Evidence map›Paper›PMID 42716705›Full record

ArticleMicrobiologyOpen2026

Quantifying Viral Lysis in Microalgae Using Cell-Free rRNA.

Saki Kikuya, Yuji Tomaru, Keizo Nagasaki, Daichi Morimoto, Yuki Yamagishi, Hiroyuki Ogata, Hisashi Endo

Abstract read
In one paragraph

Article in MicrobiologyOpen, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Saki KikuyaBioinformatics Center, Institute for Chemical Research, Kyoto University, Gokasho, Uji, Kyoto, Japan.
Yuji TomaruFisheries Technology Institute, Japan Fisheries Research and Education Agency, Hatsukaichi, Hiroshima, Japan.ORCID https://orcid.org/0000-0002-8164-6991
Keizo NagasakiFaculty of Science and Technology, Kochi University, Monobe-Otsu, Nankoku, Kochi, Japan.
Daichi MorimotoFaculty of Science and Technology, Kochi University, Monobe-Otsu, Nankoku, Kochi, Japan.ORCID https://orcid.org/0000-0002-7789-0529
Yuki YamagishiBioinformatics Center, Institute for Chemical Research, Kyoto University, Gokasho, Uji, Kyoto, Japan.
Hiroyuki OgataBioinformatics Center, Institute for Chemical Research, Kyoto University, Gokasho, Uji, Kyoto, Japan.ORCID https://orcid.org/0000-0001-6594-377X
Hisashi EndoBioinformatics Center, Institute for Chemical Research, Kyoto University, Gokasho, Uji, Kyoto, Japan.ORCID https://orcid.org/0000-0003-0016-1624

Funding

Collaborative Research Program of the Institute for Chemical Research, Kyoto University 2025-27Collaborative Research Program of the Institute for Chemical Research, Kyoto University 2025-28Collaborative Research Program of the Institute for Chemical Research, Kyoto University 2026-22Japan Science and Technology Agency PRESTO JPMJPR23G3Japan Society for the Promotion of Science KAKENHI 21H05057Japan Society for the Promotion of Science KAKENHI 22H00384Japan Society for the Promotion of Science KAKENHI 22H00385Japan Society for the Promotion of Science KAKENHI 22H02420Japan Society for the Promotion of Science KAKENHI 22K18351Japan Society for the Promotion of Science KAKENHI 24H00528Japan Society for the Promotion of Science KAKENHI JP22KJ2366Japan Society for the Promotion of Science KAKENHI JP23K14265
6 · The paper itself

Abstract

Viral lysis is a major driver of phytoplankton mortality and a key source of dissolved organic matter in the ocean, yet quantitative and taxon-resolved measurements of this process remain limited for eukaryotic plankton. Here, we demonstrate that cell-free ribosomal RNA (rRNA) dissolved in the extracellular medium serves as a quantitative proxy for viral lysis in microeukaryotes by combining laboratory infection experiments with a rate-based modeling framework. We investigated two host-virus systems: the diatom Chaetoceros tenuissimus infected by a single-stranded RNA virus (CtenRNAV) and the raphidophyte Heterosigma akashiwo infected by a large double-stranded DNA virus (HaV). By explicitly accounting for cell-free rRNA degradation, we quantified a proxy for cell lysis rate from cell-free 18S rRNA dynamics and observed up to 46- and 302-fold increases in cell-normalized lysis rates under viral infection. In C. tenuissimus, peak lysis preceded the decline in cell abundance, demonstrating that substantial viral lysis occurs while populations are still proliferating. In contrast, H. akashiwo exhibited elevated lysis in both early and late infection phases, implying that a fraction of host cells undergoes rapid, nonproductive mortality prior to viral replication, in addition to canonical lytic events. Our study provides the first experimental validation of cell-free rRNA as a quantitative marker of lytic mortality in microeukaryotes, offering a scalable approach for estimating taxon-specific mortality in natural plankton communities.

Indexed as

DiatomsMicroalgaeRNA, RibosomalRNA VirusesStramenopilesPhytoplanktonRNA, Ribosomal, 18SRNA, RibosomalRNA, Ribosomal, 18Scell‐free rRNAlysis ratemarine ecosystemsphytoplanktonviruses

Identifiers

PMID42716705
PMCPMC13557921

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.