Evidence map›Paper›PMID 38961701›Full record

ArticleGenome biology and evolution2024

Making a Pathogen? Evaluating the Impact of Protist Predation on the Evolution of Virulence in Serratia marcescens.

Heather A Hopkins, Christian Lopezguerra, Meng-Jia Lau, Kasie Raymann

Abstract read
In one paragraph

Article in Genome biology and evolution, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Genomic and phenotypic diversification ofMicrobiology spectrum · 2026
    Article
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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.

Heather A HopkinsDepartment of Plant and Microbial Biology, North Carolina State University, Raleigh, NC, USA.ORCID 0009-0001-7876-7821
Christian LopezguerraDepartment of Plant and Microbial Biology, North Carolina State University, Raleigh, NC, USA.ORCID 0009-0003-4642-3551
Meng-Jia LauDepartment of Plant and Microbial Biology, North Carolina State University, Raleigh, NC, USA.ORCID 0000-0003-2943-7022
Kasie RaymannDepartment of Plant and Microbial Biology, North Carolina State University, Raleigh, NC, USA.ORCID 0000-0001-7008-2783

Funding

Deciphering the processes of adaptation and exaptation driving the evolution of opportunism in bacteriaR01GM145747 · NIGMS · UNIVERSITY OF NORTH CAROLINA GREENSBORO · PI Kasie Tyler Raymann · 2023 to 2026
$1.3M
National Science Foundation DEB-2344788NIGMS NIH HHS R01 GM145747NIH HHS 7R01GM145747-02University of North Carolina Greensboro
6 · The paper itself

Abstract

Opportunistic pathogens are environmental microbes that are generally harmless and only occasionally cause disease. Unlike obligate pathogens, the growth and survival of opportunistic pathogens do not rely on host infection or transmission. Their versatile lifestyles make it challenging to decipher how and why virulence has evolved in opportunistic pathogens. The coincidental evolution hypothesis postulates that virulence results from exaptation or pleiotropy, i.e. traits evolved for adaptation to living in one environment that have a different function in another. In particular, adaptation to avoid or survive protist predation has been suggested to contribute to the evolution of bacterial virulence (the training ground hypothesis). Here, we used experimental evolution to determine how the selective pressure imposed by a protist predator impacts the virulence and fitness of a ubiquitous environmental opportunistic bacterial pathogen that has acquired multidrug resistance: Serratia marcescens. To this aim, we evolved S. marcescens in the presence or absence of generalist protist predator, Tetrahymena thermophila. After 60 d of evolution, we evaluated genotypic and phenotypic changes by comparing evolved S. marcescens with the ancestral strain. Whole-genome shotgun sequencing of the entire evolved populations and individual isolates revealed numerous cases of parallel evolution, many more than statistically expected by chance, in genes associated with virulence. Our phenotypic assays suggested that evolution in the presence of a predator maintained virulence, whereas evolution in the absence of a predator resulted in attenuated virulence. We also found a significant correlation between virulence, biofilm formation, growth, and grazing resistance. Overall, our results provide evidence that bacterial virulence and virulence-related traits are maintained by selective pressures imposed by protist predation.

Indexed as

Serratia marcescensTetrahymena thermophilaBiological EvolutionVirulencebacteriaevolutionexaptationopportunistic pathogenpredationvirulence

Identifiers

PMID38961701
PMCPMC11332436

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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.