Evidence map›Paper›PMID 41159752›Full record

ArticleJournal of virology2025

MicroRNA response in insect salivary glands to plant virus infection.

Yan Xiao, Guohua Liang, Jiaming Zhu, Feng Cui, Wan Zhao

Abstract read
In one paragraph

Article in Journal of virology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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.

Yan XiaoState Key Laboratory of Animal Biodiversity Conservation and Integrated Pest Management, Institute of Zoology, Chinese Academy of Sciences, Beijing, China.
Guohua LiangState Key Laboratory of Animal Biodiversity Conservation and Integrated Pest Management, Institute of Zoology, Chinese Academy of Sciences, Beijing, China.
Jiaming ZhuState Key Laboratory of Animal Biodiversity Conservation and Integrated Pest Management, Institute of Zoology, Chinese Academy of Sciences, Beijing, China.ORCID 0009-0002-1879-6994
Feng CuiState Key Laboratory of Animal Biodiversity Conservation and Integrated Pest Management, Institute of Zoology, Chinese Academy of Sciences, Beijing, China.ORCID 0000-0001-6215-7159
Wan ZhaoState Key Laboratory of Animal Biodiversity Conservation and Integrated Pest Management, Institute of Zoology, Chinese Academy of Sciences, Beijing, China.ORCID 0000-0001-6622-2157

Funding

Institute of Zoology, Chinese Academy of Sciences 2024IOZ0106,SKLA2506National Key Research and Development Program of China 2022YFD1401700National Natural Science Foundation of China 32272532National Natural Science Foundation of China 32402362Youth Innovation Promotion Association of the Chinese Academy of Sciences Y2023022
6 · The paper itself

Abstract

Most arboviruses rely on insect vectors for transmission, with salivary glands serving as a critical gateway for viral spread to new hosts. MicroRNAs (miRNAs) are key regulators of gene expression, yet their roles in salivary glands during virus infection remain poorly understood. Using the small brown planthopper (SBPH)-rice stripe virus (RSV) system, we sequenced small RNAs from salivary glands of nonviruliferous and viruliferous insects and identified 5,909 known miRNAs from 201 families. Of these, 1,143 miRNAs were differentially expressed upon RSV infection, including 1,090 upregulated from 36 families and 53 downregulated from 11 families. These differentially expressed miRNAs were predicted to target 2,876 genes. Gene Ontology analysis showed that targets of upregulated miRNA were enriched in "protein binding," while those of downregulated miRNAs were associated with "cytoskeleton" and "regulation of dephosphorylation." The neurotrophin signaling pathway was the top-enriched KEGG pathway for the upregulated miRNA targets. Two miRNAs, miR-276-5p and miR-13a-3p, were specifically modulated by RSV in the salivary glands but not in the guts. miR-276-5p was found to enhance RSV secretion from the salivary glands into rice without altering viral load in insects, whereas miR-13a-3p could play a negative role in viral accumulation in insects. Taken together, our findings highlight tissue-specific miRNA responses in vector-virus interactions and uncover distinct roles of salivary gland miRNAs in regulating viral transmission. IMPORTANCE: Most plant viruses depend on insect vectors for transmission. The salivary glands of insect vectors are the last barrier for these viruses to overcome before being transmitted to plant hosts. In this work, we dissected the microRNA (miRNA) response to plant virus infection in insect salivary glands using the model of the small brown planthopper and rice stripe virus (RSV). The abundance of hundreds of miRNAs changes in the salivary glands after RSV infection. Two specific miRNAs play distinct roles. One enhances the release of RSV from salivary glands into rice plants, and the other regulates viral accumulation within the insects. These findings deepen our understanding of small RNA reactions and potential functions of miRNAs to viral infection in the salivary glands of insect vectors.

Indexed as

HemipteraInsect VectorsMicroRNAsPlant DiseasesSalivary GlandsTenuivirusAnimalsHost-Pathogen InteractionsOryzaMicroRNAsmicroRNAplant virusrice stripe virussalivary glandssmall brown planthopperviral transmission

Identifiers

PMID41159752
PMCPMC12646003

What Socratic holds

Textmetadata
LicenceCC BY
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.