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Single-cell and population level viral infection dynamics revealed by phageFISH, a method to visualize intracellular and free viruses

Microbes drive the biogeochemical cycles that fuel planet Earth, and their viruses (phages) alter microbial population structure, genome repertoire, and metabolic capacity. However, our ability to understand and quantify phage–host interactions is technique-limited. Here, we introduce phageFISH – a...

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Autores principales: Allers, Elke, Moraru, Cristina, Duhaime, Melissa B, Beneze, Erica, Solonenko, Natalie, Barrero-Canosa, Jimena, Amann, Rudolf, Sullivan, Matthew B
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons Ltd 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3884771/
https://www.ncbi.nlm.nih.gov/pubmed/23489642
http://dx.doi.org/10.1111/1462-2920.12100
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author Allers, Elke
Moraru, Cristina
Duhaime, Melissa B
Beneze, Erica
Solonenko, Natalie
Barrero-Canosa, Jimena
Amann, Rudolf
Sullivan, Matthew B
author_facet Allers, Elke
Moraru, Cristina
Duhaime, Melissa B
Beneze, Erica
Solonenko, Natalie
Barrero-Canosa, Jimena
Amann, Rudolf
Sullivan, Matthew B
author_sort Allers, Elke
collection PubMed
description Microbes drive the biogeochemical cycles that fuel planet Earth, and their viruses (phages) alter microbial population structure, genome repertoire, and metabolic capacity. However, our ability to understand and quantify phage–host interactions is technique-limited. Here, we introduce phageFISH – a markedly improved geneFISH protocol that increases gene detection efficiency from 40% to > 92% and is optimized for detection and visualization of intra- and extracellular phage DNA. The application of phageFISH to characterize infection dynamics in a marine podovirus–gammaproteobacterial host model system corroborated classical metrics (qPCR, plaque assay, FVIC, DAPI) and outperformed most of them to reveal new biology. PhageFISH detected both replicating and encapsidated (intracellular and extracellular) phage DNA, while simultaneously identifying and quantifying host cells during all stages of infection. Additionally, phageFISH allowed per-cell relative measurements of phage DNA, enabling single-cell documentation of infection status (e.g. early vs late stage infections). Further, it discriminated between two waves of infection, which no other measurement could due to population-averaged signals. Together, these findings richly characterize the infection dynamics of a novel model phage–host system, and debut phageFISH as a much-needed tool for studying phage–host interactions in the laboratory, with great promise for environmental surveys and lineage-specific population ecology of free phages.
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spelling pubmed-38847712014-01-13 Single-cell and population level viral infection dynamics revealed by phageFISH, a method to visualize intracellular and free viruses Allers, Elke Moraru, Cristina Duhaime, Melissa B Beneze, Erica Solonenko, Natalie Barrero-Canosa, Jimena Amann, Rudolf Sullivan, Matthew B Environ Microbiol Research Articles Microbes drive the biogeochemical cycles that fuel planet Earth, and their viruses (phages) alter microbial population structure, genome repertoire, and metabolic capacity. However, our ability to understand and quantify phage–host interactions is technique-limited. Here, we introduce phageFISH – a markedly improved geneFISH protocol that increases gene detection efficiency from 40% to > 92% and is optimized for detection and visualization of intra- and extracellular phage DNA. The application of phageFISH to characterize infection dynamics in a marine podovirus–gammaproteobacterial host model system corroborated classical metrics (qPCR, plaque assay, FVIC, DAPI) and outperformed most of them to reveal new biology. PhageFISH detected both replicating and encapsidated (intracellular and extracellular) phage DNA, while simultaneously identifying and quantifying host cells during all stages of infection. Additionally, phageFISH allowed per-cell relative measurements of phage DNA, enabling single-cell documentation of infection status (e.g. early vs late stage infections). Further, it discriminated between two waves of infection, which no other measurement could due to population-averaged signals. Together, these findings richly characterize the infection dynamics of a novel model phage–host system, and debut phageFISH as a much-needed tool for studying phage–host interactions in the laboratory, with great promise for environmental surveys and lineage-specific population ecology of free phages. John Wiley & Sons Ltd 2013-08 2013-03-14 /pmc/articles/PMC3884771/ /pubmed/23489642 http://dx.doi.org/10.1111/1462-2920.12100 Text en Copyright © 2013 John Wiley & Sons Ltd http://creativecommons.org/licenses/by/2.5/ Re-use of this article is permitted in accordance with the Creative Commons Deed, Attribution 2.5, which does not permit commercial exploitation.
spellingShingle Research Articles
Allers, Elke
Moraru, Cristina
Duhaime, Melissa B
Beneze, Erica
Solonenko, Natalie
Barrero-Canosa, Jimena
Amann, Rudolf
Sullivan, Matthew B
Single-cell and population level viral infection dynamics revealed by phageFISH, a method to visualize intracellular and free viruses
title Single-cell and population level viral infection dynamics revealed by phageFISH, a method to visualize intracellular and free viruses
title_full Single-cell and population level viral infection dynamics revealed by phageFISH, a method to visualize intracellular and free viruses
title_fullStr Single-cell and population level viral infection dynamics revealed by phageFISH, a method to visualize intracellular and free viruses
title_full_unstemmed Single-cell and population level viral infection dynamics revealed by phageFISH, a method to visualize intracellular and free viruses
title_short Single-cell and population level viral infection dynamics revealed by phageFISH, a method to visualize intracellular and free viruses
title_sort single-cell and population level viral infection dynamics revealed by phagefish, a method to visualize intracellular and free viruses
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3884771/
https://www.ncbi.nlm.nih.gov/pubmed/23489642
http://dx.doi.org/10.1111/1462-2920.12100
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