Evidence map›Paper›PMID 40532126›Full record

ArticlePLoS pathogens2025

Experimental evolution of a pathogen confronted with innate immune memory increases variation in virulence.

Ana Korša, Moritz Baur, Nora K E Schulz, Jaime M Anaya-Rojas, Alexander Mellmann, Joachim Kurtz

Abstract read
In one paragraph

Article in PLoS pathogens, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
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  3. Review
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

6 authors.

Ana KoršaInstitute for Evolution and Biodiversity, University of Münster, Münster, Germany.ORCID 0000-0002-8050-0464
Moritz BaurInstitute for Evolution and Biodiversity, University of Münster, Münster, Germany.
Nora K E SchulzInstitute for Evolution and Biodiversity, University of Münster, Münster, Germany.
Jaime M Anaya-RojasInstitute for Evolution and Biodiversity, University of Münster, Münster, Germany.
Alexander MellmannInstitute for Hygiene, University of Münster, Münster, Germany.
Joachim KurtzInstitute for Evolution and Biodiversity, University of Münster, Münster, Germany.

Funding

Deutsche Forschungsgemeinschaft (DFG, German Research Foundation)Research Training Group GRK 2220
6 · The paper itself

Abstract

Understanding the drivers and mechanisms of virulence evolution is still a major goal of evolutionary biologists and epidemiologists. Theory predicts that the way virulence evolves depends on the balance between the benefits and costs it provides to pathogen fitness. Additionally, host responses to infections, such as resistance or tolerance, play a critical role in shaping virulence evolution. But, while the evolution of pathogens has been traditionally studied under the selection pressure of host adaptive immunity, less is known about their evolution when confronted to simpler and less effective forms of immunity such as immune priming. In this study, we used a well-established insect model for immune priming - red flour beetles and their bacterial pathogen Bacillus thuringiensis tenebrionis - to test how this form of innate immune memory drives the pathogen evolution. Through controlled experimental evolution of the pathogen in primed versus non-primed hosts, we found no change in average virulence after eight selection cycles in primed host. Nonetheless, we observed a notable rise in the variability of virulence, defined as the ability to kill hosts, among independent pathogen lines that evolved in primed hosts, and the bacteria were unable to develop resistance to host priming. Whole genome sequencing revealed increased activity in the bacterial mobilome (prophages and plasmids). Expression of the Cry toxin - a well-known virulence factor - was linked to evolved differences in copy number variation of the cry-carrying plasmid, though this did not correlate directly with virulence. These findings highlight that innate immune memory can drive variability in pathogen traits, which may favor adaptation to variable environments. This underscores the need to consider pathogen evolution in response to innate immune memory when applying these mechanisms in medicine, aquaculture, pest control, and insect mass production.

Indexed as

Bacillus thuringiensisHost-Pathogen InteractionsImmunity, InnateImmunologic MemoryAnimalsBiological EvolutionTrained ImmunityVirulence

Identifiers

PMID40532126
PMCPMC12176410

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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.