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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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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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.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0283676</identifier><identifier>PMID: 36996123</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Animals ; Bacteria ; Bacteria - genetics ; Bacteriophages - genetics ; Biology and Life Sciences ; Culture techniques ; E coli ; Ecosystems ; Engineering and Technology ; Feces ; Fluorescence ; Fluorescence in situ hybridization ; Genomes ; Genomics ; Health aspects ; Infections ; Intestinal microflora ; Lab Protocol ; Life cycles ; Marine ecosystems ; Metagenome ; Metagenomics ; Methods ; Microbial activity ; Microbiomes ; Microbiota ; Microbiota (Symbiotic organisms) ; Microorganisms ; Natural environment ; Nucleotide sequence ; Phages ; Population control ; Research and Analysis Methods ; Swine</subject><ispartof>PloS one, 2023-03, Vol.18 (3), p.e0283676-e0283676</ispartof><rights>Copyright: © 2023 Ostenfeld et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.</rights><rights>COPYRIGHT 2023 Public Library of Science</rights><rights>2023 Ostenfeld et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2023 Ostenfeld et al 2023 Ostenfeld et al</rights><rights>2023 Ostenfeld et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. 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subjects | Animals Bacteria Bacteria - genetics Bacteriophages - genetics Biology and Life Sciences Culture techniques E coli Ecosystems Engineering and Technology Feces Fluorescence Fluorescence in situ hybridization Genomes Genomics Health aspects Infections Intestinal microflora Lab Protocol Life cycles Marine ecosystems Metagenome Metagenomics Methods Microbial activity Microbiomes Microbiota Microbiota (Symbiotic organisms) Microorganisms Natural environment Nucleotide sequence Phages Population control Research and Analysis Methods Swine |
title | Detection of specific uncultured bacteriophages by fluorescence in situ hybridisation in pig microbiome |
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