Evidence map›Paper›PMID 27117627›Full record

ArticleScientific reports2016

Identification of miRNomes reveals ssc-miR-30d-R_1 as a potential therapeutic target for PRRS viral infection.

Chengmin Wang, Yanyu Zhang, Jing Luo, Hua Ding, Shelan Liu, Said Amer, Li Xie, Wenting Lyv, Wen Su, Meng Li and 3 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.7field-weighted citation impact, top 12% 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

12 citing papers in PubMed, 19 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Review
  5. Article
  6. miR-30d Inhibition Protects IPEC-J2 Cells AgainstFrontiers in veterinary science · 2022
    Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. 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

13 authors at 6 institutions in 2 countries.

Chengmin WangKey Lab of Animal Ecology and Conservation Biology, Institute of Zoology, Chinese Academy of Sciences, Beijing, 100101, P.R China.
Yanyu ZhangBeijing Institute of Transfusion Medicine, Academy of Military Medicine Sciences, Beijing, 100850, P.R China.
Jing LuoKey Lab of Animal Ecology and Conservation Biology, Institute of Zoology, Chinese Academy of Sciences, Beijing, 100101, P.R China.
Hua DingDepartment of Infectious Disease, Hangzhou Center for Disease Control and Prevention, Hangzhou, Zhejiang Province, 310021, P.R China.
Shelan LiuDepartment of Infectious Diseases, Zhejiang Center for Disease Control and Prevention, Hangzhou, Zhejiang Province, 310051, P.R China.
Said AmerDepartment of Zoology, Faculty of Science, Kafr El sheikh University, Kafr El sheikh 33516, Egypt.
Li XieDepartment of Infectious Disease, Hangzhou Center for Disease Control and Prevention, Hangzhou, Zhejiang Province, 310021, P.R China.
Wenting LyvKey Lab of Animal Ecology and Conservation Biology, Institute of Zoology, Chinese Academy of Sciences, Beijing, 100101, P.R China.
Wen SuKey Lab of Animal Ecology and Conservation Biology, Institute of Zoology, Chinese Academy of Sciences, Beijing, 100101, P.R China.
Meng LiKey Lab of Animal Ecology and Conservation Biology, Institute of Zoology, Chinese Academy of Sciences, Beijing, 100101, P.R China.
Qinmiao SunKey Lab of Animal Ecology and Conservation Biology, Institute of Zoology, Chinese Academy of Sciences, Beijing, 100101, P.R China.
Jiayin DaiKey Lab of Animal Ecology and Conservation Biology, Institute of Zoology, Chinese Academy of Sciences, Beijing, 100101, P.R China.
Hongxuan HeKey Lab of Animal Ecology and Conservation Biology, Institute of Zoology, Chinese Academy of Sciences, Beijing, 100101, P.R China.
Chinese Academy of Sciences · CNInstitute of Zoology · CNHangzhou Center for Disease Control and Prevention · CNAcademy of Military Medical Sciences · CNKafrelsheikh University · EGZhejiang Center for Disease Control and Prevention · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Porcine reproductive and respiratory syndrome virus (PRRSV) is known to cause reproductive disorders, such as abortion, in pregnant sows as well as immunosuppressive respiratory complications, leading to severe respiratory tract infections in young pigs. In this study, an in-depth analysis of the miRNomes in mock- and virus-infected pig lungs was carried out. We found that highly expressed ssc-miR-30d-R_1 was decreased in infected lungs, and reduced levels were significantly correlated with infection by PRRSV. Moreover, ssc-miR-30d-R_1 was shown to target Toll-like receptor 4 (TLR4) and to suppress the production of immune cytokines through inhibition of the TLR4/MyD88/NF-κB pathway. ssc-miR-30d-R_1 significantly reduced viral infections and pathological changes in pig lungs in vivo. Our current study reveals the miRNomes of PRRSV-infected pig lungs and indicates that ssc-miR-30d-R_1 is potential therapeutic agent for controlling PRRSV infection.

Indexed as

Gene Expression ProfilingAnimalsHost-Pathogen InteractionsLungMicroRNAsPorcine Reproductive and Respiratory SyndromePorcine respiratory and reproductive syndrome virusSwineMicroRNAs

Identifiers

PMID27117627
PMCPMC4846818
OpenAlexW2344847759

What OpenQuestion holds

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LicenceCC BY
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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.