Evidence map›Paper›PMID 41231926›Full record

ArticlePLoS genetics2025

Effector innovation in genome-reduced phytoplasmas and other host-dependent mollicutes.

Federico G Mirkin, Sam T Mugford, Vera Thole, Mar Marzo, Saskia A Hogenhout

Abstract read
In one paragraph

Article in PLoS genetics, 2025. 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. Article
  2. 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

5 authors.

Federico G MirkinDepartment of Crop Genetics, John Innes Centre, Norwich Research Park, Norwich, United Kingdom.ORCID https://orcid.org/0000-0002-3323-2348
Sam T MugfordDepartment of Crop Genetics, John Innes Centre, Norwich Research Park, Norwich, United Kingdom.
Vera TholeDepartment of Crop Genetics, John Innes Centre, Norwich Research Park, Norwich, United Kingdom.
Mar MarzoDepartment of Crop Genetics, John Innes Centre, Norwich Research Park, Norwich, United Kingdom.ORCID https://orcid.org/0000-0003-1591-0309
Saskia A HogenhoutDepartment of Crop Genetics, John Innes Centre, Norwich Research Park, Norwich, United Kingdom.ORCID https://orcid.org/0000-0003-1371-5606

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Obligate host-associated bacteria with reduced genomes, such as phytoplasmas, face strong evolutionary constraints, including metabolic dependence on hosts, limited opportunities for horizontal gene transfer (HGT), and frequent population bottlenecks. Despite these limitations, phytoplasmas, which are parasitic, insect-transmitted plant pathogens, maintain a diverse arsenal of secreted effectors that manipulate both plant and insect hosts to promote infection and transmission. These effectors can suppress immunity and reprogram plant development, inducing alterations such as witch's broom and leaf-like flowers, through ubiquitin-independent degradation of key transcription factors. However, how phytoplasmas diversify and maintain these effectors in the absence of frequent genetic exchange remains unclear. To address this, we analysed the effectoromes of 239 phytoplasma genomes and identified a diverse set of secreted proteins, which we designated as putative Phytoplasma Effectors (PhAMEs). We found that PhAMEs targeting evolutionarily conserved and structurally constrained surfaces of host proteins are widespread across phytoplasmas. These effectors adopt compact, efficient folds. They often function as molecular scaffolds with dual interaction surfaces capable of linking host proteins or integrating signalling pathways. Such scaffolding PhAMEs have evolved multiple times independently, providing clear evidence of convergent evolution. Despite severe genomic constrains imposed by genome reduction and limited HGT, gene duplications, interface variations, domain fusions, and repeat expansions have helped the shaping effector fold and diversity. While the overall effector repertoire of phytoplasmas appeared largely unique, some PhAME domains share similarities with proteins from other mollicutes and pathogens. Collectively, our findings shed light on how genome-reduced bacteria innovate molecular functions and offer insights into phytoplasma biology, effector evolution, and host-pathogen dynamics. They also lay the groundwork for protein engineering approaches aimed at discovering or designing novel biomolecules with biotechnological potential.

Indexed as

Bacterial ProteinsGenome, BacterialHost-Pathogen InteractionsPhytoplasmaAnimalsEvolution, MolecularGene Transfer, HorizontalPlant DiseasesBacterial Proteins

Identifiers

PMID41231926
PMCPMC12633904

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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.