Structural basis of glycan specificity in neonate-specific bovine-human reassortant rotavirus
Abstract
We report that strain-dependent variation of glycan recognition during initial cell attachment of viruses is a critical determinant of host specificity, tissue-tropism and zoonosis. Rotaviruses (RVs), which cause life-threatening gastroenteritis in infants and children, display significant genotype-dependent variations in glycan recognition resulting from sequence alterations in the VP8* domain of the spike protein VP4. The structural basis of this genotype-dependent glycan specificity, particularly in human RVs, remains poorly understood. Here, from crystallographic studies, we show how genotypic variations configure a novel binding site in the VP8* of a neonate-specific bovine-human reassortant to uniquely recognize either type I or type II precursor glycans, and to restrict type II glycan binding in the bovine counterpart. In conclusion, such a distinct glycan-binding site that allows differential recognition of the precursor glycans, which are developmentally regulated in the neonate gut and abundant in bovine and human milk provides a basis for age-restricted tropism and zoonotic transmission of G10P[11] rotaviruses.
- Authors:
-
- Baylor College of Medicine, Houston, TX (United States). Verna and Marrs McLean Department of Biochemistry and Molecular Biology
- Baylor College of Medicine, Houston, TX (United States). Department of Molecular Virology and Microbiology
- Lawrence Berkeley National Lab. (LBNL), Berkeley, CA (United States)
- Emory Univ.School of Medicine, Atlanta, GA (United States)
- Baylor College of Medicine, Houston, TX (United States). Verna and Marrs McLean Department of Biochemistry and Molecular Biology; Baylor College of Medicine, Houston, TX (United States). Department of Molecular Virology and Microbiology
- Publication Date:
- Research Org.:
- Lawrence Berkeley National Laboratory (LBNL), Berkeley, CA (United States)
- Sponsoring Org.:
- USDOE Office of Science (SC), Basic Energy Sciences (BES)
- OSTI Identifier:
- 1256040
- Grant/Contract Number:
- AC02- 05CH11231
- Resource Type:
- Accepted Manuscript
- Journal Name:
- Nature Communications
- Additional Journal Information:
- Journal Volume: 6; Journal ID: ISSN 2041-1723
- Publisher:
- Nature Publishing Group
- Country of Publication:
- United States
- Language:
- English
- Subject:
- 59 BASIC BIOLOGICAL SCIENCES
Citation Formats
Hu, Liya, Ramani, Sasirekha, Czako, Rita, Sankaran, Banumathi, Yu, Ying, Smith, David F., Cummings, Richard D., Estes, Mary K., and Venkataram Prasad, B. V. Structural basis of glycan specificity in neonate-specific bovine-human reassortant rotavirus. United States: N. p., 2015.
Web. doi:10.1038/ncomms9346.
Hu, Liya, Ramani, Sasirekha, Czako, Rita, Sankaran, Banumathi, Yu, Ying, Smith, David F., Cummings, Richard D., Estes, Mary K., & Venkataram Prasad, B. V. Structural basis of glycan specificity in neonate-specific bovine-human reassortant rotavirus. United States. https://doi.org/10.1038/ncomms9346
Hu, Liya, Ramani, Sasirekha, Czako, Rita, Sankaran, Banumathi, Yu, Ying, Smith, David F., Cummings, Richard D., Estes, Mary K., and Venkataram Prasad, B. V. Wed .
"Structural basis of glycan specificity in neonate-specific bovine-human reassortant rotavirus". United States. https://doi.org/10.1038/ncomms9346. https://www.osti.gov/servlets/purl/1256040.
@article{osti_1256040,
title = {Structural basis of glycan specificity in neonate-specific bovine-human reassortant rotavirus},
author = {Hu, Liya and Ramani, Sasirekha and Czako, Rita and Sankaran, Banumathi and Yu, Ying and Smith, David F. and Cummings, Richard D. and Estes, Mary K. and Venkataram Prasad, B. V.},
abstractNote = {We report that strain-dependent variation of glycan recognition during initial cell attachment of viruses is a critical determinant of host specificity, tissue-tropism and zoonosis. Rotaviruses (RVs), which cause life-threatening gastroenteritis in infants and children, display significant genotype-dependent variations in glycan recognition resulting from sequence alterations in the VP8* domain of the spike protein VP4. The structural basis of this genotype-dependent glycan specificity, particularly in human RVs, remains poorly understood. Here, from crystallographic studies, we show how genotypic variations configure a novel binding site in the VP8* of a neonate-specific bovine-human reassortant to uniquely recognize either type I or type II precursor glycans, and to restrict type II glycan binding in the bovine counterpart. In conclusion, such a distinct glycan-binding site that allows differential recognition of the precursor glycans, which are developmentally regulated in the neonate gut and abundant in bovine and human milk provides a basis for age-restricted tropism and zoonotic transmission of G10P[11] rotaviruses.},
doi = {10.1038/ncomms9346},
journal = {Nature Communications},
number = ,
volume = 6,
place = {United States},
year = {Wed Sep 30 00:00:00 EDT 2015},
month = {Wed Sep 30 00:00:00 EDT 2015}
}
Web of Science
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