Evidence map›Paper›PMID 40590190›Full record

ArticleMolecular ecology2025

No Mate, No Problem: Molecular Mechanisms Involved in Parthenogenesis in the Cosmopolitan Earthworm Aporrectodea trapezoides (Annelida, Clitellata).

Irene de Sosa, Marta Turon, Sergi Taboada, José Lorente-Sorolla, Rosa Fernández, Natasha Tilikj, Alberto Piris, Marta Novo, Patricia Álvarez Campos, Ana Riesgo

Abstract read
In one paragraph

Article in Molecular ecology, 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

10 authors.

Irene de SosaDepartamento de Biodiversidad y Biología Evolutiva, Museo Nacional de Ciencias Naturales (MNCN), CSIC, Madrid, Spain.ORCID 0000-0002-4020-6375
Marta TuronDepartamento de Biodiversidad y Biología Evolutiva, Museo Nacional de Ciencias Naturales (MNCN), CSIC, Madrid, Spain.ORCID 0000-0002-3806-4937
Sergi TaboadaDepartamento de Biodiversidad y Biología Evolutiva, Museo Nacional de Ciencias Naturales (MNCN), CSIC, Madrid, Spain.ORCID 0000-0003-1669-1152
José Lorente-SorollaDepartamento de Biodiversidad y Biología Evolutiva, Museo Nacional de Ciencias Naturales (MNCN), CSIC, Madrid, Spain.ORCID 0000-0002-4942-0255
Rosa FernándezMetazoa Phylogenomics Lab, Institute of Evolutionary Biology (CSIC-UPF), Barcelona, Spain.ORCID 0000-0002-4719-6640
Natasha TilikjDepartamento de Biodiversidad, Ecología y Evolución, Facultad de Ciencias Biológicas, Universidad Complutense de Madrid, Madrid, Spain.ORCID 0000-0001-7868-6936
Alberto PirisDepartamento de Biodiversidad, Ecología y Evolución, Facultad de Ciencias Biológicas, Universidad Complutense de Madrid, Madrid, Spain.ORCID 0009-0004-7605-546X
Marta NovoDepartamento de Biodiversidad, Ecología y Evolución, Facultad de Ciencias Biológicas, Universidad Complutense de Madrid, Madrid, Spain.ORCID 0000-0001-7902-3819
Patricia Álvarez CamposDepartamento de Biología (Facultad de Ciencias) y Centro de Investigación en Biodiversidad y Cambio Global (CIBC), Universidad Autónoma de Madrid, Madrid, Spain.ORCID 0000-0001-9472-2378
Ana RiesgoDepartamento de Biodiversidad y Biología Evolutiva, Museo Nacional de Ciencias Naturales (MNCN), CSIC, Madrid, Spain.ORCID 0000-0002-7993-1523

Funding

Consejo Superior de Investigaciones Científicas PIE-202030E006European Union Next Generation CNS2023-144571European Union Next Generation CNS2023-144572European Union Next Generation CNS2023-144624European Union Next Generation CNS2023-145193H2020 European Research Council 101129751H2020 European Research Council 948281Ministerio de Ciencia y Tecnología Gobierno de España FJC2020-043677-IMinisterio de Ciencia y Tecnología Gobierno de España JSPRE2020-095330Ministerio de Ciencia y Tecnología Gobierno de España MNCIN/AEI/10.13039/501100011033Ministerio de Ciencia y Tecnología Gobierno de España PID2019-105769GB-I00Ministerio de Ciencia y Tecnología Gobierno de España PID2020-117115GA-I00Ministerio de Ciencia y Tecnología Gobierno de España PID2021-122243NB-I00Ministerio de Ciencia y Tecnología Gobierno de España PID2023-148497NA-I00Ministerio de Ciencia y Tecnología Gobierno de España PRE2022-103770Ministerio de Ciencia y Tecnología Gobierno de España RYC2018-024247-IMinisterio de Ciencia y Tecnología Gobierno de España RYC2021-03152-IMSCA Postdoctoral Fellowship (HORIZON-MSCA.2022-PF-01, Project 101105716)Secretaria d'Universitats i Recerca del Departament d'Economia i Coneixement de la Generalitat de Catalunya AGAUR 2021-SGR00420
6 · The paper itself

Abstract

Approximately, 40% of earthworm species can reproduce by parthenogenesis. This is the case for the cosmopolitan species, Aporrectodea trapezoides, although sexual forms have been described sporadically. We analyse the genotypes and microbiomes of 30 individuals from four localities where both forms appear in order to understand the evolutionary mechanisms related to parthenogenesis. In all sites, heterozygosity values were approximately 30% higher in parthenogenetic individuals. However, we detected a stronger genomic structuring due to reproduction than to the geographical setting only in the Algerian population, underpinned by 195 loci that were related to gametogenesis, symbiont-like processes, and nitrate reduction. Similarly, statistical differences in the abundance of ZOTUs were only found between the Algerian sexual and parthenogenetic earthworms, with 754 ZOTUs that included the genus Romboutsia, which is involved in the production of nitric oxide, which enhances sperm motility. In summary, significant genomic and microbiome differences were found only between sexual and parthenogenetic lineages in a single locality. We hypothesise that obligate parthenogenesis evolved early, leaving traces at the genomic and microbiome levels in the Algerian parthenogens that were the earliest splitting lineage. Such obligate parthenogenesis was lost secondarily and individuals in the Iberian sites were facultative parthenogens, with the potential to copulate and therefore erase the genomic and microbial traces of obligate parthenogenesis. Our results indicate a hybrid origin of parthenogenesis in A. trapezoides and shed light on the complex interplay between genomic, microbiome, and reproductive mechanisms in A. trapezoides.

Indexed as

OligochaetaParthenogenesisAlgeriaAnimalsGenetics, PopulationGenotypeMicrobiotaReproductionmicrobiomenGBSreproductiontetraploidytranscriptomics

Identifiers

PMID40590190
PMCPMC12329633

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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.