Sialylated glycans as receptor and inhibitor of enterovirus 71 infection to DLD-1 intestinal cells

Background: Many viruses recognize specific sugar residues, particularly sulfated or sialylated glycans, as the infection receptors. A change of sialic acid (2-6)-linked galactose (SA-α2,6Gal) to SA-α2,3Gal determines the receptor for avian flu infection. The receptor for enterovirus 71 (EV71) infec...

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Main Authors: Betsy Yang, Hau Chuang, Kuender D Yang
Other Authors: The Pennsylvania State University CiteSeerX Archives
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Language:English
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Online Access:http://citeseerx.ist.psu.edu/viewdoc/summary?doi=10.1.1.628.3580
http://www.virologyj.com/content/pdf/1743-422X-6-141.pdf
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spelling ftciteseerx:oai:CiteSeerX.psu:10.1.1.628.3580 2023-05-15T15:34:32+02:00 Sialylated glycans as receptor and inhibitor of enterovirus 71 infection to DLD-1 intestinal cells Betsy Yang Hau Chuang Kuender D Yang The Pennsylvania State University CiteSeerX Archives application/pdf http://citeseerx.ist.psu.edu/viewdoc/summary?doi=10.1.1.628.3580 http://www.virologyj.com/content/pdf/1743-422X-6-141.pdf en eng http://citeseerx.ist.psu.edu/viewdoc/summary?doi=10.1.1.628.3580 http://www.virologyj.com/content/pdf/1743-422X-6-141.pdf Metadata may be used without restrictions as long as the oai identifier remains attached to it. http://www.virologyj.com/content/pdf/1743-422X-6-141.pdf text ftciteseerx 2016-01-08T15:19:41Z Background: Many viruses recognize specific sugar residues, particularly sulfated or sialylated glycans, as the infection receptors. A change of sialic acid (2-6)-linked galactose (SA-α2,6Gal) to SA-α2,3Gal determines the receptor for avian flu infection. The receptor for enterovirus 71 (EV71) infection that frequently causes fatal encephalitis in Asian children remains unclear. Currently, there is no effective vaccine or anti-virus agent for EV71 infection. Using DLD-1 intestinal cells, this study investigated whether SA-linked glycan on DLD-1 intestinal cells was a receptor for EV71, and whether natural SA-linked sugars from human milk could block EV71 infection. Results: EV71 specifically infected DLD-1 intestinal cells but not K562 myeloid cells. Depletion of O-linked glycans or glycolipids, but not N-linked glycans, significantly decreased EV71 infection of DLD-1 cells. Pretreatment of DLD-1 cells with sialidase (10 mU, 2 hours) significantly reduced 20-fold EV71 replication (p < 0.01). Taken together, these results suggest that SA-linked O-glycans and glycolipids, but not N-glycans, on DLD-1 cells were responsible for EV71 infection. Purified SA-α2,3Gal and SA-α2,6Gal from human milk significantly inhibited EV71 infection of DLD-1 cells, indicating terminal SA-linked glycans could be receptors and inhibitors of EV71 infection. Conclusion: This is the first in the literature to demonstrate that EV71 uses SA-linked glycans as receptors for infection, and natural SA-linked glycans from human milk can protect intestinal cells from EV71 infection. Further studies will test how a SA-containing glycan can prevent EV71 in the future. Text Avian flu Unknown
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description Background: Many viruses recognize specific sugar residues, particularly sulfated or sialylated glycans, as the infection receptors. A change of sialic acid (2-6)-linked galactose (SA-α2,6Gal) to SA-α2,3Gal determines the receptor for avian flu infection. The receptor for enterovirus 71 (EV71) infection that frequently causes fatal encephalitis in Asian children remains unclear. Currently, there is no effective vaccine or anti-virus agent for EV71 infection. Using DLD-1 intestinal cells, this study investigated whether SA-linked glycan on DLD-1 intestinal cells was a receptor for EV71, and whether natural SA-linked sugars from human milk could block EV71 infection. Results: EV71 specifically infected DLD-1 intestinal cells but not K562 myeloid cells. Depletion of O-linked glycans or glycolipids, but not N-linked glycans, significantly decreased EV71 infection of DLD-1 cells. Pretreatment of DLD-1 cells with sialidase (10 mU, 2 hours) significantly reduced 20-fold EV71 replication (p < 0.01). Taken together, these results suggest that SA-linked O-glycans and glycolipids, but not N-glycans, on DLD-1 cells were responsible for EV71 infection. Purified SA-α2,3Gal and SA-α2,6Gal from human milk significantly inhibited EV71 infection of DLD-1 cells, indicating terminal SA-linked glycans could be receptors and inhibitors of EV71 infection. Conclusion: This is the first in the literature to demonstrate that EV71 uses SA-linked glycans as receptors for infection, and natural SA-linked glycans from human milk can protect intestinal cells from EV71 infection. Further studies will test how a SA-containing glycan can prevent EV71 in the future.
author2 The Pennsylvania State University CiteSeerX Archives
format Text
author Betsy Yang
Hau Chuang
Kuender D Yang
spellingShingle Betsy Yang
Hau Chuang
Kuender D Yang
Sialylated glycans as receptor and inhibitor of enterovirus 71 infection to DLD-1 intestinal cells
author_facet Betsy Yang
Hau Chuang
Kuender D Yang
author_sort Betsy Yang
title Sialylated glycans as receptor and inhibitor of enterovirus 71 infection to DLD-1 intestinal cells
title_short Sialylated glycans as receptor and inhibitor of enterovirus 71 infection to DLD-1 intestinal cells
title_full Sialylated glycans as receptor and inhibitor of enterovirus 71 infection to DLD-1 intestinal cells
title_fullStr Sialylated glycans as receptor and inhibitor of enterovirus 71 infection to DLD-1 intestinal cells
title_full_unstemmed Sialylated glycans as receptor and inhibitor of enterovirus 71 infection to DLD-1 intestinal cells
title_sort sialylated glycans as receptor and inhibitor of enterovirus 71 infection to dld-1 intestinal cells
url http://citeseerx.ist.psu.edu/viewdoc/summary?doi=10.1.1.628.3580
http://www.virologyj.com/content/pdf/1743-422X-6-141.pdf
genre Avian flu
genre_facet Avian flu
op_source http://www.virologyj.com/content/pdf/1743-422X-6-141.pdf
op_relation http://citeseerx.ist.psu.edu/viewdoc/summary?doi=10.1.1.628.3580
http://www.virologyj.com/content/pdf/1743-422X-6-141.pdf
op_rights Metadata may be used without restrictions as long as the oai identifier remains attached to it.
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