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Diversity patterns of bacteriophages infecting Aggregatibacter and Haemophilus species across clades and niches

Aggregatibacter and Haemophilus species are relevant human commensals and opportunistic pathogens. Consequently, their bacteriophages may have significant impact on human microbial ecology and pathologies. Our aim was to reveal the prevalence and diversity of bacteriophages infecting Aggregatibacter...

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Autores principales: Szafrański, Szymon P., Kilian, Mogens, Yang, Ines, Bei der Wieden, Gesa, Winkel, Andreas, Hegermann, Jan, Stiesch, Meike
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6776037/
https://www.ncbi.nlm.nih.gov/pubmed/31201356
http://dx.doi.org/10.1038/s41396-019-0450-8
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author Szafrański, Szymon P.
Kilian, Mogens
Yang, Ines
Bei der Wieden, Gesa
Winkel, Andreas
Hegermann, Jan
Stiesch, Meike
author_facet Szafrański, Szymon P.
Kilian, Mogens
Yang, Ines
Bei der Wieden, Gesa
Winkel, Andreas
Hegermann, Jan
Stiesch, Meike
author_sort Szafrański, Szymon P.
collection PubMed
description Aggregatibacter and Haemophilus species are relevant human commensals and opportunistic pathogens. Consequently, their bacteriophages may have significant impact on human microbial ecology and pathologies. Our aim was to reveal the prevalence and diversity of bacteriophages infecting Aggregatibacter and Haemophilus species that colonize the human body. Genome mining with comparative genomics, screening of clinical isolates, and profiling of metagenomes allowed characterization of 346 phages grouped in 52 clusters and 18 superclusters. Less than 10% of the identified phage clusters were represented by previously characterized phages. Prophage diversity patterns varied significantly for different phage types, host clades, and environmental niches. A more diverse phage community lysogenizes Haemophilus influenzae and Haemophilus parainfluenzae strains than Aggregatibacter actinomycetemcomitans and “Haemophilus ducreyi”. Co-infections occurred more often in “H. ducreyi”. Phages from Aggregatibacter actinomycetemcomitans preferably lysogenized strains of specific serotype. Prophage patterns shared by subspecies clades of different bacterial species suggest similar ecoevolutionary drivers. Changes in frequencies of DNA uptake signal sequences and guanine–cytosine content reflect phage-host long-term coevolution. Aggregatibacter and Haemophilus phages were prevalent at multiple oral sites. Together, these findings should help exploring the ecoevolutionary forces shaping virus-host interactions in the human microbiome. Putative lytic phages, especially phiKZ-like, may provide new therapeutic options.
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spelling pubmed-67760372019-10-04 Diversity patterns of bacteriophages infecting Aggregatibacter and Haemophilus species across clades and niches Szafrański, Szymon P. Kilian, Mogens Yang, Ines Bei der Wieden, Gesa Winkel, Andreas Hegermann, Jan Stiesch, Meike ISME J Article Aggregatibacter and Haemophilus species are relevant human commensals and opportunistic pathogens. Consequently, their bacteriophages may have significant impact on human microbial ecology and pathologies. Our aim was to reveal the prevalence and diversity of bacteriophages infecting Aggregatibacter and Haemophilus species that colonize the human body. Genome mining with comparative genomics, screening of clinical isolates, and profiling of metagenomes allowed characterization of 346 phages grouped in 52 clusters and 18 superclusters. Less than 10% of the identified phage clusters were represented by previously characterized phages. Prophage diversity patterns varied significantly for different phage types, host clades, and environmental niches. A more diverse phage community lysogenizes Haemophilus influenzae and Haemophilus parainfluenzae strains than Aggregatibacter actinomycetemcomitans and “Haemophilus ducreyi”. Co-infections occurred more often in “H. ducreyi”. Phages from Aggregatibacter actinomycetemcomitans preferably lysogenized strains of specific serotype. Prophage patterns shared by subspecies clades of different bacterial species suggest similar ecoevolutionary drivers. Changes in frequencies of DNA uptake signal sequences and guanine–cytosine content reflect phage-host long-term coevolution. Aggregatibacter and Haemophilus phages were prevalent at multiple oral sites. Together, these findings should help exploring the ecoevolutionary forces shaping virus-host interactions in the human microbiome. Putative lytic phages, especially phiKZ-like, may provide new therapeutic options. Nature Publishing Group UK 2019-06-14 2019-10 /pmc/articles/PMC6776037/ /pubmed/31201356 http://dx.doi.org/10.1038/s41396-019-0450-8 Text en © The Author(s) 2019 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
Szafrański, Szymon P.
Kilian, Mogens
Yang, Ines
Bei der Wieden, Gesa
Winkel, Andreas
Hegermann, Jan
Stiesch, Meike
Diversity patterns of bacteriophages infecting Aggregatibacter and Haemophilus species across clades and niches
title Diversity patterns of bacteriophages infecting Aggregatibacter and Haemophilus species across clades and niches
title_full Diversity patterns of bacteriophages infecting Aggregatibacter and Haemophilus species across clades and niches
title_fullStr Diversity patterns of bacteriophages infecting Aggregatibacter and Haemophilus species across clades and niches
title_full_unstemmed Diversity patterns of bacteriophages infecting Aggregatibacter and Haemophilus species across clades and niches
title_short Diversity patterns of bacteriophages infecting Aggregatibacter and Haemophilus species across clades and niches
title_sort diversity patterns of bacteriophages infecting aggregatibacter and haemophilus species across clades and niches
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6776037/
https://www.ncbi.nlm.nih.gov/pubmed/31201356
http://dx.doi.org/10.1038/s41396-019-0450-8
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