Evidence map›Paper›PMID 41279535›Full record

ArticlebioRxiv : the preprint server for biology2025

Quantifying the fitness contribution of phagocytosis.

Paul E Schavemaker, Kaitlyn S Tam, Michael Lynch

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2025. 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

3 authors.

Paul E SchavemakerBiodesign Center for Mechanisms of Evolution, Arizona State University, Tempe, AZ, 85287, USA.
Kaitlyn S TamSchool of Life Sciences, Arizona State University, Tempe, AZ, 85287, USA.ORCID 0009-0008-3715-3277
Michael LynchBiodesign Center for Mechanisms of Evolution, Arizona State University, Tempe, AZ, 85287, USA.

Funding

Causes and Population-genetic Consequences of Molecular VariationR35GM122566 · NIGMS · TRUSTEES OF INDIANA UNIVERSITY · PI Michael R LYNCH · 2017 to 2026
$7.7M
NIGMS NIH HHS R35 GM122566
6 · The paper itself

Abstract

Phagocytosis, the ingestion of cells by other cells, is ubiquitous among eukaryotic life. It is required for food uptake in many single-celled species and for the immune response in multicellular species. The origin of phagocytosis and its role in the evolution of endomembranes and the eukaryotic cell remains obscure. Drawing on a wealth of empirical data, we integrate prey capture, engulfment, and internal and external digestion into a mathematical evolutionary model that quantifies the fitness of a primitive phagocytoser relative to a non-phagocytosing ancestor. We reveal the conditions under which a non-phagocytosing predator that digests its prey externally can persist. We also show that the phagocytoser can outperform the ancestor in a broad range of situations, despite the cost associated with producing a phagocytic cup. Parameter variations delineate how fast engulfment needs to be for phagocytosis to be advantageous, providing clear benchmarks for interpreting the importance of results in genetic knockout studies and mechanical models. The phagocytoser still outperforms the ancestor when food vacuoles can't fuse back to the plasma membrane, providing arguments in favor of the gradual evolution of phagocytosis and for phagocytosis as the initiator of the endomembrane system.

Identifiers

PMID41279535
PMCPMC12633225

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LicenceCC BY
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Registered trials

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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.