,3- and α2,6-linked sialic acids on glycoproteins attached via O-linked glycosylation.

ISSN 

1553-7366

Link 

http://dx.doi.org/10.1371/journal.ppat.1004172

Appears in Collections

1. Journal Articles > Journal Articles

Registered Date

2019-05-02


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