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Structural and functional analysis of the S proteins of two human coronavirus OC43 strains adapted to growth in different cells

The receptor-binding activity of strain CU (grown in MDCK I cells) and of strain VA (adapted to Vero cells) of human coronavirus OC43 was analyzed and compared with the binding activity of bovine coronavirus (BCV) and of the OC43 strain provided by the American Type Culture Collection (AT). Results...

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Autores principales: Künkel, F., Herrler, G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer-Verlag 1996
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7086633/
https://www.ncbi.nlm.nih.gov/pubmed/8712929
http://dx.doi.org/10.1007/BF01718615
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author Künkel, F.
Herrler, G.
author_facet Künkel, F.
Herrler, G.
author_sort Künkel, F.
collection PubMed
description The receptor-binding activity of strain CU (grown in MDCK I cells) and of strain VA (adapted to Vero cells) of human coronavirus OC43 was analyzed and compared with the binding activity of bovine coronavirus (BCV) and of the OC43 strain provided by the American Type Culture Collection (AT). Results obtained with resialylated erythrocytes indicated that the ability of the viruses to recognize 9-O-acetylated sialic acid in an α2,6-linkage decreased in the following order: AT>CU>BCV>VA. Only minor differences were observed with respect to the α2,3-linkage. The amino acid sequence of the S protein of strain CU and VA was derived from the nucleotide sequence of the cloned gene. Strain VA differed from strain CU in 34 positions, 18 in the S1 and 16 in the S2 subunit.
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spelling pubmed-70866332020-03-23 Structural and functional analysis of the S proteins of two human coronavirus OC43 strains adapted to growth in different cells Künkel, F. Herrler, G. Arch Virol Brief Report The receptor-binding activity of strain CU (grown in MDCK I cells) and of strain VA (adapted to Vero cells) of human coronavirus OC43 was analyzed and compared with the binding activity of bovine coronavirus (BCV) and of the OC43 strain provided by the American Type Culture Collection (AT). Results obtained with resialylated erythrocytes indicated that the ability of the viruses to recognize 9-O-acetylated sialic acid in an α2,6-linkage decreased in the following order: AT>CU>BCV>VA. Only minor differences were observed with respect to the α2,3-linkage. The amino acid sequence of the S protein of strain CU and VA was derived from the nucleotide sequence of the cloned gene. Strain VA differed from strain CU in 34 positions, 18 in the S1 and 16 in the S2 subunit. Springer-Verlag 1996 /pmc/articles/PMC7086633/ /pubmed/8712929 http://dx.doi.org/10.1007/BF01718615 Text en © Springer-Verlag 1996 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.
spellingShingle Brief Report
Künkel, F.
Herrler, G.
Structural and functional analysis of the S proteins of two human coronavirus OC43 strains adapted to growth in different cells
title Structural and functional analysis of the S proteins of two human coronavirus OC43 strains adapted to growth in different cells
title_full Structural and functional analysis of the S proteins of two human coronavirus OC43 strains adapted to growth in different cells
title_fullStr Structural and functional analysis of the S proteins of two human coronavirus OC43 strains adapted to growth in different cells
title_full_unstemmed Structural and functional analysis of the S proteins of two human coronavirus OC43 strains adapted to growth in different cells
title_short Structural and functional analysis of the S proteins of two human coronavirus OC43 strains adapted to growth in different cells
title_sort structural and functional analysis of the s proteins of two human coronavirus oc43 strains adapted to growth in different cells
topic Brief Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7086633/
https://www.ncbi.nlm.nih.gov/pubmed/8712929
http://dx.doi.org/10.1007/BF01718615
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