Evidence map›Paper›PMID 41533650›Full record

ArticleFEMS microbiology ecology2026

Risk assessment of plant-to-bacterium transgene flow associated with novel small synthetic genome (minisynplastome) platforms for plastid genetic engineering.

Aaron G Vincent, Ivette A Fuentes Quispe, Mohammad Majdi, Lezlee T Dice, Stacee A Harbison, Scott C Lenaghan, Jennifer M DeBruyn, Alessandro Occhialini

Abstract read
In one paragraph

Article in FEMS microbiology ecology, 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

8 authors.

Aaron G VincentDepartment of Plant Sciences, University of Tennessee, 301 Agriculture and Natural Resources Building, 2431 Joe Johnson Drive, Knoxville, TN 37996, United States.
Ivette A Fuentes QuispeDepartment of Biosystems Engineering and Soil Science, University of Tennessee, 2506 E. J. Chapman Drive, Knoxville, TN 37996, United States.
Mohammad MajdiDepartment of Plant Sciences, University of Tennessee, 301 Agriculture and Natural Resources Building, 2431 Joe Johnson Drive, Knoxville, TN 37996, United States.
Lezlee T DiceCenter for Agricultural Synthetic Biology (CASB), University of Tennessee, 2640 Morgan Circle Dr., Knoxville, TN 37996, United States.
Stacee A HarbisonCenter for Agricultural Synthetic Biology (CASB), University of Tennessee, 2640 Morgan Circle Dr., Knoxville, TN 37996, United States.
Scott C LenaghanCenter for Agricultural Synthetic Biology (CASB), University of Tennessee, 2640 Morgan Circle Dr., Knoxville, TN 37996, United States.
Jennifer M DeBruynDepartment of Biosystems Engineering and Soil Science, University of Tennessee, 2506 E. J. Chapman Drive, Knoxville, TN 37996, United States.ORCID 0000-0002-2993-4144
Alessandro OcchialiniDepartment of Plant Sciences, University of Tennessee, 301 Agriculture and Natural Resources Building, 2431 Joe Johnson Drive, Knoxville, TN 37996, United States.ORCID 0000-0002-1162-798X

Funding

Biotechnology Risk Assessment Research Grants Program 2022-33522-38289National Institute of Food and AgricultureUniversity of TennesseeU.S. Department of Agriculture
6 · The paper itself

Abstract

Novel cutting-edge technologies for plastid genetic engineering have a great potential in agriculture. Genetic engineering of the plastid genome (plastome) can be performed using both conventional homologous recombination vectors, and novel episomal platforms that rely on synthetic plastomes (minisynplastomes) to express transgenes from a nonintegrating plasmid. Evaluating the potential risk of horizontal gene transfer (HGT) is an important step for regulatory approval of environmental release of these novel genetic engineering tools. In particular, the endosymbiotic origin of plastids from a prokaryotic progenitor may increase the probability of HGT to the environmental microbial community. In this study, the naturally competent soil bacterium Acinetobacter baylyi has been used to test the probability of plant-to-bacterium HGT under laboratory conditions. While plant-to-bacterium HGT can be detected in vitro as a low probability event, the minisynplastome does not show an increased HGT compared to conventional transformation platforms. After a comprehensive evaluation of minisynplastome elements affecting plasmid persistence in bacteria (plastid origin of replications, plastomic regions containing rRNA genes, and regulatory elements for transgene expression), optimized minisynplastome (Gen3) platforms with no residual activity in bacteria and with undetectable HGT were characterized. This study represents a valuable resource for designing minisynplastome transformation platforms with improved environmental biosafety in agriculture.

Indexed as

AcinetobacterGenetic EngineeringGene Transfer, HorizontalGenome, PlastidPlantsPlastidsTransgenesPlasmidsRisk AssessmentAcinetobacter baylyichloroplast genetic engineeringenvironmental biosafetyhorizontal gene transferminisynplastomerisk assessment

Identifiers

PMID41533650
PMCPMC12831460

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.