Evidence map›Paper›PMID 40908793›Full record

ArticleEcology2025

Transgenerational pathogen effects: Maternal pathogen exposure reduces offspring fitness.

Kristina M McIntire, Marcin K Dziuba, Elizabeth B Haywood, Miles L Robertson, Megan Vaandrager, Emma Baird, Fiona E Corcoran, Taleah Nelson, Michael H Cortez, Meghan A Duffy

Abstract read
In one paragraph

Article in Ecology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
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

10 authors.

Kristina M McIntireDepartment of Ecology and Evolutionary Biology, University of Michigan, Ann Arbor, Michigan, USA.ORCID https://orcid.org/0000-0002-1387-5637
Marcin K DziubaDepartment of Ecology and Evolutionary Biology, University of Michigan, Ann Arbor, Michigan, USA.
Elizabeth B HaywoodDepartment of Mathematics, Florida State University, Tallahassee, Florida, USA.
Miles L RobertsonDepartment of Biological Science, Florida State University, Tallahassee, Florida, USA.
Megan VaandragerDepartment of Ecology and Evolutionary Biology, University of Michigan, Ann Arbor, Michigan, USA.
Emma BairdDepartment of Ecology and Evolutionary Biology, University of Michigan, Ann Arbor, Michigan, USA.
Fiona E CorcoranDepartment of Ecology and Evolutionary Biology, University of Michigan, Ann Arbor, Michigan, USA.
Taleah NelsonDepartment of Ecology and Evolutionary Biology, University of Michigan, Ann Arbor, Michigan, USA.
Michael H CortezDepartment of Biological Science, Florida State University, Tallahassee, Florida, USA.
Meghan A DuffyDepartment of Ecology and Evolutionary Biology, University of Michigan, Ann Arbor, Michigan, USA.ORCID https://orcid.org/0000-0002-8142-0802

Funding

Division of Environmental Biology 1748729Division of Environmental Biology 2015280Gordon and Betty Moore Foundation GBMF9202GRF 1937954
6 · The paper itself

Abstract

Pathogens can alter the phenotype not only of exposed hosts, but also of future generations. Transgenerational immune priming, where parental infection drives reduced susceptibility of offspring, has been particularly well explored, but pathogens can also alter life history traits of offspring. Here, we examined the potential for transgenerational impacts of a microsporidian pathogen, Ordospora pajunii, by experimentally measuring the impact of maternal exposure on offspring fitness in the presence and absence of parasites, and then developing mathematical models that explored the population-level impacts of these transgenerational effects. We did not find evidence of transgenerational immune priming: offspring of exposed mothers became infected at high rates, similar to offspring of unexposed mothers, and the infection burden did not differ between these two groups. We also did not find any evidence of transgenerational tolerance, where daughters of exposed mothers have higher fitness after infection. Instead, we found evidence for negative transgenerational impacts of infection: uninfected offspring of exposed mothers had substantially greater early life mortality than uninfected offspring of unexposed mothers. Offspring of exposed mothers also had reduced growth rates, fewer clutches, and fewer offspring. We propose that these observations should be considered transgenerational virulence, where a pathogen reduces the fitness of the offspring of infected hosts. Our parameterized mathematical model allowed us to explore the impacts of transgenerational virulence at the population level. If transgenerational virulence manifests as decreased reproduction or increased mortality in offspring, as we saw in the empirical portion of our study, this reduces total host density, infection prevalence, and infected host density, which could have implications for both host conservation and spillover risk. We propose that transgenerational virulence might be common and is a concept worthy of further empirical and theoretical exploration.

Indexed as

Genetic FitnessHost-Pathogen InteractionsMaternal ExposureMicrosporidiaAnimalsFemaleModels, BiologicalDaphniaimmune primingmathematical modelmicrosporidiantransgenerational effectsvirulence

Identifiers

PMID40908793
PMCPMC12411831

What OpenQuestion holds

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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.