Evidence map›Paper›PMID 42182144›Full record

ArticlebioRxiv : the preprint server for biology2026

Counting to two: how phages decide between lysis and lysogeny.

Janni Harju, Ghita Guessous, Zemer Gitai, Ned S Wingreen

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 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

4 authors.

Janni HarjuJoseph Henry Laboratories of Physics, Princeton University, Princeton, NJ, USA.ORCID 0000-0001-9696-5453
Ghita GuessousJoseph Henry Laboratories of Physics, Princeton University, Princeton, NJ, USA.ORCID 0000-0001-9597-8041
Zemer GitaiDepartment of Molecular Biology, Princeton University, Princeton, NJ 08544.ORCID 0000-0002-3280-6178
Ned S WingreenDepartment of Molecular Biology, Princeton University, Princeton, NJ 08544.ORCID 0000-0001-7384-2821

Funding

New frontiers in extracellular signalingR35GM122575 · NIGMS · CORNELL UNIVERSITY · PI CERIONE, RICHARD A. · 2017 to 2021
$3.0M
NIGMS NIH HHS R35 GM122575
6 · The paper itself

Abstract

Upon infecting a bacterium, temperate phages must decide between killing the cell to reproduce (lysis) and entering a symbiotic lifestyle (lysogeny). This choice is often informed by the cells state and by the number of infecting phage particles, or multiplicity of infection (MOI). Because the copy numbers of all phage genes scale identically with MOI, an MOI-dependent decision requires a rapidly established asymmetry between the lytic and lysogenic pathways. We introduce a minimal model showing how a simple coupling to host machinery (e.g. a protease) can generate such an asymmetry. Our analytical model yields scaling laws that predict how the lysislysogeny decision responds to perturbations of the host. It also quantitatively predicts stochastic features of infection outcomes, such as lysogeny probabilities, consistent with experimental data. By reducing complex regulatory networks to their essential components, our framework reveals the organizing principles of lysislysogeny decisions across phage species.

Identifiers

PMID42182144
PMCPMC13192843

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.