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Lifestyle of sponge symbiont phages by host prediction and correlative microscopy
Bacteriophages (phages) are ubiquitous elements in nature, but their ecology and role in animals remains little understood. Sponges represent the oldest known extant animal-microbe symbiosis and are associated with dense and diverse microbial consortia. Here we investigate the tripartite interaction...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8245591/ https://www.ncbi.nlm.nih.gov/pubmed/33603147 http://dx.doi.org/10.1038/s41396-021-00900-6 |
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author | Jahn, M. T. Lachnit, T. Markert, S. M. Stigloher, C. Pita, L. Ribes, M. Dutilh, B. E. Hentschel, U. |
author_facet | Jahn, M. T. Lachnit, T. Markert, S. M. Stigloher, C. Pita, L. Ribes, M. Dutilh, B. E. Hentschel, U. |
author_sort | Jahn, M. T. |
collection | PubMed |
description | Bacteriophages (phages) are ubiquitous elements in nature, but their ecology and role in animals remains little understood. Sponges represent the oldest known extant animal-microbe symbiosis and are associated with dense and diverse microbial consortia. Here we investigate the tripartite interaction between phages, bacterial symbionts, and the sponge host. We combined imaging and bioinformatics to tackle important questions on who the phage hosts are and what the replication mode and spatial distribution within the animal is. This approach led to the discovery of distinct phage-microbe infection networks in sponge versus seawater microbiomes. A new correlative in situ imaging approach (‘PhageFISH-CLEM‘) localised phages within bacterial symbiont cells, but also within phagocytotically active sponge cells. We postulate that the phagocytosis of free virions by sponge cells modulates phage-bacteria ratios and ultimately controls infection dynamics. Prediction of phage replication strategies indicated a distinct pattern, where lysogeny dominates the sponge microbiome, likely fostered by sponge host-mediated virion clearance, while lysis dominates in seawater. Collectively, this work provides new insights into phage ecology within sponges, highlighting the importance of tripartite animal-phage-bacterium interplay in holobiont functioning. We anticipate that our imaging approach will be instrumental to further understanding of viral distribution and cellular association in animal hosts. |
format | Online Article Text |
id | pubmed-8245591 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-82455912021-07-20 Lifestyle of sponge symbiont phages by host prediction and correlative microscopy Jahn, M. T. Lachnit, T. Markert, S. M. Stigloher, C. Pita, L. Ribes, M. Dutilh, B. E. Hentschel, U. ISME J Article Bacteriophages (phages) are ubiquitous elements in nature, but their ecology and role in animals remains little understood. Sponges represent the oldest known extant animal-microbe symbiosis and are associated with dense and diverse microbial consortia. Here we investigate the tripartite interaction between phages, bacterial symbionts, and the sponge host. We combined imaging and bioinformatics to tackle important questions on who the phage hosts are and what the replication mode and spatial distribution within the animal is. This approach led to the discovery of distinct phage-microbe infection networks in sponge versus seawater microbiomes. A new correlative in situ imaging approach (‘PhageFISH-CLEM‘) localised phages within bacterial symbiont cells, but also within phagocytotically active sponge cells. We postulate that the phagocytosis of free virions by sponge cells modulates phage-bacteria ratios and ultimately controls infection dynamics. Prediction of phage replication strategies indicated a distinct pattern, where lysogeny dominates the sponge microbiome, likely fostered by sponge host-mediated virion clearance, while lysis dominates in seawater. Collectively, this work provides new insights into phage ecology within sponges, highlighting the importance of tripartite animal-phage-bacterium interplay in holobiont functioning. We anticipate that our imaging approach will be instrumental to further understanding of viral distribution and cellular association in animal hosts. Nature Publishing Group UK 2021-02-18 2021-07 /pmc/articles/PMC8245591/ /pubmed/33603147 http://dx.doi.org/10.1038/s41396-021-00900-6 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Jahn, M. T. Lachnit, T. Markert, S. M. Stigloher, C. Pita, L. Ribes, M. Dutilh, B. E. Hentschel, U. Lifestyle of sponge symbiont phages by host prediction and correlative microscopy |
title | Lifestyle of sponge symbiont phages by host prediction and correlative microscopy |
title_full | Lifestyle of sponge symbiont phages by host prediction and correlative microscopy |
title_fullStr | Lifestyle of sponge symbiont phages by host prediction and correlative microscopy |
title_full_unstemmed | Lifestyle of sponge symbiont phages by host prediction and correlative microscopy |
title_short | Lifestyle of sponge symbiont phages by host prediction and correlative microscopy |
title_sort | lifestyle of sponge symbiont phages by host prediction and correlative microscopy |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8245591/ https://www.ncbi.nlm.nih.gov/pubmed/33603147 http://dx.doi.org/10.1038/s41396-021-00900-6 |
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