Evidence map›Paper›PMID 31416454›Full record

ArticleJournal of biomedical science2019

Exosome-delivered and Y RNA-derived small RNA suppresses influenza virus replication.

Yuag-Meng Liu, Chung-Hsin Tseng, Yi-Chun Chen, Wen-Ya Yu, Meng-Yen Ho, Chia-Yin Ho, Michael M C Lai, Wen-Chi Su

Open access · diamondAbstract read
In one paragraph

Article in Journal of biomedical science, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
4.5field-weighted citation impact, top 4% of its field
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

33 citing papers in PubMed, 73 citations in OpenAlex.

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  7. Extracellular Vesicles and Their Role in Lung Infections.International journal of molecular sciences · 2023
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  11. Extracellular Vesicles and Viruses: Two Intertwined Entities.International journal of molecular sciences · 2023
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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

8 authors at 4 institutions in 1 country.

Yuag-Meng LiuGraduate Institute of Clinical Medical Science, China Medical University, No.91, Xueshi Rd., North Dist, Taichung City, 404, Taiwan.
Chung-Hsin TsengDepartment of Microbiology and Immunology, College of Medicine, National Cheng Kung University, No. 1, Daxue Rd., East Dist, Tainan City, 701, Taiwan.
Yi-Chun ChenDivision of Infectious Diseases, Changhua Christian Medical Foundation Changhua Christian Hospital, No. 135, Nanxiao St., Changhua City, Changhua County, 500, Taiwan.
Wen-Ya YuResearch Center for Emerging Viruses, China Medical University Hospital, No.91, Xueshi Rd., North Dist, Taichung City, 404, Taiwan.
Meng-Yen HoResearch Center for Emerging Viruses, China Medical University Hospital, No.91, Xueshi Rd., North Dist, Taichung City, 404, Taiwan.
Chia-Yin HoResearch Center for Emerging Viruses, China Medical University Hospital, No.91, Xueshi Rd., North Dist, Taichung City, 404, Taiwan.
Michael M C LaiCenter of Infectious Disease and Signaling Research, National Cheng Kung University, No. 1, Daxue Rd., East Dist, Tainan City, 701, Taiwan.
Wen-Chi SuGraduate Institute of Clinical Medical Science, China Medical University, No.91, Xueshi Rd., North Dist, Taichung City, 404, Taiwan. t23514@mail.cmuh.org.tw.
China Medical University · TWChina Medical University Hospital · TWChanghua Christian Hospital · TWNational Cheng Kung University · TW

Funding

Changhua Christian Hospital 105-CCH-IRP-003Changhua Christian Hospital 106-CCH-IRP-099China Medical University Hospital DMR-107-118 to Wen-Chi SuNational Science Council 105-2628-B-039-006-MY3National Science Council 106-2314-B-371-009-MY2
6 · The paper itself

Abstract

backgroundMultiple interplays between viral and host factors are involved in influenza virus replication and pathogenesis. Several small RNAs have recently emerged as important regulators of host response to viral infections. The aim of this study was to characterize the functional role of hsa-miR-1975, a Y5 RNA-derived small RNA, in defending influenza virus and delineate the mechanisms.

methodsWe performed high throughput sequencing of small RNAs in influenza virus-infected cells to identify up- or down- regulated small RNA species. The expression of the most abundant RNA species (hsa-miR-1975) was validated by stem-loop reverse transcription-polymerase chain reaction (RT-PCR). Antiviral effects of hsa-miR-1975 were confirmed by Western Blot, RT-PCR and plaque assay. In vitro perturbation of hsa-miR-1975 combined with exosomes isolation was used to elucidate the role and mechanism of hsa-miR-1975 in the context of antiviral immunity.

resultsSmall RNA sequencing revealed that hsa-miR-1975 was the most up-regulated small RNA in influenza virus-infected cells. The amount of intracellular hsa-miR-1975 increased in the late stage of the influenza virus replication cycle. The increased hsa-miR-1975 was at least partially derived from degradation of Y5RNA as a result of cellular apoptosis. Unexpectedly, hsa-miR-1975 mimics inhibited influenza virus replication while hsa-miR-1975 sponges enhanced the virus replication. Moreover, hsa-miR-1975 was secreted in exosomes and taken up by the neighboring cells to induce interferon expression.

conclusionsOur findings unravel a critical role of Y-class small RNA in host's defense against influenza virus infection and reveal its antiviral mechanism through exosome delivery. This may provide a new candidate for targeting influenza virus.

Indexed as

Virus ReplicationA549 CellsAnimalsDogsExosomesHumansInfluenza A Virus, H1N1 SubtypeInfluenza A Virus, H3N2 SubtypeMadin Darby Canine Kidney CellsMicroRNAsMicroRNAsMIRN1975 microRNA, humanExosomeHsa-miR-1975Influenza virusInterferonY RNA

Identifiers

PMID31416454
PMCPMC6694579
OpenAlexW2968463322

What OpenQuestion holds

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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 OpenQuestion graph.