Evidence map›Paper›PMID 38003407›Full record

ArticleInternational journal of molecular sciences2023

Strain Variation Can Significantly Modulate the miRNA Response to Zika Virus Infection.

Suwipa Ramphan, Chanida Chumchanchira, Wannapa Sornjai, Thanathom Chailangkarn, Anan Jongkaewwattana, Wanchai Assavalapsakul, Duncan R Smith

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.2field-weighted citation impact, top 20% 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

4 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
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

7 authors at 4 institutions in 1 country.

Suwipa RamphanInstitute of Molecular Biosciences, Mahidol University, Nakhon Pathom 73170, Thailand.
Chanida ChumchanchiraDepartment of Biology, Faculty of Sciences, Chiang Mai University, Chiang Mai 50200, Thailand.
Wannapa SornjaiInstitute of Molecular Biosciences, Mahidol University, Nakhon Pathom 73170, Thailand.
Thanathom ChailangkarnNational Center for Genetic Engineering and Biotechnology, National Science and Technology Development Agency, Bangkok 12120, Thailand.ORCID 0000-0003-3556-1775
Anan JongkaewwattanaNational Center for Genetic Engineering and Biotechnology, National Science and Technology Development Agency, Bangkok 12120, Thailand.ORCID 0000-0003-2354-9883
Wanchai AssavalapsakulDepartment of Microbiology, Faculty of Sciences, Chulalongkorn University, Bangkok 10330, Thailand.ORCID 0000-0003-2739-3177
Duncan R SmithInstitute of Molecular Biosciences, Mahidol University, Nakhon Pathom 73170, Thailand.ORCID 0000-0002-6592-9852
Mahidol University · THNational Science and Technology Development Agency · THChiang Mai University · THChulalongkorn University · TH

Funding

Mahidol University BRF1-088/2565Thailand Research Fund IRN5802PHDW03 under IRN58W0002Thailand Research Fund and Mahidol University IRN58W0002
6 · The paper itself

Abstract

Zika virus (ZIKV) is a mosquito-transmitted virus that has emerged as a major public health concern due to its association with neurological disorders in humans, including microcephaly in fetuses. ZIKV infection has been shown to alter the miRNA profile in host cells, and these changes can contain elements that are proviral, while others can be antiviral in action. In this study, the expression of 22 miRNAs in human A549 cells infected with two different ZIKV isolates was investigated. All of the investigated miRNAs showed significant changes in expression at at least one time point examined. Markedly, 18 of the miRNAs examined showed statistically significant differences in expression between the two strains examined. Four miRNAs (miR-21, miR-34a, miR-128 and miR-155) were subsequently selected for further investigation. These four miRNAs were shown to modulate antiviral effects against ZIKV, as downregulation of their expression through anti-miRNA oligonucleotides resulted in increased virus production, whereas their overexpression through miRNA mimics reduced virus production. However, statistically significant changes were again seen when comparing the two strains investigated. Lastly, candidate targets of the miRNAs miR-34a and miR-128 were examined at the level of the mRNA and protein. HSP70 was identified as a target of miR-34a, but, again, the effects were strain type-specific. The two ZIKV strains used in this study differ by only nine amino acids, and the results highlight that consideration must be given to strain type variation when examining the roles of miRNAs in ZIKV, and probably other virus infections.

Indexed as

MicroRNAsZika VirusZika Virus InfectionAnimalsAntiviral AgentsDown-RegulationHumansVirus ReplicationAntiviral AgentsMicroRNAsheat shock protein 70 kDaHSP70microRNAmiR-34amiRNAZIKV

Identifiers

PMID38003407
PMCPMC10671159
OpenAlexW4388637162

What OpenQuestion 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 OpenQuestion graph.