Evidence map›Paper›PMID 40873037›Full record

ReviewPlant communications2025

Antiviral RNA interference in plants: Increasing complexity and integration with other biological processes.

Fangfang Li, Xue Li, Siwen Zhao, Fuan Pan, Zhaolei Li, Yuming Hao, Jiachi He, Aiming Wang, Richard Kormelink, Xueping Zhou

Abstract readReview
In one paragraph

Review in Plant communications, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

11 citing papers in PubMed.

  1. Article
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  4. Review
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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

10 authors.

Fangfang LiState Key Laboratory for Biology of Plant Diseases and Insect Pests, Institute of Plant Protection, Chinese Academy of Agricultural Sciences, Beijing 100193, China. Electronic address: lifangfang@caas.cn.
Xue LiState Key Laboratory for Biology of Plant Diseases and Insect Pests, Institute of Plant Protection, Chinese Academy of Agricultural Sciences, Beijing 100193, China.
Siwen ZhaoState Key Laboratory for Biology of Plant Diseases and Insect Pests, Institute of Plant Protection, Chinese Academy of Agricultural Sciences, Beijing 100193, China.
Fuan PanState Key Laboratory for Biology of Plant Diseases and Insect Pests, Institute of Plant Protection, Chinese Academy of Agricultural Sciences, Beijing 100193, China.
Zhaolei LiState Key Laboratory for Biology of Plant Diseases and Insect Pests, Institute of Plant Protection, Chinese Academy of Agricultural Sciences, Beijing 100193, China.
Yuming HaoState Key Laboratory for Biology of Plant Diseases and Insect Pests, Institute of Plant Protection, Chinese Academy of Agricultural Sciences, Beijing 100193, China; Laboratory of Virology, Wageningen University and Research, 6700 AA Wageningen, the Netherlands.
Jiachi HeState Key Laboratory for Biology of Plant Diseases and Insect Pests, Institute of Plant Protection, Chinese Academy of Agricultural Sciences, Beijing 100193, China; Laboratory of Virology, Wageningen University and Research, 6700 AA Wageningen, the Netherlands.
Aiming WangLondon Research and Development Centre, Agriculture and Agri-Food Canada, London, ON N5V 4T3, Canada.
Richard KormelinkLaboratory of Virology, Wageningen University and Research, 6700 AA Wageningen, the Netherlands. Electronic address: richard.kormelink@wur.nl.
Xueping ZhouState Key Laboratory for Biology of Plant Diseases and Insect Pests, Institute of Plant Protection, Chinese Academy of Agricultural Sciences, Beijing 100193, China; State Key Laboratory of Rice Biology, Institute of Biotechnology, Zhejiang University, Hangzhou, Zhejiang 310058, China. Electronic address: zzhou@zju.edu.cn.

Funding

Non-US Government Research Support type
6 · The paper itself

Abstract

RNA interference (RNAi, also known as RNA silencing) is one of the most important plant defense responses against viral invasion. Although major components of the RNAi pathway, steps leading to viral small interfering RNA biogenesis, and viral counterdefense strategies via RNAi suppressors have been well studied, the broader roles of RNAi in viral infection and seed transmission remain less thoroughly characterized. In particular, the increasing complexity of RNAi-associated mechanisms and their integration with other biological processes have not been comprehensively summarized. Increasing numbers of studies have identified non-canonical RNAi pathways, novel host factors involved in RNAi, and the possibility of small RNAs acting across kingdoms to modulate plant-virus-vector tritrophic interactions. In this review, we provide an overview of the roles of RNAi in plant viral infections and describe recent advances, with emphasis on the discoveries of novel positive and negative RNAi regulators, potential signaling pathways upstream and downstream of antiviral RNAi, and the prospects and challenges of double-stranded RNA applications, either expressed from transgenes or supplied exogenously via spraying. We also discuss how these findings reshape current views on antiviral RNAi, highlight remaining knowledge gaps, and examine how these advances influence plant-virus co-evolution while informing strategies for managing plant virus diseases and reducing their impact.

Indexed as

Plant DiseasesPlantsPlant VirusesRNA InterferenceRNA, Small InterferingRNA, Small Interferingantiviral RNA interferenceantiviral RNAi signaling pathwaysexogenous application of dsRNAnon-canonical RNAinovel RNAi regulatorsRNAi

Identifiers

PMID40873037
PMCPMC12546453

What Socratic 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 Socratic graph.