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. 2022 Feb 1;2:12. doi: 10.1038/s43705-022-00093-9

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© The Author(s) 2022

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/.

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Fig. 4 — A Schematic overview of single-cell assay for viral burst size determination by viral tagging and grow. In the latent period of infection, single viral-tagged cells (VTs) were sorted by flow cytometer from Pseudoalteromonas sp. H71 cells infected by phage HM1 at an MOI of 0.5 (see Methods for details). Following sorting single VTs into different wells of the 96-well plate containing growth medium (MSM), the plate was incubated to allow for viral progenies to release from infected cells. The number of viruses produced per VT was then determined by the number of plaques per poured plate using the traditional plaque assay. B Distribution of viral burst size from individual tagged cells. The number of progeny viruses (X-axis) per cell (Y-axis) are represented in bins of 20, with the exception of the first bin excluding single plaques. The number (n) of individual tagged cells assessed is represented at the top right corner.