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Detection of specific uncultured bacteriophages by fluorescence in situ hybridisation in pig microbiome

Microbial communities have huge impacts on their ecosystems and local environments spanning from marine and soil communities to the mammalian gut. Bacteriophages (phages) are important drivers of population control and diversity in the community, but our understanding of complex microbial communitie...

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Autores principales: Ostenfeld, Line Jensen, Munk, Patrick, Aarestrup, Frank M., Otani, Saria
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10062541/
https://www.ncbi.nlm.nih.gov/pubmed/36996123
http://dx.doi.org/10.1371/journal.pone.0283676
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author Ostenfeld, Line Jensen
Munk, Patrick
Aarestrup, Frank M.
Otani, Saria
author_facet Ostenfeld, Line Jensen
Munk, Patrick
Aarestrup, Frank M.
Otani, Saria
author_sort Ostenfeld, Line Jensen
collection PubMed
description Microbial communities have huge impacts on their ecosystems and local environments spanning from marine and soil communities to the mammalian gut. Bacteriophages (phages) are important drivers of population control and diversity in the community, but our understanding of complex microbial communities is halted by biased detection techniques. Metagenomics have provided a method of novel phage discovery independent of in vitro culturing techniques and have revealed a large proportion of understudied phages. Here, five jumbophage genomes, that were previously assembled in silico from pig faecal metagenomes, are detected and observed directly in their natural environment using a modified phageFISH approach, and combined with methods to decrease bias against large-sized phages (e.g., jumbophages). These phages are uncultured with unknown hosts. The specific phages were detected by PCR and fluorescent in situ hybridisation in their original faecal samples as well as across other faecal samples. Co-localisation of bacterial signals and phage signals allowed detection of the different stages of phage life cycle. All phages displayed examples of early infection, advanced infection, burst, and free phages. To our knowledge, this is the first detection of jumbophages in faeces, which were investigated independently of culture, host identification, and size, and based solely on the genome sequence. This approach opens up opportunities for characterisation of novel in silico phages in vivo from a broad range of gut microbiomes.
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spelling pubmed-100625412023-03-31 Detection of specific uncultured bacteriophages by fluorescence in situ hybridisation in pig microbiome Ostenfeld, Line Jensen Munk, Patrick Aarestrup, Frank M. Otani, Saria PLoS One Lab Protocol Microbial communities have huge impacts on their ecosystems and local environments spanning from marine and soil communities to the mammalian gut. Bacteriophages (phages) are important drivers of population control and diversity in the community, but our understanding of complex microbial communities is halted by biased detection techniques. Metagenomics have provided a method of novel phage discovery independent of in vitro culturing techniques and have revealed a large proportion of understudied phages. Here, five jumbophage genomes, that were previously assembled in silico from pig faecal metagenomes, are detected and observed directly in their natural environment using a modified phageFISH approach, and combined with methods to decrease bias against large-sized phages (e.g., jumbophages). These phages are uncultured with unknown hosts. The specific phages were detected by PCR and fluorescent in situ hybridisation in their original faecal samples as well as across other faecal samples. Co-localisation of bacterial signals and phage signals allowed detection of the different stages of phage life cycle. All phages displayed examples of early infection, advanced infection, burst, and free phages. To our knowledge, this is the first detection of jumbophages in faeces, which were investigated independently of culture, host identification, and size, and based solely on the genome sequence. This approach opens up opportunities for characterisation of novel in silico phages in vivo from a broad range of gut microbiomes. Public Library of Science 2023-03-30 /pmc/articles/PMC10062541/ /pubmed/36996123 http://dx.doi.org/10.1371/journal.pone.0283676 Text en © 2023 Ostenfeld et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Lab Protocol
Ostenfeld, Line Jensen
Munk, Patrick
Aarestrup, Frank M.
Otani, Saria
Detection of specific uncultured bacteriophages by fluorescence in situ hybridisation in pig microbiome
title Detection of specific uncultured bacteriophages by fluorescence in situ hybridisation in pig microbiome
title_full Detection of specific uncultured bacteriophages by fluorescence in situ hybridisation in pig microbiome
title_fullStr Detection of specific uncultured bacteriophages by fluorescence in situ hybridisation in pig microbiome
title_full_unstemmed Detection of specific uncultured bacteriophages by fluorescence in situ hybridisation in pig microbiome
title_short Detection of specific uncultured bacteriophages by fluorescence in situ hybridisation in pig microbiome
title_sort detection of specific uncultured bacteriophages by fluorescence in situ hybridisation in pig microbiome
topic Lab Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10062541/
https://www.ncbi.nlm.nih.gov/pubmed/36996123
http://dx.doi.org/10.1371/journal.pone.0283676
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