Evidence map›Paper›PMID 38649998›Full record

ReviewJournal of biomedical science2024

Dengue virus pathogenesis and host molecular machineries.

Saumya Sinha, Kinjal Singh, Y S Ravi Kumar, Riya Roy, Sushant Phadnis, Varsha Meena, Sankar Bhattacharyya, Bhupendra Verma

Open access · diamondAbstract readReview
In one paragraph

Review in Journal of biomedical science, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 59 papers.

0numbers the graph read from it
0cells of the map it votes in
59citing papers in PubMed
42.9field-weighted citation impact, top 1% 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

59 citing papers in PubMed, 79 citations in OpenAlex.

  1. The oxidative stress paradigm in arbovirus infections: mechanisms and therapeutic insights.Redox report : communications in free radical research · 2026
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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 3 institutions in 1 country.

Saumya SinhaDepartment of Biotechnology, All India Institute of Medical Sciences, Ansari Nagar, New Delhi, 110029, India.
Kinjal SinghDepartment of Biotechnology, All India Institute of Medical Sciences, Ansari Nagar, New Delhi, 110029, India.
Y S Ravi KumarDepartment of Biotechnology, M. S. Ramaiah Institute of Technology, MSR Nagar, Bengaluru, India.
Riya RoyDepartment of Biotechnology, All India Institute of Medical Sciences, Ansari Nagar, New Delhi, 110029, India.
Sushant PhadnisDepartment of Biotechnology, All India Institute of Medical Sciences, Ansari Nagar, New Delhi, 110029, India.
Varsha MeenaDepartment of Biotechnology, All India Institute of Medical Sciences, Ansari Nagar, New Delhi, 110029, India.
Sankar BhattacharyyaTranslational Health Science and Technology Institute, NCR Biotech Science Cluster, Faridabad, India.
Bhupendra VermaDepartment of Biotechnology, All India Institute of Medical Sciences, Ansari Nagar, New Delhi, 110029, India. bverma@aiims.edu.ORCID http://orcid.org/0000-0003-1731-5335
Department of Biotechnology · INM S Ramaiah University of Applied Sciences · INTranslational Health Science and Technology Institute · IN

Funding

Science and Engineering Research Board EEQ/2022/000362
6 · The paper itself

Abstract

Dengue viruses (DENV) are positive-stranded RNA viruses belonging to the Flaviviridae family. DENV is the causative agent of dengue, the most rapidly spreading viral disease transmitted by mosquitoes. Each year, millions of people contract the virus through bites from infected female mosquitoes of the Aedes species. In the majority of individuals, the infection is asymptomatic, and the immune system successfully manages to control virus replication within a few days. Symptomatic individuals may present with a mild fever (Dengue fever or DF) that may or may not progress to a more critical disease termed Dengue hemorrhagic fever (DHF) or the fatal Dengue shock syndrome (DSS). In the absence of a universally accepted prophylactic vaccine or therapeutic drug, treatment is mostly restricted to supportive measures. Similar to many other viruses that induce acute illness, DENV has developed several ways to modulate host metabolism to create an environment conducive to genome replication and the dissemination of viral progeny. To search for new therapeutic options, understanding the underlying host-virus regulatory system involved in various biological processes of the viral life cycle is essential. This review aims to summarize the complex interaction between DENV and the host cellular machinery, comprising regulatory mechanisms at various molecular levels such as epigenetic modulation of the host genome, transcription of host genes, translation of viral and host mRNAs, post-transcriptional regulation of the host transcriptome, post-translational regulation of viral proteins, and pathways involved in protein degradation.

Indexed as

DengueDengue VirusAnimalsHost-Pathogen InteractionsHumansVirus ReplicationDengue virusEpigenomic regulationPost-transcriptional modificationsPost-translational modificationsStress granule formationTranscription regulationTranslation regulation

Identifiers

PMID38649998
PMCPMC11036733
OpenAlexW4395001476

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.