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Enteric Species F Human Adenoviruses use Laminin-Binding Integrins as Co-Receptors for Infection of Ht-29 Cells

The enteric species F human adenovirus types 40 and 41 (HAdV-40 and -41) are the third most common cause of infantile gastroenteritis in the world. Knowledge about HAdV-40 and -41 cellular infection is assumed to be fundamentally different from that of other HAdVs since HAdV-40 and -41 penton bases...

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Autores principales: Rajan, Anandi, Persson, B. David, Frängsmyr, Lars, Olofsson, Annelie, Sandblad, Linda, Heino, Jyrki, Takada, Yoshikazu, Mould, A. Paul, Schnapp, Lynn M., Gall, Jason, Arnberg, Niklas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6030200/
https://www.ncbi.nlm.nih.gov/pubmed/29968781
http://dx.doi.org/10.1038/s41598-018-28255-7
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author Rajan, Anandi
Persson, B. David
Frängsmyr, Lars
Olofsson, Annelie
Sandblad, Linda
Heino, Jyrki
Takada, Yoshikazu
Mould, A. Paul
Schnapp, Lynn M.
Gall, Jason
Arnberg, Niklas
author_facet Rajan, Anandi
Persson, B. David
Frängsmyr, Lars
Olofsson, Annelie
Sandblad, Linda
Heino, Jyrki
Takada, Yoshikazu
Mould, A. Paul
Schnapp, Lynn M.
Gall, Jason
Arnberg, Niklas
author_sort Rajan, Anandi
collection PubMed
description The enteric species F human adenovirus types 40 and 41 (HAdV-40 and -41) are the third most common cause of infantile gastroenteritis in the world. Knowledge about HAdV-40 and -41 cellular infection is assumed to be fundamentally different from that of other HAdVs since HAdV-40 and -41 penton bases lack the αV-integrin-interacting RGD motif. This motif is used by other HAdVs mainly for internalization and endosomal escape. We hypothesised that the penton bases of HAdV-40 and -41 interact with integrins independently of the RGD motif. HAdV-41 transduction of a library of rodent cells expressing specific human integrin subunits pointed to the use of laminin-binding α2-, α3- and α6-containing integrins as well as other integrins as candidate co-receptors. Specific laminins prevented internalisation and infection, and recombinant, soluble HAdV-41 penton base proteins prevented infection of human intestinal HT-29 cells. Surface plasmon resonance analysis demonstrated that HAdV-40 and -41 penton base proteins bind to α6-containing integrins with an affinity similar to that of previously characterised penton base:integrin interactions. With these results, we propose that laminin-binding integrins are co-receptors for HAdV-40 and -41.
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spelling pubmed-60302002018-07-11 Enteric Species F Human Adenoviruses use Laminin-Binding Integrins as Co-Receptors for Infection of Ht-29 Cells Rajan, Anandi Persson, B. David Frängsmyr, Lars Olofsson, Annelie Sandblad, Linda Heino, Jyrki Takada, Yoshikazu Mould, A. Paul Schnapp, Lynn M. Gall, Jason Arnberg, Niklas Sci Rep Article The enteric species F human adenovirus types 40 and 41 (HAdV-40 and -41) are the third most common cause of infantile gastroenteritis in the world. Knowledge about HAdV-40 and -41 cellular infection is assumed to be fundamentally different from that of other HAdVs since HAdV-40 and -41 penton bases lack the αV-integrin-interacting RGD motif. This motif is used by other HAdVs mainly for internalization and endosomal escape. We hypothesised that the penton bases of HAdV-40 and -41 interact with integrins independently of the RGD motif. HAdV-41 transduction of a library of rodent cells expressing specific human integrin subunits pointed to the use of laminin-binding α2-, α3- and α6-containing integrins as well as other integrins as candidate co-receptors. Specific laminins prevented internalisation and infection, and recombinant, soluble HAdV-41 penton base proteins prevented infection of human intestinal HT-29 cells. Surface plasmon resonance analysis demonstrated that HAdV-40 and -41 penton base proteins bind to α6-containing integrins with an affinity similar to that of previously characterised penton base:integrin interactions. With these results, we propose that laminin-binding integrins are co-receptors for HAdV-40 and -41. Nature Publishing Group UK 2018-07-03 /pmc/articles/PMC6030200/ /pubmed/29968781 http://dx.doi.org/10.1038/s41598-018-28255-7 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Rajan, Anandi
Persson, B. David
Frängsmyr, Lars
Olofsson, Annelie
Sandblad, Linda
Heino, Jyrki
Takada, Yoshikazu
Mould, A. Paul
Schnapp, Lynn M.
Gall, Jason
Arnberg, Niklas
Enteric Species F Human Adenoviruses use Laminin-Binding Integrins as Co-Receptors for Infection of Ht-29 Cells
title Enteric Species F Human Adenoviruses use Laminin-Binding Integrins as Co-Receptors for Infection of Ht-29 Cells
title_full Enteric Species F Human Adenoviruses use Laminin-Binding Integrins as Co-Receptors for Infection of Ht-29 Cells
title_fullStr Enteric Species F Human Adenoviruses use Laminin-Binding Integrins as Co-Receptors for Infection of Ht-29 Cells
title_full_unstemmed Enteric Species F Human Adenoviruses use Laminin-Binding Integrins as Co-Receptors for Infection of Ht-29 Cells
title_short Enteric Species F Human Adenoviruses use Laminin-Binding Integrins as Co-Receptors for Infection of Ht-29 Cells
title_sort enteric species f human adenoviruses use laminin-binding integrins as co-receptors for infection of ht-29 cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6030200/
https://www.ncbi.nlm.nih.gov/pubmed/29968781
http://dx.doi.org/10.1038/s41598-018-28255-7
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