Evidence map›Paper›PMID 42535547›Full record

ArticleGenome biology and evolution2026

Interspecies Exchange of Mobile Genetic Elements During a Plant Disease Outbreak.

Daria Evseeva, Yann Pecrix, Marek Kucka, Catrin Weiler, Carolin Franzl, Markéta Vlková-Žlebková, Elena Colombi, Yingguang Frank Chan, Stéphane Poussier, Emmanuel Wicker and 1 more

Abstract read
In one paragraph

Article in Genome biology and evolution, 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

11 authors.

Daria EvseevaResearch Group for Plant Pathogen Evolution, Max Planck Institute for Biology, Tübingen, Germany.ORCID 0009-0001-6560-4572
Yann PecrixCIRAD UMR PVBMT, Saint-Pierre, La Réunion F-97410, France.ORCID 0000-0002-6537-3145
Marek KuckaFriedrich Miescher Laboratory of the Max Planck Society, Tübingen, Germany.ORCID 0000-0002-0928-4914
Catrin WeilerResearch Group for Plant Pathogen Evolution, Max Planck Institute for Biology, Tübingen, Germany.ORCID 0009-0007-2683-5734
Carolin FranzlResearch Group for Plant Pathogen Evolution, Max Planck Institute for Biology, Tübingen, Germany.ORCID 0000-0003-2467-4328
Markéta Vlková-ŽlebkováResearch Group for Plant Pathogen Evolution, Max Planck Institute for Biology, Tübingen, Germany.ORCID 0000-0002-0272-5115
Elena ColombiMacquarie University, Sydney, Australia.ORCID 0000-0002-3753-4925
Yingguang Frank ChanFriedrich Miescher Laboratory of the Max Planck Society, Tübingen, Germany.ORCID 0000-0001-6292-9681
Stéphane PoussierCIRAD UMR PVBMT, Saint-Pierre, La Réunion F-97410, France.ORCID 0000-0003-0273-3518
Emmanuel WickerCIRAD UMR-PHIM, Montpellier, France.ORCID 0000-0003-0927-7404
Honour C McCannResearch Group for Plant Pathogen Evolution, Max Planck Institute for Biology, Tübingen, Germany.ORCID 0000-0003-3061-337X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Outbreak sequencing provides insight into the origin and evolutionary processes acting on emerging pathogens. Sequencing a historic multihost outbreak of Ralstonia spp. in Martinique shows the outbreak was caused by two lineages that diverged at separate times from mainland populations. One lineage (Ralstonia pseudosolanacearum I-18) was originally introduced from Asia to South America, where it became well established prior to its dissemination to Martinique, where it retains a signature of specialization on solanaceous hosts. The novel lineage first identified during the outbreak (Ralstonia solanacearum IIB-4NPB) arose from a mainland population endemic to the Americas prior to its arrival in Martinique, where host-range expansion was observed. In contrast to minor changes in secreted effector protein repertoires, the emergent R. solanacearum IIB-4NPB acquired a novel integrative and conjugative element (ICERsoRUN1145). After identifying all Ralstonia spp. ICEs and mapping their spatial and phylogenetic distribution among Ralstonia spp. sampled during the outbreak, we found closely related ICEs circulating in mainland populations of R. pseudosolanacearum, indicating likely exchange between introduced and endemic Ralstonia spp. The family of ICEs in Ralstonia (ICERs) has a conserved bipartite structure and display a striking pattern of functional specialization in each cargo gene insertion hotspot: the first hotspot is a target for metabolic gene acquisition, and the second is a target for defense element acquisition. This work provides unparalleled phylogenetic and spatial resolution of an unusual outbreak and highlights the role of horizontal transfer in shaping the ecological success of an emerging pathogen.

Indexed as

Interspersed Repetitive SequencesPlant DiseasesRalstoniaDisease OutbreaksEvolution, MolecularGene Transfer, HorizontalPhylogenyRalstonia solanacearumbacterial plant pathogendisease emergencegenomic epidemiologyintegrative and conjugative elementsmicrobial evolutionmobile elements

Identifiers

PMID42535547
PMCPMC13540745

What OpenQuestion holds

Textmetadata
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.