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Subtypes of tail spike proteins predicts the host range of Ackermannviridae phages

Phages belonging to the Ackermannviridae family encode up to four tail spike proteins (TSPs), each recognizing a specific receptor of their bacterial hosts. Here, we determined the TSPs diversity of 99 Ackermannviridae phages by performing a comprehensive in silico analysis. Based on sequence divers...

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Autores principales: Sørensen, Anders Nørgaard, Woudstra, Cedric, Sørensen, Martine C. Holst, Brøndsted, Lone
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Research Network of Computational and Structural Biotechnology 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8432352/
https://www.ncbi.nlm.nih.gov/pubmed/34527194
http://dx.doi.org/10.1016/j.csbj.2021.08.030
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author Sørensen, Anders Nørgaard
Woudstra, Cedric
Sørensen, Martine C. Holst
Brøndsted, Lone
author_facet Sørensen, Anders Nørgaard
Woudstra, Cedric
Sørensen, Martine C. Holst
Brøndsted, Lone
author_sort Sørensen, Anders Nørgaard
collection PubMed
description Phages belonging to the Ackermannviridae family encode up to four tail spike proteins (TSPs), each recognizing a specific receptor of their bacterial hosts. Here, we determined the TSPs diversity of 99 Ackermannviridae phages by performing a comprehensive in silico analysis. Based on sequence diversity, we assigned all TSPs into distinctive subtypes of TSP1, TSP2, TSP3 and TSP4, and found each TSP subtype to be specifically associated with the genera (Kuttervirus, Agtrevirus, Limestonevirus, Taipeivirus) of the Ackermannviridae family. Further analysis showed that the N-terminal XD1 and XD2 domains in TSP2 and TSP4, hinging the four TSPs together, are preserved. In contrast, the C-terminal receptor binding modules were only conserved within TSP subtypes, except for some Kuttervirus TSP1s and TSP3s that were similar to specific TSP4s. A conserved motif in TSP1, TSP3 and TSP4 of Kuttervirus phages may allow recombination between receptor binding modules, thus altering host recognition. The receptors for numerous uncharacterized phages expressing TSPs in the same subtypes were predicted using previous host range data. To validate our predictions, we experimentally determined the host recognition of three of the four TSPs expressed by kuttervirus S117. We confirmed that S117 TSP1 and TSP2 bind to their predicted host receptors, and identified the receptor for TSP3, which is shared by 51 other Kuttervirus phages. Kuttervirus phages were thus shown encode a vast genetic diversity of potentially exchangeable TSPs influencing host recognition. Overall, our study demonstrates that comprehensive in silico and host range analysis of TSPs can predict host recognition of Ackermannviridae phages.
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spelling pubmed-84323522021-09-14 Subtypes of tail spike proteins predicts the host range of Ackermannviridae phages Sørensen, Anders Nørgaard Woudstra, Cedric Sørensen, Martine C. Holst Brøndsted, Lone Comput Struct Biotechnol J Research Article Phages belonging to the Ackermannviridae family encode up to four tail spike proteins (TSPs), each recognizing a specific receptor of their bacterial hosts. Here, we determined the TSPs diversity of 99 Ackermannviridae phages by performing a comprehensive in silico analysis. Based on sequence diversity, we assigned all TSPs into distinctive subtypes of TSP1, TSP2, TSP3 and TSP4, and found each TSP subtype to be specifically associated with the genera (Kuttervirus, Agtrevirus, Limestonevirus, Taipeivirus) of the Ackermannviridae family. Further analysis showed that the N-terminal XD1 and XD2 domains in TSP2 and TSP4, hinging the four TSPs together, are preserved. In contrast, the C-terminal receptor binding modules were only conserved within TSP subtypes, except for some Kuttervirus TSP1s and TSP3s that were similar to specific TSP4s. A conserved motif in TSP1, TSP3 and TSP4 of Kuttervirus phages may allow recombination between receptor binding modules, thus altering host recognition. The receptors for numerous uncharacterized phages expressing TSPs in the same subtypes were predicted using previous host range data. To validate our predictions, we experimentally determined the host recognition of three of the four TSPs expressed by kuttervirus S117. We confirmed that S117 TSP1 and TSP2 bind to their predicted host receptors, and identified the receptor for TSP3, which is shared by 51 other Kuttervirus phages. Kuttervirus phages were thus shown encode a vast genetic diversity of potentially exchangeable TSPs influencing host recognition. Overall, our study demonstrates that comprehensive in silico and host range analysis of TSPs can predict host recognition of Ackermannviridae phages. Research Network of Computational and Structural Biotechnology 2021-08-21 /pmc/articles/PMC8432352/ /pubmed/34527194 http://dx.doi.org/10.1016/j.csbj.2021.08.030 Text en © 2021 The Authors https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Research Article
Sørensen, Anders Nørgaard
Woudstra, Cedric
Sørensen, Martine C. Holst
Brøndsted, Lone
Subtypes of tail spike proteins predicts the host range of Ackermannviridae phages
title Subtypes of tail spike proteins predicts the host range of Ackermannviridae phages
title_full Subtypes of tail spike proteins predicts the host range of Ackermannviridae phages
title_fullStr Subtypes of tail spike proteins predicts the host range of Ackermannviridae phages
title_full_unstemmed Subtypes of tail spike proteins predicts the host range of Ackermannviridae phages
title_short Subtypes of tail spike proteins predicts the host range of Ackermannviridae phages
title_sort subtypes of tail spike proteins predicts the host range of ackermannviridae phages
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8432352/
https://www.ncbi.nlm.nih.gov/pubmed/34527194
http://dx.doi.org/10.1016/j.csbj.2021.08.030
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